How are Meloxicam adverse event reports trending over time?
This graph shows volume of adverse events submitted to the FDA by quarter for Meloxicam, as well as related generic and/or brandname drugs containing the same primary active ingredients. Adverse events are counted if Meloxicam is flagged as the suspect drug causing the adverse event.
What are the most common Meloxicam adverse events reported to the FDA?
Diarrhoea | 68 (1.45%) |
Completed Suicide | 67 (1.43%) |
Drug Ineffective | 65 (1.38%) |
Dizziness | 63 (1.34%) |
Vomiting | 61 (1.3%) |
Drug Interaction | 56 (1.19%) |
Gastrointestinal Haemorrhage | 53 (1.13%) |
Anaemia | 45 (.96%) |
Nausea | 44 (.94%) |
Confusional State | 41 (.87%) |
Headache | 39 (.83%) |
Show More |
Share/Embed Graph Export Data
This graph shows the top adverse events submitted to the FDA for Meloxicam, 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 Meloxicam 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 Meloxicam adverse events reported to the FDA?
Neurological | 257 (5.47%) |
Gastrointestinal Signs | 225 (4.79%) |
Epidermal And Dermal Conditions | 210 (4.47%) |
Gastrointestinal Hemorrhages | 189 (4.02%) |
Therapeutic And Nontherapeutic Effe... | 166 (3.53%) |
Gastrointestinal Ulceration And Per... | 129 (2.74%) |
Hematology Investigations | 113 (2.4%) |
Respiratory | 110 (2.34%) |
Gastrointestinal Motility And Defec... | 104 (2.21%) |
Joint | 101 (2.15%) |
Renal Disorders | 92 (1.96%) |
Show More |
Share/Embed Graph Export Data
This graph shows the top categories of adverse events submitted to the FDA for Meloxicam, 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 Meloxicam 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 Meloxicam, according to those reporting adverse events to the FDA?
Rheumatoid Arthritis | 647 |
Drug Use For Unknown Indication | 579 |
Product Used For Unknown Indication | 546 |
Arthritis | 443 |
Pain | 366 |
Osteoarthritis | 281 |
Show More |
Label | Labeler | Effective |
---|---|---|
Meloxicam | Bryant Ranch Prepack | 07-MAR-07 |
Meloxicam | PD-Rx Pharmaceuticals, Inc. | 23-APR-09 |
Meloxicam | Rebel Distributors Corp. | 01-JUN-09 |
Meloxicam | UDL Laboratories, Inc. | 19-NOV-09 |
Mobic | Physicians Total Care, Inc. | 01-APR-10 |
Meloxicam | Apotex Corp | 12-MAY-10 |
Meloxicam | Physicians Total Care, Inc. | 22-JUL-10 |
Meloxicam | Carlsbad Technology, Inc | 28-SEP-10 |
Meloxicam | MedVantx, Inc. | 14-OCT-10 |
Meloxicam | NCS HealthCare of KY, Inc dba Vangard Labs | 14-DEC-10 |
Meloxicam | Unit Dose Services | 16-MAR-11 |
Meloxicam | PD-Rx Pharmaceuticals, Inc. | 16-MAR-11 |
Meloxicam | Unit Dose Services | 16-MAR-11 |
Meloxicam | Zydus Pharmaceuticals (USA) Inc. | 28-APR-11 |
Meloxicam | MedVantx, Inc. | 28-APR-11 |
Meloxicam | MedVantx, Inc. | 28-APR-11 |
Meloxicam | Cadila Healthcare Limited | 29-APR-11 |
Meloxicam | REMEDYREPACK INC. | 03-MAY-11 |
Meloxicam | Cardinal Health | 17-MAY-11 |
Meloxicam | Blenheim Pharmacal, Inc. | 08-JUN-11 |
Meloxicam | Blenheim Pharmacal, Inc. | 08-JUN-11 |
Meloxicam | Roxane Laboratories, Inc. | 01-JUL-11 |
Meloxicam | REMEDYREPACK INC. | 18-JUL-11 |
Trepoxicam-7.5 | Physician Therapeutics LLC | 01-AUG-11 |
Meloxicam | STAT RX USA LLC | 18-AUG-11 |
Meloxicam | REMEDYREPACK INC. | 23-AUG-11 |
Meloxicam | REMEDYREPACK INC. | 24-AUG-11 |
Meloxicam | REMEDYREPACK INC. | 30-AUG-11 |
Meloxicam | International Labs, Inc. | 31-AUG-11 |
Meloxicam | REMEDYREPACK INC. | 08-SEP-11 |
Meloxicam | International Labs, Inc. | 16-SEP-11 |
Meloxicam | Lake Erie Medical DBA Quality Care Products LLC | 01-DEC-11 |
Meloxicam | Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC | 01-DEC-11 |
Meloxicam | McKesson Contract Packaging | 10-JAN-12 |
Meloxicam | Preferred Pharmaceuticals, Inc | 14-FEB-12 |
Meloxicam | Life Line Home Care Services, Inc. | 21-FEB-12 |
Meloxicam | International Labs, Inc. | 22-FEB-12 |
Meloxicam | STAT Rx USA LLC | 23-FEB-12 |
Mobic | Boehringer Ingelheim Pharmaceuticals, Inc. | 15-MAR-12 |
Mobic | PD-Rx Pharmaceuticals, Inc. | 15-MAR-12 |
Meloxicam | Glenmark Generics Inc., USA | 31-MAY-12 |
Meloxicam | Mylan Pharmaceuticals Inc. | 30-JUN-12 |
Meloxicam | Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC | 09-JUL-12 |
Meloxicam | PD-Rx Pharmaceuticals, Inc. | 18-JUL-12 |
Meloxicam | Unichem Pharmaceuticals (USA), Inc. | 18-JUL-12 |
Meloxicam | Medsource Pharmaceuticals | 24-JUL-12 |
Meloxicam | Teva Pharmaceuticals USA Inc | 25-JUL-12 |
Meloxicam | Aidarex Pharmaceuticals LLC | 28-SEP-12 |
Meloxicam | AvPAK | 09-OCT-12 |
Meloxicam | Lake Erie Medical DBA Quality Care Products LLC | 20-NOV-12 |
Meloxicam | International Labs, Inc. | 03-DEC-12 |
Meloxicam | Lupin Pharmaceuticals, Inc. | 07-JAN-13 |
Meloxicam | Lake Erie Medical DBA Quality Care Products LLC | 14-FEB-13 |
Meloxicam | Aurobindo Pharma Limited | 18-FEB-13 |
Meloxicam | Preferred Pharmaceuticals, Inc. | 15-MAR-13 |
Meloxicam | Cardinal Health | 22-MAR-13 |
Meloxicam | Teva Pharmaceuticals USA Inc | 25-APR-13 |
What Meloxicam safety concerns are being reported by doctors and researchers in the medical literature?
This report contains aggregated drug side effects and adverse events for Meloxicam. 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.
Share your experience with Meloxicam.