Does DIROXIMEL Cause Wrong technique in product usage process? 7 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Wrong technique in product usage process have been filed in association with DIROXIMEL (Vumerity). This represents 0.1% of all adverse event reports for DIROXIMEL.
7
Reports of Wrong technique in product usage process with DIROXIMEL
0.1%
of all DIROXIMEL reports
0
Deaths
3
Hospitalizations
How Dangerous Is Wrong technique in product usage process From DIROXIMEL?
Of the 7 reports, 3 (42.9%) required hospitalization, and 1 (14.3%) were considered life-threatening.
Is Wrong technique in product usage process Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DIROXIMEL. However, 7 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 Wrong technique in product usage process?
EVOLOCUMAB (21,664)
ALBUTEROL (17,114)
ADALIMUMAB (11,766)
PEGFILGRASTIM (10,217)
ETANERCEPT (9,835)
ERENUMAB-AOOE (9,359)
SACUBITRIL\VALSARTAN (8,022)
LEUPROLIDE (5,062)
FENTANYL (2,812)
SEMAGLUTIDE (2,538)
Which DIROXIMEL Alternatives Have Lower Wrong technique in product usage process Risk?
DIROXIMEL vs DISOPYRAMIDE
DIROXIMEL vs DISTIGMINE
DIROXIMEL vs DISULFIRAM
DIROXIMEL vs DIVALPROEX
DIROXIMEL vs DOBUTAMINE