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CO DIOVAN

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Co Diovan Adverse Events Reported to the FDA Over Time

How are Co Diovan adverse event reports trending over time?

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

Most Common Co Diovan Adverse Events Reported to the FDA

What are the most common Co Diovan adverse events reported to the FDA?

Blood Pressure Increased
28 (1.57%)
Blood Pressure Inadequately Control...
26 (1.45%)
Blood Creatinine Increased
24 (1.34%)
Fall
23 (1.29%)
Hypertension
23 (1.29%)
Hypotension
23 (1.29%)
Hyponatraemia
22 (1.23%)
Drug Ineffective
21 (1.17%)
Dizziness
19 (1.06%)
Arrhythmia
16 (.89%)
Condition Aggravated
16 (.89%)
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Death
16 (.89%)
Microalbuminuria
16 (.89%)
Myocardial Infarction
15 (.84%)
Pneumonia
15 (.84%)
Angina Pectoris
12 (.67%)
Oedema Peripheral
12 (.67%)
Syncope
12 (.67%)
Blood Creatine Phosphokinase Increa...
11 (.62%)
Cerebral Haemorrhage
11 (.62%)
Chest Pain
11 (.62%)
Malaise
11 (.62%)
Pruritus
11 (.62%)
Vomiting
11 (.62%)
Asthenia
10 (.56%)
Blood Glucose Increased
10 (.56%)
Cerebral Infarction
10 (.56%)
Chest Discomfort
10 (.56%)
Dyspnoea
10 (.56%)
Erythema
10 (.56%)
Headache
10 (.56%)
Renal Failure
10 (.56%)
Anaemia
9 (.5%)
Anxiety
9 (.5%)
Blood Pressure Decreased
9 (.5%)
Blood Sodium Decreased
9 (.5%)
Cerebrovascular Accident
9 (.5%)
Drug Interaction
9 (.5%)
Gamma-glutamyltransferase Increased
9 (.5%)
Hyperkalaemia
9 (.5%)
Pain In Extremity
9 (.5%)
Pyrexia
9 (.5%)
Swelling
9 (.5%)
Arthralgia
8 (.45%)
Blood Potassium Decreased
8 (.45%)
Muscular Weakness
8 (.45%)
Somnolence
8 (.45%)
Weight Decreased
8 (.45%)
Arthritis
7 (.39%)
Aspartate Aminotransferase Increase...
7 (.39%)
Blood Pressure Diastolic Decreased
7 (.39%)
Blood Urea Increased
7 (.39%)
Circulatory Collapse
7 (.39%)
Decreased Appetite
7 (.39%)
Dehydration
7 (.39%)
Diabetes Mellitus
7 (.39%)
Feeling Abnormal
7 (.39%)
Haematoma
7 (.39%)
Hemiplegia
7 (.39%)
Loss Of Consciousness
7 (.39%)
Renal Disorder
7 (.39%)
Renal Failure Acute
7 (.39%)
Abdominal Discomfort
6 (.34%)
Abdominal Pain Upper
6 (.34%)
Alanine Aminotransferase Increased
6 (.34%)
Back Pain
6 (.34%)
Blood Bilirubin Increased
6 (.34%)
Blood Uric Acid Increased
6 (.34%)
Cardiac Disorder
6 (.34%)
Constipation
6 (.34%)
Depression
6 (.34%)
Diarrhoea
6 (.34%)
Fatigue
6 (.34%)
Gait Disturbance
6 (.34%)
Hyperhidrosis
6 (.34%)
Hypokalaemia
6 (.34%)
Limb Discomfort
6 (.34%)
Rhabdomyolysis
6 (.34%)
Urticaria
6 (.34%)
Blister
5 (.28%)
Blood Lactate Dehydrogenase Increas...
5 (.28%)
Concomitant Disease Aggravated
5 (.28%)
Cough
5 (.28%)
Dysphagia
5 (.28%)
Eczema
5 (.28%)
Epistaxis
5 (.28%)
Haemoglobin Decreased
5 (.28%)
Hepatic Failure
5 (.28%)
Hyperuricaemia
5 (.28%)
Muscular Dystrophy
5 (.28%)
Nasopharyngitis
5 (.28%)
Normochromic Normocytic Anaemia
5 (.28%)
Pancreatitis Acute
5 (.28%)
Septic Shock
5 (.28%)
Speech Disorder
5 (.28%)
Asphyxia
4 (.22%)
Asthma
4 (.22%)
Blood Alkaline Phosphatase Increase...
4 (.22%)
Bradycardia
4 (.22%)
Bronchitis
4 (.22%)
Cardiac Arrest
4 (.22%)

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

What are the most common Co Diovan adverse events reported to the FDA?

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

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

Hypertension
337
Drug Use For Unknown Indication
14
Essential Hypertension
9
Product Used For Unknown Indication
6
Blood Pressure
5
Ill-defined Disorder
3
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Blood Pressure Increased
2
Coronary Artery Disease
2
Left Ventricular Hypertrophy
2
Suicide Attempt
1
Hypotension
1
Renal Failure Chronic
1
Oedema
1
Cerebrovascular Accident
1

Co Diovan Case Reports

What Co Diovan 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 Co Diovan. 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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