How are Acyclovir adverse event reports trending over time?
This graph shows volume of adverse events submitted to the FDA by quarter for Acyclovir, as well as related generic and/or brandname drugs containing the same primary active ingredients. Adverse events are counted if Acyclovir is flagged as the suspect drug causing the adverse event.
What are the most common Acyclovir adverse events reported to the FDA?
Renal Failure Acute | 204 (1.9%) |
Drug Ineffective | 167 (1.55%) |
Pyrexia | 131 (1.22%) |
Vomiting | 105 (.98%) |
Confusional State | 98 (.91%) |
Rash | 97 (.9%) |
Herpes Zoster | 96 (.89%) |
Blood Creatinine Increased | 93 (.87%) |
Hepatotoxicity | 89 (.83%) |
Nausea | 89 (.83%) |
Diarrhoea | 84 (.78%) |
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This graph shows the top adverse events submitted to the FDA for Acyclovir, 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 Acyclovir 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 Acyclovir adverse events reported to the FDA?
Neurological | 788 (7.34%) |
Epidermal And Dermal Conditions | 632 (5.88%) |
Renal Disorders | 423 (3.94%) |
Viral Infectious | 414 (3.85%) |
Infections - Pathogen Unspecified | 322 (3%) |
Gastrointestinal Signs | 314 (2.92%) |
Therapeutic And Nontherapeutic Effe... | 314 (2.92%) |
Hepatic And Hepatobiliary | 276 (2.57%) |
Hepatobiliary | 269 (2.5%) |
Hematology Investigations | 243 (2.26%) |
Cardiac Arrhythmias | 224 (2.09%) |
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This graph shows the top categories of adverse events submitted to the FDA for Acyclovir, 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 Acyclovir 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 Acyclovir, according to those reporting adverse events to the FDA?
Antiviral Prophylaxis | 999 |
Prophylaxis | 884 |
Drug Use For Unknown Indication | 684 |
Product Used For Unknown Indication | 683 |
Herpes Zoster | 645 |
Infection Prophylaxis | 413 |
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Label | Labeler | Effective |
---|---|---|
Acyclovir | Mylan Pharmaceuticals Inc. | 11-FEB-10 |
Acyclovir | PD-Rx Pharmaceuticals, Inc. | 11-FEB-10 |
Acyclovir | Bedford Laboratories | 06-APR-10 |
Acyclovir | DAVA Pharmaceuticals, Inc. | 14-APR-10 |
Acyclovir | Actavis Mid Atlantic LLC | 12-MAY-10 |
Acyclovir | Heritage Pharmaceuticals, Inc. | 21-MAY-10 |
Acyclovir | Hi-Tech Pharmacal Co., Inc. | 16-JUN-10 |
Acyclovir | Physicians Total Care, Inc. | 09-JUL-10 |
Acyclovir | Major Pharmaceuticals | 13-JUL-10 |
Acyclovir | UDL Laboratories, Inc. | 23-JUL-10 |
Acyclovir | Apotex Corp. | 10-DEC-10 |
Acyclovir | Boscogen, Inc. | 05-JAN-11 |
Acyclovir | Rebel Distributors Corp | 05-JAN-11 |
Zovirax | BTA PHARMACEUTICALS INC | 01-FEB-11 |
Zovirax | BTA PHARMACEUTICALS INC | 01-FEB-11 |
Acyclovir | Stat Rx USA | 10-FEB-11 |
Acyclovir | AvPAK | 10-MAR-11 |
Acyclovir | AvKARE, Inc. | 10-MAR-11 |
Acyclovir | Bryant Ranch Prepack | 28-MAR-11 |
Acyclovir | Blenheim Pharmacal, Inc. | 29-APR-11 |
Acyclovir | Blenheim Pharmacal, Inc. | 29-APR-11 |
Acyclovir | Blenheim Pharmacal, Inc. | 29-APR-11 |
Acyclovir | REMEDYREPACK INC. | 09-MAY-11 |
Acyclovir | REMEDYREPACK INC. | 09-MAY-11 |
Acyclovir | REMEDYREPACK INC. | 16-MAY-11 |
Acyclovir | Preferred Pharmaceuticals, Inc | 09-JUN-11 |
Acyclovir | RedPharm Drug Inc. | 30-JUN-11 |
Acyclovir | Golden State Medical Supply, Inc. | 01-JUL-11 |
Acyclovir | REMEDYREPACK INC. | 13-JUL-11 |
Acyclovir | REMEDYREPACK INC. | 14-JUL-11 |
Acyclovir | REMEDYREPACK INC. | 14-JUL-11 |
Acyclovir | REMEDYREPACK INC. | 28-JUL-11 |
Acyclovir | REMEDYREPACK INC. | 01-AUG-11 |
Acyclovir | REMEDYREPACK INC. | 20-SEP-11 |
Acyclovir | H.J. Harkins Company, Inc. | 27-OCT-11 |
Acyclovir | REMEDYREPACK INC. | 06-DEC-11 |
Acyclovir | PD-Rx Pharmaceuticals, Inc. | 07-DEC-11 |
Acyclovir | PD-Rx Pharmaceuticals, Inc. | 07-DEC-11 |
Acyclovir | Golden State Medical Supply, Inc. | 09-JAN-12 |
Acyclovir | Golden State Medical Supply, Inc. | 09-JAN-12 |
Acyclovir | APP Pharmaceuticals, LLC | 10-JAN-12 |
Zovirax | Rebel Distributors Corp | 09-FEB-12 |
Acyclovir | Rebel Distributors Corp | 04-APR-12 |
Acyclovir | Carlsbad Technology, Inc. | 05-APR-12 |
Acyclovir | PD-Rx Pharmaceuticals, Inc. | 05-APR-12 |
Acyclovir | Apotex Corp. | 09-APR-12 |
Zovirax | Valeant Pharmaceuticals North America LLC | 09-MAY-12 |
Zovirax | Valeant Pharmaceuticals North America LLC | 09-MAY-12 |
Acyclovir | Carlsbad Technology, Inc. | 12-JUN-12 |
Xerese | Valeant Pharmaceuticals North America LLC | 22-JUN-12 |
Acyclovir | Preferred Pharmaceuticals, Inc. | 27-JUL-12 |
Acyclovir | Mylan Pharmaceuticals Inc. | 31-JUL-12 |
Acyclovir | APP Pharmaceuticals, LLC | 15-AUG-12 |
Acyclovir | REMEDYREPACK INC. | 23-AUG-12 |
Acyclovir | Aidarex Pharmaceuticals LLC | 10-SEP-12 |
Acyclovir | Physicians Total Care, Inc. | 25-SEP-12 |
Acyclovir | Oceanside Pharmaceuticals | 03-OCT-12 |
Acyclovir | Preferred Pharmaceuticals, Inc | 03-OCT-12 |
Acyclovir | Bryant Ranch Prepack | 18-JAN-13 |
Acyclovir | Bryant Ranch Prepack | 18-JAN-13 |
Acyclovir | Teva Pharmaceuticals USA Inc | 08-FEB-13 |
Acyclovir | REMEDYREPACK INC. | 21-FEB-13 |
Acyclovir | REMEDYREPACK INC. | 27-FEB-13 |
Acyclovir | Mylan Pharmaceuticals Inc. | 28-FEB-13 |
Acyclovir | Cardinal Health | 06-MAR-13 |
Zovirax | GlaxoSmithKline LLC | 11-MAR-13 |
Acyclovir | Preferred Pharmaceuticals, Inc. | 26-MAR-13 |
Acyclovir | Preferred Pharmaceuticals, Inc | 26-MAR-13 |
Acyclovir | REMEDYREPACK INC. | 03-APR-13 |
Acyclovir | REMEDYREPACK INC. | 05-APR-13 |
What Acyclovir safety concerns are being reported by doctors and researchers in the medical literature?
This report contains aggregated drug side effects and adverse events for Acyclovir. 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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