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LISTERINE WHITENING PRE BRUSH RINSE

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Listerine Whitening Pre Brush Rinse Adverse Events Reported to the FDA Over Time

How are Listerine Whitening Pre Brush Rinse adverse event reports trending over time?

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

Most Common Listerine Whitening Pre Brush Rinse Adverse Events Reported to the FDA

What are the most common Listerine Whitening Pre Brush Rinse adverse events reported to the FDA?

Application Site Burn
24 (4.49%)
Ageusia
20 (3.75%)
Oral Mucosal Exfoliation
20 (3.75%)
Stomatitis
18 (3.37%)
Glossodynia
17 (3.18%)
Oral Discomfort
14 (2.62%)
Lip Swelling
13 (2.43%)
Application Site Irritation
12 (2.25%)
Caustic Injury
11 (2.06%)
Swelling Face
10 (1.87%)
Cheilitis
9 (1.69%)
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Gingival Pain
9 (1.69%)
Oral Pain
9 (1.69%)
Glossitis
8 (1.5%)
Pain
8 (1.5%)
Thermal Burn
8 (1.5%)
Aphthous Stomatitis
7 (1.31%)
Hypoaesthesia Oral
7 (1.31%)
Application Site Erythema
6 (1.12%)
Dysgeusia
6 (1.12%)
Dyspnoea
6 (1.12%)
Tongue Blistering
6 (1.12%)
Tongue Discolouration
6 (1.12%)
Tongue Disorder
6 (1.12%)
Tooth Disorder
6 (1.12%)
Application Site Pain
5 (.94%)
Application Site Vesicles
5 (.94%)
Burning Sensation
5 (.94%)
Gingival Disorder
5 (.94%)
Gingivitis
5 (.94%)
Infection
5 (.94%)
Lip Blister
5 (.94%)
Oropharyngeal Blistering
5 (.94%)
Paraesthesia Oral
5 (.94%)
Salivary Duct Obstruction
5 (.94%)
Swollen Tongue
5 (.94%)
Condition Aggravated
4 (.75%)
Dysphagia
4 (.75%)
Gingival Discolouration
4 (.75%)
Incorrect Dose Administered
4 (.75%)
Local Swelling
4 (.75%)
Oedema Mouth
4 (.75%)
Tooth Discolouration
4 (.75%)
Bacterial Infection
3 (.56%)
Drug Ineffective
3 (.56%)
Erythema
3 (.56%)
Gingival Erosion
3 (.56%)
Gingival Recession
3 (.56%)
Gingival Swelling
3 (.56%)
Lacrimation Increased
3 (.56%)
Lip Disorder
3 (.56%)
Medication Error
3 (.56%)
Oral Disorder
3 (.56%)
Pain In Jaw
3 (.56%)
Sensitivity Of Teeth
3 (.56%)
Tooth Injury
3 (.56%)
Anaphylactic Reaction
2 (.37%)
Anaphylactic Shock
2 (.37%)
Application Site Exfoliation
2 (.37%)
Dental Caries
2 (.37%)
Dry Mouth
2 (.37%)
Ear Pain
2 (.37%)
Eating Disorder
2 (.37%)
Expired Drug Administered
2 (.37%)
Eye Swelling
2 (.37%)
Feeling Cold
2 (.37%)
Gingival Bleeding
2 (.37%)
Gingival Blister
2 (.37%)
Gingival Erythema
2 (.37%)
Hypersensitivity
2 (.37%)
Hypoaesthesia
2 (.37%)
Hypophagia
2 (.37%)
Intentional Drug Misuse
2 (.37%)
Jaw Disorder
2 (.37%)
Lip Exfoliation
2 (.37%)
Lip Pain
2 (.37%)
Loose Tooth
2 (.37%)
Malaise
2 (.37%)
Mouth Ulceration
2 (.37%)
Neuralgia
2 (.37%)
Oral Candidiasis
2 (.37%)
Oropharyngeal Pain
2 (.37%)
Paraesthesia
2 (.37%)
Product Quality Issue
2 (.37%)
Rash Pustular
2 (.37%)
Salivary Gland Enlargement
2 (.37%)
Salivary Gland Pain
2 (.37%)
Sensation Of Heaviness
2 (.37%)
Skin Exfoliation
2 (.37%)
Skin Irritation
2 (.37%)
Swelling
2 (.37%)
Throat Tightness
2 (.37%)
Tooth Delamination
2 (.37%)
Tooth Fracture
2 (.37%)
Wrong Technique In Drug Usage Proce...
2 (.37%)
Abdominal Discomfort
1 (.19%)
Abscess
1 (.19%)
Accidental Exposure
1 (.19%)
Application Site Anaesthesia
1 (.19%)
Application Site Bleeding
1 (.19%)
Application Site Discolouration
1 (.19%)

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This graph shows the top adverse events submitted to the FDA for Listerine Whitening Pre Brush Rinse, 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 Whitening Pre Brush Rinse 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 Listerine Whitening Pre Brush Rinse

What are the most common Listerine Whitening Pre Brush Rinse adverse events reported to the FDA?

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This graph shows the top categories of adverse events submitted to the FDA for Listerine Whitening Pre Brush Rinse, 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 Whitening Pre Brush Rinse 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 Listerine Whitening Pre Brush Rinse According to Those Reporting Adverse Events

Why are people taking Listerine Whitening Pre Brush Rinse, according to those reporting adverse events to the FDA?

Dental Care
89
Dental Disorder Prophylaxis
23
Drug Use For Unknown Indication
23
Product Used For Unknown Indication
3
Accidental Exposure
1
Tooth Discolouration
1
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Listerine Whitening Pre Brush Rinse Case Reports

What Listerine Whitening Pre Brush Rinse 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 Listerine Whitening Pre Brush Rinse. 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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