Does ROTIGOTINE Cause Dopamine dysregulation syndrome? 16 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 16 reports of Dopamine dysregulation syndrome have been filed in association with ROTIGOTINE (Neupro). This represents 0.2% of all adverse event reports for ROTIGOTINE.
16
Reports of Dopamine dysregulation syndrome with ROTIGOTINE
0.2%
of all ROTIGOTINE reports
0
Deaths
9
Hospitalizations
How Dangerous Is Dopamine dysregulation syndrome From ROTIGOTINE?
Of the 16 reports, 9 (56.3%) required hospitalization, and 4 (25.0%) were considered life-threatening.
Is Dopamine dysregulation syndrome Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ROTIGOTINE. However, 16 reports have been filed with the FAERS database.
What Other Side Effects Does ROTIGOTINE Cause?
Product adhesion issue (1,718)
Off label use (646)
Drug ineffective (632)
Death (595)
Parkinson's disease (419)
Fall (412)
Device adhesion issue (383)
Overdose (353)
Application site pruritus (334)
Application site erythema (330)
What Other Drugs Cause Dopamine dysregulation syndrome?
CARBIDOPA\LEVODOPA (167)
ROPINIROLE (64)
PRAMIPEXOLE (54)
LEVODOPA (39)
CARBIDOPA\ENTACAPONE\LEVODOPA (24)
AMANTADINE (21)
BENSERAZIDE\LEVODOPA (21)
ENTACAPONE (21)
ARIPIPRAZOLE (20)
RASAGILINE (20)
Which ROTIGOTINE Alternatives Have Lower Dopamine dysregulation syndrome Risk?
ROTIGOTINE vs ROXADUSTAT
ROTIGOTINE vs ROXICODONE
ROTIGOTINE vs ROXITHROMYCIN
ROTIGOTINE vs ROZANOLIXIZUMAB
ROTIGOTINE vs ROZANOLIXIZUMAB-NOLI