Does PRAMIPEXOLE Cause Condition aggravated? 361 Reports in FDA Database
Sharpen Your Memory & Focus Naturally
NeuroZoom — 35 clinically studied ingredients. No stimulants. Pure brain support.
According to the FDA Adverse Event Reporting System (FAERS), 361 reports of Condition aggravated have been filed in association with PRAMIPEXOLE (Pramipexole Dihydrochloride). This represents 6.0% of all adverse event reports for PRAMIPEXOLE.
361
Reports of Condition aggravated with PRAMIPEXOLE
6.0%
of all PRAMIPEXOLE reports
8
Deaths
156
Hospitalizations
How Dangerous Is Condition aggravated From PRAMIPEXOLE?
Of the 361 reports, 8 (2.2%) resulted in death, 156 (43.2%) required hospitalization, and 7 (1.9%) 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 PRAMIPEXOLE. However, 361 reports have been filed with the FAERS database.
What Other Side Effects Does PRAMIPEXOLE Cause?
Drug ineffective (698)
Fatigue (373)
Dyskinesia (369)
Fall (369)
Hallucination (356)
Off label use (348)
Insomnia (341)
Dizziness (338)
Tremor (338)
Restless legs syndrome (326)
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 PRAMIPEXOLE Alternatives Have Lower Condition aggravated Risk?
PRAMIPEXOLE vs PRAMIPEXOLE\PRAMIPEXOLE
PRAMIPEXOLE vs PRAMLINTIDE
PRAMIPEXOLE vs PRASTERONE
PRAMIPEXOLE vs PRASUGREL
PRAMIPEXOLE vs PRAVASTATIN