United States skors the use of the Johnson & Johnson vacuum

Washington – United States commands martes to “pause” the administration of the vaccine against the coronavirus developed by Johnson & Johnson to investigate potentially dangerous platelet reports.

In a joint communication, the Centers for Control and Prevention of Injuries (CDC, by its seal in English) in the Administration of Medicines and Food (FDA) will hold the March that investigates detected thrombi and six females and the posterior slices the vacancy, combined with a reduced content of plaques. In the United States he has administered more than 6.8 million doses of the J&J vaccine, which is a single application.

Federal distribution channels, including the massive evacuation centers, will start using the pharmacy temporarily, and it is hoped that the states and other providers will do the same.

Other vacancies, Modern and Pfizer, include the vast majority of inoculations administered in the United States and are not affected by the break.

The Assessment Committee for the Practice of Immunization of the CDC will meet the mercenaries to study the cases. The FDA initiated its own investigation.

“As soon as the process is complete, we recommend a break in the use of this vaccine by precaution”, said doctors Anne Schuchat, Deputy Director of the CDC, and Peter Marks, Director of the FDA’s Biological Evaluation and Research Center, in a communicated joint.

The agencies recommend that women have received the J&J vaccine and have experienced cabbage paints, abdominal paints, piercing paints or failures to breathe three weeks after the injection of contacts into their medicine.

The authorities say they want to train the car manufacturers and the health professionals about the “singular treatment” corresponding to these blood clots.

Johnson & Johnson asserted that he was standing in front of the bullets, but insisted that he had not even established an angle with his car.

“We are engaged in thromboembolic events, including some with thrombocytopenia, have been reported in relation to vacuos-19 vacancies”, said the company in a statement. “Until now, we have not established a clear causal relationship between these unusual events and the vacancy,” he added.

The J&J vaccine was authorized as an emergency response by the FDA to fines in February with a large ceremony, given the hope that, in order to require a single dose and conditions of relatively easy treatment, the vaccination campaign would be impulsive and all peace. Without embargo, this vacancy constitutes a small percentage of the United States administration, debits and errors in the plant of one of its counterparts in Baltimore.

J&J suspended Dallas: