US lifts pause on Johnson & Johnson Covid-19 vaccine

Washington, April 25 : The US Food and Drug Administration (FDA) and the US Centers for Disease Control and Prevention (CDC) announced they have determined to lift the pause regarding the use of the Johnson & Johnson Covid-19 vaccine, allowing its resumed use for adults.
The decision was made following a thorough safety review, including two meetings of the CDC’s Advisory Committee on Immunization Practices (ACIP), said a joint statement of the two agencies on Friday, Xinhua news agency reported on Saturday.
The pause was recommended on April 13 after reports of six cases of a rare and severe type of blood clot in individuals following administration of the Johnson & Johnson Covid-19 vaccine.
During the pause, medical and scientific teams at the FDA and CDC examined available data to assess the risk of thrombosis involving the cerebral venous sinuses, or CVST (large blood vessels in the brain), and other sites in the body along with thrombocytopenia, or low blood platelet counts, according to the statement.
The teams at FDA and CDC also conducted extensive outreach to providers and clinicians to ensure they were made aware of the potential for these adverse events and could properly manage and recognize these events due to the unique treatment required for these blood clots and low platelets.
The FDA has determined that the available data show that the vaccine’s known and potential benefits outweigh its known and potential risks in individuals 18 years of age and older.