Does ROTIGOTINE Cause Incorrect dose administered? 108 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 108 reports of Incorrect dose administered have been filed in association with ROTIGOTINE (Neupro). This represents 1.4% of all adverse event reports for ROTIGOTINE.
108
Reports of Incorrect dose administered with ROTIGOTINE
1.4%
of all ROTIGOTINE reports
5
Deaths
14
Hospitalizations
How Dangerous Is Incorrect dose administered From ROTIGOTINE?
Of the 108 reports, 5 (4.6%) resulted in death, 14 (13.0%) required hospitalization, and 1 (0.9%) were considered life-threatening.
Is Incorrect dose administered Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ROTIGOTINE. However, 108 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 Incorrect dose administered?
TIRZEPATIDE (23,301)
ADALIMUMAB (14,000)
DUPILUMAB (9,907)
RANITIDINE (9,337)
INSULIN LISPRO (8,318)
ACETAMINOPHEN (5,316)
DULAGLUTIDE (5,207)
SECUKINUMAB (4,524)
INSULIN GLARGINE (3,070)
SOMATROPIN (2,772)
Which ROTIGOTINE Alternatives Have Lower Incorrect dose administered Risk?
ROTIGOTINE vs ROXADUSTAT
ROTIGOTINE vs ROXICODONE
ROTIGOTINE vs ROXITHROMYCIN
ROTIGOTINE vs ROZANOLIXIZUMAB
ROTIGOTINE vs ROZANOLIXIZUMAB-NOLI