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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 GEMFIBROZIL Cause Hypertransaminasaemia? 16 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 16 reports of Hypertransaminasaemia have been filed in association with GEMFIBROZIL (Gemfibrozil). This represents 1.5% of all adverse event reports for GEMFIBROZIL.

16
Reports of Hypertransaminasaemia with GEMFIBROZIL
1.5%
of all GEMFIBROZIL reports
0
Deaths
16
Hospitalizations

How Dangerous Is Hypertransaminasaemia From GEMFIBROZIL?

Of the 16 reports, 16 (100.0%) required hospitalization.

Is Hypertransaminasaemia Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for GEMFIBROZIL. However, 16 reports have been filed with the FAERS database.

What Other Side Effects Does GEMFIBROZIL Cause?

Drug hypersensitivity (242) Drug ineffective (77) Rhabdomyolysis (63) Fatigue (60) Drug interaction (59) Myalgia (58) Nausea (54) Acute kidney injury (52) Diarrhoea (43) Rash (41)

What Other Drugs Cause Hypertransaminasaemia?

METHOTREXATE (436) ACETAMINOPHEN (326) PACLITAXEL (318) CARBOPLATIN (304) PEMBROLIZUMAB (231) ATORVASTATIN (207) CYCLOPHOSPHAMIDE (202) PREDNISONE (198) GEMCITABINE (196) DEXAMETHASONE (169)

Which GEMFIBROZIL Alternatives Have Lower Hypertransaminasaemia Risk?

GEMFIBROZIL vs GEMTUZUMAB OZOGAMICIN GEMFIBROZIL vs GEMZAR GEMFIBROZIL vs GENTAMICIN GEMFIBROZIL vs GEODON GEMFIBROZIL vs GILENYA

Related Pages

GEMFIBROZIL Full Profile All Hypertransaminasaemia Reports All Drugs Causing Hypertransaminasaemia GEMFIBROZIL Demographics