Does DROXIDOPA Cause Product administration error? 19 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 19 reports of Product administration error have been filed in association with DROXIDOPA (Droxidopa). This represents 0.1% of all adverse event reports for DROXIDOPA.
19
Reports of Product administration error with DROXIDOPA
0.1%
of all DROXIDOPA reports
0
Deaths
1
Hospitalizations
How Dangerous Is Product administration error From DROXIDOPA?
Of the 19 reports, 1 (5.3%) required hospitalization.
Is Product administration error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DROXIDOPA. However, 19 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 Product administration error?
HYDROXYPROGESTERONE CAPROATE (972)
ACETAMINOPHEN (666)
CENEGERMIN-BKBJ (613)
LEUPROLIDE (595)
EVOLOCUMAB (565)
ADALIMUMAB (543)
METHYLPHENIDATE (414)
OLMESARTAN MEDOXOMIL (314)
ASPIRIN (241)
SECUKINUMAB (225)
Which DROXIDOPA Alternatives Have Lower Product administration error Risk?
DROXIDOPA vs DULAGLUTIDE
DROXIDOPA vs DULERA
DROXIDOPA vs DULOXETINE
DROXIDOPA vs DUPILUMAB
DROXIDOPA vs DURAGESIC