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TARGRETIN

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Targretin Adverse Events Reported to the FDA Over Time

How are Targretin adverse event reports trending over time?

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

Most Common Targretin Adverse Events Reported to the FDA

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

Headache
20 (2.29%)
Fatigue
16 (1.83%)
Hypertriglyceridaemia
16 (1.83%)
Hypothyroidism
16 (1.83%)
Asthenia
14 (1.6%)
Dehydration
14 (1.6%)
Pneumonia
14 (1.6%)
Dyspnoea
13 (1.49%)
Pyrexia
11 (1.26%)
Anaemia
10 (1.14%)
Disease Progression
10 (1.14%)
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General Physical Health Deteriorati...
10 (1.14%)
Confusional State
9 (1.03%)
Leukopenia
9 (1.03%)
Malignant Neoplasm Progression
9 (1.03%)
Cardiac Failure
8 (.92%)
Febrile Neutropenia
8 (.92%)
Skin Exfoliation
8 (.92%)
Condition Aggravated
7 (.8%)
Erythema
7 (.8%)
Insomnia
7 (.8%)
Myalgia
7 (.8%)
Nausea
7 (.8%)
Neoplasm Malignant
7 (.8%)
Oedema Peripheral
7 (.8%)
Visual Impairment
7 (.8%)
Chills
6 (.69%)
Choroiditis
6 (.69%)
Depressed Mood
6 (.69%)
Drug Interaction
6 (.69%)
Dysuria
6 (.69%)
Hyperhidrosis
6 (.69%)
Hypoxia
6 (.69%)
International Normalised Ratio
6 (.69%)
Mycosis Fungoides
6 (.69%)
Pain
6 (.69%)
Pruritus
6 (.69%)
Blood Triglycerides Increased
5 (.57%)
Cardiac Failure Congestive
5 (.57%)
Cough
5 (.57%)
Haematochezia
5 (.57%)
International Normalised Ratio Incr...
5 (.57%)
Oxygen Saturation Decreased
5 (.57%)
Sepsis
5 (.57%)
Subdural Haematoma
5 (.57%)
Thrombocytopenia
5 (.57%)
Abdominal Pain
4 (.46%)
Arthralgia
4 (.46%)
Cerebrovascular Accident
4 (.46%)
Deafness
4 (.46%)
Death
4 (.46%)
Dizziness
4 (.46%)
Drug Ineffective
4 (.46%)
Face Oedema
4 (.46%)
Granuloma
4 (.46%)
Haematuria
4 (.46%)
Haemoglobin Decreased
4 (.46%)
Haemoptysis
4 (.46%)
Lymphoma
4 (.46%)
Pulmonary Fibrosis
4 (.46%)
Rash
4 (.46%)
Renal Failure Acute
4 (.46%)
Vomiting
4 (.46%)
White Blood Cell Count Increased
4 (.46%)
Abasia
3 (.34%)
Acute Coronary Syndrome
3 (.34%)
Blood Cholesterol Abnormal
3 (.34%)
Blood Creatinine Increased
3 (.34%)
Blood Triglycerides Abnormal
3 (.34%)
Cardiac Arrest
3 (.34%)
Coagulopathy
3 (.34%)
Delirium
3 (.34%)
Dermatitis Exfoliative
3 (.34%)
Diverticulitis
3 (.34%)
Dry Skin
3 (.34%)
Ecchymosis
3 (.34%)
Flank Pain
3 (.34%)
Hyperlipidaemia
3 (.34%)
Hypoglycaemia
3 (.34%)
Hypotension
3 (.34%)
Infection
3 (.34%)
Lung Infection
3 (.34%)
Lymphadenopathy
3 (.34%)
Myoglobin Blood Increased
3 (.34%)
Nephrolithiasis
3 (.34%)
Night Sweats
3 (.34%)
Pancreatic Carcinoma
3 (.34%)
Pericardial Effusion
3 (.34%)
Pleural Effusion
3 (.34%)
Pulmonary Hypertension
3 (.34%)
Pulmonary Mass
3 (.34%)
Retinoic Acid Syndrome
3 (.34%)
Skin Necrosis
3 (.34%)
Sudden Hearing Loss
3 (.34%)
Abnormal Dreams
2 (.23%)
Acne
2 (.23%)
Anaemia Haemolytic Autoimmune
2 (.23%)
Anxiety
2 (.23%)
Aortic Dilatation
2 (.23%)
Apathy
2 (.23%)
Atrial Flutter
2 (.23%)

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

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

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

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

Mycosis Fungoides
93
T-cell Lymphoma
16
Acute Myeloid Leukaemia
12
Non-small Cell Lung Cancer
11
Lymphoma
6
Lymphomatoid Papulosis
6
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Thyroid Cancer
5
Thyroid Cancer Metastatic
4
Myelodysplastic Syndrome
3
Peripheral T-cell Lymphoma Unspecif...
3
Metastasis
3
Bladder Cancer
2
Non-small Cell Lung Cancer Stage Iv
2
Mesothelioma
2
Lung Cancer Metastatic
2
Colorectal Cancer Metastatic
1
Fibrosis
1
Oesophageal Cancer Metastatic
1
Bladder Transitional Cell Carcinoma
1
Carcinoma In Situ Of Skin
1
Adult T-cell Lymphoma/leukaemia
1
Thyroid Gland Cancer
1
Thymoma
1
Lung Neoplasm Malignant
1
Neoplasm Malignant
1
Product Used For Unknown Indication
1

Drug Labels

LabelLabelerEffective
TargretinEisai Inc.01-NOV-11
TargretinEisai Inc.15-NOV-11

Targretin Case Reports

What Targretin 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 Targretin. 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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