Does PRAMIPEXOLE Cause Product prescribing error? 32 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), 32 reports of Product prescribing error have been filed in association with PRAMIPEXOLE (Pramipexole Dihydrochloride). This represents 0.5% of all adverse event reports for PRAMIPEXOLE.
32
Reports of Product prescribing error with PRAMIPEXOLE
0.5%
of all PRAMIPEXOLE reports
0
Deaths
24
Hospitalizations
How Dangerous Is Product prescribing error From PRAMIPEXOLE?
Of the 32 reports, 24 (75.0%) required hospitalization.
Is Product prescribing error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PRAMIPEXOLE. However, 32 reports have been filed with the FAERS database.
What Other Side Effects Does PRAMIPEXOLE Cause?
Drug ineffective (698)
Fatigue (373)
Dyskinesia (369)
Fall (369)
Condition aggravated (361)
Hallucination (356)
Off label use (348)
Insomnia (341)
Dizziness (338)
Tremor (338)
What Other Drugs Cause Product prescribing error?
SOMATROPIN (1,123)
SACUBITRIL\VALSARTAN (1,023)
SECUKINUMAB (821)
TOFACITINIB (805)
DUPILUMAB (725)
NIRMATRELVIR\RITONAVIR (611)
PREGABALIN (476)
METHOTREXATE (434)
TORSEMIDE (352)
METOPROLOL (325)
Which PRAMIPEXOLE Alternatives Have Lower Product prescribing error Risk?
PRAMIPEXOLE vs PRAMIPEXOLE\PRAMIPEXOLE
PRAMIPEXOLE vs PRAMLINTIDE
PRAMIPEXOLE vs PRASTERONE
PRAMIPEXOLE vs PRASUGREL
PRAMIPEXOLE vs PRAVASTATIN