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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 Haematemesis? 26 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 26 reports of Haematemesis have been filed in association with MOLNUPIRAVIR (LAGEVRIO). This represents 0.5% of all adverse event reports for MOLNUPIRAVIR.

26
Reports of Haematemesis with MOLNUPIRAVIR
0.5%
of all MOLNUPIRAVIR reports
18
Deaths
2
Hospitalizations

How Dangerous Is Haematemesis From MOLNUPIRAVIR?

Of the 26 reports, 18 (69.2%) resulted in death, 2 (7.7%) required hospitalization, and 14 (53.8%) were considered life-threatening.

Is Haematemesis Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for MOLNUPIRAVIR. However, 26 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 Haematemesis?

ASPIRIN (1,538) RIVAROXABAN (1,085) CLOPIDOGREL BISULFATE (954) IBUPROFEN (836) APIXABAN (650) ADALIMUMAB (563) ACETAMINOPHEN (454) WARFARIN (426) SERTRALINE (412) ENOXAPARIN (404)

Which MOLNUPIRAVIR Alternatives Have Lower Haematemesis 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 Haematemesis Reports All Drugs Causing Haematemesis MOLNUPIRAVIR Demographics