Prescribing Information for ▼PAXLOVID (nirmatrelvir / ritonavir) can be found here. Adverse event reporting information can be found at the bottom of the page.
Paxlovid has a Conditional Marketing Authorisation in the United Kingdom. A Conditional Marketing Authorisation means that further evidence on this medicinal product is awaited. New information on this medicinal product will be reviewed when any relevant information of significance becomes available and at least every year and the product information will be updated as necessary.
NICE has recommended treatments for patients who do not need supplemental oxygen and are at increased risk for progression to severe COVID-19, as defined by the Independent Advisory Group Report1,2
Remdesivir is also recommended as a treatment option in hospitals for adults and paediatric patients (weighing at least 40kg)6
The decision to treat and choice of treatment is based on the individual patient’s eligibility criteria, clinical circumstances and is ultimately at the discretion of the individual prescriber. Please refer to the SmPC5 before making any prescribing decisions.
Summary of the high risk adult patients who may be eligible for COVID-19 treatment.
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Learn about PAXLOVID dosing, potential drug interactions, and how to prescribe.
Explore downloadable materials to further support both you and your patients.
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Watch short educational key-opinion-leader (KOL) videos from Healthcare Professionals on their experience in managing patients at risk of severe COVID-19.
Adverse Events
Adverse Events should be reported. Reporting forms and information can be found at https://coronavirus-yellowcard.mhra.gov.uk/ or search
for MHRA Yellow Card in Google Play or Apple App Store
Adverse events should also be reported to Pfizer Medical Information on 01304 616161
To access further materials, resources and receive communication about medicines and vaccines promoted by Pfizer.
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