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CABAZITAXEL

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Cabazitaxel Adverse Events Reported to the FDA Over Time

How are Cabazitaxel adverse event reports trending over time?

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

Most Common Cabazitaxel Adverse Events Reported to the FDA

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

Pulmonary Embolism
51 (5.01%)
Sepsis
29 (2.85%)
Neutropenia
26 (2.56%)
Death
25 (2.46%)
Diarrhoea
25 (2.46%)
Pancytopenia
24 (2.36%)
Pneumonia
20 (1.97%)
Syncope
20 (1.97%)
Anaemia
19 (1.87%)
Thrombocytopenia
19 (1.87%)
Cholecystitis
18 (1.77%)
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Gastrointestinal Haemorrhage
17 (1.67%)
Duodenal Ulcer
16 (1.57%)
Gastritis
14 (1.38%)
Hypocalcaemia
14 (1.38%)
Pyrexia
14 (1.38%)
Cardio-respiratory Arrest
13 (1.28%)
Disseminated Intravascular Coagulat...
13 (1.28%)
Hypotension
13 (1.28%)
Deep Vein Thrombosis
12 (1.18%)
Dehydration
12 (1.18%)
Febrile Neutropenia
11 (1.08%)
Cardiac Failure
10 (.98%)
Cystitis Radiation
10 (.98%)
Fall
10 (.98%)
Haematuria
10 (.98%)
Nausea
10 (.98%)
Neutropenic Sepsis
10 (.98%)
Pneumonitis
10 (.98%)
Renal Failure Acute
10 (.98%)
Sudden Death
10 (.98%)
Asthenia
9 (.88%)
Cerebral Haemorrhage
9 (.88%)
Haemorrhagic Anaemia
9 (.88%)
Leukopenia
9 (.88%)
Septic Shock
9 (.88%)
Agranulocytosis
8 (.79%)
Colitis
8 (.79%)
Diabetes Mellitus
8 (.79%)
Small Intestinal Haemorrhage
8 (.79%)
Cardiac Failure Congestive
7 (.69%)
Disease Progression
7 (.69%)
Multi-organ Failure
7 (.69%)
Neoplasm Progression
7 (.69%)
Pulmonary Oedema
7 (.69%)
Urinary Tract Infection
7 (.69%)
Vomiting
7 (.69%)
Acute Coronary Syndrome
6 (.59%)
Atrial Fibrillation
6 (.59%)
Back Pain
6 (.59%)
Cachexia
6 (.59%)
Chemical Cystitis
6 (.59%)
Diverticulum Intestinal Haemorrhagi...
6 (.59%)
Febrile Bone Marrow Aplasia
6 (.59%)
Gastric Ulcer
6 (.59%)
Hypoglycaemia
6 (.59%)
Myocardial Infarction
6 (.59%)
Pain In Extremity
6 (.59%)
Phlebitis Infective
6 (.59%)
Respiratory Failure
6 (.59%)
Small Intestinal Obstruction
6 (.59%)
Acute Myocardial Infarction
5 (.49%)
Duodenal Ulcer Haemorrhage
5 (.49%)
General Physical Health Deteriorati...
5 (.49%)
Abdominal Pain
4 (.39%)
Accidental Overdose
4 (.39%)
Acute Respiratory Failure
4 (.39%)
Aortic Dissection
4 (.39%)
Cataract
4 (.39%)
Circulatory Collapse
4 (.39%)
Confusional State
4 (.39%)
Diabetic Ketoacidosis
4 (.39%)
Duodenal Perforation
4 (.39%)
Embolism
4 (.39%)
Erysipelas
4 (.39%)
Gastric Ulcer Haemorrhage
4 (.39%)
Generalised Oedema
4 (.39%)
Haematochezia
4 (.39%)
Haemoptysis
4 (.39%)
Hydronephrosis
4 (.39%)
Hyperglycaemia
4 (.39%)
Implant Site Reaction
4 (.39%)
Large Intestinal Haemorrhage
4 (.39%)
Neutropenic Infection
4 (.39%)
Oedema
4 (.39%)
Paraparesis
4 (.39%)
Pleurisy
4 (.39%)
Spinal Cord Compression
4 (.39%)
Transaminases Increased
4 (.39%)
Weight Increased
4 (.39%)
Blood Creatinine Increased
3 (.29%)
Ejection Fraction Decreased
3 (.29%)
Hyponatraemia
3 (.29%)
Ileus Paralytic
3 (.29%)
Jaundice
3 (.29%)
Metastases To Central Nervous Syste...
3 (.29%)
Renal Failure
3 (.29%)
Rhabdomyolysis
3 (.29%)
Shock
3 (.29%)
Abdominal Distension
2 (.2%)
Arrhythmia
2 (.2%)

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

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

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

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

Prostate Cancer
133
Prostate Cancer Metastatic
104
Product Used For Unknown Indication
7
Colon Cancer
3
Metastatic Gastric Cancer
2
Gastric Cancer
2
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Adenocarcinoma Of The Cervix
1
Sarcoma Metastatic
1
Lung Neoplasm Malignant
1
Oesophageal Carcinoma
1

Drug Labels

LabelLabelerEffective
JevtanaSanofi-Aventis U.S. LLC12-OCT-12
JevtanaSanofi-Aventis U.S. LLC29-APR-13

Cabazitaxel Case Reports

What Cabazitaxel 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 Cabazitaxel. 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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