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ZOPHREN

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Zophren Adverse Events Reported to the FDA Over Time

How are Zophren adverse event reports trending over time?

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

Most Common Zophren Adverse Events Reported to the FDA

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

Erythema
51 (2.11%)
Malaise
50 (2.07%)
Vomiting
48 (1.99%)
Pyrexia
41 (1.7%)
Dyspnoea
39 (1.61%)
Chills
34 (1.41%)
Pruritus
34 (1.41%)
Cytolytic Hepatitis
31 (1.28%)
Nausea
30 (1.24%)
Hypotension
29 (1.2%)
Cardiac Arrest
27 (1.12%)
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Rash
27 (1.12%)
Paraesthesia
26 (1.08%)
Chest Pain
24 (.99%)
Hyperhidrosis
24 (.99%)
Abdominal Pain
23 (.95%)
Loss Of Consciousness
20 (.83%)
Hypersensitivity
18 (.75%)
Back Pain
17 (.7%)
Cholestasis
17 (.7%)
Gamma-glutamyltransferase Increased
17 (.7%)
Anaemia
16 (.66%)
Respiratory Distress
16 (.66%)
Acute Generalised Exanthematous Pus...
15 (.62%)
Condition Aggravated
15 (.62%)
Confusional State
15 (.62%)
Feeling Hot
15 (.62%)
Headache
15 (.62%)
Asthenia
14 (.58%)
Bradycardia
14 (.58%)
Diarrhoea
14 (.58%)
Hypoxia
14 (.58%)
Interstitial Lung Disease
14 (.58%)
Thrombocytopenia
14 (.58%)
Toxic Skin Eruption
14 (.58%)
Haemorrhage
13 (.54%)
Hyperthermia
13 (.54%)
Myalgia
13 (.54%)
Neutropenia
13 (.54%)
Oxygen Saturation Decreased
13 (.54%)
Transaminases Increased
13 (.54%)
Hypertension
12 (.5%)
Shock
12 (.5%)
Anaphylactic Shock
11 (.46%)
Cyanosis
11 (.46%)
Face Oedema
11 (.46%)
Hypothyroidism
11 (.46%)
Pallor
11 (.46%)
Renal Failure
11 (.46%)
Urticaria
11 (.46%)
Alanine Aminotransferase Increased
10 (.41%)
Cardiogenic Shock
10 (.41%)
Death
10 (.41%)
Diplopia
10 (.41%)
Drug Exposure During Pregnancy
10 (.41%)
Oedema Peripheral
10 (.41%)
Rash Maculo-papular
10 (.41%)
Septic Shock
10 (.41%)
Toxic Epidermal Necrolysis
10 (.41%)
Aspartate Aminotransferase Increase...
9 (.37%)
Bronchospasm
9 (.37%)
Convulsion
9 (.37%)
Inflammation
9 (.37%)
Pancreatitis Acute
9 (.37%)
Rash Erythematous
9 (.37%)
Renal Failure Acute
9 (.37%)
Tachycardia
9 (.37%)
Blood Alkaline Phosphatase Increase...
8 (.33%)
Blood Pressure Decreased
8 (.33%)
Cardiac Failure
8 (.33%)
Colitis Ischaemic
8 (.33%)
Cough
8 (.33%)
Leukopenia
8 (.33%)
Pericardial Effusion
8 (.33%)
Skin Exfoliation
8 (.33%)
Ventricular Extrasystoles
8 (.33%)
Cardio-respiratory Arrest
7 (.29%)
Chest Discomfort
7 (.29%)
Circulatory Collapse
7 (.29%)
Disorientation
7 (.29%)
Encephalopathy
7 (.29%)
Hepatitis Cholestatic
7 (.29%)
Hepatocellular Injury
7 (.29%)
Infusion Related Reaction
7 (.29%)
Jaundice
7 (.29%)
Leukodystrophy
7 (.29%)
Lung Disorder
7 (.29%)
Pain
7 (.29%)
Palmar-plantar Erythrodysaesthesia ...
7 (.29%)
Pleural Effusion
7 (.29%)
Pulmonary Oedema
7 (.29%)
Pupils Unequal
7 (.29%)
Rash Papular
7 (.29%)
Ventricular Tachycardia
7 (.29%)
Amaurosis
6 (.25%)
Anxiety
6 (.25%)
Coma
6 (.25%)
Depressed Level Of Consciousness
6 (.25%)
Dermatitis Bullous
6 (.25%)
Drug Interaction
6 (.25%)
Dysphagia
6 (.25%)

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

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

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

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

Premedication
148
Drug Use For Unknown Indication
106
Nausea
65
Prophylaxis Of Nausea And Vomiting
64
Vomiting
47
Product Used For Unknown Indication
40
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Prophylaxis
33
Breast Cancer
8
Antiemetic Supportive Care
8
Chemotherapy
8
Lymphoma
7
Colon Cancer
5
Ill-defined Disorder
4
Non-hodgkins Lymphoma
4
Acute Myeloid Leukaemia
3
Breast Cancer Metastatic
3
Prophylactic Chemotherapy
3
Oligodendroglioma
3
Postoperative Care
3
Vomiting In Pregnancy
3
Systemic Lupus Erythematosus
2
B-cell Lymphoma
2
Wegeners Granulomatosis
2
Unevaluable Event
2
Abdominal Pain
2
Neuropathy
1
Drug Exposure During Pregnancy
1
Procedural Vomiting
1
Prostate Cancer
1
Squamous Cell Carcinoma
1
Myeloid Leukaemia
1
Optic Tract Glioma
1
Mixed Connective Tissue Disease
1
Hodgkins Disease
1
Vomiting Projectile
1
Therapeutic Procedure
1
Post Procedural Nausea
1
Bladder Cancer
1
Glioblastoma
1
Rectal Cancer
1
Gastric Cancer
1
Myelodysplastic Syndrome
1
Scleroderma
1
Supplementation Therapy
1
Bile Duct Cancer
1
Teratoma
1

Zophren Case Reports

What Zophren 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 Zophren. 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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