How are Nitroglycerin adverse event reports trending over time?
This graph shows volume of adverse events submitted to the FDA by quarter for Nitroglycerin, as well as related generic and/or brandname drugs containing the same primary active ingredients. Adverse events are counted if Nitroglycerin is flagged as the suspect drug causing the adverse event.
What are the most common Nitroglycerin adverse events reported to the FDA?
Hypotension | 137 (2.19%) |
Drug Ineffective | 94 (1.5%) |
Completed Suicide | 84 (1.34%) |
Chest Pain | 78 (1.25%) |
Dyspnoea | 74 (1.18%) |
Syncope | 71 (1.14%) |
Myocardial Infarction | 67 (1.07%) |
Fall | 58 (.93%) |
Dehydration | 54 (.86%) |
Nausea | 53 (.85%) |
Confusional State | 52 (.83%) |
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This graph shows the top adverse events submitted to the FDA for Nitroglycerin, 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 Nitroglycerin 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 Nitroglycerin adverse events reported to the FDA?
Neurological | 358 (5.73%) |
Epidermal And Dermal Conditions | 222 (3.55%) |
Decreased And Nonspecific Blood Pre... | 213 (3.41%) |
Respiratory | 187 (2.99%) |
Coronary Artery | 186 (2.98%) |
Infections - Pathogen Unspecified | 185 (2.96%) |
Cardiac Arrhythmias | 176 (2.82%) |
Therapeutic And Nontherapeutic Effe... | 176 (2.82%) |
Gastrointestinal Signs | 165 (2.64%) |
Cardiac And Vascular Investigations | 123 (1.97%) |
Renal Disorders | 122 (1.95%) |
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This graph shows the top categories of adverse events submitted to the FDA for Nitroglycerin, 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 Nitroglycerin 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 Nitroglycerin, according to those reporting adverse events to the FDA?
Chest Pain | 942 |
Product Used For Unknown Indication | 877 |
Angina Pectoris | 728 |
Drug Use For Unknown Indication | 707 |
Cardiac Disorder | 218 |
Hypertension | 117 |
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Label | Labeler | Effective |
---|---|---|
Nitroglycerin In Dextrose | Baxter Healthcare Corporation | 06-OCT-00 |
Nitroglycerin | Mylan Pharmaceuticals Inc. | 15-OCT-08 |
Nitro-bid | E. FOUGERA & CO., A division of Nycomed US Inc. | 03-MAR-09 |
Nitroglycerin | Glenmark Generics Inc., USA | 09-SEP-09 |
Nitroglycerin | Preferred Pharmaceuticals, Inc | 09-SEP-09 |
Nitroglycerin | Greenstone LLC | 22-SEP-09 |
Nitroglycerin | Physicians Total Care, Inc. | 30-SEP-09 |
Nitroglycerin Transdermal Delivery System | Graceway Pharmaceuticals, LLC | 18-NOV-09 |
Nitroglycerin Transdermal Delivery System | Physicians Total Care, Inc. | 18-NOV-09 |
Nitroglycerin Transdermal System | Hercon Laboratories Corporation | 08-APR-10 |
Nitroglycerin Transdermal System | Harvard Drug Group, LLC | 08-APR-10 |
Nitroglyceriner | PD-Rx Pharmaceuticals, Inc. | 10-MAY-10 |
Nitroglyceriner | PD-Rx Pharmaceuticals, Inc. | 10-MAY-10 |
Nitroglyceriner | PD-Rx Pharmaceuticals, Inc. | 10-MAY-10 |
Nitroglycerin | American Regent, Inc. | 24-JUL-10 |
Nitroglycerin | Rebel Distributors Corp | 08-OCT-10 |
Nitroglycerin Transdermal Delivery System | Alvogen, Inc. | 10-NOV-10 |
Nitroglycerin Slocaps | Rebel Distributors Corp | 03-JAN-11 |
Nitrostat | Physicians Total Care, Inc. | 12-JAN-11 |
Nitroglycerin | Kremers Urban Pharmaceuticals Inc. | 01-FEB-11 |
Nitrostat | Parke-Davis Division of Pfizer Inc | 07-JUN-11 |
Nitroglycerin Transdermal System | Cardinal Health | 22-JUN-11 |
Rectiv | ProStrakan, Inc. | 30-JUN-11 |
Rectiv | Aptalis Pharma US, Inc. | 30-JAN-12 |
Nitromist | Akrimax Pharmaceuticals, LLC | 15-FEB-12 |
Nitrostat | Rebel Distributors Corp | 16-FEB-12 |
Nitroglycerin | General Injectables and Vaccines, Inc. | 20-FEB-12 |
Nitrostat | General Injectables & Vaccines, Inc | 28-MAR-12 |
Nitroglycerin | Rouses Point Pharmaceuticals, LLC | 08-MAY-12 |
Nitro-dur | Merck Sharp & Dohme Corp. | 30-MAY-12 |
Nitro-bid | SAVAGE LABORATORIES, A division of Fougera Pharmaceuticals Inc. | 12-JUN-12 |
Nitroglycerin In Dextrose | Hospira, Inc. | 10-JUL-12 |
Nitro-time | Major Pharmaceuticals | 18-JUL-12 |
Nitroglycerin Lingual | Wilshire Pharmaceuticals, Inc. | 30-JUL-12 |
Nitroglyceriner | AvKARE, Inc. | 19-DEC-12 |
Nitrolingual Pumpspray | Arbor Pharmaceuticals, Inc. | 28-FEB-13 |
What Nitroglycerin safety concerns are being reported by doctors and researchers in the medical literature?
This report contains aggregated drug side effects and adverse events for Nitroglycerin. 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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