How are Listerine adverse event reports trending over time?
This graph shows volume of adverse events submitted to the FDA by quarter for Listerine, as well as related generic and/or brandname drugs containing the same primary active ingredients. Adverse events are counted if Listerine is flagged as the suspect drug causing the adverse event.
What are the most common Listerine adverse events reported to the FDA?
Application Site Burn | 222 (3.71%) |
Incorrect Route Of Drug Administrat... | 194 (3.24%) |
Intentional Drug Misuse | 153 (2.56%) |
Oral Discomfort | 129 (2.16%) |
Product Quality Issue | 115 (1.92%) |
Glossodynia | 94 (1.57%) |
Ageusia | 90 (1.5%) |
Oral Pain | 86 (1.44%) |
Stomatitis | 86 (1.44%) |
Lip Swelling | 83 (1.39%) |
Oral Mucosal Exfoliation | 73 (1.22%) |
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This graph shows the top adverse events submitted to the FDA for Listerine, 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 Listerine 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 Listerine adverse events reported to the FDA?
Oral Soft Tissue Conditions | 840 (14.04%) |
Medication Errors | 445 (7.44%) |
Administration Site Reactions | 440 (7.35%) |
Dental And Gingival Conditions | 376 (6.28%) |
Neurological | 368 (6.15%) |
Tongue Conditions | 352 (5.88%) |
Psychiatric | 257 (4.3%) |
Epidermal And Dermal Conditions | 203 (3.39%) |
Gastrointestinal Signs | 200 (3.34%) |
Respiratory | 195 (3.26%) |
Product Quality Issues | 163 (2.72%) |
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This graph shows the top categories of adverse events submitted to the FDA for Listerine, 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 Listerine 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 Listerine, according to those reporting adverse events to the FDA?
Dental Disorder Prophylaxis | 542 |
Dental Care | 349 |
Drug Use For Unknown Indication | 182 |
Product Used For Unknown Indication | 158 |
Breath Odour | 40 |
Accidental Exposure | 39 |
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Label | Labeler | Effective |
---|---|---|
Listerinetotal Care | Johnson & Johnson Healthcare Products, Division of McNEIL-PPC, Inc. | 18-NOV-09 |
Listerine Total Care Plus Whitening | Johnson & Johnson Healthcare Products, Division of McNEIL-PPC, Inc. | 11-MAY-10 |
Listerine Cool Mint Antiseptic | Johnson & Johnson Healthcare Products, Division of McNEIL-PPC, Inc. | 22-FEB-12 |
Listerine Freshburst Antiseptic | Johnson & Johnson Healthcare Products, Division of McNEIL-PPC, Inc. | 22-FEB-12 |
Listerine Antiseptic | Johnson & Johnson Healthcare Products, Division of McNEIL-PPC, Inc. | 23-FEB-12 |
Listerine Essential Care | Johnson & Johnson Healthcare Products, Division of McNEIL-PPC, Inc. | 13-MAR-12 |
Listerine Essential Care Tartar Control | Johnson & Johnson Healthcare Products, Division of McNEIL-PPC, Inc. | 13-MAR-12 |
Listerine Whitening Restoring | Johnson & Johnson Healthcare Products, Division of McNEIL-PPC, Inc. | 02-MAY-12 |
Listerine Total Care Anticavity Cinnamint | Johnson & Johnson Healthcare Products, Division of McNEIL-PPC, Inc. | 15-MAY-12 |
Listerine Ultraclean Antiseptic Artic Mint | Johnson & Johnson Healthcare Products, Division of McNEIL-PPC, Inc. | 06-JUL-12 |
Listerine Ultraclean Antiseptic Cool Mint | Johnson & Johnson Healthcare Products, Division of McNEIL-PPC, Inc. | 11-JUL-12 |
Listerine Ultraclean Antiseptic Fresh Citrus | Johnson & Johnson Healthcare Products, Division of McNEIL-PPC, Inc. | 12-JUL-12 |
Listerine Smart Rinse Phineas And Ferb Bubble Blast | Johnson & Johnson Healthcare Products, Division of McNEIL-PPC, Inc. | 26-JUL-12 |
Listerine Smart Rinse Barbie | Johnson & Johnson Healthcare Products, Division of McNEIL-PPC, Inc. | 26-JUL-12 |
Listerine Total Care Zero Freshmint | Johnson & Johnson Healthcare Products, Division of McNEIL-PPC, Inc. | 26-JUL-12 |
Listerine Total Care Zero Fresh Mint | Johnson & Johnson Healthcare Products, Division of McNEIL-PPC, Inc. | 27-JUL-12 |
Listerine Smart Rinse Bubble Gum Shield | Johnson & Johnson Healthcare Products, Division of McNEIL-PPC, Inc. | 27-JUL-12 |
Listerine Smart Rinse Mint Shield | Johnson & Johnson Healthcare Products, Division of McNEIL-PPC, Inc. | 27-JUL-12 |
Listerine Smart Rinse Berry Shield | Johnson & Johnson Healthcare Products, Division of McNEIL-PPC, Inc. | 28-JUL-12 |
Listerine Fluoride Defense | Johnson & Johnson Healthcare Products, Division of McNEIL-PPC, Inc. | 21-AUG-12 |
Listerine Whitening Fluoride Anticavity Original | Johnson & Johnson Healthcare Products, Division of McNEIL-PPC, Inc. | 27-NOV-12 |
Soft Mint Listerine Antiseptic | Johnson & Johnson Healthcare Products, Division of McNEIL-PPC, Inc. | 29-NOV-12 |
Listerine Essential Care Tartar Control | Johnson & Johnson Healthcare Products, Division of McNEIL-PPC, Inc. | 01-MAR-13 |
What Listerine safety concerns are being reported by doctors and researchers in the medical literature?
This report contains aggregated drug side effects and adverse events for Listerine. 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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