Does ROTIGOTINE Cause Abnormal behaviour? 27 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 27 reports of Abnormal behaviour have been filed in association with ROTIGOTINE (Neupro). This represents 0.3% of all adverse event reports for ROTIGOTINE.
27
Reports of Abnormal behaviour with ROTIGOTINE
0.3%
of all ROTIGOTINE reports
0
Deaths
13
Hospitalizations
How Dangerous Is Abnormal behaviour From ROTIGOTINE?
Of the 27 reports, 13 (48.1%) required hospitalization, and 1 (3.7%) were considered life-threatening.
Is Abnormal behaviour Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ROTIGOTINE. However, 27 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 Abnormal behaviour?
PIMAVANSERIN (1,364)
ARIPIPRAZOLE (903)
METHYLPHENIDATE (779)
MONTELUKAST (672)
LEVETIRACETAM (655)
RISPERIDONE (642)
QUETIAPINE (612)
OLANZAPINE (530)
OXYCODONE (486)
DULOXETINE (483)
Which ROTIGOTINE Alternatives Have Lower Abnormal behaviour Risk?
ROTIGOTINE vs ROXADUSTAT
ROTIGOTINE vs ROXICODONE
ROTIGOTINE vs ROXITHROMYCIN
ROTIGOTINE vs ROZANOLIXIZUMAB
ROTIGOTINE vs ROZANOLIXIZUMAB-NOLI