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FDA limits use of the J&J Janssen COVID-19 vaccine

The U.S. Food and Drug Administration has limited the use of the Johnson & Johnson Janssen COVID-19 vaccine due to rare blood clotting instances of thrombosis with thrombocytopenia syndrome (TTS) after receiving the vaccine. TTS is a syndrome in which an individual develops blood clots in the veins or arteries in addition to low platelet counts. Symptoms occur one to two weeks
United States Johnson Janssen Peter Marks Centers For Disease Pharmacovigilance Risk Assessment Committee Drug Administration

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