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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 Haematochezia? 61 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 61 reports of Haematochezia have been filed in association with CLOFIBRATE. This represents 75.3% of all adverse event reports for CLOFIBRATE.

61
Reports of Haematochezia with CLOFIBRATE
75.3%
of all CLOFIBRATE reports
0
Deaths
61
Hospitalizations

How Dangerous Is Haematochezia From CLOFIBRATE?

Of the 61 reports, 61 (100.0%) required hospitalization.

Is Haematochezia Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for CLOFIBRATE. However, 61 reports have been filed with the FAERS database.

What Other Side Effects Does CLOFIBRATE Cause?

Pain (73) Chronic sinusitis (64) Dyspepsia (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)

What Other Drugs Cause Haematochezia?

VEDOLIZUMAB (5,215) ADALIMUMAB (4,008) INFLIXIMAB (3,539) ASPIRIN (2,379) RIVAROXABAN (1,623) MESALAMINE (1,456) CLOPIDOGREL BISULFATE (1,390) APIXABAN (1,312) METHOTREXATE (1,133) TOFACITINIB (1,118)

Related Pages

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