Does ROTIGOTINE Cause Disorientation? 42 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 42 reports of Disorientation have been filed in association with ROTIGOTINE (Neupro). This represents 0.5% of all adverse event reports for ROTIGOTINE.
42
Reports of Disorientation with ROTIGOTINE
0.5%
of all ROTIGOTINE reports
3
Deaths
23
Hospitalizations
How Dangerous Is Disorientation From ROTIGOTINE?
Of the 42 reports, 3 (7.1%) resulted in death, 23 (54.8%) required hospitalization, and 2 (4.8%) were considered life-threatening.
Is Disorientation Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ROTIGOTINE. However, 42 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 Disorientation?
OLANZAPINE (612)
QUETIAPINE (551)
CARBIDOPA\LEVODOPA (543)
PREGABALIN (521)
TRAMADOL (506)
SERTRALINE (483)
GABAPENTIN (428)
DULOXETINE (427)
LORAZEPAM (404)
SODIUM OXYBATE (393)
Which ROTIGOTINE Alternatives Have Lower Disorientation Risk?
ROTIGOTINE vs ROXADUSTAT
ROTIGOTINE vs ROXICODONE
ROTIGOTINE vs ROXITHROMYCIN
ROTIGOTINE vs ROZANOLIXIZUMAB
ROTIGOTINE vs ROZANOLIXIZUMAB-NOLI