Posted on 05/16/2021 3:36:19 PM PDT by BeauBo
(President Trump's Operation Warp Speed Update)
(A bigger uptick in first shots today - second day in a row - May be a noteworthy change)
Total Vaccine Doses Delivered: 344,503,395 (20,195,100 J&J)
Administered: 273,545,207 (9,654,031 J&J)
People Vaccinated, At Least One Dose: 157,485,596
Fully Vaccinated: 123,282,685
(Excerpt) Read more at covid.cdc.gov ...
That’s what I’m doing.
I think the safety data is more clear. I read thousands of VAERS reports starting a month ago when I found out about it. At first I was concerned and I posted about that. But after someone pointed out the comparable populations it was clear there was a lot of coincidence and low quality reporting in VAERS (leaving out medical history). I don't think the vaccines are as safe as most others, e.g. flu. That should not be a surprise to anyone.
As for COVID, it's killing 1% of known cases, vaccinated or not. Fortunately breakthrough cases are rare with about 20k acknowledged and perhaps 2-3 times more untested and hidden. The toll from COVID was a majority of the excess deaths last year (about 500k excess). Hard to break it down further because there were serious consequences to shutdowns and deferred healthcare.
National Vaccine Information Center Your Health. Your Family. Your Choice. | MedAlerts Home |
Case Details (Sorted by Vaccination Date) |
Administered by: Unknown Purchased by: ? |
Life Threatening? No
Birth Defect? No
Died? Yes
Date died: 2021-04-26
Days after onset: 0
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: Unknown
Current Illness: None
Preexisting Conditions: Hypertension Atrial fibrillation with two prior ablations
Allergies: None
Diagnostic Lab Data: See above -cardiac catheterization
CDC Split Type:
Write-up: Patient (per family member) received 1st dose of Pfizer COVID vaccine on 4/24/2021. On 4/26/2021 at 6 AM patient presented to hospital with chest pain for 2 hours. EKG showed inferior ST segment elevation myocardial infarction (a "heart attack") and the patient was brought emergently for cardiac catheterization. Catheterization showed an occluded right coronary artery, and angioplasty/stenting was performed. Following brief restoration of blood flow to the heart, the artery re-occluded and the patient arrested. After 90 minutes of CPR, the patient expired.
Administered by: Pharmacy Purchased by: ? Life Threatening? No Write-up: Shortness of Breath Fever Body Pains - Shoulder, Hand pain | |||||||||||||||||
Administered by: Other Purchased by: ? Life Threatening? No Write-up: Cough and diarrhea the day after receiving vaccine. The next day, had difficulty breathing and collapsed. | |||||||||||||||||
Administered by: Private Purchased by: ? Life Threatening? No Write-up: Patient collapsed and became unresponsive 24 hours after receiving second dose of vaccine. | |||||||||||||||||
Administered by: Public Purchased by: ? Life Threatening? No Write-up: The decedent was found in her bedroom by her daughter. Medical history only includes previous blood clots. Decedent has been complaining of coughing and shortness of breath the past few days. There is no history of drug use. The decedent had a foam cone when found. | |||||||||||||||||
Administered by: Private Purchased by: ? Life Threatening? No Write-up: Patient suffered a seizure and pulmonary edema four days after receiving second Pfizer shot. He was pronounced dead several hours later. Patient had no health issues and was 45 years old. | |||||||||||||||||
Administered by: Unknown Purchased by: ? Life Threatening? No Write-up: 80 yo woman with hx of HTN, anxiety dneies any other conditions, presented to ER due to epigastric pain, vomiting x1. In Er presented with elevated heart rate, EKG with sinus tachycardia, regular rythm. CXR with COPD changes. There are bibasilar infiltrates suspicious for pneumonitis in the appropriate clinical setting. PAtient admitted to unit for further treatment and workup. WBC 16.91 4/27/2021 | |||||||||||||||||
Administered by: Pharmacy Purchased by: ? Life Threatening? No Write-up: Neck pain and stiffness starting shortly after vaccine admin of 2nd dose | |||||||||||||||||
Administered by: Private Purchased by: ? Life Threatening? No Write-up: I was notified that patient passed away at Hospital 10:37 am today. Per message to medical office from Coroner, it was reported that patient collapsed this morning while walking his dog. Patient was brought in by ALS complaint of FULL ARREST to Hospital 10:10 am and pronounced at 10:37 am 4/24/2021 by Dr. at Hospital. | |||||||||||||||||
Administered by: Pharmacy Purchased by: ? Life Threatening? No Write-up: Family friend of the wife, called our pharmacy on 04/28/2021 and reported that wife''s appointment would need to be canceled for 04/29/2021 because her spouse passed away the previous night. This prompted our staff to look further and it was noted that her spouse, received his first Moderna vaccine on 4/26/2021 at our pharmacy. Friend was not reporting his death due to the belief that the injection was the cause. Only to report, so upcoming appointment for his wife could be canceled. It was reported to our Medical staff that Patient n has Chronic COPD and had difficulty breathing on the evening of 4/27/2021 and was taken to the hospital where he later passed away. Patient was on portable oxygen and resembled shortness of breath while ambulating at the time of his vaccination appointment on 4/26/2021. Patient immediately recovered from Shortness of Breath once seated in exam room for injection for a few minutes. | |||||||||||||||||
Administered by: Other Purchased by: ? Life Threatening? No Write-up: Death on April 28, 2021 1AM | |||||||||||||||||
Administered by: Private Purchased by: ? Life Threatening? No Write-up: Patient is a 80 y.o. male with significant PMHx of CAD, HTN, HLD, CKD who is admitted to ICU as a transfer from hospital for acute liver failure and cardiac arrest. Pt presented to hospital on 04/28 w/ complaints of nausea and vomiting. He stated that he had recently gotten his COVID vaccine. Pt was found to be in acute liver failure in the ED w/ AST and ALT $g 1000. Lactate $g 15.0. BMP showed AKI on CKD and BG $g500. Pt did have cardiac arrest while undergoing CT Scan and ROSC was achieved after CPR x 20 mins. Pt was hence transferred to the ICU for higher level management and admitted for cardiac arrest and acute liver failure. Upon arrival, Pt was intubated and sedated. He was non-responsive to verbal and physical stimuli. Pt was acidotic. ABG: 6.99 / 28 / 165 / 7. 1 amp of HCO3 was given upon arrival. Pt was started on insulin gtt for DKA and was started on Levophed for low BP. Pt underwent cardiac arrest shortly after arrival to the ICU. CPR was performed for $g 20 mins without ROSC. Family arrived at bedside and decision was made to stop CPR at 0205 on 04/29/2021. | |||||||||||||||||
Administered by: Other Purchased by: ? Life Threatening? No Write-up: This was a 58 year old female who received her 1st dose Pfizer on 4/6/21 (Lot# EW0175) and 2nd dose Pfizer on 4/27/21 (Lot# EW0151). Of note, the patient was in a motor vehicle accident on 4/12/21 with a diagnosis of concussion and cervical/thoracic strain/sprain (see history under patient information). On 4/29/21, the patient''s sister contacted the patient''s primary care clinic with the following documented concern: "Pt''s sister calling to report that two days ago pt got 2nd dose Pfizer vaccine and has been sick. This morning they found her passed out against the her bedroom door. Pt reports that she can''t remember much other than going to the bathroom. Pt''s sister states that patient totaled her car a week ago, and that it was determined she had a concussion. "She hasn''t been herself since the wreck and I am very concerned." This caller recommenced the Ed or UC but caller denied stating that either needs to see her today. This writer is reaching out to nurse to see if they can advise from here." A RN assessed the patient virtually with the following documentation: "RN note: Call transferred from patient''s sister. Pt noted to be found on her floor this morning. Pt unsure if she hit her head. Spoke to patient. She reports body aches, and feeling weak. Pt is slow to answer questions, and had a lot of difficulty hearing me (sister did not have any difficulty hearing me). Pt is noted to have more rapid breathing, and some slight wheezing. Speech is clear when she is speaking. Sister gave patient water to drink. She drank out of bottle and was able to hold on her own (though had difficulty with this at first). Sister noted some water dripping down face, but was able to swallow okay. Sister also noted that patient''s lips seem to be pursed. Plan: Given recent concussion, and patients change in behavior per sister (pt more irritable, speaking more slowly, moving slowly, breathing faster, and wheezing), recommended patient be taken to the ED today--recommended ambulance since it took 2 men to help patient back to bed this morning. Sister states patient is not agreeable to going to ED at this time. Advised to try to encourage her to drink more fluids, and continue to monitor her sxs, and if any worsening, to call for ambulance transport. Sister agreeable to plan, and will discuss with sister, and recommend ED visit today." On 4/30/21, the patient''s sister contacted the clinic to inform them that the patient was found dead that morning. The medical examiner is completing the further investigation. If additional information is needed from the primary care physician for this patient. | |||||||||||||||||
Administered by: Pharmacy Purchased by: ? Life Threatening? No Write-up: 27 year old male with Down''s Syndrome and no other past medical history received second COVID-19 vaccine on 4/27/2021. On 4/30/2021 began "feeling poorly" with nausea/vomiting and possible chest discomfort. Originally presented to ED on morning of 4/30 - EKG completed demonstrated diffused ST elevation. Patient was transferred to Medical Center for heart catheterization. Left heart catheterization demonstrated normal coronary arteries and LVEDP of 25. Stat ECHO demonstrated pericardial effusion and concern raised for myopericarditis. Patient subsequently transferred to a different Medical Center for higher level of care. Upon arrival to Medical Center plan was to intubate and take to cath lab for heart biopsy and PA catheter placement. However, upon intubation patient began to decompensate and subsequently developed cardiac arrest. During ACLS, VA ECMO was placed and therapeutic hypothermia was initiated. Following VA ECMO placement patient received IVIG, high dose methylprednisolone (1000 mg), anakinra 100 mg, and broad spectrum antibiotics (vancomycin and Zosyn). Despite these efforts the patient continued to have hemodynamic instability and was on high dose vasopressors (epinephrine, norepinephrine, dopamine, angiotensin II, vasopressin). Patient subsequently suffered another cardiac arrest, briefly regained pulse with high dose vasopressors, but subsequently lost pulse despite best efforts and died on 5/1/2021 at approximately 13:00. | |||||||||||||||||
Administered by: Private Purchased by: ? Life Threatening? No Write-up: Patient suffered cardiac arrest today | |||||||||||||||||
Administered by: Private Purchased by: ? Life Threatening? No Write-up: Vomiting and diarrhea starting 4/28/21 (day after vaccine). Came to ED today for these symptoms, feeling weak, had a cardiopulmonary arrest and died. | |||||||||||||||||
Administered by: Pharmacy Purchased by: ? Life Threatening? No Write-up: Expired within 72 hours of receiving vaccine. | |||||||||||||||||
Administered by: Senior Living Purchased by: ? Life Threatening? No Write-up: on 04/29/2021 Resident was checked at 1830 and found to be at baseline status. At approximately 1855, resident was found pulses and apneic. CPR initiated and resident transferred to medical center. Resident expired 1939. | |||||||||||||||||
Administered by: Pharmacy Purchased by: ? Life Threatening? No Write-up: On 4/13 Patient underwent aortic root replacement with saphenous vein graft reconstruction of the right coronary artery. He had no prior coronary disease. This operation was done for an enlarging aortic root aneurysm in the setting of Marfan syndrome. The right coronary was anomalous and needed vein extension for reimplantation. He recovered very well and was seen in our clinic on 4/23, with no unusual findings. He had a normal echo, EKG and DVT study performed. On 4/28 he had his first Moderna COVID19 dose. on 5/1, he developed malaise, myalgias, painful lymph nodes, chills, and chest pain. He called my clinic and was instructed to go to the ER, but then felt better and didn''t go. He was then found unresponsive later that afternoon and was pronounced dead on arrival of EMS. | |||||||||||||||||
Administered by: Private Purchased by: ? Life Threatening? No Write-up: Tired, headache. | |||||||||||||||||
Link To This Search Result:
https://www.medalerts.org/vaersdb/findfield.php?EVENTS=ON&PAGENO=202&PERPAGE=20&ESORT=VAX-DATE&VAX=COVID19&DIED=Yes
Copyright © 2021 National Vaccine Information Center. All rights reserved.
21525 Ridgetop Circle, Suite 100, Sterling, VA 20166
Animal models are always imperfect. They’re designed and intended to be a first-look basic test for safety and efficacy. If you give a new medicine to a bunch of rhesus monkeys and half of them die, that’s really bad news. That might not entirely translate to humans, but it’s enough of a risk that your trials are over; you aren’t moving on to humans.
The other thing you can do with animals that you usually can’t do with humans is challenge trials, where you test how well the vaccine works after an intentional exposure. You often can’t do this with humans because some of them may die. Same reason you can’t do clinical trial testing on pregnant women or children until far, far into the process: the risk is just too high. So there’s a process that’s been built out over decades. You start with animals and see how that goes. Animals having problems? Don’t go forward. Animals all fine and medicine seems to work with them? Great, now move on to a small group of humans (Phase 1 clinical trial) so you limit the amount of risk. Here you just check safety. You don’t even care if it works; your entire trial exists only to confirm that this small group shows no signs of problems. That went okay? Great, expand the group (Phase 2 clinical trial). Here you can begin to look at how well it works, but 95% of what you’re doing is still solely focused on seeing if any ill effects show up. Still good? Now the big one: Phase 3 clinical trials. This is where you check for both safety and effectiveness in a massive group of people (thousands to tens of thousands). This is where 90% of new medicines fail. They’re safe in small groups, but in larger groups, problems emerge. Or it’s just not as effective as you expected.
You typically have to track all these people for quite some time (a year or two most often) after you’ve gathered all the FDA’s required data. You do this to ensure that the situation doesn’t change later. But at some point, you have to reach a point where you say “we’re good now” because the alternative is that we never get another medicine out of trials ever again. We just perpetually test everything; never actually releasing anything. Given decades of experience with tens of thousands of different medicines, there are established timelines for what constitutes the end of testing.
The COVID-19 vaccines have all gone through animal trials and full Phase 1, Phase 2, and Phase 3 clinical trials. That happened before the EUAs got issued. The first humans got COVID-19 vaccines back on March 16, 2020. Over a year ago. Two of the vaccines will be fully FDA approved by the end of this summer or early fall. And there’s nothing abnormal about that. They’re still on all the normal paths that medicines go on every year. Dozens of new medicines get an EUA every year. Dozens gain priority review. There are two other accelerated pathways through FDA as well which are routinely used to speed up availability of new medicines, but they ALL have strict testing guidelines they must pass to get there.
But to respond to your first point, yes, I’m completely against forced vaccinations. I find that to be an affront to the dignity of a human being and an assault on individual liberty.
No, they haven’t. And you making that claim doesn’t make it true. You have zero evidence to back that claim. You have zero death certificates that even list a COVID-19 vaccine as a cause of death. What you have is VAERS, a system for reporting adverse events which occur at some point after vaccination. And literally anyone who dies for any reason after getting a COVID-19 vaccine goes in there. If someone gets shot on their way out of the vaccine clinic, that goes in VAERS. By law. That’s the data you’re working with.
And VAERS reports can be filed by anyone on Earth. A man in the UK reported that a vaccine turned his daughter into Wonder Woman. That report was accepted by VAERS. A US doctor reported that a flu shot turned him into the Incredible Hulk. That report was accepted. This is the data you bring to us and you expect to be taken seriously?
The entire purpose of VAERS is for researchers to check the data in there against normal rates so any outliers (i.e. potential problems) can be identified and investigated. VAERS is how we find unusual patterns that lead to unexpected side effects which would never otherwise be linked to a vaccine. With that information, warnings can be issued and people can be protected. So what you’re attempting to do is valid, but I can tell you that there are quite a number of people whose entire job is running those numbers constantly and they have more complete datasets. Not saying you shouldn’t do it; just pointing out that the methods are being continuously applied at scale and the results acted upon.
As for low quality reporting, you should check out the guy in the UK who filed a report that a vaccine turned his daughter into Wonder Woman. VAERS accepted the report with no question (as it always does). That wasn’t even someone in the US. At least the doctor who filed a VAERS report that a flu shot turned him into the Incredible Hulk (yes that’s real, and yes, VAERS accepted the report) was from the US.
You can keep spamming VAERS data all you like. Doesn’t make it statistically valid. Doesn’t include 95% of the details necessary to make a judgement about an individual case. Doesn’t have anyone screening the reports.
You don’t even have to be in the US to file reports in VAERS. People from China can file reports all day just as easily as the guy in the UK filed the report about a vaccine turning his daughter into Wonder Woman. Your data set is low quality, unfiltered, unverified, and statistically speaking mostly noise.
But go ahead and continue spamming FR with massive walls of text you copied and pasted from elsewhere. I’m sure somebody somewhere is getting real value out of that.
That's 7 days / 365 * 0.008 * number of vaccinees / underreporting ratio. Assuming there are 4 times as many real events as reports, that's 3836 deaths in VAERS. So that's ballpark expected deaths assuming 100 million vaccinees.
For reactions other than deaths you need every shot, or 250,000 and typically day-of-vaccination or at most the day after. With 800,000 heart attacks annually / 330 million Americans that's 415 heart attacks with 250 million shots assuming 25% reporting into VAERS.
This is not difficult to understand nor controversial. Same numbers for stroke as heart attack, and I have not looked up the rest. That's what should be in VAERS, and any large excess of those numbers indicates unexpected adverse reactions.
For deaths, about the expected number of reports. For adverse reactions, more than expected, but I have to do more careful filtering to reduce the false positives and negatives.
There’s a lot of assumptions built into those calculations, any one of which could significantly alter the outcome. I appreciate your attempt to apply a reasoned analysis, but there’s a lot of noise in VAERS to consider. It’s very difficult to pull real signal out of it without much more complete data sets and more in-depth analysis going report-by-report.
Covid19 vax, death,
https://www.medalerts.org/vaersdb/findfield.php?TABLE=ON&GROUP1=MAN&EVENTS=ON&PERPAGE=20&ESORT=VAX-DATE&VAX=COVID19&DIED=Yes
Covid19 vax, disabled,
https://www.medalerts.org/vaersdb/findfield.php?TABLE=ON&GROUP1=MAN&EVENTS=ON&PERPAGE=20&ESORT=VAX-DATE&VAX=COVID19&DISABLE=Yes
Covid19 vax, life threatening
https://www.medalerts.org/vaersdb/findfield.php?TABLE=ON&GROUP1=MAN&EVENTS=ON&PERPAGE=20&ESORT=VAX-DATE&VAX=COVID19&L_THREAT=Yes
Covid19 vax, serious
https://www.medalerts.org/vaersdb/findfield.php?TABLE=ON&GROUP1=MAN&EVENTS=ON&PERPAGE=20&ESORT=VAX-DATE&VAX=COVID19&SERIOUS=ON
Thank you for shortening this at least.
The data is still unverified, incomplete, inaccurate, and implies no causation, but at least this is quicker to scroll past.
“More Americans have died from the poisonous vax than on 9-11.”
Not true.
“after” vaccination, is not “from” vaccination.
Aside from the rare allergic/anaphylactic reactions and those common to vaccines in general, I have not (nor have the many regulatory agencies around the world) seen any unique causative mechanism of death from the COVID vaccines - that includes the blood clotting issue that was hyped and debunked upon formal investigation.
People will continue to die of all other causes after vaccination - it only protects from COVID.
“The data is still unverified, incomplete, inaccurate, and implies no causation, but at least this is quicker to scroll past.”
Opinion.
Correlation is a logical place to start looking for causation. And it’s against the law to submit false VAERS reports. Those are facts no matter how zealously you deny them.
National Vaccine Information Center Your Health. Your Family. Your Choice. | MedAlerts Home |
Table |
Case Details (Sorted by Vaccination Date) |
Administered by: Unknown Purchased by: ? |
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:
CDC Split Type: USPFIZER INC2021018771
Write-up: Several back operations of stimulator in the back and in pain management; This is a spontaneous report from a contactable Consumer. This adult female Consumer(patient) reported that: An adult female patient received bnt162b2 (BNT162B2) at single dose on an unspecified date for Covid-19 immunisation. Medical history was none. No known allergies. The patient''s concomitant medications were not reported. Patient was not pregnant a time of vaccination. The patient had not received any other vaccines within 4 weeks prior to the BNT162B2 vaccine. The patient had not experienced Covid-19 prior to vaccination. The patient experienced several back operations of stimulator in the back and in pain management on an unspecified date, resulted in disability or permanent damage. Post the vaccination, the patient has not been tested for COVID-19. The outcome of events was unknown. Information on the lot/batch number has been requested.
Administered by: Work Purchased by: ? Life Threatening? No Write-up: Asthma attack within 60 minutes, dry throat immediately after vaccination, stuffy nose, short of breath, abdominal pain and diarrhea headache within 12 hours, temp of 101.3, chills, weakness and fatigue for 24 hours. GI symptoms stopped after 4 days. Wheezing, SOB, fatigue, headache continue until now (2 weeks post vaccine). I''ve been put on prednisone, multiple inhalers, and had a cortisone injection. The lower I get on the prednisone, the weaker and more fatigued I feel. I''ve missed work for 2 weeks now. Cannot fulfill my job duties with this weakness, fatigue, lightheaded and dizziness. I am on disability for now. | ||||||||||||||
Administered by: Unknown Purchased by: ? Life Threatening? Yes Write-up: ON Jan 16 complained of lightheadedness then felt better after supper and nap. Next day ok On Jan 22 did not get up, had stroke, taken by ambulance to hospital and transferred to medical facility. | ||||||||||||||
Administered by: Private Purchased by: ? Life Threatening? No Write-up: None stated. | ||||||||||||||
Administered by: Unknown Purchased by: ? Life Threatening? No Write-up: Dexcom Continuous Glucose Sensor failed. Contacted Dexcom explained the problem (failed sensor). They declined to help and blamed Tandum and transferred to them. They said NO NO this is a Dexcom problem and transferred me back! Dexcom identified the problem and offed to send a replacement vis 3-7 days vis ground shipping! A week without a CGM sensor!!! I expressed concern and asked for overnight. One week ago I got the Moderna vaccine and suffered Diabetic Ketoacidosis. Failed sensor has resulted in elevated BG. Last week I had Ketoacidosis following moderna Covid-19 vaccine. Being without continuous BG testing is dangerous. Raised my concerns with Dexcom. Asked for call back and action. | ||||||||||||||
Administered by: Unknown Purchased by: ? Life Threatening? No Write-up: cold extremities; fever; chills; fatigue; rheumatoid arthritis; This is a spontaneous report from a non-contactable physician. A 39-years-old female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on an unspecified date at single dose for COVID-19 immunization. The patient medical history was none. There were no concomitant medications. Historical Vaccine included received first dose of BNT162B2 intramuscular at the age of 39-year-old on 16Dec2020 at single dose for COVID-19 immunization and did fine. The patient did fine after first dose, after second dose had 36 hours of fever and chills. Covid test negative. Several weeks later she developed fatigue and cold extremities. She was found to have elevated CCP (Cyclic Citrullinated Peptide) antibodies, dx (diagnosis) rheumatoid arthritis. All events occurred on 04Jan2021. The events resulted in doctor or other healthcare professional office/clinic visit, disability or permanent damage. Treatment received for the events included medication for pain, specialist referral. There was no other vaccine received in four weeks. The patient was no pregnant. The patient had no COVID prior vaccination. Covid test (Nasal Swab) post vaccination was Negative. The outcome of the events was not recovered. No follow-up attempts are possible; information about lot/batch number cannot be obtained.; Sender''s Comments: Based on the time association and drug''s safety profile, the events fever, chills, fatigue, and cold extremities are possibly related to suspect vaccine BNT162B2 administration. The event rheumatoid arthritis is more likely underlying/intercurrent condition, unrelated to suspect vaccine BNT162B2 injection given the product''s safety profile and the pathophysiology of rheumatoid arthritis. 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. | ||||||||||||||
Administered by: Unknown Purchased by: ? Life Threatening? No Write-up: I couldn''t re stand; This is a spontaneous report from a contactable pharmacist (patient). A female patient of an unspecified age started to receive first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number and expiry date not reported), via an unspecified route of administration from an unspecified date at a single dose for Covid-19 immunization. The patient medical history included multiple sclerosis (MS). The patient''s concomitant medications were not reported. The patient stated she has MS and have both of her Pfizer vaccine doses. She called her doctor and he said it was ok to get the vaccine, even though it had only been 48 days since her IV Immunotherapy. Then the next day his office sent a letter stating to wait 60 days after IV immunotherapy. On an unspecified date, after the first dose, she sat and she couldn''t re stand with her Multiple sclerosis. She had to call to help to her with her my wheelchair. She called her HCP and he said to take acetaminophen (TYLENOL) 4x/day and it would get better and it did get better. The dose was similar reaction per caller and she stated she has reported this information to the Pfizer safety dept. The patient stated, she was not even sure it was the vaccine that caused inability to stand for a few hours, with M.S. it could just flare up on it''s own. Outcome of the event was unknown. Information about batch/lot number has been requested. | ||||||||||||||
Administered by: Pharmacy Purchased by: ? Life Threatening? Yes Write-up: Patient admitted to hospital pontine stroke following day. | ||||||||||||||
Administered by: Unknown Purchased by: ? Life Threatening? No Write-up: Myelitis transverse; A spontaneous report report was received from a physician concerning a male patient of an unknown age, who received Moderna''s COVID-19 vaccine (mRNA-1273) and who developed transverse myelitis. The patient''s medical history was not provided nor was concomitant medication use. On an unknown date, approximately nine days prior to the onset of the event, the patient received his first of two scheduled doses of mRNA-1273 (LOT unknown) intramuscularly for prophylaxis of Covid-19 infection. It was reported that the patient, a physician, after an extensive neurological workup, was diagnosed with transverse myelitis. His symptoms began, according to report, approximately nine days following vaccine administration. Treatment for the reported event was not provided. Action taken with mRNA-1273 in response to the event was not reported. The outcome of the event, transverse myelitis, was considered unknown. .; Reporter''s Comments: Very limited information regarding this event has been provided at this time. Further information has been requested. | ||||||||||||||
Administered by: Unknown Purchased by: ? Life Threatening? No Write-up: Facial palsy reaction; A spontaneous report was received from a consumer (patients wife) concerning an male patient of unknown age who experienced the event facial paralysis. The patient''s medical history was not provided. Concomitant product use was not provided by the reporter. On unknown date, prior to the onset of the events, the patient received their first of two planned doses of mRNA-1273 (lot/batch: unknown) via unknown route at unknown anatomical location for prophylaxis of COVID-19 infection. On an unknown date, the patient experienced the event facial palsy. Information about treatment was not provided. Action taken with mRNA-1273 in response to the event was unknown. The outcome of the event facial palsy was unknown. ; Reporter''s Comments: Very limited information regarding this event has been provided at this time. Further information has been requested. | ||||||||||||||
Administered by: Unknown Purchased by: ? Life Threatening? Yes Write-up: Caller says the the pt started having really bad headache the day after taking the vax that lasted about a week and half. She had 4 hours of amnesia. Pts husband took her to Hospital ER where she had a brain scan and was diagnosed w/ TGA and then admitted. | ||||||||||||||
Administered by: Other Purchased by: ? Life Threatening? No Write-up: STROKE SYMPTOMS, DIFFICULTY AMBULATING, IMPAIRED SPEECH | ||||||||||||||
Administered by: Private Purchased by: ? Life Threatening? No Write-up: Circulatory burning within 10 minutes, blurry vision, chest pressure, confusion & inability to concentrate , extreme weakness & fatigue, extreme focused joint pain, headache, coughing and difficulty breathing requiring multiple nebulizer uses every 2 hours over 2 weeks, headache. Face & body rash, . Persistent exhaustion continues requiring 2-3 hour daily naps & non Fibro brain fog continues at 3 weeks. | ||||||||||||||
Administered by: Unknown Purchased by: ? Life Threatening? No Write-up: Gullian-Barre Syndrome; Paralyzed from the waist down, lost use of both arms; Severe pain; A spontaneous report was received from a consumer (patient''s brother) concerning a 62-year-old, female patient who received Moderna''s COVID-19 vaccine (mRNA-1273) and experienced severe pain, was paralyzed form waist down and was diagnosed with Guillan-Barre Syndrome. The patient''s medical history was not provided. No concomitant product use was reported. On an unknown date the patient received her first dose of two planned doses of mRNA-1273 (Lot number: unknown) via unknown route at unknown anatomical location for prophylaxis of COVID-19 infection. On 24-Feb-2021, the patient received her second of two planned doses of mRNA-1273 (Lot number: unknown) intramuscularly at unknown anatomical location for prophylaxis of COVID-19 infection. On 24-Feb-2021, the patient experienced severe pain in a few hours and was taken to the emergency room, then, discharged. The patient was taken back to the emergency room on 25-Feb-2021 (Thursday night), and on 26-Feb-2021 (Friday), she was paralyzed from the waist down, losing use of both arms. The patient was tested at the hospital for transverse myelitis, which was negative. Spinal tap for GBS (Guillan Barre Syndrome) was protein positive and she was given a definitive diagnosis of GBS. There was movement in fingers but could not pick up objects. Seriousness criteria for the events of Gullian-Barre Syndrome and paralyzed from the waist down, lost use of both arms was medically significant. Action taken with mRNA-1273 in response to events was not applicable. The outcome of all the events was unknown. No further information was provided.; Reporter''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. | ||||||||||||||
Administered by: Private Purchased by: ? Life Threatening? No Write-up: Hardness in arm, extreme soreness in injection site 6 weeks out, after 2 days extreme pain in arm extending from shoulder, collar bone area to elbow,.restricted circulation ( hand, lower arm much colder than other arm) x-ray revealed narrowing of joint in shoulder. Still painful | ||||||||||||||
Administered by: Unknown Purchased by: ? Life Threatening? No Write-up: cannot currently walk without assistance; no sensation from the waist; severe reaction to vaccine; A spontaneous report was received from an unknown (age and race) female consumer who received Moderna''s COVID-19 Vaccine (mRNA-1273) and experienced severe vaccination adverse reaction, no sensation from the waist down and cannot currently walk without assistance. The consumer''s medical history was not provided. No relevant concomitant medications were reported. On an unknown date the consumer received their first dose of mRNA-1273 (lot# unknown) intramuscularly for prophylaxis of COVID-19 infection. On an unknown date, the consumer experienced severe vaccination adverse reaction,no sensation from the waist down and cannot currently walk without assistance. She was hospitalized for three days since the event started. No information on discharge from the hospital. No treatment information was provided. Action taken with mRNA-1273 in response to the events was unknown. The outcome of the events were unknown. The assessment for the events was not provided.; Reporter''s Comments: Very limited information regarding these events has been provided at this time. Further information has been requested. | ||||||||||||||
Administered by: Pharmacy Purchased by: ? Life Threatening? Yes Write-up: Acute diastolic congestive heart failure, Accelerated hypertension, Acute injury to kidney, Hypomagnesemia, Hyperkalemia,Syncope and collapse | ||||||||||||||
Administered by: Unknown Purchased by: ? Life Threatening? No Write-up: serious reaction and is on disability. She described it as continuous anaphylaxis; This is a spontaneous report received from a non-contactable consumer. An unspecified aged female patient received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE; Solution for injection, Lot Number: unknown) via an unspecified route of administration on an unspecified date at a single dose for COVID-19 immunization. The patient medical history was not provided. Concomitant medications were reported as none. On an unspecified date patient was reported as she received her first Pfizer COVID vaccine and had a serious reaction and is on disability. She described it as continuous anaphylaxis. It was unknown if the patient received any treatment. The outcome of the event was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained. | ||||||||||||||
Administered by: Unknown Purchased by: ? Life Threatening? No Write-up: anaphylaxis; A Spontaneous report was received from a nurse concerning unknown patient who received Modern''s COVID-19 vaccine (mRNA-1273) and experienced Anaphylactic reaction. The patient''s medical history was unknown. Concomitant medications are not reported. On unknown date prior to the onset of the events, the patient received their first of two planned doses of mRNA-1273 (lot/batch: unknown) for prophylaxis of COVID-19 infection. On an unknown date the patient experienced Anaphylactic reactions. The event is considered as medically significant. No treatment was given. No lab details are provided. No Action taken with mRNA-1273 in response to the events was not reported. At the time of this report, the outcome of the events were unknown.; Reporter''s Comments: Very limited information regarding this event has been provided at this time. Further information has been requested. | ||||||||||||||
Administered by: Public Purchased by: ? Life Threatening? No Write-up: stroke in left arm, arm is weaker than the other, strength never came back; This is a spontaneous report from a contactable nurse. An 86-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), second dose intramuscular, administered in the left arm on an unspecified date (also reported as 12Feb2021 12:00; pending clarification) (batch/lot number: EM9810) as a single dose, and first dose intramuscular, administered in the left arm on 12Feb2021 12:00 (batch/lot number: EL3249) as a single dose for COVID-19 immunisation. Medical history included cancer, prostate to bone from an unknown date. The patient has no known drug allergies. The patient''s concomitant medications were not reported. Facility type vaccine was public health clinic facility. No other vaccine in four weeks. No other medications in two weeks. No Covid prior to vaccination and no Covid tested post vaccination. On 12Mar2021 (as reported, however, also reported as 13Mar2021; pending clarification), the patient experienced stroke in left arm, arm was weaker than the other, strength never came back. The adverse event resulted in disability or permanent damage. No treatment was received for the event. The outcome of the event was not recovered. No follow-up attempts are possible. No further information is expected.; Sender''s Comments: Based on the information provided, it is unlikely that the reported event is related to suspect product. The reported event is related to this patients underlying morbidity of prostate cancer with metastases to the bone. 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 Regulatory Authorities, Ethics Committees and Investigators, as appropriate | ||||||||||||||
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
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Posting this demonstrates a lack of understanding for how a US Standard Certificate of Death is filled out. Specifically, Section 32 Parts I and II. Where COVID-19 is the underlying cause of death ("UCoD"), it's a death caused by COVID-19 and included in the death statistics as such. The UCoD is the disease or injury which initiates the chain of events leading directly to death.
"Then notice how the covid vaccine deaths are often argued the opposite from covid deaths, that there were many other factors meaning the death can't be attributed to the covid vaccine. Can't logically argue covid deaths and covid vaccine deaths opposite ways."
By all means, let's be consistent. Locate for me the number of US Standard Certificates of Death listing COVID-19 vaccine as the UCoD. Let's be consistent. VAERS is not the official government document listing the cause of death. The US Standard Certificate of Death is. The number of US Standard Certificates of Death listing COVID-19 vaccine as the UCoD is - as of today - zero. The number listing COVID-19 is nearly 600,000.
So yes, by all means, let's stay consistent.
Here’s a search limited to vaccines administered in nursing homes, why would they submit “unverified, incomplete, inaccurate” reports? Are they liars?
“VAERS is not documentation that a vaccine caused the event”
Obviously that doesn’t automatically mean the vaccine did not cause the event. You act like all the events can be blown off.
“The COVID-19 vaccines have all gone through animal trials”
Ok, but are you saying the results, from a safety standpoint, wouldn’t be relevant to publish? Or indeterminate? Or is it simply that none of us have found them?
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