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CT Pauses Use of Johnson & Johnson COVID-19 Vaccine After Rare Complications

CT Pauses Use of Johnson & Johnson COVID-19 Vaccine After Rare Complications © SOPA Images/LightRocket via Gett file photo j&J The state of Connecticut is pausing the administration of the one-dose Johnson & Johnson vaccine for the time being while the FDA and CDC investigate reports of potentially dangerous blood clots. Johnson & Johnson Impacts Conn. Replay Video UP NEXT In a joint statement issued on Tuesday morning, the Centers for Disease Control and Prevention and the Food and Drug Administration said they were investigating unusual clots in six women that occurred 6 to 13 days after vaccination. The clots occurred in veins that drain blood from the brain and occurred together with low platelets. All six cases were in women between the ages of 18 and 48.

US Calls For Pause On J&J COVID Vaccine Due To Deadly Blood Clots

US Calls For Pause On J&J COVID Vaccine Due To Deadly Blood Clots April 13th 2021, 11:34 am The FDA left open the possibility that new cases of blood clots could be brought to its attention. Image Credit: Share Email Update (1010ET): The health officials who spoke on today’s call started by reiterating details about the decision to halt the J&J shared with the press earlier. Officials said they would update doctors with new vaccine “fact sheets” designated certain medications that could be associated with higher risks of blood clots. After they said they were only seeing symptoms in patients who received the JNJ vaccine, the first question from the press (asked by an FT reporter) was: what about AstraZeneca? In Europe, governments have been imposing age limits on who can receive the AstraZeneca jab for similar reasons.

Johnson & Johnson Delays Rollout Of COVID-19 Vaccine In Europe

Johnson & Johnson Delays Rollout Of COVID-19 Vaccine In Europe Share this article Johnson & Johnson is delaying the rollout of its single-dose vaccine in Europe because of concerns over very rare blood clots. It comes just days before it was due to start being rolled out across the EU. Earlier today the regulator in the US recommended a “pause” in the vaccine s deployment there. The decision was in response to six cases of blood clotting identified among the nearly seven million people who d received it. Officials said such cases appeared to be extremely rare, but they were recommending the pause out of an abundance of caution while they investigate the cases.

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