FDA tightens warning of heart issues after J&J COVID vaccine

The FDA is strengthening its warning of possible severe adverse effects of the Johnson & Johnson COVID vaccine. On Wednesday, the federal health agency said the Johnson & Johnson vaccine must not be administered to people with past histories of blood clots and thrombosis.

The FDA also said other adeno-virus based vaccines must not be used in such patients. This came after the Vaccine Adverse Event Reporting System (VAERS) self-reporting system posted almost 20,000 Americans died post-vaccination so far and 100,000 were hospitalized.
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