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Johnson & Johnson Vaccine Decision from EMA

Johnson & Johnson Vaccine Decision from EMA

Johnson & Johnson Vaccine Decision from EMA

Johnson & Johnson Vaccine Decision from EMA. The European Medicines Agency (EMA) has reaffirmed that the vaccine developed by Johnson & Johnson (J&J) against the coronavirus (Covid-19) is safe and effective.

The effect of the vaccine developed by Johnson & Johnson from the European Medicines Agency against the corona virus (Covid-19) has been approved again.

In a written statement by the EMA, the use of the J&J vaccine was recommended on the grounds that it rarely causes blood clotting.

Stating that the risk / benefit balance of the J&J vaccine remained positive, EMA stated that the benefits of the vaccine outweigh the risks.

Emphasizing that one of the 7.5 million people vaccinated by the J&J vaccine died, EMA noted that they believe that blood clotting should be added to the list of rare side effects of the vaccine.

On the other hand, the J&J Covid-19 vaccine was examined by many health institutions and organizations, including EMA, on the grounds that it caused blood clots in the people who were administered the vaccine. In addition, the use of the vaccine was suspended by many countries due to suspected side effects.

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