DrugCite
Search

ARZERRA

Adverse Events
Drug Profile
Learn More
Reference
About Results
Comments

Arzerra Adverse Events Reported to the FDA Over Time

How are Arzerra adverse event reports trending over time?

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

Most Common Arzerra Adverse Events Reported to the FDA

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

Death
18 (2.36%)
Dyspnoea
18 (2.36%)
Infusion Related Reaction
17 (2.23%)
Neutropenia
17 (2.23%)
Pyrexia
17 (2.23%)
Pneumonia
16 (2.1%)
Rash
14 (1.83%)
Febrile Neutropenia
13 (1.7%)
Neuropathy Peripheral
12 (1.57%)
Disease Progression
11 (1.44%)
Urticaria
11 (1.44%)
Show More Show More
Diarrhoea
10 (1.31%)
Nausea
10 (1.31%)
Pruritus
10 (1.31%)
Chest Pain
9 (1.18%)
Lymphadenopathy
9 (1.18%)
Platelet Count Decreased
9 (1.18%)
Thrombocytopenia
9 (1.18%)
Anaemia
8 (1.05%)
Sepsis
8 (1.05%)
Chronic Lymphocytic Leukaemia
7 (.92%)
Vomiting
7 (.92%)
Asthenia
6 (.79%)
Flushing
6 (.79%)
Hyperhidrosis
6 (.79%)
Neutrophil Count Decreased
6 (.79%)
Weight Decreased
6 (.79%)
White Blood Cell Count Decreased
6 (.79%)
Adverse Drug Reaction
5 (.66%)
Chills
5 (.66%)
Fatigue
5 (.66%)
Hypoaesthesia
5 (.66%)
Local Swelling
5 (.66%)
Tremor
5 (.66%)
Abdominal Pain Upper
4 (.52%)
Bradycardia
4 (.52%)
Cardiac Arrest
4 (.52%)
Deep Vein Thrombosis
4 (.52%)
Dizziness
4 (.52%)
Drug Administration Error
4 (.52%)
Erythema
4 (.52%)
General Physical Health Deteriorati...
4 (.52%)
Off Label Use
4 (.52%)
Oxygen Saturation Decreased
4 (.52%)
Pain In Extremity
4 (.52%)
Rash Vesicular
4 (.52%)
Throat Tightness
4 (.52%)
White Blood Cell Count Increased
4 (.52%)
Abdominal Discomfort
3 (.39%)
Alanine Aminotransferase Increased
3 (.39%)
Back Pain
3 (.39%)
Blister
3 (.39%)
Blood Bilirubin Increased
3 (.39%)
Cellulitis
3 (.39%)
Cough
3 (.39%)
Drug Ineffective
3 (.39%)
Electrocardiogram Qt Prolonged
3 (.39%)
Enterococcal Sepsis
3 (.39%)
Escherichia Sepsis
3 (.39%)
Feeling Hot
3 (.39%)
Gait Disturbance
3 (.39%)
Hepatic Enzyme Increased
3 (.39%)
Hepatitis B
3 (.39%)
Hepatomegaly
3 (.39%)
Hepatorenal Syndrome
3 (.39%)
Herpes Virus Infection
3 (.39%)
Hypertension
3 (.39%)
Infection
3 (.39%)
Liver Function Test Abnormal
3 (.39%)
Lymphocyte Count Increased
3 (.39%)
Lymphoma
3 (.39%)
Pancytopenia
3 (.39%)
Paraesthesia
3 (.39%)
Paraesthesia Oral
3 (.39%)
Product Quality Issue
3 (.39%)
Productive Cough
3 (.39%)
Progressive Multifocal Leukoencepha...
3 (.39%)
Throat Irritation
3 (.39%)
Acute Respiratory Distress Syndrome
2 (.26%)
Adenovirus Infection
2 (.26%)
Anosmia
2 (.26%)
Arrhythmia
2 (.26%)
Arthralgia
2 (.26%)
Ascites
2 (.26%)
Balance Disorder
2 (.26%)
Basal Cell Carcinoma
2 (.26%)
Blood Glucose Increased
2 (.26%)
Bone Pain
2 (.26%)
Burning Sensation
2 (.26%)
C-reactive Protein Increased
2 (.26%)
Cerebrovascular Accident
2 (.26%)
Chest Discomfort
2 (.26%)
Coagulopathy
2 (.26%)
Cognitive Disorder
2 (.26%)
Colitis
2 (.26%)
Coma Hepatic
2 (.26%)
Confusional State
2 (.26%)
Dehydration
2 (.26%)
Delirium
2 (.26%)
Diabetes Mellitus
2 (.26%)
Ear Infection
2 (.26%)

ExportShare/Embed GraphExport Export Data

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

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

Show More Show More

ExportShare/Embed Graph Export Export Data

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

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

Chronic Lymphocytic Leukaemia
87
Product Used For Unknown Indication
24
Drug Use For Unknown Indication
9
B-cell Lymphoma
5
Non-hodgkins Lymphoma
5
Lymphoma
5
Show More Show More
Chronic Lymphocytic Leukaemia Refra...
3
Multiple Myeloma
2
Diffuse Large B-cell Lymphoma Recur...
2
Diffuse Large B-cell Lymphoma
1
Rheumatoid Arthritis
1
Malignant Melanoma
1
Leukaemia
1
Richters Syndrome
1
Waldenstroms Macroglobulinaemia
1
Mantle Cell Lymphoma
1
Lymphadenopathy
1
Hodgkins Disease
1

Drug Labels

LabelLabelerEffective
ArzerraGlaxoSmithKline LLC12-SEP-11

Arzerra Case Reports

What Arzerra safety concerns are being reported by doctors and researchers in the medical literature?

Powered by Google

About Results

This report contains aggregated drug side effects and adverse events for Arzerra. 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.

Comments

Share your experience with Arzerra.