How are Fluticasone Propionate adverse event reports trending over time?
This graph shows volume of adverse events submitted to the FDA by quarter for Fluticasone Propionate, as well as related generic and/or brandname drugs containing the same primary active ingredients. Adverse events are counted if Fluticasone Propionate is flagged as the suspect drug causing the adverse event.
What are the most common Fluticasone Propionate adverse events reported to the FDA?
Drug Ineffective | 4998 (6.36%) |
Dyspnoea | 3725 (4.74%) |
Product Quality Issue | 2698 (3.43%) |
Asthma | 2605 (3.31%) |
Dysphonia | 2030 (2.58%) |
Cough | 2015 (2.56%) |
Pneumonia | 1097 (1.4%) |
Headache | 949 (1.21%) |
Death | 801 (1.02%) |
Dizziness | 779 (.99%) |
Chest Discomfort | 766 (.97%) |
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This graph shows the top adverse events submitted to the FDA for Fluticasone Propionate, 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 Fluticasone Propionate 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 Fluticasone Propionate adverse events reported to the FDA?
Respiratory | 12203 (15.52%) |
Therapeutic And Nontherapeutic Effe... | 6354 (8.08%) |
Bronchial Disorders | 4165 (5.3%) |
Neurological | 3639 (4.63%) |
Infections - Pathogen Unspecified | 3166 (4.03%) |
Product Quality Issues | 2833 (3.6%) |
Epidermal And Dermal Conditions | 1787 (2.27%) |
Gastrointestinal Signs | 1786 (2.27%) |
Medication Errors | 1695 (2.16%) |
Fungal Infectious | 1581 (2.01%) |
Upper Respiratory Tract Disorders | 1531 (1.95%) |
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This graph shows the top categories of adverse events submitted to the FDA for Fluticasone Propionate, 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 Fluticasone Propionate 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 Fluticasone Propionate, according to those reporting adverse events to the FDA?
Asthma | 16226 |
Chronic Obstructive Pulmonary Disea... | 6648 |
Drug Use For Unknown Indication | 5944 |
Product Used For Unknown Indication | 3936 |
Hypersensitivity | 833 |
Emphysema | 812 |
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Label | Labeler | Effective |
---|---|---|
Fluticasone Propionate | GW Laboratories, Inc | 04-SEP-08 |
Fluticasone Propionate | Physicians Total Care, Inc. | 22-DEC-09 |
Advairdiskus | Dispensing Solutions Inc. | 02-MAR-10 |
Fluticasone Propionate | Physicians Total Care, Inc. | 20-MAY-10 |
Advair Diskus | Physicians Total Care, Inc. | 21-JUN-10 |
Fluticasone Propionate | Roxane Laboratories, Inc | 30-JUN-10 |
Fluticasone Propionate | Perrigo New York Inc | 21-JUL-10 |
Fluticasone Propionate | Physicians Total Care, Inc. | 21-JUL-10 |
Cutivate | PHARMADERM., A division of Nycomed US Inc. | 06-AUG-10 |
Advairdiskus | Rebel Distributors Corp. | 01-SEP-10 |
Fluticasone Propionate | Rebel Distributors Corp | 03-JAN-11 |
Fluticasone Propionate | Apotex Corp. | 17-JAN-11 |
Fluticasone Propionate | Golden State Medical Supply, Inc. | 06-MAY-11 |
Cutivate | PharmaDerm, A division of Nycomed US Inc. | 31-MAY-11 |
Fluticasone Propionate | Perrigo New York Inc | 06-JUL-11 |
Advairdiskus | Rebel Distributors Corp | 20-JUL-11 |
Floventdiskus | GlaxoSmithKline LLC | 01-SEP-11 |
Fluticasone Propionate | G & W LABORATORIES, INC. | 07-SEP-11 |
Advairdiskus | GlaxoSmithKline LLC | 14-SEP-11 |
Flonase | GlaxoSmithKline LLC | 27-OCT-11 |
Fluticasone Propionate | Hi-Tech Pharmacal Co., Inc. | 17-NOV-11 |
Fluticasone Propionate | Apotex Corp. | 28-NOV-11 |
Floventhfa | GlaxoSmithKline LLC | 12-JAN-12 |
Fluticasone | Morton Grove Pharmaceuticals, Inc. | 13-JAN-12 |
Floventhfa | Physicians Total Care, Inc. | 16-JAN-12 |
Fluticasone Propionate | Preferred Pharmaceuticals, Inc | 18-JAN-12 |
Advairdiskus | Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC | 05-MAR-12 |
Fluticasone Propionate | Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC | 12-MAR-12 |
Fluticasone Propionate | Glenmark Generics Inc., USA | 28-MAR-12 |
Fluticasone Propionate | E. FOUGERA & CO. A division of Fougera Pharmaceuticals Inc. | 17-MAY-12 |
Floventhfa | Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC | 14-JUN-12 |
Fluticasone Propionate | Taro Pharmaceuticals U.S.A., Inc. | 19-JUL-12 |
Fluticasone Propionate | Apotex Corp. | 10-AUG-12 |
Cutivate | PharmaDerm a division of Fougera Pharmaceuticals Inc. | 14-AUG-12 |
Dymista | Meda Pharmaceuticals Inc. | 17-AUG-12 |
Advairdiskus | Aidarex Pharmaceuticals LLC | 10-SEP-12 |
Fluticasone Propionate | Global Pharmaceuticals, Division of IMPAX Laboratories Inc. | 18-SEP-12 |
Fluticasone Propionate | Prasco Laboratories | 16-OCT-12 |
Fluticasone Propionate | E. FOUGERA & CO. A division of Fougera Pharmaceuticals Inc. | 09-JAN-13 |
Cutivate | PharmaDerm A division of Fougera Pharmaceuticals Inc. | 17-JAN-13 |
Advair Hfa | GlaxoSmithKline LLC | 05-MAR-13 |
Fluticasone Propionate | E. Fougera & Co. a division of Fougera Pharmaceuticals Inc. | 07-MAR-13 |
Cutivate | PharmaDerm, A division of Fougera Pharmaceuticals Inc. | 11-MAR-13 |
Fluticasone Propionate | Preferred Pharmaceuticals, Inc. | 22-APR-13 |
What Fluticasone Propionate safety concerns are being reported by doctors and researchers in the medical literature?
This report contains aggregated drug side effects and adverse events for Fluticasone Propionate. 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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