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ADVAFERON

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Advaferon Adverse Events Reported to the FDA Over Time

How are Advaferon adverse event reports trending over time?

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

Most Common Advaferon Adverse Events Reported to the FDA

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

Injection Site Necrosis
13 (3%)
Malaise
13 (3%)
Bacterial Infection
10 (2.31%)
Injection Site Ulcer
10 (2.31%)
Peritonsillitis
10 (2.31%)
White Blood Cell Count Decreased
9 (2.08%)
Anorexia
8 (1.85%)
Neutrophil Count Decreased
8 (1.85%)
Prostate Cancer
8 (1.85%)
Weight Decreased
8 (1.85%)
Alanine Aminotransferase Increased
7 (1.62%)
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Convulsion
7 (1.62%)
Platelet Count Decreased
7 (1.62%)
Pyrexia
7 (1.62%)
Skin Ulcer
7 (1.62%)
Interstitial Lung Disease
6 (1.39%)
Skin Necrosis
6 (1.39%)
Ascites
5 (1.15%)
Cerebral Haemorrhage
5 (1.15%)
Deafness
5 (1.15%)
Depression
5 (1.15%)
Erythema
5 (1.15%)
Pneumonia
5 (1.15%)
Rhabdomyolysis
5 (1.15%)
Anxiety
4 (.92%)
Aspartate Aminotransferase Increase...
4 (.92%)
Depressed Level Of Consciousness
4 (.92%)
Diabetes Mellitus
4 (.92%)
Electrocardiogram St Segment Depres...
4 (.92%)
Face Oedema
4 (.92%)
Insomnia
4 (.92%)
Intestinal Ischaemia
4 (.92%)
Oedema Peripheral
4 (.92%)
Staphylococcal Infection
4 (.92%)
Abdominal Distension
3 (.69%)
Affect Lability
3 (.69%)
Ammonia Increased
3 (.69%)
Autoimmune Disorder
3 (.69%)
Endocrine Ophthalmopathy
3 (.69%)
Enterococcal Infection
3 (.69%)
General Physical Health Deteriorati...
3 (.69%)
Generalised Oedema
3 (.69%)
Hepatic Neoplasm Malignant
3 (.69%)
Injection Site Induration
3 (.69%)
Mental Disorder
3 (.69%)
Nasopharyngitis
3 (.69%)
Pallor
3 (.69%)
Pancytopenia
3 (.69%)
Retinal Vein Occlusion
3 (.69%)
Vomiting
3 (.69%)
Weight Increased
3 (.69%)
Antinuclear Antibody Positive
2 (.46%)
Anuria
2 (.46%)
Arthralgia
2 (.46%)
Blood Lactate Dehydrogenase Increas...
2 (.46%)
Blood Pressure Decreased
2 (.46%)
Breast Cancer Male
2 (.46%)
Cellulitis
2 (.46%)
Completed Suicide
2 (.46%)
Diabetic Ketoacidosis
2 (.46%)
Dizziness
2 (.46%)
Eating Disorder
2 (.46%)
Emotional Disorder
2 (.46%)
Feeling Abnormal
2 (.46%)
Haemophilus Infection
2 (.46%)
Hemiplegia
2 (.46%)
Hyperamylasaemia
2 (.46%)
Hypertension
2 (.46%)
Hypothyroidism
2 (.46%)
Immunodeficiency
2 (.46%)
Injection Site Erythema
2 (.46%)
Injection Site Pruritus
2 (.46%)
Loss Of Consciousness
2 (.46%)
Meningitis
2 (.46%)
Mydriasis
2 (.46%)
Pain
2 (.46%)
Pain In Extremity
2 (.46%)
Pancreatitis Acute
2 (.46%)
Proteinuria
2 (.46%)
Pupillary Reflex Impaired
2 (.46%)
Rash
2 (.46%)
Rectal Cancer
2 (.46%)
Respiratory Failure
2 (.46%)
Retinal Haemorrhage
2 (.46%)
Sepsis
2 (.46%)
Skin Warm
2 (.46%)
Subcutaneous Haematoma
2 (.46%)
Systemic Sclerosis
2 (.46%)
Thalamus Haemorrhage
2 (.46%)
Thirst
2 (.46%)
Abdominal Pain Upper
1 (.23%)
Acute Prerenal Failure
1 (.23%)
Affective Disorder
1 (.23%)
Anaemia
1 (.23%)
Angina Pectoris
1 (.23%)
Anti-gad Antibody Positive
1 (.23%)
Anti-neutrophil Cytoplasmic Antibod...
1 (.23%)
Antibody Test Abnormal
1 (.23%)
Autoimmune Hepatitis
1 (.23%)
Autophony
1 (.23%)
Azotaemia
1 (.23%)

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

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

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

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

Hepatitis C
274
Hepatitis Chronic Active
5
Hepatic Cirrhosis
5
Chronic Hepatitis
4
Hepatitis C Virus
2
Hepatitis Fulminant
2
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Viral Hepatitis Carrier
1
Hepatitis Acute
1

Advaferon Case Reports

What Advaferon 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 Advaferon. 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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