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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 misuse? 45 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 45 reports of Intentional product misuse have been filed in association with MOLNUPIRAVIR (LAGEVRIO). This represents 0.9% of all adverse event reports for MOLNUPIRAVIR.

45
Reports of Intentional product misuse with MOLNUPIRAVIR
0.9%
of all MOLNUPIRAVIR reports
0
Deaths
4
Hospitalizations

How Dangerous Is Intentional product misuse From MOLNUPIRAVIR?

Of the 45 reports, 4 (8.9%) required hospitalization.

Is Intentional product misuse Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for MOLNUPIRAVIR. However, 45 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 misuse?

ETANERCEPT (3,992) PREGABALIN (3,731) BUDESONIDE\FORMOTEROL (3,399) ACETAMINOPHEN (2,924) ESOMEPRAZOLE (2,852) MINOXIDIL (2,418) TOFACITINIB (2,331) CINACALCET (2,092) QUETIAPINE (1,855) ALPRAZOLAM (1,709)

Which MOLNUPIRAVIR Alternatives Have Lower Intentional product misuse 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 misuse Reports All Drugs Causing Intentional product misuse MOLNUPIRAVIR Demographics