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This is very effective. I've used Lasix to lower down my blood pressure....Keep Reading

metoprolol seems to cause my BP to drop too lw and makes me dizzy....Keep Reading

feet swollen 3x size.. not supposed to take lasix or K with ...Keep Reading

Have been on Orencia several mo,s and developed lower leg edema 3+ and ...Keep Reading

Head Aches, stomach cramps, nausea and lethargic, normally suffer with high ...Keep Reading

Initially a great releif with not being out of breathwith the slightest exertion, ...Keep Reading

Try co-pretor. The swelling is a known side-effect, if you continue with ...Keep Reading

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Indicate Your Lasix Side Effects
Shortness Of Breath (3)
Sever Dehydration (2)
Shortness Of Breath, Sever Dehydration (2)
Anorexia (1)
Bradycardia Blood Urea Increase Stevens -johnson S (1)
CANT SLEEP (1)
Glare (1)
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Common Lasix Side Effects

top 5 Lasix|Shortness |Sever dehy|Shortness |Anorexia|Bradycardi|CANT SLEEP|Glare adverse effects>>See All Lasix Side Effects

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Lasix adverse events reported to FDA.

Have You Experienced unusual Lasix symptoms? PatientsVille.com collects and analyzes Lasix side effect and adverse reports submitted by Lasix users, such as renal failure, elevated bun and creatinine,extreme fatigue,anorexia,nausea|difficulties with breathing and vomiting |Muscle spasms across back, into R kidney|.

Summary

FDA Adverse Reports: 910. View All

Lasix FDA safety alerts: No

Reported deaths: 148

Reported hospitalizations: 550

Lasix Dosage, Warnings, Usage.

Post Your Unusual Symptoms:

Most Reported
1Shortness Of Breath, Sever Dehydration
2Shortness Of Breath
3Sever Dehydration
4Glare
5Starbursts Around Night Lights
6One Vitr
7Glare, Starbursts Around Night Lights And One Vitr
8Renal Failure Acute, Bradycardia Blood Urea Increase Stevens -johnson Syndrome
9Glare, Starbursts Around Night Lights And One Vitreous Gel Detachment
10Severe Morning Constipation/Using Duphalac
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Recent Drug Reports

renal failure, elevated bun and creatinine,extreme fatigue,anorexia,nausea

difficulties with breathing and vomiting

Muscle spasms across back, into R kidney

More Lasix Side Effect Reports

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Often additional risks of using a medication, such as Lasix, 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 Lasix users, Learn more about unwanted side effects & find ways to reduce them. Browse Lasix Adverse Reports reported to FDA and participate in Lasix discussion, find alternative treatments and find ways to avoid or reduce risks associated with using Lasix. 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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Lasix Adverse Effect Reports (FDA)

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6843699-2 | Convulsion, Heart Rate Decreased
on Jul 06, 2010 Female patient from JAPAN , 80 years of age, was diagnosed with oedema, angina pectoris and was treated with Lasix (View Usage). Patient experienced the following unwanted or unexpected effects: convulsion, heart rate decreased. Lasix dosage: . During the same period patient was treated with LANIRAPID (View Lanirapid Review and Lanirapid Label ).

6840131-X | Abasia, Abdominal Pain, Confusional State, Feeling Abnormal, Oedema Peripheral, Urine Output Decreased
Patient was taking Lasix (View Usage). Patient had the following side effects: abasia, abdominal pain (What is abdominal pain?), confusional state, feeling abnormal, oedema peripheral, urine output decreased on Jul 13, 2010 from UNITED STATES Additional patient health information: Female patient , weighting 204.0 lb, was diagnosed with cardiac failure congestive and. Lasix dosage: Lasix Once A Day. During the same period patient was treated with TRIAMETERENE 37.5MG + HCTZ 25MG (Triameterene + Hctz Once A Day) (View Triameterene 37.5mg + Hctz 25mg Review and Triameterene 37.5mg + Hctz 25mg Label ).

6836511-9 | Hypokalaemia, Off Label Use, Pseudo-bartter Syndrome
Adverse event was reported on Jul 07, 2010 by a Female patient taking Lasix (View Usage) (Dosage: Once Or Twice A Week.) was diagnosed with oedema and. Location: JAPAN , 33 years of age, After Lasix was administered, patient had the following side effects: hypokalaemia, off label use, pseudo-bartter syndrome. During the same period patient was treated with SLOW K (View Slow-k Review and Slow-k Label ).

6831700-1 | Diarrhoea, Normochromic Normocytic Anaemia, Renal Failure Acute
on Jun 28, 2010 Male patient from FRANCE , 61 years of age, weighting 154.3 lb, was treated with Lasix (View Usage). Patient experienced the following unwanted or unexpected effects: diarrhoea, normochromic normocytic anaemia, renal failure acute. Lasix dosage: . During the same period patient was treated with TRIATEC (View Triatec Review and Triatec Label ), MYFORTIC (View Myfortic Review and Myfortic Label ), TARDYFERON B(9) (View Tardyferon B(9) Review and Tardyferon B(9) Label ), SODIUM BICARBONATE (View Sodium Bicarbonate Review and Sodium Bicarbonate Label ), EUPRESSYL (View Eupressyl Review and Eupressyl Label ), AMLOR (View Amlor Review and Amlor Label ), AVLOCARDYL (View Avlocardyl Review and Avlocardyl Label ), LESCOL (View Lescol Review and Lescol Label ). Patient was hospitalized.


6831683-4 | Interstitial Lung Disease
on Apr 21, 2010 Male patient from JAPAN , 62 years of age, was treated with Lasix (View Usage). Patient had the following side effects: interstitial lung disease. Lasix dosage: . During the same period patient was treated with TAXOTERE (View Taxotere Review and Taxotere Label ), NORVASC (View Norvasc Review and Norvasc Label ), CRESTOR (View Crestor Review and Crestor Label ). Patient was hospitalized.

6814386-1 | Febrile Neutropenia
Patient was taking Lasix (View Usage). After Lasix was administered, patient had the following side effects: febrile neutropenia on Jun 28, 2010 from FRANCE Additional patient health information: Male patient , 70 years of age, . Lasix dosage: . During the same period patient was treated with BACTRIM (View Bactrim Review and Bactrim Label ), ACYCLOVIR (View Acyclovir Review and Acyclovir Label ), VANCOMYCIN HCL (View Vancomycin Hcl Review and Vancomycin Hcl Label ), PIPERACILLIN (View Piperacillin Review and Piperacillin Label ), ESOMEPRAZOLE MAGNESIUM (View Esomeprazole Magnesium Review and Esomeprazole Magnesium Label ), ARANESP (View Aranesp Review and Aranesp Label ), GRANOCYTE (View Granocyte Review and Granocyte Label ), GENTAMICIN (View Gentamicin Review and Gentamicin Label ). Patient was hospitalized.

6809681-6 | Asthenia, Blood Glucose Decreased, Fall, Gastrointestinal Disorder, Hypotension, Injury, Loss Of Consciousness
Adverse event was reported on Jun 17, 2010 by a Male patient taking Lasix (View Usage) (Dosage: ) was diagnosed with hypertension and. Location: UNITED STATES , 74 years of age, Patient experienced the following unwanted or unexpected effects: asthenia, blood glucose decreased, fall (What is fall?), gastrointestinal disorder, hypotension, injury, loss of consciousness. During the same period patient was treated with DIGOXIN (View Digoxin Review and Digoxin Label ), COUMADIN (View Coumadin Review and Coumadin Label ), ATORVASTATIN CALCIUM (View Atorvastatin Calcium Review and Atorvastatin Calcium Label ), POTASSIUM (View Potassium Review and Potassium Label ). Patient was hospitalized.

6802942-6 | Cataract, Intraocular Pressure Increased, Pigmentation Disorder, Retinal Haemorrhage
on Jun 18, 2010 Female patient from JAPAN , 46 years of age, was treated with Lasix (View Usage). Patient had the following side effects: cataract (What is cataract?), intraocular pressure increased, pigmentation disorder, retinal haemorrhage. Lasix dosage: . During the same period patient was treated with ATELEC (View Atelec Review and Atelec Label ), LONGES (View Longes Review and Longes Label ), BASEN (View Basen Review and Basen Label ), EPADEL (View Epadel Review and Epadel Label ).

6802923-2 | Dizziness, Hypotension, Malaise, Sinus Bradycardia
on Jun 17, 2010 Male patient from ITALY , 93 years of age, was diagnosed with hypertension, benign prostatic hyperplasia and was treated with Lasix (View Usage). After Lasix was administered, patient had the following side effects: dizziness (What is dizziness?), hypotension, malaise, sinus bradycardia. Lasix dosage: Dose:1 Unit(s). During the same period patient was treated with ZESTORETIC (Dose:.5 Unit(s)) (View Zestoretic Review and Zestoretic Label ), TERAPROST (Dose:1 Unit(s)) (View Teraprost Review and Teraprost Label ), TICLOPIDINE HCL (View Ticlopidine Hcl Review and Ticlopidine Hcl Label ), OMEPRAZOLE (View Omeprazole Review and Omeprazole Label ), AVODART (View Avodart Review and Avodart Label ), SIVASTIN (View Sivastin Review and Sivastin Label ), LENDORMIN (View Lendormin Review and Lendormin Label ), NITRODERM (View Nitroderm Review and Nitroderm Label ). Patient was hospitalized.

6801301-X | Anaemia, Renal Failure
Patient was taking Lasix (View Usage). Patient experienced the following unwanted or unexpected effects: anaemia, renal failure on Jun 21, 2010 from UNITED STATES Additional patient health information: Male patient , 76 years of age, . Lasix dosage: . During the same period patient was treated with ADVAIR DISKUS 100/50 (100/50 Mcg Strength Dose:2 Puff(s)) (View Advair Diskus 100/50 Review and Advair Diskus 100/50 Label ). Patient was hospitalized.

6801294-5 | Cheilitis, Dermatitis Exfoliative, Eczema, Eczema Asteatotic, Pruritus, Skin Lesion, Weight Decreased
Adverse event was reported on Jun 17, 2010 by a Male patient taking Lasix (View Usage) (Dosage: ) . Location: FRANCE , 89 years of age, Patient had the following side effects: cheilitis, dermatitis exfoliative, eczema (What is eczema?), eczema asteatotic, pruritus, skin lesion, weight decreased. During the same period patient was treated with AERIUS (View Aerius Review and Aerius Label ), ATARAX (View Atarax Review and Atarax Label ), MONO TILDIEM LP (View Mono Tildiem Lp Review and Mono Tildiem Lp Label ), NITRODERM (View Nitroderm Review and Nitroderm Label ), PREVISCAN (View Previscan Review and Previscan Label ), ZOLPIDEM (View Zolpidem Review and Zolpidem Label ). Patient was hospitalized.

6801291-X | Hypokalaemia, Off Label Use, Pseudo-bartter Syndrome
on Jun 23, 2010 Female patient from JAPAN , 33 years of age, was diagnosed with oedema and was treated with Lasix (View Usage). After Lasix was administered, patient had the following side effects: hypokalaemia, off label use, pseudo-bartter syndrome. Lasix dosage: Once Or Twice A Week.. During the same period patient was treated with SLOW K (View Slow-k Review and Slow-k Label ).

6801256-8 | International Normalised Ratio Increased
on Jun 18, 2010 Male patient from ITALY , 79 years of age, was treated with Lasix (View Usage). Patient experienced the following unwanted or unexpected effects: international normalised ratio increased. Lasix dosage: . During the same period patient was treated with COUMADIN (View Coumadin Review and Coumadin Label ), AMOXICILLIN (View Amoxicillin Review and Amoxicillin Label ), SELES BETA (View Seles Beta Review and Seles Beta Label ), AMLODIPINE BESYLATE (View Amlodipine Besylate Review and Amlodipine Besylate Label ), MONOCINQUE (Dose:1 Unit(s)) (View Monocinque Review and Monocinque Label ), ROSUVASTATIN (Dose:1 Unit(s)) (View Rosuvastatin Review and Rosuvastatin Label ), ASPIRIN (Dose:1 Unit(s)) (View Aspirin Review and Aspirin Label ), OMEPRAZEN (Dose:1 Unit(s)) (View Omeprazen Review and Omeprazen Label ).

6790326-9 | Bradycardia, Hypotension, Malaise
Patient was taking Lasix (View Usage). Patient had the following side effects: bradycardia, hypotension, malaise on Jun 15, 2010 from FRANCE Additional patient health information: Female patient , 92 years of age, . Lasix dosage: . During the same period patient was treated with PERINDOPRIL (View Perindopril Review and Perindopril Label ), BISOPROLOL (View Bisoprolol Review and Bisoprolol Label ), KARDEGIC (View Kardegic Review and Kardegic Label ). Patient was hospitalized.

6790316-6 | Convulsion, Depressed Level Of Consciousness, Hypertension, Reversible Posterior Leukoencephalopathy Syndrome, Visual Impairment, Vomiting
Adverse event was reported on Jun 15, 2010 by a Female patient taking Lasix (View Usage) (Dosage: ) . Location: FRANCE , 45 years of age, After Lasix was administered, patient had the following side effects: convulsion, depressed level of consciousness, hypertension, reversible posterior leukoencephalopathy syndrome, visual impairment, vomiting. During the same period patient was treated with TRIATEC (View Triatec Review and Triatec Label ), GARDENAL (View Gardenal Review and Gardenal Label ), EUPRESSYL (View Eupressyl Review and Eupressyl Label ), HYPERIUM (View Hyperium Review and Hyperium Label ), ATENOLOL (View Atenolol Review and Atenolol Label ), SOLU MEDROL (View Solu-medrol Review and Solu-medrol Label ). Patient was hospitalized.

6783488-0 | International Normalised Ratio Increased
on Jun 15, 2010 Female patient from ITALY , 79 years of age, was diagnosed with pulmonary oedema, atrial fibrillation (What is atrial fibrillation?) and was treated with Lasix (View Usage). Patient experienced the following unwanted or unexpected effects: international normalised ratio increased. Lasix dosage: . During the same period patient was treated with COUMADIN (View Coumadin Review and Coumadin Label ), LEVOTHYROXINE SODIUM (View Levothyroxine Sodium Review and Levothyroxine Sodium Label ), BISOPROLOL (View Bisoprolol Review and Bisoprolol Label ), VALPROATE SODIUM/VALPROIC ACID (View Valproate Sodium/valproic Acid Review and Valproate Sodium/valproic Acid Label ), VALPRESSION (View Valpression Review and Valpression Label ), CALCITRIOL (View Calcitriol Review and Calcitriol Label ), AMIODARONE HCL (View Amiodarone Hcl Review and Amiodarone Hcl Label ).

6783467-3 | Fall, Orthostatic Hypotension, Traumatic Brain Injury
on Jun 14, 2010 Female patient from FRANCE , 79 years of age, was treated with Lasix (View Usage). Patient had the following side effects: fall (What is fall?), orthostatic hypotension, traumatic brain injury (What is traumatic brain injury?). Lasix dosage: Dose Unit: 40 Mg. During the same period patient was treated with TAREG (View Tareg Review and Tareg Label ), MONICOR (Dose Unit: 20 Mg) (View Monicor Review and Monicor Label ), VASTAREL ^BIOPHARMA^ (View Vastarel ^biopharma^ Review and Vastarel ^biopharma^ Label ), RISPERDAL (Dose Unit: 1 Mg) (View Risperdal Review and Risperdal Label ), SOTALOL (View Sotalol Review and Sotalol Label ). Patient was hospitalized.

6781528-6 | Abasia, Abdominal Discomfort, Diarrhoea, Muscle Spasms, Oedema Peripheral
Patient was taking Lasix (View Usage). After Lasix was administered, patient had the following side effects: abasia, abdominal discomfort, diarrhoea, muscle spasms, oedema peripheral on Jun 17, 2010 from UNITED STATES Additional patient health information: Female patient , weighting 206.0 lb, was diagnosed with fluid retention, pollakiuria, pulmonary hypertension (What is pulmonary hypertension?) and. Lasix dosage: .

6781454-2 | Dementia, Renal Impairment
Adverse event was reported on Jun 09, 2010 by a Female patient taking Lasix (View Usage) (Dosage: ) . Location: JAPAN , 88 years of age, Patient experienced the following unwanted or unexpected effects: dementia (What is dementia?), renal impairment. During the same period patient was treated with ALDACTONE (View Aldactone Review and Aldactone Label ).

6781449-9 | Fall, Fracture
on Jun 14, 2010 Female patient from FRANCE , 86 years of age, was treated with Lasix (View Usage). Patient had the following side effects: fall (What is fall?), fracture (What is fracture?). Lasix dosage: Dose Unit: 40 Mg. During the same period patient was treated with RENITEC /NET/ (Dose Unit: 5 Mg) (View Renitec /net/ Review and Renitec /net/ Label ), LANZOR (View Lanzor Review and Lanzor Label ), FOSAMAX (View Fosamax Review and Fosamax Label ), SINTROM (View Sintrom Review and Sintrom Label ). Patient was hospitalized.

6779492-9 | Axonal Neuropathy, Blood Creatine Phosphokinase Increased, Myalgia, Osteoporosis, Renal Failure Chronic
on Jun 09, 2010 Female patient from FRANCE , 69 years of age, weighting 130.1 lb, was diagnosed with osteoporosis (What is osteoporosis?), gastroduodenal ulcer and was treated with Lasix (View Usage). After Lasix was administered, patient had the following side effects: axonal neuropathy, blood creatine phosphokinase increased, myalgia, osteoporosis (What is osteoporosis?), renal failure chronic. Lasix dosage: . During the same period patient was treated with ALLOPURINOL (View Allopurinol Review and Allopurinol Label ), ROSUVASTATIN (View Rosuvastatin Review and Rosuvastatin Label ), STRONTIUM RANELATE (View Strontium Ranelate Review and Strontium Ranelate Label ), INIPOMP (View Inipomp Review and Inipomp Label ), PREDNISONE (View Prednisone Review and Prednisone Label ), DIFFU K (View Diffu K Review and Diffu K Label ), VERAPAMIL (View Verapamil Review and Verapamil Label ). Patient was hospitalized.

6766214-0 | Activities Of Daily Living Impaired, Aortic Stenosis, Back Pain, Cardiac Arrest, Cardiac Failure, Chronic Obstructive Pulmonary Disease, Cough, Depression, Hypertension
Patient was taking Lasix (View Usage). Patient experienced the following unwanted or unexpected effects: activities of daily living impaired, aortic stenosis, back pain (What is back pain?), cardiac arrest (What is cardiac arrest?), cardiac failure, chronic obstructive pulmonary disease, cough, depression (What is depression?), hypertension on Jun 08, 2010 from UNITED STATES Additional patient health information: Female patient , 72 years of age, weighting 173.5 lb, was diagnosed with lipids abnormal, arthritis (What is arthritis?), hypertension, insomnia, pain (What is pain?) and. Lasix dosage: . During the same period patient was treated with LIPITOR (View Lipitor Review and Lipitor Label ), CELEBREX (View Celebrex Review and Celebrex Label ), NORVASC (View Norvasc Review and Norvasc Label ), VERAPAMIL (View Verapamil Review and Verapamil Label ), TRAZODONE (View Trazodone Review and Trazodone Label ), HYDROCODONE (Dose:7.5 Unit(s)) (View Hydrocodone Review and Hydrocodone Label ). Patient was hospitalized.

6760176-8 | Atrial Fibrillation
Adverse event was reported on May 27, 2010 by a Male patient taking Lasix (View Usage) (Dosage: ) . Location: UNITED STATES , 83 years of age, Patient had the following side effects: atrial fibrillation (What is atrial fibrillation?). During the same period patient was treated with WARFARIN SODIUM (View Warfarin Sodium Review and Warfarin Sodium Label ), DIGOXIN (View Digoxin Review and Digoxin Label ), VITAMINS (View Vitamins Review and Vitamins Label ).

6760166-5 | Grand Mal Convulsion, Hypocalcaemia, Hypokalaemia, Hypomagnesaemia, Pseudoaldosteronism
on May 27, 2010 Female patient from JAPAN , 87 years of age, was diagnosed with dementia (What is dementia?) and was treated with Lasix (View Usage). After Lasix was administered, patient had the following side effects: grand mal convulsion, hypocalcaemia, hypokalaemia, hypomagnesaemia, pseudoaldosteronism. Lasix dosage: . During the same period patient was treated with GLYCYRRHIZIC ACID (View Glycyrrhizic Acid Review and Glycyrrhizic Acid Label ). Patient was hospitalized.

6756042-4 | Pneumonia, Pyrexia
on May 26, 2010 Male patient from JAPAN , 65 years of age, was treated with Lasix (View Usage). Patient experienced the following unwanted or unexpected effects: pneumonia (What is pneumonia?), pyrexia. Lasix dosage: . During the same period patient was treated with ASPIRIN (View Aspirin Review and Aspirin Label ), WARFARIN SODIUM (View Warfarin Sodium Review and Warfarin Sodium Label ), OLMETEC (View Olmetec Review and Olmetec Label ), SUNRYTHM (View Sunrythm Review and Sunrythm Label ), LANIRAPID (View Lanirapid Review and Lanirapid Label ).

6753660-4 | Haemoglobin Decreased
Patient was taking Lasix (View Usage). Patient had the following side effects: haemoglobin decreased on May 17, 2010 from JAPAN Additional patient health information: Female patient , 94 years of age, was diagnosed with hypertension and. Lasix dosage: Start Date: At Least 2 Years Ago. During the same period patient was treated with DIOVAN (Start Date: Quite A Long Time Ago) (View Diovan Review and Diovan Label ). Patient was hospitalized.

6751167-1 | Malaise
Adverse event was reported on May 21, 2010 by a Female patient taking Lasix (View Usage) (Dosage: ) was diagnosed with osteoarthritis (What is osteoarthritis?) and. Location: UNITED STATES , 78 years of age, weighting 169.1 lb, After Lasix was administered, patient had the following side effects: malaise. During the same period patient was treated with NEXIUM /UNK/ (View Nexium /unk/ Review and Nexium /unk/ Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), ATENOLOL (View Atenolol Review and Atenolol Label ), SYNTHROID (View Synthroid Review and Synthroid Label ), VERAPAMIL (View Verapamil Review and Verapamil Label ), LISINOPRIL (View Lisinopril Review and Lisinopril Label ), SIMVASTATIN (View Simvastatin Review and Simvastatin Label ). Patient was hospitalized.

6742066-X | Coma, Overdose
on May 18, 2010 Female patient from FRANCE , 77 years of age, was diagnosed with agitation, insomnia and was treated with Lasix (View Usage). Patient experienced the following unwanted or unexpected effects: coma, overdose. Lasix dosage: . During the same period patient was treated with MEPRONIZINE (View Mepronizine Review and Mepronizine Label ), SECTRAL (View Sectral Review and Sectral Label ), TOPALGIC (View Topalgic Review and Topalgic Label ), TERCIAN (Dose:40 Milligram(s)/millilitre) (View Tercian Review and Tercian Label ), LOXAPAC (View Loxapac Review and Loxapac Label ), TRIHEXYPHENIDYL HCL (View Trihexyphenidyl Hcl Review and Trihexyphenidyl Hcl Label ).

6742051-8 | Cytolytic Hepatitis, Pancreatitis Acute
on May 18, 2010 Female patient from FRANCE , 76 years of age, was treated with Lasix (View Usage). Patient had the following side effects: cytolytic hepatitis, pancreatitis acute. Lasix dosage: . During the same period patient was treated with PREDNISONE TAB (View Prednisone Tab Review and Prednisone Tab Label ), TAHOR (View Tahor Review and Tahor Label ), ZOPICLONE (View Zopiclone Review and Zopiclone Label ), ATENOLOL (View Atenolol Review and Atenolol Label ), AMLOR (View Amlor Review and Amlor Label ), OMEPRAZOLE (View Omeprazole Review and Omeprazole Label ), OROCAL D(3) (View Orocal D(3) Review and Orocal D(3) Label ), MINISINTROM (View Minisintrom Review and Minisintrom Label ).

6723212-0 | Fall, Haematoma, Pubis Fracture, Traumatic Brain Injury
Patient was taking Lasix (View Usage). After Lasix was administered, patient had the following side effects: fall (What is fall?), haematoma, pubis fracture, traumatic brain injury (What is traumatic brain injury?) on Apr 29, 2010 from FRANCE Additional patient health information: Female patient , 89 years of age, . Lasix dosage: . During the same period patient was treated with DIFFU K (View Diffu K Review and Diffu K Label ), ALLOPURINOL (View Allopurinol Review and Allopurinol Label ), PREVISCAN (View Previscan Review and Previscan Label ), COVERSYL 2 MG TABLET (Daily Dose: 2 Milligram(s)) (View Coversyl 2 Mg Tablet Review and Coversyl 2 Mg Tablet Label ). Patient was hospitalized.

6711376-4 | Heart Rate Increased, Hyperthermia, Pruritus
Adverse event was reported on Apr 29, 2010 by a Female patient taking Lasix (View Usage) (Dosage: ) was diagnosed with ascites and. Location: FRANCE , 16 years of age, Patient experienced the following unwanted or unexpected effects: heart rate increased, hyperthermia, pruritus. During the same period patient was treated with ALBUMIN HUMAN ^MERIEUX^ (Dose:200 Milligram(s)/millilitre) (View Albumin Human ^merieux^ Review and Albumin Human ^merieux^ Label ). Patient was hospitalized.

6709937-1 | Hallucination, Auditory, Tinnitus
on Jan 28, 2010 Female patient from FRANCE , 83 years of age, was treated with Lasix (View Usage). Patient had the following side effects: hallucination, auditory, tinnitus (What is tinnitus?). Lasix dosage: .

6706162-5 | International Normalised Ratio Increased
on Apr 28, 2010 Male patient from ITALY , 79 years of age, was treated with Lasix (View Usage). After Lasix was administered, patient had the following side effects: international normalised ratio increased. Lasix dosage: . During the same period patient was treated with COUMADIN (View Coumadin Review and Coumadin Label ), AMOXICILLIN (View Amoxicillin Review and Amoxicillin Label ), SELES BETA (View Seles Beta Review and Seles Beta Label ), AMLODIPINE BESYLATE (View Amlodipine Besylate Review and Amlodipine Besylate Label ), MONOCINQUE (Dose:1 Unit(s)) (View Monocinque Review and Monocinque Label ), ROSUVASTATIN (Dose:1 Unit(s)) (View Rosuvastatin Review and Rosuvastatin Label ), ASPIRIN (Dose:1 Unit(s)) (View Aspirin Review and Aspirin Label ), OMEPRAZEN (Dose:1 Unit(s)) (View Omeprazen Review and Omeprazen Label ).

6703798-2 | Cataract, Intraocular Pressure Increased, Pigmentation Disorder, Retinal Haemorrhage
Patient was taking Lasix (View Usage). Patient experienced the following unwanted or unexpected effects: cataract (What is cataract?), intraocular pressure increased, pigmentation disorder, retinal haemorrhage on Apr 26, 2010 from JAPAN Additional patient health information: Female patient , 46 years of age, . Lasix dosage: .

6703783-0 | Toxic Epidermal Necrolysis
Adverse event was reported on Apr 20, 2010 by a Female patient taking Lasix (View Usage) (Dosage: ) . Location: FRANCE , 87 years of age, Patient had the following side effects: toxic epidermal necrolysis. During the same period patient was treated with ZYLORIC ^GLAXO WELLCOME^ (View Zyloric ^glaxo Wellcome^ Review and Zyloric ^glaxo Wellcome^ Label ), DIAMICRON (View Diamicron Review and Diamicron Label ), FENOFIBRATE (View Fenofibrate Review and Fenofibrate Label ), COTRIATEC, COMPRIME (View Cotriatec, Comprime Review and Cotriatec, Comprime Label ), ASPEGIC 1000 (View Aspegic 1000 Review and Aspegic 1000 Label ), TAHOR (View Tahor Review and Tahor Label ), VASTAREL ^SERVIER^ (View Vastarel ^servier^ Review and Vastarel ^servier^ Label ), NOVONORM (View Novonorm Review and Novonorm Label ). Patient was hospitalized.

6703759-3 | Renal Failure Acute
on Apr 19, 2010 Female patient from UNITED STATES , 60 years of age, was diagnosed with rheumatoid arthritis (What is rheumatoid arthritis?) and was treated with Lasix (View Usage). After Lasix was administered, patient had the following side effects: renal failure acute. Lasix dosage: Dose As Used: Unk. During the same period patient was treated with METHOTREXATE (View Methotrexate Review and Methotrexate Label ), FOLIC ACID (View Folic Acid Review and Folic Acid Label ), ADVAIR DISKUS 100/50 (View Advair Diskus 100/50 Review and Advair Diskus 100/50 Label ), CARVEDILOL (View Carvedilol Review and Carvedilol Label ), MONTELUKAST SODIUM (View Montelukast Sodium Review and Montelukast Sodium Label ), WARFARIN SODIUM (View Warfarin Sodium Review and Warfarin Sodium Label ). Patient was hospitalized.

6700157-3 | Hepatic Enzyme Abnormal
on Mar 25, 2010 Male patient from FRANCE , 75 years of age, was diagnosed with hepatitis b (What is hepatitis b?) and was treated with Lasix (View Usage). Patient experienced the following unwanted or unexpected effects: hepatic enzyme abnormal. Lasix dosage: . During the same period patient was treated with RULID (View Rulid Review and Rulid Label ), CALCIUM CARBONATE (View Calcium Carbonate Review and Calcium Carbonate Label ), ALLOPURINOL (View Allopurinol Review and Allopurinol Label ), LEXOMIL (View Lexomil Review and Lexomil Label ), METEOXANE (View Meteoxane Review and Meteoxane Label ), MYFORTIC (View Myfortic Review and Myfortic Label ), HYPERIUM (View Hyperium Review and Hyperium Label ), ZEFFIX (View Zeffix Review and Zeffix Label ). Patient was hospitalized.

6694023-X |
Patient was taking Lasix (View Usage). on Apr 14, 2010 from AUSTRALIA Additional patient health information: Female patient , 64 years of age, was diagnosed with hypertension, bipolar disorder (What is bipolar disorder?), iron deficiency and. Lasix dosage: . During the same period patient was treated with PERINDOPRIL (View Perindopril Review and Perindopril Label ), CLOPINE (View Clopine Review and Clopine Label ), EPILIM (View Epilim Review and Epilim Label ), FERROUS FUMARATE/FOLIC ACID (View Ferrous Fumarate/folic Acid Review and Ferrous Fumarate/folic Acid Label ).

6689926-6 | Renal Failure Acute
Adverse event was reported on Apr 20, 2010 by a Male patient taking Lasix (View Usage) (Dosage: ) . Location: FRANCE , 77 years of age, After Lasix was administered, patient had the following side effects: renal failure acute. Patient was hospitalized.

6689917-5 | International Normalised Ratio Increased
on Apr 13, 2010 Male patient from FRANCE , 85 years of age, was treated with Lasix (View Usage). Patient experienced the following unwanted or unexpected effects: international normalised ratio increased. Lasix dosage: . During the same period patient was treated with PREVISCAN (View Previscan Review and Previscan Label ), EUPANTOL (View Eupantol Review and Eupantol Label ), METFORMIN HCL (View Metformin Hcl Review and Metformin Hcl Label ), HEMIGOXINE NATIVELLE (View Hemigoxine Nativelle Review and Hemigoxine Nativelle Label ). Patient was hospitalized.

6688178-0 | Bradycardia, Hyperkalaemia, Renal Failure
on Apr 13, 2010 Male patient from FRANCE , 79 years of age, was treated with Lasix (View Usage). Patient had the following side effects: bradycardia, hyperkalaemia, renal failure. Lasix dosage: . During the same period patient was treated with COVERSYL /FRA/ (View Coversyl /fra/ Review and Coversyl /fra/ Label ), ALDACTONE (View Aldactone Review and Aldactone Label ), AMIODARONE (View Amiodarone Review and Amiodarone Label ), CARDENSIEL (View Cardensiel Review and Cardensiel Label ), INEGY (View Inegy Review and Inegy Label ), DOXAZOSIN (View Doxazosin Review and Doxazosin Label ), BUFLOMEDIL (View Buflomedil Review and Buflomedil Label ), PREVISCAN (View Previscan Review and Previscan Label ). Patient was hospitalized.

6688172-X | Cerebral Infarction
Patient was taking Lasix (View Usage). After Lasix was administered, patient had the following side effects: cerebral infarction on Apr 12, 2010 from JAPAN Additional patient health information: Male patient , 62 years of age, weighting 165.3 lb, . Lasix dosage: . During the same period patient was treated with ALDACTONE (View Aldactone Review and Aldactone Label ), PLAVIX (View Plavix Review and Plavix Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), HEPARIN (Dose:10000 Unit(s)) (View Heparin Review and Heparin Label ). Patient was hospitalized.

6682663-3 | Toxic Epidermal Necrolysis
Adverse event was reported on Apr 02, 2010 by a Female patient taking Lasix (View Usage) (Dosage: ) . Location: FRANCE , 87 years of age, Patient experienced the following unwanted or unexpected effects: toxic epidermal necrolysis. During the same period patient was treated with ZYLORIC ^GLAXO WELLCOME^ (View Zyloric ^glaxo Wellcome^ Review and Zyloric ^glaxo Wellcome^ Label ), DIAMICRON (View Diamicron Review and Diamicron Label ), FENOFIBRATE (View Fenofibrate Review and Fenofibrate Label ), COTRIATEC, COMPRIME (View Cotriatec, Comprime Review and Cotriatec, Comprime Label ), ASPEGIC 1000 (View Aspegic 1000 Review and Aspegic 1000 Label ), TAHOR (View Tahor Review and Tahor Label ), VASTAREL ^SERVIER^ (View Vastarel ^servier^ Review and Vastarel ^servier^ Label ), NOVONORM (View Novonorm Review and Novonorm Label ). Patient was hospitalized.

6682596-2 | Toxic Epidermal Necrolysis
on Apr 02, 2010 Male patient from JAPAN , 76 years of age, weighting 130.1 lb, was diagnosed with hypertension and was treated with Lasix (View Usage). Patient had the following side effects: toxic epidermal necrolysis. Lasix dosage: Dose Unit: 20 Mg. During the same period patient was treated with NU LOTAN (Dose Unit: 50 Mg) (View Nu-lotan Review and Nu-lotan Label ), NU LOTAN (Dose Unit: 50 Mg) (View Nu-lotan Review and Nu-lotan Label ), LIPITOR (Dose As Used: 1 Tablet/day) (View Lipitor Review and Lipitor Label ), ALLOPURINOL (Dose As Used: 1 Tablet/day) (View Allopurinol Review and Allopurinol Label ), NORVASC (Dose Unit: 5 Mg) (View Norvasc Review and Norvasc Label ), KREMEZIN (Dose Unit: 2 G) (View Kremezin Review and Kremezin Label ), FLUITRAN (Dose As Used: 0.5 Tablet/day) (View Fluitran Review and Fluitran Label ). Patient was hospitalized.

6674948-1 | Dermatitis Allergic, Eosinophilia, Pruritus, Toxic Skin Eruption
on Apr 08, 2010 Male patient from FRANCE , 80 years of age, was treated with Lasix (View Usage). After Lasix was administered, patient had the following side effects: dermatitis allergic, eosinophilia, pruritus, toxic skin eruption. Lasix dosage: . During the same period patient was treated with CORDARONE (View Cordarone Review and Cordarone Label ), LERCAN (View Lercan Review and Lercan Label ), TAHOR (View Tahor Review and Tahor Label ), ASPEGIC 1000 (View Aspegic 1000 Review and Aspegic 1000 Label ), HYPERIUM (View Hyperium Review and Hyperium Label ). Patient was hospitalized.

6674923-7 | Febrile Neutropenia
Patient was taking Lasix (View Usage). Patient experienced the following unwanted or unexpected effects: febrile neutropenia on Apr 07, 2010 from FRANCE Additional patient health information: Male patient , 70 years of age, . Lasix dosage: . During the same period patient was treated with BACTRIM (View Bactrim Review and Bactrim Label ), ACYCLOVIR SODIUM (View Acyclovir Sodium Review and Acyclovir Sodium Label ), VANCOMYCIN HCL (View Vancomycin Hcl Review and Vancomycin Hcl Label ), PIPERACILLIN (View Piperacillin Review and Piperacillin Label ), ESOMEPRAZOLE (View Esomeprazole Review and Esomeprazole Label ), ARANESP (View Aranesp Review and Aranesp Label ), GRANOCYTE (View Granocyte Review and Granocyte Label ), GENTAMICIN (View Gentamicin Review and Gentamicin Label ). Patient was hospitalized.

6673492-5 | Hypoglycaemia, Sopor
Adverse event was reported on Mar 30, 2010 by a Female patient taking Lasix (View Usage) (Dosage: Dose:1 Unit(s)) was diagnosed with diabetes mellitus and. Location: ITALY , 80 years of age, Patient had the following side effects: hypoglycaemia, sopor. During the same period patient was treated with METFORMIN (Dose:2 Unit(s)) (View Metformin Review and Metformin Label ), LEVOTHYROXINE SODIUM (Dose:1 Unit(s)) (View Levothyroxine Sodium Review and Levothyroxine Sodium Label ), MODURETIC 5 50 (Dose:1 Unit(s)) (View Moduretic 5-50 Review and Moduretic 5-50 Label ), KCL RETARD (Dose:1 Unit(s)) (View Kcl-retard Review and Kcl-retard Label ), LANSOPRAZOLE (Dose:1 Unit(s)) (View Lansoprazole Review and Lansoprazole Label ), ISOSORBIDE MONONITRATE (Dose:1 Unit(s)) (View Isosorbide Mononitrate Review and Isosorbide Mononitrate Label ), INSULIN (View Insulin Review and Insulin Label ). Patient was hospitalized.

6673478-0 | Fall, Injury, Syncope, Traumatic Fracture
on Mar 30, 2010 Female patient from ITALY , 83 years of age, was treated with Lasix (View Usage). After Lasix was administered, patient had the following side effects: fall (What is fall?), injury, syncope, traumatic fracture. Lasix dosage: . During the same period patient was treated with ATENOLOL (View Atenolol Review and Atenolol Label ), AMLODIPINE (View Amlodipine Review and Amlodipine Label ), ASPIRIN (View Aspirin Review and Aspirin Label ). Patient was hospitalized.

6669093-5 | Condition Aggravated, Confusional State, Leukopenia, Lymphopenia, Neutropenia, Renal Failure Acute
on Mar 25, 2010 Male patient from FRANCE , 80 years of age, was diagnosed with atrial fibrillation (What is atrial fibrillation?), insomnia, agitation and was treated with Lasix (View Usage). Patient experienced the following unwanted or unexpected effects: condition aggravated, confusional state, leukopenia, lymphopenia, neutropenia, renal failure acute. Lasix dosage: . During the same period patient was treated with IMOVANE (View Imovane Review and Imovane Label ), THERALENE (View Theralene Review and Theralene Label ), LANSOPRAZOLE (View Lansoprazole Review and Lansoprazole Label ), TAREG (View Tareg Review and Tareg Label ), COUMADIN (View Coumadin Review and Coumadin Label ). Patient was hospitalized.

6657588-X | Electrocardiogram Qt Prolonged, Malaise
Patient was taking Lasix (View Usage). Patient had the following side effects: electrocardiogram qt prolonged, malaise on Mar 23, 2010 from FRANCE Additional patient health information: Female patient , 84 years of age, . Lasix dosage: . During the same period patient was treated with CORDARONE (5 Times Per Week) (View Cordarone Review and Cordarone Label ), KARDEGIC (View Kardegic Review and Kardegic Label ), PREVISCAN (10 Mg Daily In Alternation With 5 Mg Daily) (View Previscan Review and Previscan Label ), ATORVASTATIN CALCIUM (View Atorvastatin Calcium Review and Atorvastatin Calcium Label ), KALEORID (View Kaleorid Review and Kaleorid Label ), PERINDOPRIL (View Perindopril Review and Perindopril Label ), LANSOPRAZOLE (View Lansoprazole Review and Lansoprazole Label ), DOLIPRANE (View Doliprane Review and Doliprane Label ). Patient was hospitalized.

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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 Lasix 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 Lasix quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Lasix 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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During the same period patient was treated with LASIX (View Lasix Review and Lasix Label ), ZAROXOLYN (View Zaroxolyn Review and Zaroxolyn Label ), COUMADIN (View Coumadin ...<<<<

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Lasix Reactions
Anorexia
Aspartate Aminotransferase Increased
Asthenia
Blister
Blood Creatinine Increased
Blood Urea Increased
Bradycardia
Cardiac Failure
Condition Aggravated
Confusional State
Dehydration
Diarrhoea
DizzinessWhat is Dizziness?
Dyspnoea
FallWhat is Fall?
Hyperkalaemia
Hypokalaemia
Hyponatraemia
Hypotension
Malaise
NauseaWhat is Nausea?
Pancytopenia
Pemphigoid
Pruritus
Pseudo-bartter Syndrome
Renal Failure
Renal Failure Acute
Stevens-johnson Syndrome
Syncope
Toxic Epidermal Necrolysis
Lasix 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 Lasix 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!