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Mevacor Adverse Events Reported to the FDA Over Time

How are Mevacor adverse event reports trending over time?

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

Most Common Mevacor Adverse Events Reported to the FDA

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

Myalgia
30 (3.9%)
Rhabdomyolysis
27 (3.51%)
Drug Interaction
24 (3.12%)
Completed Suicide
19 (2.47%)
Muscle Spasms
17 (2.21%)
Pain In Extremity
17 (2.21%)
Muscular Weakness
13 (1.69%)
Asthenia
12 (1.56%)
Headache
12 (1.56%)
Alanine Aminotransferase Increased
11 (1.43%)
Fall
11 (1.43%)
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Fatigue
11 (1.43%)
Aspartate Aminotransferase Increase...
10 (1.3%)
Drug Ineffective
9 (1.17%)
Blood Creatine Phosphokinase Increa...
8 (1.04%)
Pain
8 (1.04%)
Back Pain
7 (.91%)
Disturbance In Attention
7 (.91%)
Influenza Like Illness
7 (.91%)
Nausea
7 (.91%)
Renal Failure Acute
7 (.91%)
Abdominal Pain Upper
6 (.78%)
Amyotrophic Lateral Sclerosis
6 (.78%)
Depression
6 (.78%)
Diarrhoea
6 (.78%)
Insomnia
6 (.78%)
Malaise
6 (.78%)
Nervous System Disorder
6 (.78%)
Overdose
6 (.78%)
Anxiety
5 (.65%)
Arthralgia
5 (.65%)
Dizziness
5 (.65%)
Feeling Abnormal
5 (.65%)
Gait Disturbance
5 (.65%)
Movement Disorder
5 (.65%)
Muscle Injury
5 (.65%)
Myocardial Infarction
5 (.65%)
Myopathy
5 (.65%)
Thinking Abnormal
5 (.65%)
Urinary Tract Infection
5 (.65%)
Weight Decreased
5 (.65%)
Adverse Event
4 (.52%)
Arthropathy
4 (.52%)
Balance Disorder
4 (.52%)
Blood Cholesterol Increased
4 (.52%)
Bone Marrow Disorder
4 (.52%)
Constipation
4 (.52%)
Drug Dose Omission
4 (.52%)
Dyspnoea
4 (.52%)
Dysstasia
4 (.52%)
Hot Flush
4 (.52%)
Palpitations
4 (.52%)
Abasia
3 (.39%)
Alopecia
3 (.39%)
Anorexia
3 (.39%)
Bradyarrhythmia
3 (.39%)
Burning Sensation
3 (.39%)
Chest Pain
3 (.39%)
Circulatory Collapse
3 (.39%)
Convulsion
3 (.39%)
Drug Administration Error
3 (.39%)
Drug Intolerance
3 (.39%)
Drug Toxicity
3 (.39%)
Foot Fracture
3 (.39%)
Hepatitis
3 (.39%)
Hyperkalaemia
3 (.39%)
Hypersensitivity
3 (.39%)
Hypertension
3 (.39%)
Hypokalaemia
3 (.39%)
Liver Function Test Abnormal
3 (.39%)
Memory Impairment
3 (.39%)
Musculoskeletal Stiffness
3 (.39%)
Nervousness
3 (.39%)
Papilloedema
3 (.39%)
Paraesthesia
3 (.39%)
Tachycardia
3 (.39%)
Tremor
3 (.39%)
Vomiting
3 (.39%)
Weight Increased
3 (.39%)
Wrong Technique In Drug Usage Proce...
3 (.39%)
Blindness Unilateral
2 (.26%)
Blood Alkaline Phosphatase Increase...
2 (.26%)
Blood Bilirubin Increased
2 (.26%)
Blood Pressure Decreased
2 (.26%)
Bone Marrow Transplant
2 (.26%)
Bradycardia
2 (.26%)
Cardiac Arrest
2 (.26%)
Cataract
2 (.26%)
Cerebral Disorder
2 (.26%)
Cerebral Haemorrhage
2 (.26%)
Cerebrovascular Accident
2 (.26%)
Cerebrovascular Disorder
2 (.26%)
Condition Aggravated
2 (.26%)
Coordination Abnormal
2 (.26%)
Deep Vein Thrombosis
2 (.26%)
Diplopia
2 (.26%)
Dysarthria
2 (.26%)
Erectile Dysfunction
2 (.26%)
Erythema
2 (.26%)
Fungal Infection
2 (.26%)
Gallbladder Disorder
2 (.26%)

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

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

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

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

Blood Cholesterol Increased
119
Hypercholesterolaemia
72
Blood Cholesterol
59
Hyperlipidaemia
27
Product Used For Unknown Indication
26
Drug Use For Unknown Indication
26
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Ischaemic Stroke
5
Hypertension
4
Blood Cholesterol Abnormal
4
Lipids
4
Dyslipidaemia
4
Ill-defined Disorder
3
Lipids Increased
3
Low Density Lipoprotein Increased
3
Blood Triglycerides Increased
2
Type Iia Hyperlipidaemia
2
Coronary Artery Disease
2
Suicidal Ideation
1
Arteriosclerosis
1
Cardiac Disorder
1
Hypertriglyceridaemia
1
Cardiovascular Event Prophylaxis
1
Type Ii Hyperlipidaemia
1
Lipid Metabolism Disorder
1

Drug Labels

LabelLabelerEffective
MevacorMerck Sharp & Dohme Corp.31-OCT-12

Mevacor Case Reports

What Mevacor 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 Mevacor. 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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