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ARACYTINE

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Aracytine Adverse Events Reported to the FDA Over Time

How are Aracytine adverse event reports trending over time?

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

Most Common Aracytine Adverse Events Reported to the FDA

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

Pyrexia
32 (2.51%)
Thrombocytopenia
23 (1.8%)
Renal Failure Acute
22 (1.72%)
Cytolytic Hepatitis
18 (1.41%)
Febrile Bone Marrow Aplasia
17 (1.33%)
Pancytopenia
17 (1.33%)
Bone Marrow Failure
15 (1.17%)
Renal Failure
15 (1.17%)
Pneumonia
14 (1.1%)
Pleural Effusion
13 (1.02%)
Cerebellar Syndrome
12 (.94%)
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Confusional State
12 (.94%)
Pancreatitis Acute
12 (.94%)
Respiratory Distress
12 (.94%)
Blood Bilirubin Increased
11 (.86%)
Diarrhoea
11 (.86%)
Sepsis
11 (.86%)
Toxic Skin Eruption
11 (.86%)
Condition Aggravated
10 (.78%)
Hypotension
10 (.78%)
Leukopenia
10 (.78%)
Coma
9 (.7%)
Gamma-glutamyltransferase Increased
9 (.7%)
Hyperthermia
9 (.7%)
Mydriasis
9 (.7%)
Somnolence
9 (.7%)
Agranulocytosis
8 (.63%)
Blood Alkaline Phosphatase Increase...
8 (.63%)
Cardio-respiratory Arrest
8 (.63%)
Cholestasis
8 (.63%)
Convulsion
8 (.63%)
Lung Disorder
8 (.63%)
Neutropenia
8 (.63%)
Vasculitis Cerebral
8 (.63%)
Abdominal Pain
7 (.55%)
Acute Myeloid Leukaemia
7 (.55%)
Alanine Aminotransferase Increased
7 (.55%)
Aspartate Aminotransferase Increase...
7 (.55%)
Bronchopulmonary Aspergillosis
7 (.55%)
Cardiac Failure
7 (.55%)
Hepatic Failure
7 (.55%)
Hypertension
7 (.55%)
Septic Shock
7 (.55%)
Tachycardia
7 (.55%)
Tachypnoea
7 (.55%)
Vomiting
7 (.55%)
Anaemia
6 (.47%)
Aplasia
6 (.47%)
Balance Disorder
6 (.47%)
Bilirubin Conjugated Increased
6 (.47%)
Cardiac Arrest
6 (.47%)
Death
6 (.47%)
Dermatitis Bullous
6 (.47%)
Febrile Neutropenia
6 (.47%)
Hyperbilirubinaemia
6 (.47%)
Hypernatraemia
6 (.47%)
Interstitial Lung Disease
6 (.47%)
Mucosal Inflammation
6 (.47%)
Staphylococcal Infection
6 (.47%)
Stevens-johnson Syndrome
6 (.47%)
Tremor
6 (.47%)
Venoocclusive Liver Disease
6 (.47%)
Acute Pulmonary Oedema
5 (.39%)
Anuria
5 (.39%)
Ataxia
5 (.39%)
Blood Creatinine Increased
5 (.39%)
Dysarthria
5 (.39%)
Escherichia Infection
5 (.39%)
Eye Movement Disorder
5 (.39%)
Hepatitis Cholestatic
5 (.39%)
Nausea
5 (.39%)
Oedema Peripheral
5 (.39%)
Oxygen Saturation Decreased
5 (.39%)
Sinus Bradycardia
5 (.39%)
Ventricular Fibrillation
5 (.39%)
Acute Leukaemia
4 (.31%)
Acute Respiratory Distress Syndrome
4 (.31%)
Arrhythmia
4 (.31%)
Ascites
4 (.31%)
Bacteraemia
4 (.31%)
Blood Lactate Dehydrogenase Increas...
4 (.31%)
Body Temperature Increased
4 (.31%)
Cerebral Haemorrhage
4 (.31%)
Cheilitis
4 (.31%)
Chills
4 (.31%)
Decerebration
4 (.31%)
Drug Toxicity
4 (.31%)
Dyspnoea
4 (.31%)
Encephalopathy
4 (.31%)
Escherichia Sepsis
4 (.31%)
Gait Disturbance
4 (.31%)
Haemoglobin Decreased
4 (.31%)
Haemoptysis
4 (.31%)
Hepatic Steatosis
4 (.31%)
Hypoxia
4 (.31%)
Jaundice
4 (.31%)
Lipase Increased
4 (.31%)
Liver Disorder
4 (.31%)
Lymphadenitis
4 (.31%)
Myocardial Infarction
4 (.31%)
Necrotising Ulcerative Gingivostoma...
4 (.31%)

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

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

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

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

Acute Myeloid Leukaemia
70
Acute Lymphocytic Leukaemia
37
Lymphoma
20
Non-hodgkins Lymphoma
16
Mantle Cell Lymphoma
16
Diffuse Large B-cell Lymphoma
10
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Leukaemia
10
Drug Use For Unknown Indication
10
Myelodysplastic Syndrome
9
Chronic Myeloid Leukaemia
8
B-cell Lymphoma
6
B-cell Type Acute Leukaemia
6
Acute Leukaemia
5
Leukaemia Recurrent
4
Myeloid Leukaemia
4
Lymphocytic Leukaemia
4
Brain Neoplasm
3
Central Nervous System Lymphoma
3
Bone Pain
3
Chemotherapy
2
Hodgkins Disease
2
Acute Myeloid Leukaemia Recurrent
2
Burkitts Lymphoma Stage Iv
2
T-cell Type Acute Leukaemia
2
Drug Exposure During Pregnancy
2
Acute Monocytic Leukaemia
2
Product Used For Unknown Indication
2
Refractory Anaemia With An Excess O...
1
Acute Biphenotypic Leukaemia
1
T-cell Lymphoma
1
Non-hodgkins Lymphoma Stage Iv
1
Chronic Lymphocytic Leukaemia
1
Non-hodgkins Lymphoma Recurrent
1
High Grade B-cell Lymphoma Burkitt-...
1
Burkitts Lymphoma
1

Aracytine Case Reports

What Aracytine 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 Aracytine. 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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