Does ROTIGOTINE Cause Wrong technique in product usage process? 216 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 216 reports of Wrong technique in product usage process have been filed in association with ROTIGOTINE (Neupro). This represents 2.8% of all adverse event reports for ROTIGOTINE.
216
Reports of Wrong technique in product usage process with ROTIGOTINE
2.8%
of all ROTIGOTINE reports
16
Deaths
48
Hospitalizations
How Dangerous Is Wrong technique in product usage process From ROTIGOTINE?
Of the 216 reports, 16 (7.4%) resulted in death, 48 (22.2%) required hospitalization, and 1 (0.5%) were considered life-threatening.
Is Wrong technique in product usage process Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ROTIGOTINE. However, 216 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 Wrong technique in product usage process?
EVOLOCUMAB (21,664)
ALBUTEROL (17,114)
ADALIMUMAB (11,766)
PEGFILGRASTIM (10,217)
ETANERCEPT (9,835)
ERENUMAB-AOOE (9,359)
SACUBITRIL\VALSARTAN (8,022)
LEUPROLIDE (5,062)
FENTANYL (2,812)
SEMAGLUTIDE (2,538)
Which ROTIGOTINE Alternatives Have Lower Wrong technique in product usage process Risk?
ROTIGOTINE vs ROXADUSTAT
ROTIGOTINE vs ROXICODONE
ROTIGOTINE vs ROXITHROMYCIN
ROTIGOTINE vs ROZANOLIXIZUMAB
ROTIGOTINE vs ROZANOLIXIZUMAB-NOLI