Does DIROXIMEL Cause Product dose omission issue? 759 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 759 reports of Product dose omission issue have been filed in association with DIROXIMEL (Vumerity). This represents 7.1% of all adverse event reports for DIROXIMEL.
759
Reports of Product dose omission issue with DIROXIMEL
7.1%
of all DIROXIMEL reports
2
Deaths
55
Hospitalizations
How Dangerous Is Product dose omission issue From DIROXIMEL?
Of the 759 reports, 2 (0.3%) resulted in death, 55 (7.2%) required hospitalization, and 1 (0.1%) 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 DIROXIMEL. However, 759 reports have been filed with the FAERS database.
What Other Side Effects Does DIROXIMEL Cause?
Flushing (1,518)
Multiple sclerosis (978)
Multiple sclerosis relapse (892)
Diarrhoea (836)
Fatigue (715)
Nausea (709)
Headache (571)
Pruritus (552)
Memory impairment (517)
Fall (500)
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 DIROXIMEL Alternatives Have Lower Product dose omission issue Risk?
DIROXIMEL vs DISOPYRAMIDE
DIROXIMEL vs DISTIGMINE
DIROXIMEL vs DISULFIRAM
DIROXIMEL vs DIVALPROEX
DIROXIMEL vs DOBUTAMINE