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Dicynone Adverse Events Reported to the FDA Over Time

How are Dicynone adverse event reports trending over time?

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

Most Common Dicynone Adverse Events Reported to the FDA

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

Atrial Septal Defect
17 (10.3%)
Drug Exposure During Pregnancy
16 (9.7%)
Congenital Musculoskeletal Anomaly
15 (9.09%)
Premature Baby
14 (8.48%)
Leukocytoclastic Vasculitis
7 (4.24%)
Polyhydramnios
7 (4.24%)
Caesarean Section
6 (3.64%)
Acute Generalised Exanthematous Pus...
5 (3.03%)
Maternal Drugs Affecting Foetus
5 (3.03%)
Breech Presentation
4 (2.42%)
Toxic Skin Eruption
4 (2.42%)
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Inflammation
3 (1.82%)
Thrombocytopenia
3 (1.82%)
Vascular Purpura
3 (1.82%)
Alanine Aminotransferase Increased
2 (1.21%)
Anaemia
2 (1.21%)
Aspartate Aminotransferase Increase...
2 (1.21%)
Cholestasis
2 (1.21%)
Dyspnoea
2 (1.21%)
Gamma-glutamyltransferase Increased
2 (1.21%)
Generalised Erythema
2 (1.21%)
Hepatitis C
2 (1.21%)
Hyperglobulinaemia
2 (1.21%)
Lip Disorder
2 (1.21%)
Normochromic Normocytic Anaemia
2 (1.21%)
Oral Disorder
2 (1.21%)
Purpura
2 (1.21%)
Rash Pustular
2 (1.21%)
Skin Exfoliation
2 (1.21%)
Abdominal Pain
1 (.61%)
Antinuclear Antibody Positive
1 (.61%)
Aplasia
1 (.61%)
Blood Alkaline Phosphatase Increase...
1 (.61%)
Brain Oedema
1 (.61%)
Cerebral Haemorrhage
1 (.61%)
Cholecystitis
1 (.61%)
Cholelithiasis
1 (.61%)
Cholelithiasis Obstructive
1 (.61%)
Chromaturia
1 (.61%)
Complement Factor C4 Decreased
1 (.61%)
Congenital Anomaly
1 (.61%)
Congenital Jaw Malformation
1 (.61%)
Cryoglobulinaemia
1 (.61%)
Death
1 (.61%)
Disease Progression
1 (.61%)
Drug Withdrawal Syndrome Neonatal
1 (.61%)
Escherichia Bacteraemia
1 (.61%)
Eye Pain
1 (.61%)
Faeces Discoloured
1 (.61%)
Haemoglobin Decreased
1 (.61%)
Maternal Death Affecting Foetus
1 (.61%)
Pancreatitis Acute
1 (.61%)
Pancytopenia
1 (.61%)
Renal Failure
1 (.61%)
Small For Dates Baby
1 (.61%)

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

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

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

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

Epistaxis
7
Thrombotic Thrombocytopenic Purpura
5
Pain
3
Drug Use For Unknown Indication
3
Thrombocytopenia
2
Haematoma
2
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Haematuria
1
Flushing
1
Procedural Complication
1
Menorrhagia
1
Erythema
1
Haemorrhage
1
Prophylaxis
1
Haemoptysis
1
Product Used For Unknown Indication
1

Dicynone Case Reports

What Dicynone 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 Dicynone. 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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