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FRUSEMIDE

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Frusemide Adverse Events Reported to the FDA Over Time

How are Frusemide adverse event reports trending over time?

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

Most Common Frusemide Adverse Events Reported to the FDA

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

Dyspnoea
39 (2.79%)
Renal Failure Acute
35 (2.5%)
Lower Respiratory Tract Infection
21 (1.5%)
Convulsion
20 (1.43%)
Dizziness
20 (1.43%)
Hyperthermia
20 (1.43%)
Musculoskeletal Stiffness
20 (1.43%)
Neuroleptic Malignant Syndrome
20 (1.43%)
Hypotension
17 (1.22%)
Dehydration
16 (1.14%)
Oedema Peripheral
16 (1.14%)
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Pyrexia
16 (1.14%)
Atrial Fibrillation
15 (1.07%)
Drug Interaction
15 (1.07%)
Pulmonary Oedema
15 (1.07%)
Disseminated Intravascular Coagulat...
14 (1%)
Vomiting
14 (1%)
Tachycardia
13 (.93%)
Tubulointerstitial Nephritis
13 (.93%)
Diarrhoea
12 (.86%)
Gastrointestinal Haemorrhage
12 (.86%)
Hypoglycaemia
12 (.86%)
Multi-organ Failure
12 (.86%)
Overdose
12 (.86%)
Ventricular Tachycardia
12 (.86%)
Acute Myocardial Infarction
11 (.79%)
Cardiac Arrest
11 (.79%)
Colon Cancer
11 (.79%)
Fatigue
11 (.79%)
Feeling Abnormal
11 (.79%)
Lactic Acidosis
11 (.79%)
Malaise
11 (.79%)
Renal Failure
11 (.79%)
Cardiac Murmur
10 (.72%)
Hyperkalaemia
10 (.72%)
Laryngospasm
10 (.72%)
Loss Of Consciousness
10 (.72%)
Paraesthesia
10 (.72%)
Somnolence
10 (.72%)
Stridor
10 (.72%)
Tonic Convulsion
10 (.72%)
Chronic Obstructive Pulmonary Disea...
9 (.64%)
Hypokalaemia
9 (.64%)
Laryngeal Oedema
9 (.64%)
Left Ventricular Dysfunction
9 (.64%)
Nausea
9 (.64%)
Obstructive Airways Disorder
9 (.64%)
Toxic Epidermal Necrolysis
9 (.64%)
Venous Pressure Jugular Increased
9 (.64%)
Blood Creatinine Increased
8 (.57%)
Hyponatraemia
8 (.57%)
Renal Impairment
8 (.57%)
Blood Creatine Phosphokinase Increa...
7 (.5%)
Bradycardia
7 (.5%)
Confusional State
7 (.5%)
Dyspnoea Exertional
7 (.5%)
Nocturnal Dyspnoea
7 (.5%)
Renal Failure Chronic
7 (.5%)
Alanine Aminotransferase Increased
6 (.43%)
Anaemia
6 (.43%)
Aspartate Aminotransferase Increase...
6 (.43%)
Asthenia
6 (.43%)
Blood Amylase Increased
6 (.43%)
Blood Sodium Decreased
6 (.43%)
Bronchospasm
6 (.43%)
Dissociation
6 (.43%)
Drug Level Increased
6 (.43%)
Oedema
6 (.43%)
Oxygen Saturation Decreased
6 (.43%)
Paralysis
6 (.43%)
Respiratory Failure
6 (.43%)
Sepsis
6 (.43%)
Abdominal Pain
5 (.36%)
Back Pain
5 (.36%)
Blood Potassium Increased
5 (.36%)
Burning Sensation
5 (.36%)
Cardio-respiratory Arrest
5 (.36%)
Coronary Artery Bypass
5 (.36%)
Cough
5 (.36%)
Drug Exposure During Pregnancy
5 (.36%)
Graft Dysfunction
5 (.36%)
Increased Upper Airway Secretion
5 (.36%)
Insomnia
5 (.36%)
Palpitations
5 (.36%)
Pulmonary Embolism
5 (.36%)
Tension
5 (.36%)
Wheezing
5 (.36%)
Agitation
4 (.29%)
Angioedema
4 (.29%)
Anorexia
4 (.29%)
Asthma Late Onset
4 (.29%)
Atrioventricular Block Complete
4 (.29%)
Blood Alkaline Phosphatase Increase...
4 (.29%)
Blood Pressure Decreased
4 (.29%)
Blood Urea Increased
4 (.29%)
Cardiomegaly
4 (.29%)
Completed Suicide
4 (.29%)
Cystitis
4 (.29%)
Gamma-glutamyltransferase Increased
4 (.29%)
International Normalised Ratio Incr...
4 (.29%)
Myositis
4 (.29%)

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

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

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

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

Drug Use For Unknown Indication
186
Hypertension
58
Cardiac Failure Congestive
47
Product Used For Unknown Indication
43
Ill-defined Disorder
39
Cardiac Failure
35
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Fluid Retention
34
Oedema
28
Diuretic Therapy
26
Myocardial Ischaemia
20
Oedema Peripheral
17
Ascites
16
Essential Hypertension
15
Left Ventricular Failure
12
Joint Swelling
8
Pulmonary Oedema
8
Polyuria
7
Cardiovascular Disorder
7
Fluid Overload
7
Fallots Tetralogy
6
Cardiac Valve Disease
5
Blood Pressure
5
Cardiovascular Event Prophylaxis
4
Atrial Fibrillation
4
Coronary Artery Disease
4
Pulmonary Embolism
3
Hypertensive Heart Disease
3
Blood Pressure Increased
3
Pulmonary Congestion
3
Dyspnoea
3
Congestive Cardiomyopathy
3
Cardiac Disorder
2
Cardiac Failure Acute
2
Glomerulonephritis Chronic
2
Oliguria
2
Haemorrhoidal Haemorrhage
2
Systemic Lupus Erythematosus
2
Drug Therapy
2
Brain Oedema
2
Angina Pectoris
2
Nephrotic Syndrome
2
Pulmonary Arterial Hypertension
2
Aortic Valve Incompetence
2
Hepatic Vein Thrombosis
2
Heart Disease Congenital
2
Lymphoedema
1
Hepatic Cirrhosis
1
Urinary Retention
1
Cardiomyopathy
1
Urine Output Decreased
1
Cardiac Failure Chronic
1

Frusemide Case Reports

What Frusemide 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 Frusemide. 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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