Does DIROXIMEL Cause Product dose omission in error? 481 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 481 reports of Product dose omission in error have been filed in association with DIROXIMEL (Vumerity). This represents 4.5% of all adverse event reports for DIROXIMEL.
481
Reports of Product dose omission in error with DIROXIMEL
4.5%
of all DIROXIMEL reports
0
Deaths
24
Hospitalizations
How Dangerous Is Product dose omission in error From DIROXIMEL?
Of the 481 reports, 24 (5.0%) required hospitalization.
Is Product dose omission in error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DIROXIMEL. However, 481 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)
Product dose omission issue (759)
Fatigue (715)
Nausea (709)
Headache (571)
Pruritus (552)
Memory impairment (517)
What Other Drugs Cause Product dose omission in error?
DUPILUMAB (7,586)
TOFACITINIB (2,461)
LENALIDOMIDE (618)
PALBOCICLIB (592)
ABALOPARATIDE (457)
NIRAPARIB (428)
RUXOLITINIB (425)
TERIFLUNOMIDE (371)
DIMETHYL (308)
RELUGOLIX (293)
Which DIROXIMEL Alternatives Have Lower Product dose omission in error Risk?
DIROXIMEL vs DISOPYRAMIDE
DIROXIMEL vs DISTIGMINE
DIROXIMEL vs DISULFIRAM
DIROXIMEL vs DIVALPROEX
DIROXIMEL vs DOBUTAMINE