How are Atorvastatin adverse event reports trending over time?
This graph shows volume of adverse events submitted to the FDA by quarter for Atorvastatin, as well as related generic and/or brandname drugs containing the same primary active ingredients. Adverse events are counted if Atorvastatin is flagged as the suspect drug causing the adverse event.
What are the most common Atorvastatin adverse events reported to the FDA?
Myalgia | 5383 (3.74%) |
Pain In Extremity | 2613 (1.82%) |
Muscle Spasms | 2092 (1.45%) |
Arthralgia | 1995 (1.39%) |
Blood Cholesterol Increased | 1961 (1.36%) |
Muscular Weakness | 1911 (1.33%) |
Death | 1865 (1.3%) |
Rhabdomyolysis | 1824 (1.27%) |
Fatigue | 1789 (1.24%) |
Asthenia | 1770 (1.23%) |
Pain | 1666 (1.16%) |
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This graph shows the top adverse events submitted to the FDA for Atorvastatin, 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 Atorvastatin 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 Atorvastatin adverse events reported to the FDA?
Muscle | 13802 (9.6%) |
Neurological | 6061 (4.21%) |
Musculoskeletal And Connective Tiss... | 5740 (3.99%) |
Gastrointestinal Signs | 4347 (3.02%) |
Lipid Analyses | 4035 (2.81%) |
Epidermal And Dermal Conditions | 3823 (2.66%) |
Joint | 3642 (2.53%) |
Hepatobiliary | 3456 (2.4%) |
Hepatic And Hepatobiliary | 3422 (2.38%) |
Therapeutic And Nontherapeutic Effe... | 2881 (2%) |
Injuries | 2709 (1.88%) |
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This graph shows the top categories of adverse events submitted to the FDA for Atorvastatin, 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 Atorvastatin 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 Atorvastatin, according to those reporting adverse events to the FDA?
Blood Cholesterol Increased | 15892 |
Hypercholesterolaemia | 6181 |
Hyperlipidaemia | 5128 |
Product Used For Unknown Indication | 4124 |
Drug Use For Unknown Indication | 3795 |
Blood Cholesterol | 3153 |
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Label | Labeler | Effective |
---|---|---|
Lipitor | Physicians Total Care, Inc | 06-AUG-09 |
Lipitor | A-S Medication Solutions LLC | 04-SEP-09 |
Lipitor | PHARMAKON, LLC | 02-DEC-10 |
Lipitor | Rebel Distributors Corp | 03-JAN-11 |
Atorvastatin Calcium | Rebel Distributors Corp | 28-DEC-11 |
Atorvastatin Calcium | Golden State Medical Supply, Inc. | 09-JAN-12 |
Atorvastatin Calcium | Dispensing Solutions, Inc. | 20-FEB-12 |
Lipitor | PD-Rx Pharmaceuticals, Inc. | 29-FEB-12 |
Lipitor | PD-Rx Pharmaceuticals, Inc. | 29-FEB-12 |
Lipitor | PD-Rx Pharmaceuticals, Inc. | 29-FEB-12 |
Atorvastatin Calcium | Mylan Pharmaceuticals Inc. | 01-MAR-12 |
Atorvastatin Calcium | Mylan Institutional Inc. | 01-MAR-12 |
Lipitor | Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC | 05-MAR-12 |
Atorvastatin Calcium | Watson Laboratories, Inc. | 07-MAR-12 |
Atorvastatin Calcium | PD-Rx Pharmaceuticals, Inc. | 12-APR-12 |
Atorvastatin Calcium | Unit Dose Services | 04-JUN-12 |
Atorvastatin Calcium | American Health Packaging | 04-JUN-12 |
Atorvastatin Calcium | Unit Dose Services | 04-JUN-12 |
Atorvastatin Calcium | Unit Dose Services | 04-JUN-12 |
Atorvastatin Calcium | Unit Dose Services | 04-JUN-12 |
Atorvastatin Calcium | Major Pharmaceuticals | 25-JUN-12 |
Amlodipine Besylate And Atorvastatin Calcium | Physicians Total Care, Inc. | 27-JUN-12 |
Atorvastatin Calcium | Rebel Distributors Corp | 10-JUL-12 |
Atorvastatin Calcium | American Health Packaging | 11-JUL-12 |
Atorvastatin Calcium | Rebel Distributors Corp | 31-JUL-12 |
Atorvastatin Calcium | Rebel Distributors Corp | 26-SEP-12 |
Amlodipine Besylate And Atorvastatin Calcium | Ranbaxy Pharmaceuticals Inc | 01-OCT-12 |
Amlodipine Besylate/atorvastatin Calcium | Mylan Pharmaceuticals Inc. | 01-OCT-12 |
Atorvastatin Calcium | Legacy Pharmaceutical Packaging | 17-OCT-12 |
Lipitor | Parke-Davis Div of Pfizer Inc | 31-OCT-12 |
Atorvastatin Calcium | Greenstone LLC | 01-NOV-12 |
Caduet | Pfizer Laboratories Div Pfizer Inc | 16-NOV-12 |
Atorvastatin Calcium | Ranbaxy Pharmaceuticals Inc. | 26-NOV-12 |
Atorvastatin Calcium | Dr. Reddy's Laboratories Limited | 11-DEC-12 |
Atorvastatin Calcium | Dr. Reddy's Laboratories Limited | 11-DEC-12 |
Atorvastatin Calcium | Apotex Corp. | 31-DEC-12 |
Atorvastatin Calcium | Kremers Urban Pharmaceuticals Inc. | 31-DEC-12 |
Atorvastatin Calcium | Sandoz Inc | 14-JAN-13 |
Atorvastatin Calcium | Dispensing Solutions, Inc. | 14-JAN-13 |
Lipitor | Bryant Ranch Prepack | 17-JAN-13 |
Lipitor | Bryant Ranch Prepack | 17-JAN-13 |
Atorvastatin Calcium | Bryant Ranch Prepack | 18-JAN-13 |
Atorvastatin Calcium | Bryant Ranch Prepack | 18-JAN-13 |
Atorvastatin Calcium | Bryant Ranch Prepack | 18-JAN-13 |
Atorvastatin Calcium | Bryant Ranch Prepack | 21-JAN-13 |
Lipitor | Bryant Ranch Prepack | 21-JAN-13 |
Atorvastatin Calcium | Bryant Ranch Prepack | 21-JAN-13 |
Lipitor | Bryant Ranch Prepack | 21-JAN-13 |
Atorvastatin Calcium | Legacy Pharmaceutical Packaging | 07-FEB-13 |
Atorvastatin Calcium | Physicians Total Care, Inc. | 21-FEB-13 |
Atorvastatin Calcium | Cardinal Health | 06-MAR-13 |
Lipitor | Cardinal Health | 07-MAR-13 |
Atorvastatin Calcium | Legacy Pharmaceutical Packaging | 03-MAY-13 |
What Atorvastatin safety concerns are being reported by doctors and researchers in the medical literature?
This report contains aggregated drug side effects and adverse events for Atorvastatin. 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 Atorvastatin.