DrugCite
Search

BETA BLOCKER

Adverse Events
Drug Profile
Learn More
Reference
About Results
Comments

Beta Blocker Adverse Events Reported to the FDA Over Time

How are Beta Blocker adverse event reports trending over time?

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

Most Common Beta Blocker Adverse Events Reported to the FDA

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

Completed Suicide
110 (16.44%)
Death
26 (3.89%)
Poisoning
26 (3.89%)
Drug Toxicity
23 (3.44%)
Cardiac Arrest
18 (2.69%)
Bradycardia
14 (2.09%)
Multiple Drug Overdose
14 (2.09%)
Respiratory Arrest
13 (1.94%)
Drug Interaction
12 (1.79%)
Loss Of Consciousness
10 (1.49%)
Heart Rate Decreased
9 (1.35%)
Show More Show More
Intentional Drug Misuse
9 (1.35%)
Hypotension
8 (1.2%)
Syncope
8 (1.2%)
Unresponsive To Stimuli
8 (1.2%)
Atrioventricular Block First Degree
7 (1.05%)
Diarrhoea
7 (1.05%)
Haematuria
7 (1.05%)
Abdominal Pain Upper
6 (.9%)
Malaise
6 (.9%)
Multiple Drug Overdose Intentional
6 (.9%)
Ventricular Extrasystoles
6 (.9%)
Agitation
5 (.75%)
Dizziness Postural
5 (.75%)
Expired Drug Administered
5 (.75%)
Fatigue
5 (.75%)
Hypertension
5 (.75%)
Pain
5 (.75%)
Cardiac Failure
4 (.6%)
Cardio-respiratory Arrest
4 (.6%)
Dizziness
4 (.6%)
Flatulence
4 (.6%)
Overdose
4 (.6%)
Palpitations
4 (.6%)
Tachycardia
4 (.6%)
Atrial Fibrillation
3 (.45%)
Blood Pressure Systolic Increased
3 (.45%)
Cardiac Murmur
3 (.45%)
Chest Pain
3 (.45%)
Drug Abuse
3 (.45%)
Fall
3 (.45%)
Hyperkalaemia
3 (.45%)
Renal Cyst
3 (.45%)
Tremor
3 (.45%)
Acidosis
2 (.3%)
Adverse Drug Reaction
2 (.3%)
Anxiety
2 (.3%)
Apnoea
2 (.3%)
Atrioventricular Block
2 (.3%)
Bladder Trabeculation
2 (.3%)
Blindness
2 (.3%)
Blood Albumin Decreased
2 (.3%)
Blood Creatinine Increased
2 (.3%)
Blood Pressure Decreased
2 (.3%)
Blood Pressure Immeasurable
2 (.3%)
Blood Pressure Inadequately Control...
2 (.3%)
Blood Pressure Increased
2 (.3%)
Cardiac Failure Congestive
2 (.3%)
Clonus
2 (.3%)
Condition Aggravated
2 (.3%)
Convulsion
2 (.3%)
Deep Vein Thrombosis
2 (.3%)
Depressed Level Of Consciousness
2 (.3%)
Depression
2 (.3%)
Disease Recurrence
2 (.3%)
Drug Exposure During Pregnancy
2 (.3%)
Drug Ineffective
2 (.3%)
Dyskinesia
2 (.3%)
Dystonia
2 (.3%)
Electrocardiogram Abnormal
2 (.3%)
Eyelid Oedema
2 (.3%)
Foreign Body Sensation In Eyes
2 (.3%)
General Physical Health Deteriorati...
2 (.3%)
Heart Valve Incompetence
2 (.3%)
Hypothermia
2 (.3%)
Ill-defined Disorder
2 (.3%)
Influenza Like Illness
2 (.3%)
Intraocular Pressure Increased
2 (.3%)
Lethargy
2 (.3%)
Mood Altered
2 (.3%)
Multi-organ Failure
2 (.3%)
Muscle Spasms
2 (.3%)
Muscular Weakness
2 (.3%)
Myoclonus
2 (.3%)
Ocular Hyperaemia
2 (.3%)
Oedema Peripheral
2 (.3%)
Pneumonia Aspiration
2 (.3%)
Prostatic Disorder
2 (.3%)
Prostatic Specific Antigen Increase...
2 (.3%)
Renal Failure Acute
2 (.3%)
Respiratory Disorder
2 (.3%)
Sinus Bradycardia
2 (.3%)
Somnolence
2 (.3%)
Suicide Attempt
2 (.3%)
Therapeutic Agent Toxicity
2 (.3%)
Tricuspid Valve Incompetence
2 (.3%)
Tunnel Vision
2 (.3%)
Vision Blurred
2 (.3%)
Weight Increased
2 (.3%)
Accidental Exposure
1 (.15%)
Ageusia
1 (.15%)

ExportShare/Embed GraphExport Export Data

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

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

Show More Show More

ExportShare/Embed Graph Export Export Data

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

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

Drug Use For Unknown Indication
127
Product Used For Unknown Indication
100
Hypertension
51
Cardiac Disorder
15
Tachycardia
10
Atrial Fibrillation
6
Show More Show More
Angina Pectoris
5
Anxiety
5
Blood Pressure
5
Myocarditis
4
Heart Rate Irregular
4
Acute Myocardial Infarction
4
Pericarditis
4
Long Qt Syndrome Congenital
4
Heart Rate Increased
3
Blood Pressure Management
3
Cardiac Failure
3
Migraine
2
Glaucoma
2
Arrhythmia
2
Chest Pain
2
Acute Coronary Syndrome
2
Coronary Artery Disease
2
Suicide Attempt
2
Drug Administration Error
1
Hypertensive Heart Disease
1
Extrasystoles
1
Vascular Calcification
1
Hypotension
1
Migraine Prophylaxis
1
Asthma
1
Atrial Flutter
1
Essential Hypertension
1
Ischaemia
1
Heart Rate Decreased
1
Drug Withdrawal Syndrome
1
Myocardial Infarction
1
Mitral Valve Stenosis
1
Ill-defined Disorder
1

Beta Blocker Case Reports

What Beta Blocker safety concerns are being reported by doctors and researchers in the medical literature?

Powered by Google

About Results

This report contains aggregated drug side effects and adverse events for Beta Blocker. 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.

Comments

Share your experience with Beta Blocker.