Does PRAMIPEXOLE Cause Product administration error? 11 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 11 reports of Product administration error have been filed in association with PRAMIPEXOLE (Pramipexole Dihydrochloride). This represents 0.2% of all adverse event reports for PRAMIPEXOLE.
11
Reports of Product administration error with PRAMIPEXOLE
0.2%
of all PRAMIPEXOLE reports
0
Deaths
10
Hospitalizations
How Dangerous Is Product administration error From PRAMIPEXOLE?
Of the 11 reports, 10 (90.9%) required hospitalization, and 10 (90.9%) were considered life-threatening.
Is Product administration error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PRAMIPEXOLE. However, 11 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 administration error?
HYDROXYPROGESTERONE CAPROATE (972)
ACETAMINOPHEN (666)
CENEGERMIN-BKBJ (613)
LEUPROLIDE (595)
EVOLOCUMAB (565)
ADALIMUMAB (543)
METHYLPHENIDATE (414)
OLMESARTAN MEDOXOMIL (314)
ASPIRIN (241)
SECUKINUMAB (225)
Which PRAMIPEXOLE Alternatives Have Lower Product administration error Risk?
PRAMIPEXOLE vs PRAMIPEXOLE\PRAMIPEXOLE
PRAMIPEXOLE vs PRAMLINTIDE
PRAMIPEXOLE vs PRASTERONE
PRAMIPEXOLE vs PRASUGREL
PRAMIPEXOLE vs PRAVASTATIN