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CORDAREX

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Cordarex Adverse Events Reported to the FDA Over Time

How are Cordarex adverse event reports trending over time?

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

Most Common Cordarex Adverse Events Reported to the FDA

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

Renal Failure Acute
29 (4.52%)
Drug Interaction
15 (2.34%)
Nausea
13 (2.03%)
Tubulointerstitial Nephritis
13 (2.03%)
Hepatitis Acute
11 (1.72%)
Multi-organ Failure
10 (1.56%)
Shock
10 (1.56%)
Bradycardia
9 (1.4%)
Interstitial Lung Disease
9 (1.4%)
Left Ventricular Failure
9 (1.4%)
Small Intestinal Perforation
9 (1.4%)
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Aspartate Aminotransferase Increase...
8 (1.25%)
Hyperthyroidism
8 (1.25%)
Loss Of Consciousness
8 (1.25%)
Renal Failure
8 (1.25%)
Alveolitis
7 (1.09%)
Dizziness
7 (1.09%)
Alanine Aminotransferase Increased
6 (.94%)
Apnoea
6 (.94%)
Blood Lactate Dehydrogenase Increas...
6 (.94%)
Hypothyroidism
6 (.94%)
Lung Disorder
6 (.94%)
Vomiting
6 (.94%)
Weight Decreased
6 (.94%)
Atrial Fibrillation
5 (.78%)
Blood Pressure Increased
5 (.78%)
Chest Pain
5 (.78%)
Convulsion
5 (.78%)
Gamma-glutamyltransferase Increased
5 (.78%)
Heart Rate Increased
5 (.78%)
Hyperkalaemia
5 (.78%)
Hyponatraemia
5 (.78%)
Long Qt Syndrome
5 (.78%)
Lung Infiltration
5 (.78%)
Pancreatitis Acute
5 (.78%)
Paraesthesia
5 (.78%)
Tachycardia
5 (.78%)
Torsade De Pointes
5 (.78%)
Blood Creatine Phosphokinase Increa...
4 (.62%)
Blood Creatinine Increased
4 (.62%)
Cardiac Failure
4 (.62%)
Condition Aggravated
4 (.62%)
Drug Ineffective
4 (.62%)
Fatigue
4 (.62%)
Gastrointestinal Haemorrhage
4 (.62%)
General Physical Health Deteriorati...
4 (.62%)
Heart Rate Decreased
4 (.62%)
Infusion Related Reaction
4 (.62%)
Muscle Spasms
4 (.62%)
Pneumonia Primary Atypical
4 (.62%)
Pulmonary Hypertension
4 (.62%)
Retching
4 (.62%)
Acute Respiratory Distress Syndrome
3 (.47%)
Anaemia
3 (.47%)
Blood Alkaline Phosphatase Increase...
3 (.47%)
Constipation
3 (.47%)
Dehydration
3 (.47%)
Diarrhoea
3 (.47%)
Drug Effect Decreased
3 (.47%)
Eyelid Oedema
3 (.47%)
Haemoglobin Decreased
3 (.47%)
Hepatic Failure
3 (.47%)
Hepatocellular Injury
3 (.47%)
Hepatotoxicity
3 (.47%)
Injection Site Erythema
3 (.47%)
Injection Site Necrosis
3 (.47%)
Injection Site Vesicles
3 (.47%)
Nephrogenic Anaemia
3 (.47%)
Pneumonitis
3 (.47%)
Pulmonary Fibrosis
3 (.47%)
Pulmonary Oedema
3 (.47%)
Renal Failure Chronic
3 (.47%)
Rhabdomyolysis
3 (.47%)
Abdominal Pain
2 (.31%)
Acute Hepatic Failure
2 (.31%)
Ageusia
2 (.31%)
Arrhythmia
2 (.31%)
Asthenia
2 (.31%)
Blister
2 (.31%)
Blood Pressure Decreased
2 (.31%)
Blood Pressure Diastolic Increased
2 (.31%)
Blood Urea Increased
2 (.31%)
Brain Natriuretic Peptide Increased
2 (.31%)
Bronchitis Chronic
2 (.31%)
Cardioactive Drug Level Decreased
2 (.31%)
Circulatory Collapse
2 (.31%)
Clostridium Colitis
2 (.31%)
Cough
2 (.31%)
Death
2 (.31%)
Diabetes Mellitus
2 (.31%)
Dyspnoea
2 (.31%)
Escherichia Infection
2 (.31%)
Flatulence
2 (.31%)
Gastrointestinal Disorder
2 (.31%)
General Physical Condition Abnormal
2 (.31%)
Glutamate Dehydrogenase Increased
2 (.31%)
Groin Pain
2 (.31%)
Haemodialysis
2 (.31%)
Haemoptysis
2 (.31%)
Haemorrhagic Erosive Gastritis
2 (.31%)
Haemorrhoidal Haemorrhage
2 (.31%)

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

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

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

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

Atrial Fibrillation
80
Arrhythmia
20
Drug Use For Unknown Indication
16
Product Used For Unknown Indication
11
Tachyarrhythmia
11
Atrial Flutter
7
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Ventricular Tachycardia
5
Tachycardia
5
Hypertension
4
Supraventricular Tachycardia
4
Bradycardia
3
Ventricular Fibrillation
3
Congestive Cardiomyopathy
2
Ventricular Extrasystoles
2
Coronary Artery Surgery
2
Cardiomyopathy
2
Tachycardia Paroxysmal
1
Coronary Artery Disease
1
Cardioversion
1
Atrial Tachycardia
1
Cardiac Disorder
1
Bradyarrhythmia
1
Ventricular Arrhythmia
1
Arrhythmia Prophylaxis
1
Cardiac Failure
1

Cordarex Case Reports

What Cordarex 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 Cordarex. 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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