Unfortunately, you won't know about "side effects" as much as you'd like. "Immediate" ones or those that show up later?
Traditionally when vaccines have had critical side effects or a bad batch was created the side effects show up within days.
Once again you are spouting nonsense. If my group was inline before old people then I would be happy to get the vaccine. This is in no way supporting old people dying.
You've been outed. You clearly stated that you would not allow yourself to be jabbed until others had been and demonstrated safety.
Nice fantasy you have there. I stated that I really had no worries about safety because so many others would be jabbed before I was allowed to have a turn. If any safety issues showed up they would be pretty obvious (and re-called by the government) before they got to my number. Obviously if safety issues are found then most people would not get jabbed until they are fixed. Assuming that politicians do not force the vaccine to be delivered before safety trials are complete then I expect the COVID vaccine to be perfectly safe. Most of the proposed vaccines require two doses about 1 month apart -- and the expectation is that immunity would last for two or three years before fading. Most likely most people would have to get a next-generation booster three years down the road that would provide life-time immunity to COVID-19.
Clearly you are OK with Trump releasing a vaccine early without completing proper safety trials just so he can get re-elected. It's impossible to underestimate you.
Rather, I am not certain that a vaccine is even necessary. The pandemic, if you can even call it that, has been over for months in my view and the last vestiges of cases are filtering through now. I believe we are very close, if not at, herd immunity on this strain of Kung Flu.
still up for it? https://www.reuters.com/article/us-...ld-jeopardize-testing-of-others-idUSKBN25K2M0 Exclusive: Fauci says rushing out a vaccine could jeopardize testing of others CHICAGO/NEW YORK (Reuters) - The top U.S. infectious diseases expert is warning that distributing a COVID-19 vaccine under special emergency use guidelines before it has been proved safe and effective in large trials is a bad idea that could have a chilling effect on the testing of other vaccines. Scientists and health experts have expressed concern that President Donald Trump will apply pressure on the U.S. Food and Drug Administration to deliver a vaccine before November to boost his chances of re-election. Anthony Fauci, director of the National Institute of Allergy and Infectious Diseases, declined to comment on the president, but said there are risks in rushing out a vaccine despite the urgent need. “The one thing that you would not want to see with a vaccine is getting an EUA (emergency use authorization) before you have a signal of efficacy,” Fauci told Reuters in a phone interview. “One of the potential dangers if you prematurely let a vaccine out is that it would make it difficult, if not impossible, for the other vaccines to enroll people in their trial,” Fauci said. Large-scale clinical trials of the leading vaccine candidates from Moderna Inc (MRNA.O), Pfizer Inc (PFE.N) andAstraZeneca Plc (AZN.L), which aim to enroll tens of thousands of volunteers, were launched in recent weeks. Johnson & Johnson (JNJ.N) last week said it hopes to include 60,000 subjects in its Phase III vaccine trial. Trump stoked concerns of politicizing the regulatory approval process with an announcement on Sunday of an emergency use authorization for plasma from recovered COVID-19 patients to treat current patients before its benefits have been assessed in randomized, placebo-controlled clinical trials. Trump had tweeted on Saturday that “deep state” elements at the FDA were delaying progress on drugs and vaccines until after the Nov. 3 election in order to hurt his reelection bid. Safe and effective vaccines are seen as essential to ending the pandemic that has claimed the lives of more than 800,000 people worldwide, over 177,000 of them in the United States. But vaccine experts worry that the White House may apply pressure on the FDA to push out a vaccine via an EUA before it has been fully tested - a pathway that has never been used to approve a vaccine intended for widespread use. “I would be very worried about using an EUA mechanism for something like a vaccine. It’s very different from plasma therapy,” said Dr. Peter Hotez, an infectious disease expert and vaccine researcher at Baylor College of Medicine. Fauci said the FDA’s guidance on vaccines - both for full approval and for an EUA - explicitly requires a demonstration that it is both safe and effective. An EUA is typically used for products to “diagnose, prevent and treat serious or life-threatening diseases where the known benefits outweigh the potential risks of the product,” Fauci said. An EUA might be appropriate once studies have shown safety and effectiveness, but before the FDA has completed its formal review of the company’s marketing application, he said. “To me, it’s absolutely paramount that you definitively show that a vaccine is safe and effective, both,” Fauci said. “We would hope that nothing interferes with the full demonstration that a vaccine is safe and effective.”