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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 CLOFIBRATE Cause Dyspepsia? 64 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 64 reports of Dyspepsia have been filed in association with CLOFIBRATE. This represents 79.0% of all adverse event reports for CLOFIBRATE.

64
Reports of Dyspepsia with CLOFIBRATE
79.0%
of all CLOFIBRATE reports
0
Deaths
64
Hospitalizations

How Dangerous Is Dyspepsia From CLOFIBRATE?

Of the 64 reports, 64 (100.0%) required hospitalization.

Is Dyspepsia Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for CLOFIBRATE. However, 64 reports have been filed with the FAERS database.

What Other Side Effects Does CLOFIBRATE Cause?

Pain (73) Chronic sinusitis (64) Infusion related reaction (64) Malaise (64) Procedural pain (64) Therapeutic product effect incomplete (64) Female genital tract fistula (63) Nausea (63) Off label use (63) Paraesthesia oral (63)

What Other Drugs Cause Dyspepsia?

ADALIMUMAB (3,586) METHOTREXATE (2,690) RITUXIMAB (2,289) TOFACITINIB (2,264) PREDNISONE (2,224) APREMILAST (2,207) ETANERCEPT (2,100) ESOMEPRAZOLE (2,064) TOCILIZUMAB (2,046) LEFLUNOMIDE (1,981)

Related Pages

CLOFIBRATE Full Profile All Dyspepsia Reports All Drugs Causing Dyspepsia CLOFIBRATE Demographics