Health
What you need to know as a change in federal guidance – NBC Chicago
The Food and Drug Administration has been advising Americans for several months to get the Pfizer or Moderna series COVID vaccine instead of the Johnson & Johnson one-shot vaccine, but because authorities have severely restricted its use. The guidance has been strengthened. Of medicine.
On Thursday, the FDA severely restricted those who could receive the Johnson & Johnson vaccine amid concerns about rare but serious side effects that could cause life-threatening blood clots in patients who received the shot. Announced that it will impose.
This is the latest in what we know Changes to FDA guidance.
How has the FDA guidance changed?
As of Thursday, U.S. regulators should be warned that patients are at risk of receiving the Johnson & Johnson vaccine and should only be given the Johnson & Johnson vaccine if they meet certain other criteria. It states that there is.
Federal authorities say that patients who require a first dose of COVID vaccine or booster immunization Receive a Pfizer or Moderna vaccine.
Due to the rare but serious blood clotting concerns associated with the Johnson & Johnson COVID vaccine, the CDC Panel recommends that individuals look for either the Pfizer vaccine or the Moderna vaccine. See ViNguyen on NBC5 for more details.
Why did the FDA make the changes?
The FDA has warned of the small risks of potentially life-threatening conditions associated with the Johnson & Johnson vaccine, but continued investigation of these findings has led the department to make changes to its recommendations.
During research and analysis, the FDA states that there is a risk of a condition called thrombosis with thrombocytopenia syndrome (TTS) associated with Johnson & Johnson vaccination.
Although this condition is rare, it can cause low platelet levels and cause life-threatening blood clots. Several cases have been reported to federal regulators, they say, justifying “restricting the authorized use of vaccines.”
How rare is TTS?
Although the FDA advises patients to receive other COVID vaccines, the incidence of TTS in patients vaccinated with Johnson & Johnson remains very rare.
Federal officials say that 3.23 cases of illness occurred per million doses of the vaccine given. Deaths associated with TTS occur at a rate of 0.48 per million doses of vaccine administered.
According to the FDA, TTS can have long-term, debilitating health effects, and the syndrome has a high mortality rate.
Can Americans still receive the Johnson & Johnson Vaccine?
Certain Americans need to be warned about the risk of TTS, but they can continue to receive the Johnson & Johnson vaccine.
According to the FDA, these groups will continue to receive single-dose shot series.
-Individuals who have experienced an anaphylactic reaction after vaccination with Pfizer or Moderna COVID vaccine.
-Individuals with personal or religious concerns about RNA vaccination.
-Individuals who have not been vaccinated with COVID-19 due to restricted access to the mRNA vaccine.
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