DrugCite
Search

VESANOID

Adverse Events
Drug Profile
Learn More
Reference
About Results
Comments

Vesanoid Adverse Events Reported to the FDA Over Time

How are Vesanoid adverse event reports trending over time?

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

Most Common Vesanoid Adverse Events Reported to the FDA

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

Retinoic Acid Syndrome
60 (3.78%)
Pyrexia
47 (2.96%)
Respiratory Failure
20 (1.26%)
Hypoxia
18 (1.13%)
Blood Potassium Increased
17 (1.07%)
Pleural Effusion
17 (1.07%)
Renal Failure
17 (1.07%)
Acute Promyelocytic Leukaemia Diffe...
16 (1.01%)
Pulmonary Alveolar Haemorrhage
16 (1.01%)
Myalgia
15 (.94%)
Neutropenia
15 (.94%)
Show More Show More
Renal Failure Acute
15 (.94%)
Infection
14 (.88%)
Condition Aggravated
13 (.82%)
Grand Mal Convulsion
13 (.82%)
Pancytopenia
13 (.82%)
Sepsis
13 (.82%)
Confusional State
12 (.76%)
Death
12 (.76%)
Cardiac Failure
11 (.69%)
Disseminated Intravascular Coagulat...
11 (.69%)
Drug Exposure During Pregnancy
11 (.69%)
Hypotension
11 (.69%)
Septic Shock
11 (.69%)
Acute Promyelocytic Leukaemia
10 (.63%)
Anaemia
10 (.63%)
Arthralgia
10 (.63%)
Benign Intracranial Hypertension
10 (.63%)
Diarrhoea
10 (.63%)
Dry Skin
10 (.63%)
Insomnia
10 (.63%)
Interstitial Lung Disease
10 (.63%)
Myocardial Infarction
10 (.63%)
Myositis
10 (.63%)
Blood Creatine Phosphokinase Increa...
9 (.57%)
Cerebral Haemorrhage
9 (.57%)
Dyspnoea
9 (.57%)
Gamma-glutamyltransferase Increased
9 (.57%)
Haemorrhage
9 (.57%)
Myelodysplastic Syndrome
9 (.57%)
Paraesthesia
9 (.57%)
Transaminases Increased
9 (.57%)
Alanine Aminotransferase Increased
8 (.5%)
Aspartate Aminotransferase Increase...
8 (.5%)
Asthenia
8 (.5%)
Blindness Unilateral
8 (.5%)
Cellulitis
8 (.5%)
Embolism
8 (.5%)
Febrile Neutropenia
8 (.5%)
Flushing
8 (.5%)
Headache
8 (.5%)
Phlebitis
8 (.5%)
Platelet Count Decreased
8 (.5%)
Pulmonary Embolism
8 (.5%)
Rash
8 (.5%)
Respiratory Distress
8 (.5%)
Abortion Spontaneous
7 (.44%)
Agitation
7 (.44%)
Alopecia
7 (.44%)
Anxiety
7 (.44%)
Bipolar Disorder
7 (.44%)
Caesarean Section
7 (.44%)
Cerebral Haemorrhage Neonatal
7 (.44%)
Dizziness
7 (.44%)
Fatigue
7 (.44%)
Foetal Distress Syndrome
7 (.44%)
Haemoptysis
7 (.44%)
Histiocytosis Haematophagic
7 (.44%)
Hypercalcaemia
7 (.44%)
Hyperglycaemia
7 (.44%)
Necrotising Ulcerative Gingivostoma...
7 (.44%)
Abdominal Pain
6 (.38%)
Abnormal Behaviour
6 (.38%)
Apgar Score Low
6 (.38%)
Atrioventricular Block Complete
6 (.38%)
Blood Bilirubin Increased
6 (.38%)
Chest Pain
6 (.38%)
Drug Interaction
6 (.38%)
Guillain-barre Syndrome
6 (.38%)
Haemorrhage Intracranial
6 (.38%)
Hyperbilirubinaemia
6 (.38%)
Hypernatraemia
6 (.38%)
Hypoaesthesia
6 (.38%)
Lung Infiltration
6 (.38%)
Nausea
6 (.38%)
Pancreatic Enzymes Increased
6 (.38%)
Pneumonia
6 (.38%)
Suicide Attempt
6 (.38%)
Alveolitis
5 (.31%)
Ascites
5 (.31%)
Blood Alkaline Phosphatase Increase...
5 (.31%)
Blood Lactate Dehydrogenase Increas...
5 (.31%)
Coma
5 (.31%)
Drug Eruption
5 (.31%)
Hepatic Enzyme Increased
5 (.31%)
Medication Error
5 (.31%)
Oliguria
5 (.31%)
Osteonecrosis
5 (.31%)
Premature Baby
5 (.31%)
Progressive Multifocal Leukoencepha...
5 (.31%)
Psychotic Disorder
5 (.31%)

ExportShare/Embed GraphExport Export Data

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

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

Show More Show More

ExportShare/Embed Graph Export Export Data

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

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

Acute Promyelocytic Leukaemia
187
Acute Myeloid Leukaemia
51
Drug Use For Unknown Indication
42
Leukaemia
7
Product Used For Unknown Indication
7
Acute Leukaemia
6
Show More Show More
Chemotherapy
4
Myelodysplastic Syndrome
2
Acne
2
Acute Lymphocytic Leukaemia
2
Prolymphocytic Leukaemia
1
Breast Cancer Metastatic
1
Unevaluable Event
1
Chloasma
1
Carcinoid Tumour Of The Small Bowel
1
Hepatitis C
1

Vesanoid Case Reports

What Vesanoid safety concerns are being reported by doctors and researchers in the medical literature?

Powered by Google

About Results

This report contains aggregated drug side effects and adverse events for Vesanoid. 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.

Comments

Share your experience with Vesanoid.