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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 Off label use? 63 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 63 reports of Off label use have been filed in association with CLOFIBRATE. This represents 77.8% of all adverse event reports for CLOFIBRATE.

63
Reports of Off label use with CLOFIBRATE
77.8%
of all CLOFIBRATE reports
0
Deaths
63
Hospitalizations

How Dangerous Is Off label use From CLOFIBRATE?

Of the 63 reports, 63 (100.0%) required hospitalization.

Is Off label use Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for CLOFIBRATE. However, 63 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) Paraesthesia oral (63)

What Other Drugs Cause Off label use?

RITUXIMAB (39,751) INFLIXIMAB (34,801) DENOSUMAB (34,612) METHOTREXATE (24,020) VEDOLIZUMAB (21,017) ETANERCEPT (20,178) TOCILIZUMAB (18,256) PREDNISONE (17,867) LENALIDOMIDE (17,017) ADALIMUMAB (16,417)

Related Pages

CLOFIBRATE Full Profile All Off label use Reports All Drugs Causing Off label use CLOFIBRATE Demographics