DrugCite
Search

SENSODYNE F

Adverse Events
Drug Profile
Learn More
Reference
About Results
Comments

Sensodyne F Adverse Events Reported to the FDA Over Time

How are Sensodyne F adverse event reports trending over time?

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

Most Common Sensodyne F Adverse Events Reported to the FDA

What are the most common Sensodyne F adverse events reported to the FDA?

Age 1-9 Years

All Ages and Genders

Dyspnoea
12 (4.65%)
Oral Pain
8 (3.1%)
Asthma
7 (2.71%)
Balance Disorder
6 (2.33%)
Gingival Pain
6 (2.33%)
Lower Respiratory Tract Infection
6 (2.33%)
Fatigue
5 (1.94%)
Lethargy
5 (1.94%)
Weight Decreased
5 (1.94%)
Cough
4 (1.55%)
Dizziness
4 (1.55%)
Show More Show More
Dysgeusia
4 (1.55%)
Feeling Abnormal
4 (1.55%)
Glossitis
4 (1.55%)
Malaise
4 (1.55%)
Pain
4 (1.55%)
Poor Quality Drug Administered
4 (1.55%)
Sensitivity Of Teeth
4 (1.55%)
Swollen Tongue
4 (1.55%)
Chest Discomfort
3 (1.16%)
Gingival Atrophy
3 (1.16%)
Glossodynia
3 (1.16%)
Hypersensitivity
3 (1.16%)
Oral Discomfort
3 (1.16%)
Stomatitis
3 (1.16%)
Tongue Disorder
3 (1.16%)
Tongue Ulceration
3 (1.16%)
Anaphylactic Shock
2 (.78%)
Anxiety
2 (.78%)
Arthralgia
2 (.78%)
Bronchitis
2 (.78%)
Candidiasis
2 (.78%)
Cardiac Disorder
2 (.78%)
Chest Pain
2 (.78%)
Choking
2 (.78%)
Condition Aggravated
2 (.78%)
Conduction Disorder
2 (.78%)
Deafness Unilateral
2 (.78%)
Dysphonia
2 (.78%)
Ear Pain
2 (.78%)
Eating Disorder
2 (.78%)
Exercise Tolerance Decreased
2 (.78%)
Fibromyalgia
2 (.78%)
Gingival Recession
2 (.78%)
Headache
2 (.78%)
Hypoaesthesia Oral
2 (.78%)
Monoplegia
2 (.78%)
Movement Disorder
2 (.78%)
Muscle Tightness
2 (.78%)
Ovarian Cancer
2 (.78%)
Pain In Extremity
2 (.78%)
Palpitations
2 (.78%)
Paraesthesia
2 (.78%)
Pharyngitis
2 (.78%)
Tongue Coated
2 (.78%)
Vomiting
2 (.78%)
Wrist Fracture
2 (.78%)
Abnormal Dreams
1 (.39%)
Anaphylactic Reaction
1 (.39%)
Angioedema
1 (.39%)
Aphthous Stomatitis
1 (.39%)
Apnoea
1 (.39%)
Apparent Death
1 (.39%)
Aspiration
1 (.39%)
Atrial Fibrillation
1 (.39%)
Blindness
1 (.39%)
Blood Glucose Abnormal
1 (.39%)
Burning Sensation
1 (.39%)
Cardiac Valve Disease
1 (.39%)
Cheilitis
1 (.39%)
Clostridial Infection
1 (.39%)
Convulsion
1 (.39%)
Coronary Artery Disease
1 (.39%)
Coronary Artery Occlusion
1 (.39%)
Cyanosis
1 (.39%)
Diarrhoea
1 (.39%)
Diarrhoea Haemorrhagic
1 (.39%)
Drug Ineffective
1 (.39%)
Dry Mouth
1 (.39%)
Erythema
1 (.39%)
Exposure To Toxic Agent
1 (.39%)
Eye Haemorrhage
1 (.39%)
Facial Palsy
1 (.39%)
Facial Spasm
1 (.39%)
Food Poisoning
1 (.39%)
Gait Disturbance
1 (.39%)
Gingival Bleeding
1 (.39%)
Gingival Disorder
1 (.39%)
Haematoma
1 (.39%)
Haemorrhage
1 (.39%)
Heart Rate Decreased
1 (.39%)
Heart Rate Increased
1 (.39%)
Hepatic Enzyme Increased
1 (.39%)
Herpes Zoster
1 (.39%)
Hip Swelling
1 (.39%)
Hypoaesthesia
1 (.39%)
Insomnia
1 (.39%)
Intentional Drug Misuse
1 (.39%)
Intranasal Hypoaesthesia
1 (.39%)
Lip Swelling
1 (.39%)
Lymphadenopathy
1 (.39%)

ExportShare/Embed GraphExport Export Data

This graph shows the top adverse events submitted to the FDA for Sensodyne F, 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 Sensodyne F 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 Sensodyne F

What are the most common Sensodyne F adverse events reported to the FDA?

Age 1-9 Years

All Ages and Genders

Show More Show More

ExportShare/Embed Graph Export Export Data

This graph shows the top categories of adverse events submitted to the FDA for Sensodyne F, 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 Sensodyne F 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 Sensodyne F According to Those Reporting Adverse Events

Why are people taking Sensodyne F, according to those reporting adverse events to the FDA?

Sensitivity Of Teeth
24
Dental Cleaning
17
Drug Use For Unknown Indication
10
Dental Care
4
Ill-defined Disorder
2

Child Safety Precautions


Sensodyne F Case Reports

What Sensodyne F safety concerns are being reported by doctors and researchers in the medical literature?

Powered by Google

About Results

This report contains aggregated drug side effects and adverse events for Sensodyne F. 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.

Comments

Share your experience with Sensodyne F.