Italian Medicines Agency Agenzia Italiana del Farmaco

Meeting highlights from the Pharmacovigilance Risk Assessment Committee (PRAC) 5-8 February 2024 - Meeting highlights from the Pharmacovigilance Risk Assessment Committee (PRAC) 5-8 February 2024

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Meeting highlights from the Pharmacovigilance Risk Assessment Committee (PRAC) 5-8 February 2024

EMA’s safety committee (PRAC) is reminding healthcare professionals of the risk of serious and potentially fatal adverse reactions with Paxlovid (nirmatrelvir, ritonavir) when used in combination with certain immunosuppressants that have a narrow safe dosage range (where small changes in the dose can lead to serious adverse reactions), due to drug-drug interactions reducing the body’s ability to eliminate these medicines.

The PRAC reviewed all available evidence, including reports of serious adverse reactions, some of which were fatal, resulting from drug-drug interactions between Paxlovid and these immunosuppressants. In several cases, blood levels of these immunosuppressants increased rapidly to toxic levels resulting in life-threatening conditions. Therefore, the PRAC agreed on a direct healthcare professional communication (DHPC) to remind healthcare professionals of the risk of these interactions, which is known and already described in the product information for this medicine.
 


Published on: 09 February 2024

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