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EMA investigates Covid-19 drug Paxlovid

Friday, 11/19/2021 5:56 PM by

dpa-AFX

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AMSTERDAM (dpa-AFX) – The European Medicines Agency EMA started an investigation of the Covid-19 drug Paxlovid from the manufacturer Pfizer started in order to enable countries to use it at an early stage even before market approval. The EMA announced on Friday in Amsterdam that existing data from tests with paxlovid in sick people at risk of a severe course would be evaluated. Preliminary results indicated that paxlovid reduced the risk of hospital treatment or a fatal outcome from corona infection. Data on the quality and safety of the drug would also be examined.

Pfizer has just filed for emergency approval for paxlovid in the United States. According to the company from the beginning of November, the corona pill is very successful in preventing serious illnesses in high-risk patients. An interim analysis of test results found the drug reduced the risk of hospital admissions and death in Covid-19 patients by 89 percent, according to Pfizer.

As the EMA explained, the investigation that is now under way is intended to enable health authorities in the EU countries to use the drug at short notice before the drug is approved. There are currently three drugs approved for the treatment of Covid patients in the EU. Applications for approval have been made for a further four in total./evs/DP/ngu

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