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TREOSULFAN

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Treosulfan Adverse Events Reported to the FDA Over Time

How are Treosulfan adverse event reports trending over time?

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

Most Common Treosulfan Adverse Events Reported to the FDA

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

Graft Versus Host Disease
28 (4.12%)
Convulsion
24 (3.53%)
Acute Graft Versus Host Disease
22 (3.24%)
Cytomegalovirus Infection
20 (2.95%)
Multi-organ Failure
18 (2.65%)
Pneumonitis
16 (2.36%)
Adenovirus Infection
14 (2.06%)
Acute Graft Versus Host Disease In ...
13 (1.91%)
Chronic Graft Versus Host Disease
13 (1.91%)
Epstein-barr Virus Infection
13 (1.91%)
Rash
12 (1.77%)
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Hypertension
11 (1.62%)
Mucosal Inflammation
11 (1.62%)
Adenoviral Hepatitis
9 (1.33%)
Evans Syndrome
9 (1.33%)
Nephrotic Syndrome
8 (1.18%)
Sepsis
8 (1.18%)
Acute Graft Versus Host Disease In ...
7 (1.03%)
Cerebral Haemorrhage
7 (1.03%)
Pyrexia
7 (1.03%)
Renal Failure
7 (1.03%)
Acute Graft Versus Host Disease In ...
6 (.88%)
Blood Bilirubin Increased
6 (.88%)
Capillary Leak Syndrome
6 (.88%)
Human Herpesvirus 6 Infection
6 (.88%)
Pulmonary Haemorrhage
6 (.88%)
Respiratory Failure
6 (.88%)
Toxic Encephalopathy
6 (.88%)
Toxic Epidermal Necrolysis
6 (.88%)
C-reactive Protein Increased
5 (.74%)
Cardiac Failure
5 (.74%)
Death
5 (.74%)
Pericarditis
5 (.74%)
Platelet Count Decreased
5 (.74%)
Venoocclusive Liver Disease
5 (.74%)
Cholestasis
4 (.59%)
Depression Suicidal
4 (.59%)
Disease Progression
4 (.59%)
Drug Toxicity
4 (.59%)
Febrile Neutropenia
4 (.59%)
Fungal Infection
4 (.59%)
Gastroenteritis Viral
4 (.59%)
Herpes Zoster
4 (.59%)
Hypertonia
4 (.59%)
Optic Neuritis
4 (.59%)
Pancytopenia
4 (.59%)
Retinitis
4 (.59%)
Septic Shock
4 (.59%)
Staphylococcal Skin Infection
4 (.59%)
Tracheostomy
4 (.59%)
Venoocclusive Disease
4 (.59%)
Candidiasis
3 (.44%)
Cholecystitis
3 (.44%)
Haemoglobin Decreased
3 (.44%)
Hepatic Encephalopathy
3 (.44%)
Hepatorenal Syndrome
3 (.44%)
Lymphoproliferative Disorder
3 (.44%)
Neurological Decompensation
3 (.44%)
Pain
3 (.44%)
Pancreatitis Necrotising
3 (.44%)
Paraparesis
3 (.44%)
Paroxysmal Arrhythmia
3 (.44%)
Peritonitis Bacterial
3 (.44%)
Pneumonia
3 (.44%)
Pulmonary Hypertension
3 (.44%)
Staphylococcal Scalded Skin Syndrom...
3 (.44%)
Stupor
3 (.44%)
Subarachnoid Haemorrhage
3 (.44%)
Thrombocytopenia
3 (.44%)
Vanishing Bile Duct Syndrome
3 (.44%)
Abdominal Pain
2 (.29%)
Acute Myeloid Leukaemia
2 (.29%)
Acute Respiratory Failure
2 (.29%)
Anaphylactic Shock
2 (.29%)
Anuria
2 (.29%)
Arrhythmia Supraventricular
2 (.29%)
Bacterial Infection
2 (.29%)
Blood Amylase Increased
2 (.29%)
Blood Creatinine Increased
2 (.29%)
Bone Marrow Failure
2 (.29%)
Bronchopulmonary Aspergillosis
2 (.29%)
Central Nervous System Infection
2 (.29%)
Cerebral Infarction
2 (.29%)
Complications Of Bone Marrow Transp...
2 (.29%)
Constipation
2 (.29%)
Cystitis Haemorrhagic
2 (.29%)
Dehydration
2 (.29%)
Diabetes Mellitus
2 (.29%)
Disease Recurrence
2 (.29%)
Dizziness
2 (.29%)
Drug Ineffective
2 (.29%)
Dyspnoea
2 (.29%)
Ear Infection
2 (.29%)
Ear Infection Bacterial
2 (.29%)
Engraftment Syndrome
2 (.29%)
Epstein-barr Virus Associated Lymph...
2 (.29%)
Erythema
2 (.29%)
Eye Infection Fungal
2 (.29%)
Fatigue
2 (.29%)
Fungus Serology Test Positive
2 (.29%)
Fusarium Infection
2 (.29%)

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

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

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

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

Bone Marrow Conditioning Regimen
58
Stem Cell Transplant
44
Combined Immunodeficiency
35
Prophylaxis Against Transplant Reje...
27
Cord Blood Transplant Therapy
21
Multiple Myeloma
10
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Bone Marrow Transplant
8
Lymphohistiocytosis
7
Primary Immunodeficiency Syndrome
6
Omenn Syndrome
6
Acute Myeloid Leukaemia
6
Myelodysplastic Syndrome
5
Allogenic Bone Marrow Transplantati...
4
Off Label Use
4
Immunodeficiency Congenital
4
Wiskott-aldrich Syndrome
4
Acute Lymphocytic Leukaemia
4
Mantle Cell Lymphoma
3
Ovarian Cancer
3
Chronic Granulomatous Disease
3
Ovarian Epithelial Cancer
3
Drug Use For Unknown Indication
3
Immunosuppression
2
Product Used For Unknown Indication
2
Haematological Malignancy
2
Endocrine Disorder
2
Immunodeficiency
2
Autoimmune Lymphoproliferative Synd...
2
Immunosuppressant Drug Therapy
2
Cartilage-hair Hypoplasia
1
Surgical Preconditioning
1
Thalassaemia
1
Hodgkins Disease
1
Juvenile Chronic Myelomonocytic Leu...
1
Osteopetrosis
1

Treosulfan Case Reports

What Treosulfan 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 Treosulfan. 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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