[link to www.zerohedge.com (secure)]

And from the horses mouth or ASS
[link to www.ema.europa.eu (secure)]

You all stepped in some shit!!!

The European Medicines Agency’s Pharmacovigilance Risk Assessment Committee (PRAC) concluded that the use of the J&J vaccine is possibly linked with vein clotting and an immune condition that causes the immune system to attack blood platelets.

Venous thromboembolism “is a condition in which a blood clot forms in a deep vein, usually in a leg, arm, or groin, and may travel to the lungs causing a blockage of the blood supply, with possible life-threatening consequences,” the committee said.

After reviewing new evidence, PRAC concluded that there is a “reasonable possibility” that the clotting condition is linked with vaccination using the J&J vaccine.

The committee also found that the use of the J&J and the AstraZeneca vaccines is linked to an immune condition that causes the body’s immune system to target healthy platelets needed for normal blood clotting. and have serious health consequences,” the committee said.


The communications about the immune thrombocytopenia (ITP) mentions that cases of the condition have been reported in the first four weeks after vaccination and “included serious cases with very low platelet counts.”

“If an individual has a history of ITP, healthcare professionals should consider the risk of developing low platelet levels prior to administering the vaccine. In individuals with a history of ITP, it is recommended to monitor platelet levels following vaccination with COVID-19 Vaccine Janssen,” the direct communication to doctors stated.

The message to doctors regarding venous thromboembolism (VTE) The message also noted that patients presenting with one of the two conditions should be checked for the other.

“This is important, to assess a potential diagnosis of thrombosis with thrombocytopenia syndrome (TTS), which requires specialized clinical management,” the communication said.

The U.S. Food and Drug Administration (FDA) authorized the J&J vaccine for emergency use on Feb. 27, 2021.

Less than two months later, on April 23, the FDA amended the authorization to include information “about a very rare and serious type of blood clot in people who receive the vaccine.” The clotting condition in that case was separate from the one flagged by the European regulator on Oct. 1.