“Right now, we found no causal relationship with vaccination and we will continue our investigation and analysis of these cases, “the regulator said in a statement.
The FDA recognized information on “some individuals” suffering from thrombi and low platelet levels in the blood after receiving the vaccine Janssen:
“Both conditions can have different causes,” the FDA said. “We will keep the public informed because we have more data,” he added.
The European Medicines Agency (EMA) announced this Friday that it is investigating a possible link about the J&J combination and gossip,
“One case occurred in a clinical trial and three occurred during vaccination in the United States. One of them was fatal,” the EMA said.
The FDA found that the statement from the European Bureau was based on information contained therein.
The J&J vaccine – one of the few administered in one dose, which was also approved in Colombia and will arrive soon – was authorized for emergency use in the United States in late February, after the regulator gave the green light. immunizers from the pharmaceutical companies Pfizer / BioNTech and Moderna.