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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does DROXIDOPA Cause Adverse event? 46 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 46 reports of Adverse event have been filed in association with DROXIDOPA (Droxidopa). This represents 0.2% of all adverse event reports for DROXIDOPA.

46
Reports of Adverse event with DROXIDOPA
0.2%
of all DROXIDOPA reports
0
Deaths
10
Hospitalizations

How Dangerous Is Adverse event From DROXIDOPA?

Of the 46 reports, 10 (21.7%) required hospitalization, and 1 (2.2%) were considered life-threatening.

Is Adverse event Listed in the Official Label?

Yes, Adverse event is listed as a known adverse reaction in the official FDA drug label for DROXIDOPA.

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 Adverse event?

ABATACEPT (4,028) APIXABAN (3,871) ETANERCEPT (3,096) LENALIDOMIDE (2,426) INFLIXIMAB (2,269) ADALIMUMAB (2,121) METHOTREXATE (1,846) LEFLUNOMIDE (1,476) RIVAROXABAN (1,465) ALENDRONATE (1,462)

Which DROXIDOPA Alternatives Have Lower Adverse event Risk?

DROXIDOPA vs DULAGLUTIDE DROXIDOPA vs DULERA DROXIDOPA vs DULOXETINE DROXIDOPA vs DUPILUMAB DROXIDOPA vs DURAGESIC

Related Pages

DROXIDOPA Full Profile All Adverse event Reports All Drugs Causing Adverse event DROXIDOPA Demographics