As COVID-19 vaccinations roll out to more and more people, health authorities are keeping a close watch for any unexpected side effects.
On Tuesday, a health worker in Alaska suffered a severe allergic reaction after receiving the Pfizer-BioNTech COVID-19 vaccine. She is in the hospital for another night under observation while another worker, vaccinated Wednesday, has recovered. Doctors already knew to be on the lookout after Britain reported two similar cases last week.
In the U.S. and Canada, vaccine recipients are supposed to hang around after the injection in case signs of an allergy appear and they need immediate treatment. That is exactly what happened when the health worker in Juneau became flushed and short of breath 10 minutes after the shot. The second worker experienced eye puffiness, light headedness and scratchy throat.
Allergies are always a question with a new medical product, but monitoring COVID-19 vaccines for any other, unexpected side effects is a bigger challenge than usual.
It’s not just because so many people need to be vaccinated over the next year. Never before have so many vaccines made in different ways converged at the same time — and it’s possible that one shot option will come with different side effects than another.
WATCH | Allergist addresses concerns about adverse events after pandemic shots:
The first vaccine beginning widespread use in the U.S. and many Western countries, made by Pfizer Inc. and Germany’s BioNTech, and a second option expected soon from competitor Moderna Inc. both are made the same way.
The U.S. Food and Drug Administration says huge studies of each have uncovered no major safety risks.
But the allergy concern “points out again the importance of real-time safety monitoring,” said Dr. Jesse Goodman of Georgetown University, a former FDA vaccine chief.
And authorities have multiple ways of tracking how people fare as these COVID-19 vaccines, and hopefully additional ones in coming months, get into more arms.
How will I feel after vaccination?
Getting either the Pfizer-BioNTech shot or the Moderna version can cause some temporary discomfort, just as many vaccines do.
In addition to a sore arm, people can experience a fever and some flu-like symptoms — fatigue, aches, chills, headache. They last about a day, sometimes bad enough that recipients miss work, and are more common after the second dose and in younger people.
These reactions are a sign that the immune system is revving up. COVID-19 vaccines tend to cause more of those reactions than a flu shot, about what people experience with shingles vaccinations. But some are similar to early coronavirus symptoms, one reason hospitals are staggering when their employees get vaccinated.
What about serious risks?
The FDA found no serious side effects in the tens of thousands enrolled in studies of the two vaccines.
Still, problems so rare they don’t occur in even very large studies sometimes crop up when a vaccine is used more widely and without the stringent rules of a clinical trial.
The first allergy reports from England were in people with a history of serious allergies, and British authorities warned those with severe prior experiences to hold off vaccination as they determine what ingredient might be a problem.
U.S. health authorities are giving more nuanced advice. People always are asked about allergies before vaccinations, and instructions for the Pfizer-BioNTech shot say to avoid it if you’re severely allergic to one of its ingredients or had a severe reaction to a prior dose. Health workers can go over the ingredient list.
The U.S. Centers for Disease Control and Prevention advises people to stick around for 15 minutes after vaccination, and those with a history of other allergies for 30 minutes, so they can be treated immediately if they have a reaction.
What is Health Canada doing?
Health Canada advised earlier this week that people with allergies to any of the ingredients in the Pfizer-BioNTech COVID 19 vaccine should not receive it and should speak with their health professional about any serious allergies or other health conditions they may have before they receive this vaccine.
“Health Canada has reviewed the available evidence and has concluded that the current Product Monograph and available public health guidance are appropriate, and is not recommending any changes to the product’s use at this time,” the department said in an advisory to the general public and health professionals.
Health Canada collaborates with international regulators to share information about coronavirus vaccines as they are rolled out around the world.
“If any new safety issues are confirmed, Health Canada will take appropriate action, which could include communicating any new risks to Canadians and health-care providers or changing the recommended use of the product,” the regulator said in an advisory to the general public and health professionals.
What happened in Alaska?
The Alaska health worker, who doctors said had no history of allergies, was following that advice and got prompt care for a particularly severe reaction called anaphylaxis. She has recovered after a night of observation in the hospital — but won’t be allowed a second vaccine dose.
Alaska doctors alerted U.S. authorities, who will continue the monitoring required to tell just how common this kind of reaction really is.
That will be especially important as enough vaccine arrives for injections to be given outside of health-care settings that have lots of experience handling this type of reaction.
“Balancing any potential risks with the benefits the vaccine provides in the pandemic is an ongoing process,” CDC’s Dr. Jay Butler cautioned Wednesday.
What if other risks crop up?
The challenge is telling whether the vaccine caused a health problem or if it’s coincidence. Health authorities have stressed that people should not jump to conclusions that there’s a connection.
The way to tell: Comparing any reports of possible side effects with data showing how often that same condition occurs routinely in the population.
The government has multiple ways to do that. Doctors are required to report any patient problems.
But the FDA is scrutinizing massive databases of insurance claims for early red flags that any health problems are occurring more often in the newly vaccinated than everyone else.
Lots of concern over the 4 subjects (out of over 40,000) in the Pfizer trial who developed Bell’s palsy. That’s 0.01%. The incidence of Bell’s Palsy in the gen population is roughly 30/100 K or 0.03%. Doubtful the vaccine had much to do with this <a href=”https://twitter.com/hashtag/MathIsTruth?src=hash&ref_src=twsrc%5Etfw”>#MathIsTruth</a>
On its list to check is Bell’s palsy, a temporary facial paralysis that occurred in a handful of people in both vaccine studies. The FDA said it’s probably coincidence, but will track to be sure.
Vaccine recipients can help with the extra safety tracking. Called “v-safe,” the program run by the CDC automatically sends a daily text the first week after each vaccine dose asking how people feel, and then a weekly text for the next five weeks. Any responses that suggest concern prompt a phone call for further information.
In Canada, members of the general public who experience a potential side effect following immunization are asked to report it to their health-care professional who can also help manage any side effects.
Health Canada asks health-care professionals who have a patient that experiences a potential side effect following immunization to complete the Adverse Events Following Immunization (AEFI) form appropriate for their province or territory and send it to their local health unit.
The Associated Press Health and Science Department receives support from the Howard Hughes Medical Institute’s Department of Science Education. The AP is solely responsible for all content.
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