How are Vinorelbine Tartrate adverse event reports trending over time?
This graph shows volume of adverse events submitted to the FDA by quarter for Vinorelbine Tartrate, as well as related generic and/or brandname drugs containing the same primary active ingredients. Adverse events are counted if Vinorelbine Tartrate is flagged as the suspect drug causing the adverse event.
What are the most common Vinorelbine Tartrate adverse events reported to the FDA?
Neutropenia | 426 (3.38%) |
Febrile Neutropenia | 285 (2.26%) |
Pyrexia | 254 (2.01%) |
Vomiting | 228 (1.81%) |
Diarrhoea | 219 (1.74%) |
Dyspnoea | 185 (1.47%) |
Nausea | 178 (1.41%) |
Pneumonia | 142 (1.13%) |
Dehydration | 141 (1.12%) |
Leukopenia | 140 (1.11%) |
Anaemia | 132 (1.05%) |
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This graph shows the top adverse events submitted to the FDA for Vinorelbine Tartrate, 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 Vinorelbine Tartrate 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 Vinorelbine Tartrate adverse events reported to the FDA?
White Blood Cell | 894 (7.09%) |
Infections - Pathogen Unspecified | 751 (5.96%) |
Gastrointestinal Signs | 670 (5.31%) |
Respiratory | 546 (4.33%) |
Hematology Investigations | 474 (3.76%) |
Gastrointestinal Motility And Defec... | 350 (2.78%) |
Neurological | 343 (2.72%) |
Lower Respiratory Tract Disorders | 298 (2.36%) |
Anemias Nonhemolytic And Marrow Dep... | 294 (2.33%) |
Electrolyte And Fluid Balance Condi... | 292 (2.32%) |
Body Temperature Conditions | 277 (2.2%) |
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This graph shows the top categories of adverse events submitted to the FDA for Vinorelbine Tartrate, 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 Vinorelbine Tartrate 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 Vinorelbine Tartrate, according to those reporting adverse events to the FDA?
Non-small Cell Lung Cancer | 1048 |
Breast Cancer | 622 |
Breast Cancer Metastatic | 560 |
Lung Neoplasm Malignant | 198 |
Drug Use For Unknown Indication | 145 |
Hodgkins Disease | 102 |
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Label | Labeler | Effective |
---|---|---|
Vinorelbine Tartrate | Pierre Fabre Medicament | 17-AUG-11 |
Vinorelbine Tartrate | Sandoz Inc. | 19-SEP-11 |
Navelbine | Pierre Fabre Medicament | 02-FEB-12 |
Vinorelbine Tartrate | Hospira Worldwide, Inc. | 08-JUN-12 |
Vinorelbine Tartrate | Teva Parenteral Medicines, Inc. | 13-AUG-12 |
Vinorelbine Tartrate | Jiangsu Hengrui Medicine Co.,Ltd. | 11-OCT-12 |
What Vinorelbine Tartrate safety concerns are being reported by doctors and researchers in the medical literature?
This report contains aggregated drug side effects and adverse events for Vinorelbine Tartrate. 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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