Does ROTIGOTINE Cause Transient ischaemic attack? 22 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 22 reports of Transient ischaemic attack have been filed in association with ROTIGOTINE (Neupro). This represents 0.3% of all adverse event reports for ROTIGOTINE.
22
Reports of Transient ischaemic attack with ROTIGOTINE
0.3%
of all ROTIGOTINE reports
13
Deaths
18
Hospitalizations
How Dangerous Is Transient ischaemic attack From ROTIGOTINE?
Of the 22 reports, 13 (59.1%) resulted in death, 18 (81.8%) required hospitalization, and 1 (4.5%) were considered life-threatening.
Is Transient ischaemic attack Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ROTIGOTINE. However, 22 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 Transient ischaemic attack?
APIXABAN (1,157)
RIVAROXABAN (820)
LENALIDOMIDE (655)
ADALIMUMAB (604)
ASPIRIN (587)
ROSIGLITAZONE (585)
NAPROXEN (521)
LEVOTHYROXINE (517)
DABIGATRAN ETEXILATE (471)
CLOPIDOGREL BISULFATE (454)
Which ROTIGOTINE Alternatives Have Lower Transient ischaemic attack Risk?
ROTIGOTINE vs ROXADUSTAT
ROTIGOTINE vs ROXICODONE
ROTIGOTINE vs ROXITHROMYCIN
ROTIGOTINE vs ROZANOLIXIZUMAB
ROTIGOTINE vs ROZANOLIXIZUMAB-NOLI