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Amlodin Adverse Events Reported to the FDA Over Time

How are Amlodin adverse event reports trending over time?

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

Most Common Amlodin Adverse Events Reported to the FDA

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

Hypotension
17 (1.71%)
Renal Failure Acute
17 (1.71%)
Platelet Count Decreased
15 (1.51%)
Bradycardia
14 (1.41%)
Overdose
14 (1.41%)
Haemoglobin Decreased
13 (1.31%)
Tubulointerstitial Nephritis
13 (1.31%)
Blood Pressure Decreased
12 (1.21%)
Pancytopenia
12 (1.21%)
Pyrexia
12 (1.21%)
Rhabdomyolysis
12 (1.21%)
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Depressed Level Of Consciousness
11 (1.11%)
Leukocytoclastic Vasculitis
11 (1.11%)
White Blood Cell Count Decreased
11 (1.11%)
Blood Creatinine Increased
9 (.91%)
Blood Lactate Dehydrogenase Increas...
9 (.91%)
C-reactive Protein Increased
9 (.91%)
Haematocrit Decreased
9 (.91%)
Alanine Aminotransferase Increased
8 (.8%)
Aspartate Aminotransferase Increase...
8 (.8%)
Atrial Fibrillation
8 (.8%)
Blood Urea Increased
8 (.8%)
Dyspnoea
8 (.8%)
Hyperkalaemia
8 (.8%)
Hypoglycaemia
8 (.8%)
Intentional Overdose
8 (.8%)
Liver Disorder
8 (.8%)
Malaise
8 (.8%)
Shock
8 (.8%)
Vomiting
8 (.8%)
Cardiac Failure
7 (.7%)
Interstitial Lung Disease
7 (.7%)
Nausea
7 (.7%)
Nephrotic Syndrome
7 (.7%)
Rash
7 (.7%)
Red Blood Cell Count Decreased
7 (.7%)
Blood Alkaline Phosphatase Increase...
6 (.6%)
Blood Creatine Phosphokinase Increa...
6 (.6%)
Duodenal Ulcer Perforation
6 (.6%)
Gait Disturbance
6 (.6%)
Gamma-glutamyltransferase Increased
6 (.6%)
Glomerulonephritis Membranous
6 (.6%)
Hepatic Function Abnormal
6 (.6%)
Oedema
6 (.6%)
Pleural Effusion
6 (.6%)
Pneumonia
6 (.6%)
Renal Disorder
6 (.6%)
Renal Impairment
6 (.6%)
Suicide Attempt
6 (.6%)
Thrombocytopenia
6 (.6%)
Toxic Epidermal Necrolysis
6 (.6%)
Tremor
6 (.6%)
Urine Output Decreased
6 (.6%)
Agranulocytosis
5 (.5%)
Blood Bilirubin Increased
5 (.5%)
Cardio-respiratory Arrest
5 (.5%)
Cerebral Infarction
5 (.5%)
Drug Interaction
5 (.5%)
Femur Fracture
5 (.5%)
Hemiplegia
5 (.5%)
Hepatitis Acute
5 (.5%)
Hyponatraemia
5 (.5%)
Iga Nephropathy
5 (.5%)
Loss Of Consciousness
5 (.5%)
Nephropathy
5 (.5%)
Oedema Peripheral
5 (.5%)
Parkinsonism
5 (.5%)
Sepsis
5 (.5%)
Abdominal Pain
4 (.4%)
Accidental Overdose
4 (.4%)
Allergic Granulomatous Angiitis
4 (.4%)
Anorexia
4 (.4%)
Aortic Dissection
4 (.4%)
Atrioventricular Block
4 (.4%)
Cardiac Arrest
4 (.4%)
Cardiac Failure Congestive
4 (.4%)
Convulsion
4 (.4%)
Dermatitis Contact
4 (.4%)
Diabetic Hyperosmolar Coma
4 (.4%)
Diabetic Nephropathy
4 (.4%)
Disseminated Intravascular Coagulat...
4 (.4%)
Drug Eruption
4 (.4%)
Gamma-glutamyltransferase Abnormal
4 (.4%)
Hepatitis Fulminant
4 (.4%)
Lymphocyte Stimulation Test Positiv...
4 (.4%)
Metabolic Acidosis
4 (.4%)
Muscular Weakness
4 (.4%)
Neurogenic Bladder
4 (.4%)
Neurosis
4 (.4%)
Penile Ulceration
4 (.4%)
Phlebitis
4 (.4%)
Renal Failure
4 (.4%)
Scrotal Ulcer
4 (.4%)
Thrombotic Thrombocytopenic Purpura
4 (.4%)
Acute Myocardial Infarction
3 (.3%)
Altered State Of Consciousness
3 (.3%)
Anaemia
3 (.3%)
Aplastic Anaemia
3 (.3%)
Bleeding Time Prolonged
3 (.3%)
Blood Creatine Increased
3 (.3%)
Blood Creatinine Abnormal
3 (.3%)

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

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

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

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

Hypertension
1015
Drug Use For Unknown Indication
47
Essential Hypertension
13
Angina Pectoris
8
Prophylaxis
5
Product Used For Unknown Indication
5
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Blood Pressure Increased
4
Ill-defined Disorder
3
Blood Pressure Management
3
Arteriosclerosis Coronary Artery
2
Renal Failure Chronic
2
Dyslipidaemia
2
Hypertrophic Cardiomyopathy
2
Heart Rate Irregular
2
Breast Cancer Recurrent
2
Suicide Attempt
2
Therapeutic Response Decreased
1
Completed Suicide
1
Hyperlipidaemia
1
Pulmonary Hypertension
1
Hypertonia
1
Oncologic Complication
1
Cancer Pain
1
Blood Pressure Decreased
1
Cardiac Failure Chronic
1
Renal Cell Carcinoma Stage Iv
1
Ankylosing Spondylitis
1
Cardiac Failure
1

Amlodin Case Reports

What Amlodin 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 Amlodin. 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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