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Low Blood Pressure (1)
Nausea,gastric Upset,increase In Depression (1)
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Common Frusemide Side Effects

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Frusemide adverse events reported to FDA.

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Summary

FDA Adverse Reports: 68. View All

Frusemide FDA safety alerts: No

Reported deaths: 19

Reported hospitalizations: 30

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Most Reported
1Wet Feet
2Nausea,gastric Upset,increase In Depression
3Low Blood Pressure
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sleeplessness, sweating, low sex drive

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Often additional risks of using a medication, such as Frusemide, become known after product is used by a larger number of patients, for a longer period of time, and by patients with different health characteristics from those studied before drug approval. This page allows You to Find answers and discuss health symptoms with other Frusemide users, Learn more about unwanted side effects & find ways to reduce them. Browse Frusemide Adverse Reports reported to FDA and participate in Frusemide discussion, find alternative treatments and find ways to avoid or reduce risks associated with using Frusemide. You can also Post a question to users community or Ask a Doctor. PatientsVille.com is Your Complete Guide to all common, undocumented and undisclosed side effects associated with drugs and vaccines. Browse More Drug Reports Here: A  B  C  D  E  F  G  H  I  J  K  L  M  N  O  P  Q  R  S  T  U  V  W  X  Y  Z

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Frusemide Adverse Effect Reports (FDA)

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Showing 1-50 of 68  Next Page  >

7001494-8 | Malaise, Oedema Peripheral
on Sep 08, 2010 Male patient from UNITED KINGDOM , 74 years of age, weighting 149.9 lb, was treated with Frusemide (View Usage). Patient experienced the following unwanted or unexpected effects: malaise, oedema peripheral. Frusemide dosage: . During the same period patient was treated with ASPIRIN (View Aspirin Review and Aspirin Label ), FELODIPINE (View Felodipine Review and Felodipine Label ), SEREVENT (View Serevent Review and Serevent Label ).

6931992-4 | Malaise
Patient was taking Frusemide (View Usage). Patient had the following side effects: malaise on Aug 11, 2010 from UNITED KINGDOM Additional patient health information: Male patient , 55 years of age, was diagnosed with schizophrenia and. Frusemide dosage: . During the same period patient was treated with CLOZARIL (View Clozaril Review and Clozaril Label ).

6479948-2 | Cardiac Arrest, Hypokalaemia, Ventricular Tachycardia
Adverse event was reported on Nov 17, 2009 by a Female patient taking Frusemide (View Usage) (Dosage: ) was diagnosed with wound infection, hypertension, pain (What is pain?) and. Location: UNITED KINGDOM , 77 years of age, After Frusemide was administered, patient had the following side effects: cardiac arrest (What is cardiac arrest?), hypokalaemia, ventricular tachycardia. During the same period patient was treated with VANCOMYCIN (View Vancomycin Review and Vancomycin Label ), AMILORIDE HYDROCHLORIDE (View Amiloride Hydrochloride Review and Amiloride Hydrochloride Label ), ATENOLOL (View Atenolol Review and Atenolol Label ), BENDROFLUMETHIAZIDE (View Bendroflumethiazide Review and Bendroflumethiazide Label ), OPIOIDS (View Opioids Review and Opioids Label ), RAMIPRIL (View Ramipril Review and Ramipril Label ), SPIRONOLACTONE (View Spironolactone Review and Spironolactone Label ).

6335960-5 | Blood Osmolarity Decreased, Burning Sensation
on Aug 21, 2009 Female patient from UNITED KINGDOM , 51 years of age, weighting 227.0 lb, was diagnosed with joint swelling, depression (What is depression?), pain (What is pain?), schizoaffective disorder and was treated with Frusemide (View Usage). Patient experienced the following unwanted or unexpected effects: blood osmolarity decreased, burning sensation. Frusemide dosage: 20 Mg, Unk. During the same period patient was treated with AMITRIPTYLINE (150 Mg, Qd) (View Amitriptyline Review and Amitriptyline Label ), IBUPROFEN (400 Mg, Tid) (View Ibuprofen Review and Ibuprofen Label ), RISPERIDONE (3 Mg, Bid) (View Risperidone Review and Risperidone Label ), DIHYDROCODEINE TARTRATE (View Dihydrocodeine Tartrate Review and Dihydrocodeine Tartrate Label ), FYBOGEL (View Fybogel Review and Fybogel Label ), LACTULOSE (View Lactulose Review and Lactulose Label ), LANSOPRAZOLE (View Lansoprazole Review and Lansoprazole Label ), MAXEPA (View Maxepa Review and Maxepa Label ). Patient was hospitalized.


6329651-4 | Burning Sensation, Hyponatraemia
on Aug 12, 2009 Female patient from UNITED KINGDOM , 51 years of age, weighting 227.0 lb, was diagnosed with joint swelling, schizoaffective disorder, depression (What is depression?), pain (What is pain?) and was treated with Frusemide (View Usage). Patient had the following side effects: burning sensation, hyponatraemia. Frusemide dosage: . During the same period patient was treated with RISPERIDONE (View Risperidone Review and Risperidone Label ), AMITRIPTYLINE HYDROCHLORIDE (View Amitriptyline Hydrochloride Review and Amitriptyline Hydrochloride Label ), IBUPROFEN (View Ibuprofen Review and Ibuprofen Label ), DIHYDROCODEINE BITARTRATE INJ (View Dihydrocodeine Bitartrate Inj Review and Dihydrocodeine Bitartrate Inj Label ), FYBOGEL (View Fybogel Review and Fybogel Label ), LACTULOSE (View Lactulose Review and Lactulose Label ), LANSOPRAZOLE (View Lansoprazole Review and Lansoprazole Label ), MAXEPA /00931501/ (View Maxepa /00931501/ Review and Maxepa /00931501/ Label ).

6321532-5 | Blood Osmolarity Decreased, Burning Sensation
Patient was taking Frusemide (View Usage). After Frusemide was administered, patient had the following side effects: blood osmolarity decreased, burning sensation on Aug 11, 2009 from UNITED KINGDOM Additional patient health information: Female patient , 51 years of age, weighting 227.0 lb, was diagnosed with joint swelling, depression (What is depression?), pain (What is pain?), schizoaffective disorder and. Frusemide dosage: 20 Mg, Unk. During the same period patient was treated with AMITRIPTYLINE (150 Mg, Qd) (View Amitriptyline Review and Amitriptyline Label ), IBUPROFEN (400 Mg, Tid) (View Ibuprofen Review and Ibuprofen Label ), RISPERIDONE (3 Mg, Bid) (View Risperidone Review and Risperidone Label ), DIHYDROCODEINE TARTRATE (View Dihydrocodeine Tartrate Review and Dihydrocodeine Tartrate Label ), FYBOGEL (View Fybogel Review and Fybogel Label ), LACTULOSE (View Lactulose Review and Lactulose Label ), LANSOPRAZOLE (View Lansoprazole Review and Lansoprazole Label ), MAXEPA (View Maxepa Review and Maxepa Label ).

6287033-8 | Off Label Use, Renal Failure
Adverse event was reported on Jul 14, 2009 by a Male patient taking Frusemide (View Usage) (Dosage: ) was diagnosed with cardiac failure congestive and. Location: UNITED KINGDOM , 76 years of age, Patient experienced the following unwanted or unexpected effects: off label use, renal failure. During the same period patient was treated with IBUPROFEN (View Ibuprofen Review and Ibuprofen Label ), RAMIPRIL (View Ramipril Review and Ramipril Label ). Patient was hospitalized.

6278913-8 | Off Label Use, Renal Failure
on Jul 14, 2009 Male patient from UNITED KINGDOM , 76 years of age, was diagnosed with cardiac failure congestive and was treated with Frusemide (View Usage). Patient had the following side effects: off label use, renal failure. Frusemide dosage: 40 Mg, Unk. During the same period patient was treated with RAMIPRIL (5 Mg, Unk) (View Ramipril Review and Ramipril Label ), IBUPROFEN (View Ibuprofen Review and Ibuprofen Label ). Patient was hospitalized.

6257522-0 | Renal Failure
on Jun 24, 2009 Female patient from AUSTRALIA , 83 years of age, was treated with Frusemide (View Usage). After Frusemide was administered, patient had the following side effects: renal failure. Frusemide dosage: . During the same period patient was treated with PARACETAMOL (Dose: 1 G 4-hourly) (View Paracetamol Review and Paracetamol Label ), IRBESARTAN (View Irbesartan Review and Irbesartan Label ), MELOXICAM (View Meloxicam Review and Meloxicam Label ), PANTOPRAZOLE SODIUM (View Pantoprazole Sodium Review and Pantoprazole Sodium Label ), SIGMACORT /00028601/ (View Sigmacort /00028601/ Review and Sigmacort /00028601/ Label ), HYPROMELLOSE EYE DROPS (Dose: 2 Drops) (View Hypromellose Eye Drops Review and Hypromellose Eye Drops Label ), SERETIDE /01420901/ (Dose: 2 Puffs) (View Seretide /01420901/ Review and Seretide /01420901/ Label ), CARDIZEM (View Cardizem Review and Cardizem Label ).

6228143-0 | Hypoglycaemia, Lactic Acidosis, Renal Failure Acute, Shock
Patient was taking Frusemide (View Usage). Patient experienced the following unwanted or unexpected effects: hypoglycaemia, lactic acidosis, renal failure acute, shock on Jun 05, 2009 from Additional patient health information: Female patient , 61 years of age, . Frusemide dosage: . During the same period patient was treated with METFORMIN HYDROCHLORIDE (View Metformin Hydrochloride Review and Metformin Hydrochloride Label ), GLICLAZIDE (View Gliclazide Review and Gliclazide Label ), QUINAPRIL (View Quinapril Review and Quinapril Label ), CANDESARTAN W/HYDROCHLOROTHIAZIDE (View Candesartan W/hydrochlorothiazide Review and Candesartan W/hydrochlorothiazide Label ).

6219642-6 | Lactic Acidosis, Renal Failure Acute
Adverse event was reported on Jun 02, 2009 by a Female patient taking Frusemide (View Usage) (Dosage: ) . Location: , 61 years of age, Patient had the following side effects: lactic acidosis, renal failure acute. During the same period patient was treated with METFORMIN (View Metformin Review and Metformin Label ), GLICLAZIDE (View Gliclazide Review and Gliclazide Label ), QUINAPRIL (View Quinapril Review and Quinapril Label ), CANDESARTAN W/HYDROCHLOROTHIAZIDE (View Candesartan W/hydrochlorothiazide Review and Candesartan W/hydrochlorothiazide Label ).

6206784-4 | Dizziness, Loss Of Consciousness, Road Traffic Accident
on May 18, 2009 Male patient from AUSTRALIA , 75 years of age, was treated with Frusemide (View Usage). After Frusemide was administered, patient had the following side effects: dizziness (What is dizziness?), loss of consciousness, road traffic accident. Frusemide dosage: . During the same period patient was treated with SIMVASTATIN (View Simvastatin Review and Simvastatin Label ), PLAVIX (View Plavix Review and Plavix Label ), DIGESIC (View Digesic Review and Digesic Label ), CENTRUM /00554501/ (View Centrum /00554501/ Review and Centrum /00554501/ Label ), POTASSIUM CHLORIDE (View Potassium Chloride Review and Potassium Chloride Label ), NEXIUM (View Nexium Review and Nexium Label ), MONODUR (View Monodur Review and Monodur Label ), GLUCOSAMINE (View Glucosamine Review and Glucosamine Label ). Patient was hospitalized.

6197507-6 | Dizziness, Loss Of Consciousness, Road Traffic Accident
on May 11, 2009 Male patient from AUSTRALIA , 75 years of age, was treated with Frusemide (View Usage). Patient experienced the following unwanted or unexpected effects: dizziness (What is dizziness?), loss of consciousness, road traffic accident. Frusemide dosage: . During the same period patient was treated with SIMVASTATIN (View Simvastatin Review and Simvastatin Label ), PLAVIX (View Plavix Review and Plavix Label ), DIGESIC (View Digesic Review and Digesic Label ), CENTRUM /00554501/ (View Centrum /00554501/ Review and Centrum /00554501/ Label ), POTASSIUM CHLORIDE (View Potassium Chloride Review and Potassium Chloride Label ), NEXIUM (View Nexium Review and Nexium Label ), MONODUR (View Monodur Review and Monodur Label ), GLUCOSAMINE (View Glucosamine Review and Glucosamine Label ). Patient was hospitalized.

6169906-X | Convulsion, Disseminated Intravascular Coagulation, Hyperthermia, Hyperthermia Malignant, Multi-organ Failure, Musculoskeletal Stiffness, Neuroleptic Malignant Syndrome, Tachycardia
Patient was taking Frusemide (View Usage). Patient had the following side effects: convulsion, disseminated intravascular coagulation, hyperthermia, hyperthermia malignant, multi-organ failure, musculoskeletal stiffness, neuroleptic malignant syndrome, tachycardia on Apr 07, 2009 from Additional patient health information: Male patient , 82 years of age, was diagnosed with cardiac failure congestive, depression (What is depression?), cardiac failure chronic, atrial fibrillation (What is atrial fibrillation?), emphysema and. Frusemide dosage: . During the same period patient was treated with PAXIL (View Paxil Review and Paxil Label ), ARTIST (View Artist Review and Artist Label ), KLARICID (View Klaricid Review and Klaricid Label ), CERCINE (View Cercine Review and Cercine Label ), DIGOXIN (View Digoxin Review and Digoxin Label ), SEREVENT (View Serevent Review and Serevent Label ). Patient was hospitalized.

6165596-0 | Convulsion, Hyperthermia, Hyperthermia Malignant, Multi-organ Failure, Musculoskeletal Stiffness, Neuroleptic Malignant Syndrome, Tachycardia
Adverse event was reported on Apr 07, 2009 by a Male patient taking Frusemide (View Usage) (Dosage: ) was diagnosed with cardiac failure congestive, depression (What is depression?), cardiac failure chronic, atrial fibrillation (What is atrial fibrillation?), emphysema and. Location: , 82 years of age, After Frusemide was administered, patient had the following side effects: convulsion, hyperthermia, hyperthermia malignant, multi-organ failure, musculoskeletal stiffness, neuroleptic malignant syndrome, tachycardia. During the same period patient was treated with PAXIL (View Paxil Review and Paxil Label ), ARTIST (View Artist Review and Artist Label ), KLARICID (View Klaricid Review and Klaricid Label ), CERCINE (View Cercine Review and Cercine Label ), DIGOXIN (View Digoxin Review and Digoxin Label ), SEREVENT (View Serevent Review and Serevent Label ). Patient was hospitalized.

6145943-6 | Convulsion, Hyperthermia, Hyperthermia Malignant, Musculoskeletal Stiffness, Neuroleptic Malignant Syndrome
on Mar 26, 2009 Male patient from , 82 years of age, was diagnosed with depression (What is depression?) and was treated with Frusemide (View Usage). Patient experienced the following unwanted or unexpected effects: convulsion, hyperthermia, hyperthermia malignant, musculoskeletal stiffness, neuroleptic malignant syndrome. Frusemide dosage: Dose: Unk. During the same period patient was treated with PAROXETINE HYDROCHLORIDE (Dose: Unk) (View Paroxetine Hydrochloride Review and Paroxetine Hydrochloride Label ), CARVEDILOL (Dose: Unk) (View Carvedilol Review and Carvedilol Label ), CLARITHROMYCIN (Dose: Unk) (View Clarithromycin Review and Clarithromycin Label ), DIAZEPAM (Dose: Unk) (View Diazepam Review and Diazepam Label ), DIGOXIN (Dose: Unk) (View Digoxin Review and Digoxin Label ), SALMETEROL XINAFOATE (Dose: Unk) (View Salmeterol Xinafoate Review and Salmeterol Xinafoate Label ), SULPIRIDE (Dose: Unk) (View Sulpiride Review and Sulpiride Label ), THEOPHYLLINE (Dose: Unk) (View Theophylline Review and Theophylline Label ). Patient was hospitalized.

6131895-1 | Coronary Artery Bypass
on Mar 17, 2009 Male patient from , 63 years of age, was treated with Frusemide (View Usage). Patient had the following side effects: coronary artery bypass (What is coronary artery bypass?). Frusemide dosage: . During the same period patient was treated with APROVEL (View Aprovel Review and Aprovel Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), ATORVASTATIN (View Atorvastatin Review and Atorvastatin Label ). Patient was hospitalized.

6110933-6 | Coronary Artery Bypass
Patient was taking Frusemide (View Usage). After Frusemide was administered, patient had the following side effects: coronary artery bypass (What is coronary artery bypass?) on Mar 04, 2009 from Additional patient health information: Male patient , 63 years of age, . Frusemide dosage: . During the same period patient was treated with APROVEL (View Aprovel Review and Aprovel Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), ATORVASTATIN (View Atorvastatin Review and Atorvastatin Label ). Patient was hospitalized.

5870757-1 | Asthma Late Onset, Bronchospasm, Chronic Obstructive Pulmonary Disease, Cough, Dyspnoea, Loss Of Consciousness, Malaise, Wheezing
Adverse event was reported on Aug 27, 2008 by a Female patient taking Frusemide (View Usage) (Dosage: ) was diagnosed with hypothyroidism, prophylaxis against gastrointestinal ulcer and. Location: , 68 years of age, Patient experienced the following unwanted or unexpected effects: asthma late onset, bronchospasm, chronic obstructive pulmonary disease, cough, dyspnoea, loss of consciousness, malaise, wheezing. During the same period patient was treated with RAMIPRIL (View Ramipril Review and Ramipril Label ), DIHYDROCODEINE BITARTRATE INJ (View Dihydrocodeine Bitartrate Inj Review and Dihydrocodeine Bitartrate Inj Label ), IBUPROFEN (View Ibuprofen Review and Ibuprofen Label ), LEVOTHYROXINE SODIUM (View Levothyroxine Sodium Review and Levothyroxine Sodium Label ), OMEPRAZOLE (View Omeprazole Review and Omeprazole Label ).

5505977-9 | Gastric Cancer
on Oct 29, 2007 Male patient from UNITED KINGDOM , 70 years of age, was diagnosed with chronic myeloid leukaemia and was treated with Frusemide (View Usage). Patient had the following side effects: gastric cancer. Frusemide dosage: 20 Mg, Qd. During the same period patient was treated with LANSOPRAZOLE (30 Mg, Qd) (View Lansoprazole Review and Lansoprazole Label ), OXYNORM (10 Mg, Tid) (View Oxynorm Review and Oxynorm Label ), GLIVEC (200mg / Day) (View Glivec Review and Glivec Label ).

5479696-1 | Hyperglycaemia
on Sep 19, 2007 Male patient from , weighting 10.14 lb, was diagnosed with hyperinsulinaemia and was treated with Frusemide (View Usage). After Frusemide was administered, patient had the following side effects: hyperglycaemia. Frusemide dosage: . During the same period patient was treated with DIAZOXIDE (View Diazoxide Review and Diazoxide Label ), SPIRONOLACTONE (View Spironolactone Review and Spironolactone Label ), ACETYLSALICYLIC ACID (View Acetylsalicylic Acid Review and Acetylsalicylic Acid Label ).

5470784-2 | Hyperglycaemia
Patient was taking Frusemide (View Usage). Patient experienced the following unwanted or unexpected effects: hyperglycaemia on Sep 19, 2007 from Additional patient health information: Male patient , weighting 10.14 lb, was diagnosed with hyperinsulinaemia and. Frusemide dosage: . During the same period patient was treated with DIAZOXIDE (View Diazoxide Review and Diazoxide Label ), SPIRONOLACTONE (View Spironolactone Review and Spironolactone Label ), ASPIRIN (View Aspirin Review and Aspirin Label ).

5386313-8 | Bradycardia, Hypotension, Intentional Overdose, Somnolence
Adverse event was reported on Jul 09, 2007 by a Male patient taking Frusemide (View Usage) (Dosage: ) was diagnosed with hypertension, depression (What is depression?) and. Location: UNITED KINGDOM , 56 years of age, weighting 254.9 lb, Patient had the following side effects: bradycardia, hypotension, intentional overdose, somnolence. During the same period patient was treated with BISOPROLOL (View Bisoprolol Review and Bisoprolol Label ), AMLODIPINE (View Amlodipine Review and Amlodipine Label ), ESCITALOPRAM OXALATE (View Escitalopram Oxalate Review and Escitalopram Oxalate Label ), GTN SPRAY (Dose: 1-2 Puffs) (View Gtn Spray Review and Gtn Spray Label ), NICORANDIL (View Nicorandil Review and Nicorandil Label ), BENDROFLUMETHIAZIDE (View Bendroflumethiazide Review and Bendroflumethiazide Label ), IBERSARTAN (View Ibersartan Review and Ibersartan Label ), ISOSORBIDE MONONITRATE SR (View Isosorbide Mononitrate Sr Review and Isosorbide Mononitrate Sr Label ).

5349221-4 | Pemphigoid
on May 29, 2007 Male patient from , 73 years of age, weighting 180.8 lb, was diagnosed with cardiac failure congestive, hypertension, oedema, hypercholesterolaemia, pain (What is pain?) and was treated with Frusemide (View Usage). After Frusemide was administered, patient had the following side effects: pemphigoid. Frusemide dosage: . During the same period patient was treated with BENDROFLUMETHIAZIDE (View Bendroflumethiazide Review and Bendroflumethiazide Label ), ATORVASTATIN (View Atorvastatin Review and Atorvastatin Label ), CODEINE PHOSPHATE AND ACETAMINOPHEN (Dose: 1 Df) (View Codeine Phosphate And Acetaminophen Review and Codeine Phosphate And Acetaminophen Label ), PERINDOPRIL (View Perindopril Review and Perindopril Label ).

5329879-6 | Hyperglycaemia
on May 09, 2007 Male patient from , weighting 10.14 lb, was diagnosed with hyperinsulinaemia and was treated with Frusemide (View Usage). Patient experienced the following unwanted or unexpected effects: hyperglycaemia. Frusemide dosage: . During the same period patient was treated with DIAZOXIDE (View Diazoxide Review and Diazoxide Label ), SPIRONOLACTONE (View Spironolactone Review and Spironolactone Label ), ACETYLSALICYLIC ACID SRT (View Acetylsalicylic Acid Srt Review and Acetylsalicylic Acid Srt Label ).

4999274-8 | Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Blood Alkaline Phosphatase Increased, Cardiac Arrest, Dehydration, Hypotension, Renal Failure Acute, Rhabdomyolysis
Patient was taking Frusemide (View Usage). Patient had the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood alkaline phosphatase increased, cardiac arrest (What is cardiac arrest?), dehydration, hypotension, renal failure acute, rhabdomyolysis on Aug 15, 2005 from Additional patient health information: Female patient , 65 years of age, weighting 176.4 lb, was diagnosed with hyperlipidaemia, pain (What is pain?) and. Frusemide dosage: . During the same period patient was treated with SIMVASTATIN (View Simvastatin Review and Simvastatin Label ), DICLOFENAC (View Diclofenac Review and Diclofenac Label ), LISINOPRIL (View Lisinopril Review and Lisinopril Label ), CLOPIDOGREL (View Clopidogrel Review and Clopidogrel Label ), ESOMEPRAZOLE (View Esomeprazole Review and Esomeprazole Label ), ALLOPURINOL (View Allopurinol Review and Allopurinol Label ), ATENOLOL (View Atenolol Review and Atenolol Label ), AMITRIPTYLINE HCL (View Amitriptyline Hcl Review and Amitriptyline Hcl Label ).

4993850-4 | Liver Function Test Abnormal, Renal Failure Acute
Adverse event was reported on Apr 18, 2006 by a Male patient taking Frusemide (View Usage) (Dosage: 80 Mg Freq Unk Po) was diagnosed with polyuria, atrial fibrillation (What is atrial fibrillation?), arthritis (What is arthritis?), blood pressure increased and. Location: UNITED KINGDOM , 91 years of age, After Frusemide was administered, patient had the following side effects: liver function test abnormal, renal failure acute. During the same period patient was treated with DIGOXIN (125 Ug Daily Po) (View Digoxin Review and Digoxin Label ), AMIODARONE (200 Mg Freq Unk Po) (View Amiodarone Review and Amiodarone Label ), SPIRONOLACTONE (25 Mg Daily Po) (View Spironolactone Review and Spironolactone Label ), ARCOXIA (80 Mg Daily Po) (View Arcoxia Review and Arcoxia Label ), COVERSYL (4 Mg Daily Po) (View Coversyl Review and Coversyl Label ), CEPHALEXIN (View Cephalexin Review and Cephalexin Label ), BISOPROLOL (View Bisoprolol Review and Bisoprolol Label ), SALBUTAMOL (View Salbutamol Review and Salbutamol Label ). Patient was hospitalized.

4979152-0 | Acute Myocardial Infarction, Colon Cancer, Gastrointestinal Haemorrhage, Laryngeal Oedema, Laryngospasm, Lower Respiratory Tract Infection, Obstructive Airways Disorder, Overdose, Pulmonary Oedema
on Aug 08, 2005 Female patient from , 75 years of age, was diagnosed with hypertension and was treated with Frusemide (View Usage). Patient experienced the following unwanted or unexpected effects: acute myocardial infarction, colon cancer, gastrointestinal haemorrhage, laryngeal oedema, laryngospasm, lower respiratory tract infection, obstructive airways disorder, overdose, pulmonary oedema. Frusemide dosage: . During the same period patient was treated with LISINOPRIL (View Lisinopril Review and Lisinopril Label ), LANSOPRAZOLE (Dose: Unk) (View Lansoprazole Review and Lansoprazole Label ), ASPIRIN (Dose: Unk) (View Aspirin Review and Aspirin Label ), ATENOLOL (Dose: Unk) (View Atenolol Review and Atenolol Label ), GLYCERYL TRINITRATE (Dose: Unk) (View Glyceryl Trinitrate Review and Glyceryl Trinitrate Label ), ATORVASTATIN (Dose: Unk) (View Atorvastatin Review and Atorvastatin Label ), NITROGLYCERIN (View Nitroglycerin Review and Nitroglycerin Label ).

4977986-X | Acute Myocardial Infarction, Colon Cancer, Gastrointestinal Haemorrhage, Laryngeal Oedema, Laryngospasm, Lower Respiratory Tract Infection, Obstructive Airways Disorder, Overdose, Pulmonary Oedema
on Aug 08, 2005 Female patient from , 75 years of age, was diagnosed with hypertension and was treated with Frusemide (View Usage). Patient had the following side effects: acute myocardial infarction, colon cancer, gastrointestinal haemorrhage, laryngeal oedema, laryngospasm, lower respiratory tract infection, obstructive airways disorder, overdose, pulmonary oedema. Frusemide dosage: . During the same period patient was treated with LISINOPRIL (View Lisinopril Review and Lisinopril Label ), LANSOPRAZOLE (Dose: Unk) (View Lansoprazole Review and Lansoprazole Label ), ASPIRIN (Dose: Unk) (View Aspirin Review and Aspirin Label ), ATENOLOL (Dose: Unk) (View Atenolol Review and Atenolol Label ), GLYCERYL TRINITRATE (Dose: Unk) (View Glyceryl Trinitrate Review and Glyceryl Trinitrate Label ), ATORVASTATIN (Dose: Unk) (View Atorvastatin Review and Atorvastatin Label ), NITROGLYCERIN (View Nitroglycerin Review and Nitroglycerin Label ).

4950379-7 | Pemphigoid
Patient was taking Frusemide (View Usage). After Frusemide was administered, patient had the following side effects: pemphigoid on Mar 15, 2006 from UNITED KINGDOM Additional patient health information: Male patient , 66 years of age, was diagnosed with cardiac failure and. Frusemide dosage: .

4934000-X | Blood Sodium Decreased, Fall
Adverse event was reported on Feb 24, 2006 by a Male patient taking Frusemide (View Usage) (Dosage: ) was diagnosed with diabetes mellitus non-insulin-dependent, hypertension, anaemia and. Location: , 78 years of age, Patient experienced the following unwanted or unexpected effects: blood sodium decreased, fall (What is fall?). During the same period patient was treated with OMEPRAZOLE (View Omeprazole Review and Omeprazole Label ), GLICLAZIDE (View Gliclazide Review and Gliclazide Label ), METFORMIN (View Metformin Review and Metformin Label ), ENALAPRIL MALEATE (View Enalapril Maleate Review and Enalapril Maleate Label ), IRON (FERROUS SULFATE) (View Iron (ferrous Sulfate) Review and Iron (ferrous Sulfate) Label ). Patient was hospitalized.

4931775-0 | Blood Bicarbonate Decreased, Blood Potassium Increased, Blood Urea Increased, Dehydration, Diarrhoea, Hypotension, Renal Failure Acute, Vomiting
on Feb 24, 2006 Male patient from , 64 years of age, was diagnosed with nephrotic syndrome and was treated with Frusemide (View Usage). Patient had the following side effects: blood bicarbonate decreased, blood potassium increased, blood urea increased, dehydration, diarrhoea, hypotension, renal failure acute, vomiting. Frusemide dosage: . During the same period patient was treated with LISINOPRIL (View Lisinopril Review and Lisinopril Label ), SPIRONOLACTONE (View Spironolactone Review and Spironolactone Label ), AMILORIDE HCL (View Amiloride Hcl Review and Amiloride Hcl Label ), ALLOPURINOL (View Allopurinol Review and Allopurinol Label ), CETIRIZINE (View Cetirizine Review and Cetirizine Label ), SALBUTAMOL (Dose: 2 Puffs) (View Salbutamol Review and Salbutamol Label ), DERMOVATE (View Dermovate Review and Dermovate Label ). Patient was hospitalized.

4931775-0 | Blood Bicarbonate Decreased, Blood Potassium Increased, Blood Urea Increased, Dehydration, Diarrhoea, Hypotension, Renal Failure Acute, Vomiting
on Feb 24, 2006 Male patient from , 64 years of age, was diagnosed with nephrotic syndrome and was treated with Frusemide (View Usage). After Frusemide was administered, patient had the following side effects: blood bicarbonate decreased, blood potassium increased, blood urea increased, dehydration, diarrhoea, hypotension, renal failure acute, vomiting. Frusemide dosage: . During the same period patient was treated with LISINOPRIL (View Lisinopril Review and Lisinopril Label ), SPIRONOLACTONE (View Spironolactone Review and Spironolactone Label ), AMILORIDE HYDROCHLORIDE (View Amiloride Hydrochloride Review and Amiloride Hydrochloride Label ), ALLOPURINOL (View Allopurinol Review and Allopurinol Label ), CETIRIZINE (View Cetirizine Review and Cetirizine Label ), SALBUTAMOL (Dose: 2 Puffs) (View Salbutamol Review and Salbutamol Label ), DERMOVATE (View Dermovate Review and Dermovate Label ). Patient was hospitalized.

4845990-8 | Cystitis
Patient was taking Frusemide (View Usage). Patient experienced the following unwanted or unexpected effects: cystitis on Jul 21, 2005 from Additional patient health information: Female patient , 75 years of age, was diagnosed with hypertension, osteoporosis (What is osteoporosis?), platelet aggregation, hypercholesterolaemia, pain (What is pain?), depression (What is depression?), dyspepsia, cardiac failure and. Frusemide dosage: . During the same period patient was treated with ADCAL D3 (View Adcal-d3 Review and Adcal-d3 Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), ATORVASTATIN CALCIUM (View Atorvastatin Calcium Review and Atorvastatin Calcium Label ), CODEINE (View Codeine Review and Codeine Label ), FLUOXETINE (View Fluoxetine Review and Fluoxetine Label ), ISOTARD XL (View Isotard Xl Review and Isotard Xl Label ), LANSOPRAZOLE (View Lansoprazole Review and Lansoprazole Label ), NICORANDIL (View Nicorandil Review and Nicorandil Label ).

4826386-1 | Acute Myocardial Infarction, Colon Cancer, Gastrointestinal Haemorrhage, Laryngeal Oedema, Laryngospasm, Lower Respiratory Tract Infection, Obstructive Airways Disorder, Overdose, Pulmonary Oedema
Adverse event was reported on Aug 08, 2005 by a Female patient taking Frusemide (View Usage) (Dosage: ) was diagnosed with hypertension and. Location: , 75 years of age, Patient had the following side effects: acute myocardial infarction, colon cancer, gastrointestinal haemorrhage, laryngeal oedema, laryngospasm, lower respiratory tract infection, obstructive airways disorder, overdose, pulmonary oedema. During the same period patient was treated with LISINOPRIL (View Lisinopril Review and Lisinopril Label ), ZOTON (Dose: Unk) (View Zoton Review and Zoton Label ), ASPIRIN (Dose: Unk) (View Aspirin Review and Aspirin Label ), ATENOLOL (Dose: Unk) (View Atenolol Review and Atenolol Label ), GLYCERYL TRINITRATE (Dose: Unk) (View Glyceryl Trinitrate Review and Glyceryl Trinitrate Label ), ATORVASTATIN CALCIUM (Dose: Unk) (View Atorvastatin Calcium Review and Atorvastatin Calcium Label ), NITROGLYCERIN (View Nitroglycerin Review and Nitroglycerin Label ).

4815693-4 | Bile Duct Stone, Cholecystitis
on Oct 30, 2003 Female patient from UNITED KINGDOM , weighting 154.3 lb, was diagnosed with ill-defined disorder, cardiac failure congestive and was treated with Frusemide (View Usage). After Frusemide was administered, patient had the following side effects: bile duct stone, cholecystitis. Frusemide dosage: . During the same period patient was treated with PERINDOPRIL ERBUMINE (View Perindopril Erbumine Review and Perindopril Erbumine Label ), DOXAZOSIN (View Doxazosin Review and Doxazosin Label ), CODEINE PHOSPHATE AND ACETAMINOPHEN (View Codeine Phosphate And Acetaminophen Review and Codeine Phosphate And Acetaminophen Label ). Patient was hospitalized.

4814560-X | Diverticulitis
on Sep 08, 2003 Female patient from UNITED KINGDOM , weighting 149.9 lb, was diagnosed with ill-defined disorder, cardiac failure congestive and was treated with Frusemide (View Usage). Patient experienced the following unwanted or unexpected effects: diverticulitis. Frusemide dosage: . During the same period patient was treated with PERINDOPRIL ERBUMINE (Daily Dose: 4 Milligram(s)) (View Perindopril Erbumine Review and Perindopril Erbumine Label ), LOSARTAN (View Losartan Review and Losartan Label ), SIMVASTATIN (View Simvastatin Review and Simvastatin Label ), THYROXIN (View Thyroxin Review and Thyroxin Label ). Patient was hospitalized.

4811790-8 | Atrial Fibrillation, Cardiac Failure Congestive, Cardiomegaly, Constipation, Dyspnoea, Lower Respiratory Tract Infection, Pleural Effusion, Pulmonary Oedema, Rectal Haemorrhage
Patient was taking Frusemide (View Usage). Patient had the following side effects: atrial fibrillation (What is atrial fibrillation?), cardiac failure congestive, cardiomegaly, constipation (What is constipation?), dyspnoea, lower respiratory tract infection, pleural effusion, pulmonary oedema, rectal haemorrhage on Jan 30, 2002 from IRELAND Additional patient health information: Male patient , weighting 187.4 lb, was diagnosed with ill-defined disorder, cardiac failure congestive, cardiac valve disease and. Frusemide dosage: . During the same period patient was treated with COVERSYL (View Coversyl Review and Coversyl Label ), LOSEC (View Losec Review and Losec Label ), ALLOPURINOL (View Allopurinol Review and Allopurinol Label ), WARFARIN (View Warfarin Review and Warfarin Label ), DIGOXIN (View Digoxin Review and Digoxin Label ), BUMETANIDE (View Bumetanide Review and Bumetanide Label ), CAPTOPRIL (View Captopril Review and Captopril Label ). Patient was hospitalized.

4811224-3 | Chronic Obstructive Pulmonary Disease
Adverse event was reported on Mar 13, 2003 by a Female patient taking Frusemide (View Usage) (Dosage: ) was diagnosed with ill-defined disorder, cardiac failure congestive and. Location: UNITED KINGDOM , weighting 222.7 lb, After Frusemide was administered, patient had the following side effects: chronic obstructive pulmonary disease. During the same period patient was treated with PERINDOPRIL ERBUMINE (Daily Dose: 4 Milligram(s)) (View Perindopril Erbumine Review and Perindopril Erbumine Label ), RAMIPRIL (View Ramipril Review and Ramipril Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), PHYLLOCONTIN (View Phyllocontin Review and Phyllocontin Label ), SERETIDE (View Seretide Review and Seretide Label ), FUROSEMIDE (View Furosemide Review and Furosemide Label ). Patient was hospitalized.

4811219-X | Myocardial Infarction
on May 28, 2003 Female patient from UNITED KINGDOM , weighting 220.5 lb, was diagnosed with ill-defined disorder, cardiac failure congestive and was treated with Frusemide (View Usage). Patient experienced the following unwanted or unexpected effects: myocardial infarction. Frusemide dosage: . During the same period patient was treated with PERINDOPRIL (Daily Dose: 4 Milligram(s)) (View Perindopril Review and Perindopril Label ), DIAMICRON (Daily Dose: 30 Milligram(s)) (View Diamicron Review and Diamicron Label ), SIMVASTATIN (View Simvastatin Review and Simvastatin Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), GTN (View Gtn Review and Gtn Label ), FOLIC ACID (View Folic Acid Review and Folic Acid Label ), DOXEPIN HCL (View Doxepin Hcl Review and Doxepin Hcl Label ), GABAPENTIN (View Gabapentin Review and Gabapentin Label ).

4811210-3 | Angina Pectoris, Carotid Artery Stenosis, Diverticulum
on Oct 23, 2003 Male patient from UNITED KINGDOM , weighting 138.9 lb, was diagnosed with ill-defined disorder, cardiac failure congestive and was treated with Frusemide (View Usage). Patient had the following side effects: angina pectoris, carotid artery stenosis, diverticulum. Frusemide dosage: . During the same period patient was treated with PERINDOPRIL (Daily Dose: 4 Milligram(s)) (View Perindopril Review and Perindopril Label ), SPIRONOLACTONE (View Spironolactone Review and Spironolactone Label ). Patient was hospitalized.

4811205-X | Alcohol Use, Bronchopneumonia, Fall, Lumbar Vertebral Fracture
Patient was taking Frusemide (View Usage). After Frusemide was administered, patient had the following side effects: alcohol use, bronchopneumonia, fall (What is fall?), lumbar vertebral fracture on May 19, 2003 from IRELAND Additional patient health information: Male patient , weighting 164.0 lb, was diagnosed with ill-defined disorder, cardiac failure congestive and. Frusemide dosage: . During the same period patient was treated with PERINDOPRIL ERBUMINE (Daily Dose: 4 Milligram(s)) (View Perindopril Erbumine Review and Perindopril Erbumine Label ), DIGOXIN (View Digoxin Review and Digoxin Label ), VALPROATE SODIUM (View Valproate Sodium Review and Valproate Sodium Label ). Patient was hospitalized.

4808704-3 | Bronchopneumonia, Cardiac Failure, Dyspnoea, Fall
Adverse event was reported on Aug 19, 2004 by a Male patient taking Frusemide (View Usage) (Dosage: ) was diagnosed with ill-defined disorder, cardiac failure congestive and. Location: UNITED KINGDOM , weighting 112.4 lb, Patient experienced the following unwanted or unexpected effects: bronchopneumonia, cardiac failure, dyspnoea, fall (What is fall?). During the same period patient was treated with PERINDOPRIL (Daily Dose: 2 Milligram(s)) (View Perindopril Review and Perindopril Label ), DIGOXIN (View Digoxin Review and Digoxin Label ), ASPIRIN (View Aspirin Review and Aspirin Label ). Patient was hospitalized.

4801616-0 | Acute Myocardial Infarction, Angioneurotic Oedema, Colon Cancer, Gastrointestinal Haemorrhage, Lower Respiratory Tract Infection, Overdose, Pulmonary Oedema, Respiratory Failure
on Aug 08, 2005 Female patient from , 75 years of age, was treated with Frusemide (View Usage). Patient had the following side effects: acute myocardial infarction, angioneurotic oedema, colon cancer, gastrointestinal haemorrhage, lower respiratory tract infection, overdose, pulmonary oedema, respiratory failure. Frusemide dosage: . During the same period patient was treated with LISINOPRIL (View Lisinopril Review and Lisinopril Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), ATENOLOL (View Atenolol Review and Atenolol Label ), ATORVASTATIN CALCIUM (View Atorvastatin Calcium Review and Atorvastatin Calcium Label ), LANSOPRAZOLE (View Lansoprazole Review and Lansoprazole Label ), NITROGLYCERIN (View Nitroglycerin Review and Nitroglycerin Label ).

4718333-8 | Renal Failure Acute
on Jul 07, 2005 Female patient from , 70 years of age, was treated with Frusemide (View Usage). After Frusemide was administered, patient had the following side effects: renal failure acute. Frusemide dosage: Dose: Unk. During the same period patient was treated with SPIRONOLACTONE (Dose: Unk) (View Spironolactone Review and Spironolactone Label ), PERINDOPRIL (Dose: Unk) (View Perindopril Review and Perindopril Label ), METFORMIN HCL (View Metformin Hcl Review and Metformin Hcl Label ), GLICLAZIDE (View Gliclazide Review and Gliclazide Label ), LANSOPRAZOLE (View Lansoprazole Review and Lansoprazole Label ), ATORVASTATIN CALCIUM (View Atorvastatin Calcium Review and Atorvastatin Calcium Label ), PROPRANOLOL (View Propranolol Review and Propranolol Label ), LOPERAMIDE (View Loperamide Review and Loperamide Label ). Patient was hospitalized.

4712111-1 | Pneumonia, Toxic Epidermal Necrolysis
Patient was taking Frusemide (View Usage). Patient experienced the following unwanted or unexpected effects: pneumonia (What is pneumonia?), toxic epidermal necrolysis on Jun 29, 2005 from Additional patient health information: Male patient , 85 years of age, was diagnosed with cardiac failure, gastritis erosive, anaemia, hypothyroidism and. Frusemide dosage: . During the same period patient was treated with CIMETIDINE (View Cimetidine Review and Cimetidine Label ), FERROUS SULFATE TAB (View Ferrous Sulfate Tab Review and Ferrous Sulfate Tab Label ), THYROXINE (View Thyroxine Review and Thyroxine Label ). Patient was hospitalized and became disabled.

4706585-X | Asthenia, Coordination Abnormal, Hyponatraemia
Adverse event was reported on Jun 27, 2005 by a Male patient taking Frusemide (View Usage) (Dosage: ) was diagnosed with immunosuppression, sleep disorder (What is sleep disorder?), pulmonary embolism (What is pulmonary embolism?), atrial fibrillation (What is atrial fibrillation?), hyperuricaemia and. Location: , 60 years of age, weighting 202.8 lb, Patient had the following side effects: asthenia, coordination abnormal, hyponatraemia. During the same period patient was treated with FLUOXETINE (View Fluoxetine Review and Fluoxetine Label ), MYCOPHENOLATE MOFETIL (View Mycophenolate Mofetil Review and Mycophenolate Mofetil Label ), PREDNISOLONE (View Prednisolone Review and Prednisolone Label ), DIAZEPAM (View Diazepam Review and Diazepam Label ), WARFARIN (View Warfarin Review and Warfarin Label ), SOTALOL HCL (View Sotalol Hcl Review and Sotalol Hcl Label ), ALLOPURINOL (View Allopurinol Review and Allopurinol Label ), DIGOXIN (View Digoxin Review and Digoxin Label ). Patient was hospitalized.

4691724-X | Encephalopathy, Gastrointestinal Haemorrhage, Hepatic Cirrhosis, Hepatic Failure, Hepatitis, Varices Oesophageal
on Jun 07, 2005 Male patient from , 66 years of age, was diagnosed with metabolic disorder (What is metabolic disorder?) and was treated with Frusemide (View Usage). After Frusemide was administered, patient had the following side effects: encephalopathy, gastrointestinal haemorrhage, hepatic cirrhosis, hepatic failure, hepatitis (What is hepatitis?), varices oesophageal. Frusemide dosage: . During the same period patient was treated with AMIODARONE (View Amiodarone Review and Amiodarone Label ), OMEPRAZOLE (View Omeprazole Review and Omeprazole Label ), SIMVASTATIN (View Simvastatin Review and Simvastatin Label ).

4691723-8 | Prothrombin Time Shortened
on Jun 07, 2005 Male patient from , 77 years of age, was diagnosed with cardiac failure congestive, arrhythmia (What is arrhythmia?), candidiasis and was treated with Frusemide (View Usage). Patient experienced the following unwanted or unexpected effects: prothrombin time shortened. Frusemide dosage: . During the same period patient was treated with AMIODARONE (View Amiodarone Review and Amiodarone Label ), WARFARIN SODIUM (View Warfarin Sodium Review and Warfarin Sodium Label ), DAKTARIN ORAL GEL (View Daktarin Oral Gel Review and Daktarin Oral Gel Label ).

4691722-6 | Bradycardia, Hypoxia, Nausea, Orthostatic Hypotension, Pallor, Pulmonary Fibrosis, Syncope
Patient was taking Frusemide (View Usage). Patient had the following side effects: bradycardia, hypoxia, nausea (What is nausea?), orthostatic hypotension, pallor, pulmonary fibrosis (What is pulmonary fibrosis?), syncope on Jun 07, 2005 from Additional patient health information: Male patient , 83 years of age, . Frusemide dosage: . During the same period patient was treated with INDAPAMIDE (View Indapamide Review and Indapamide Label ), PRAZOSIN HCL (View Prazosin Hcl Review and Prazosin Hcl Label ), AMIODARONE (View Amiodarone Review and Amiodarone Label ), ROFECOXIB (View Rofecoxib Review and Rofecoxib Label ), GLIPIZIDE (View Glipizide Review and Glipizide Label ), PANTOPRAZOLE (View Pantoprazole Review and Pantoprazole Label ), RAMIPRIL (View Ramipril Review and Ramipril Label ).

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To find out about documented side effects or safety concerns read either the drug label or the drug's package insert. You may also want to speak with your pharmacist or healthcare provider. All medicines have benefits and risks. The risks are the chances that something unwanted or unexpected could happen to you when you use them. You can protect yourself by searching summaries of recent safety alerts, adverse reports. Sometimes there are risks that only come to light after a medical product gets on the market and is used in a larger number of patients, for a longer period of time, and in patients whose health characteristics are different from those of the patients studied before approval.

Be aware of the following potential Frusemide risks to be aware of: 1. Watch for any Serious adverse events, such as life-threatening situation, which can require an admission to hospital or longer-than-expected hospital stay, permanent disability, birth defect, miscarriage, stillbirth, or birth with serious disease requires medical care to prevent permanent damage
2. Any potential Frusemide quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Frusemide use error: mixing up products with similar drug names or packaging, taking wrong dose of a drug because of confusing dosing instructions on label
4. When applicable, Problems with different manufacturer of same medicine: not getting same results from a generic drug as a brand name drug, or from another generic

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Frusemide Reactions
Acute Myocardial Infarction
Alanine Aminotransferase Increased
Blood Potassium Increased
Bradycardia
Burning Sensation
Cardiac ArrestWhat is Cardiac arrest?
Colon Cancer
Convulsion
Dehydration
DizzinessWhat is Dizziness?
Dyspnoea
FallWhat is Fall?
Gastrointestinal Haemorrhage
Hyperglycaemia
Hyperthermia
Hyperthermia Malignant
Hyperthyroidism
Hypotension
Lactic Acidosis
Laryngeal Oedema
Laryngospasm
Loss Of Consciousness
Lower Respiratory Tract Infection
Malaise
Musculoskeletal Stiffness
Overdose
Pulmonary FibrosisWhat is Pulmonary fibrosis?
Pulmonary Oedema
Renal Failure
Renal Failure Acute
Frusemide Side Effects Notice - The material on this site is for informational purposes only, and is not a substitute for medical advice, diagnosis or treatment provided by a qualified health care provider. PatientsVille.com does not provide medical advice, diagnosis or treatment. The information regarding Frusemide adverse reports, reviews and polls contained on PatientsVille.com site has not been scientifically or otherwise verified as to a cause and effect relationship and cannot be used to estimate the incidence of adverse drug reactions or for establishing or changing of patient treatments. Thank you for visiting Patientsville.com!