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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 BETA.-CAROTENE Cause Off label use? 29 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 29 reports of Off label use have been filed in association with BETA.-CAROTENE. This represents 58.0% of all adverse event reports for BETA.-CAROTENE.

29
Reports of Off label use with BETA.-CAROTENE
58.0%
of all BETA.-CAROTENE reports
29
Deaths
21
Hospitalizations

How Dangerous Is Off label use From BETA.-CAROTENE?

Of the 29 reports, 29 (100.0%) resulted in death, 21 (72.4%) required hospitalization, and 19 (65.5%) 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 BETA.-CAROTENE. However, 29 reports have been filed with the FAERS database.

What Other Side Effects Does BETA.-CAROTENE Cause?

Hyponatraemia (38) Abdominal distension (37) Vomiting (37) Abdominal pain (34) Appendicitis (34) Appendicolith (34) Ascites (34) Nausea (34) Constipation (33) Ventricular fibrillation (33)

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

BETA.-CAROTENE Full Profile All Off label use Reports All Drugs Causing Off label use BETA.-CAROTENE Demographics