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BETA BLOCKING AGENTS

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Beta Blocking Agents Adverse Events Reported to the FDA Over Time

How are Beta Blocking Agents adverse event reports trending over time?

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

Most Common Beta Blocking Agents Adverse Events Reported to the FDA

What are the most common Beta Blocking Agents adverse events reported to the FDA?

Completed Suicide
82 (9.08%)
Poisoning
28 (3.1%)
Death
17 (1.88%)
Loss Of Consciousness
17 (1.88%)
Haematuria
13 (1.44%)
Ventricular Extrasystoles
13 (1.44%)
Intentional Drug Misuse
12 (1.33%)
Atrioventricular Block First Degree
11 (1.22%)
Blood Pressure Increased
11 (1.22%)
Bradycardia
11 (1.22%)
Dizziness
11 (1.22%)
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Drug Ineffective
10 (1.11%)
Hypotension
10 (1.11%)
Heart Rate Increased
9 (1%)
Rash
9 (1%)
Tremor
9 (1%)
Chest Pain
8 (.89%)
Drug Interaction
8 (.89%)
Overdose
8 (.89%)
Somnolence
8 (.89%)
Cardiac Arrest
7 (.78%)
Dizziness Postural
7 (.78%)
Dyspnoea
7 (.78%)
Electrocardiogram St Segment Depres...
7 (.78%)
Suicide Attempt
7 (.78%)
Syncope
7 (.78%)
Blood Bilirubin Increased
6 (.66%)
Blood Pressure Systolic Increased
6 (.66%)
Coma
6 (.66%)
Confusional State
6 (.66%)
Convulsion
6 (.66%)
Cough
6 (.66%)
Drug Toxicity
6 (.66%)
Haemoglobin Decreased
6 (.66%)
Intentional Overdose
6 (.66%)
Multiple Drug Overdose
6 (.66%)
Muscular Weakness
6 (.66%)
Myocardial Infarction
6 (.66%)
Pneumonia
6 (.66%)
Abnormal Dreams
5 (.55%)
Agitation
5 (.55%)
Duodenal Ulcer
5 (.55%)
Fear
5 (.55%)
Full Blood Count Abnormal
5 (.55%)
Gastrointestinal Haemorrhage
5 (.55%)
Heart Valve Incompetence
5 (.55%)
Lethargy
5 (.55%)
Neutropenia
5 (.55%)
Palpitations
5 (.55%)
Panic Attack
5 (.55%)
Platelet Count Decreased
5 (.55%)
Premature Labour
5 (.55%)
Respiratory Arrest
5 (.55%)
Visual Acuity Reduced
5 (.55%)
Vomiting
5 (.55%)
Wrong Technique In Drug Usage Proce...
5 (.55%)
Angina Pectoris
4 (.44%)
Atrioventricular Block
4 (.44%)
Blood Creatinine Increased
4 (.44%)
Cardiac Disorder
4 (.44%)
Cardio-respiratory Arrest
4 (.44%)
Drug Screen Positive
4 (.44%)
Electrocardiogram Pr Prolongation
4 (.44%)
Fatigue
4 (.44%)
Feeling Abnormal
4 (.44%)
Hyperkalaemia
4 (.44%)
Nausea
4 (.44%)
Oxygen Saturation Decreased
4 (.44%)
Speech Disorder
4 (.44%)
Tachycardia
4 (.44%)
Weight Increased
4 (.44%)
Accidental Exposure
3 (.33%)
Arthralgia
3 (.33%)
Aspiration
3 (.33%)
Bipolar Disorder
3 (.33%)
Blood Cholesterol Increased
3 (.33%)
Blood Glucose Increased
3 (.33%)
Cardiac Failure Congestive
3 (.33%)
Cardiac Murmur
3 (.33%)
Colitis
3 (.33%)
Diarrhoea
3 (.33%)
Drug Abuser
3 (.33%)
Drug Level Increased
3 (.33%)
Fall
3 (.33%)
Gout
3 (.33%)
Heart Rate Decreased
3 (.33%)
Hyperglycaemia
3 (.33%)
Lymphocytic Infiltration
3 (.33%)
Nervous System Disorder
3 (.33%)
Nightmare
3 (.33%)
Pain
3 (.33%)
Po2 Decreased
3 (.33%)
Psoriasis
3 (.33%)
Renal Cyst
3 (.33%)
Adenoma Benign
2 (.22%)
Alanine Aminotransferase Increased
2 (.22%)
Aortic Bruit
2 (.22%)
Aspartate Aminotransferase Increase...
2 (.22%)
Asthenia
2 (.22%)
Asthma
2 (.22%)
Atrial Fibrillation
2 (.22%)

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This graph shows the top adverse events submitted to the FDA for Beta Blocking Agents, 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 Beta Blocking Agents 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 Beta Blocking Agents

What are the most common Beta Blocking Agents adverse events reported to the FDA?

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

Why are people taking Beta Blocking Agents, according to those reporting adverse events to the FDA?

Product Used For Unknown Indication
116
Hypertension
95
Drug Use For Unknown Indication
92
Atrial Fibrillation
14
Blood Pressure Management
12
Blood Pressure
8
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Blood Pressure Increased
6
Cardiac Disorder
5
Ill-defined Disorder
5
Tachycardia
5
Arrhythmia
3
Coronary Artery Disease
3
Angina Pectoris
3
Glaucoma
2
Myocardial Infarction
2
Suicide Attempt
2
Cardiac Failure
2
Cardiac Failure Congestive
2
Atrial Flutter
2
Palpitations
2
Heart Rate
2
Cardiac Failure Chronic
2
Cardiovascular Disorder
2
Ischaemia
2
Accidental Exposure
1
Essential Hypertension
1
Cardiomyopathy
1
Chest Pain
1
Completed Suicide
1
Basedows Disease
1
Hypertensive Heart Disease
1
Drug Therapy
1
Myocardial Ischaemia
1
Migraine
1
Asthma
1
Open Angle Glaucoma
1
Supraventricular Tachycardia
1
Heart Rate Abnormal
1
Cardiovascular Event Prophylaxis
1

Beta Blocking Agents Case Reports

What Beta Blocking Agents 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 Beta Blocking Agents. 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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