Does PRAMIPEXOLE Cause Product dose omission? 12 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 12 reports of Product dose omission have been filed in association with PRAMIPEXOLE (Pramipexole Dihydrochloride). This represents 0.2% of all adverse event reports for PRAMIPEXOLE.
12
Reports of Product dose omission with PRAMIPEXOLE
0.2%
of all PRAMIPEXOLE reports
0
Deaths
5
Hospitalizations
How Dangerous Is Product dose omission From PRAMIPEXOLE?
Of the 12 reports, 5 (41.7%) required hospitalization.
Is Product dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PRAMIPEXOLE. However, 12 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 dose omission?
APREMILAST (4,567)
DUPILUMAB (2,729)
ALBUTEROL (1,742)
USTEKINUMAB (1,653)
INSULIN GLARGINE (1,500)
ETANERCEPT (1,400)
LENALIDOMIDE (1,400)
RUXOLITINIB (1,376)
ALIROCUMAB (1,354)
DIMETHYL (1,248)
Which PRAMIPEXOLE Alternatives Have Lower Product dose omission Risk?
PRAMIPEXOLE vs PRAMIPEXOLE\PRAMIPEXOLE
PRAMIPEXOLE vs PRAMLINTIDE
PRAMIPEXOLE vs PRASTERONE
PRAMIPEXOLE vs PRASUGREL
PRAMIPEXOLE vs PRAVASTATIN