Does FENFLURAMINE Cause Product dose omission issue? 61 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 61 reports of Product dose omission issue have been filed in association with FENFLURAMINE (Fintepla). This represents 1.6% of all adverse event reports for FENFLURAMINE.
61
Reports of Product dose omission issue with FENFLURAMINE
1.6%
of all FENFLURAMINE reports
0
Deaths
24
Hospitalizations
How Dangerous Is Product dose omission issue From FENFLURAMINE?
Of the 61 reports, 24 (39.3%) required hospitalization, and 1 (1.6%) were considered life-threatening.
Is Product dose omission issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for FENFLURAMINE. However, 61 reports have been filed with the FAERS database.
What Other Side Effects Does FENFLURAMINE Cause?
Seizure (1,566)
Drug ineffective (585)
Off label use (526)
Decreased appetite (467)
Tricuspid valve incompetence (454)
Somnolence (378)
Weight decreased (329)
Mitral valve incompetence (276)
Diarrhoea (265)
Fatigue (253)
What Other Drugs Cause Product dose omission issue?
DUPILUMAB (18,189)
USTEKINUMAB (9,405)
GUSELKUMAB (9,267)
LENALIDOMIDE (8,145)
MEPOLIZUMAB (5,873)
TOFACITINIB (5,646)
VOXELOTOR (5,122)
BELIMUMAB (4,671)
SECUKINUMAB (4,572)
APREMILAST (4,460)
Which FENFLURAMINE Alternatives Have Lower Product dose omission issue Risk?
FENFLURAMINE vs FENOFIBRATE
FENFLURAMINE vs FENOFIBRIC ACID
FENFLURAMINE vs FENOTEROL
FENFLURAMINE vs FENOTEROL HYDROBROMIDE
FENFLURAMINE vs FENOTEROL HYDROBROMIDE\IPRATROPIUM