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PEG INTERFERON ALFA

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Peg Interferon Alfa Adverse Events Reported to the FDA Over Time

How are Peg Interferon Alfa adverse event reports trending over time?

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

Most Common Peg Interferon Alfa Adverse Events Reported to the FDA

What are the most common Peg Interferon Alfa adverse events reported to the FDA?

Anaemia
212 (2.48%)
Nausea
133 (1.56%)
Vomiting
130 (1.52%)
Dehydration
129 (1.51%)
Syncope
118 (1.38%)
Thrombocytopenia
110 (1.29%)
Pyrexia
108 (1.26%)
Pneumonia
105 (1.23%)
Haemoglobin Decreased
99 (1.16%)
Platelet Count Decreased
88 (1.03%)
Asthenia
87 (1.02%)
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Hypokalaemia
81 (.95%)
Dyspnoea
75 (.88%)
Fatigue
69 (.81%)
Diarrhoea
68 (.8%)
Dizziness
67 (.78%)
Pancytopenia
62 (.73%)
Weight Decreased
61 (.71%)
Convulsion
60 (.7%)
Renal Failure Acute
56 (.66%)
Depression
55 (.64%)
Grand Mal Convulsion
55 (.64%)
Ascites
53 (.62%)
Neutropenia
53 (.62%)
White Blood Cell Count Decreased
52 (.61%)
Headache
47 (.55%)
Cholelithiasis
44 (.52%)
Confusional State
44 (.52%)
Retinal Detachment
42 (.49%)
Rash
41 (.48%)
Deep Vein Thrombosis
40 (.47%)
Blood Glucose Increased
39 (.46%)
Pleural Effusion
39 (.46%)
Leukopenia
38 (.44%)
Fall
37 (.43%)
Gastritis
37 (.43%)
Renal Failure
37 (.43%)
Death
36 (.42%)
Loss Of Consciousness
36 (.42%)
Malaise
36 (.42%)
Vertigo
36 (.42%)
Gastroenteritis
35 (.41%)
Guillain-barre Syndrome
34 (.4%)
Mental Status Changes
34 (.4%)
Gingival Bleeding
33 (.39%)
Appendicitis
31 (.36%)
Hypotension
31 (.36%)
Sepsis
31 (.36%)
Alanine Aminotransferase Increased
30 (.35%)
Aspartate Aminotransferase Increase...
30 (.35%)
Chest Pain
30 (.35%)
Hepatic Cirrhosis
29 (.34%)
Oedema Peripheral
29 (.34%)
Urinary Tract Infection
29 (.34%)
Cellulitis
28 (.33%)
Myocardial Infarction
28 (.33%)
Transplant Rejection
28 (.33%)
Cough
27 (.32%)
Decreased Appetite
27 (.32%)
Diabetic Ketoacidosis
27 (.32%)
General Physical Health Deteriorati...
27 (.32%)
Abdominal Pain
26 (.3%)
Haematocrit Decreased
26 (.3%)
Orthostatic Hypotension
26 (.3%)
Staphylococcal Infection
26 (.3%)
Anorexia
25 (.29%)
Cholecystitis Acute
25 (.29%)
Disorientation
25 (.29%)
Pruritus
25 (.29%)
Vision Blurred
25 (.29%)
Anxiety
24 (.28%)
Septic Shock
24 (.28%)
Atrial Fibrillation
23 (.27%)
Cholecystitis
23 (.27%)
Hepatic Encephalopathy
23 (.27%)
Hepatic Neoplasm Malignant
23 (.27%)
Hypertension
23 (.27%)
Metabolic Acidosis
23 (.27%)
Migraine
23 (.27%)
Cognitive Disorder
22 (.26%)
Neutrophil Count Decreased
22 (.26%)
Cardiac Failure
21 (.25%)
Haemorrhage
21 (.25%)
Red Blood Cell Count Decreased
21 (.25%)
Splenomegaly
21 (.25%)
Arthralgia
20 (.23%)
Facial Palsy
20 (.23%)
Hepatitis C
20 (.23%)
Hypothyroidism
20 (.23%)
Influenza Like Illness
20 (.23%)
Jaundice
20 (.23%)
Asthma
19 (.22%)
Back Pain
19 (.22%)
Epistaxis
19 (.22%)
Gastrointestinal Haemorrhage
19 (.22%)
Hyponatraemia
19 (.22%)
Pallor
19 (.22%)
Tachycardia
19 (.22%)
Chills
18 (.21%)
Myalgia
18 (.21%)
Delirium
17 (.2%)

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This graph shows the top adverse events submitted to the FDA for Peg Interferon Alfa, 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 Peg Interferon Alfa 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 Peg Interferon Alfa

What are the most common Peg Interferon Alfa adverse events reported to the FDA?

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

Why are people taking Peg Interferon Alfa, according to those reporting adverse events to the FDA?

Hepatitis C
707
Drug Use For Unknown Indication
45
Hepatitis B
26
Hepatitis C Virus
18
Chronic Hepatitis
6
Chronic Myeloid Leukaemia
6
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Hepatitis C Virus Test
4
Hepatic Cirrhosis
4
Malignant Melanoma
4
Anaemia Of Chronic Disease
3
Hepatitis
3
Disease Recurrence
2
Antiviral Treatment
2
Renal Cell Carcinoma Stage Unspecif...
2
Product Used For Unknown Indication
1
Carcinoid Tumour
1
Hiv Infection
1
Small Intestine Carcinoma
1
Cryoglobulinaemia
1
Neoplasm Prophylaxis
1
Hepatitis Acute
1
Kaposis Sarcoma Aids Related
1

Peg Interferon Alfa Case Reports

What Peg Interferon Alfa 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 Peg Interferon Alfa. 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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