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JEVTANA KIT

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Jevtana Kit Adverse Events Reported to the FDA Over Time

How are Jevtana Kit adverse event reports trending over time?

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

Most Common Jevtana Kit Adverse Events Reported to the FDA

What are the most common Jevtana Kit adverse events reported to the FDA?

Death
61 (6.2%)
Neutropenia
34 (3.46%)
Thrombocytopenia
30 (3.05%)
Anaemia
25 (2.54%)
Diarrhoea
22 (2.24%)
Pulmonary Embolism
18 (1.83%)
Renal Failure
18 (1.83%)
Asthenia
17 (1.73%)
Pancytopenia
16 (1.63%)
Disease Progression
15 (1.52%)
Dyspnoea
15 (1.52%)
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Pneumonia
15 (1.52%)
Abdominal Pain
14 (1.42%)
Gastrointestinal Haemorrhage
14 (1.42%)
Pyrexia
14 (1.42%)
Atrial Fibrillation
12 (1.22%)
Decreased Appetite
12 (1.22%)
Nausea
12 (1.22%)
Sepsis
12 (1.22%)
Constipation
11 (1.12%)
Disseminated Intravascular Coagulat...
10 (1.02%)
General Physical Health Deteriorati...
10 (1.02%)
Hypotension
10 (1.02%)
Febrile Neutropenia
9 (.91%)
Ileus
9 (.91%)
Chest Pain
8 (.81%)
Fatigue
8 (.81%)
Respiratory Failure
8 (.81%)
Spinal Cord Compression
8 (.81%)
Arrhythmia
7 (.71%)
Confusional State
7 (.71%)
Convulsion
7 (.71%)
Febrile Bone Marrow Aplasia
7 (.71%)
Lung Infiltration
7 (.71%)
Pleural Effusion
7 (.71%)
Rectal Haemorrhage
7 (.71%)
Septic Shock
7 (.71%)
Weight Decreased
7 (.71%)
Condition Aggravated
6 (.61%)
Delirium
6 (.61%)
Hallucination
6 (.61%)
Vomiting
6 (.61%)
Bacterial Sepsis
5 (.51%)
Dizziness
5 (.51%)
Gastric Haemorrhage
5 (.51%)
Haemoglobin Decreased
5 (.51%)
Haemoptysis
5 (.51%)
Multi-organ Failure
5 (.51%)
Neuropathy Peripheral
5 (.51%)
Oedema Peripheral
5 (.51%)
Sudden Death
5 (.51%)
Abscess
4 (.41%)
Anuria
4 (.41%)
Atrial Flutter
4 (.41%)
Blood Glucose Abnormal
4 (.41%)
Blood Lactate Dehydrogenase Increas...
4 (.41%)
Bone Pain
4 (.41%)
Cardiac Arrest
4 (.41%)
Cholestasis
4 (.41%)
Chronic Obstructive Pulmonary Disea...
4 (.41%)
Clostridium Difficile Colitis
4 (.41%)
Cold Type Haemolytic Anaemia
4 (.41%)
Dehydration
4 (.41%)
Disorientation
4 (.41%)
Drug Ineffective
4 (.41%)
Extravasation
4 (.41%)
Flushing
4 (.41%)
Haematuria
4 (.41%)
Hepatic Failure
4 (.41%)
Hypovolaemia
4 (.41%)
Melaena
4 (.41%)
Muscle Rigidity
4 (.41%)
Muscle Spasms
4 (.41%)
Neurotoxicity
4 (.41%)
Neutropenic Infection
4 (.41%)
Pneumonitis
4 (.41%)
Pulmonary Haemorrhage
4 (.41%)
Renal Failure Acute
4 (.41%)
Tremor
4 (.41%)
Unresponsive To Stimuli
4 (.41%)
White Blood Cell Count Decreased
4 (.41%)
Acute Coronary Syndrome
3 (.3%)
Acute Pulmonary Oedema
3 (.3%)
Acute Respiratory Distress Syndrome
3 (.3%)
Ageusia
3 (.3%)
Alanine Aminotransferase Increased
3 (.3%)
Aphagia
3 (.3%)
Aspartate Aminotransferase Increase...
3 (.3%)
Blood Alkaline Phosphatase Decrease...
3 (.3%)
Blood Bilirubin Increased
3 (.3%)
Coronary Artery Occlusion
3 (.3%)
Diverticular Perforation
3 (.3%)
Intestinal Perforation
3 (.3%)
Pain
3 (.3%)
Petechiae
3 (.3%)
Proctitis
3 (.3%)
Prostate Cancer
3 (.3%)
Prostatic Specific Antigen Increase...
3 (.3%)
Stevens-johnson Syndrome
3 (.3%)
Syncope
3 (.3%)
Tachycardia
3 (.3%)

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

What are the most common Jevtana Kit adverse events reported to the FDA?

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

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

Prostate Cancer
101
Prostate Cancer Metastatic
50
Prostate Cancer Recurrent
3
Product Used For Unknown Indication
3
Chemotherapy
2
Breast Cancer
1
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Palliative Care
1

Jevtana Kit Case Reports

What Jevtana Kit 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 Jevtana Kit. 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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