UK Regulator Approves Paxlovid Covid-19 Antiviral Drug

Healthcare

A novel corona virus treatment drug called as Paxlovid has now received the approval by the MHRA (Medicines and Healthcare products Regulatory Agency) of the United Kingdom after the agency has found for being safe and effective at the decreasing risk of deaths and hospitalizations in the people suffering with the moderate and mild corona virus infection, who are at an increased risk of developing the serious illness.

This approval has also been following a review of the safety of the people, along with the effectiveness and quality by the regulator of the United Kingdom along with the advice from the health experts of the United Kingdom’s independent scientific advisory board known as the Commission on the Human Medicines.

Paxlovid, which has been developed by Pfizer is an antiviral medicine along with a combination of the active ingredients that has been working by inhibiting a required replication of the novel corona virus, and this medicine has been preventing the novel corona virus from spreading along with keeping the levels of the corona virus low and also providing help to the people for overcoming the infections.

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The medicine has also been responsible for decreasing the breakdown of the second ingredient known as PF-07321332 in the body of the infected people, along with the increasing effectiveness of the medicine, and the two active substances in the medicine has been coming as separate tablets that have been packaged and taken together two times a day for a time period of 5 days.

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