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Molnupiravir not to be included in Covid treatment now

By Payal Banerjee
January 11, 2022 18:04 IST
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The Indian Council of Medical Research's national task force for COVID-19 has decided against including antiviral drug Molnupiravir in the clinical management protocol for COVID-19 as of now, official sources said on Tuesday.

IMAGE: Dr Lingaiah Amidyala, director of Yashoda Hospitals showing the latest COVID drug 'Molnupiravir' ahead of its Phase III clinical trials in Hyderabad, May 21, 2021. Photograph: ANI Photo

The experts of the task force cited safety concerns and argued that Molnupiravir was not of much benefit in COVID treatment to arrive at the decision in a meeting held on Monday.


According to the health ministry, Molnupiravir is an antiviral drug that inhibits SARS-CoV-2 replication by viral mutagenesis.

This anti-Covid pill got the Drug Regulator General of India's approval on December 28 for restricted use in emergencies.

"Members of the National Task Force for COVID-19 were not in favour of including the drug in the national treatment guidelines citing that it does not have much benefit in the treatment of coronavirus infection and that there were safety concerns," an official source told PTI.

ICMR chief Dr Balram Bhargava had last week said that Molnupiravir has major safety concerns.

He added that the World Health Organisation and the UK have not included it for treatment.

"We have to remember that this drug has major safety concerns. It can cause teratogenicity, mutagenicity and cartilage damage. It can damage the muscles also," the ICMR chief had said.

"Contraception will have to be done for three months for male and female if this drug is given because the child born could be problematic due to teratogenic influence," he had said.

The UK medicines and healthcare products regulatory agency had on December 4 granted approval for Molnupiravir under special conditions for treatment of mild to moderate COVID-19 in adults who have at least one risk factor for developing severe illness.

The United States Food and Drug Administration on December 23 granted emergency use authorisation for the drug for treating mild-to-moderate COVID-19 in adults at high risk for progression to severe disease, including hospitalisation or death, and for whom alternative treatment options are not accessible or clinically appropriate.

According to conditions, the drug should be sold by retail only under the prescription of medical specialists and the recommended dose should be 800 mg twice daily for five days.

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Payal Banerjee in New Delhi
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