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RODOGYL

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Rodogyl Adverse Events Reported to the FDA Over Time

How are Rodogyl adverse event reports trending over time?

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

Most Common Rodogyl Adverse Events Reported to the FDA

What are the most common Rodogyl adverse events reported to the FDA?

Pyrexia
15 (6.02%)
Vomiting
10 (4.02%)
Diarrhoea
8 (3.21%)
Urticaria
8 (3.21%)
Pruritus
7 (2.81%)
Asthenia
6 (2.41%)
Multiple Drug Overdose Intentional
6 (2.41%)
Rash
6 (2.41%)
Cholestasis
5 (2.01%)
Acute Generalised Exanthematous Pus...
4 (1.61%)
Autoimmune Disorder
4 (1.61%)
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Dermatitis Exfoliative
4 (1.61%)
Hyperthermia
4 (1.61%)
Myocarditis
4 (1.61%)
Pallor
4 (1.61%)
Acute Pulmonary Oedema
3 (1.2%)
Ataxia
3 (1.2%)
Cardiac Valve Disease
3 (1.2%)
Cell Death
3 (1.2%)
Ejection Fraction Decreased
3 (1.2%)
Encephalopathy
3 (1.2%)
Erythema
3 (1.2%)
Headache
3 (1.2%)
Lymphadenopathy
3 (1.2%)
Nausea
3 (1.2%)
Agranulocytosis
2 (.8%)
Arthralgia
2 (.8%)
Aspartate Aminotransferase Increase...
2 (.8%)
Blood Alkaline Phosphatase Increase...
2 (.8%)
Blood Bilirubin Increased
2 (.8%)
Cough
2 (.8%)
Dermatitis Bullous
2 (.8%)
Dizziness
2 (.8%)
Drug Rash With Eosinophilia And Sys...
2 (.8%)
Dysarthria
2 (.8%)
Dyspnoea
2 (.8%)
Eosinophilic Pneumonia
2 (.8%)
Fluid Overload
2 (.8%)
Gastric Lavage
2 (.8%)
Haemoglobin Decreased
2 (.8%)
Hypoaesthesia
2 (.8%)
Inflammation
2 (.8%)
Insomnia
2 (.8%)
Intentional Overdose
2 (.8%)
Leukocytosis
2 (.8%)
Liver Disorder
2 (.8%)
Malaise
2 (.8%)
Mitral Valve Incompetence
2 (.8%)
Myocardial Infarction
2 (.8%)
Neck Pain
2 (.8%)
Pancytopenia
2 (.8%)
Paraparesis
2 (.8%)
Petechiae
2 (.8%)
Pruritus Generalised
2 (.8%)
Rash Maculo-papular
2 (.8%)
Rash Pustular
2 (.8%)
Suicide Attempt
2 (.8%)
Thrombocytopenia
2 (.8%)
Toxic Skin Eruption
2 (.8%)
Tremor
2 (.8%)
Ventricular Hypokinesia
2 (.8%)
Vertigo
2 (.8%)
Viral Infection
2 (.8%)
Abnormal Behaviour
1 (.4%)
Abscess Oral
1 (.4%)
Alanine Aminotransferase Increased
1 (.4%)
Angiopathy
1 (.4%)
Anorexia
1 (.4%)
Antinuclear Antibody Positive
1 (.4%)
Balanitis
1 (.4%)
Blood Bilirubin Unconjugated Increa...
1 (.4%)
Blood Immunoglobulin E Increased
1 (.4%)
Cardiomyopathy
1 (.4%)
Cellulitis
1 (.4%)
Cheilitis
1 (.4%)
Chills
1 (.4%)
Chromaturia
1 (.4%)
Cytolytic Hepatitis
1 (.4%)
Dehydration
1 (.4%)
Dysgeusia
1 (.4%)
Fall
1 (.4%)
Fatigue
1 (.4%)
Fixed Eruption
1 (.4%)
Gamma-glutamyltransferase Increased
1 (.4%)
General Physical Health Deteriorati...
1 (.4%)
Hallucination
1 (.4%)
Hallucinations, Mixed
1 (.4%)
Hepatotoxicity
1 (.4%)
Hypotension
1 (.4%)
Iatrogenic Injury
1 (.4%)
Jaundice
1 (.4%)
Leukopenia
1 (.4%)
Liver Injury
1 (.4%)
Lymphocyte Count Abnormal
1 (.4%)
Monocyte Count Abnormal
1 (.4%)
Mucous Membrane Disorder
1 (.4%)
Myalgia
1 (.4%)
No Therapeutic Response
1 (.4%)
Oliguria
1 (.4%)
Oral Infection
1 (.4%)
Persecutory Delusion
1 (.4%)

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

What are the most common Rodogyl adverse events reported to the FDA?

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

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

Drug Use For Unknown Indication
7
Tooth Abscess
5
Tooth Infection
5
Tooth Extraction
4
Toothache
3
Tonsillitis
2
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Wisdom Teeth Removal
2
Pyrexia
2
Intentional Overdose
2
Dental Care
1
Brain Abscess
1
Coma Hepatic
1
Dental Discomfort
1
Pericardial Disease
1
Abscess
1
Local Swelling
1
Dental Operation
1
Periodontitis
1
Infection
1
Gingivitis
1
Bacterial Infection
1

Rodogyl Case Reports

What Rodogyl 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 Rodogyl. 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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