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EZETROL

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Ezetrol Adverse Events Reported to the FDA Over Time

How are Ezetrol adverse event reports trending over time?

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

Most Common Ezetrol Adverse Events Reported to the FDA

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

Myalgia
48 (3.66%)
Fatigue
43 (3.27%)
Dyspnoea
39 (2.97%)
Paraesthesia
39 (2.97%)
Atrial Fibrillation
37 (2.82%)
Dizziness
36 (2.74%)
Blood Creatine Phosphokinase Increa...
33 (2.51%)
Cardiac Murmur
29 (2.21%)
Venous Pressure Jugular Increased
28 (2.13%)
Ventricular Tachycardia
28 (2.13%)
Feeling Abnormal
26 (1.98%)
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Oedema Peripheral
26 (1.98%)
Oedema
21 (1.6%)
Left Ventricular Dysfunction
19 (1.45%)
Drug Interaction
15 (1.14%)
Alanine Aminotransferase Increased
14 (1.07%)
Rhabdomyolysis
13 (.99%)
Chest Pain
12 (.91%)
Muscle Spasms
12 (.91%)
Aspartate Aminotransferase Increase...
11 (.84%)
Bulbar Palsy
11 (.84%)
Dysphagia
11 (.84%)
Gamma-glutamyltransferase Increased
11 (.84%)
Ageusia
10 (.76%)
Anosmia
10 (.76%)
Arthralgia
10 (.76%)
Dry Eye
10 (.76%)
Lip Swelling
10 (.76%)
Nausea
10 (.76%)
Cardiac Arrest
9 (.69%)
Dissociation
9 (.69%)
Glossodynia
9 (.69%)
Liver Function Test Abnormal
9 (.69%)
Pyrexia
9 (.69%)
Tracheitis
9 (.69%)
C-reactive Protein Increased
8 (.61%)
Dyspnoea Exertional
8 (.61%)
Organising Pneumonia
8 (.61%)
Renal Failure Acute
8 (.61%)
Speech Disorder
8 (.61%)
Swollen Tongue
8 (.61%)
Abdominal Pain
7 (.53%)
Cough
7 (.53%)
Encephalopathy
7 (.53%)
Eye Pruritus
7 (.53%)
Gait Disturbance
7 (.53%)
Renal Failure
7 (.53%)
Vomiting
7 (.53%)
Asthenia
6 (.46%)
Blood Bilirubin Increased
6 (.46%)
Blood Lactate Dehydrogenase Increas...
6 (.46%)
Cardiac Fibrillation
6 (.46%)
Cheilitis
6 (.46%)
Condition Aggravated
6 (.46%)
Jaundice
6 (.46%)
Seasonal Allergy
6 (.46%)
Ventricular Dysfunction
6 (.46%)
Blood Alkaline Phosphatase Increase...
5 (.38%)
Blood Creatinine Increased
5 (.38%)
Blood Triglycerides Increased
5 (.38%)
Death
5 (.38%)
Gastrointestinal Pain
5 (.38%)
Granulomatous Liver Disease
5 (.38%)
Hallucination, Auditory
5 (.38%)
Hepatitis
5 (.38%)
Hyperbilirubinaemia
5 (.38%)
Leukocytoclastic Vasculitis
5 (.38%)
Melaena
5 (.38%)
Memory Impairment
5 (.38%)
Renal Impairment
5 (.38%)
Restless Legs Syndrome
5 (.38%)
Sleep Apnoea Syndrome
5 (.38%)
Acute Hepatic Failure
4 (.3%)
Amnesia
4 (.3%)
Coma
4 (.3%)
Drug Ineffective
4 (.3%)
Eosinophilia
4 (.3%)
Gastrooesophageal Reflux Disease
4 (.3%)
Hepatic Necrosis
4 (.3%)
Hepatitis Acute
4 (.3%)
Hepatorenal Syndrome
4 (.3%)
Hyperkalaemia
4 (.3%)
Immune System Disorder
4 (.3%)
Insomnia
4 (.3%)
International Normalised Ratio Incr...
4 (.3%)
Lactic Acidosis
4 (.3%)
Lip Disorder
4 (.3%)
Multi-organ Failure
4 (.3%)
Neutropenia
4 (.3%)
Peripheral Sensory Neuropathy
4 (.3%)
Pulmonary Embolism
4 (.3%)
Skin Fissures
4 (.3%)
Somnolence
4 (.3%)
Vertigo
4 (.3%)
Abdominal Pain Upper
3 (.23%)
Activities Of Daily Living Impaired
3 (.23%)
Anaemia
3 (.23%)
Aphonia
3 (.23%)
Ataxia
3 (.23%)
Axonal Neuropathy
3 (.23%)
Biliary Cirrhosis Primary
3 (.23%)

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

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

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

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

Hypercholesterolaemia
122
Drug Use For Unknown Indication
106
Hyperlipidaemia
48
Dyslipidaemia
28
Product Used For Unknown Indication
26
Blood Cholesterol Increased
24
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Blood Cholesterol
18
Ill-defined Disorder
8
Acute Myocardial Infarction
7
Lipids Increased
7
Diabetes Mellitus
7
Type Iia Hyperlipidaemia
6
Cardiovascular Event Prophylaxis
4
Lipids
4
Myocardial Infarction
3
Prophylaxis
3
Obesity
2
Hypertriglyceridaemia
2
Coronary Artery Disease
2
Ischaemic Cardiomyopathy
2
Metabolic Disorder
1
Lipid Metabolism Disorder
1
Peripheral Arterial Occlusive Disea...
1
Low Density Lipoprotein Increased
1
Heart Transplant
1
Unevaluable Event
1
Mixed Hyperlipidaemia
1
Essential Hypertension
1
Blood Cholesterol Abnormal
1
Ischaemic Heart Disease Prophylaxis
1
Coronary Artery Restenosis
1
Myocardial Ischaemia
1
Dementia
1

Ezetrol Case Reports

What Ezetrol 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 Ezetrol. 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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