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European drug regulators are examining new reports of possible side effects seen in a small number of people who have received the Pfizer and Moderna mRNA COVID-19 vaccines, according to a Reuters article.
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Reports of the conditions – a skin condition and two kidney disorders – prompted the European Medicines Agency to seek additional information from Moderna and Pfizer and its partner BioNTech.
It is not known how many cases of erythema multiforme, a form of allergic skin reaction; glomerulonephritis or kidney inflammation; and nephrotic syndrome, a kidney disorder that causes heavy loss of urine protein, have been reported.
Erythema multiforme causes round skin lesions while kidney problems can cause fatigue, bloody or foamy urine, and edema – or swelling of the eyelids, limbs, or abdomen.
Over 330 million doses of the Pfizer-BioNTech vaccine have been administered in Europe, compared to over 43 million doses of the Moderna vaccine.
Last month, the EMA discovered a possible link between rare cases of heart inflammation and COVID-19 mRNA vaccines.
Despite the possible side effects of mRNA vaccines, the EMA stressed that it believes the benefits of the vaccines far outweigh the risks.
EMA is a European Union (EU) agency responsible for the scientific assessment, supervision and control of the safety of medicines in the EU. The organization said it would not recommend any changes to vaccine labeling yet.
According to the organization, the EMA has seven scientific committees that assess drugs throughout their lifecycle, from early stages of development, through marketing authorization and safety monitoring. once they are on the market.
© 2021 Cox Media Group
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