Does DIROXIMEL Cause Intentional product misuse? 180 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 180 reports of Intentional product misuse have been filed in association with DIROXIMEL (Vumerity). This represents 1.7% of all adverse event reports for DIROXIMEL.
180
Reports of Intentional product misuse with DIROXIMEL
1.7%
of all DIROXIMEL reports
0
Deaths
9
Hospitalizations
How Dangerous Is Intentional product misuse From DIROXIMEL?
Of the 180 reports, 9 (5.0%) required hospitalization.
Is Intentional product misuse Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DIROXIMEL. However, 180 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 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 DIROXIMEL Alternatives Have Lower Intentional product misuse Risk?
DIROXIMEL vs DISOPYRAMIDE
DIROXIMEL vs DISTIGMINE
DIROXIMEL vs DISULFIRAM
DIROXIMEL vs DIVALPROEX
DIROXIMEL vs DOBUTAMINE