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FUROSEMIDE

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Furosemide Adverse Events Reported to the FDA Over Time

How are Furosemide adverse event reports trending over time?

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

Most Common Furosemide Adverse Events Reported to the FDA

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

Renal Failure Acute
973 (3.22%)
Dehydration
538 (1.78%)
Hypotension
521 (1.72%)
Dizziness
446 (1.48%)
Drug Interaction
431 (1.43%)
Hyperkalaemia
362 (1.2%)
Hypokalaemia
361 (1.19%)
Dyspnoea
360 (1.19%)
Renal Failure
343 (1.13%)
Hyponatraemia
292 (.97%)
Oedema Peripheral
270 (.89%)
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Blood Creatinine Increased
262 (.87%)
Atrial Fibrillation
254 (.84%)
Fall
243 (.8%)
Asthenia
241 (.8%)
Vomiting
239 (.79%)
Diarrhoea
237 (.78%)
Fatigue
233 (.77%)
Nausea
233 (.77%)
Syncope
228 (.75%)
Confusional State
227 (.75%)
Drug Ineffective
224 (.74%)
Cardiac Failure
193 (.64%)
Malaise
183 (.61%)
Condition Aggravated
182 (.6%)
Renal Impairment
181 (.6%)
Cardiac Arrest
165 (.55%)
Oedema
162 (.54%)
Toxic Epidermal Necrolysis
161 (.53%)
Ventricular Tachycardia
161 (.53%)
Bradycardia
158 (.52%)
Somnolence
153 (.51%)
Completed Suicide
146 (.48%)
Anaemia
145 (.48%)
Paraesthesia
142 (.47%)
Cardiac Failure Congestive
138 (.46%)
Loss Of Consciousness
134 (.44%)
Death
130 (.43%)
Cardiac Murmur
129 (.43%)
Hypertension
129 (.43%)
General Physical Health Deteriorati...
126 (.42%)
Feeling Abnormal
124 (.41%)
Overdose
119 (.39%)
Hypovolaemia
118 (.39%)
Blood Urea Increased
115 (.38%)
Electrocardiogram Qt Prolonged
114 (.38%)
Torsade De Pointes
112 (.37%)
Weight Decreased
112 (.37%)
Pneumonia
110 (.36%)
Rhabdomyolysis
109 (.36%)
Headache
108 (.36%)
Pulmonary Oedema
107 (.35%)
Pyrexia
104 (.34%)
Hallucination
102 (.34%)
Orthostatic Hypotension
100 (.33%)
Left Ventricular Dysfunction
97 (.32%)
Sepsis
97 (.32%)
Blood Pressure Decreased
94 (.31%)
Tachycardia
93 (.31%)
Blood Creatine Phosphokinase Increa...
92 (.3%)
Chronic Obstructive Pulmonary Disea...
92 (.3%)
Abdominal Pain
91 (.3%)
Hypoglycaemia
91 (.3%)
Pruritus
91 (.3%)
Weight Increased
90 (.3%)
Haemoglobin Decreased
89 (.29%)
Renal Failure Chronic
89 (.29%)
Venous Pressure Jugular Increased
88 (.29%)
Lactic Acidosis
86 (.28%)
Decreased Appetite
85 (.28%)
Blood Potassium Increased
83 (.27%)
Blood Sodium Decreased
82 (.27%)
Convulsion
81 (.27%)
International Normalised Ratio Incr...
79 (.26%)
Thrombocytopenia
79 (.26%)
Blood Pressure Increased
78 (.26%)
Fluid Retention
77 (.25%)
Gastrointestinal Haemorrhage
77 (.25%)
Respiratory Failure
77 (.25%)
Drug Toxicity
75 (.25%)
Urinary Tract Infection
75 (.25%)
Erythema
74 (.24%)
Metabolic Acidosis
73 (.24%)
Abdominal Distension
71 (.23%)
Blood Potassium Decreased
71 (.23%)
Disorientation
71 (.23%)
Dyspnoea Exertional
71 (.23%)
Hypomagnesaemia
71 (.23%)
Medication Error
71 (.23%)
Blood Glucose Increased
70 (.23%)
Haemodialysis
69 (.23%)
Drug Exposure During Pregnancy
68 (.22%)
Therapeutic Agent Toxicity
67 (.22%)
Agitation
66 (.22%)
Cardiogenic Shock
66 (.22%)
Constipation
65 (.21%)
Cough
64 (.21%)
Rash
64 (.21%)
Chest Pain
62 (.21%)
Multi-organ Failure
62 (.21%)
Shock
62 (.21%)

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

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

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

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

Drug Use For Unknown Indication
2867
Hypertension
2619
Product Used For Unknown Indication
2373
Fluid Retention
1048
Oedema
954
Cardiac Failure Congestive
898
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Diuretic Therapy
896
Cardiac Failure
873
Oedema Peripheral
561
Ill-defined Disorder
233
Polyuria
212
Cardiac Disorder
209
Renal Failure
187
Ascites
182
Prophylaxis
176
Cardiac Failure Chronic
163
Blood Pressure
147
Swelling
136
Myocardial Ischaemia
104
Essential Hypertension
96
Fluid Overload
95
Renal Failure Chronic
92
Joint Swelling
74
Pulmonary Oedema
58
Atrial Fibrillation
54
Hepatic Cirrhosis
53
Renal Impairment
53
Left Ventricular Failure
51
Myocardial Infarction
50
Coronary Artery Disease
49
Renal Disorder
47
Pulmonary Arterial Hypertension
44
Pleural Effusion
41
Nephrotic Syndrome
37
Pulmonary Hypertension
37
Blood Pressure Increased
36
Cardiomyopathy
33
Urine Output Decreased
31
Cardiovascular Disorder
30
Dyspnoea
29
Congestive Cardiomyopathy
29
Oliguria
26
Fluid Imbalance
25
Blood Pressure Abnormal
23
Angina Pectoris
23
Renal Failure Acute
21
Ischaemic Cardiomyopathy
21
Hypertonia
20
Ventricular Tachycardia
18
Acute Myocardial Infarction
17
Cardiovascular Event Prophylaxis
17

Drug Labels

LabelLabelerEffective
FurosemideDAVA Pharmaceuticals, Inc.30-JUN-07
FurosemideMylan Pharmaceuticals Inc.01-JUL-08
FurosemideUDL Laboratories, Inc.10-JUL-08
FurosemideBryant Ranch Prepack29-JAN-09
FurosemideMcKesson Packaging Services Business unit of McKesson Corporation11-JAN-10
FurosemideContract Pharmacy Services-PA12-APR-10
FurosemideState of Florida DOH Central Pharmacy02-JUN-10
FurosemideState of Florida DOH Central Pharmacy02-JUN-10
FurosemideMorton Grove Pharmaceuticals, Inc.25-JUN-10
FurosemideGeneral Injectables & Vaccines, Inc24-AUG-10
FurosemidePhysicians Total Care, Inc.07-SEP-10
FurosemideGeneral Injectables & Vaccines, Inc08-SEP-10
FurosemideRebel Distirbutors Corp28-SEP-10
Furosemide REMEDYREPACK INC. 01-NOV-10
FurosemideREMEDYREPACK INC. 22-NOV-10
FurosemideContract Pharmacy Services-PA09-DEC-10
FurosemideRebel Distributors Corp28-DEC-10
FurosemideUnit Dose Services11-FEB-11
Furosemide Ranbaxy Pharmaceuticals Inc.11-FEB-11
FurosemideUnit Dose Services11-FEB-11
FurosemideMedVantx, Inc.11-FEB-11
FurosemideGeneral Injectables & Vaccines, Inc25-APR-11
FurosemideAmerican Health Packaging26-APR-11
FurosemideCardinal Health05-MAY-11
FurosemideMcKesson Packaging Services Business Unit of McKesson Corporation13-JUN-11
FurosemidePD-Rx Pharmaceuticals, Inc.16-JUN-11
FurosemidePD-Rx Pharmaceuticals, Inc.16-JUN-11
FurosemideREMEDYREPACK INC. 27-JUN-11
FurosemideAmerican Regent, Inc.29-JUN-11
FurosemideRedPharm Drug Inc.25-JUL-11
FurosemideREMEDYREPACK INC. 26-SEP-11
FurosemideREMEDYREPACK INC. 10-OCT-11
FurosemideREMEDYREPACK INC. 13-OCT-11
FurosemideMcKesson Contract Packaging03-NOV-11
FurosemideMcKesson Contract Packaging03-NOV-11
FurosemideMcKesson Packaging Services a business unit of McKesson Corporation21-NOV-11
FurosemideContract Pharmacy Services-PA30-NOV-11
FurosemideLake Erie Medical & Surgical Supply DBA Quality Care Products LLC30-NOV-11
FurosemidePhysicians Total Care, Inc.01-MAR-12
FurosemideNCS HealthCare of KY, Inc dba Vangard Labs13-MAR-12
FurosemideMedVantx, Inc.16-MAR-12
Furosemide General Injectables & Vaccines, Inc.27-MAR-12
FurosemideRoxane Laboratories, Inc05-APR-12
FurosemideCardinal Health10-APR-12
FurosemideCardinal Health16-APR-12
FurosemideIVAX Pharmaceuticals, Inc.21-MAY-12
FurosemideHospira, Inc.22-MAY-12
FurosemideQualitest Pharmaceuticals06-JUN-12
FurosemideSandoz Inc12-JUN-12
FurosemideMajor Pharmaceuticals09-JUL-12
Furosemide PD-Rx Pharmaceuticals, Inc.28-AUG-12
Furosemide PD-Rx Pharmaceuticals, Inc.28-AUG-12
Furosemide Excellium Pharmaceutical Inc.28-AUG-12
FurosemideAPP Pharmaceuticals, LLC04-SEP-12
FurosemideSTAT Rx USA LLC06-SEP-12
FurosemideCardinal Health19-NOV-12
FurosemideBryant Ranch Prepack15-JAN-13
FurosemidePrecision Dose Inc.17-JAN-13
FurosemidePrecision Dose Inc.18-JAN-13
FurosemideBryant Ranch Prepack18-JAN-13
LasixSanofi-Aventis U.S. LLC06-FEB-13
FurosemideNCS HealthCare of KY, Inc dba Vangard Labs18-FEB-13
FurosemideIngenus Pharmaceuticals, LLC07-MAR-13
FurosemideREMEDYREPACK INC. 14-MAR-13
FurosemideCardinal Health14-MAR-13
FurosemideREMEDYREPACK INC. 18-MAR-13
FurosemidePreferred Pharmaceuticals, Inc.20-MAR-13
FurosemidePreferred Pharmaceuticals, Inc20-MAR-13
FurosemideCardinal Health22-MAR-13
FurosemideCardinal Health22-MAR-13
FurosemidePreferred Pharmaceuticals, Inc.25-MAR-13
FurosemideREMEDYREPACK INC. 04-APR-13
Furosemide REMEDYREPACK INC. 05-APR-13
FurosemideCardinal Health29-APR-13
FurosemideCardinal Health08-MAY-13

Furosemide Case Reports

What Furosemide 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 Furosemide. 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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