How are Betamethasone adverse event reports trending over time?
This graph shows volume of adverse events submitted to the FDA by quarter for Betamethasone, as well as related generic and/or brandname drugs containing the same primary active ingredients. Adverse events are counted if Betamethasone is flagged as the suspect drug causing the adverse event.
What are the most common Betamethasone adverse events reported to the FDA?
Drug Exposure During Pregnancy | 144 (1.58%) |
Condition Aggravated | 106 (1.17%) |
Drug Ineffective | 97 (1.07%) |
Pruritus | 86 (.95%) |
Erythema | 85 (.93%) |
Insomnia | 76 (.84%) |
Premature Baby | 73 (.8%) |
Dyspnoea | 72 (.79%) |
Pyrexia | 69 (.76%) |
Malaise | 68 (.75%) |
Caesarean Section | 66 (.73%) |
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This graph shows the top adverse events submitted to the FDA for Betamethasone, 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 Betamethasone 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 Betamethasone adverse events reported to the FDA?
Epidermal And Dermal Conditions | 744 (8.18%) |
Neurological | 359 (3.95%) |
Infections - Pathogen Unspecified | 316 (3.48%) |
Respiratory | 306 (3.37%) |
Chemical Injury And Poisoning | 208 (2.29%) |
Therapeutic And Nontherapeutic Effe... | 197 (2.17%) |
Hematology Investigations | 184 (2.02%) |
Gastrointestinal Signs | 170 (1.87%) |
Allergic Conditions | 151 (1.66%) |
Cardiac And Vascular Investigations | 133 (1.46%) |
Administration Site Reactions | 126 (1.39%) |
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This graph shows the top categories of adverse events submitted to the FDA for Betamethasone, 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 Betamethasone 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 Betamethasone, according to those reporting adverse events to the FDA?
Drug Use For Unknown Indication | 327 |
Psoriasis | 240 |
Product Used For Unknown Indication | 229 |
Rash | 127 |
Rheumatoid Arthritis | 89 |
Eczema | 71 |
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Label | Labeler | Effective |
---|---|---|
Betamethasone Dipropionateaugmented | Physicians Total Care, Inc. | 15-JUL-09 |
Betamethasone Valerate | Physicians Total Care, Inc. | 23-OCT-09 |
Betamethasone Clotrimazole | Stat Rx USA | 27-OCT-09 |
Betamethasone Dipropionate | Sandoz Inc | 16-NOV-09 |
Taclonex | Warner Chilcott (US), LLC | 10-DEC-09 |
Betamethasone Dipropionate | Physicians Total Care, Inc. | 29-DEC-09 |
Betamethasone Dipropionate | Actavis Mid Atlantic LLC | 01-APR-10 |
Betamethasone Dipropionate | Actavis Mid Atlantic LLC | 01-APR-10 |
Betamethasone Sodium Phosphate And Betamethasone Acetate | American Regent, Inc. | 04-MAY-10 |
Luxiq | Physicians Total Care, Inc. | 29-JUN-10 |
Betamethasone Dipropionate | STAT RX USA LLC | 11-AUG-10 |
Clotrimazole And Betamethasone Dipropionate | Actavis Mid Atlantic LLC | 02-SEP-10 |
Betamethasone Valerate | Rebel Distributors Corp. | 14-SEP-10 |
Betamethasone Dipropionate | Rebel Distributors Corp. | 14-SEP-10 |
Betamethasone Dipropionate | Rebel Distributors Corp. | 14-SEP-10 |
Betamethasone Valerate | Rebel Distributors Corp | 22-SEP-10 |
Clotrimazole And Betamethasone Dipropionate | Rebel Distributors Corp | 24-SEP-10 |
Betamethasone Dipropionate | Actavis Mid Atlantic LLC | 27-OCT-10 |
Betamethasone Valerate | Actavis Mid Atlantic LLC | 03-NOV-10 |
Betamethasone Dipropionate | Preferred Pharmaceuticals, Inc | 09-NOV-10 |
Betamethasone Dipropionate | Physicians Total Care, Inc. | 01-MAR-11 |
Betamethasone Valerate | STAT RX USA LLC | 07-APR-11 |
Betamethasone Dipropionate | Perrigo New York Inc | 01-SEP-11 |
Betamethasone Dipropionate | Taro Pharmaceuticals U.S.A., Inc. | 22-SEP-11 |
Betamethasone Valerate | Taro Pharmaceuticals U.S.A., Inc. | 17-OCT-11 |
Betamethasone Dipropionate | Taro Pharmaceuticals U.S.A., Inc. | 28-NOV-11 |
Betamethasone Valerate | STI Pharma | 01-DEC-11 |
Betamethasone Dipropionate | H.J. Harkins Company, Inc. | 22-DEC-11 |
Betamethasone Dipropionate | H.J. Harkins Company, Inc. | 03-JAN-12 |
Betamethasone Dipropionate | Physicians Total Care, Inc. | 03-JAN-12 |
Betamethasone Dipropionate | Taro Pharmaceuticals U.S.A., Inc. | 10-JAN-12 |
Clotrimazole And Betamethasone Dipropionate | Taro Pharmaceuticals U.S.A., Inc. | 03-FEB-12 |
Betamethasone Dipropionate | Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC | 26-MAR-12 |
Calcipotriene And Betamethasone Dipropionate | Perrigo New York Inc | 09-APR-12 |
Betamethasone Dipropionate | Taro Pharmaceuticals U.S.A., Inc. | 10-APR-12 |
Betamethasone Dipropionate | Taro Pharmaceuticals U.S.A., Inc. | 13-APR-12 |
Betamethasone Dipropionate | Preferred Pharmaceuticals, Inc | 23-APR-12 |
Clotrimazole And Betamethasone Dipropionate | Physicians Total Care, Inc. | 01-MAY-12 |
Betamethasone Dipropionate | E. FOUGERA & CO. A division of Fougera Pharmaceuticals Inc. | 03-MAY-12 |
Betamethasone Dipropionate | Prasco Laboratories | 15-MAY-12 |
Clotrimazole And Betamethasone Dipropionate | E. FOUGERA & CO. A division of Fougera Pharmaceuticals Inc. | 21-MAY-12 |
Clotrimazole And Betamethasone Dipropionate | Prasco Laboratories | 25-MAY-12 |
Lotrisone | Merck Sharp & Dohme Corp. | 25-MAY-12 |
Taclonex | Physicians Total Care, Inc. | 29-MAY-12 |
Clotrimazole And Betamethasone Dipropionate | E. FOUGERA & CO., A division of Fougera Pharmaceuticals Inc. | 30-MAY-12 |
Betamethasone Valerate | Teva Pharmaceuticals USA Inc | 29-JUN-12 |
Betamethasone Dipropionate | Glenmark Generics Inc., USA | 01-JUL-12 |
Betamethasone Dipropionate | E. FOUGERA & CO. A division of Fougera Pharmaceuticals Inc. | 03-JUL-12 |
Betamethasone Dipropionate | E. FOUGERA & CO., A division of Fougera Pharmaceuticals Inc. | 06-JUL-12 |
Betamethasone Dipropionate | E. FOUGERA & CO., A division of Fougera Pharmaceuticals Inc. | 06-JUL-12 |
Betamethasone | Global Pharmaceuticals, Division of Impax Laboratories Inc. | 18-SEP-12 |
Clotrimazole And Betamethasone Dipropionate | Lake Erie Medical DBA Quality Care Products LLC | 19-OCT-12 |
Taclonex | LEO Pharma Inc. | 10-DEC-12 |
Taclonex | LEO Pharma Inc. | 11-DEC-12 |
Betamethasone Valerate | Perrigo New York Inc | 22-JAN-13 |
Betamethasone Dipropionate | Perrigo New York Inc | 20-FEB-13 |
Betamethasone Dipropionate | E. Fougera & Co. a division of Fougera Pharmaceuticals Inc. | 18-MAR-13 |
Betamethasone Valerate | E. Fougera & Co., a division of Fougera Pharmaceuticals Inc. | 18-MAR-13 |
What Betamethasone safety concerns are being reported by doctors and researchers in the medical literature?
This report contains aggregated drug side effects and adverse events for Betamethasone. 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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