Does PRAMIPEXOLE Cause Intentional product use issue? 45 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 45 reports of Intentional product use issue have been filed in association with PRAMIPEXOLE (Pramipexole Dihydrochloride). This represents 0.7% of all adverse event reports for PRAMIPEXOLE.
45
Reports of Intentional product use issue with PRAMIPEXOLE
0.7%
of all PRAMIPEXOLE reports
1
Deaths
11
Hospitalizations
How Dangerous Is Intentional product use issue From PRAMIPEXOLE?
Of the 45 reports, 1 (2.2%) resulted in death, 11 (24.4%) required hospitalization.
Is Intentional product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PRAMIPEXOLE. However, 45 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 Intentional product use issue?
INFLIXIMAB (11,028)
RITUXIMAB (9,602)
INFLIXIMAB-DYYB (7,549)
TOCILIZUMAB (5,078)
METHOTREXATE (4,087)
PREDNISONE (3,961)
ABATACEPT (3,693)
ADALIMUMAB (3,557)
NIVOLUMAB (3,297)
LEFLUNOMIDE (3,280)
Which PRAMIPEXOLE Alternatives Have Lower Intentional product use issue Risk?
PRAMIPEXOLE vs PRAMIPEXOLE\PRAMIPEXOLE
PRAMIPEXOLE vs PRAMLINTIDE
PRAMIPEXOLE vs PRASTERONE
PRAMIPEXOLE vs PRASUGREL
PRAMIPEXOLE vs PRAVASTATIN