Does LUTEIN Cause Intentional product misuse? 32 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 32 reports of Intentional product misuse have been filed in association with LUTEIN. This represents 32.0% of all adverse event reports for LUTEIN.
32
Reports of Intentional product misuse with LUTEIN
32.0%
of all LUTEIN reports
32
Deaths
32
Hospitalizations
How Dangerous Is Intentional product misuse From LUTEIN?
Of the 32 reports, 32 (100.0%) resulted in death, 32 (100.0%) required hospitalization, and 30 (93.8%) were considered life-threatening.
Is Intentional product misuse Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for LUTEIN. However, 32 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 Intentional product misuse?
ETANERCEPT (3,992)
PREGABALIN (3,731)
BUDESONIDE\FORMOTEROL (3,399)
ACETAMINOPHEN (2,924)
ESOMEPRAZOLE (2,852)
MINOXIDIL (2,418)
TOFACITINIB (2,331)
CINACALCET (2,092)
QUETIAPINE (1,855)
ALPRAZOLAM (1,709)
Which LUTEIN Alternatives Have Lower Intentional product misuse 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