Does LUTEIN Cause Condition aggravated? 55 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 55 reports of Condition aggravated have been filed in association with LUTEIN. This represents 55.0% of all adverse event reports for LUTEIN.
55
Reports of Condition aggravated with LUTEIN
55.0%
of all LUTEIN reports
55
Deaths
40
Hospitalizations
How Dangerous Is Condition aggravated From LUTEIN?
Of the 55 reports, 55 (100.0%) resulted in death, 40 (72.7%) required hospitalization, and 36 (65.5%) 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 LUTEIN. However, 55 reports have been filed with the FAERS database.
What Other Side Effects Does LUTEIN Cause?
Abdominal distension (65)
Appendicitis (63)
Ascites (63)
Hyponatraemia (63)
Vomiting (63)
Abdominal pain (62)
Appendicolith (62)
Ventricular fibrillation (62)
General physical health deterioration (61)
Stress (61)
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)
Which LUTEIN Alternatives Have Lower Condition aggravated Risk?
LUTEIN vs LUTETIUM LU-177
LUTEIN vs LUTETIUM LU-177 VIPIVOTIDE TETRAXETAN
LUTEIN vs LUTETIUM OXODOTREOTIDE LU-177
LUTEIN vs LUTROPIN ALFA
LUTEIN vs LYMECYCLINE