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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 ROPINIROLE Cause Product dose omission? 10 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 10 reports of Product dose omission have been filed in association with ROPINIROLE (ropinirole hydrochloride). This represents 0.2% of all adverse event reports for ROPINIROLE.

10
Reports of Product dose omission with ROPINIROLE
0.2%
of all ROPINIROLE reports
0
Deaths
4
Hospitalizations

How Dangerous Is Product dose omission From ROPINIROLE?

Of the 10 reports, 4 (40.0%) required hospitalization.

Is Product dose omission Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for ROPINIROLE. However, 10 reports have been filed with the FAERS database.

What Other Side Effects Does ROPINIROLE Cause?

Drug ineffective (452) Hallucination (303) Somnolence (256) Nausea (244) Fall (239) Dyskinesia (223) Parkinson's disease (218) Condition aggravated (200) Dizziness (194) Insomnia (192)

What Other Drugs Cause Product dose omission?

APREMILAST (4,567) DUPILUMAB (2,729) ALBUTEROL (1,742) USTEKINUMAB (1,653) INSULIN GLARGINE (1,500) ETANERCEPT (1,400) LENALIDOMIDE (1,400) RUXOLITINIB (1,376) ALIROCUMAB (1,354) DIMETHYL (1,248)

Which ROPINIROLE Alternatives Have Lower Product dose omission Risk?

ROPINIROLE vs ROPIVACAINE ROPINIROLE vs ROSIGLITAZONE ROPINIROLE vs ROSUVASTATIN ROPINIROLE vs ROSUVASTATIN\ROSUVASTATIN ROPINIROLE vs ROTIGOTINE

Related Pages

ROPINIROLE Full Profile All Product dose omission Reports All Drugs Causing Product dose omission ROPINIROLE Demographics