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COREG CR

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Coreg Cr Adverse Events Reported to the FDA Over Time

How are Coreg Cr adverse event reports trending over time?

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

Most Common Coreg Cr Adverse Events Reported to the FDA

What are the most common Coreg Cr adverse events reported to the FDA?

Dizziness
224 (5.61%)
Fatigue
200 (5.01%)
Drug Ineffective
162 (4.06%)
Dyspnoea
109 (2.73%)
Blood Pressure Increased
80 (2%)
Nausea
79 (1.98%)
Hypotension
76 (1.9%)
Weight Increased
66 (1.65%)
Headache
64 (1.6%)
Diarrhoea
56 (1.4%)
Asthenia
53 (1.33%)
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Feeling Abnormal
48 (1.2%)
Blood Pressure Decreased
45 (1.13%)
Insomnia
41 (1.03%)
Oedema Peripheral
39 (.98%)
Heart Rate Decreased
37 (.93%)
Hypertension
37 (.93%)
Pain In Extremity
35 (.88%)
Vision Blurred
35 (.88%)
Malaise
34 (.85%)
Rash
34 (.85%)
Somnolence
34 (.85%)
Palpitations
33 (.83%)
Chest Pain
30 (.75%)
Death
29 (.73%)
Heart Rate Increased
29 (.73%)
Pain
28 (.7%)
Alopecia
27 (.68%)
Cough
27 (.68%)
Blood Glucose Increased
26 (.65%)
Muscle Spasms
26 (.65%)
Adverse Event
24 (.6%)
Blood Pressure Fluctuation
24 (.6%)
Loss Of Consciousness
24 (.6%)
Abdominal Pain Upper
23 (.58%)
Arthralgia
23 (.58%)
Hypoaesthesia
23 (.58%)
Hyperhidrosis
22 (.55%)
Pruritus
22 (.55%)
Arrhythmia
21 (.53%)
Chest Discomfort
21 (.53%)
Oedema
21 (.53%)
Product Quality Issue
21 (.53%)
Fall
20 (.5%)
Heart Rate Irregular
19 (.48%)
Overdose
19 (.48%)
Paraesthesia
19 (.48%)
Anxiety
18 (.45%)
Depression
18 (.45%)
Myalgia
18 (.45%)
Weight Decreased
18 (.45%)
Abdominal Discomfort
16 (.4%)
Muscular Weakness
16 (.4%)
Syncope
16 (.4%)
Balance Disorder
15 (.38%)
Blood Pressure Inadequately Control...
15 (.38%)
Pollakiuria
15 (.38%)
Visual Impairment
15 (.38%)
Bradycardia
14 (.35%)
Drug Interaction
14 (.35%)
Dry Eye
14 (.35%)
Gait Disturbance
14 (.35%)
Lethargy
14 (.35%)
Medication Error
14 (.35%)
Abdominal Distension
13 (.33%)
Constipation
13 (.33%)
Flatulence
13 (.33%)
Joint Swelling
13 (.33%)
Peripheral Coldness
13 (.33%)
Rhinorrhoea
13 (.33%)
Tachycardia
12 (.3%)
Therapeutic Response Unexpected
12 (.3%)
Vomiting
12 (.3%)
Adverse Drug Reaction
11 (.28%)
Anorexia
11 (.28%)
Dry Mouth
11 (.28%)
Dysgeusia
11 (.28%)
Feeling Hot
11 (.28%)
Fluid Retention
11 (.28%)
Ill-defined Disorder
11 (.28%)
Neck Pain
11 (.28%)
Nervousness
11 (.28%)
Abdominal Pain
10 (.25%)
Atrial Fibrillation
10 (.25%)
Cardiac Arrest
10 (.25%)
Cerebrovascular Accident
10 (.25%)
Dyspepsia
10 (.25%)
Dysphagia
10 (.25%)
Hypersensitivity
10 (.25%)
Tinnitus
10 (.25%)
Visual Acuity Reduced
10 (.25%)
Abasia
9 (.23%)
Burning Sensation
9 (.23%)
Cardiac Failure Congestive
9 (.23%)
Drug Administration Error
9 (.23%)
Ejection Fraction Decreased
9 (.23%)
Flushing
9 (.23%)
Swelling
9 (.23%)
Treatment Noncompliance
9 (.23%)
Tremor
9 (.23%)
Urticaria
9 (.23%)

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

What are the most common Coreg Cr adverse events reported to the FDA?

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

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

Hypertension
583
Drug Use For Unknown Indication
387
Product Used For Unknown Indication
50
Left Ventricular Dysfunction
33
Cardiac Failure Congestive
27
Cardiomyopathy
23
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Cardiac Disorder
22
Atrial Fibrillation
22
Arrhythmia
14
Cardiac Failure
12
Blood Pressure
11
Coronary Artery Disease
6
Heart Rate Increased
6
Ejection Fraction Decreased
6
Blood Pressure Abnormal
6
Tachycardia
5
Myocardial Infarction
4
Pain
4
Prophylaxis
4
Congestive Cardiomyopathy
3
Oesophageal Spasm
3
Heart Rate
2
Heart Rate Decreased
2
Implantable Defibrillator Insertion
2
Prinzmetal Angina
2
Mitral Valve Prolapse
1
Postoperative Care
1
Ill-defined Disorder
1
Hypotension
1
Cardiac Operation
1
Myocarditis
1
Mitral Valve Replacement
1
Ventricular Tachycardia
1
Cardiac Valve Disease
1
Chest Pain
1
Angina Pectoris
1
Cardiac Failure Chronic
1
Ventricular Arrhythmia
1
Supplementation Therapy
1
Postural Orthostatic Tachycardia Sy...
1
Obstruction
1
Heart Valve Replacement
1
Anxiety
1
Ejection Fraction Abnormal
1
Angina Unstable
1
Blood Pressure Inadequately Control...
1
Cardiopulmonary Failure
1
Arterial Stenosis
1
Blood Cholesterol
1
Cardiac Pacemaker Insertion
1
Cardiac Septal Defect
1

Drug Labels

LabelLabelerEffective
CoregcrcrPhysicians Total Care, Inc.08-SEP-10
CoregcrGlaxoSmithKline LLC16-AUG-11

Coreg Cr Case Reports

What Coreg Cr 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 Coreg Cr. 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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