How are Levofloxacin adverse event reports trending over time?
This graph shows volume of adverse events submitted to the FDA by quarter for Levofloxacin, as well as related generic and/or brandname drugs containing the same primary active ingredients. Adverse events are counted if Levofloxacin is flagged as the suspect drug causing the adverse event.
What are the most common Levofloxacin adverse events reported to the FDA?
Drug Interaction | 204 (1.39%) |
Pyrexia | 185 (1.26%) |
Tendon Rupture | 174 (1.18%) |
Arthralgia | 172 (1.17%) |
Tendonitis | 158 (1.07%) |
Dyspnoea | 156 (1.06%) |
Diarrhoea | 150 (1.02%) |
Renal Failure Acute | 147 (1%) |
Nausea | 141 (.96%) |
Pneumonia | 126 (.86%) |
Pain In Extremity | 121 (.82%) |
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This graph shows the top adverse events submitted to the FDA for Levofloxacin, 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 Levofloxacin 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 Levofloxacin adverse events reported to the FDA?
Epidermal And Dermal Conditions | 945 (6.42%) |
Neurological | 657 (4.46%) |
Infections - Pathogen Unspecified | 590 (4.01%) |
Respiratory | 503 (3.42%) |
Hepatic And Hepatobiliary | 431 (2.93%) |
Gastrointestinal Signs | 424 (2.88%) |
Joint | 353 (2.4%) |
Tendon, Ligament And Cartilage | 347 (2.36%) |
Hematology Investigations | 337 (2.29%) |
Injuries | 335 (2.27%) |
Therapeutic And Nontherapeutic Effe... | 334 (2.27%) |
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This graph shows the top categories of adverse events submitted to the FDA for Levofloxacin, 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 Levofloxacin 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 Levofloxacin, according to those reporting adverse events to the FDA?
Product Used For Unknown Indication | 570 |
Drug Use For Unknown Indication | 553 |
Pneumonia | 534 |
Urinary Tract Infection | 324 |
Infection Prophylaxis | 225 |
Prophylaxis | 209 |
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Label | Labeler | Effective |
---|---|---|
Iquix | Vistakon Pharmaceuticals LLC | 18-MAR-10 |
Levaquin | PD-Rx Pharmaceuticals, Inc. | 26-APR-10 |
Levaquin | PD-Rx Pharmaceuticals, Inc. | 26-APR-10 |
Levaquin | Rebel Distributors Corp | 28-DEC-10 |
Levofloxacin | Akorn Inc. | 31-DEC-10 |
Levofloxacin | PACK Pharmaceuticals, LLC | 04-MAY-11 |
Levaquin | Cardinal Health | 26-MAY-11 |
Levofloxacin | Akorn, Inc. | 08-JUN-11 |
Levofloxacin | PD-Rx Pharmaceuticals, Inc. | 20-JUN-11 |
Levofloxacin | PD-Rx Pharmaceuticals, Inc. | 20-JUN-11 |
Levofloxacin | Torrent Pharmaceuticals Limited | 23-JUN-11 |
Levaquin | Physicians Total Care, Inc. | 23-JUN-11 |
Levofloxacin | American Health Packaging | 30-JUN-11 |
Levofloxacin | Major Pharmaceuticals | 14-JUL-11 |
Levofloxacin | Rebel Distributors Corp | 19-JUL-11 |
Levaquin | RedPharm Drug Inc. | 27-JUL-11 |
Levaquin | RedPharm Drug Inc. | 27-JUL-11 |
Levaquin | RedPharm Drug Inc. | 27-JUL-11 |
Levofloxacin | Unit Dose Services | 04-AUG-11 |
Quixin | Vistakon Pharmaceuticals LLC | 17-AUG-11 |
Levofloxacin | STAT RX USA LLC | 31-AUG-11 |
Levaquin | PD-Rx Pharmaceuticals, Inc. | 24-OCT-11 |
Levofloxacin | Mylan Institutional Inc. | 16-DEC-11 |
Levofloxacin | Mylan Pharmaceuticals Inc. | 12-JAN-12 |
Levofloxacin | West-ward Pharmaceutical Corp | 31-JAN-12 |
Levofloxacin | Northstar Rx LLC | 10-FEB-12 |
Levofloxacin | Hi-Tech Pharmacal Co., Inc. | 13-APR-12 |
Levofloxacin | H.J. Harkins Company, Inc. | 16-APR-12 |
Levofloxacin | Physicians Total Care, Inc. | 24-APR-12 |
Levaquin | Janssen Pharmaceuticals, Inc. | 30-APR-12 |
Levofloxacin | Macleods Pharmaceuticals Limited | 15-MAY-12 |
Levofloxacin | Sagent Pharmaceuticals | 22-MAY-12 |
Levofloxacin | Sagent Pharmaceuticals | 24-MAY-12 |
Levofloxacin | Dr. Reddy's Laboratories Limited | 08-JUN-12 |
Levofloxacin | Sandoz Inc | 20-JUN-12 |
Levofloxacin | Boca Pharmacal Inc. | 25-JUN-12 |
Levofloxacin | Sagent Pharmaceuticals | 29-JUN-12 |
Levofloxacin | Sandoz Inc | 22-JUL-12 |
Levofloxacin | Hi-Tech Pharmacal Co., Inc. | 06-SEP-12 |
Levofloxacin | Aurobindo Pharma Limited | 25-SEP-12 |
Levofloxacin | Teva Pharmaceuticals USA Inc | 25-SEP-12 |
Levaquin | Bryant Ranch Prepack | 12-OCT-12 |
Levaquin | Lake Erie Medical DBA Quality Care Products LLC | 15-OCT-12 |
Levofloxacin | Wockhardt USA LLC. | 17-OCT-12 |
Levofloxacin | Wockhardt Limited | 17-OCT-12 |
Levofloxacin | Bryant Ranch Prepack | 23-OCT-12 |
Levofloxacin | Greenstone LLC | 05-NOV-12 |
Levofloxacin | Zydus Pharmaceuticals (USA) Inc. | 07-NOV-12 |
Levofloxacin | Cadila Healthcare Limited | 07-NOV-12 |
Levofloxacin | Lake Erie Medical DBA Quality Care Products LLC | 21-NOV-12 |
Levofloxacin | Lupin Pharmaceuticals, Inc. | 03-JAN-13 |
Levofloxacin | Bryant Ranch Prepack | 17-JAN-13 |
Levofloxacin | Heritage Pharmaceuticals Inc. | 28-JAN-13 |
Levofloxacin | Preferred Pharmaceuticals, Inc. | 29-JAN-13 |
Levofloxacin | AuroMedics Pharma LLC | 02-FEB-13 |
Levofloxacin | Preferred Pharmaceuticals, Inc. | 04-FEB-13 |
Levofloxacin | Lake Erie Medical DBA Quality Care Products LLC | 14-FEB-13 |
Levofloxacin | REMEDYREPACK INC. | 08-MAR-13 |
Levofloxacin | Preferred Pharmaceuticals, Inc | 13-MAR-13 |
Levofloxacin | Preferred Pharmaceuticals, Inc | 15-MAR-13 |
Levofloxacin | Preferred Pharmaceuticals, Inc. | 27-MAR-13 |
Levaquin | REMEDYREPACK INC. | 10-APR-13 |
Levaquin | REMEDYREPACK INC. | 11-APR-13 |
Levofloxacin | Cardinal Health | 29-APR-13 |
What Levofloxacin safety concerns are being reported by doctors and researchers in the medical literature?
This report contains aggregated drug side effects and adverse events for Levofloxacin. 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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