How are Prochlorperazine adverse event reports trending over time?
This graph shows volume of adverse events submitted to the FDA by quarter for Prochlorperazine, as well as related generic and/or brandname drugs containing the same primary active ingredients. Adverse events are counted if Prochlorperazine is flagged as the suspect drug causing the adverse event.
What are the most common Prochlorperazine adverse events reported to the FDA?
Nausea | 95 (2.46%) |
Vomiting | 86 (2.22%) |
Completed Suicide | 75 (1.94%) |
Drug Ineffective | 58 (1.5%) |
Anxiety | 52 (1.34%) |
Dyspnoea | 50 (1.29%) |
Dystonia | 50 (1.29%) |
Tremor | 46 (1.19%) |
Insomnia | 45 (1.16%) |
Hypersensitivity | 44 (1.14%) |
Constipation | 43 (1.11%) |
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This graph shows the top adverse events submitted to the FDA for Prochlorperazine, 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 Prochlorperazine 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 Prochlorperazine adverse events reported to the FDA?
Gastrointestinal Signs | 231 (5.97%) |
Neurological | 199 (5.15%) |
Movement Disorders | 197 (5.09%) |
Epidermal And Dermal Conditions | 175 (4.53%) |
Anxiety Disorders | 133 (3.44%) |
Respiratory | 133 (3.44%) |
Therapeutic And Nontherapeutic Effe... | 111 (2.87%) |
Infections - Pathogen Unspecified | 110 (2.84%) |
Muscle | 109 (2.82%) |
Suicidal And Self-injurious Behavio... | 108 (2.79%) |
Allergic Conditions | 98 (2.53%) |
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This graph shows the top categories of adverse events submitted to the FDA for Prochlorperazine, 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 Prochlorperazine 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 Prochlorperazine, according to those reporting adverse events to the FDA?
Nausea | 2410 |
Drug Use For Unknown Indication | 733 |
Vomiting | 566 |
Product Used For Unknown Indication | 426 |
Prophylaxis | 158 |
Prophylaxis Of Nausea And Vomiting | 144 |
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Label | Labeler | Effective |
---|---|---|
Prochlorperazine Maleate | Bryant Ranch Prepack | 01-MAR-98 |
Prochlorperazine | G & W LABORATORIES, INC. | 18-DEC-08 |
Prochlorperazine | STAT RX USA LLC | 24-SEP-09 |
Prochlorperazine Maleate | Physicians Total Care, Inc. | 16-MAR-10 |
Prochlorperazine Edisylate | Physicians Total Care, Inc. | 21-APR-10 |
Prochlorperazine Edisylate | Bedford Laboratories | 21-APR-10 |
Prochlorperazine | Physicians Total Care, Inc. | 09-AUG-10 |
Prochlorperazine Edisylate | General Injectables & Vaccines, Inc | 25-AUG-10 |
Prochlorperazine Maleate | Mylan Pharmaceuticals Inc. | 15-SEP-10 |
Prochlorperazine Maleate | PD-Rx Pharmaceuticals, Inc. | 15-SEP-10 |
Prochlorperazine Maleate | PD-Rx Pharmaceuticals, Inc. | 15-SEP-10 |
Prochlorperazine Maleate | PD-Rx Pharmaceuticals, Inc. | 15-SEP-10 |
Prochlorperazine Maleate | PD-Rx Pharmaceuticals, Inc. | 15-SEP-10 |
Prochlorperazine Maleate | UDL Laboratories, Inc. | 17-DEC-10 |
Compro | PD-Rx Pharmaceuticals, Inc. | 22-DEC-10 |
Compro | Paddock Laboratories, Inc. | 22-DEC-10 |
Prochlorperazine Maleate | Rebel Distributors Corp | 04-JAN-11 |
Prochlorperazine Edisylate | Baxter Healthcare Corporation | 04-JAN-11 |
Prochlorperazine Maleate | JUBILANT CADISTA PHARMACEUTICALS, INC. | 01-MAR-11 |
Prochlorperazine Maleate | REMEDYREPACK INC. | 11-APR-11 |
Prochlorperazine Maleate | REMEDYREPACK INC. | 30-JUN-11 |
Prochlorperazine Maleate | Sandoz Inc | 21-OCT-11 |
Prochlorperazine Maleate | Lake Erie Medical & Surgical Supply DBA Quality Care Prodcuts LLC | 06-DEC-11 |
Prochlorperazine Maleate | Dispensing Solutions, Inc. | 07-FEB-12 |
Prochlorperazine Maleate | Preferred Pharmaceuticals, Inc | 05-APR-12 |
Prochlorperazine Maleate | NCS HealthCare of KY, Inc dba Vangard Labs | 20-APR-12 |
Prochlorperazine Edisylate | Cardinal Health | 29-MAY-12 |
Prochlorperazine Maleate | Preferred Pharmaceuticals, Inc. | 25-JUL-12 |
Prochlorperazine Maleate | Teva Pharmaceuticals USA Inc | 06-SEP-12 |
Prochlorperazine Maleate | REMEDYREPACK INC. | 12-SEP-12 |
Prochlorperazine Maleate | Bryant Ranch Prepack | 18-JAN-13 |
Prochlorperazine Maleate | Lake Erie Medical DBA Quality Care Products LLC | 14-FEB-13 |
Prochlorperazine Maleate | Preferred Pharmaceuticals, Inc. | 14-MAR-13 |
Prochlorperazine Maleate | Cardinal Health | 19-MAR-13 |
What Prochlorperazine safety concerns are being reported by doctors and researchers in the medical literature?
This report contains aggregated drug side effects and adverse events for Prochlorperazine. 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.
Share your experience with Prochlorperazine.