Joint CDC and FDA Statement on Johnson & Johnson COVID-19 Vaccine | CDC Online Newsroom

As of April twelve, a lot more than six.eight million doses of the Johnson & Johnson (Janssen ) vaccine have been administered in the U.S. CDC and Food and drug administration are examining knowledge involving six reported U.S. cases of a exceptional and critical type of blood clot in folks after getting the J&J vaccine. In these cases, a type of blood clot identified as cerebral venous sinus thrombosis (CVST) was found in mix with low concentrations of blood platelets (thrombocytopenia). All six cases occurred among the girls between the ages of 18 and 48, and signs or symptoms occurred six to thirteen times after vaccination. Treatment method of this specific type of blood clot is different from the therapy that may well ordinarily be administered. Ordinarily, an anticoagulant drug identified as heparin is utilized to handle blood clots. In this environment, administration of heparin might be harmful, and substitute remedies want to be specified.

CDC will convene a conference of the Advisory Committee on Immunization Techniques (ACIP) on Wednesday to further more evaluate these cases and assess their probable importance. Food and drug administration will evaluate that analysis as it also investigates these cases. Until that method is total, we are recommending a pause in the use of this vaccine out of an abundance of caution. This is significant, in portion, to make sure that the wellbeing treatment provider local community is aware of the probable for these adverse events and can prepare for correct recognition and administration due to the one of a kind therapy necessary with this type of blood clot.

Ideal now, these adverse events look to be incredibly exceptional. COVID-19 vaccine protection is a major precedence for the federal govt, and we get all experiences of wellbeing complications subsequent COVID-19 vaccination very significantly. People today who have gained the J&J vaccine who acquire critical headache, abdominal suffering, leg suffering, or shortness of breath inside three weeks after vaccination should get in touch with their wellbeing treatment provider. Overall health treatment providers are requested to report adverse events to the Vaccine Adverse Event Reporting Technique at icon

CDC and Food and drug administration will offer supplemental details and answer issues later right now at a media briefing. A recording of that media get in touch with will be offered on the FDA’s YouTube channel.