Wednesday, 1 May, 2024
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UK regulatory body warns about Paxlovid risks

Britain’s health regulator has issued a warning about Covid-19 medication Paxlovid and the potential for risk of harmful drug interactions because of the ritonavir component – due to its inhibition of the enzyme CYP3A that metabolises many commonly used drugs.

The Medicines and Healthcare products Regulatory Agency (MHRA) has recommended prescribers obtain a detailed patient history of current medications before prescribing Paxlovid.

Ritonavir is a potent CYP3A4 inhibitor that acts to boost the plasma levels of the nirmatrelvir component of Paxlovid by preventing its degradation; as many commonly used drugs are metabolised by CYP3A4, the risk of harmful drug interactions with Paxlovid is significant, it said.

Additionally, drug interactions may also reduce its effectiveness in the treatment of Covid-19.

While the drug was approved for use in South Africa earlier this year, MedicalBrief reported last week that it is very expensive in this country, and not easily available.

 

MHRA article – Nirmatrelvir, ritonavir (Paxlovid): be alert to the risk of drug interactions with ritonavir (Open access)

 

See more from MedicalBrief archives:

 

The quest for pills to thwart long Covid – is it worth it?

 

Covid drug Paxlovid now approved for use in SA

 

Paxlovid as a treatment for long COVID

 

 

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