Does DROXIDOPA Cause Product dose omission issue? 366 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 366 reports of Product dose omission issue have been filed in association with DROXIDOPA (Droxidopa). This represents 1.8% of all adverse event reports for DROXIDOPA.
366
Reports of Product dose omission issue with DROXIDOPA
1.8%
of all DROXIDOPA reports
8
Deaths
53
Hospitalizations
How Dangerous Is Product dose omission issue From DROXIDOPA?
Of the 366 reports, 8 (2.2%) resulted in death, 53 (14.5%) required hospitalization.
Is Product dose omission issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DROXIDOPA. However, 366 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 issue?
DUPILUMAB (18,189)
USTEKINUMAB (9,405)
GUSELKUMAB (9,267)
LENALIDOMIDE (8,145)
MEPOLIZUMAB (5,873)
TOFACITINIB (5,646)
VOXELOTOR (5,122)
BELIMUMAB (4,671)
SECUKINUMAB (4,572)
APREMILAST (4,460)
Which DROXIDOPA Alternatives Have Lower Product dose omission issue Risk?
DROXIDOPA vs DULAGLUTIDE
DROXIDOPA vs DULERA
DROXIDOPA vs DULOXETINE
DROXIDOPA vs DUPILUMAB
DROXIDOPA vs DURAGESIC