Does DROXIDOPA Cause Product dose omission? 382 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 382 reports of Product dose omission have been filed in association with DROXIDOPA (Droxidopa). This represents 1.9% of all adverse event reports for DROXIDOPA.
382
Reports of Product dose omission with DROXIDOPA
1.9%
of all DROXIDOPA reports
1
Deaths
49
Hospitalizations
How Dangerous Is Product dose omission From DROXIDOPA?
Of the 382 reports, 1 (0.3%) resulted in death, 49 (12.8%) required hospitalization, and 2 (0.5%) were considered life-threatening.
Is Product dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DROXIDOPA. However, 382 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 dose omission?
APREMILAST (4,567)
DUPILUMAB (2,729)
ALBUTEROL (1,742)
USTEKINUMAB (1,653)
INSULIN GLARGINE (1,500)
ETANERCEPT (1,400)
LENALIDOMIDE (1,400)
RUXOLITINIB (1,376)
ALIROCUMAB (1,354)
DIMETHYL (1,248)
Which DROXIDOPA Alternatives Have Lower Product dose omission Risk?
DROXIDOPA vs DULAGLUTIDE
DROXIDOPA vs DULERA
DROXIDOPA vs DULOXETINE
DROXIDOPA vs DUPILUMAB
DROXIDOPA vs DURAGESIC