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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 UNSPECIFIED INGREDIENT Cause Off label use? 1,306 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 1,306 reports of Off label use have been filed in association with UNSPECIFIED INGREDIENT. This represents 5.0% of all adverse event reports for UNSPECIFIED INGREDIENT.

1,306
Reports of Off label use with UNSPECIFIED INGREDIENT
5.0%
of all UNSPECIFIED INGREDIENT reports
324
Deaths
483
Hospitalizations

How Dangerous Is Off label use From UNSPECIFIED INGREDIENT?

Of the 1,306 reports, 324 (24.8%) resulted in death, 483 (37.0%) required hospitalization, and 158 (12.1%) were considered life-threatening.

Is Off label use Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for UNSPECIFIED INGREDIENT. However, 1,306 reports have been filed with the FAERS database.

What Other Side Effects Does UNSPECIFIED INGREDIENT Cause?

Death (2,090) Drug ineffective (1,227) Completed suicide (1,190) Nausea (1,041) Fatigue (1,020) Dyspnoea (934) Pneumonia (903) Asthenia (894) Vomiting (877) Diarrhoea (821)

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)

Which UNSPECIFIED INGREDIENT Alternatives Have Lower Off label use Risk?

UNSPECIFIED INGREDIENT vs UPADACITINIB UNSPECIFIED INGREDIENT vs URAPIDIL UNSPECIFIED INGREDIENT vs UREA UNSPECIFIED INGREDIENT vs URIDINE TRIACETATE UNSPECIFIED INGREDIENT vs UROFOLLITROPIN

Related Pages

UNSPECIFIED INGREDIENT Full Profile All Off label use Reports All Drugs Causing Off label use UNSPECIFIED INGREDIENT Demographics