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DILATREND

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Dilatrend Adverse Events Reported to the FDA Over Time

How are Dilatrend adverse event reports trending over time?

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

Most Common Dilatrend Adverse Events Reported to the FDA

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

Death
34 (4.85%)
Hypotension
30 (4.28%)
Bradycardia
24 (3.42%)
Loss Of Consciousness
16 (2.28%)
Drug Interaction
14 (2%)
Hypoglycaemia
14 (2%)
Asthenia
13 (1.85%)
Dyspnoea
13 (1.85%)
Cardiac Arrest
11 (1.57%)
Dizziness
11 (1.57%)
Cardiac Failure
10 (1.43%)
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Syncope
8 (1.14%)
Vertigo
8 (1.14%)
Abdominal Pain
7 (1%)
Atrial Fibrillation
7 (1%)
Fall
7 (1%)
Psoriasis
7 (1%)
Somnolence
7 (1%)
Hyperkalaemia
6 (.86%)
Nausea
6 (.86%)
Renal Failure
6 (.86%)
Sinus Bradycardia
6 (.86%)
Urticaria
6 (.86%)
Circulatory Collapse
5 (.71%)
Dehydration
5 (.71%)
Diarrhoea
5 (.71%)
Malaise
5 (.71%)
Muscular Weakness
5 (.71%)
Vision Blurred
5 (.71%)
Vomiting
5 (.71%)
Abdominal Pain Upper
4 (.57%)
Bronchospasm
4 (.57%)
Depression
4 (.57%)
Disease Progression
4 (.57%)
Hallucination
4 (.57%)
Hyperhidrosis
4 (.57%)
Hypothermia
4 (.57%)
Macular Degeneration
4 (.57%)
Myocardial Infarction
4 (.57%)
Oedema Peripheral
4 (.57%)
Retinal Oedema
4 (.57%)
Transplant Rejection
4 (.57%)
Abnormal Behaviour
3 (.43%)
Anaphylactic Reaction
3 (.43%)
Asthma
3 (.43%)
Atrioventricular Block
3 (.43%)
Blood Pressure Decreased
3 (.43%)
Bone Marrow Failure
3 (.43%)
Cardiac Failure Congestive
3 (.43%)
Confusional State
3 (.43%)
Delirium
3 (.43%)
Dermatitis Allergic
3 (.43%)
Electrocardiogram Qt Prolonged
3 (.43%)
Extrasystoles
3 (.43%)
Fatigue
3 (.43%)
Fluid Retention
3 (.43%)
General Physical Health Deteriorati...
3 (.43%)
Hepatocellular Injury
3 (.43%)
Hypertension
3 (.43%)
Hypoaesthesia
3 (.43%)
Hypoglycaemic Coma
3 (.43%)
Neutrophilia
3 (.43%)
Orthopnoea
3 (.43%)
Orthostatic Hypotension
3 (.43%)
Presyncope
3 (.43%)
Rash
3 (.43%)
Rhabdomyolysis
3 (.43%)
Stridor
3 (.43%)
Suicidal Ideation
3 (.43%)
Thrombocytopenia
3 (.43%)
Visual Impairment
3 (.43%)
White Blood Cell Count Increased
3 (.43%)
Anaemia
2 (.29%)
Angiopathy
2 (.29%)
Atrioventricular Block Second Degre...
2 (.29%)
Back Disorder
2 (.29%)
Blood Cholesterol Increased
2 (.29%)
Cardiovascular Disorder
2 (.29%)
Chronic Myeloid Leukaemia
2 (.29%)
Condition Aggravated
2 (.29%)
Corneal Disorder
2 (.29%)
Cough
2 (.29%)
Drug Administration Error
2 (.29%)
Drug Exposure During Pregnancy
2 (.29%)
Drug Intolerance
2 (.29%)
Dysuria
2 (.29%)
Erythema
2 (.29%)
Erythropenia
2 (.29%)
Eye Irritation
2 (.29%)
Feeling Abnormal
2 (.29%)
Fluid Overload
2 (.29%)
Haemorrhage
2 (.29%)
Headache
2 (.29%)
Hepatic Encephalopathy
2 (.29%)
Hepatic Function Abnormal
2 (.29%)
Incontinence
2 (.29%)
Incorrect Dose Administered
2 (.29%)
Insomnia
2 (.29%)
Intentional Overdose
2 (.29%)
Intracranial Haematoma
2 (.29%)
Keratoconjunctivitis Sicca
2 (.29%)

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

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

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

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

Drug Use For Unknown Indication
127
Hypertension
125
Product Used For Unknown Indication
60
Cardiac Failure
20
Coronary Artery Disease
18
Cardiac Failure Congestive
14
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Essential Hypertension
13
Cardiomyopathy
7
Cardiac Disorder
5
Hyperparathyroidism
4
Atrial Fibrillation
3
Myocardial Ischaemia
3
Tachycardia Paroxysmal
2
Ischaemic Cardiomyopathy
2
Arrhythmia
2
Ill-defined Disorder
2
Hypertonia
2
Coronary Angioplasty
2
Arrhythmia Supraventricular
1
Blood Pressure
1
Cardiovascular Disorder
1
Tachycardia
1
Arteriosclerosis Coronary Artery
1
Left Ventricular Hypertrophy
1
Acute Myocardial Infarction
1
Stent Placement
1
Angina Pectoris
1
Prophylaxis
1
Muscle Rupture
1
Hypertensive Crisis
1
Congestive Cardiomyopathy
1
Ventricular Tachycardia
1

Dilatrend Case Reports

What Dilatrend 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 Dilatrend. 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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