Does DROXIDOPA Cause Intentional product use issue? 105 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 105 reports of Intentional product use issue have been filed in association with DROXIDOPA (Droxidopa). This represents 0.5% of all adverse event reports for DROXIDOPA.
105
Reports of Intentional product use issue with DROXIDOPA
0.5%
of all DROXIDOPA reports
0
Deaths
5
Hospitalizations
How Dangerous Is Intentional product use issue From DROXIDOPA?
Of the 105 reports, 5 (4.8%) required hospitalization.
Is Intentional product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DROXIDOPA. However, 105 reports have been filed with the FAERS database.
What Other Side Effects Does DROXIDOPA Cause?
Dizziness (2,823)
Death (1,985)
Blood pressure increased (1,862)
Drug ineffective (1,602)
Headache (1,555)
Fall (1,351)
Hypotension (1,180)
Fatigue (1,142)
Hypertension (1,133)
Nausea (1,032)
What Other Drugs Cause Intentional product use issue?
INFLIXIMAB (11,028)
RITUXIMAB (9,602)
INFLIXIMAB-DYYB (7,549)
TOCILIZUMAB (5,078)
METHOTREXATE (4,087)
PREDNISONE (3,961)
ABATACEPT (3,693)
ADALIMUMAB (3,557)
NIVOLUMAB (3,297)
LEFLUNOMIDE (3,280)
Which DROXIDOPA Alternatives Have Lower Intentional product use issue Risk?
DROXIDOPA vs DULAGLUTIDE
DROXIDOPA vs DULERA
DROXIDOPA vs DULOXETINE
DROXIDOPA vs DUPILUMAB
DROXIDOPA vs DURAGESIC