I’m not surprised at the growth of vaccine hesitancy, based on the absolutely ham-handed approach that the media and the Democrat machine managed their messaging.

Harris did her best to bad-mouth the vax, going so far as to say that it was tainted by Trump, and she didn’t trust it.

Then their “woke” rollout, scheduling doses based on race raised more than a few eyebrows. The J+J pause, and the absurd and transparently political CDC guidance that after the vax, everyone has to carry on as before wearing masks, social distancing, and going broke.

Now, their heavy-handed messaging and coercion is the icing on the cake.

There will always be a small contingent of dedicated anti-vaxers who will never be convinced, but their numbers are too small to make any difference. The broader messaging is just terrible.

This junta destroys everything it touches.

No clue.

The summary you linked to indicates that the 88 year old woman was unresponsive at the time and 14 days post COVID (not sure if that was test result, start of symptoms, or observed recovery).

Could have been a mandate, family / POA request, a long shot attemp to try something, a nefarious plot to kill her off. There is nothing in the report indicating why the shot was given, but there is indication that the staff thought she was soon to pass.

To: frogjerk

I personally know of 2 kids it messed up, like $15K in Hospital scans later we can’t explain why your Athletic 19 year old SMU honor student can’t form words anymore, but thank god she got her vaccine two days ago.

Don’t plan on the media contacting you about this.

7 posted on 04/12/2021 6:46:13 PM PDT by UNGN

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To: MinorityRepublican

Today hit a milestone: More people I personally know have been Hospitalized for bad reactions to the vaccine than people I personally know that were hospitalized for Covid.

The vaccine requirement for healthy kids is borderline criminal.

Dumbest “pandemic” ever.

5 posted on 04/12/2021 6:41:05 PM PDT by UNGN

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To: Dave Wright

My mother and father took the first Moderna vaccine shot about six weeks ago. Within a week my mother went from a very active person in her mid 80s to an invalid unable to make it from the bed to the bathroom. She has progressively gotten worse to the point that she now looks like a little death camp survivor. We and her doctors expect her to die soon. It wasn’t an allergic reaction. So your explanation fails miserably, but I am sure you can come up with something better to push these experimental vaccines on those of us who are skeptical.

I spent years working as a Hazmat Officer in charge of a Hazmat team. It was my responsibility to make risk assessments for bio and chemical hazards. I probably have had ten times as many vaccinations as most people. It is amazing to me how many of my former subordinates have refused to take these vaccines at the risk of losing their positions. The risk involved in taking an experimental vaccine should be left up to the individual and their doctor not the all knowing government, big tech and the corporate media.

10 posted on 04/09/2021 5:38:39 PM PDT by fireman15

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To: ProtectOurFreedom

I worked as a Hazmat Officer for ten years in charge of a big city Hazmat Team. I have had ten times as many vaccines as most people in my life and never had any complications and very few times when even my arm got sore. A week after my mother got the first Moderna shot she went from very active and going to the YMCA every day to an invalid who can’t make it from her bed to the bathroom without assistance. She has lost so much weight that she looks like a little death camp survivor and she cries and says that she is in so much pain that she just wants to die. These shots are not safe for everyone, and in many cases are most likely much worse for some individuals than getting Covid itself.

12 posted on 04/10/2021 9:53:18 AM PDT by fireman15

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To: Pollard

A friend of mine passed last week from Covid. He was 77 and he had the jab.

15 posted on 05/02/2021 8:38:41 AM PDT by Ben Dover

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To: Cathi

I just had a friend die 24 hours after getting the vaccine. A 52 year old male with no health issues. His death certificate says he died of cardiac arrest, which is the typical “Heart Stopped” report when no other condition can be found. There will be no VAERS report. He is not the first to die suddenly after the jab without a VAERS report.

17 posted on 05/05/2021 7:32:04 AM PDT by CodeToad (Arm up! They Have!)

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“but there is indication that the staff thought she was soon to pass.”

Pass within days, not hours.

Check out post 60.

Did you read the reports you posted? The last one has a mile-long list of lethal pre-existing conditions and on morphine. But they gave her the shot anyway and she died. I'm wondering what you expected.

I am very familiar with an assisted living where everyone was pressured to get the shot, no matter what the risk was from the shot. It's not a safe shot. This is not a flu shot. But then, COVID is not the flu.

Did you happen to read those reports?

Yeah I read that one, but I didn’t read all 550 of them. The point is, like you say, this isn’t a 100% safe shot like some make it out to be.

Not all 550.

Here's more searching covid 19 vaccine, 0 days onset, and disabled;

This is page 1 out of 27

Result pages: 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 next

VAERS ID:	919022 (history)
Form:	Version 2.0
Age:	28.0
Sex:	Male
Location:	Maryland

Vaccinated:	2020-09-02
Onset:	2020-09-02
Days after vaccination:	0
Submitted:	0000-00-00
Entered:	2021-01-04

Vaccination / Manufacturer	Lot / Dose	Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA	- / 2	LA / IM

Administered by: Private Purchased by: ?
Symptoms: Autoantibody positive, Blindness unilateral, Computerised tomogram coronary artery, Echocardiogram, Electrocardiogram, Electrocardiogram ambulatory, Magnetic resonance imaging brain, Ophthalmological examination, Postural orthostatic tachycardia syndrome, Pyrexia, Tachycardia
SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Glaucoma (broad), Optic nerve disorders (broad), Retinal disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Dehydration (broad), Immune-mediated/autoimmune disorders (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? Yes
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Dutastride 0.5 mg/day, Wellbutrin XL 300 mg/day, Truvada (emtricitabine 200 mg and tenofovir disoproxil fumarate 300 mg)/day.
Current Illness:
Preexisting Conditions:
Allergies: doxycycline-gastrointestinal.
Diagnostic Lab Data: Eye exam, MRI of brain and orbits, Holter monitor, EKG, Echocardiogram, CT cardiac calcium score.
CDC Split Type:

Write-up: Complete loss of vision in the left eye 12 hours after receiving second dose (Moderna mRNA-1273) while having a fever of 102 F for 6 hours. Loss of vision lasted for 1 minute. Loss of vision occurred while standing. Referral to primary care and ophthalmology specialist found normal eye exam and MRI of orbits but presence of tachycardia especially while standing (fluctuations between 60 beats at rest/laying down to 130 beats per minute standing). Postural tachycardia syndrome (POTS) is suspected. Currently pursuing cardiac workup with cardiologist and Covid POTS specialist. POTS specialist believes autoantibody development after vaccination could be suspected as recovering covid patients similarly present to clinic with POTS like symptoms.

VAERS ID:	1100464 (history)
Form:	Version 2.0
Age:	74.0
Sex:	Female
Location:	California

Vaccinated:	2020-12-01
Onset:	2020-12-01
Days after vaccination:	0
Submitted:	0000-00-00
Entered:	2021-03-15

Vaccination / Manufacturer	Lot / Dose	Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH	- / 1	- / -

Administered by: Senior Living Purchased by: ?
Symptoms: Nervous system disorder, SARS-CoV-2 test
SMQs:, COVID-19 (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? Yes
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: COVID-19 (if covid prior vaccination: yes); Diabetes; Multiple sclerosis (advanced stages)
Allergies:
Diagnostic Lab Data: Test Date: 202101; Test Name: Unknown COVID-19 test (nasal swab); Test Result: Negative
CDC Split Type: USPFIZER INC2021205876

Write-up: suffered a neurological setback following the first injection; This is a spontaneous report from a contactable consumer. A 74-year-old female patient received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection; batch/lot number and expiration date were unknown), via an unspecified route of administration on an unspecified date in Dec2020 at a single dose for COVID-19 immunization. The vaccine facility type was reported as the nursing home/senior living facility. Relevant medical history included multiple sclerosis (advanced stages), diabetes, and COVID-19 prior vaccination; all from an unknown date and unknown if ongoing. The patient had other medications in two weeks, which included diabetic medications (meds, pills), anti depressants, etc. The patient had no other vaccine in four weeks. The patient was not pregnant at the time of vaccination. On an unspecified date in Dec2020, the patient suffered a neurological setback following the first injection, although it wasn''t terribly obvious at that time. The event was considered serious as it resulted in disability or permanent damage. The patient underwent lab tests and procedures, which included an unknown COVID-19 test via nasal swab: negative on an unspecified date in Jan2021. It was unknown if the patient received any treatment for the adverse event (AE). The patient was not recovered from the event. Information on the batch/lot number has been requested.

VAERS ID:	904385 (history)
Form:	Version 2.0
Age:	83.0
Sex:	Female
Location:	Texas

Vaccinated:	2020-12-16
Onset:	2020-12-16
Days after vaccination:	0
Submitted:	0000-00-00
Entered:	2020-12-20

Vaccination / Manufacturer	Lot / Dose	Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH	- / 1	AR / IM

Administered by: Private Purchased by: ?
Symptoms: Comminuted fracture, Epistaxis, Facial bones fracture, Haemorrhage, Loss of consciousness, Subcutaneous haematoma, Tenderness
SMQs:, Torsade de pointes/QT prolongation (broad), Haemorrhage terms (excl laboratory terms) (narrow), Hyperglycaemia/new onset diabetes mellitus (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Accidents and injuries (narrow), Hypotonic-hyporesponsive episode (broad), Generalised convulsive seizures following immunisation (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? Yes
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, 3 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications: amLODIPine, 7.5 mg, oral, Nightly ? cevimeline, 30 mg, oral, TID ? cholecalciferol (vitamin D3), 2,000 Units, oral, Daily ? irbesartan-hydrochlorothiazide, 1 tablet, oral, QAM ? levothyroxine, 50 mcg, oral, Daily at 0600 ? metoprolol s
Current Illness: None
Preexisting Conditions: Sjogrens Syndrome, Hypertension, Hypothyroidism
Allergies: Quinilones, Sulfa
Diagnostic Lab Data: There is a comminuted fracture of the nasal bones bilaterally with Left orbital floor blowout fracture with hemorrhagic opacification of the left maxillary sinus and slight inferior displacement with slight extraconal fat protrusion. There is associated left orbital preseptal and postseptal emphysema. Comminuted fracture involving the anterior and posterior wall of the left maxillary sinus with hemorrhagic opacification of the sinus and left malar subcutaneous hematoma
CDC Split Type:

Write-up: Patient is a pleasant 83 y.o. female pediatrician with history of Sjogren''s, hypothyroidism, hyperlipidemia, hypertension who had been at Hospital to get her Covid vaccine. 30 minutes after doing so she reports being in the lobby and about to walk upstairs and feeling fine. The next thing she knows she wakes up on the stairs with her nose and face bleeding surrounded by healthcare team. She denies any precipitating symptoms such as chest pain, shortness of breath, fevers dizziness, headache. She reports feeling well otherwise in the last few days. I did a thorough bony palpation exam including spine and he only point of tenderness besides on her face was the area above her right ankle. She does not have a history of syncope or collapse

VAERS ID:	944270 (history)
Form:	Version 2.0
Age:	58.0
Sex:	Male
Location:	Massachusetts

Vaccinated:	2020-12-16
Onset:	2020-12-16
Days after vaccination:	0
Submitted:	0000-00-00
Entered:	2021-01-14

Vaccination / Manufacturer	Lot / Dose	Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH	- / 1	- / OT

Administered by: Private Purchased by: ?
Symptoms: Basal ganglia haemorrhage, Blood pressure increased, Brain oedema, Cerebrovascular accident, Coagulation test normal, Computerised tomogram head abnormal, Culture negative, Fatigue, Hemiparesis, Impaired work ability, Intracranial mass, Muscular weakness, Myalgia, Platelet count decreased, Pyrexia, Syncope
SMQs:, Torsade de pointes/QT prolongation (broad), Rhabdomyolysis/myopathy (broad), Haematopoietic thrombocytopenia (narrow), Peripheral neuropathy (broad), Haemorrhage terms (excl laboratory terms) (narrow), Neuroleptic malignant syndrome (broad), Systemic lupus erythematosus (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Ischaemic central nervous system vascular conditions (narrow), Haemorrhagic central nervous system vascular conditions (narrow), Embolic and thrombotic events, vessel type unspecified and mixed arterial and venous (narrow), Guillain-Barre syndrome (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Hyponatraemia/SIADH (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Hypertension (narrow), Cardiomyopathy (broad), Eosinophilic pneumonia (broad), Conditions associated with central nervous system haemorrhages and cerebrovascular accidents (narrow), Hypotonic-hyporesponsive episode (broad), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad)

Life Threatening? Yes
Birth Defect? No
Died? No
Permanent Disability? Yes
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 22 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Hypertension; Stress
Allergies:
Diagnostic Lab Data: Test Date: 20201218; Test Name: BP; Result Unstructured Data: Test Result:high as 200s/100; Test Date: 20201218; Test Name: BP; Result Unstructured Data: Test Result:179/101; Test Date: 20201218; Test Name: head CT; Result Unstructured Data: Test Result:Rt basal ganglia hemorrhage w/ edema and mass effe; Comments: Rt basal ganglia hemorrhage w/ edema and mass effect; Test Name: platelets; Result Unstructured Data: Test Result:normal coags; Test Date: 20201218; Test Name: platelets; Result Unstructured Data: Test Result:114 (unknown baseline); Test Date: 20201218; Test Name: platelets; Result Unstructured Data: Test Result:Low; Test Date: 20201218; Test Name: Nasal Swab; Result Unstructured Data: Test Result:Negative
CDC Split Type: USPFIZER INC2021014540

Write-up: He collapsed with left sided hemiparesis; Stroke; Rt basal ganglia hemorrhage w/ edema and mass effect.; Rt basal ganglia hemorrhage w/ edema and mass effect.; Low platelets, 114; His bp as high as 200s/100; Hand weakness; Myalgia; Fever; Severe fatigue; This is a spontaneous report from a contactable physician. A 58-year-old male patient received first dose of bnt162b2 (Pfizer BioNTech COVID vaccine), intramuscularly on 16Dec2020 at a single dose for COVID-19 immunization. Medical history included hypertension with reported med noncompliance in the last few months due to stress. Concomitant medication included hypertension medications in two weeks. The patient was presumed neg covid status prior to vaccine. He worked as a Pulm/critical care physician. He reported fever, myalgia, fatigue on 16Dec2020. Next day (17Dec2020), he took off from work due to his symptoms. The following day (18Dec2020), he came to work. He c/o ongoing severe fatigue & hand weakness in am. Staff noted him to be evaluating his hands during clinic. At 12:15, he collapsed with left sided hemiparesis. The reporter had suspicion for stroke. He was transported to the Emergency Room (ER), head CT showed Rt basal ganglia hemorrhage w/ edema and mass effect. Labs notable for Low platelets, 114 (unknown baseline) on 18Dec2020, normal coags on an unspecified date. BP recorded as 179/101, but it was noted in trauma room his bp as high as 200s/100. He had a history of hypertension with reported med noncompliance in the last few months due to stress. Patient was transferred for further care. Full course was unknown but had rebleed there with low plts. Adverse event (he collapsed with left sided hemiparesis) resulted in hospitalization (22 days), life threatening illness (immediate risk of death from the event), disability/incapacitating or permanent damage. Treatment was received for adverse events. Results of tests and procedures for investigation of the patient: on 18Dec2020, Nasal Swab test: negative. The outcome of events was not recovered. Unknown if any other vaccines within 4 weeks prior to the COVID vaccine. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient was not tested for COVID-19. Information on the lot/batch number has been requested.; Sender''s Comments: Collapsed with left sided hemiparesis/suspicion for stroke are as consequences of basal ganglia hemorrhage with edema, which is caused by worsening of hypertension. Low platelet also contributes to brain hemorrhage. All these serious events are unrelated to the vaccine use. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to Regulatory Authorities, Ethics Committees and Investigators, as appropriate.

VAERS ID:	1113923 (history)
Form:	Version 2.0
Age:	36.0
Sex:	Female
Location:	Unknown

Vaccinated:	2020-12-16
Onset:	2020-12-16
Days after vaccination:	0
Submitted:	0000-00-00
Entered:	2021-03-19

Vaccination / Manufacturer	Lot / Dose	Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH	- / 1	LA / OT

Administered by: Work Purchased by: ?
Symptoms: Biopsy, Chillblains, Fatigue, Headache, Hypoaesthesia, Investigation, SARS-CoV-2 test
SMQs:, Peripheral neuropathy (broad), Guillain-Barre syndrome (broad), Accidents and injuries (broad), COVID-19 (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? Yes
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Allergies:
Diagnostic Lab Data: Test Date: 20201216; Test Name: biopsy; Result Unstructured Data: Test Result:perniosis of bilateral hands; Test Name: lupus and other autoimmune work up; Test Result: Negative ; Test Name: Nasal Swab; Test Result: Negative
CDC Split Type: USPFIZER INC2021233857

Write-up: severe biopsy proven perniosis of bilateral hands; headaches; fatigue; left sided facial numbness; This is a spontaneous report from a contactable physician. A 36-year-old female patient received her first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number and expiration date were not provided), intramuscular on left arm on 16Dec2020 at single dose for COVID-19 immunization. Medical history was reported as none. The patient''s concomitant medications were not reported. The patient has no known allergies and was not pregnant. She was not diagnosed with COVID prior to vaccination and has no other vaccine in four weeks. The patient received her vaccine at a clinic. On 16Dec2020, the patient developed severe biopsy proven perniosis of bilateral hands, right after the vaccine which was still lasting. She also had headaches, fatigue for 2 weeks post vaccination (as reported) and left sided facial numbness for hours post vaccination. She had pain and swelling of the fingers which inhibits her from working as an nurse. She has been on disability leave from work. All lupus and other autoimmune work up have been negative. The events resulted in doctor or other healthcare professional office/clinic visit and emergency room/ department or urgent care. Therapeutic measures were taken as a result of the events and included treatment with amlodipine, prednisone course, topical steroids and pentoxifylline. The patient underwent lab test and procedure which included nasal swab which was negative post vaccination on an unspecified date. The outcome of the events was not recovered. The events were assessed as serious causing disability or permanent damage. Information on the lot/batch number has been requested.; Sender''s Comments: Based on available information, a possible contributory role of the subject product, BNT162B2 vaccine, cannot be excluded for the perniosis of bilateral hands and other reported events due to temporal relationship Additional information is needed to better assess the case, including complete medical history, diagnostics, counteractive treatment measures and concomitant medications. There is limited information provided in this report. This case will be reassessed upon receipt of follow-up information. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to Regulatory Authorities, Ethics Committees and Investigators, as appropriate.

VAERS ID:	910649 (history)
Form:	Version 2.0
Age:	36.0
Sex:	Female
Location:	North Carolina

Vaccinated:	2020-12-17
Onset:	2020-12-17
Days after vaccination:	0
Submitted:	0000-00-00
Entered:	2020-12-28

Vaccination / Manufacturer	Lot / Dose	Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH	EK5730 / UNK	LA / -

Administered by: Unknown Purchased by: ?
Symptoms: Blood pressure increased, Dizziness, Dyspnoea, Headache, Hypertension, Malaise, Nervousness, Pyrexia
SMQs:, Anaphylactic reaction (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Hypertension (narrow), Cardiomyopathy (broad), Vestibular disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? Yes
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: Test Date: 202012; Test Name: blood pressure; Result Unstructured Data: Test Result:It was 160''s over 105; Test Date: 202012; Test Name: blood pressure; Result Unstructured Data: Test Result:not come down/ still really high; Test Date: 20201218; Test Name: blood pressure; Result Unstructured Data: Test Result:Her blood pressure was high; Test Date: 20201219; Test Name: blood pressure; Result Unstructured Data: Test Result:138/90; Test Date: 20201220; Test Name: blood pressure; Result Unstructured Data: Test Result:156/100; Test Date: 20201220; Test Name: blood pressure; Result Unstructured Data: Test Result:her blood pressure was up; Test Date: 20201220; Test Name: blood pressure; Result Unstructured Data: Test Result:had been high all day; Test Date: 20201218; Test Name: Body temperature; Result Unstructured Data: Test Result:low grade fever; Comments: night; Test Date: 202012; Test Name: heart rate; Result Unstructured Data: Test Result:in the low 100''s, around 105; Test Date: 20201218; Test Name: heart rate; Result Unstructured Data: Test Result:in the 100''s
CDC Split Type: USPFIZER INC2020510499

Write-up: low grade fever; Her blood pressure was high/ still really high/ blood pressure was up; headache; Fifteen to twenty minutes after she received the vaccine she became light headed and dizzy/ light headedness and dizziness; This is a spontaneous report from a contactable nurse (patient). A 36-year-old female patient received BNT162B2 (Lot#: EK5730) via an unspecified route of administration on 17Dec2020 afternoon at single dose in the left arm for COVID-19 immunization. Caller was unable to confirm the manufacturer of the vaccine that she received. It is not written on the card, and she didn''t see the vial. The patient medical history was not reported. Concomitant medications included oral contraception pill, but the name was unknown. Fifteen to twenty minutes after she received the vaccine on 17Dec2020 she became light headed and dizzy. She had to catch her breath. She couldn''t shake it off. The light headedness and dizziness lasted at that intensity for 10 minutes, but it never went away. They encouraged her to be admitted in the emergency room (ER). She would say that the seriousness of being light headed and dizzy was disabling. Caller didn''t remember the exact numbers for her blood pressure. It was 160''s over 105. Her heart rate was in the low 100''s, around 105. She stayed at the first monitoring station in the vaccine area for 2 hours. They were taking her blood pressure every five minutes. She was given diphenhydramine hydrochloride (BENADRYL) there and lots of water. After 3 hours and she was not improving they called a "code medic" that got the medical director and nursing supervisor to come. They encouraged her to go to the ER for continual monitoring. She stayed in the ER for4 hours and was given meds to help with the blood pressure. She was discharged from the ER home. She was nervous because of all this stemming from the vaccine. She had a low grade fever on 18Dec2020 (Friday) night. Caller stated her work had already reported her reaction. Occupational safety and the medical director are aware. Caller does not have reference number to provide. On 18Dec2020 (Friday) she was not overly concerned because it was the next day. Her blood pressure was high and her heart rate was in the 100''s. They monitored her for a couple of hours and she was given a diphenhydramine hydrochloride (BENADRYL). She went to the emergency room (ER) for a few more hours and received additional treatment. They sent her home to be monitored at home. She has been taking her blood pressure every day since and it had not come down. It was still really high. She called her primary care doctor. He was wanting her to start blood pressure for medication it. She was concerned about starting it with the assumption that it was related to the vaccine. She would like to know the right thing to do. It seems safe to take the medicine, but it was unknown that whether it was going to mask the blood pressure and something else be going on. On 18Dec2020 she still had a headache and didn''t feel well, but she thought she needed to give it some time. She had been anticipating not to feel well on 18Dec2020 (Friday). On 19Dec2020 she felt better considering she didn''t have a headache. On 19Dec2020 (Saturday) her blood pressure was 138/90 and she felt good. Then on 20Dec2020 she had the bad headache and her blood pressure was up. On 20Dec2020 (Sunday) she had a bad headache and her blood pressure was 156/100. She came to work today and her blood pressure had been high all day. She still had a headache and the light headedness continued. The outcome of the event low grade fever was unknown, of other remain events was not recovered.; Sender''s Comments: A causal association between BNT162B2 and the event dizziness cannot be excluded based on a compatible temporal relation. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to RAs, Ethics Committees, and Investigators, as appropriate.

VAERS ID:	906782 (history)
Form:	Version 2.0
Age:	44.0
Sex:	Male
Location:	California

Vaccinated:	2020-12-18
Onset:	2020-12-18
Days after vaccination:	0
Submitted:	0000-00-00
Entered:	2020-12-22

Vaccination / Manufacturer	Lot / Dose	Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH	CK5730 / 1	LA / IM

Administered by: Other Purchased by: ?
Symptoms: Cold sweat, Dizziness, Dysgeusia, Feeling abnormal, Hot flush, Hypoaesthesia, Pallor, Paraesthesia, Peripheral coldness
SMQs:, Peripheral neuropathy (broad), Taste and smell disorders (narrow), Anticholinergic syndrome (broad), Dementia (broad), Guillain-Barre syndrome (broad), Vestibular disorders (broad), Hypotonic-hyporesponsive episode (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? Yes
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: multivitamines
Current Illness: none
Preexisting Conditions: none
Allergies: noe
Diagnostic Lab Data: Rapid Response was called BP and SpO2 was checked, I don''t know the results, on 12/18/2020.
CDC Split Type:

Write-up: Received COVID-19 vaccine on 12/18/2020 around 1225pm, ten minutes later while being monitored I started to feel hot flash, got dizzy like about to pass out, I asked to let me lay down, I felt the medication bitter taste in the back of my throat, I was clammy pale, I lay on a stretcher and put my feet up elevated, rapid response was called and BP was checked and Spo2, my hands were getting cold and tingling I was talking to RN, another RN, after laying down for ten minutes I sit up I was getting my BP back to normal, I sat down in the chair again for another 10 minutes, I was offered to go to the ER but I decline, I said I was getting better, after 15 minutes I left monitored by my supervisor I felt the medication in my stomach, after the tingling my fingers were numbed for the next days until present.

VAERS ID:	934937 (history)
Form:	Version 2.0
Age:	64.0
Sex:	Female
Location:	New Mexico

Vaccinated:	2020-12-18
Onset:	2020-12-18
Days after vaccination:	0
Submitted:	0000-00-00
Entered:	2021-01-11

Vaccination / Manufacturer	Lot / Dose	Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH	EKS730 / 1	LA / OT

Administered by: Unknown Purchased by: ?
Symptoms: Chills, Headache, Nausea, Pain in extremity, Retching, Skin warm
SMQs:, Acute pancreatitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Tendinopathies and ligament disorders (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? Yes
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Allergies:
Diagnostic Lab Data: Test Name: temperature; Result Unstructured Data: Test Result:Unknown result
CDC Split Type: USPFIZER INC2021007689

Write-up: blasting headaches; chills all night; dry heaving all night; Nausea; no fever but her skin felt hot; sore left arm; This is a spontaneous report from a contactable nurse for herself. This 64-year-old female patient started to receive BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE), intramuscular on 18Dec2020 at single dose on left upper arm (lot: EKS730), via an unspecified route of administration on 05Jan2021 14:30 at single dose (lot: EL1284 or EKI284) for COVID-19 immunisation. Medical history and concomitant medications were none. The patient did not have anything with the first shot except a sore left arm on 18Dec2020. She stated that if she lays on left side it is sore. The patient had the sore left arm both times that she got the vaccine. She got second dose of vaccine on 05Jan2021 at 2:30pm and had a blasting headache and just had chills that went away about hour ago on 05Jan2021. She did not have a fever but her skin felt hot on 05Jan2021. She stated that she had dry heaves on 05Jan2021. The patient started that she had a blasting headache within a few hours of the vaccine and it gradually got worst by the time she went to bed. Stated that the chills and dry heaves started then and throughout the night. The chills stopped an hour before she got up. Stated that she went to check her temperature and did not have a fever despite having chills and her skin feeling hot. Stated that nausea started about 10 at night on 05Jan2021. Seriousness for blasting headache, chills and dry heaves was disabling, for nausea was medically significant, for other events was non-serious. The patient took Ibuprofen for the headache. Stated that she was going to try to drink something. The outcome of sore left arm was not recovered; of chills was recovered on 06Jan2021. The outcome of other events was recovering. The causality for blasting headache, chills, dry heaves, nausea and skin felt hot was related (Source of assessment: Primary Source Reporter, Method of assessment: Agency Information on the batch number has been requested.; Sender''s Comments: Based on available information, a possible contributory role of the subject product, BNT162B2 vaccine, cannot be excluded for the headache, chills, dry heaves and other reported events due to temporal relationship. There is limited information provided in this report. Additional information is needed to better assess the case, including complete medical history, diagnostics, counteractive treatment measures and concomitant medications. This case will be reassessed once additional information is available. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to Regulatory Authorities, Ethics Committees and Investigators, as appropriate.

VAERS ID:	996740 (history)
Form:	Version 2.0
Age:	37.0
Sex:	Female
Location:	Illinois

Vaccinated:	2020-12-18
Onset:	2020-12-18
Days after vaccination:	0
Submitted:	0000-00-00
Entered:	2021-02-03

Vaccination / Manufacturer	Lot / Dose	Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH	EK5730 / 1	RA / -

Administered by: Private Purchased by: ?
Symptoms: Adverse event, Exposure during pregnancy, Facial paresis, Guillain-Barre syndrome, Immunoglobulin therapy, Muscular weakness, SARS-CoV-2 test negative
SMQs:, Rhabdomyolysis/myopathy (broad), Peripheral neuropathy (narrow), Guillain-Barre syndrome (narrow), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Demyelination (narrow), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Immune-mediated/autoimmune disorders (narrow), COVID-19 (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? Yes
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 7 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: Test Date: 20210110; Test Name: COVID-19 PCR test (Nasal Swab); Test Result: Negative
CDC Split Type: USPFIZER INC2021046591

Write-up: Patient developed GBS with 4 extremity weakness and facial weakness; Patient developed GBS with 4 extremity weakness and facial weakness; Patient developed GBS with 4 extremity weakness and facial weakness; This is a spontaneous report from a contactable pharmacist (patient). A 37-year-old non-pregnant female patient received the first dose of BNT162B2 (Pfizer-Biontech Covid-19 Vaccine, Lot. Ek5730) at single dose, in the right arm, on 18Dec2020, at 03:30 PM, for COVID-19 immunisation. Relevant medical history and concomitant medications were unknown. The patient had not received any other vaccines within 4 weeks prior to the BNT162B2 vaccine. The patient had not experienced Covid-19 prior vaccination. On 18Dec2020, at 07:00 PM, the patient developed Guillain-Barre syndrome (GBS) with 4 extremity weakness and facial weakness. Emergency Room Visit required. Hospitalization required (7 days admission in hospital). Treatment required: IVIG. The adverse events were assessed as serious (hospitalization and disability). Clinical outcome of the adverse events was recovering at time of this report. Post the vaccination, on 10Jan2021, the patient has been tested for COVID-19 and resulted negative. COVID-19 test type post vaccination: COVID-19 PCR test (Nasal Swab).; Sender''s Comments: Based on the close temporal relationship, the association between the events Guillain-Barre syndrome (GBS) with 4 extremity weakness and facial weakness with BNT162b2 can not be completely excluded. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to regulatory authorities, Ethics Committees, and Investigators, as appropriate.

VAERS ID:	1009954 (history)
Form:	Version 2.0
Age:	59.0
Sex:	Female
Location:	Pennsylvania

Vaccinated:	2020-12-18
Onset:	2020-12-18
Days after vaccination:	0
Submitted:	0000-00-00
Entered:	2021-02-07

Vaccination / Manufacturer	Lot / Dose	Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH	- / 1	- / IM

Administered by: Private Purchased by: ?
Symptoms: Arthralgia, Pain
SMQs:, Arthritis (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? Yes
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Omepraxole Escitalopram Provastanin
Current Illness: None
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data:
CDC Split Type:

Write-up: Shoulder pain when rotating arm around

VAERS ID:	1178300 (history)
Form:	Version 2.0
Age:	44.0
Sex:	Female
Location:	Illinois

Vaccinated:	2020-12-18
Onset:	2020-12-18
Days after vaccination:	0
Submitted:	0000-00-00
Entered:	2021-04-07

Vaccination / Manufacturer	Lot / Dose	Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH	- / UNK	RA / -

Administered by: Private Purchased by: ?
Symptoms: Dizziness, Palpitations, Pharyngeal swelling, SARS-CoV-2 test
SMQs:, Anaphylactic reaction (broad), Angioedema (narrow), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Cardiomyopathy (broad), Vestibular disorders (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), COVID-19 (broad)

Life Threatening? Yes
Birth Defect? No
Died? No
Permanent Disability? Yes
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 5 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Food allergy
Allergies:
Diagnostic Lab Data: Test Name: Covid test; Result Unstructured Data: Test Result:Negative
CDC Split Type: USPFIZER INC2021355529

Write-up: dizzy; throat started to swell; Within five minutes of the immunization my heart was racing; This is a spontaneous report from a contactable healthcare professional (patient). A 44-year-old female patient received BNT162B2 (lot number and expiry date were not reported), via an unspecified route of administration, administered in right arm on 18Dec2020 09:00 (at the age of 44-year-old) at single dose for COVID-19 immunization. Medical history included dairy allergy. The patient is not pregnant at the time of vaccination. The patient''s concomitant medications were not reported. No other vaccines within 4 weeks prior to the COVID vaccine nor any other medications the patient received within 2 weeks. Within five minutes of the immunization on 18Dec2020 the patient''s heart was racing, she was dizzy, her throat started to swell, and she was brought to the ER where they gave her epinephrine and Benadryl. She was admitted to the hospital (Dec2020) two times within a week due to the same symptoms; continuous heart palpitations. She was still having heart palpitations. The adverse events resulted in Doctor or other healthcare professional office/clinic visit, Emergency room/department or urgent care, Hospitalization, Life threatening illness (immediate risk of death from the event), Disability or permanent damage. The patient was hospitalized for 5 days. Since the vaccination, has the patient been tested for COVID-19. Covid test was negative on unspecified date. The outcome of the event heart was racing was not recovered and the outcome of the remaining events was recovering. Information on the lot/batch number has been requested.; Sender''s Comments: Based on the information available, a possible contributory role of the suspect BNT162B2 cannot be excluded for the reported events palpitations, dizziness and pharyngeal swelling occurred in a plausible temporal relationship. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to Regulatory Authorities, Ethics Committees and Investigators, as appropriate.

VAERS ID:	928318 (history)
Form:	Version 2.0
Age:	50.0
Sex:	Female
Location:	Colorado

Vaccinated:	2020-12-19
Onset:	2020-12-19
Days after vaccination:	0
Submitted:	0000-00-00
Entered:	2021-01-08

Vaccination / Manufacturer	Lot / Dose	Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH	EH 9899 / 1	LA / IM

Administered by: Private Purchased by: ?
Symptoms: Arthralgia, Asthenia, Axillary pain, Fatigue, Headache, Insomnia, Malaise, Oropharyngeal pain, Pain in extremity, Pyrexia, Rhinorrhoea, Sleep disorder, Spinal pain
SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Guillain-Barre syndrome (broad), Arthritis (broad), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? Yes
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Flu vaccine/ quaderavlent every year/ symptoms last about 5 days then goes away. face swelling, body aches, pains, joint pain, l
Other Medications: none
Current Illness: none
Preexisting Conditions: Raynaud''s syndrome, spondylolisthesis
Allergies: preservatives in clothing and furniture.
Diagnostic Lab Data: None
CDC Split Type:

Write-up: headache, sore throat, runny nose, arm pain that migrated to the axilla and down the side of the body, joint pain ( hands, wrist, feet, hips, knees, spine, neck), insomnia, general malaise, fatigue, and lower grade fever. Most symptoms lasted about 7 -10 days. However, it is now day 20 after the initial vaccine and I still have joint pain that has not gone away. esp in hands, wrists, and feet. When I sleep I still wake up with all my joints hurting it gets better as I start moving but the wrist, hands, and feet pain has not gone away. This pain will wake me in the night when I change positions. I called my doctor today to inquire if it is a good idea if I should take the second dose because the first dose made me so dibiliated. Awaiting for a response. I am due to take the second vaccine on 2/9/21.

VAERS ID:	1023358 (history)
Form:	Version 2.0
Age:
Sex:	Female
Location:	California

Vaccinated:	2020-12-19
Onset:	2020-12-19
Days after vaccination:	0
Submitted:	0000-00-00
Entered:	2021-02-11

Vaccination / Manufacturer	Lot / Dose	Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH	- / 1	- / -

Administered by: Unknown Purchased by: ?
Symptoms: Amnesia, Anosmia, Blood electrolytes, Blood pressure increased, Blood pressure measurement, Blood pressure systolic increased, Blood test, Chest discomfort, Chest pain, Computerised tomogram, Deafness, Dizziness, Dyspnoea, Encephalitis, Fall, Fibrin D dimer increased, Full blood count, Gait disturbance, Headache, Laboratory test, Lymphadenopathy, Magnetic resonance imaging, Magnetic resonance imaging brain, Memory impairment, Nausea, Neck pain, Pain, Paraesthesia, Physical examination, Presyncope, Rhinitis, SARS-CoV-2 test, Taste disorder, Visual impairment
SMQs:, Anaphylactic reaction (broad), Acute pancreatitis (broad), Peripheral neuropathy (broad), Haemorrhage laboratory terms (broad), Neuroleptic malignant syndrome (broad), Taste and smell disorders (narrow), Anticholinergic syndrome (broad), Dementia (broad), Parkinson-like events (broad), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Guillain-Barre syndrome (broad), Noninfectious encephalitis (narrow), Noninfectious encephalopathy/delirium (broad), Accidents and injuries (narrow), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Glaucoma (broad), Hypertension (narrow), Optic nerve disorders (broad), Cardiomyopathy (broad), Lens disorders (broad), Retinal disorders (broad), Depression (excl suicide and self injury) (broad), Hearing impairment (narrow), Vestibular disorders (broad), Hypotonic-hyporesponsive episode (broad), Arthritis (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad), Immune-mediated/autoimmune disorders (broad), COVID-19 (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? Yes
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Food allergy (food allergies (clams, escargot)); Ovarian cancer (age 29); Sulfonamide allergy (Allergies to Bactrim/Sulfa)
Allergies:
Diagnostic Lab Data: Test Date: 20210103; Test Name: electrolytes; Result Unstructured Data: Test Result:WNL (within normal limits); Test Date: 20210103; Test Name: BP; Result Unstructured Data: Test Result:elevated BP; Test Date: 20210108; Test Name: BP; Result Unstructured Data: Test Result:elevated SBP 190-200; Test Date: 20210103; Test Name: DDimer; Result Unstructured Data: Test Result:elevated; Test Date: 20210108; Test Name: CT head; Result Unstructured Data: Test Result:CT head negative; Test Date: 20210103; Test Name: CT Scan of Chest/Abdomen; Result Unstructured Data: Test Result:L axilla lymphadenopathy; Test Date: 20210103; Test Name: CBC, Electrolytes; Result Unstructured Data: Test Result:WNL (within normal limits); Comments: CBC, Electrolytes WNL (within normal limits).; Test Date: 20210108; Test Name: pheochromocytoma; Test Result: Negative ; Test Date: 20210108; Test Name: MRI; Result Unstructured Data: Test Result:MRI negative; Test Name: Brain MRI; Result Unstructured Data: Test Result:Unknown result; Comments: no diagnosis has been yet identified; Test Date: 20210103; Test Name: PE; Test Result: Negative ; Test Date: 20210108; Test Name: COVID tests; Test Result: Negative
CDC Split Type: USPFIZER INC2021100197

Write-up: encephalitis-like symptoms; Hearing loss; memory loss; parathesias; visual disturbances; taste disturbances; dizziness; Lsided chest pain; staggering; elevated SBP 190-200; severe L-sided chest tightness; pre-syncope; elevated BP; DDimer was elevated; fell; intermittent memory lapses; nausea episodes; cant smell that last 1-2 hrs; L neck /head pain; L neck /head pain; Left axilla lymphadenopathy; rhinitis; lightheaded/lightheadedness; had an episode of pain all over; SOB; This is a spontaneous report from a contactable physician (patient). A 46-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot/batch number and expiration date were unknown), via an unspecified route of administration from on 19Dec2020 at a single dose for COVID-19 immunization. Medical history included ovarian cancer at age 29, food allergy to clams and escargot, and allergy to sulfa. The patient''s concomitant medications were not reported. The patient previously took bactrim and experienced allergies. On 19Dec2020, immediately after vaccine had rhinitis, lightheaded, given Zyrtec and water and observed for a duration of 30 min. Three hours postvaccination on 19Dec2020, at home had an episode of pain all over and SOB (shortness of breath). 3 days later (22Dec2020), patient had L (left) neck /head pain and left axilla lymphadenopathy. On 23Dec2020, she fell in the shower. On the same day (23Dec2020) the patient had intermittent memory lapses, lightheadedness, nausea episodes, can''t smell that last 1-2 hours a few times a day. Symptoms worsened on 03Jan2021, with severe L-sided chest tightness, pre-syncope, was seen in the ER with elevated BP. DDimer was elevated, CT Scan of Chest/Abdomen showed L axilla lymphadenopathy, negative for PE. CBC, Electrolytes WNL (within normal limits), still on 03Jan2021. Observed in ER for 7 hrs. and then discharged home. Intermittent symptoms continued. On 08Jan2021, patient had another severe episode while at work. She was noted to be staggering, and again was complaining of left-sided chest pain. She was taken to the ER by her colleagues on 08Jan2021 and noted to have elevated SBP 190-200. On 08Jan2021, patient underwent CT head negative, MRI negative, w/u (workup) for pheochromocytoma negative and COVID negative. She was started on prednisone and Norvasc and discharged home. She continues to have intermittent episodes however they have decreased in intensity and last for about 1 hour. She described her symptoms as encephalitis-like symptoms. These include memory loss, paresthesia, visual disturbances, hearing loss, taste disturbances, and dizziness. These symptoms when severe have been incapacitating. She had been hospitalized for a neurological and infectious work up (including Brain MRI and multiple COVID tests) but no diagnosis has been yet identified. This symptom kcomplex (unspecified) has persisted to now. She has not received the second dose of vaccine. She is asking how long mRNA, the lipid nanoparticles and the protein spike lasts in the body. Outcome of the events was unknown. Information on the lot/batch number has been requested.; Sender''s Comments: Based on the limited information currently available, a possible contributory role of the suspect drug in the reported events cannot be completely excluded given the implied temporal association. However, underlying medical conditions may provide the alternate explanations. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to Regul atory Authorities, Ethics Committees and Investigators, as appropriate.

VAERS ID:	1255242 (history)
Form:	Version 2.0
Age:	40.0
Sex:	Female
Location:	Vermont

Vaccinated:	2020-12-19
Onset:	2020-12-19
Days after vaccination:	0
Submitted:	0000-00-00
Entered:	2021-04-25

Vaccination / Manufacturer	Lot / Dose	Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH	- / 1	RA / OT

Administered by: Private Purchased by: ?
Symptoms: Asthenia, Blood follicle stimulating hormone, Blood follicle stimulating hormone increased, Chills, Hot flush, Infertility female, Migraine, Nausea, Ovarian disorder, Pyrexia, SARS-CoV-2 test, Ultrasound scan, Vertigo, Vomiting
SMQs:, Acute pancreatitis (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Guillain-Barre syndrome (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Vestibular disorders (narrow), Fertility disorders (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), COVID-19 (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? Yes
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: WELLBUTRIN; LOESTRIN
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Asthma (other medical history: Eosinophilic esophagitis, asthma); Eosinophilic esophagitis (other medical history: Eosinophilic esophagitis, asthma)
Allergies:
Diagnostic Lab Data: Test Name: FSH; Result Unstructured Data: Test Result:Unknown results; Comments: previous values; Test Date: 20201219; Test Name: FSH; Result Unstructured Data: Test Result:skyrocketed from previous values; Comments: They obtained an FSH level and it had skyrocketed from previous values not long before my ovaries had shrunk in size by approximately half; Test Date: 20210314; Test Name: nasal swab/Covid test; Test Result: Negative ; Test Date: 20201219; Test Name: ultrasound; Result Unstructured Data: Test Result:ovaries had shrunk in size; Comments: ovaries had shrunk in size by approximately half
CDC Split Type: USPFIZER INC2021392945

Write-up: Diminished ovarian reserve/diminished reserve; fever; chills; hot flashes; nausea; vomiting; migraine headache; vertigo; weakness; They obtained an FSH level and it had skyrocketed from previous values not long before; my ovaries had shrunk in size by approximately half; This is a spontaneous report from a contactable nurse (patient). A 40-years-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE, Solution for injection), first dose via intramuscular, administered in right arm on 19Dec2020 09:30 at a single dose (lot number and expiry date were not reported); and then received the second dose on 02Jan2021 09:30 (lot number and expiry date not reported), intramuscularly administered in right arm as a single dose; for COVID-19 immunisation. Medical history included eosinophilic esophagitis and asthma. The patient had no known allergies. The patient was not pregnant at the time of the report and vaccination. The patient had no covid prior vaccination. Concomitant medications which were taken in two weeks prior to vaccination included bupropion hydrochloride (WELLBUTRIN) and ethinylestradiol, norethisterone acetate (LOESTRIN), taken for an unspecified indication, start and stop date were not reported. The patient had no other vaccine in four weeks. On 19Dec2020, the patient experienced diminished ovarian reserve. Patient stated that she was extremely symptomatic after both vaccines and starting on 19Dec2020 had experienced fever, chills, hot flashes, nausea, vomiting, migraine headache, vertigo and weakness. The hot flashes persisted and worsened after each subsequent vaccine, prompting her to go to my MD. They obtained an FSH level on 19Dec2020 and it had skyrocketed from previous values (dates unspecified; unknown results) not long before. An ultrasound on 19Dec2020, showed that her ovaries had shrunk in size by approximately half and she had diminished reserve. Patient was now on supplemental hormones and will be for many years to come as she was only 40. Patient know the vaccine caused this. It was too great of a coincidence. Adverse events resulted in doctor or other healthcare professional office/clinic visit, disability or permanent damage. As a result of the events reported patient was now on hormonal replacement therapy. The patient was tested for covid post vaccination which included nasal swab/Covid test on 14Mar2021 as negative. The outcome of the events reported was not recovered. Information about lot/batch number has been requested.; Sender''s Comments: A possible contributory effect of suspect BNT162B2 on reported events cannot be excluded, for events fever, chills, hot flashes, nausea, vomiting, migraine headache, vertigo and weakness, conversely the suspect drug is considered very unlikely related for other gynecological disturbances. The impact of this report on the benefit/risk profile of the Pfizer drug is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to Committees and Investigators, as appropriate.

VAERS ID:	920958 (history)
Form:	Version 2.0
Age:	51.0
Sex:	Female
Location:	California

Vaccinated:	2020-12-21
Onset:	2020-12-21
Days after vaccination:	0
Submitted:	0000-00-00
Entered:	2021-01-05

Vaccination / Manufacturer	Lot / Dose	Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH	EH9899 / 1	LA / -

Administered by: Private Purchased by: ?
Symptoms: Fall, Musculoskeletal disorder, Neurological symptom, Pain in extremity, Pruritus, SARS-CoV-2 test negative
SMQs:, Rhabdomyolysis/myopathy (broad), Anaphylactic reaction (broad), Accidents and injuries (narrow), Hypersensitivity (broad), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), COVID-19 (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? Yes
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Allergies:
Diagnostic Lab Data: Test Date: 202012; Test Name: COVID; Test Result: Negative
CDC Split Type: USPFIZER INC2020510713

Write-up: felt like she had a stroke; fell down; Pain in leg; itchiness in her head; left leg not functioning normally; This is a spontaneous report from a contactable nurse (reporting for herself). A 51-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE; Lot number: EH9899), via an unspecified route of administration in the left deltoid on 21Dec2020 at 10:00 (at the age of 51-years-old) as a single dose for COVID-19 immunization. Medical history was none. There were no concomitant medications. There were no prior vaccinations within 4 weeks prior to the first administration of the suspect vaccine. On 21Dec2020, the patient experienced left leg not functioning normally, which was reported with the seriousness criteria of disability. On 21Dec2020, the patient had itchiness in her head. The patient felt like she had a stroke, fell down and pain in leg on 22Dec2020, which were all reported with the seriousness criteria of disability. The patient called the doctor office and spoke with the doctor on call and was told to use diphenhydramine hydrochloride (BENADRYL). No further details provided. The patient was sent home for 10 days and she was sent back to work. The patient underwent lab tests and procedures which included COVID: negative in Dec2020. The outcome of the events was not recovered. The reported assessed the events related to the suspect product, BNT162B2.; Sender''s Comments: The reported events leg dragging, leg pain and fall and suspected stroke were possibly related to the use of first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), due to temporal relationship. However, stroke was not diagnosed. The case will be reassessed should additional information become available. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to Regulatory Authorities, Ethics Committees and Investigators, as appropriate.

VAERS ID:	915612 (history)
Form:	Version 2.0
Age:	33.0
Sex:	Male
Location:	Illinois

Vaccinated:	2020-12-22
Onset:	2020-12-22
Days after vaccination:	0
Submitted:	0000-00-00
Entered:	2020-12-31

Vaccination / Manufacturer	Lot / Dose	Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH	EJ1685 / 1	LA / IM

Administered by: Private Purchased by: ?
Symptoms: Flushing, Hypoaesthesia, Neuralgia, Paraesthesia, Rash, Small fibre neuropathy
SMQs:, Anaphylactic reaction (broad), Peripheral neuropathy (narrow), Guillain-Barre syndrome (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? Yes
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: None
Current Illness: None
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data: My ID docs called a neurologist in our group, Dr. He saw me on December 29th in which he said this could potentially be guillain barre or it could just be a allergy reaction, both due to the covid vaccine. He did a full evaluation and found that I had neuropathic pain in my right hand and right foot. As of the 29th, the numbness and tingling was back to my right foot also and would come and go. He gave me a shot of decadron 1g (even though it would blunt my antibody titer response to the vaccine) and gave me extended release gabapentin to start on the evening of the 29th. He also had me start a Medrol dose pack starting on the 30th (today). 12-30-2020 Dr. did a STAT EMG which came back fairly normal. He can almost definitively say this is not guillain barre although he still concerned about some of the more rare de-myelinating brain disorders caused from vaccines. he said the most likely on the differential is a small fiber peripheral neuropathy stimulated from the lipid moiety that encompasses the messenger RNA of the mRNA vaccine. He told me to continue the prescribed meds and he is going to do a biopsy on Monday to try to diagnose the small fiber peripheral neuropathy.
CDC Split Type:

Write-up: Received my vaccine on December 22nd, 2020 at around 830 Am. That afternoon, about 3 PM, I started to have a reaction. It started with tingling/numbness in my right hand which progressed up my arm into my elbow. About 10 minutes later, it then progressed into my right foot, and my left foot. About 10 minutes after that, I started to get flushed and a neck rash (diagnosed from Dr.). I took Benadryl and Ibuprofen 800mg PO every 6 hours for the next 24 hours. The numbness in my right foot and left foot along with the flushness went away a couple hours later. Although, the numbness in my right hand never went away. It came and went for the next 4 days until December 27th and 28th when it started getting worse. On December 28th evening, it got so bad that I was debating going to the emergency room around 1 am. The numbness and tingling was in my right hand and started shooting up my arm. The nerve pain around my wrist was unbearable. I finally fell asleep and the next morning, it was not nearly as bad, but was still there. The numbness and tingling moved from my right hand mainly to right hand, right foot, right leg, left foot and left hand today (12-30-2020).

VAERS ID:	926473 (history)
Form:	Version 2.0
Age:	30.0
Sex:	Female
Location:	South Dakota

Vaccinated:	2020-12-22
Onset:	2020-12-22
Days after vaccination:	0
Submitted:	0000-00-00
Entered:	2021-01-07

Vaccination / Manufacturer	Lot / Dose	Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH	EK9231 / 1	LA / IM

Administered by: Other Purchased by: ?
Symptoms: Arthralgia, Immediate post-injection reaction, Inflammation, Joint range of motion decreased, Magnetic resonance imaging joint, Muscular weakness, Musculoskeletal discomfort, Pain, X-ray limb
SMQs:, Rhabdomyolysis/myopathy (broad), Peripheral neuropathy (broad), Guillain-Barre syndrome (broad), Noninfectious encephalopathy/delirium (broad), Hypersensitivity (narrow), Arthritis (broad), Tendinopathies and ligament disorders (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? Yes
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Novolog, Trokendi, Metoprolol, Biotin, Vitamin D, Vitamin C, Potassium
Current Illness:
Preexisting Conditions: Type 1 Diabetic POTS Migraines
Allergies: Morphine Tomatoes
Diagnostic Lab Data: xrays 12/31/2020 (orthopedic provider recommended) MRI 12/31/2020 (orthopedic provider recommended) upcoming surgical consultation d/t this ongoing issue
CDC Split Type:

Write-up: When vaccine was administered, seemed high on my arm. I had immediate soreness and shoulder discomfort, I was told this was normal. It continued to progress and I eventually had decreased ROM, weakness and sharp shooting pain in my shoulder. Working at OI, I consulted provider, xrays were obtained and I was evaluated. He strongly suggested an MRI be obtained as well. That was completed the same day as my evaluation on 12/31/2020 (1 week and 2 days after the vaccine was administered). The provider informed me that they have had patients with similar situations that were evaluated for frozen shoulder after having a vaccine d/t administration site and vaccine going into subacromial space. He does report that this was my case/situation, upon my exam, I had severe inflammation with this as well-he is now having me follow up for a surgical consultation for my shoulder to be repaired. Today''s date is 1/7/2021, I have these same ongoing symptoms that have continued since day of administration, without diminishing in severity. He is unable to provide an injection d/t my upcoming second dose of the COVID vaccine this next week, 1/12/2021. He strongly suggests that my 2nd vaccine be administered elsewhere-advised NOT be administered in the same shoulder OR in opposite to cause these symptoms to flare. He advised in gluteus if possible to avoid any further issues if at all possible.

VAERS ID:	1045888 (history)
Form:	Version 2.0
Age:	36.0
Sex:	Female
Location:	Massachusetts

Vaccinated:	2020-12-22
Onset:	2020-12-22
Days after vaccination:	0
Submitted:	0000-00-00
Entered:	2021-02-22

Vaccination / Manufacturer	Lot / Dose	Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH	EL0140 / 1	LA / IM

Administered by: Work Purchased by: ?
Symptoms: Condition aggravated, Erythema, Hyperaesthesia, Paraesthesia, Pruritus, Swelling, Temperature intolerance
SMQs:, Anaphylactic reaction (broad), Angioedema (broad), Peripheral neuropathy (broad), Guillain-Barre syndrome (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Hypersensitivity (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? Yes
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: none
Current Illness: none
Preexisting Conditions: none
Allergies: none
Diagnostic Lab Data:
CDC Split Type:

Write-up: after receiving the vaccine, I have developed a skin intolerance to heat (hot water, hit items touching skin), heat causes itching and tingling and well as redness and swelling with hotter temperatures at longer durations. This has been occurring since after receiving the first vaccine, with increased severity after the second. The symptoms last from 20-2 hours after exposure and then resolve.

VAERS ID:	913469 (history)
Form:	Version 2.0
Age:	67.0
Sex:	Female
Location:	New York

Vaccinated:	2020-12-23
Onset:	2020-12-23
Days after vaccination:	0
Submitted:	0000-00-00
Entered:	2020-12-30

Vaccination / Manufacturer	Lot / Dose	Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH	EK9231 / 1	LA / IM

Administered by: Other Purchased by: ?
Symptoms: Arthralgia, Blood test, Chest X-ray, Chills, Dyspnoea, Electrocardiogram, Pyrexia, SARS-CoV-2 test, Urticaria
SMQs:, Anaphylactic reaction (narrow), Angioedema (narrow), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Cardiomyopathy (broad), Hypersensitivity (narrow), Arthritis (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), COVID-19 (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? Yes
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: Eliquis
Current Illness: None
Preexisting Conditions: I was diagnosed with with COVID 19 in April 2020 and was diagnosed with pulmonary embolus , pneumonia sob. I had no other medical conditions prior to having COVID 19.
Allergies: IV contrast dye
Diagnostic Lab Data: Blood test, chest X-ray and CoVID pcr test was done EKG 12/25/2020
CDC Split Type:

Write-up: Shortness of breath Hives, Fever, chills joint pains. I was Tx in the ER with Pepcid IV Solumedrol IV, Benadryl IV ,Tylenol and IV fluids. I was discharged on prednisone , Benadryl and Tylenol.

VAERS ID:	929162 (history)
Form:	Version 2.0
Age:	47.0
Sex:	Female
Location:	Indiana

Vaccinated:	2020-12-23
Onset:	2020-12-23
Days after vaccination:	0
Submitted:	0000-00-00
Entered:	2021-01-08

Vaccination / Manufacturer	Lot / Dose	Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH	EL1284 / 1	LA / IM

Administered by: Other Purchased by: ?
Symptoms: Arthralgia, Body temperature abnormal, Chest pain, Fatigue, Malaise, Myalgia
SMQs:, Rhabdomyolysis/myopathy (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (broad), Cardiomyopathy (broad), Eosinophilic pneumonia (broad), Arthritis (broad), Tendinopathies and ligament disorders (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? Yes
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: Lexapro, Wellbutrin, synthroid, elequis, ambien,acyclovir
Current Illness: Environmental stress?
Preexisting Conditions: Hypothyroid, depression, anxiety, insomnia, Covid19 3/2020- resulting in 2 Bliood clots in my leg , micro clots in my lungs, scattered bilateral opacities and pneumonia.
Allergies: Avelox,tizanadine, shellfish, eggs, peanut butter, mold, dogs,cats, dust and other misc environmental allergies.
Diagnostic Lab Data:
CDC Split Type:

Write-up: Cp initially that resolved in seconds. Then severe muscle aches, fatigue, temp 1 week,excruciating joint pain continues now. Malaise.

Result pages: 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 next

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Link To This Search Result:

https://www.medalerts.org/vaersdb/findfield.php?TABLE=ON&GROUP1=MAN&EVENTS=ON&PERPAGE=20&ESORT=VAX-DATE&VAX=COVID19&DISABLE=Yes&NUMDAYS=0

Copyright © 2021 National Vaccine Information Center. All rights reserved.
21525 Ridgetop Circle, Suite 100, Sterling, VA 20166

I just did - thanks for posting.

“ Write-up: My grandmother died a few hours after receiving the moderna covid vaccine booster 1. While I don?t expect that the events are related, the treating hospital did not acknowledge this and I wanted to be sure a report was made.”

“ Write-up: pt received vaccine at covid clinic on 12/30 at approximately 3:30, pt vomited 4 minutes after receiving shot—dark brown vomit, staff reported pt had vomited night before. Per staff report pt became short of breath between 6 and 7 pm that night. Pt had DNR on file. pt passed away at approximately 10pm. Staff reported pt was 14 + days post covid”

“ Age 99
Other Medications: Refused anything PO for about one week prior to death.
Current Illness: Refused food for one week prior to death.
Other Medications: Refused anything PO for about one week prior to death.
Current Illness: Refused food for one week prior to death.”

“ Current Illness: Resident was living in an assisted living facility. She fell on 11/24/2020 and was seen in the ER. There, she tested positive for COVID 19. She was admitted to this facility for rehab. She showed a decline after admission and was referred to hospice.
Preexisting Conditions: Vitamin deficiency, hyperlipidemia, hypertension, anemia, dementia, chronic kidney disease III, osteoporosis, history of breast cancer/MI/pulmonary embolism, depression.
Write-up: Resident received vaccine in am and expired that afternoon.“

“ Preexisting Conditions: ACUTE ON CHRONIC DIASTOLIC (CONGESTIVE) HEART FAILURE RHEUMATOID ARTHRITIS, UNSPECIFIED ANEMIA, UNSPECIFIED HYPOTHYROIDISM, UNSPECIFIED CACHEXIA ESSENTIAL (PRIMARY) HYPERTENSION DEMENTIA IN OTHER DISEASES CLASSIFIED ELSEWHERE WITHOUT BEHAVIORAL DISTURBANCE AGE-RELATED PHYSICAL DEBILITY OTHER CHRONIC PAIN DILATED CARDIOMYOPATHY ERYTHEMATOUS CONDITION, UNSPECIFIED UNSPECIFIED OSTEOARTHRITIS, UNSPECIFIED SITE PRIMARY GENERALIZED (OSTEO)ARTHRITIS OTHER SPONDYLOSIS WITH RADICULOPATHY, LUMBAR REGION HYPERKALEMIA OTHER INTERVERTEBRAL DISC DEGENERATION, LUMBAR REGION AGE-RELATED OSTEOPOROSIS WITHOUT CURRENT PATHOLOGICAL FRACTURE CERVICALGIA OTHER BIOMECHANICAL LESIONS OF LUMBAR REGION �� BILATERAL PRIMARY OSTEOARTHRITIS OF KNEE LOCALIZED EDEMA HYPO-OSMOLALITY AND HYPONATREMIA OTHER SPECIFIED DISORDERS OF BONE DENSITY AND STRUCTURE, UNSPECIFIED SITE HISTORY OF FALLING WEAKNESS”

Every single one of these need to be looked into no doubt.

But posting that the 99 year old that didn’t eat for a week prior to getting the vaccine is proof that the vaccine killed him might be a stretch...

“But posting that the 99 year old that didn’t eat for a week prior to getting the vaccine is proof that the vaccine killed him might be a stretch...”

I didn’t do that.

even though the CDC is withholding from VAERS more than 75% of the actual reports of adverse events it received for Covid vaccines.

And you know this, HOW, exactly?

I'm getting kind of exasperated by the "fun with numbers" that people seem to like doing on this. The official numbers don't match the doom and gloom scenario, so OF COURSE the "real" numbers (the ones the super secret evil bad guys aren't sharing with us!) are SO much worse! But of course, there's never any PROOF that these numbers truly ARE worse..we're supposed to trust that they are..cuz it's all a plot by the super secret evil shadowy bad guys to "depopulate the planet" (or something). OK..got it.

~~~~~~~~~~~~~~~~~~~~~

Oh, but I've been thoroughly sickened by the "deny everything" crowd who demands that the public believe experimental vaccines based on failed technology and never tested on people with co-morbidities, and only tested a few months at a time (no long-term studies) are as safe as, or safer than, those traditional vaccines from our childhood.

Most who ridicule me for posting about vaccine risks provide posts that are research and content-free and which instead rely on ad hominem attacks. Yesterday someone pretended to refute information I posted by whining that he doesn't consider videos of research valid and would only read said research in print. That works well - censorship is in full force so content ends up on personal blogs and is then ridiculed for not being present in traditional publications.

THIS IS WHY RISK IS CENSORED AND PURGED. The CDC closed ranks with big tech and the universities, publications which receive funding (and threats) and so it is the Lancet publishes fake news and quietly retracts it later, having falsely protected the CDC party line when it was needed most.

The first, and OBVIOUS, proof I offer is that an unprecedented number of deaths are occurring following Covid-19 vaccinations and the CDC says that there are ZERO deaths attributed to the Covid vaccines. The CDC is obviously lying, as it has lied every step of the way through this plandemic (lied about illness, lied about medications, lied about lockdowns, lied about masks etc.) This is your first hint that maybe there's more the CDC is not telling us.

COVID Vaccine Killing Huge Numbers, Warns Leading Doctor – Liberty Sentinel [32 minute video] (freerepublic.com)

Note that Dr. McCullough states that in the past, 25 deaths following vaccination would get a vaccine pulled from the market, yet Covid vaccines have over 4000 deaths in VAERS, and the CDC says there's nothing to see here...

In early April of 2021, only about 25% of reports that the CDC received either from family members or medical staff/institutions had been published to VAERS, so back then, a fair rule of thumb was to multiply counts of various adverse events recorded by a factor of 4 to guestimate approximate numbers. That information was based on a number cruncher following CDC reports of and I'll ping Cathi here to see if she has that link.

But since them the CDC has cut back on data entry, even as administration continued to increase. Some believe graphed data of reports versus vaccinations indicate that the CDC started throttling back reporting of adverse events starting January 9 (i.e., weekly updates on Fridays).

Bitchute user welcometheeagle88 has plotted the number of vaccinations delivered against the number of reports the CDC published to VAERS. Note that 51% of all records the CDC published for Covid-19 vaccinations thus far are dated December 2020 and January 2021. Vaccinations began mid-December so that's roughly 7 weeks of administration.

During December and January, 36 million doses of Covid 'vaccines' were administered. According to usafacts.org, as of yesterday 268,438,666 doses had been administered.

Then, in the last 94 days, another 232 million doses of the Covid 'vaccine' were administered, and which accounts for 49% of all reports for Covid vax now in VAERS. So using this method, as opposed to the method for which I am pinging Cathi, we can see that the CDC is not entering most of the records it has received.

VAERS 5/14/2021. Throttling data and even deleted 18 deaths from last week! Let's dive in. (bitchute.com)

In the graphs below, the blue line indicates elevated mortality after vaccination.

The full video has more charts from around the world: Impact of COVID Vaccinations on Mortality - YouTube

You're the one with the credibility problem. You can't demonstrate that these 'vaccines' are safe. You can quote the CDC and PHarma, but you can't prove they were tested adequately over co-morbidities and age ranges, long enough with large enough sample sizes. You can't prove the trials are valid given they used the PCR test with a 90%+ false positive rate.

Lies, Damned Lies and Health Statistics – the Deadly Danger of False Positives (freerepublic.com)

https://i.imgflip.com/57x2j2.jpg

You can't explain why, historically, 25 deaths would get a vaccine pulled but 4000 deaths are dismissed with an inadequate review unlike any previous review (see the first link I posted.) There's so much you can't demonstrate because these vaccines are not safe and in spite of all the censorship, the truth is leaking out.

The truth is not on your side so you start throwing 'conspiracy' because that's all you have - attack the messenger.

From the 5/7/2021 release of VAERS data:

Found 3,578 cases where Onset Interval is 0 and Vaccine is COVID19 and Serious

Case Details (Sorted by Vaccination Date)

This is page 178 out of 179

Result pages: prev 159 160 161 162 163 164 165 166 167 168 169 170 171 172 173 174 175 176 177 178 179 next

VAERS ID:	1288437 (history)
Form:	Version 2.0
Age:	30.0
Sex:	Female
Location:	Michigan

Vaccinated:	2021-04-16
Onset:	2021-04-16
Days after vaccination:	0
Submitted:	0000-00-00
Entered:	2021-05-05

Vaccination / Manufacturer	Lot / Dose	Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH	- / 1	LA / OT

Administered by: Unknown Purchased by: ?
Symptoms: Arthralgia, Asthenia, Fatigue, Headache, Insomnia, Myalgia, Oropharyngeal pain
SMQs:, Rhabdomyolysis/myopathy (broad), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Guillain-Barre syndrome (broad), Eosinophilic pneumonia (broad), Arthritis (broad), Tendinopathies and ligament disorders (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? Yes
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: CONCERTA; BUPROPION
Current Illness: Asthma
Preexisting Conditions: Medical History/Concurrent Conditions: Attention deficit disorder; COVID-19 (her brother had covid); Depression
Allergies:
Diagnostic Lab Data:
CDC Split Type: USPFIZER INC2021459172

Write-up: exhausted / Fatigue; she could hardly sleep; Mild sore throat; Headache; No energy; Myalgia; Arthralgia; This is a spontaneous report from a contactable physician. A 30-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE, Lot unknown, first dose) solution for injection intramuscular in the left arm on 16Apr2021 at 18:30 (at the age of 30-years-old) as a single dose for COVID-19 vaccination. Medical history included ongoing asthma, attention deficit disorder, and depression. Concomitant medications included ongoing methylphenidate hydrochloride (CONCERTA) for attention deficit hyperactivity disorder and ongoing bupropion for depression. Family history included brother had Covid. The patient did not receive any other vaccine within 4 weeks prior to the vaccine. On 16Apr2021, the patient developed headache (important medical event - IME), no energy (disability), myalgia (disability), arthralgia (IME), and mild sore throat. On 18Apr2021, she could hardly sleep and exhausted/fatigue (disability). The patient had no shortness of breath, even though she has asthma and it was not an anaphylactic reaction. The patient took TYLENOL for the events which helped somewhat but didn''t relieve it fully. It resolved as time passed. The outcome of the events headache, no energy, myalgia, arthralgia, mild sore throat was recovered on 18Apr2021. The outcome of the events could hardly sleep and exhausted/fatigue was recovered in Apr2021. Information on the lot/batch number has been requested.; Sender''s Comments: Based on chronological connection to the vaccine and known product safety profile, causality between reported events and BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE0 cannot be excluded. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to Regulatory Authorities, Ethics Committees and Investigators, as appropriate.

VAERS ID:	1241805 (history)
Form:	Version 2.0
Age:	45.0
Sex:	Male
Location:	Arizona

Vaccinated:	2021-04-17
Onset:	2021-04-17
Days after vaccination:	0
Submitted:	0000-00-00
Entered:	2021-04-22

Vaccination / Manufacturer	Lot / Dose	Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH	- / 1	LA / SYR

Administered by: School Purchased by: ?
Symptoms: Cyanosis, Death, Feeling abnormal, Headache, Vomiting
SMQs:, Anaphylactic reaction (broad), Acute pancreatitis (broad), Dementia (broad), Acute central respiratory depression (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Hypotonic-hyporesponsive episode (broad)

Life Threatening? No
Birth Defect? No
Died? Yes
Date died: 2021-04-18
Days after onset: 1
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: none
Current Illness: none
Preexisting Conditions: none
Allergies: none
Diagnostic Lab Data: Body examined by medical examiner, Case Number #2021-04116
CDC Split Type:

Write-up: Patient experienced a headache within 4 hours of vaccination. Took recommended dose of Tylenol. 4 hours after that (8 hours after vaccination) he was still experiencing extreme headache and also vomiting and took another dose of Tylenol. Was still feeling poor at 1am but coherent and talking, not thinking that it was serious enough to warrant going to hospital, as he believed it was just a bad headache and the vomiting was from the headache. At 6am, he was found blue/dead in his bed.

VAERS ID:	1278704 (history)
Form:	Version 2.0
Age:	26.0
Sex:	Male
Location:	Colorado

Vaccinated:	2021-04-17
Onset:	2021-04-17
Days after vaccination:	0
Submitted:	0000-00-00
Entered:	2021-05-01

Vaccination / Manufacturer	Lot / Dose	Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH	ER8735 / 1	RA / -

Administered by: Unknown Purchased by: ?
Symptoms: Memory impairment, Road traffic accident, Seizure
SMQs:, Systemic lupus erythematosus (broad), Dementia (broad), Convulsions (narrow), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Accidents and injuries (narrow), Depression (excl suicide and self injury) (broad), Generalised convulsive seizures following immunisation (narrow), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 1 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications: BUPROPION; EFFEXOR
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Penicillin allergy
Allergies:
Diagnostic Lab Data:
CDC Split Type: USPFIZER INC2021424222

Write-up: Seizure; crashed my car.; don''t remember 45 minutes of my life; This is a spontaneous report from a Contactable Consumer (patient). A 26-years-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), dose 1 via an unspecified route of administration, administered in Arm Right on 17Apr2021 13:15 (Batch/Lot Number: ER8735) as SINGLE DOSE for covid-19 immunisation at a vaccine facility, at 26 years old. Medical history included known allergies: Penicillin from an unknown date. No other vaccine in four weeks. Patient did not COVID prior vaccination and has not been tested for COVID post vaccination. Concomitant medication included bupropion; and venlafaxine hydrochloride (EFFEXOR) taken for an unspecified indication, start and stop date were not reported. Patient waited 15 minutes and felt normal. Patient stopped for gas and soda and then patient stated to be honest he woke up surprised with EMT, police and fire just telling him he started having a seizure and crashed his car on 17Apr2021 13:30. Patient stated "that''s craziest laser I don''t remember 45 minutes of my life (onset 17Apr2021). Thought I would be like 140. It was 3 pm which leave a large gap. This is really scary for me and my family". The events resulted in emergency room visit for seizure and crashed his car. The patient was hospitalized for seizure and for crashed his car for 1 day. Therapeutic measures were taken as a result of seizure and crashed my car (Some things to regulate my heart rhythm). Outcome of the events seizure and crashed his car was not recovered while unknown for don''t remember 45 minutes of his life.

VAERS ID:	1237511 (history)
Form:	Version 2.0
Age:	68.0
Sex:	Male
Location:	New York

Vaccinated:	2021-04-18
Onset:	2021-04-18
Days after vaccination:	0
Submitted:	0000-00-00
Entered:	2021-04-21

Vaccination / Manufacturer	Lot / Dose	Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA	039B21A / 2	UN / IM

Administered by: Private Purchased by: ?
Symptoms: Anticoagulant therapy, Asthenia, Breath sounds abnormal, Cardiac arrest, Chest X-ray abnormal, Computerised tomogram head normal, Endotracheal intubation, Lung opacity, Pneumonia aspiration, Therapeutic hypothermia, Unresponsive to stimuli, Vomiting
SMQs:, Torsade de pointes/QT prolongation (broad), Anaphylactic reaction (broad), Acute pancreatitis (broad), Angioedema (broad), Hyperglycaemia/new onset diabetes mellitus (broad), Interstitial lung disease (narrow), Neuroleptic malignant syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Shock-associated circulatory or cardiac conditions (excl torsade de pointes) (narrow), Acute central respiratory depression (narrow), Guillain-Barre syndrome (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Cardiomyopathy (broad), Eosinophilic pneumonia (broad), Hypotonic-hyporesponsive episode (broad), Respiratory failure (narrow), Hypoglycaemia (broad), Infective pneumonia (broad)

Life Threatening? No
Birth Defect? No
Died? Yes
   Date died: 2021-04-20
   Days after onset: 2
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 2 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: Allopurinol 300mg tablet, amiodarone 200mg tablet, aspirin 81mg tablet, atorvastatin 40mg tablet, carvedilol 12.5mg tablet, clopidogrel 75mg tablet, folic acid 1mg, Levemir, Humalog, losartan-HCTZ 100/25mg tablet, omeprazole 40mg capsule, p
Current Illness:
Preexisting Conditions: Diabetes Mellitus Type 2, ICD Pacemaker, Renal disorder, gout
Allergies: Unable to assess at the time of hospitalization
Diagnostic Lab Data: CT Head done - no acute findings suggestive of stroke, hemorrhage Chest XRay showed Bilateral R$gL opacities and lung sounds coarse
CDC Split Type:

Write-up: Patient brought in by ambulance after cardiac arrest witnessed by patient''s wife at 4/19/21 1:37AM. Per ED, the wife reports he had complained of feeling weak over the last few days without clear reason, then this morning patient had episode of emesis after which he told wife to call 911 and then suddenly became unresponsive. In ED was intubated, started on hypothermia protocol, Patient sedated on Propofol and started on a heparin drip, clopidogrel, aspirin and empiric antibiotics for aspiration Pneumonia

VAERS ID:	1254026 (history)
Form:	Version 2.0
Age:	57.0
Sex:	Female
Location:	Unknown

Vaccinated:	2021-04-18
Onset:	2021-04-18
Days after vaccination:	0
Submitted:	0000-00-00
Entered:	2021-04-24

Vaccination / Manufacturer	Lot / Dose	Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA	042B21-2A / 1	- / OT

Administered by: Unknown Purchased by: ?
Symptoms: Chest pain, Swelling face, Swollen tongue
SMQs:, Anaphylactic reaction (narrow), Angioedema (narrow), Oropharyngeal allergic conditions (narrow), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Gastrointestinal nonspecific symptoms and therapeutic procedures (broad), Cardiomyopathy (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, ? days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: USMODERNATX, INC.MOD20210

Write-up: Tongue swelling; Face swelling; Chest pains left side of chest; This spontaneous case was reported by an other health care professional (subsequently medically confirmed) and describes the occurrence of SWOLLEN TONGUE (Tongue swelling) and SWELLING FACE (Face swelling) in a 57-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 042B21-2A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 18-Apr-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 18-Apr-2021, the patient experienced SWOLLEN TONGUE (Tongue swelling) (seriousness criterion hospitalization), SWELLING FACE (Face swelling) (seriousness criterion hospitalization) and CHEST PAIN (Chest pains left side of chest). At the time of the report, SWOLLEN TONGUE (Tongue swelling), SWELLING FACE (Face swelling) and CHEST PAIN (Chest pains left side of chest) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. Concomitant product use was not provided. Treatment included Benadryl IM and Steroid IV. Based on the current available information and temporal association between the use of the product and the start date of the events, a causal relationship cannot be excluded.; Sender''s Comments: Based on the current available information and temporal association between the use of the product and the start date of the events, a causal relationship cannot be excluded.

VAERS ID:	1284755 (history)
Form:	Version 2.0
Age:	49.0
Sex:	Female
Location:	New York

Vaccinated:	2021-04-18
Onset:	2021-04-18
Days after vaccination:	0
Submitted:	0000-00-00
Entered:	2021-05-04

Vaccination / Manufacturer	Lot / Dose	Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH	EW0161 / 1	LA / -

Administered by: Unknown Purchased by: ?
Symptoms: Blood pressure measurement, Body temperature increased, Chest discomfort, Dizziness, Dyspnoea, Heart rate, Hypertension, Musculoskeletal stiffness, Oropharyngeal discomfort, Palpitations, SARS-CoV-2 test
SMQs:, Anaphylactic reaction (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Dystonia (broad), Parkinson-like events (broad), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Noninfectious encephalitis (broad), Noninfectious meningitis (broad), Hypertension (narrow), Cardiomyopathy (broad), Vestibular disorders (broad), Arthritis (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), COVID-19 (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 1 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications: METOPROLOL; TYLENOL
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: COVID-19; Hypertension
Allergies:
Diagnostic Lab Data: Test Date: 20210418; Test Name: blood pressure; Result Unstructured Data: Test Result:high blood pressure around 180/123 mmHg; Test Date: 20210418; Test Name: heart palpitations; Result Unstructured Data: Test Result:rapid; Test Date: 20210109; Test Name: COVID; Test Result: Positive
CDC Split Type: USPFIZER INC2021432028

Write-up: light headed; heat inside her left arm then her chest; heart palpitations rapid; high blood pressure around 180/123mmhg; Neck stiffness; throat becoming stiff; Very difficult breathing; tightness in her chest; This is a spontaneous report from a contactable other health professional (patient). A 49-year-old female patient (not pregnant) received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EW0161), via an unspecified route of administration, administered in left arm on 18Apr2021 11:45 am (at 49-year-old, not pregnant at the time of vaccination) at single dose for COVID-19 immunisation. Medical history included hypertension, Covid-19 from 09Jan2021. Tested positive for COVID on 09Jan2021 and have antibodies after infection. Patient took vaccine under 100 days after COVID infection. No known allergies. Concomitant medications included metoprolol; paracetamol (TYLENOL extra strength), and multi vitamin. No other vaccine in four weeks. On 18Apr2021 11:52 (reported as 7 minutes after BNT162B2 1st dose), the patient experienced light headed, heat inside her left arm then her chest, tightness in her chest, felt heart palpitations rapid, high blood pressure around 180/123 mmhg. Neck stiffness and throat becoming stiff. Very difficult breathing after all symptoms were present. The events resulted in emergency room/department or urgent care, hospitalization. The days of hospitalization was 1 day. Therapeutic measures were taken as a result of the events, which included aspirin/ 2 bags of 1000 ml Sodium chloride. The outcome of the events was recovering. No COVID tested post vaccination.; Sender''s Comments: Based on the current available information and the plausible drug-event temporal association, a possible contributory role of the suspect product BNT162B2 to the development of reported events cannot be excluded. The case will be reassessed if additional information becomes available. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to Regulatory Authorities, Ethics Committees and Investigators, as appropriate.

VAERS ID:	1243311 (history)
Form:	Version 2.0
Age:	68.0
Sex:	Female
Location:	Pennsylvania

Vaccinated:	2021-04-19
Onset:	2021-04-19
Days after vaccination:	0
Submitted:	0000-00-00
Entered:	2021-04-22

Vaccination / Manufacturer	Lot / Dose	Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA	046B21A / 2	RA / IM

Administered by: Other Purchased by: ?
Symptoms: Death, Depressed level of consciousness, Fatigue, Unresponsive to stimuli
SMQs:, Hyperglycaemia/new onset diabetes mellitus (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Guillain-Barre syndrome (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Hypotonic-hyporesponsive episode (broad), Generalised convulsive seizures following immunisation (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? Yes
   Date died: 2021-04-21
   Days after onset: 2
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, 1 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: Arthritis, DM Type II, ESRD on dialysis, hypertension, hyperlipidemia, Obesity, sleep apnea, stroke, Valvular disease
Allergies: Latex
Diagnostic Lab Data:
CDC Split Type:

Write-up: PER hospital note: Patient received Covid-19 vaccine on Monday (4/19/21), since then has been feeling fatigued. Per patients husband she was difficult to arouse this morning (4/21/21) and ultimately unresponsive. Patient was transported to hospital via EMS (4/21/21)where she expired a short time later.

VAERS ID:	1291274 (history)
Form:	Version 2.0
Age:	54.0
Sex:	Female
Location:	New Jersey

Vaccinated:	2021-04-19
Onset:	2021-04-19
Days after vaccination:	0
Submitted:	0000-00-00
Entered:	2021-05-05

Vaccination / Manufacturer	Lot / Dose	Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH	EW0162 / 2	RA / -

Administered by: Private Purchased by: ?
Symptoms: Hypersensitivity, SARS-CoV-2 test
SMQs:, Angioedema (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), COVID-19 (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 1 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Autoimmune disorder; Food allergy
Allergies:
Diagnostic Lab Data: Test Date: 20210419; Test Name: Nasal Swab; Test Result: Negative
CDC Split Type: USPFIZER INC2021442629

Write-up: Severe allergic reaction; This is a spontaneous report from a contactable consumer (patient). A 54-year-old female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection; Lot Number: EW0162) via an unspecified route of administration, administered in Arm Right, at the age of 54-year-old, on 19Apr2021 11:45, as SINGLE DOSE for covid-19 immunisation. Medical history included Auto Immune Mixed Connective Tissue Disease and allergies to sesame seeds. The patient is not pregnant at the time of vaccination. There were no concomitant medications. The patient previously took codeine and experienced drug hypersensitivity and first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection; lot Number ER8727) via an unspecified route of administration, administered in Arm Right, at the age of 54-year-old on 29Mar2021 11:30, as SINGLE DOSE for covid-19 immunisation. There are no other vaccines received in four weeks and no other medications in two weeks. On 19Apr2021 12:00 PM, the patient experienced severe allergic reaction requiring ambulance to er hospital and administration of epipen injection, IV steroids, antihistamines and histamine blockers. The patient was admitted in the hospital in Apr2021 for 1 day. Covid test (nasal swab) on 19Apr2021 showed negative result. Outcome was recovering.

VAERS ID:	1238733 (history)
Form:	Version 2.0
Age:	61.0
Sex:	Female
Location:	Tennessee

Vaccinated:	2021-04-20
Onset:	2021-04-20
Days after vaccination:	0
Submitted:	0000-00-00
Entered:	2021-04-21

Vaccination / Manufacturer	Lot / Dose	Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA	004M20A / 1	RA / IM

Administered by: Senior Living Purchased by: ?
Symptoms: Cardio-respiratory arrest, Death, Posture abnormal
SMQs:, Torsade de pointes/QT prolongation (broad), Anaphylactic reaction (broad), Arrhythmia related investigations, signs and symptoms (broad), Shock-associated circulatory or cardiac conditions (excl torsade de pointes) (narrow), Dystonia (broad), Acute central respiratory depression (broad), Respiratory failure (broad)

Life Threatening? No
Birth Defect? No
Died? Yes
Date died: 2021-04-20
Days after onset: 0
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Resident was found kneeling over walker with face down in the bathtub right before 1700. Code called and initiated. Resident pronounced dead at 1721 by EMS.

VAERS ID:	1266071 (history)
Form:	Version 2.0
Age:	74.0
Sex:	Female
Location:	Pennsylvania

Vaccinated:	2021-04-20
Onset:	2021-04-20
Days after vaccination:	0
Submitted:	0000-00-00
Entered:	2021-04-28

Vaccination / Manufacturer	Lot / Dose	Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH	- / 2	- / -

Administered by: Unknown Purchased by: ?
Symptoms: Cardiac arrest, Circulatory collapse, Heart rate, Pulseless electrical activity, Unresponsive to stimuli
SMQs:, Torsade de pointes/QT prolongation (broad), Anaphylactic reaction (narrow), Hyperglycaemia/new onset diabetes mellitus (broad), Neuroleptic malignant syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Shock-associated circulatory or cardiac conditions (excl torsade de pointes) (narrow), Torsade de pointes, shock-associated conditions (narrow), Hypovolaemic shock conditions (narrow), Toxic-septic shock conditions (narrow), Anaphylactic/anaphylactoid shock conditions (narrow), Hypoglycaemic and neurogenic shock conditions (narrow), Acute central respiratory depression (broad), Guillain-Barre syndrome (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Cardiomyopathy (broad), Cardiac arrhythmia terms, nonspecific (narrow), Hypotonic-hyporesponsive episode (broad), Hypersensitivity (narrow), Respiratory failure (broad), Hypoglycaemia (broad)

Life Threatening? Yes
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 2 days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Acute respiratory failure; Cardiac arrest; Diabetes; Hypoxia; Transaminitis
Allergies:
Diagnostic Lab Data: Test Name: initial rhythm; Result Unstructured Data: Test Result:PEA
CDC Split Type: USPFIZER INC2021448526

Write-up: post-cardiac arrest; collapsed; initial rhythm was PEA; unresponsive; This is a spontaneous report received from a contactable pharmacist. A 74-year-old female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number unknown), on 20Apr2021 (at the age of 74-year-old) at single dose for COVID-19 immunisation. It was reported that patient was not pregnant. Facility type vaccine was reported as unknown. The patient''s medical history included acute respiratory failure with hypoxia, cardiac arrest, transaminitis, and diabetes. It was unknown if patient had COVID prior vaccination. The patient''s concomitant medications were not reported. It was unknown if patient received other medications in two weeks and if she received any other vaccine in four weeks. The patient previously received first dose of BNT162B2 on unspecified date at single dose for COVID-19 immunisation, lisinopril and hydrochlorothiazide/triamterene (DYAZIDE) both reported as known allergies. It was reported that patient was brought in by emergency medical services (EMS) status post-cardiac arrest. Per EMS she was driving to urgent care (unclear why). She just got her second Pfizer vaccine. At urgent care she collapsed and cardiopulmonary resuscitation (CPR) was initiated immediately. EMS arrived and her initial rhythm was pulseless electrical activity (PEA). They placed a gel and administered 3 rounds of CPR with 3 onset epinephrine. No shockable rhythm. Patient arrived at hospital intubated and unresponsive on 20Apr2021. Duration of hospitalization was reported as two days. The events were reported as serious with criteria hospitalization and life-threatening illness (immediate risk of death from the event). The events resulted in doctor or other healthcare professional office/clinic visit and emergency room/department or urgent care. It was unknown if patient was tested for COVID post-vaccination. The outcome of the events was resolving Information on lot number/batch number has been requested.; Sender''s Comments: The reported events would seem unlikely related to suspect vaccine BNT162B2, but more likely due to underlying cardiovascular morbidities. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to Regulatory Authorities, Ethics Committees and Investigators, as appropriate.

VAERS ID:	1237552 (history)
Form:	Version 2.0
Age:	39.0
Sex:	Female
Location:	Alabama

Vaccinated:	2021-04-21
Onset:	2021-04-21
Days after vaccination:	0
Submitted:	0000-00-00
Entered:	2021-04-21

Vaccination / Manufacturer	Lot / Dose	Site / Route
COVID19: COVID19 (COVID19 (JANSSEN)) / JANSSEN	041A21A / 1	LA / IM

Administered by: Other Purchased by: ?
Symptoms: Dyspnoea, Muscle spasms
SMQs:, Anaphylactic reaction (broad), Dystonia (broad), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Cardiomyopathy (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, ? days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patient C/O shortness of Breath and cramping in lower extremities on 4/14/21. She was sent to local ER for evaluation and was admitted for observation.

VAERS ID:	1268044 (history)
Form:	Version 2.0
Age:	68.0
Sex:	Male
Location:	Tennessee

Vaccinated:	2021-04-21
Onset:	2021-04-21
Days after vaccination:	0
Submitted:	0000-00-00
Entered:	2021-04-28

Vaccination / Manufacturer	Lot / Dose	Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA	044B21A / 2	RA / IM

Administered by: Other Purchased by: ?
Symptoms: Death, Unresponsive to stimuli
SMQs:, Hyperglycaemia/new onset diabetes mellitus (broad), Neuroleptic malignant syndrome (broad), Guillain-Barre syndrome (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Hypotonic-hyporesponsive episode (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? Yes
Date died: 2021-04-21
Days after onset: 0
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: ESRD,o Diabeteso Non ST Elevation Myocardial Infarction o Rheumatic Mitral Valve Insufficiency
Allergies: Hydralazine and Betadine
Diagnostic Lab Data:
CDC Split Type:

Write-up: Clinic was informed that patient patient went unresponsive at home at 2pm on 4/21/21 and patient expired.

VAERS ID:	1242950 (history)
Form:	Version 2.0
Age:	65.0
Sex:	Male
Location:	Michigan

Vaccinated:	2021-04-22
Onset:	2021-04-22
Days after vaccination:	0
Submitted:	0000-00-00
Entered:	2021-04-22

Vaccination / Manufacturer	Lot / Dose	Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA	025B21A / UNK	UN / UN

Administered by: Public Purchased by: ?
Symptoms: Blood test, Death
SMQs:

Life Threatening? No
Birth Defect? No
Died? Yes
Date died: 2021-04-22
Days after onset: 0
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Atorvastatin, Pantoprazole, Metoprolol, Lisinopril
Current Illness: unk
Preexisting Conditions: A-fib, HTN
Allergies: Penicillian
Diagnostic Lab Data: Blood draw done on decedent 04-22-2021
CDC Split Type:

Write-up: Receiver of vaccine was reported dead on 04-22-2021 TOD 0809 to Medical Examiner''s Office Report # 052-EMF-79-21

VAERS ID:	1246486 (history)
Form:	Version 2.0
Age:	53.0
Sex:	Male
Location:	Virginia

Vaccinated:	2021-04-22
Onset:	2021-04-22
Days after vaccination:	0
Submitted:	0000-00-00
Entered:	2021-04-23

Vaccination / Manufacturer	Lot / Dose	Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA	048B21A / 2	- / IM

Administered by: Work Purchased by: ?
Symptoms: Cardiac arrest, Cardiac assistance device user, Death, Dyspnoea, Endotracheal intubation, Malaise, Resuscitation, Vomiting
SMQs:, Torsade de pointes/QT prolongation (broad), Anaphylactic reaction (narrow), Acute pancreatitis (broad), Angioedema (broad), Arrhythmia related investigations, signs and symptoms (broad), Shock-associated circulatory or cardiac conditions (excl torsade de pointes) (narrow), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Cardiomyopathy (broad), Respiratory failure (broad)

Life Threatening? No
Birth Defect? No
Died? Yes
Date died: 2021-04-22
Days after onset: 0
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Unknown
Current Illness:
Preexisting Conditions: Hypertension
Allergies:
Diagnostic Lab Data: Unknown
CDC Split Type:

Write-up: Patient reported to onsite health clinic to see nurse at 1930. Complaints of not feeling well. Vomited then dyspnea. Went into cardiac arrest, AED used x1. EMS called at 1945. CPR, intubation until 2055. Time of death 2055.

VAERS ID:	1262166 (history)
Form:	Version 2.0
Age:	82.0
Sex:	Female
Location:	California

Vaccinated:	2021-04-22
Onset:	2021-04-22
Days after vaccination:	0
Submitted:	0000-00-00
Entered:	2021-04-27

Vaccination / Manufacturer	Lot / Dose	Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH	ER8735 / 2	LA / IM

Administered by: Private Purchased by: ?
Symptoms: Cardiac arrest, Fall, Pain, Restlessness
SMQs:, Torsade de pointes/QT prolongation (broad), Anaphylactic reaction (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Shock-associated circulatory or cardiac conditions (excl torsade de pointes) (narrow), Dementia (broad), Akathisia (broad), Acute central respiratory depression (broad), Noninfectious encephalopathy/delirium (broad), Accidents and injuries (narrow), Cardiomyopathy (broad), Respiratory failure (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? Yes
Date died: 0000-00-00
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Losartan, HCTZ
Current Illness:
Preexisting Conditions: Acute resp. failure with hypoxia, Stage 4 CKD, Renal artery stenosis, Dyspnea on exertion, obesity, palpitations, Gout
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: was fine until Thursday evening 4/22/2021. Started feeling body aches and restless. Friday morniing 4/23/2021. She woke up and went to the bathroom. Go out and fell and went into cardiac arrest. #12: GAD, Fibromyalgia, migraine, ventral hernia, hypothyroid, hypercholesterolemia, neuropathy, Hx of Covid-19

VAERS ID:	1267795 (history)
Form:	Version 2.0
Age:	63.0
Sex:	Male
Location:	Nevada

Vaccinated:	2021-04-22
Onset:	2021-04-22
Days after vaccination:	0
Submitted:	0000-00-00
Entered:	2021-04-28

Vaccination / Manufacturer	Lot / Dose	Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH	- / 1	- / IM

Administered by: Other Purchased by: ?
Symptoms: Asthenia, Lethargy
SMQs:, Guillain-Barre syndrome (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? Yes
Date died: 2021-04-27
Days after onset: 5
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Levothyroxine; Metformin
Current Illness: After receiving the vaccine, the decedent complained of extreme weakness and lethargy.
Preexisting Conditions: Liver Disease; Diabetes; Neuropathy; Degenerative Hip Disease; Chronic Back pain; cholecystectomy
Allergies: Unknown
Diagnostic Lab Data: Refused medical attention
CDC Split Type:

Write-up: After receiving the initial dose, the decedent had complaints of extreme weakness and lethargy.

VAERS ID:	1260018 (history)
Form:	Version 2.0
Age:	50.0
Sex:	Male
Location:	Florida

Vaccinated:	2021-04-23
Onset:	2021-04-23
Days after vaccination:	0
Submitted:	0000-00-00
Entered:	2021-04-26

Vaccination / Manufacturer	Lot / Dose	Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA	018B21A / 1	LA / IM

Administered by: Pharmacy Purchased by: ?
Symptoms: Death, Hyperhidrosis, Hypopnoea, Unresponsive to stimuli
SMQs:, Hyperglycaemia/new onset diabetes mellitus (broad), Neuroleptic malignant syndrome (broad), Acute central respiratory depression (narrow), Guillain-Barre syndrome (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Hypotonic-hyporesponsive episode (broad), Respiratory failure (narrow), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? Yes
Date died: 2021-04-01
Days after onset: 22
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: n/a
Current Illness: n/a
Preexisting Conditions: n/a
Allergies: n/a
Diagnostic Lab Data: n/a
CDC Split Type:

Write-up: Was sweaty, unresponsive, and breathing shallow a few mins after administration. BP 97/68. Within a few mins, patient became responsive and BP 146/81. Patient chose not to go with EMS and walked out of store after they were feeling better. Today (3 days later) received report from medical examiner that patient passed away.

VAERS ID:	1264249 (history)
Form:	Version 2.0
Age:	68.0
Sex:	Female
Location:	New York

Vaccinated:	2021-04-23
Onset:	2021-04-23
Days after vaccination:	0
Submitted:	0000-00-00
Entered:	2021-04-27

Vaccination / Manufacturer	Lot / Dose	Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH	EW0171 / 2	RA / IM

Administered by: Senior Living Purchased by: ?
Symptoms: Chills, Dizziness, Dyspnoea
SMQs:, Anaphylactic reaction (broad), Anticholinergic syndrome (broad), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Cardiomyopathy (broad), Vestibular disorders (broad)

Life Threatening? No
Birth Defect? No
Died? Yes
   Date died: 2021-04-25
   Days after onset: 2
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, ? days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: chills, dizziness. shortness of breath developed a few hours later .

VAERS ID:	1269772 (history)
Form:	Version 2.0
Age:	43.0
Sex:	Male
Location:	Wisconsin

Vaccinated:	2021-04-23
Onset:	2021-04-23
Days after vaccination:	0
Submitted:	0000-00-00
Entered:	2021-04-29

Vaccination / Manufacturer	Lot / Dose	Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH	EW0169 / 2	LA / OT

Administered by: Private Purchased by: ?
Symptoms: Arrhythmia, Body temperature, Cardiac arrest, Computerised tomogram head, Echocardiogram, Electrocardiogram, Exercise electrocardiogram abnormal, Fall, Investigation, Pyrexia, SARS-CoV-2 test, Seizure, Troponin
SMQs:, Torsade de pointes/QT prolongation (broad), Anaphylactic reaction (broad), Neuroleptic malignant syndrome (broad), Systemic lupus erythematosus (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Shock-associated circulatory or cardiac conditions (excl torsade de pointes) (narrow), Convulsions (narrow), Acute central respiratory depression (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Accidents and injuries (narrow), Cardiomyopathy (broad), Cardiac arrhythmia terms, nonspecific (narrow), Other ischaemic heart disease (broad), Generalised convulsive seizures following immunisation (narrow), Respiratory failure (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad), COVID-19 (broad)

Life Threatening? Yes
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, ? days
Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Obstructive sleep apnea syndrome; Peanut allergy; Sneezing
Allergies:
Diagnostic Lab Data: Test Date: 20210423; Test Name: Febrile; Result Unstructured Data: Test Result:38+; Comments: on arrival requiring active cooling measures to maintain normothermia; Test Date: 20210423; Test Name: CT of head; Test Result: Negative ; Comments: for acute intracranial process; Test Date: 20210423; Test Name: Transthoracic echo; Result Unstructured Data: Test Result:Without regional wall abnormalities; Comments: or significant findings; Test Date: 20210423; Test Name: EKG; Result Unstructured Data: Test Result:without ischemic changes, arrhythmia; Test Date: 20210423; Test Name: Rhythm; Result Unstructured Data: Test Result:PEA; Test Date: 20210423; Test Name: PCR; Test Result: Negative ; Comments: Nasal Swab; Test Date: 20210423; Test Name: Troponin; Result Unstructured Data: Test Result:12
CDC Split Type: USPFIZER INC2021458331

Write-up: Seizure; Cardiac arrest; Arrhythmia; Began convulsing and then tipped over; Began convulsing and then tipped over; 12 lead EKG without ischemic changes, arrhythmia; Febrile 38+; This is a spontaneous report from a contactable other HCP. A 43-years-old male patient received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot Number: EW0169) via intramuscular route in arm left on 23Apr2021 at 12:45 as single dose for covid-19 immunisation. Historical Vaccine included first dose of bnt162b2 (Lot Number: EW0150) via intramuscular, administered in arm left on 02Apr2021at 14:15 for covid-19 immunisation. Medical history included obstructive sleep apnea, food allergy and intolerant of peanuts-causes sneezing and there were no concomitant medications. On 23Apr2021 at 18:30 the patient experienced a seizure resulting in cardiac arrest. Witnesses described patient began convulsing and then tipped over. AED applied with no shock advised. Unknown down time prior to initiation of CPR. Rhythm PEA upon arrival of EMS. 7 mins CPR before ROSC obtained. Initial Troponin 12. 12 lead EKG without ischemic changes, arrhythmia, etc. Transthoracic echo without regional wall abnormalities or significant findings. CT of head negative for acute intracranial process. No history of seizure, cardiac issues, drug use, etc. Intubated and sedated. Febrile 38+ on arrival requiring active cooling measures to maintain normothermia. The case classified as serious emergency room/department or urgent care, Hospitalization, Life threatening illness (immediate risk of death from the event). On 23Apr2021, the patient underwent lab tests and procedures which included body temperature: 38+ on arrival requiring active cooling measures to maintain normothermia, computerised tomogram head: negative for acute intracranial process, echocardiogram: without regional wall abnormalities or significant findings, electrocardiogram: without ischemic changes, arrhythmia, investigation: pea, sars-cov-2 test: negative Nasal Swab and troponin: 12. Treatment received included multiple life support measures, treatment for seizures, etc. No covid prior vaccination. Patient had covid tested post vaccination. No other vaccine in four weeks. The outcome of the events was not recovered.; Sender''s Comments: Based on strong temporal association the causal association between the reported events seizure, cardiac arrest, arrhythmia, began convulsing and then tipped over, febrile 38+ and the usage of the vaccine are considered related. The case will be reassessed once new information is available. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to regulatory authorities, Ethics Committees, and Investigators, as appropriate.

VAERS ID:	1270749 (history)
Form:	Version 2.0
Age:	50.0
Sex:	Male
Location:	Florida

Vaccinated:	2021-04-23
Onset:	2021-04-23
Days after vaccination:	0
Submitted:	0000-00-00
Entered:	2021-04-29

Vaccination / Manufacturer	Lot / Dose	Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA	018B21A / 1	LA / IM

Administered by: Pharmacy Purchased by: ?
Symptoms: Arteriosclerosis coronary artery, Autopsy, Cold sweat, Coronary artery occlusion, Death, Dyspnoea, Hypotension, Paraesthesia
SMQs:, Anaphylactic reaction (narrow), Peripheral neuropathy (broad), Neuroleptic malignant syndrome (broad), Myocardial infarction (narrow), Embolic and thrombotic events, arterial (narrow), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Guillain-Barre syndrome (broad), Cardiomyopathy (broad), Other ischaemic heart disease (narrow), Hypoglycaemia (broad), Dehydration (broad), Hypokalaemia (broad)

Life Threatening? No
Birth Defect? No
Died? Yes
Date died: 2021-04-24
Days after onset: 1
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: SWEET DREAMS NEUROSLEEP, DREAM WATER, & NATURAL VITALITY CALM
Current Illness: NONE
Preexisting Conditions: ALCOHOLISM (CIRRHOSIS), HTN, TOBACCO ABUSE, ASHD
Allergies: UNKNOWN CATERPILLAR (ANIMAL)
Diagnostic Lab Data: MEDICAL EXAMINER AUTOPSY - MARKED ATHEROSCLEROSIS OF CORONARY ARTERIES WITH ACUTE OCCLUSION OF THE LAD
CDC Split Type:

Write-up: HYPOTENSION (SARASOTA EMS RESPONDED TO PHARMACY); CLAMMY/SOB, EXTREMITY TINGLES; DEATH WITHIN 6-7 HRS

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https://www.medalerts.org/vaersdb/findfield.php?EVENTS=ON&PAGENO=178&PERPAGE=20&ESORT=VAX-DATE&VAX=COVID19&SERIOUS=ON&NUMDAYS=0

By now anyone who doesn’t know that claims based on VAERS reports are BOGUS is beyond hope. Everyone knows, as you know, that the reports can't be used that way.

Assumptions from them are just not possible.

“We’re at a little over 66% now so should reach 70% in a week or so.”

On tomorrow’s report, the USA should hit 60% of adults having had a first shot.

So Maryland is ahead of the curve.

This is the endgame, finally.

I can tell you a lot about the pressure. First there's the lawyers for the assisted living making sure every resident has someone to sign for them. Second, the Mass governor sending the national guard on shot day back in Jan. when everyone gets them all at the same time (and three weeks later in Feb).

Lots of people got shots who were in no shape to withstand it, that day, or any other day.

what a waste of time you are

You could be honest and put that notice on your posts about VAERS.
Or the notice at the site.

what a waste of time you are

What I tell you about arguing with retarded kids.

Brilliant post as usual.

Imagine that the CDC, NIH, FDA and any other relevant health authorities had proposed a plan for therapeutic treatment of cv19 starting last May, when Dr. Pierre Kory said that his team already had the MATH+ protocol (as I understand it, also a protocol used for sepsis). Imagine they had been reasonable, and avoided fearmongering. People would have been more accepting of their recommendations going forward. Of course...the vaccine would no longer have been needed, as we would have been out of the plandemic in a couple months. But it would have been nice to now that we could at least trust that our authorities were looking out for us, and not for the interests of parties known and unknown.

As it stands right now, the people calling the shots on matters of health worldwide appear to be about as benevolent as SPECTRE...

...appear to be about as benevolent as SPECTRE...

Its much worse than that.

Its KAOS.