How are Zidovudine adverse event reports trending over time?
This graph shows volume of adverse events submitted to the FDA by quarter for Zidovudine, as well as related generic and/or brandname drugs containing the same primary active ingredients. Adverse events are counted if Zidovudine is flagged as the suspect drug causing the adverse event.
What are the most common Zidovudine adverse events reported to the FDA?
Drug Exposure During Pregnancy | 1113 (5.64%) |
Immune Reconstitution Syndrome | 326 (1.65%) |
Anaemia | 320 (1.62%) |
Premature Baby | 293 (1.49%) |
Maternal Drugs Affecting Foetus | 292 (1.48%) |
Pyrexia | 237 (1.2%) |
Cardiac Murmur | 178 (.9%) |
Congenital Anomaly | 173 (.88%) |
Neutropenia | 172 (.87%) |
Vomiting | 167 (.85%) |
Caesarean Section | 163 (.83%) |
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This graph shows the top adverse events submitted to the FDA for Zidovudine, 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 Zidovudine 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 Zidovudine adverse events reported to the FDA?
Chemical Injury And Poisoning | 1501 (7.61%) |
Hepatic And Hepatobiliary | 863 (4.38%) |
Infections - Pathogen Unspecified | 592 (3%) |
Gastrointestinal Signs | 546 (2.77%) |
Anemias Nonhemolytic And Marrow Dep... | 522 (2.65%) |
Respiratory | 518 (2.63%) |
Neonatal And Perinatal Conditions | 498 (2.53%) |
Cardiac And Vascular Disorders Cong... | 420 (2.13%) |
Therapeutic And Nontherapeutic Effe... | 373 (1.89%) |
Neurological | 353 (1.79%) |
Hepatobiliary | 346 (1.75%) |
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This graph shows the top categories of adverse events submitted to the FDA for Zidovudine, 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 Zidovudine 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 Zidovudine, according to those reporting adverse events to the FDA?
Hiv Infection | 3485 |
Drug Exposure During Pregnancy | 650 |
Prophylaxis Against Hiv Infection | 311 |
Human Immunodeficiency Virus Transm... | 289 |
Drug Use For Unknown Indication | 262 |
Antiretroviral Therapy | 256 |
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Label | Labeler | Effective |
---|---|---|
Combivir | Stat Rx USA | 27-OCT-09 |
Zidovudine | State of Florida DOH Central Pharmacy | 13-APR-10 |
Combivir | Rebel Distributors Corp | 24-SEP-10 |
Zidovudine | Rebel Distributors Corp | 26-JAN-11 |
Zidovudine | American Health Packaging | 08-FEB-11 |
Zidovudine | American Health Packaging | 10-MAR-11 |
Combivir | GlaxoSmithKline LLC | 14-MAR-11 |
Combivir | PD-Rx Pharmaceuticals, Inc. | 14-MAR-11 |
Retrovir | GlaxoSmithKline LLC | 14-MAR-11 |
Trizivir | GlaxoSmithKline LLC | 13-JUL-11 |
Retrovir | GlaxoSmithKline LLC | 13-JUL-11 |
Zidovudine | Camber Pharmaceuticals | 11-AUG-11 |
Zidovudine | Greenstone LLC | 27-OCT-11 |
Lamivudine And Zidovudine | PD-Rx Pharmaceuticals, Inc. | 23-DEC-11 |
Combivir | HHS/Program Support Center/Supply Service Center | 03-JAN-12 |
Zidovudine | Mylan Pharmaceuticals Inc. | 01-FEB-12 |
Combivir | H.J. Harkins Company, Inc. | 02-FEB-12 |
Zidovudine | Edenbridge Pharmaceuticals, LLC | 01-APR-12 |
Zidovudine | Edenbridge Pharmaceuticals, LLC | 01-APR-12 |
Lamivudine And Zidovudine | Rebel Distributors Corp | 04-APR-12 |
Lamivudine And Zidovudine | Lupin Pharmaceuticals, Inc. | 24-APR-12 |
Lamivudine And Zidovudine | Aurobindo Pharma Limited | 15-MAY-12 |
Lamivudine And Zidovudine | Teva Pharmaceuticals USA Inc | 21-MAY-12 |
Trizivir | ViiV Healthcare Company | 22-MAY-12 |
Retrovir | ViiV Healthcare Company | 31-MAY-12 |
Retrovir | ViiV Healthcare Company | 31-MAY-12 |
Zidovudine | Sunshine Lake Pharma Co., Ltd. | 08-JUN-12 |
Lamivudine And Zidovudine | H.J. Harkins Company, Inc. | 25-JUN-12 |
Zidovudine | Cipla Limited | 28-JUN-12 |
Zidovudine | Cipla Limited | 10-JUL-12 |
Zidovudine | Boca Pharmacal Inc. | 10-JUL-12 |
Zidovudine | Boca Pharmacal Inc. | 10-JUL-12 |
Zidovudine | Aurobindo Pharma Limited | 25-JUL-12 |
Lamivudine And Zidovudine | St Marys Medical Park Pharmacy | 29-AUG-12 |
Zidovudine | Bryant Ranch Prepack | 12-OCT-12 |
Zidovudine | Roxane Laboratories, Inc | 22-NOV-12 |
Zidovudine | Cipla Limited | 23-NOV-12 |
Zidovudine | Prodigy Health Supplier | 23-DEC-12 |
Combivir | ViiV Healthcare Company | 16-JAN-13 |
Lamivudine And Zidovudine | Bryant Ranch Prepack | 18-JAN-13 |
Combivir | REMEDYREPACK INC. | 11-MAR-13 |
Retrovir | Physicians Total Care, Inc. | 27-MAR-13 |
Zidovudine | Aurobindo Pharma Limited | 29-MAR-13 |
Zidovudine | Aurobindo Pharma Limited | 29-MAR-13 |
Lamivudine And Zidovudine | REMEDYREPACK INC. | 11-APR-13 |
Lamivudine And Zidovudine | REMEDYREPACK INC. | 11-APR-13 |
Zidovudine | REMEDYREPACK INC. | 15-APR-13 |
Zidovudine | REMEDYREPACK INC. | 15-APR-13 |
Zidovudine | REMEDYREPACK INC. | 15-APR-13 |
Zidovudine | REMEDYREPACK INC. | 15-APR-13 |
Combivir | REMEDYREPACK INC. | 23-APR-13 |
Combivir | REMEDYREPACK INC. | 23-APR-13 |
Combivir | REMEDYREPACK INC. | 23-APR-13 |
What Zidovudine safety concerns are being reported by doctors and researchers in the medical literature?
This report contains aggregated drug side effects and adverse events for Zidovudine. 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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