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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does MOLNUPIRAVIR Cause Intentional product use issue? 21 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 21 reports of Intentional product use issue have been filed in association with MOLNUPIRAVIR (LAGEVRIO). This represents 0.4% of all adverse event reports for MOLNUPIRAVIR.

21
Reports of Intentional product use issue with MOLNUPIRAVIR
0.4%
of all MOLNUPIRAVIR reports
0
Deaths
3
Hospitalizations

How Dangerous Is Intentional product use issue From MOLNUPIRAVIR?

Of the 21 reports, 3 (14.3%) required hospitalization.

Is Intentional product use issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for MOLNUPIRAVIR. However, 21 reports have been filed with the FAERS database.

What Other Side Effects Does MOLNUPIRAVIR Cause?

Product use issue (706) No adverse event (614) Covid-19 (396) Wrong technique in product usage process (380) Product use in unapproved indication (296) Diarrhoea (259) Accidental underdose (207) Product use complaint (206) Rash (200) Underdose (183)

What Other Drugs Cause Intentional product use issue?

INFLIXIMAB (11,028) RITUXIMAB (9,602) INFLIXIMAB-DYYB (7,549) TOCILIZUMAB (5,078) METHOTREXATE (4,087) PREDNISONE (3,961) ABATACEPT (3,693) ADALIMUMAB (3,557) NIVOLUMAB (3,297) LEFLUNOMIDE (3,280)

Which MOLNUPIRAVIR Alternatives Have Lower Intentional product use issue Risk?

MOLNUPIRAVIR vs MOLSIDOMINE MOLNUPIRAVIR vs MOMELOTINIB MOLNUPIRAVIR vs MOMETASONE MOLNUPIRAVIR vs MOMETASONE FUROATE MOLNUPIRAVIR vs MOMETASONE FUROATE\OLOPATADINE

Related Pages

MOLNUPIRAVIR Full Profile All Intentional product use issue Reports All Drugs Causing Intentional product use issue MOLNUPIRAVIR Demographics