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Zanamivir Adverse Events Reported to the FDA Over Time

How are Zanamivir adverse event reports trending over time?

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

Most Common Zanamivir Adverse Events Reported to the FDA

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

Death
26 (4.48%)
Acute Respiratory Distress Syndrome
20 (3.44%)
Cytolytic Hepatitis
17 (2.93%)
Multi-organ Failure
17 (2.93%)
Respiratory Failure
17 (2.93%)
Drug Exposure During Pregnancy
16 (2.75%)
Renal Failure
16 (2.75%)
Pancytopenia
13 (2.24%)
Haemodynamic Instability
12 (2.07%)
Cardiac Arrest
10 (1.72%)
Hypoxia
10 (1.72%)
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Thrombocytopenia
10 (1.72%)
Blood Creatinine Increased
9 (1.55%)
Bradycardia
9 (1.55%)
Encephalopathy
9 (1.55%)
Haemoglobin Decreased
9 (1.55%)
Pathogen Resistance
9 (1.55%)
Drug Ineffective
8 (1.38%)
Pyrexia
7 (1.2%)
Abortion Spontaneous
6 (1.03%)
Accidental Overdose
6 (1.03%)
Hepatocellular Injury
6 (1.03%)
Hypotension
6 (1.03%)
Ileus Paralytic
6 (1.03%)
Renal Impairment
6 (1.03%)
Alanine Aminotransferase Increased
5 (.86%)
Aspartate Aminotransferase Increase...
5 (.86%)
Drug Resistance
5 (.86%)
Gamma-glutamyltransferase Increased
5 (.86%)
Live Birth
5 (.86%)
Renal Failure Acute
5 (.86%)
Shock
5 (.86%)
Sinus Arrest
5 (.86%)
Agitation
4 (.69%)
Aplasia
4 (.69%)
Cholestasis
4 (.69%)
Hepatic Failure
4 (.69%)
Neutropenia
4 (.69%)
Pneumonia
4 (.69%)
Pneumonia Viral
4 (.69%)
Pneumothorax
4 (.69%)
Septic Shock
4 (.69%)
Torsade De Pointes
4 (.69%)
Anxiety
3 (.52%)
Arrhythmia
3 (.52%)
Aspergillosis
3 (.52%)
Cardiogenic Shock
3 (.52%)
Circulatory Collapse
3 (.52%)
Delirium
3 (.52%)
Extubation
3 (.52%)
General Physical Health Deteriorati...
3 (.52%)
Hepatic Enzyme Increased
3 (.52%)
Hepatic Function Abnormal
3 (.52%)
Hepatotoxicity
3 (.52%)
Hyperlactacidaemia
3 (.52%)
Leukopenia
3 (.52%)
Mechanical Ventilation
3 (.52%)
Pneumonia Staphylococcal
3 (.52%)
Pneumonitis
3 (.52%)
Pulmonary Embolism
3 (.52%)
Tachycardia
3 (.52%)
Tachypnoea
3 (.52%)
Ventricular Arrhythmia
3 (.52%)
Acidosis
2 (.34%)
Anuria
2 (.34%)
Ascites
2 (.34%)
Cardio-respiratory Arrest
2 (.34%)
Chills
2 (.34%)
Condition Aggravated
2 (.34%)
Convulsion
2 (.34%)
Cough
2 (.34%)
Drug Toxicity
2 (.34%)
Dyspnoea
2 (.34%)
Febrile Neutropenia
2 (.34%)
Gastrointestinal Haemorrhage
2 (.34%)
Haematotoxicity
2 (.34%)
Haemolysis
2 (.34%)
Haemorrhagic Stroke
2 (.34%)
Hepatomegaly
2 (.34%)
Hypocapnia
2 (.34%)
Hyporeflexia
2 (.34%)
Influenza
2 (.34%)
Intravascular Haemolysis
2 (.34%)
Ischaemia
2 (.34%)
Ischaemic Stroke
2 (.34%)
Lactic Acidosis
2 (.34%)
Linear Iga Disease
2 (.34%)
Malaise
2 (.34%)
Metabolic Alkalosis
2 (.34%)
Mutism
2 (.34%)
Nervous System Disorder
2 (.34%)
No Adverse Event
2 (.34%)
Overdose
2 (.34%)
Pregnancy
2 (.34%)
Pulmonary Fibrosis
2 (.34%)
Pulmonary Haemorrhage
2 (.34%)
Pupil Fixed
2 (.34%)
Respiratory Disorder
2 (.34%)
Retrograde Portal Vein Flow
2 (.34%)
Rhabdomyolysis
2 (.34%)
Transaminases Increased
2 (.34%)

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

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

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

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

H1n1 Influenza
86
Influenza
65
Drug Use For Unknown Indication
2
Product Used For Unknown Indication
2
Pneumonitis
2
Pathogen Resistance
2
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Antiviral Treatment
1
Influenza Virus Test Positive
1
Anti-infective Therapy
1
Ill-defined Disorder
1

Drug Labels

LabelLabelerEffective
RelenzaDispensing Solutions Inc.02-MAR-10
RelenzaPhysicians Total Care, Inc.02-MAR-10
RelenzaGlaxoSmithKline LLC03-JAN-12

Zanamivir Case Reports

What Zanamivir 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 Zanamivir. 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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