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EUPRESSYL

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Eupressyl Adverse Events Reported to the FDA Over Time

How are Eupressyl adverse event reports trending over time?

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

Most Common Eupressyl Adverse Events Reported to the FDA

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

Fall
34 (4.03%)
Hypotension
27 (3.2%)
Anaemia
26 (3.08%)
Cytolytic Hepatitis
24 (2.84%)
Renal Failure
22 (2.61%)
Thrombocytopenia
21 (2.49%)
Renal Impairment
17 (2.01%)
Dizziness
15 (1.78%)
Cholestasis
14 (1.66%)
Hyponatraemia
12 (1.42%)
Pancreatitis Acute
12 (1.42%)
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Nephropathy
11 (1.3%)
Orthostatic Hypotension
11 (1.3%)
Sudden Death
11 (1.3%)
Cerebral Haematoma
10 (1.18%)
Drug Rash With Eosinophilia And Sys...
10 (1.18%)
Pruritus
10 (1.18%)
Tubulointerstitial Nephritis
10 (1.18%)
Condition Aggravated
8 (.95%)
Dyspnoea
8 (.95%)
Pain
8 (.95%)
Haemoglobin Decreased
7 (.83%)
Hyperkalaemia
7 (.83%)
Malaise
7 (.83%)
Rash Maculo-papular
7 (.83%)
Renal Failure Acute
7 (.83%)
Sepsis
7 (.83%)
Vascular Purpura
7 (.83%)
Venous Insufficiency
7 (.83%)
Cardio-respiratory Arrest
6 (.71%)
Drug Interaction
6 (.71%)
Gamma-glutamyltransferase Increased
6 (.71%)
General Physical Health Deteriorati...
6 (.71%)
Hepatitis
6 (.71%)
Hypokalaemia
6 (.71%)
International Normalised Ratio Incr...
6 (.71%)
Leukocytoclastic Vasculitis
6 (.71%)
Atrial Fibrillation
5 (.59%)
Blood Creatinine Increased
5 (.59%)
Depression
5 (.59%)
Disorientation
5 (.59%)
Eosinophilia
5 (.59%)
Guillain-barre Syndrome
5 (.59%)
Head Injury
5 (.59%)
Hydrocephalus
5 (.59%)
Hypertension
5 (.59%)
Hyperthermia
5 (.59%)
Joint Injury
5 (.59%)
Nausea
5 (.59%)
Oedema Peripheral
5 (.59%)
Pyrexia
5 (.59%)
Ventricular Arrhythmia
5 (.59%)
Wrist Fracture
5 (.59%)
Asthenia
4 (.47%)
Blood Alkaline Phosphatase Increase...
4 (.47%)
Bronchospasm
4 (.47%)
Cerebrovascular Accident
4 (.47%)
Colitis Ischaemic
4 (.47%)
Dermatitis Bullous
4 (.47%)
Headache
4 (.47%)
Pulmonary Oedema
4 (.47%)
Red Blood Cell Count Decreased
4 (.47%)
Tuberculosis
4 (.47%)
Acute Hepatic Failure
3 (.36%)
Aortic Dissection
3 (.36%)
Bacterial Test Positive
3 (.36%)
Blood Urea Increased
3 (.36%)
Cardiac Arrest
3 (.36%)
Cardiac Murmur Functional
3 (.36%)
Cerebral Ischaemia
3 (.36%)
Confusional State
3 (.36%)
Device Related Infection
3 (.36%)
Ecchymosis
3 (.36%)
Haematoma
3 (.36%)
Loss Of Consciousness
3 (.36%)
Lung Disorder
3 (.36%)
Mental Impairment
3 (.36%)
Priapism
3 (.36%)
Sarcoidosis
3 (.36%)
Seasonal Allergy
3 (.36%)
Septic Shock
3 (.36%)
Skin Lesion
3 (.36%)
Toxic Skin Eruption
3 (.36%)
Urinary Retention
3 (.36%)
Abdominal Pain Upper
2 (.24%)
Acute Generalised Exanthematous Pus...
2 (.24%)
Agranulocytosis
2 (.24%)
Aortic Bruit
2 (.24%)
Aortic Dilatation
2 (.24%)
Back Pain
2 (.24%)
Blood Pressure Increased
2 (.24%)
Bradycardia
2 (.24%)
Bronchiolitis
2 (.24%)
Coma
2 (.24%)
Decreased Appetite
2 (.24%)
Dehydration
2 (.24%)
Depressed Level Of Consciousness
2 (.24%)
Diarrhoea
2 (.24%)
Diffuse Alveolar Damage
2 (.24%)
Electrocardiogram Abnormal
2 (.24%)
Electrocardiogram Qrs Complex Prolo...
2 (.24%)

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

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

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

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

Hypertension
124
Drug Use For Unknown Indication
70
Product Used For Unknown Indication
36
Essential Hypertension
9
Ill-defined Disorder
4
Aortic Dissection
3
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Pulmonary Hypertension
3
Hypertensive Cardiomyopathy
2
Aneurysm
1
Blood Pressure Increased
1

Eupressyl Case Reports

What Eupressyl 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 Eupressyl. 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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