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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.

RESMETIROM for Steatohepatitis: Side Effects & Safety Data

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There are 5 adverse event reports in the FDA FAERS database where RESMETIROM was used for Steatohepatitis.

Most Reported Side Effects for RESMETIROM

Side Effect Reports % Deaths Hosp.
Diarrhoea 182 20.7% 0 7
Nausea 162 18.4% 1 7
Pruritus 147 16.7% 0 6
Alanine aminotransferase increased 98 11.1% 0 7
Aspartate aminotransferase increased 97 11.0% 0 7
Fatigue 72 8.2% 1 3
Abdominal pain upper 69 7.8% 0 3
Dizziness 68 7.7% 0 4
Vomiting 60 6.8% 0 6
Weight decreased 47 5.3% 0 1
Blood bilirubin increased 41 4.7% 0 6
Rash 40 4.5% 0 0
Hepatic enzyme increased 38 4.3% 0 0
Abdominal pain 37 4.2% 0 3
Headache 37 4.2% 0 1

Other Indications for RESMETIROM

Metabolic dysfunction-associated steatohepatitis (451) Product used for unknown indication (194) Non-alcoholic steatohepatitis (125) Hepatic steatosis (63) Hepatic fibrosis (40) Hepatic cirrhosis (24)

Related Pages

RESMETIROM Full Profile All Steatohepatitis Drugs RESMETIROM Demographics RESMETIROM Timeline