Does DROXIDOPA Cause Product use complaint? 41 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 41 reports of Product use complaint have been filed in association with DROXIDOPA (Droxidopa). This represents 0.2% of all adverse event reports for DROXIDOPA.
41
Reports of Product use complaint with DROXIDOPA
0.2%
of all DROXIDOPA reports
1
Deaths
6
Hospitalizations
How Dangerous Is Product use complaint From DROXIDOPA?
Of the 41 reports, 1 (2.4%) resulted in death, 6 (14.6%) required hospitalization.
Is Product use complaint Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DROXIDOPA. However, 41 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 use complaint?
TROFINETIDE (472)
ENZALUTAMIDE (336)
LIFITEGRAST (326)
VOXELOTOR (298)
CLASCOTERONE (285)
NIRMATRELVIR\RITONAVIR (248)
ABALOPARATIDE (224)
ESTRADIOL (208)
MOLNUPIRAVIR (206)
ACETAMINOPHEN (202)
Which DROXIDOPA Alternatives Have Lower Product use complaint Risk?
DROXIDOPA vs DULAGLUTIDE
DROXIDOPA vs DULERA
DROXIDOPA vs DULOXETINE
DROXIDOPA vs DUPILUMAB
DROXIDOPA vs DURAGESIC