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Adenoscan Adverse Events Reported to the FDA Over Time

How are Adenoscan adverse event reports trending over time?

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

Most Common Adenoscan Adverse Events Reported to the FDA

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

Dyspnoea
48 (4.74%)
Chest Pain
29 (2.87%)
Blood Pressure Decreased
22 (2.17%)
Respiratory Arrest
20 (1.98%)
Tremor
20 (1.98%)
Nausea
18 (1.78%)
Cardiac Arrest
17 (1.68%)
Body Temperature Increased
16 (1.58%)
Infusion Related Reaction
16 (1.58%)
Bronchospasm
15 (1.48%)
Atrioventricular Block Complete
14 (1.38%)
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Chills
14 (1.38%)
Headache
14 (1.38%)
Dizziness
13 (1.28%)
Loss Of Consciousness
13 (1.28%)
Vomiting
13 (1.28%)
Atrioventricular Block
12 (1.19%)
Blood Pressure Increased
12 (1.19%)
Cardio-respiratory Arrest
12 (1.19%)
Coronary Artery Disease
12 (1.19%)
Diarrhoea
12 (1.19%)
Hypotension
12 (1.19%)
Arteriospasm Coronary
11 (1.09%)
Oxygen Saturation Decreased
11 (1.09%)
Atrioventricular Block Second Degre...
10 (.99%)
Pyrexia
10 (.99%)
Chest Discomfort
9 (.89%)
Procedural Complication
9 (.89%)
Pulmonary Oedema
9 (.89%)
Convulsion
8 (.79%)
Hypertension
8 (.79%)
Pain In Jaw
8 (.79%)
Syncope
8 (.79%)
Heart Rate Decreased
7 (.69%)
Hyperhidrosis
7 (.69%)
Insomnia
7 (.69%)
Post Procedural Complication
7 (.69%)
Ventricular Fibrillation
7 (.69%)
Anxiety
6 (.59%)
Atrial Fibrillation
6 (.59%)
Bradycardia
6 (.59%)
Drug Hypersensitivity
6 (.59%)
Electrocardiogram St Segment Elevat...
6 (.59%)
Facial Pain
6 (.59%)
Flushing
6 (.59%)
Supraventricular Tachycardia
6 (.59%)
Unresponsive To Stimuli
6 (.59%)
Ventricular Tachycardia
6 (.59%)
Angina Pectoris
5 (.49%)
Asthenia
5 (.49%)
Coronary Artery Stenosis
5 (.49%)
Electrocardiogram St Segment Depres...
5 (.49%)
Feeling Cold
5 (.49%)
Haemoptysis
5 (.49%)
Hypoaesthesia
5 (.49%)
Lacrimation Increased
5 (.49%)
Nervousness
5 (.49%)
Panic Reaction
5 (.49%)
Poor Quality Drug Administered
5 (.49%)
Respiratory Distress
5 (.49%)
Respiratory Failure
5 (.49%)
Sepsis
5 (.49%)
Shock
5 (.49%)
Tachycardia
5 (.49%)
Aura
4 (.4%)
Bacterial Culture Positive
4 (.4%)
Disorientation
4 (.4%)
Dysphagia
4 (.4%)
Escherichia Infection
4 (.4%)
Feeling Abnormal
4 (.4%)
Heart Rate Increased
4 (.4%)
Malaise
4 (.4%)
Migraine
4 (.4%)
Myocardial Ischaemia
4 (.4%)
Nervous System Disorder
4 (.4%)
Neurological Symptom
4 (.4%)
Neuropathy Peripheral
4 (.4%)
Nodal Rhythm
4 (.4%)
Palpitations
4 (.4%)
Pharyngeal Oedema
4 (.4%)
Septic Shock
4 (.4%)
Acute Respiratory Failure
3 (.3%)
Anaphylactic Reaction
3 (.3%)
Atrioventricular Block First Degree
3 (.3%)
Blood Pressure Immeasurable
3 (.3%)
Cardiac Failure
3 (.3%)
Cyanosis
3 (.3%)
Drug Ineffective
3 (.3%)
Drug Interaction
3 (.3%)
Electrocardiogram Abnormal
3 (.3%)
Electrocardiogram Change
3 (.3%)
Electrocardiogram T Wave Inversion
3 (.3%)
Enterobacter Infection
3 (.3%)
Enterobacter Sepsis
3 (.3%)
Fatigue
3 (.3%)
Groin Pain
3 (.3%)
Heart Rate Irregular
3 (.3%)
Hypersensitivity
3 (.3%)
Ischaemia
3 (.3%)
Left Ventricular Failure
3 (.3%)
Medication Error
3 (.3%)

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

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

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

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

Scan Myocardial Perfusion
253
Cardiac Stress Test
23
Drug Use For Unknown Indication
5
Multiple Gated Acquisition Scan
3
Chest Pain
2
Angina Pectoris
2
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Scan
2
Dizziness
1
Product Used For Unknown Indication
1
Stress
1
Coronary Artery Disease
1
Myocardial Ischaemia
1
Diagnostic Procedure
1

Drug Labels

LabelLabelerEffective
AdenoscanAstellas Pharma US, Inc.01-MAY-12

Adenoscan Case Reports

What Adenoscan 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 Adenoscan. 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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