How are Ropinirole adverse event reports trending over time?
This graph shows volume of adverse events submitted to the FDA by quarter for Ropinirole, as well as related generic and/or brandname drugs containing the same primary active ingredients. Adverse events are counted if Ropinirole is flagged as the suspect drug causing the adverse event.
What are the most common Ropinirole adverse events reported to the FDA?
Drug Ineffective | 972 (4.53%) |
Nausea | 639 (2.98%) |
Somnolence | 589 (2.75%) |
Insomnia | 462 (2.16%) |
Hallucination | 365 (1.7%) |
Dizziness | 354 (1.65%) |
Restless Legs Syndrome | 350 (1.63%) |
Fatigue | 280 (1.31%) |
Pathological Gambling | 265 (1.24%) |
Vomiting | 257 (1.2%) |
Tremor | 256 (1.19%) |
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This graph shows the top adverse events submitted to the FDA for Ropinirole, as well as related generic and/or brandname drugs containing the same primary active ingredients, from Q1 2004 to Q3 2012. Adverse events are counted if Ropinirole is flagged as a suspect drug causing the adverse event. For each adverse event listed, percent (%) represents percentage of the adverse event to all adverse events reported for the drug. Percent does not represent a rate related to drug utilization.
What are the most common Ropinirole adverse events reported to the FDA?
Neurological | 2331 (10.87%) |
Therapeutic And Nontherapeutic Effe... | 1558 (7.27%) |
Gastrointestinal Signs | 1180 (5.5%) |
Movement Disorders | 872 (4.07%) |
Sleep Disorders | 827 (3.86%) |
Disturbances In Thinking | 669 (3.12%) |
Anxiety Disorders | 585 (2.73%) |
Medication Errors | 554 (2.58%) |
Impulse Control | 404 (1.88%) |
Injuries | 400 (1.87%) |
Musculoskeletal And Connective Tiss... | 394 (1.84%) |
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This graph shows the top categories of adverse events submitted to the FDA for Ropinirole, as well as related generic and/or brandname drugs containing the same primary active ingredients, from Q1 2004 to Q3 2012. Adverse events are counted if Ropinirole is flagged as a suspect drug causing the adverse event. For each adverse event listed, percent (%) represents percentage of the adverse event to all adverse events reported for the drug. Percent does not represent a rate related to drug utilization.
Why are people taking Ropinirole, according to those reporting adverse events to the FDA?
Restless Legs Syndrome | 3774 |
Parkinsons Disease | 2618 |
Drug Use For Unknown Indication | 865 |
Product Used For Unknown Indication | 346 |
Parkinsonism | 105 |
Muscle Spasms | 55 |
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Label | Labeler | Effective |
---|---|---|
Ropinirole Hydrochloride | Major Pharmaceuticals | 01-SEP-09 |
Ropinirole Hydrochloride | Bryant Ranch Prepack | 18-SEP-09 |
Ropinirole Hydrochloride | Heritage Pharmaceuticals Inc. | 29-APR-10 |
Ropinirole Hydrochloride | Rebel Distributors Corp | 11-NOV-10 |
Ropinirole Hydrochloride | Zydus Pharmaceuticals (USA) Inc. | 30-APR-11 |
Ropinirole Hydrochloride | Cadila Healthcare Limited | 02-MAY-11 |
Ropinirole Hydrochloride | American Health Packaging | 20-JUN-11 |
Ropinirole Hydrochloride | STAT RX USA LLC | 23-JUN-11 |
Ropinirole Hydrochloride | Rebel Distributors Corp | 30-JUN-11 |
Ropinirole | Actavis Elizabeh LLC | 23-JUL-11 |
Requip | PD-Rx Pharmaceuticals, Inc. | 25-AUG-11 |
Ropinirole Hydrochloride | Corepharma LLC. | 30-AUG-11 |
Ropinirole Hydrochloride | Solco Healthcare US LLC | 31-AUG-11 |
Ropinirole Hydrochloride | Mylan Pharmaceuticals Inc. | 01-SEP-11 |
Ropinirole Hydrochloride | Zhejiang Huahai Pharmaceutical Co., Ltd. | 14-SEP-11 |
Ropinirole | Dr. Reddys Laboratories Limited | 31-OCT-11 |
Ropinirole Hydrochloride | Watson Laboratories, Inc. | 01-DEC-11 |
Requipxl | Physicians Total Care, Inc. | 27-DEC-11 |
Ropinirole Hydrochloride | Physicians Total Care, Inc. | 15-FEB-12 |
Ropinirole | Glenmark Generics Inc., USA | 06-MAR-12 |
Ropinirole Hydrochloride | Wockhardt USA LLC. | 18-MAY-12 |
Ropinirole Hydrochloride | AvKARE, Inc. | 28-JUN-12 |
Ropinirole Hydrochloride | Wockhardt Limited | 10-JUL-12 |
Requip | GlaxoSmithKline LLC | 11-JUL-12 |
Ropinirole | Sandoz Inc | 12-JUL-12 |
Ropinirole Hydrochloride | Teva Pharmaceuticals USA Inc | 09-AUG-12 |
Ropinirole Hydrochloride | Mylan Pharmaceuticals Inc. | 16-AUG-12 |
Ropinirole | Northstar Rx LLC | 05-DEC-12 |
Requipxl | GlaxoSmithKline LLC | 18-DEC-12 |
Requip | Bryant Ranch Prepack | 18-JAN-13 |
Ropinirole Hydrochloride | NCS HealthCare of KY, Inc dba Vangard Labs | 14-FEB-13 |
Ropinirole Hydrochloride | Bryant Ranch Prepack | 15-FEB-13 |
Ropinirole Hydrochloride | Bryant Ranch Prepack | 15-FEB-13 |
Ropinirole | Apotex Corp. | 18-FEB-13 |
Ropinirole | Roxane Laboratories, Inc | 25-FEB-13 |
Ropinirole Hydrochloride | Wockhardt Limited | 05-MAR-13 |
Ropinirole Hydrochloride | Wockhardt USA LLC. | 05-MAR-13 |
Ropinirole4 Mg | Trigen Laboratories, Inc. | 26-APR-13 |
Ropinirole2 Mg | Trigen Laboratories, Inc. | 26-APR-13 |
Ropinirole8 Mg | Trigen Laboratories, Inc. | 26-APR-13 |
Ropinirole6 Mg | Trigen Laboratories, Inc. | 26-APR-13 |
Ropinirole12 Mg | Trigen Laboratories, Inc. | 26-APR-13 |
What Ropinirole safety concerns are being reported by doctors and researchers in the medical literature?
This report contains aggregated drug side effects and adverse events for Ropinirole. The data has been pulled from the United States Food and Drug Administration's (US FDA) Adverse Event Reporting System (AERS), a database containing more than 4,000,000 adverse event reports.
DrugCite expands your query using the Unified Medical Language System (UMLS) to include generic drugs and primary active ingredients. While the core of DrugCite's advanced drug filtering algorithm is based on the industry standard UMLS, DrugCite's proprietary filtering system also includes dozens of additional steps to reconcile malformed drug names in the FDA's data.
DrugCite only counts a drug if the submitter of the adverse event indicates that the drug is suspected to have caused the adverse event.
Depending on how the data is aggregated, different counts may occur. When someone submits an adverse event to the FDA, the submitter can attribute multiple adverse events to one or more drugs. For example, an individual taking Paxil could submit the adverse events "anxiety" and "suicidal ideation" for the same individual safety report (ISR). This means when DrugCite aggregates by adverse event, two distinct adverse events are counted in the adverse event graph; once for "anxiety" and again for "suicidal ideation". However, when DrugCite aggregates by individual safety reports irrespective of the details of the adverse events contained within the safety report, the report is only counted once.
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