Posted on 02/10/2021 5:00:32 PM PST by ebb tide
NDIA, February 10, 2021 (LifeSiteNews) – US-based COVID-19 vaccine maker Pfizer has withdrawn its application for emergency-use authorization of its product in India after the country’s health authorities demanded local safety testing.
India’s drug regulator last weekdeclined Pfizer’s request that its experimental COVID-19 mRNA vaccine “BioNTech” (BNT162b) be approved without a local trial of the product’s safety on the country’s population.
The country’s Central Drugs Standard Control Organisation formed a Subject Expert Committee that met on Feb. 3 to discuss Pfizer’s proposal for the emergency use authorization of its COVID-19 experimental vaccine.
“The committee noted that incidents of palsy, anaphylaxis and other SAE’s have been reported during post marketing and the causality of the events with the vaccine is being investigated,” the committee reported.
“Further, the firm [Pfizer] has not proposed any plan to generate safety and immunogenicity data in Indian population. After detailed deliberation, the committee has not recommended for grant of permission for emergency use in the country at this stage,” the committee added.
Pfizer in turn withdrew its application.
“Based on the deliberations at the meeting and our understanding of additional information that the regulator may need, the company has decided to withdraw its application at this time,” the company stated, as reported by Reuters.
“Pfizer will continue to engage with the authority and re-submit its approval request with additional information as it becomes available in the near future.”
India’s concerns about the safety of Pfizer’s mRNA gene-altering technology are not misplaced.
Data from the US-based National Vaccine Information Center shows that as of Jan. 29, there have been 501 deaths — a subset of 11,249 total adverse events — following COVID-19 vaccinations. Pfizer’s vaccine was taken by 59 percent of those who died while Moderna’s vaccine was taken by 41 percent.
The Norwegian Medicines Agency reported on Jan. 14 that twenty-three people died within days of receiving the first dose of Pfizer’s product.
California officials are investigating the Jan. 7 death of a 60-year-old healthcare worker who died four days after receiving his second injection of Pfizer’s product. A reportedly “perfectly healthy” 56-year-old Miami obstetrician died 16 days after receiving the Pfizer shot. State along with federal officials are investigating the Jan. 30 death of a 58-year-old Virginia woman who died hours after receiving the first dose of Pfizer’s vaccine.
America’s Frontline Doctors are urging the Biden administration to take note of India’s decision to deny Pfizer’s application based on a lack of safety.
“President Biden and his COVID-19 task force need to immediately and clearly explain to the American people why the Pfizer-BioNTech experimental vaccine is safe for Americans despite Indian drug regulators denying its emergency use based on concerns about potential side effects, immunogenicity, and other data,” the doctors’ group stated.
“The burden of proof should fall on the Biden White House to provide Americans with greater transparency and information so that they can make informed decisions about their own healthcare. Science should guide this administration’s COVID response plan not public relations, polls, and politics.”
While India has rejected Pfizer’s vaccine, it has approved the use of Oxford University’s AstraZeneca vaccine and another one developed on home soil by Bharat Biotech with the Indian Council of Medical Research, reports Reuters.
LifeSiteNews has produced an extensive COVID-19 vaccines resources page. View it here.
Ping
“Safety? Safety? There’s no money in that.”
Those of us familiar with Bill Gates’ forays into vaccines in India and the horrific effects they had in India understand the people of India’s reticence to allow any vaccine into their country that’s not fully tested at this point.
But...but, the pro vaxxers here at FR have assured us the vaccines are safe. Wait 2 minutes and they will repost preparred responses to that effect. And attacking anyone that fails to take the government and big pharma at its word.
Love it! India does sell HCQ
India has already approved its own domestically produced vaccine, called Covavax. The Phillipines also ordered 30 million doses of it. A US based company has obtained the US marketing rights for it and will apply for an EUA.
If India has HCQ then why would India need vaccines?
and ivermectin
Don’t worry they’ll have guinea pigs lining up for it all over America.
Oh great.. I got my 1st shot and getting booster on 23rd....was not going to get it but because I am retiring and spending time in FL with friends I thought “what the heck. It will prob be a good idea so I don’t bring anything to their hones”. I should have stuck with my instincts of not bothering.
Just wait, India. US citizens will happily stand n line to be safety testers for your people.
The truth about this so-called vaccine is that it’s not really a vaccine at all. Once one has received both doses, one is still capable of contracting and transmitting COVID. I’m sorry to say that if your intention was to avoid spreading the disease to others, taking this vaccine for that reason is pointless.
There’s no proof or even evidence that a vaccinated person can not still transmit the virus to others.
Let the Indians develop their own damn vaccine. Screw ‘em.
Actually that is smart thinking. Or else they want to make money off their own.
“Safety Testing??!!...We don’t do no stinkin’ Safety Testing!!”
They already have. And it’s safer an not immoral.
They had bad experiences with Bill Gates, maybe they think he’s involved.
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