TENORMIN
Tenormin Adverse Events Reported to the FDA Over Time
How are Tenormin adverse event reports trending over time?
This graph shows volume of adverse events submitted to the FDA by quarter for Tenormin, as well as related generic and/or brandname drugs containing the same primary active ingredients. Adverse events are counted if Tenormin is flagged as the suspect drug causing the adverse event.
Most Common Tenormin Adverse Events Reported to the FDA
What are the most common Tenormin adverse events reported to the FDA?
| Bradycardia | 143 (2.92%) |
| Drug Interaction | 78 (1.59%) |
| Drug Ineffective | 66 (1.35%) |
| Hypertension | 64 (1.31%) |
| Malaise | 60 (1.23%) |
| Dizziness | 58 (1.18%) |
| Fall | 52 (1.06%) |
| Hypotension | 52 (1.06%) |
| Myocardial Infarction | 52 (1.06%) |
| Suicide Attempt | 52 (1.06%) |
| Cytolytic Hepatitis | 45 (.92%) |
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Share/Embed Graph Export Data
This graph shows the top adverse events submitted to the FDA for Tenormin, 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 Tenormin 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.
Adverse Event Categories for Tenormin
What are the most common Tenormin adverse events reported to the FDA?
| Cardiac Arrhythmias | 422 (8.62%) |
| Neurological | 309 (6.31%) |
| Hepatic And Hepatobiliary | 209 (4.27%) |
| Therapeutic And Nontherapeutic Effe... | 172 (3.51%) |
| Decreased And Nonspecific Blood Pre... | 164 (3.35%) |
| Medication Errors | 161 (3.29%) |
| Cardiac And Vascular Investigations | 149 (3.04%) |
| Epidermal And Dermal Conditions | 134 (2.74%) |
| Respiratory | 122 (2.49%) |
| Renal Disorders | 121 (2.47%) |
| Injuries | 93 (1.9%) |
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Share/Embed Graph Export Data
This graph shows the top categories of adverse events submitted to the FDA for Tenormin, 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 Tenormin 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.
Common Uses of Tenormin According to Those Reporting Adverse Events
Why are people taking Tenormin, according to those reporting adverse events to the FDA?
| Hypertension | 1432 |
| Drug Use For Unknown Indication | 245 |
| Product Used For Unknown Indication | 150 |
| Essential Hypertension | 78 |
| Atrial Fibrillation | 75 |
| Blood Pressure | 59 |
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Drug Labels
| Label | Labeler | Effective |
|---|---|---|
| Tenormin | AstraZeneca Pharmaceuticals LP | 31-OCT-12 |
Tenormin Case Reports
What Tenormin safety concerns are being reported by doctors and researchers in the medical literature?
About Results
This report contains aggregated drug side effects and adverse events for Tenormin. 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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