Does BETA.-CAROTENE Cause Condition aggravated? 25 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 25 reports of Condition aggravated have been filed in association with BETA.-CAROTENE. This represents 50.0% of all adverse event reports for BETA.-CAROTENE.
25
Reports of Condition aggravated with BETA.-CAROTENE
50.0%
of all BETA.-CAROTENE reports
25
Deaths
21
Hospitalizations
How Dangerous Is Condition aggravated From BETA.-CAROTENE?
Of the 25 reports, 25 (100.0%) resulted in death, 21 (84.0%) required hospitalization, and 19 (76.0%) were considered life-threatening.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BETA.-CAROTENE. However, 25 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 Condition aggravated?
TOFACITINIB (16,925)
INFLIXIMAB (16,616)
DUPILUMAB (16,459)
ETANERCEPT (15,897)
METHOTREXATE (14,938)
ADALIMUMAB (13,527)
PREDNISONE (10,751)
INFLIXIMAB-DYYB (10,275)
HYDROXYCHLOROQUINE (8,848)
RITUXIMAB (8,627)