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ADENOSINE

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Adenosine Adverse Events Reported to the FDA Over Time

How are Adenosine adverse event reports trending over time?

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

Most Common Adenosine Adverse Events Reported to the FDA

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

Drug Interaction
29 (2.77%)
Bronchospasm
26 (2.49%)
Dyspnoea
26 (2.49%)
Pleural Effusion
24 (2.29%)
Supraventricular Tachycardia
24 (2.29%)
Myositis
23 (2.2%)
Pericardial Effusion
22 (2.1%)
Pulmonary Embolism
22 (2.1%)
Liver Function Test Abnormal
21 (2.01%)
Cardiac Arrest
20 (1.91%)
Asthenia
18 (1.72%)
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Pneumonia
17 (1.63%)
Respiratory Arrest
16 (1.53%)
Infusion Related Reaction
15 (1.43%)
Myalgia
14 (1.34%)
Myopathy
14 (1.34%)
Alanine Aminotransferase Increased
13 (1.24%)
Bradycardia
13 (1.24%)
Aspartate Aminotransferase Increase...
12 (1.15%)
Hypokinesia
12 (1.15%)
Infection
12 (1.15%)
Loss Of Consciousness
12 (1.15%)
Atrial Fibrillation
11 (1.05%)
Cardio-respiratory Arrest
11 (1.05%)
Drug Ineffective
11 (1.05%)
Arteriospasm Coronary
10 (.96%)
Blood Creatine Phosphokinase Increa...
10 (.96%)
Hypokalaemia
10 (.96%)
Medication Error
10 (.96%)
Respiratory Distress
10 (.96%)
Headache
9 (.86%)
Hypotension
9 (.86%)
Nausea
9 (.86%)
Tachycardia
9 (.86%)
Chest Pain
8 (.76%)
Flushing
8 (.76%)
Ventricular Tachycardia
8 (.76%)
Dizziness
7 (.67%)
Pain
7 (.67%)
Renal Failure
7 (.67%)
Convulsion
6 (.57%)
Heart Rate Increased
6 (.57%)
Hypoxia
6 (.57%)
Metabolic Acidosis
6 (.57%)
Oxygen Saturation Decreased
6 (.57%)
Procedural Complication
6 (.57%)
Wheezing
6 (.57%)
Apnoea
5 (.48%)
Atrioventricular Block
5 (.48%)
Atrioventricular Block Complete
5 (.48%)
Chest Discomfort
5 (.48%)
Electrocardiogram St Segment Elevat...
5 (.48%)
Facial Pain
5 (.48%)
Tachypnoea
5 (.48%)
Abdominal Pain
4 (.38%)
Anaphylactic Reaction
4 (.38%)
Breath Sounds Abnormal
4 (.38%)
Circumstance Or Information Capable...
4 (.38%)
Condition Aggravated
4 (.38%)
Device Occlusion
4 (.38%)
Dilatation Atrial
4 (.38%)
Electrocardiogram St Segment Depres...
4 (.38%)
Fatigue
4 (.38%)
Haemoglobin Decreased
4 (.38%)
Hepatitis Fulminant
4 (.38%)
Left Ventricular Dysfunction
4 (.38%)
Livedo Reticularis
4 (.38%)
Neurological Symptom
4 (.38%)
Respiratory Gas Exchange Disorder
4 (.38%)
Sinus Arrest
4 (.38%)
Sinus Bradycardia
4 (.38%)
Vision Blurred
4 (.38%)
Acute Respiratory Failure
3 (.29%)
Atrial Flutter
3 (.29%)
Basal Cell Carcinoma
3 (.29%)
Blood Pressure Decreased
3 (.29%)
Blood Pressure Systolic Increased
3 (.29%)
Circulatory Collapse
3 (.29%)
Confusional State
3 (.29%)
Coronary Artery Stenosis
3 (.29%)
Cyanosis
3 (.29%)
Depressed Level Of Consciousness
3 (.29%)
Device Failure
3 (.29%)
Drug Hypersensitivity
3 (.29%)
Ejection Fraction Decreased
3 (.29%)
Extravasation
3 (.29%)
Feeling Abnormal
3 (.29%)
Hyperhidrosis
3 (.29%)
Hyperkalaemia
3 (.29%)
Hypersensitivity
3 (.29%)
Hypertension
3 (.29%)
Incorrect Route Of Drug Administrat...
3 (.29%)
Movement Disorder
3 (.29%)
Pain In Extremity
3 (.29%)
Pallor
3 (.29%)
Post Procedural Complication
3 (.29%)
Pulmonary Oedema
3 (.29%)
Respiratory Depression
3 (.29%)
Rhabdomyolysis
3 (.29%)
Syringe Issue
3 (.29%)
Urticaria
3 (.29%)

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

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

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

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

Supraventricular Tachycardia
75
Cardiac Stress Test
48
Drug Use For Unknown Indication
28
Product Used For Unknown Indication
26
Dizziness
14
Tachycardia
12
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Sinus Arrhythmia
12
Scan Myocardial Perfusion
7
Diagnostic Procedure
7
Otic Cancer Metastatic
5
Surgery
5
Cerebral Infarction
5
Cardiac Arrest
4
Cardiac Pharmacologic Stress Test
4
Aneurysm Repair
4
Cardiovascular Disorder
4
Percutaneous Coronary Intervention
4
Pharyngitis
3
Coronary Artery Disease
3
Chest Pain
3
Spinal Muscular Atrophy
3
Atrial Tachycardia
3
Arrhythmia
3
Cardioversion
3
Myocardial Infarction
3
Cytomegalovirus Enterocolitis
2
Viith Nerve Paralysis
2
Prophylaxis
2
Menieres Disease
2
Atrial Flutter
2
Heart Rate Irregular
2
Tinnitus
2
Coronary Artery Thrombosis
2
Ill-defined Disorder
2
Venous Insufficiency
2
Cerebral Circulatory Failure
2
Presbyacusis
2
Palpitations
2
Atrial Fibrillation
2
Ventricular Tachycardia
2
Arterial Therapeutic Procedure
1
Nutritional Support
1
Gastric Disorder
1
Coronary No-reflow Phenomenon
1
Single Photon Emission Computerised...
1
Cardiac Operation
1
Dementia Alzheimers Type
1
Blood Triglycerides
1
Asthma
1
Hypertension
1
Off Label Use
1

Drug Labels

LabelLabelerEffective
AdenosineBedford Laboratories14-JAN-10
AdenosinePhysicians Total Care, Inc.14-JAN-10
AdenosineSagent Pharmaceuticals, Inc30-JUN-10
AdenosineBaxter Healthcare Corporation15-JUL-10
AdenosineBaxter Healthcare Corporation15-JUL-10
AdenosineGeneral Injectables & Vaccines, Inc23-JUL-10
AdenosineGeneral Injectables & Vaccines, Inc05-OCT-11
AdenosineAkorn, Inc.06-OCT-11
AdenosineWest-ward Pharmaceutical Corp.09-DEC-11
AdenosineAPP Pharmaceuticals, LLC16-JAN-12
AdenosineSagent Pharmaceuticals09-APR-12
AdenoscanAstellas Pharma US, Inc.01-MAY-12
AdenocardAstellas Pharma US, Inc.01-MAY-12
AdenosineWOCKHARDT LIMITED30-OCT-12
AdenosineWOCKHARDT USA LLC.30-OCT-12
AdenosineCardinal Health17-APR-13

Adenosine Case Reports

What Adenosine 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 Adenosine. 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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