Does DROXIDOPA Cause Condition aggravated? 533 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 533 reports of Condition aggravated have been filed in association with DROXIDOPA (Droxidopa). This represents 2.7% of all adverse event reports for DROXIDOPA.
533
Reports of Condition aggravated with DROXIDOPA
2.7%
of all DROXIDOPA reports
14
Deaths
82
Hospitalizations
How Dangerous Is Condition aggravated From DROXIDOPA?
Of the 533 reports, 14 (2.6%) resulted in death, 82 (15.4%) required hospitalization, and 5 (0.9%) were considered life-threatening.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DROXIDOPA. However, 533 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 Condition aggravated?
TOFACITINIB (16,925)
INFLIXIMAB (16,616)
DUPILUMAB (16,459)
ETANERCEPT (15,897)
METHOTREXATE (14,938)
ADALIMUMAB (13,527)
PREDNISONE (10,751)
INFLIXIMAB-DYYB (10,275)
HYDROXYCHLOROQUINE (8,848)
RITUXIMAB (8,627)
Which DROXIDOPA Alternatives Have Lower Condition aggravated Risk?
DROXIDOPA vs DULAGLUTIDE
DROXIDOPA vs DULERA
DROXIDOPA vs DULOXETINE
DROXIDOPA vs DUPILUMAB
DROXIDOPA vs DURAGESIC