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BLINDED BEVACIZUMAB

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Blinded Bevacizumab Adverse Events Reported to the FDA Over Time

How are Blinded Bevacizumab adverse event reports trending over time?

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

Most Common Blinded Bevacizumab Adverse Events Reported to the FDA

What are the most common Blinded Bevacizumab adverse events reported to the FDA?

Febrile Neutropenia
262 (11.58%)
Pyrexia
51 (2.25%)
Dehydration
49 (2.17%)
Diarrhoea
46 (2.03%)
Neutropenia
44 (1.94%)
Pneumonia
37 (1.63%)
Convulsion
34 (1.5%)
Pulmonary Embolism
34 (1.5%)
Septic Shock
30 (1.33%)
Renal Failure Acute
28 (1.24%)
Mucosal Inflammation
26 (1.15%)
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Anaemia
25 (1.1%)
Haemoglobin Decreased
25 (1.1%)
Respiratory Failure
24 (1.06%)
Dyspnoea
23 (1.02%)
Blood Sodium Decreased
21 (.93%)
Gastric Perforation
21 (.93%)
Fatigue
20 (.88%)
Hypokalaemia
20 (.88%)
Pancytopenia
20 (.88%)
Platelet Count Decreased
18 (.8%)
Nausea
17 (.75%)
Sepsis
17 (.75%)
Vomiting
17 (.75%)
White Blood Cell Count Decreased
17 (.75%)
Ascites
16 (.71%)
Confusional State
16 (.71%)
Abdominal Pain
15 (.66%)
Death
15 (.66%)
Gastrointestinal Haemorrhage
15 (.66%)
General Physical Health Deteriorati...
15 (.66%)
Leukopenia
15 (.66%)
Lymphopenia
15 (.66%)
Rectal Ulcer
15 (.66%)
Haematochezia
14 (.62%)
Cerebral Ischaemia
13 (.57%)
Upper Gastrointestinal Haemorrhage
13 (.57%)
Asthenia
12 (.53%)
Ejection Fraction Decreased
12 (.53%)
Peritonitis
12 (.53%)
Atrial Fibrillation
11 (.49%)
Disease Progression
11 (.49%)
Neutropenic Sepsis
11 (.49%)
Stomatitis
11 (.49%)
Deep Vein Thrombosis
10 (.44%)
Hyponatraemia
10 (.44%)
Infection
10 (.44%)
Blood Creatinine Increased
9 (.4%)
Lower Limb Fracture
9 (.4%)
Mental Status Changes
9 (.4%)
Pneumonia Aspiration
9 (.4%)
Thrombocytopenia
9 (.4%)
Acute Respiratory Distress Syndrome
8 (.35%)
Alanine Aminotransferase Increased
8 (.35%)
Blood Potassium Increased
8 (.35%)
Cerebral Haemorrhage
8 (.35%)
Chest Pain
8 (.35%)
Malignant Neoplasm Progression
8 (.35%)
Pleural Effusion
8 (.35%)
Pneumothorax
8 (.35%)
Small Intestinal Obstruction
8 (.35%)
Splenic Abscess
8 (.35%)
Anorexia
7 (.31%)
Blood Urea Increased
7 (.31%)
Cardiac Failure
7 (.31%)
Cerebral Infarction
7 (.31%)
Cerebrovascular Accident
7 (.31%)
Decreased Appetite
7 (.31%)
Headache
7 (.31%)
Hyperglycaemia
7 (.31%)
Hypotension
7 (.31%)
Intestinal Obstruction
7 (.31%)
Laboratory Test Abnormal
7 (.31%)
Lethargy
7 (.31%)
Malaise
7 (.31%)
Muscular Weakness
7 (.31%)
Neutropenic Infection
7 (.31%)
Peripheral Sensory Neuropathy
7 (.31%)
Pneumonitis
7 (.31%)
Aspartate Aminotransferase Increase...
6 (.27%)
Colitis
6 (.27%)
Cystitis
6 (.27%)
Hypovolaemic Shock
6 (.27%)
Ileus
6 (.27%)
Neutrophil Count Decreased
6 (.27%)
Partial Seizures
6 (.27%)
Renal Failure
6 (.27%)
Somnolence
6 (.27%)
Sudden Death
6 (.27%)
Angina Pectoris
5 (.22%)
Blood Lactic Acid Increased
5 (.22%)
Constipation
5 (.22%)
Cough
5 (.22%)
Haemoptysis
5 (.22%)
Hepatic Artery Thrombosis
5 (.22%)
Hyperkalaemia
5 (.22%)
Metastases To Meninges
5 (.22%)
Multi-organ Failure
5 (.22%)
Oedema Peripheral
5 (.22%)
Opportunistic Infection
5 (.22%)
Oral Candidiasis
5 (.22%)

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

What are the most common Blinded Bevacizumab adverse events reported to the FDA?

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

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

Diffuse Large B-cell Lymphoma
368
Gastric Cancer
105
Breast Cancer Metastatic
47
Breast Cancer
47
Metastatic Renal Cell Carcinoma
36
Glioblastoma
30
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Non-small Cell Lung Cancer
20
Non-hodgkins Lymphoma
20
Glioblastoma Multiforme
16
B-cell Lymphoma
13
Metastatic Gastric Cancer
10
Prostate Cancer
10
Ovarian Cancer
9
Ovarian Epithelial Cancer
8
Metastatic Malignant Melanoma
7
Drug Use For Unknown Indication
7
Colorectal Cancer
6
Colorectal Cancer Metastatic
6
Multiple Myeloma
5
Lymphoma
4
Transitional Cell Carcinoma
3
Neoplasm Malignant
2
Fallopian Tube Cancer
2
Pancreatic Carcinoma Metastatic
1
Ovarian Cancer Metastatic
1
Mesothelioma Malignant
1
Hodgkins Disease
1
Adenocarcinoma Pancreas
1
Product Used For Unknown Indication
1

Blinded Bevacizumab Case Reports

What Blinded Bevacizumab 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 Blinded Bevacizumab. 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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