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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does ROTIGOTINE Cause Hypoxia? 14 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 14 reports of Hypoxia have been filed in association with ROTIGOTINE (Neupro). This represents 0.2% of all adverse event reports for ROTIGOTINE.

14
Reports of Hypoxia with ROTIGOTINE
0.2%
of all ROTIGOTINE reports
13
Deaths
13
Hospitalizations

How Dangerous Is Hypoxia From ROTIGOTINE?

Of the 14 reports, 13 (92.9%) resulted in death, 13 (92.9%) required hospitalization, and 1 (7.1%) were considered life-threatening.

Is Hypoxia Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for ROTIGOTINE. However, 14 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 Hypoxia?

TREPROSTINIL (1,322) PREDNISONE (898) MACITENTAN (845) ALBUTEROL (763) CYCLOPHOSPHAMIDE (749) PACLITAXEL (684) DEXAMETHASONE (628) AMBRISENTAN (613) TIOTROPIUM (582) ACETAMINOPHEN (545)

Which ROTIGOTINE Alternatives Have Lower Hypoxia Risk?

ROTIGOTINE vs ROXADUSTAT ROTIGOTINE vs ROXICODONE ROTIGOTINE vs ROXITHROMYCIN ROTIGOTINE vs ROZANOLIXIZUMAB ROTIGOTINE vs ROZANOLIXIZUMAB-NOLI

Related Pages

ROTIGOTINE Full Profile All Hypoxia Reports All Drugs Causing Hypoxia ROTIGOTINE Demographics