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The Hague, The Netherlands (AP) — European Union pharmaceutical institutions began reviewing Merck’s COVID-19 treatment on Monday. This has allowed us to quickly advise national drug authorities in blocks of 27 countries before obtaining formal approval.
In a statement, the European Medicines Agency said, “Providing EU-wide recommendations in the shortest possible time frame to help national authorities determine the possibility of early use of medicines, such as in an emergency use environment. I will do it. “
The Amsterdam-based agency provides recommendations while a comprehensive review of Molnupiravir continues ahead of possible applications for selling the drug.
Currently, most COVID-19 treatments require IV or injection. Merck’s COVID-19 pill has already been reviewed by the US Food and Drug Administration after showing strong initial results. On Thursday, Britain became the first country to accept it.
In the UK, the pill tested positive for COVID-19 and was approved for adults over the age of 18 who have at least one risk factor for developing serious illnesses such as obesity and heart disease. Patients with mild to moderate COVID-19 take 4 tablets twice daily for 5 days.
In the United States, the FDA set up a public meeting later this month to consider Molnupiravir. The company reported in September that the drug reduced hospitalization and mortality by 50%.
The drug targets the enzyme that the coronavirus uses to replicate itself, inserting errors into the genetic code and delaying the ability of human cells to spread and take over. Its genetic activity has led some independent experts to question whether the drug can cause mutations that lead to birth defects and tumors.
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EU Pharmaceuticals Reviewing Data on Merck’s COVID-19 Pills | WGN Radio 720
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