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Zenapax Adverse Events Reported to the FDA Over Time

How are Zenapax adverse event reports trending over time?

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

Most Common Zenapax Adverse Events Reported to the FDA

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

Pyrexia
38 (1.89%)
Cytomegalovirus Infection
37 (1.84%)
Transplant Rejection
34 (1.69%)
Blood Creatinine Increased
32 (1.59%)
Infection
29 (1.44%)
Kidney Transplant Rejection
29 (1.44%)
Pyelonephritis
26 (1.29%)
Complications Of Transplanted Kidne...
25 (1.24%)
Diarrhoea
23 (1.14%)
Sepsis
21 (1.04%)
Drug Ineffective
19 (.94%)
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Haemoglobin Decreased
19 (.94%)
Anaemia Haemolytic Autoimmune
18 (.89%)
Blood Glucose Increased
16 (.79%)
Abdominal Pain
15 (.74%)
Dehydration
15 (.74%)
Hypotension
15 (.74%)
Acute Respiratory Distress Syndrome
14 (.69%)
Anaemia
14 (.69%)
Urinary Tract Infection
14 (.69%)
Aplasia Pure Red Cell
13 (.65%)
Graft Dysfunction
13 (.65%)
Haematocrit Decreased
13 (.65%)
Hypertension
13 (.65%)
Atelectasis
12 (.6%)
Enterococcal Infection
12 (.6%)
Vomiting
12 (.6%)
Pleural Effusion
11 (.55%)
Renal Failure
11 (.55%)
Haemodialysis
10 (.5%)
Hepatic Enzyme Increased
10 (.5%)
Nausea
10 (.5%)
Acute Pulmonary Oedema
9 (.45%)
Bone Marrow Failure
9 (.45%)
Condition Aggravated
9 (.45%)
Dyspnoea
9 (.45%)
Graft Versus Host Disease
9 (.45%)
Renal Failure Acute
9 (.45%)
Blood Urea Increased
8 (.4%)
Candidiasis
8 (.4%)
Fatigue
8 (.4%)
Febrile Neutropenia
8 (.4%)
Hypoxia
8 (.4%)
Immunosuppression
8 (.4%)
Liver Transplant Rejection
8 (.4%)
Lung Disorder
8 (.4%)
Multi-organ Failure
8 (.4%)
Oedema Peripheral
8 (.4%)
Septic Shock
8 (.4%)
Tachycardia
8 (.4%)
Toxoplasmosis
8 (.4%)
White Blood Cell Count Decreased
8 (.4%)
Alanine Aminotransferase Increased
7 (.35%)
Aspartate Aminotransferase Increase...
7 (.35%)
Bacterial Infection
7 (.35%)
Bile Duct Stenosis
7 (.35%)
Deep Vein Thrombosis
7 (.35%)
Drug Toxicity
7 (.35%)
Gastrointestinal Haemorrhage
7 (.35%)
Hallucination
7 (.35%)
Hepatotoxicity
7 (.35%)
Renal Impairment
7 (.35%)
Renal Tubular Necrosis
7 (.35%)
Staphylococcal Infection
7 (.35%)
Aspergillosis
6 (.3%)
Bk Virus Infection
6 (.3%)
Blood Culture Positive
6 (.3%)
Blood Sodium Decreased
6 (.3%)
Bronchitis
6 (.3%)
Cellulitis
6 (.3%)
Chest Pain
6 (.3%)
Complications Of Transplanted Liver
6 (.3%)
Cytomegalovirus Antigen Positive
6 (.3%)
Escherichia Infection
6 (.3%)
Escherichia Urinary Tract Infection
6 (.3%)
Headache
6 (.3%)
Hepatic Failure
6 (.3%)
Hepatic Steatosis
6 (.3%)
Human Herpesvirus 8 Infection
6 (.3%)
Morganella Infection
6 (.3%)
Pancytopenia
6 (.3%)
Pelvic Abscess
6 (.3%)
Transaminases Increased
6 (.3%)
Ventricular Tachycardia
6 (.3%)
Asphyxia
5 (.25%)
Brain Oedema
5 (.25%)
Cardiac Arrest
5 (.25%)
Drug Ineffective For Unapproved Ind...
5 (.25%)
Dysuria
5 (.25%)
Fluid Overload
5 (.25%)
Fungal Infection
5 (.25%)
Gastroenteritis
5 (.25%)
Haematoma Infection
5 (.25%)
Hepatic Neoplasm Malignant
5 (.25%)
Hyperkalaemia
5 (.25%)
Hypokalaemia
5 (.25%)
Hypovolaemia
5 (.25%)
Ileus
5 (.25%)
Immunosuppressant Drug Level Increa...
5 (.25%)
Interstitial Lung Disease
5 (.25%)
Klebsiella Infection
5 (.25%)

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

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

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

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

Prophylaxis Against Transplant Reje...
142
Renal Transplant
37
Multiple Sclerosis
17
Liver Transplant
17
Drug Use For Unknown Indication
15
Graft Versus Host Disease
12
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Immunosuppression
12
Adult T-cell Lymphoma/leukaemia
9
Transplant Rejection
3
Retinopathy
3
Product Used For Unknown Indication
3
Heart Transplant
3
Hodgkins Disease
2
Hepatitis C
2
Prophylaxis Against Graft Versus Ho...
2
Small Intestine Transplant
2
Immunosuppressant Drug Therapy
1
Pemphigoid
1
Polymyositis
1
Acute Graft Versus Host Disease
1
Organ Transplant
1
Relapsing-remitting Multiple Sclero...
1
Intestinal Transplant
1
Human T-cell Lymphotropic Virus Inf...
1

Zenapax Case Reports

What Zenapax 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 Zenapax. 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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