Does ROTIGOTINE Cause Incorrect dose administered by device? 7 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Incorrect dose administered by device have been filed in association with ROTIGOTINE (Neupro). This represents 0.1% of all adverse event reports for ROTIGOTINE.
7
Reports of Incorrect dose administered by device with ROTIGOTINE
0.1%
of all ROTIGOTINE reports
0
Deaths
3
Hospitalizations
How Dangerous Is Incorrect dose administered by device From ROTIGOTINE?
Of the 7 reports, 3 (42.9%) required hospitalization.
Is Incorrect dose administered by device Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ROTIGOTINE. However, 7 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 by device?
EXENATIDE (3,332)
EVOLOCUMAB (2,840)
SOMATROPIN (2,486)
ALBUTEROL (1,236)
ETANERCEPT (1,032)
SECUKINUMAB (996)
ERENUMAB-AOOE (973)
BUDESONIDE\FORMOTEROL (753)
INSULIN GLARGINE (753)
BUDESONIDE\FORMOTEROL\GLYCOPYRROLATE (674)
Which ROTIGOTINE Alternatives Have Lower Incorrect dose administered by device Risk?
ROTIGOTINE vs ROXADUSTAT
ROTIGOTINE vs ROXICODONE
ROTIGOTINE vs ROXITHROMYCIN
ROTIGOTINE vs ROZANOLIXIZUMAB
ROTIGOTINE vs ROZANOLIXIZUMAB-NOLI