Does ROTIGOTINE Cause On and off phenomenon? 55 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 55 reports of On and off phenomenon have been filed in association with ROTIGOTINE (Neupro). This represents 0.7% of all adverse event reports for ROTIGOTINE.
55
Reports of On and off phenomenon with ROTIGOTINE
0.7%
of all ROTIGOTINE reports
0
Deaths
30
Hospitalizations
How Dangerous Is On and off phenomenon From ROTIGOTINE?
Of the 55 reports, 30 (54.5%) required hospitalization.
Is On and off phenomenon Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ROTIGOTINE. However, 55 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 On and off phenomenon?
CARBIDOPA\LEVODOPA (3,509)
FOSCARBIDOPA\FOSLEVODOPA (391)
PRAMIPEXOLE (116)
APOMORPHINE (107)
LEVODOPA (106)
AMANTADINE (81)
CLOZAPINE (73)
ROPINIROLE (72)
BENSERAZIDE\LEVODOPA (65)
ENTACAPONE (59)
Which ROTIGOTINE Alternatives Have Lower On and off phenomenon Risk?
ROTIGOTINE vs ROXADUSTAT
ROTIGOTINE vs ROXICODONE
ROTIGOTINE vs ROXITHROMYCIN
ROTIGOTINE vs ROZANOLIXIZUMAB
ROTIGOTINE vs ROZANOLIXIZUMAB-NOLI