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An influential vaccine panel’s task force will be led by a member who has previously expressed distrust in the Covid vaccine, ...
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MedPage Today on MSNIn Abrupt Reversal, FDA Yanks Ixchiq Vaccine Over Safety Concern
According to the vaccine's maker, Valneva, the FDA based its decision to suspend the shot on four new serious adverse events ...
Reports of serious adverse events after administration of the updated COVID-19 booster shots were rare, according to a new study from experts at the Centers for Disease Control and Prevention and ...
CDC and FDA identified 39 confirmed reports of people who got the J&J/Janssen COVID-19 Vaccine and later developed TTS. Women younger than 50 years old especially should be aware of the rare but ...
A post posted to Instagram read, “The latest CDC Data show reports of adverse events from COVID Vaccines surpass 220,000, including 943 among 12-17 year olds.” The post came from the ...
From December 2020 to July 2021, the FDA received adverse event reports describing 22 patients who ingested products containing delta-8 THC.
The CDC is tasked with performing a proportional reporting ratio, or PRR, data mining analysis on a weekly basis to determine whether the amount of reported “adverse events” following the ...
The CDC stated that most events resolved themselves within the 15-minute observation period that’s required after receiving the vaccine. Thirteen people were taken to an emergency department ...
Moderna Vaccine The CDC report tracking allergic reactions to Moderna’s COVID-19 vaccine found “adverse” events in reaction to the vaccine were reported just .03% of the time.
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