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EMA grants conditional marketing approval for Paxlovid to treat COVID 19 infection. Pfizer
The European Medicines Agency issued a conditional marketing authorization for Paxlovid, an antiviral treatment taken orally to treat Covid-19. Produced by Pfizer, the pills were approved for use in adults who tested positive for the coronavirus, and who do not yet need to be put on oxygen, but whose symptoms of the disease are worsening.
The treatment consists of a total of 30 pills administered over a five-day period. Two 150-milligram tablets of Paxlovid and one 100-milligram tablet of the drug ritonavir are to be given together to a patient twice daily. A single carton distributed by the company will include all pills required for the full course of treatment. Paxlovid reduces the ability of the SARS-CoV-2 coronavirus to replicate in the body, while ritonavir extends the effectiveness of the Pfizer medication. This enables “it to remain longer in the body at levels that affect the multiplication of the virus".
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Condition: Coronavirus/COVID-19 Infection
Type: drug