How are Lovastatin adverse event reports trending over time?
This graph shows volume of adverse events submitted to the FDA by quarter for Lovastatin, as well as related generic and/or brandname drugs containing the same primary active ingredients. Adverse events are counted if Lovastatin is flagged as the suspect drug causing the adverse event.
What are the most common Lovastatin adverse events reported to the FDA?
Myalgia | 129 (3.5%) |
Rhabdomyolysis | 105 (2.85%) |
Drug Interaction | 72 (1.95%) |
Asthenia | 64 (1.74%) |
Arthralgia | 61 (1.66%) |
Fatigue | 58 (1.57%) |
Muscle Spasms | 56 (1.52%) |
Pain In Extremity | 56 (1.52%) |
Completed Suicide | 55 (1.49%) |
Blood Creatine Phosphokinase Increa... | 49 (1.33%) |
Muscular Weakness | 45 (1.22%) |
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This graph shows the top adverse events submitted to the FDA for Lovastatin, 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 Lovastatin 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 Lovastatin adverse events reported to the FDA?
Muscle | 390 (10.58%) |
Neurological | 194 (5.26%) |
Musculoskeletal And Connective Tiss... | 121 (3.28%) |
Therapeutic And Nontherapeutic Effe... | 117 (3.18%) |
Gastrointestinal Signs | 115 (3.12%) |
Joint | 83 (2.25%) |
Hepatic And Hepatobiliary | 81 (2.2%) |
Hepatobiliary | 81 (2.2%) |
Epidermal And Dermal Conditions | 80 (2.17%) |
Renal Disorders | 74 (2.01%) |
Suicidal And Self-injurious Behavio... | 74 (2.01%) |
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This graph shows the top categories of adverse events submitted to the FDA for Lovastatin, 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 Lovastatin 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 Lovastatin, according to those reporting adverse events to the FDA?
Blood Cholesterol Increased | 1061 |
Product Used For Unknown Indication | 513 |
Drug Use For Unknown Indication | 358 |
Blood Cholesterol | 277 |
Hyperlipidaemia | 271 |
Hypercholesterolaemia | 192 |
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Label | Labeler | Effective |
---|---|---|
Lovastatin | McKesson Packaging Services Business Unit of McKesson Corporation | 21-DEC-09 |
Lovastatin | REMEDYREPACK INC. | 17-OCT-10 |
Lovastatin | Carlsbad Technology, Inc. | 22-OCT-10 |
Lovastatin | NCS HealthCare of KY, Inc dba Vangard Labs | 27-OCT-10 |
Lovastatin | PD-Rx Pharmaceuticals, Inc. | 27-OCT-10 |
Lovastatin | PD-Rx Pharmaceuticals, Inc. | 27-OCT-10 |
Lovastatin | Physicians Total Care, Inc. | 03-JAN-11 |
Lovastatin | Rebel Distributors Corp | 03-JAN-11 |
Lovastatin | AvKARE, Inc. | 25-FEB-11 |
Lovastatin | REMEDYREPACK INC. | 09-MAR-11 |
Lovastatin | REMEDYREPACK INC. | 16-MAR-11 |
Lovastatin | REMEDYREPACK INC. | 17-JUN-11 |
Lovastatin | KAISER FOUNDATION HOSPITALS | 02-AUG-11 |
Lovastatin | REMEDYREPACK INC. | 23-SEP-11 |
Lovastatin | REMEDYREPACK INC. | 20-OCT-11 |
Lovastatin | REMEDYREPACK INC. | 24-OCT-11 |
Lovastatin | REMEDYREPACK INC. | 02-DEC-11 |
Lovastatin | REMEDYREPACK INC. | 12-DEC-11 |
Lovastatin | Rebel Distributors Corp | 13-DEC-11 |
Lovastatin | Golden State Medical Supply, Inc. | 09-JAN-12 |
Lovastatin | American Health Packaging | 31-JAN-12 |
Lovastatin | Dispensing Solutions, Inc. | 03-FEB-12 |
Lovastatin | APHENA PHARMA SOLUTIONS - TENNESSEE, INC. | 28-FEB-12 |
Lovastatin | Actavis Inc. | 13-MAR-12 |
Lovastatin | NCS HealthCare of KY, Inc dba Vangard Labs | 15-MAR-12 |
Lovastatin | Cardinal Health | 12-APR-12 |
Lovastatin | Mylan Institutional Inc. | 04-MAY-12 |
Lovastatin | Lupin Pharmaceuticals, Inc. | 15-AUG-12 |
Lovastatin | REMEDYREPACK INC. | 11-SEP-12 |
Lovastatin | STAT Rx USA LLC | 27-SEP-12 |
Advicor | Physicians Total Care, Inc. | 04-OCT-12 |
Mevacor | Merck Sharp & Dohme Corp. | 31-OCT-12 |
Advicor | Abbott Laboratories | 05-NOV-12 |
Lovastatin | Mutual Pharmaceutical Company, Inc. | 19-NOV-12 |
Altoprev | Shionogi Inc. | 01-DEC-12 |
Lovastatin | Mylan Pharmaceuticals Inc. | 28-DEC-12 |
Lovastatin | International Labs, Inc. | 15-JAN-13 |
Lovastatin | Bryant Ranch Prepack | 18-JAN-13 |
Lovastatin | NCS HealthCare of KY, Inc dba Vangard Labs | 22-JAN-13 |
Lovastatin | NCS HealthCare of KY, Inc dba Vangard Labs | 25-JAN-13 |
Lovastatin | Teva Pharmaceuticals USA Inc | 08-FEB-13 |
Lovastatin | International Labs, Inc. | 12-FEB-13 |
Lovastatin | REMEDYREPACK INC. | 13-FEB-13 |
Lovastatin | Eon Labs, Inc. | 14-FEB-13 |
Lovastatin | REMEDYREPACK INC. | 15-FEB-13 |
Lovastatin | Preferred Pharmaceuticals, Inc | 18-MAR-13 |
Lovastatin | Preferred Pharmaceuticals, Inc | 18-MAR-13 |
Lovastatin | Cardinal Health | 18-MAR-13 |
Lovastatin | Preferred Pharmaceuticals, Inc. | 18-MAR-13 |
Lovastatin | Preferred Pharmaceuticals, Inc | 18-MAR-13 |
Lovastatin | Apotex Corp. | 08-APR-13 |
Lovastatin | REMEDYREPACK INC. | 09-APR-13 |
Lovastatin | Mylan Pharmaceuticals Inc. | 22-APR-13 |
Lovastatin | International Labs, Inc. | 01-MAY-13 |
What Lovastatin safety concerns are being reported by doctors and researchers in the medical literature?
This report contains aggregated drug side effects and adverse events for Lovastatin. 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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