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DANATROL

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Danatrol Adverse Events Reported to the FDA Over Time

How are Danatrol adverse event reports trending over time?

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

Most Common Danatrol Adverse Events Reported to the FDA

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

Pleural Effusion
6 (4%)
Asthenia
5 (3.33%)
Weight Increased
5 (3.33%)
Alanine Aminotransferase Increased
4 (2.67%)
Aspartate Aminotransferase Increase...
4 (2.67%)
Cholestasis
4 (2.67%)
Cough
4 (2.67%)
Cytolytic Hepatitis
4 (2.67%)
Dyspnoea
4 (2.67%)
Fluid Retention
4 (2.67%)
Oedema Peripheral
4 (2.67%)
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Orthopnoea
4 (2.67%)
Sodium Retention
4 (2.67%)
Cholelithiasis
3 (2%)
Diabetes Mellitus
3 (2%)
Renal Failure
3 (2%)
Weight Decreased
3 (2%)
Abdominal Pain
2 (1.33%)
Blood Creatine Phosphokinase Increa...
2 (1.33%)
Blood Lactate Dehydrogenase Increas...
2 (1.33%)
Cardiac Failure
2 (1.33%)
Cardiomegaly
2 (1.33%)
Cardiomyopathy
2 (1.33%)
Chest Pain
2 (1.33%)
Creatinine Renal Clearance Increase...
2 (1.33%)
Gamma-glutamyltransferase Increased
2 (1.33%)
Hepatitis
2 (1.33%)
Hypertension
2 (1.33%)
Interstitial Lung Disease
2 (1.33%)
Lung Disorder
2 (1.33%)
Mitral Valve Incompetence
2 (1.33%)
Oestradiol Increased
2 (1.33%)
Ovarian Hyperfunction
2 (1.33%)
Pain In Extremity
2 (1.33%)
Pulmonary Oedema
2 (1.33%)
Ventricular Hypertrophy
2 (1.33%)
Angina Unstable
1 (.67%)
Aphasia
1 (.67%)
Atrial Fibrillation
1 (.67%)
Bilirubin Conjugated Increased
1 (.67%)
Blood Alkaline Phosphatase Increase...
1 (.67%)
Blood Bilirubin Increased
1 (.67%)
Calculus Bladder
1 (.67%)
Cerebral Haemorrhage
1 (.67%)
Cerebral Venous Thrombosis
1 (.67%)
Convulsion
1 (.67%)
Demyelination
1 (.67%)
Dermatitis Exfoliative
1 (.67%)
Drug Exposure During Pregnancy
1 (.67%)
Drug Ineffective
1 (.67%)
Drug Interaction
1 (.67%)
Ejection Fraction Decreased
1 (.67%)
Glomerulonephritis Minimal Lesion
1 (.67%)
Haematuria
1 (.67%)
Haemoptysis
1 (.67%)
Hemiplegia
1 (.67%)
Hepatomegaly
1 (.67%)
Hyperbilirubinaemia
1 (.67%)
Hyperphagia
1 (.67%)
Hypotension
1 (.67%)
International Normalised Ratio Incr...
1 (.67%)
Intra-uterine Death
1 (.67%)
Jaundice
1 (.67%)
Jaundice Cholestatic
1 (.67%)
Keratitis Interstitial
1 (.67%)
Lung Cyst
1 (.67%)
Muscular Weakness
1 (.67%)
Nephropathy
1 (.67%)
Nephrotic Syndrome
1 (.67%)
Nocardiosis
1 (.67%)
Opportunistic Infection
1 (.67%)
Pancreatic Disorder
1 (.67%)
Pericardial Effusion
1 (.67%)
Personality Change Due To A General...
1 (.67%)
Polydipsia
1 (.67%)
Polyuria
1 (.67%)
Pulmonary Embolism
1 (.67%)
Pyrexia
1 (.67%)
Splenomegaly
1 (.67%)
Toxic Skin Eruption
1 (.67%)

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

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

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

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

Drug Use For Unknown Indication
12
Idiopathic Thrombocytopenic Purpura
5
Thrombocytopenia
3
Splenomegaly
3
Endometriosis
3
Aplastic Anaemia
2
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Epistaxis
2
Autoimmune Thrombocytopenia
1
Myelodysplastic Syndrome
1
Angioneurotic Oedema
1
Myelofibrosis
1
Metrorrhagia
1

Danatrol Case Reports

What Danatrol 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 Danatrol. 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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