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COOL MINT LISTERINE

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Cool Mint Listerine Adverse Events Reported to the FDA Over Time

How are Cool Mint Listerine adverse event reports trending over time?

This graph shows volume of adverse events submitted to the FDA by quarter for Cool Mint Listerine, as well as related generic and/or brandname drugs containing the same primary active ingredients. Adverse events are counted if Cool Mint Listerine is flagged as the suspect drug causing the adverse event.

Most Common Cool Mint Listerine Adverse Events Reported to the FDA

What are the most common Cool Mint Listerine adverse events reported to the FDA?

Accidental Exposure
27 (3.49%)
Incorrect Route Of Drug Administrat...
27 (3.49%)
Intentional Drug Misuse
23 (2.98%)
Application Site Burn
22 (2.85%)
Product Quality Issue
20 (2.59%)
Oral Discomfort
16 (2.07%)
Nausea
15 (1.94%)
Malaise
12 (1.55%)
Blister
9 (1.16%)
Glossodynia
9 (1.16%)
Vision Blurred
9 (1.16%)
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Ageusia
8 (1.03%)
Dysphagia
8 (1.03%)
Gingival Bleeding
8 (1.03%)
Oral Pain
8 (1.03%)
Pain
8 (1.03%)
Tongue Disorder
8 (1.03%)
Anorexia
7 (.91%)
Asthenia
7 (.91%)
Blood Potassium Decreased
7 (.91%)
Diarrhoea
7 (.91%)
Disturbance In Attention
7 (.91%)
Gingival Infection
7 (.91%)
Oropharyngeal Blistering
7 (.91%)
Syncope
7 (.91%)
Application Site Pain
6 (.78%)
Burning Sensation
6 (.78%)
Fatigue
6 (.78%)
Glossitis
6 (.78%)
Hypersensitivity
6 (.78%)
Oxygen Saturation Decreased
6 (.78%)
Stomatitis
6 (.78%)
Vomiting
6 (.78%)
Abdominal Pain Upper
5 (.65%)
Blindness Unilateral
5 (.65%)
Dyspnoea
5 (.65%)
Erythema
5 (.65%)
Expired Drug Administered
5 (.65%)
Eye Pain
5 (.65%)
Feeling Abnormal
5 (.65%)
Oral Mucosal Exfoliation
5 (.65%)
Product Contamination
5 (.65%)
Sinus Disorder
5 (.65%)
Swollen Tongue
5 (.65%)
Abdominal Pain
4 (.52%)
Application Site Irritation
4 (.52%)
Application Site Vesicles
4 (.52%)
Dizziness Postural
4 (.52%)
Drug Abuse
4 (.52%)
Dyspepsia
4 (.52%)
Eye Irritation
4 (.52%)
Fibromyalgia
4 (.52%)
Gingival Pain
4 (.52%)
Hypoaesthesia
4 (.52%)
Inflammation
4 (.52%)
Lip And/or Oral Cavity Cancer
4 (.52%)
Mouth Ulceration
4 (.52%)
Oropharyngeal Pain
4 (.52%)
Product Taste Abnormal
4 (.52%)
Tongue Blistering
4 (.52%)
Toothache
4 (.52%)
Wrong Technique In Drug Usage Proce...
4 (.52%)
Accidental Drug Intake By Child
3 (.39%)
Alcohol Poisoning
3 (.39%)
Alcohol Use
3 (.39%)
Caustic Injury
3 (.39%)
Chest Pain
3 (.39%)
Confusional State
3 (.39%)
Dizziness
3 (.39%)
Drug Ineffective
3 (.39%)
Drug Toxicity
3 (.39%)
Eye Disorder
3 (.39%)
Feeling Drunk
3 (.39%)
Gastritis
3 (.39%)
Heart Rate Increased
3 (.39%)
Hypoaesthesia Oral
3 (.39%)
Impaired Driving Ability
3 (.39%)
Incorrect Dose Administered
3 (.39%)
Incorrect Drug Administration Durat...
3 (.39%)
Lymphadenopathy
3 (.39%)
Ocular Hyperaemia
3 (.39%)
Oesophagitis
3 (.39%)
Oral Disorder
3 (.39%)
Overdose
3 (.39%)
Pharyngeal Erythema
3 (.39%)
Pharyngeal Oedema
3 (.39%)
Rash
3 (.39%)
Sinus Headache
3 (.39%)
Swelling
3 (.39%)
Throat Irritation
3 (.39%)
Throat Tightness
3 (.39%)
Tongue Ulceration
3 (.39%)
Visual Acuity Reduced
3 (.39%)
Abnormal Behaviour
2 (.26%)
Aphagia
2 (.26%)
Auricular Swelling
2 (.26%)
Blood Pressure Increased
2 (.26%)
Condition Aggravated
2 (.26%)
Convulsion
2 (.26%)
Corneal Abrasion
2 (.26%)
Crying
2 (.26%)

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This graph shows the top adverse events submitted to the FDA for Cool Mint 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 Cool Mint 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.

Adverse Event Categories for Cool Mint Listerine

What are the most common Cool Mint Listerine adverse events reported to the FDA?

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This graph shows the top categories of adverse events submitted to the FDA for Cool Mint 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 Cool Mint 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.

Common Uses of Cool Mint Listerine According to Those Reporting Adverse Events

Why are people taking Cool Mint Listerine, according to those reporting adverse events to the FDA?

Dental Disorder Prophylaxis
84
Drug Use For Unknown Indication
26
Accidental Exposure
11
Breath Odour
11
Alcohol Use
8
Product Used For Unknown Indication
5
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Intentional Overdose
4
Intentional Drug Misuse
3
Gingivitis
3
Toothache
3
Alcoholic
3
Alcoholism
3
Dental Care
2
Nasopharyngitis
2
Feeling Drunk
2
Intentional Misuse
2
Poisoning
2
Smoking Cessation Therapy
2
Pharyngolaryngeal Pain
1
Sleep Disorder
1
Hangover
1
Dry Mouth
1
Alcohol Poisoning
1
Overdose
1
Social Problem
1
Gingival Pain
1
Euphoric Mood
1

Cool Mint Listerine Case Reports

What Cool Mint Listerine safety concerns are being reported by doctors and researchers in the medical literature?

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About Results

This report contains aggregated drug side effects and adverse events for Cool Mint 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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