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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 Intentional dose omission? 25 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 25 reports of Intentional dose omission have been filed in association with DROXIDOPA (Droxidopa). This represents 0.1% of all adverse event reports for DROXIDOPA.

25
Reports of Intentional dose omission with DROXIDOPA
0.1%
of all DROXIDOPA reports
0
Deaths
4
Hospitalizations

How Dangerous Is Intentional dose omission From DROXIDOPA?

Of the 25 reports, 4 (16.0%) required hospitalization.

Is Intentional dose omission Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for DROXIDOPA. However, 25 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 Intentional dose omission?

DUPILUMAB (2,269) CERTOLIZUMAB PEGOL (1,253) ADALIMUMAB (845) TOFACITINIB (845) INFLIXIMAB (815) ABALOPARATIDE (623) ETANERCEPT (615) AMBRISENTAN (595) SODIUM OXYBATE (580) CALCIUM OXYBATE\MAGNESIUM OXYBATE\POTASSIUM OXYBATE\SODIUM OXYBATE (518)

Which DROXIDOPA Alternatives Have Lower Intentional dose omission Risk?

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

Related Pages

DROXIDOPA Full Profile All Intentional dose omission Reports All Drugs Causing Intentional dose omission DROXIDOPA Demographics