FUROSEMIDE Side Effects

7008845-9 | Malaise, Oedema Peripheral
on Sep 08, 2010 Male patient from UNITED KINGDOM , 74 years of age, was diagnosed with joint swelling, hypertension and was treated with Furosemide (View Usage). Patient experienced the following unwanted or unexpected effects: malaise, oedema peripheral. Furosemide 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 ), CORTICOSTEROID NOS (View Corticosteroid Nos Review and Corticosteroid Nos Label ).

7007759-8 | Hepatic Encephalopathy, Hepatic Failure, Hepatitis B, Peritonitis Bacterial
Patient was taking Furosemide (View Usage). Patient had the following side effects: hepatic encephalopathy, hepatic failure, hepatitis b (What is hepatitis b?), peritonitis bacterial on Sep 17, 2010 from Additional patient health information: Male patient , 81 years of age, was diagnosed with non-hodgkin's lymphoma and. Furosemide dosage: . During the same period patient was treated with PREDNISONE (View Prednisone Review and Prednisone Label ), LANSOPRAZOLE (View Lansoprazole Review and Lansoprazole Label ), PRAVASTATIN (View Pravastatin Review and Pravastatin Label ), TAMSULOSINE (View Tamsulosine Review and Tamsulosine Label ), ALLOPURINOL (View Allopurinol Review and Allopurinol Label ), CYCLOSPORINE (View Cyclosporine Review and Cyclosporine Label ), VINCRISTINE (View Vincristine Review and Vincristine Label ), RITUXIMAB (View Rituximab Review and Rituximab Label ). Patient was hospitalized.

7001107-5 | Renal Impairment
Adverse event was reported on Sep 09, 2010 by a Female patient taking Furosemide (View Usage) (Dosage: ) was diagnosed with renal cell carcinoma and. Location: GERMANY , 81 years of age, weighting 153.2 lb, After Furosemide was administered, patient had the following side effects: renal impairment. During the same period patient was treated with EVEROLIMUS (View Everolimus Review and Everolimus Label ), METAMIZOLE (View Metamizole Review and Metamizole Label ), AMLODIPINE/VALSARTAN (View Amlodipine/valsartan Review and Amlodipine/valsartan Label ), GABAPENTIN (View Gabapentin Review and Gabapentin Label ). Patient was hospitalized.

6993718-8 | Orthostatic Hypotension, Syncope
on Sep 11, 2009 Female patient from UNITED STATES , 75 years of age, weighting 131.0 lb, was diagnosed with cardiomyopathy (What is cardiomyopathy?) and was treated with Furosemide (View Usage). Patient experienced the following unwanted or unexpected effects: orthostatic hypotension, syncope. Furosemide dosage: . During the same period patient was treated with CONTRAST MEDIA (View Contrast Media Review and Contrast Media Label ), GEMCITABINE (View Gemcitabine Review and Gemcitabine Label ), CARBOPLATIN (2 Auc;qw; Iv) (View Carboplatin Review and Carboplatin Label ), PLAVIX (View Plavix Review and Plavix Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), DIGOXIN (View Digoxin Review and Digoxin Label ). Patient was hospitalized.


6992363-8 | Gait Disturbance, Monarthritis, Nephrocalcinosis, Overdose, Renal Injury, Renal Tubular Necrosis, Tubulointerstitial Nephritis
on Sep 06, 2010 Female patient from ISRAEL , 60 years of age, weighting 114.6 lb, was diagnosed with arthralgia and was treated with Furosemide (View Usage). Patient had the following side effects: gait disturbance, monarthritis, nephrocalcinosis, overdose, renal injury, renal tubular necrosis, tubulointerstitial nephritis. Furosemide dosage: 40-60 Mg Daily, 1000 Mg/day, Over The Preceding 5 Years. During the same period patient was treated with ORLISTAT (120-240 Mg /day, Over Previous 3 Years) (View Orlistat Review and Orlistat Label ), ETORICOXIB (90 Mg/day) (View Etoricoxib Review and Etoricoxib Label ). Patient was hospitalized.

6979416-5 | Dizziness
Patient was taking Furosemide (View Usage). After Furosemide was administered, patient had the following side effects: dizziness (What is dizziness?) on Sep 10, 2010 from UNITED STATES Additional patient health information: Male patient , 91 years of age, weighting 202.8 lb, was diagnosed with cardiac failure congestive and. Furosemide dosage: 120 Mg Bid Po. Patient was hospitalized.

6972915-1 | Monarthritis, Renal Failure Acute, Renal Failure Chronic
Adverse event was reported on Sep 03, 2010 by a Female patient taking Furosemide (View Usage) (Dosage: ) was diagnosed with renal failure acute, monarthritis, arthralgia and. Location: , 60 years of age, weighting 114.6 lb, Patient experienced the following unwanted or unexpected effects: monarthritis, renal failure acute, renal failure chronic. During the same period patient was treated with PREDNISONE (40 Mg) (View Prednisone Review and Prednisone Label ), ORLISTAT (View Orlistat Review and Orlistat Label ), NSAID (View Nsaid Review and Nsaid Label ), ETORICOXIB (90 Mg) (View Etoricoxib Review and Etoricoxib Label ). Patient was hospitalized.

6969460-6 | Dizziness, Fall, Femur Fracture
on Aug 23, 2010 Female patient from UNITED STATES , 91 years of age, weighting 141.1 lb, was diagnosed with hypertension and was treated with Furosemide (View Usage). Patient had the following side effects: dizziness (What is dizziness?), fall (What is fall?), femur fracture. Furosemide dosage: 40 Mg, Intravenous. During the same period patient was treated with CLEVIDIPINE (CLEVIDIPINE) EMULSION FOR INFUSION (4-16 Ml, Hr, Intravenous) (View Clevidipine (clevidipine) Emulsion For Infusion Review and Clevidipine (clevidipine) Emulsion For Infusion Label ). Patient was hospitalized.

6968798-6 | Glomerulosclerosis, Kidney Fibrosis, Nephrocalcinosis, Renal Failure, Renal Tubular Necrosis
on Aug 26, 2010 Female patient from ISRAEL , 60 years of age, was treated with Furosemide (View Usage). After Furosemide was administered, patient had the following side effects: glomerulosclerosis, kidney fibrosis, nephrocalcinosis, renal failure, renal tubular necrosis. Furosemide dosage: 40 To 60 Mg Daily Then Increased To Around 1000 Mg/day. During the same period patient was treated with ORLISTAT (120 To 240 Mg/day, Over The Previous 3 Years.) (View Orlistat Review and Orlistat Label ), ANTIINFLAMMATORY/ANTIRHEUMATIC NON STEROIDS (View Antiinflammatory/antirheumatic Non-steroids Review and Antiinflammatory/antirheumatic Non-steroids Label ).

6965124-3 | Myocardial Ischaemia
Patient was taking Furosemide (View Usage). Patient experienced the following unwanted or unexpected effects: myocardial ischaemia on Aug 23, 2010 from ITALY Additional patient health information: Male patient , 78 years of age, was diagnosed with nephrotic syndrome and. Furosemide dosage: . During the same period patient was treated with LANSOPRAZOLE (View Lansoprazole Review and Lansoprazole Label ), ACETYLSALICYLIC ACID (View Acetylsalicylic Acid Review and Acetylsalicylic Acid Label ), EPOETIN ALFA (View Epoetin Alfa Review and Epoetin Alfa Label ). Patient was hospitalized.

6964387-8 | Deafness Neurosensory, Fluid Retention, Gout, Renal Failure Acute, Renal Failure Chronic, Tinnitus
Adverse event was reported on Aug 20, 2010 by a Male patient taking Furosemide (View Usage) (Dosage: 80 Mg, Bid) was diagnosed with congestive cardiomyopathy, cardiac disorder, renal disorder, gout (What is gout?), fluid retention and. Location: UNITED KINGDOM , 41 years of age, Patient had the following side effects: deafness neurosensory, fluid retention, gout (What is gout?), renal failure acute, renal failure chronic, tinnitus (What is tinnitus?). During the same period patient was treated with INDOMETHACIN SODIUM (25 Mg, Tid) (View Indomethacin Sodium Review and Indomethacin Sodium Label ), RAMIPRIL (10 Mg, Qd) (View Ramipril Review and Ramipril Label ), AMIODARONE (200 Mg, Qd) (View Amiodarone Review and Amiodarone Label ), BISOPROLOL FUMARATE (10 Mg, Qd) (View Bisoprolol Fumarate Review and Bisoprolol Fumarate Label ), METOLAZONE (2.5 Mg, Qd) (View Metolazone Review and Metolazone Label ), SPIRONOLACTONE (View Spironolactone Review and Spironolactone Label ). Patient was hospitalized and became disabled.

6964107-7 | Renal Failure
on Aug 23, 2010 Female patient from ISRAEL , 60 years of age, was diagnosed with arthritis (What is arthritis?) and was treated with Furosemide (View Usage). After Furosemide was administered, patient had the following side effects: renal failure. Furosemide dosage: 40-60 Mg/day. During the same period patient was treated with ORLISTAT (120-240 Mg/day) (View Orlistat Review and Orlistat Label ), ETORICOXIB (View Etoricoxib Review and Etoricoxib Label ).

6962512-6 | Hepatitis Chronic Active, Hepatocellular Injury, Hepatotoxicity
on Aug 20, 2010 Female patient from UNITED STATES , 30 years of age, was treated with Furosemide (View Usage). Patient experienced the following unwanted or unexpected effects: hepatitis chronic active, hepatocellular injury, hepatotoxicity. Furosemide dosage: 20 Mg, Daily For Almost 6.5 Years, Oral. During the same period patient was treated with LISINOPRIL (10 Mg, Daily For 8 Months, Oral) (View Lisinopril Review and Lisinopril Label ).

6960394-X | Renal Failure
Patient was taking Furosemide (View Usage). Patient had the following side effects: renal failure on Aug 23, 2010 from ISRAEL Additional patient health information: Female patient , 60 years of age, . Furosemide dosage: 40-60mg. During the same period patient was treated with ETORICOXIB (View Etoricoxib Review and Etoricoxib Label ), ORLISTAT (120-240 Mg/day) (View Orlistat Review and Orlistat Label ).

6957458-3 | Deafness Neurosensory, Fluid Retention, Gout, Renal Failure Chronic, Tinnitus
Adverse event was reported on Aug 17, 2010 by a Male patient taking Furosemide (View Usage) (Dosage: 80 Mg, Bid) was diagnosed with congestive cardiomyopathy, cardiac disorder, renal disorder, gout (What is gout?), fluid retention and. Location: UNITED KINGDOM , 41 years of age, After Furosemide was administered, patient had the following side effects: deafness neurosensory, fluid retention, gout (What is gout?), renal failure chronic, tinnitus (What is tinnitus?). During the same period patient was treated with INDOMETHACIN SODIUM (25 Mg, Tid) (View Indomethacin Sodium Review and Indomethacin Sodium Label ), RAMIPRIL (10 Mg, Qd) (View Ramipril Review and Ramipril Label ), AMIODARONE (200 Mg, Qd) (View Amiodarone Review and Amiodarone Label ), BISOPROLOL FUMARATE (10 Mg, Qd) (View Bisoprolol Fumarate Review and Bisoprolol Fumarate Label ), METOLAZONE (2.5 Mg, Qd) (View Metolazone Review and Metolazone Label ), SPIRONOLACTONE (View Spironolactone Review and Spironolactone Label ). Patient was hospitalized and became disabled.

6943525-7 | Malaise
on Aug 13, 2010 Male patient from UNITED KINGDOM , 55 years of age, was diagnosed with schizophrenia and was treated with Furosemide (View Usage). Patient experienced the following unwanted or unexpected effects: malaise. Furosemide dosage: . During the same period patient was treated with CLOZARIL (View Clozaril Review and Clozaril Label ).

6943509-9 | Deafness Neurosensory, Renal Failure Acute
on Aug 13, 2010 Male patient from UNITED KINGDOM , 41 years of age, was diagnosed with atrial fibrillation (What is atrial fibrillation?), gout (What is gout?), blood creatinine increased and was treated with Furosemide (View Usage). Patient had the following side effects: deafness neurosensory, renal failure acute. Furosemide dosage: . During the same period patient was treated with INDOMETHACIN SODIUM (View Indomethacin Sodium Review and Indomethacin Sodium Label ), RAMIPRIL (View Ramipril Review and Ramipril Label ), WARFARIN SODIUM (View Warfarin Sodium Review and Warfarin Sodium Label ), AMIODARONE (View Amiodarone Review and Amiodarone Label ), BISOPROLOL (View Bisoprolol Review and Bisoprolol Label ), METOLAZONE (View Metolazone Review and Metolazone Label ). Patient was hospitalized and became disabled.

6941967-7 | Deafness Neurosensory, Fluid Retention, Gout, Renal Failure Acute
Patient was taking Furosemide (View Usage). After Furosemide was administered, patient had the following side effects: deafness neurosensory, fluid retention, gout (What is gout?), renal failure acute on Aug 12, 2010 from UNITED KINGDOM Additional patient health information: Male patient , 41 years of age, was diagnosed with congestive cardiomyopathy, gout (What is gout?), fluid retention and. Furosemide dosage: 80 Mg, Bid. During the same period patient was treated with INDOMETHACIN SODIUM (25 Mg, Tid) (View Indomethacin Sodium Review and Indomethacin Sodium Label ), RAMIPRIL (10 Mg, Qd) (View Ramipril Review and Ramipril Label ), AMIODARONE (200 Mg, Qd) (View Amiodarone Review and Amiodarone Label ), BISOPROLOL (10 Mg, Qd) (View Bisoprolol Review and Bisoprolol Label ), METOLAZONE (2.5 Mg, Qd) (View Metolazone Review and Metolazone Label ), SPIRONOLACTONE (View Spironolactone Review and Spironolactone Label ), WARFARIN SODIUM (View Warfarin Sodium Review and Warfarin Sodium Label ). Patient was hospitalized.

6941429-7 | Blood Creatine Phosphokinase Increased, Narcotic Intoxication, Renal Failure Acute
Adverse event was reported on Aug 11, 2010 by a Male patient taking Furosemide (View Usage) (Dosage: ) was diagnosed with fluid overload, diabetes mellitus, hypertension, left ventricular failure, hypercholesterolaemia, polyuria, phantom pain, breakthrough pain and. Location: UNITED KINGDOM , 79 years of age, Patient experienced the following unwanted or unexpected effects: blood creatine phosphokinase increased, narcotic intoxication, renal failure acute. During the same period patient was treated with METFORMIN HCL (View Metformin Hcl Review and Metformin Hcl Label ), RAMIPRIL (View Ramipril Review and Ramipril Label ), ATORVASTATIN (View Atorvastatin Review and Atorvastatin Label ), BENDROFLUMETHAZIDE (View Bendroflumethazide Review and Bendroflumethazide Label ), OXYCONTIN (View Oxycontin Review and Oxycontin Label ), OXYCODONE HCL (View Oxycodone Hcl Review and Oxycodone Hcl Label ), ASPIRIN (View Aspirin Review and Aspirin Label ). Patient was hospitalized.

6941428-5 | Blood Creatine Phosphokinase Increased, Narcotic Intoxication, Renal Failure Acute
on Aug 11, 2010 Male patient from UNITED KINGDOM , 79 years of age, was diagnosed with fluid overload, diabetes mellitus, hypertension, left ventricular failure, hypercholesterolaemia, polyuria, phantom pain, breakthrough pain and was treated with Furosemide (View Usage). Patient had the following side effects: blood creatine phosphokinase increased, narcotic intoxication, renal failure acute. Furosemide dosage: . During the same period patient was treated with METFORMIN HCL (View Metformin Hcl Review and Metformin Hcl Label ), RAMIPRIL (View Ramipril Review and Ramipril Label ), ATORVASTATIN (View Atorvastatin Review and Atorvastatin Label ), BENDROFLUMETHAZIDE (View Bendroflumethazide Review and Bendroflumethazide Label ), OXYCONTIN (View Oxycontin Review and Oxycontin Label ), OXYCODONE HCL (View Oxycodone Hcl Review and Oxycodone Hcl Label ), ASPIRIN (View Aspirin Review and Aspirin Label ). Patient was hospitalized.

6941426-1 | Blood Creatine Phosphokinase Increased, Narcotic Intoxication, Renal Failure Acute
on Aug 11, 2010 Male patient from UNITED KINGDOM , 79 years of age, was diagnosed with fluid overload, diabetes mellitus, hypertension, left ventricular failure, hypercholesterolaemia, polyuria, phantom pain, breakthrough pain and was treated with Furosemide (View Usage). After Furosemide was administered, patient had the following side effects: blood creatine phosphokinase increased, narcotic intoxication, renal failure acute. Furosemide dosage: . During the same period patient was treated with METFORMIN HCL (View Metformin Hcl Review and Metformin Hcl Label ), RAMIPRIL (View Ramipril Review and Ramipril Label ), ATORVASTATIN (View Atorvastatin Review and Atorvastatin Label ), BENDROFLUMETHAZIDE (View Bendroflumethazide Review and Bendroflumethazide Label ), OXYCONTIN (View Oxycontin Review and Oxycontin Label ), OXYCODONE HCL (View Oxycodone Hcl Review and Oxycodone Hcl Label ), ASPIRIN (View Aspirin Review and Aspirin Label ). Patient was hospitalized.

6936832-5 | Asthenia, Gait Disturbance, Neuropathy Peripheral, Renal Failure Acute, Rhabdomyolysis
Patient was taking Furosemide (View Usage). Patient experienced the following unwanted or unexpected effects: asthenia, gait disturbance, neuropathy peripheral, renal failure acute, rhabdomyolysis on Aug 09, 2010 from ITALY Additional patient health information: Male patient , 42 years of age, was diagnosed with dyslipidaemia and. Furosemide dosage: 30 Mg. During the same period patient was treated with EZETIMIBE/SIMVASTATIN (10mg/20mg) (View Ezetimibe/simvastatin Review and Ezetimibe/simvastatin Label ), INSULIN LISPRO AND INSULIN GLARGINE (Total 72 U) (View Insulin Lispro And Insulin Glargine Review and Insulin Lispro And Insulin Glargine Label ), RAMIPRIL (10mg) (View Ramipril Review and Ramipril Label ), GABAPENTIN (300 Mg) (View Gabapentin Review and Gabapentin Label ), ASPIRIN (100 Mg) (View Aspirin Review and Aspirin Label ), ALLOPURINOL (300mg) (View Allopurinol Review and Allopurinol Label ). Patient was hospitalized.

6935968-2 | Arthralgia
Adverse event was reported on Aug 02, 2010 by a Female patient taking Furosemide (View Usage) (Dosage: ) . Location: UNITED KINGDOM , 82 years of age, Patient had the following side effects: arthralgia. During the same period patient was treated with CO CODAMOL (PANADEINE CO) (View Co-codamol (panadeine Co) Review and Co-codamol (panadeine Co) Label ), ETODOLAC (View Etodolac Review and Etodolac Label ), METHOTREXATE (View Methotrexate Review and Methotrexate Label ), ACETAMINOPHEN (View Acetaminophen Review and Acetaminophen Label ).

6928938-1 | Deafness, Fluid Retention, Gout, Renal Failure Chronic
on Aug 03, 2010 Male patient from UNITED KINGDOM , 41 years of age, was diagnosed with congestive cardiomyopathy, gout (What is gout?), fluid retention and was treated with Furosemide (View Usage). After Furosemide was administered, patient had the following side effects: deafness, fluid retention, gout (What is gout?), renal failure chronic. Furosemide dosage: . During the same period patient was treated with INDOMETHACIN (View Indomethacin Review and Indomethacin Label ), AMIODARONE (View Amiodarone Review and Amiodarone Label ), BISOPROLOL (View Bisoprolol Review and Bisoprolol Label ), METOLAZONE (View Metolazone Review and Metolazone Label ), RAMIPRIL (View Ramipril Review and Ramipril Label ), SPIRONOLACTONE (View Spironolactone Review and Spironolactone Label ), WARFARIN (View Warfarin Review and Warfarin Label ). Patient was hospitalized.

6928937-X | Deafness, Fluid Retention, Gout, Renal Failure Chronic
on Aug 03, 2010 Male patient from UNITED KINGDOM , 41 years of age, was diagnosed with congestive cardiomyopathy, gout (What is gout?), fluid retention and was treated with Furosemide (View Usage). Patient experienced the following unwanted or unexpected effects: deafness, fluid retention, gout (What is gout?), renal failure chronic. Furosemide dosage: . During the same period patient was treated with INDOMETHACIN (View Indomethacin Review and Indomethacin Label ), AMIODARONE (View Amiodarone Review and Amiodarone Label ), BISOPROLOL (View Bisoprolol Review and Bisoprolol Label ), METOLAZONE (View Metolazone Review and Metolazone Label ), RAMIPRIL (View Ramipril Review and Ramipril Label ), SPIRONOLACTONE (View Spironolactone Review and Spironolactone Label ), WARFARIN (View Warfarin Review and Warfarin Label ). Patient was hospitalized.

6925377-4 | Cardiogenic Shock, Continuous Haemodiafiltration, Disorientation, Electrocardiogram Qrs Complex Prolonged, Electrocardiogram Qt Prolonged, Heart Rate Decreased, Renal Failure
Patient was taking Furosemide (View Usage). Patient had the following side effects: cardiogenic shock, continuous haemodiafiltration, disorientation, electrocardiogram qrs complex prolonged, electrocardiogram qt prolonged, heart rate decreased, renal failure on Jul 30, 2010 from NETHERLANDS Additional patient health information: Male patient , 75 years of age, . Furosemide dosage: Ingested 800 Mg. During the same period patient was treated with DIGOXIN (Ingested 7.125mg) (View Digoxin Review and Digoxin Label ), SOTALOL HCL (Ingested 7200mg) (View Sotalol Hcl Review and Sotalol Hcl Label ), ISOSORBIDE MONONITRATE (Ingested 6000mg) (View Isosorbide Mononitrate Review and Isosorbide Mononitrate Label ), ACENOCOUMAROL (Ingested 98mg) (View Acenocoumarol Review and Acenocoumarol Label ), ATORVASTATIN CALCIUM (Ingested 1200mg) (View Atorvastatin Calcium Review and Atorvastatin Calcium Label ), PERINDOPRIL (Ingested 200mg) (View Perindopril Review and Perindopril Label ), AMLODIPINE (Ingested 300mg) (View Amlodipine Review and Amlodipine Label ). Patient was hospitalized.

6919257-8 | Hypotension, Tachycardia
Adverse event was reported on Jul 12, 2010 by a Male patient taking Furosemide (View Usage) (Dosage: ) was diagnosed with chronic obstructive pulmonary disease and. Location: SWEDEN , 79 years of age, After Furosemide was administered, patient had the following side effects: hypotension, tachycardia. During the same period patient was treated with RAMIPRIL (View Ramipril Review and Ramipril Label ), CAPTOPRIL (View Captopril Review and Captopril Label ), FALICARD ^DRESDEN^ (View Falicard ^dresden^ Review and Falicard ^dresden^ Label ), THEOPHYLLINE (Dose As Used: 400mg, 2 In Day) (View Theophylline Review and Theophylline Label ), XIPAMIDE (View Xipamide Review and Xipamide Label ), DOMPERIDONE (Dose As Used: 10mg, 3 In Day) (View Domperidone Review and Domperidone Label ), PANTOZOL (Dose As Used: 40mg, 2 In Day) (View Pantozol Review and Pantozol Label ). Patient was hospitalized.

6916418-9 | Granulomatous Liver Disease, Hypercalcaemia
on Aug 06, 2010 Male patient from , 62 years of age, was diagnosed with hypercalcaemia, type 2 diabetes mellitus, hyperuricaemia and was treated with Furosemide (View Usage). Patient experienced the following unwanted or unexpected effects: granulomatous liver disease, hypercalcaemia. Furosemide dosage: . During the same period patient was treated with METFORMIN HCL (View Metformin Hcl Review and Metformin Hcl Label ), ALLOPURINOL (View Allopurinol Review and Allopurinol Label ).

6915062-7 | Arthralgia
on Jul 26, 2010 Female patient from UNITED KINGDOM , 82 years of age, weighting 191.8 lb, was treated with Furosemide (View Usage). Patient had the following side effects: arthralgia. Furosemide dosage: . During the same period patient was treated with ACETAMINOPHEN AND CODEINE PHOSPHATE (View Acetaminophen And Codeine Phosphate Review and Acetaminophen And Codeine Phosphate Label ), ETODOLAC (View Etodolac Review and Etodolac Label ), METHOTREXATE (View Methotrexate Review and Methotrexate Label ), PARACETAMOL (View Paracetamol Review and Paracetamol Label ).

6914876-7 | Rash
Patient was taking Furosemide (View Usage). After Furosemide was administered, patient had the following side effects: rash (What is rash?) on Aug 04, 2010 from UNITED STATES Additional patient health information: Male patient , 72 years of age, . Furosemide dosage: . Patient was hospitalized.

6914859-7 | Thrombocytopenia
Adverse event was reported on Aug 04, 2010 by a Male patient taking Furosemide (View Usage) (Dosage: ) . Location: UNITED STATES , 80 years of age, Patient experienced the following unwanted or unexpected effects: thrombocytopenia. Patient was hospitalized.

6905762-7 | Blood Creatine Phosphokinase Increased, Narcotic Intoxication, Renal Failure Acute
on Jul 21, 2010 Male patient from UNITED KINGDOM , 79 years of age, was diagnosed with fluid overload, diabetes mellitus, hypertension, left ventricular failure, hypercholesterolaemia, polyuria, phantom pain, breakthrough pain and was treated with Furosemide (View Usage). Patient had the following side effects: blood creatine phosphokinase increased, narcotic intoxication, renal failure acute. Furosemide dosage: . During the same period patient was treated with METFORMIN HCL (View Metformin Hcl Review and Metformin Hcl Label ), RAMIPRIL (View Ramipril Review and Ramipril Label ), ATORVASTATIN (View Atorvastatin Review and Atorvastatin Label ), BENDROFLUMETHAZIDE (View Bendroflumethazide Review and Bendroflumethazide Label ), OXYCONTIN (View Oxycontin Review and Oxycontin Label ), OXYCODONE HCL (View Oxycodone Hcl Review and Oxycodone Hcl Label ), ASPIRIN (View Aspirin Review and Aspirin Label ). Patient was hospitalized.

6905761-5 | Blood Creatine Phosphokinase Increased, Narcotic Intoxication, Renal Failure Acute
on Jul 21, 2010 Male patient from UNITED KINGDOM , 79 years of age, was diagnosed with fluid overload, diabetes mellitus, hypertension, left ventricular failure, hypercholesterolaemia, polyuria, phantom pain, breakthrough pain and was treated with Furosemide (View Usage). After Furosemide was administered, patient had the following side effects: blood creatine phosphokinase increased, narcotic intoxication, renal failure acute. Furosemide dosage: . During the same period patient was treated with METFORMIN HCL (View Metformin Hcl Review and Metformin Hcl Label ), RAMIPRIL (View Ramipril Review and Ramipril Label ), ATORVASTATIN (View Atorvastatin Review and Atorvastatin Label ), BENDROFLUMETHAZIDE (View Bendroflumethazide Review and Bendroflumethazide Label ), OXYCONTIN (View Oxycontin Review and Oxycontin Label ), OXYCODONE HCL (View Oxycodone Hcl Review and Oxycodone Hcl Label ), ASPIRIN (View Aspirin Review and Aspirin Label ). Patient was hospitalized.

6905758-5 | Blood Creatine Phosphokinase Increased, Narcotic Intoxication, Renal Failure Acute
Patient was taking Furosemide (View Usage). Patient experienced the following unwanted or unexpected effects: blood creatine phosphokinase increased, narcotic intoxication, renal failure acute on Jul 21, 2010 from UNITED KINGDOM Additional patient health information: Male patient , 79 years of age, was diagnosed with fluid overload, diabetes mellitus, hypertension, left ventricular failure, hypercholesterolaemia, polyuria, phantom pain, breakthrough pain and. Furosemide dosage: . During the same period patient was treated with METFORMIN HCL (View Metformin Hcl Review and Metformin Hcl Label ), RAMIPRIL (View Ramipril Review and Ramipril Label ), ATORVASTATIN (View Atorvastatin Review and Atorvastatin Label ), BENDROFLUMETHAZIDE (View Bendroflumethazide Review and Bendroflumethazide Label ), OXYCONTIN (View Oxycontin Review and Oxycontin Label ), OXYCODONE HCL (View Oxycodone Hcl Review and Oxycodone Hcl Label ), ASPIRIN (View Aspirin Review and Aspirin Label ). Patient was hospitalized.

6902426-0 | Diarrhoea, Diverticulum, Lymphadenopathy, Pancreatitis
Adverse event was reported on Aug 02, 2010 by a Male patient taking Furosemide (View Usage) (Dosage: 120 Mg Every Day Po) was diagnosed with cardiac failure congestive and. Location: UNITED STATES , 79 years of age, weighting 200.4 lb, Patient had the following side effects: diarrhoea, diverticulum, lymphadenopathy, pancreatitis. Patient was hospitalized.

6900780-7 | Arthralgia
on Jul 23, 2010 Female patient from UNITED KINGDOM , 82 years of age, weighting 191.8 lb, was treated with Furosemide (View Usage). After Furosemide was administered, patient had the following side effects: arthralgia. Furosemide dosage: . During the same period patient was treated with ACETAMINOPHEN AND CODEINE PHOSPHATE (View Acetaminophen And Codeine Phosphate Review and Acetaminophen And Codeine Phosphate Label ), ETODOLAC (View Etodolac Review and Etodolac Label ), METHOTREXATE (View Methotrexate Review and Methotrexate Label ).

6885346-X | Bacterial Infection, Dermatitis Infected, Pain, Product Contamination, Product Quality Issue
on Jul 09, 2010 Female patient from UNITED STATES , 41 years of age, was diagnosed with cardiac failure congestive, lung disorder, arthritis (What is arthritis?) and was treated with Furosemide (View Usage). Patient experienced the following unwanted or unexpected effects: bacterial infection (What is bacterial infection?), dermatitis infected, pain (What is pain?), product contamination, product quality issue. Furosemide dosage: 80 Mg Twice Daily;. During the same period patient was treated with ACETAMINOPHEN (1950 Mg, 3 In 1 D,) (View Acetaminophen Review and Acetaminophen Label ).

6882286-7 | Cardiac Failure Congestive, Dizziness, Renal Failure Acute
Patient was taking Furosemide (View Usage). Patient had the following side effects: cardiac failure congestive, dizziness (What is dizziness?), renal failure acute on Jul 28, 2010 from UNITED STATES Additional patient health information: Male patient , 80 years of age, weighting 152.1 lb, was diagnosed with cardiac failure congestive and. Furosemide dosage: 40 Mg Bid Po. Patient was hospitalized.

6882282-X | Dehydration, Dizziness, Renal Injury
Adverse event was reported on Jul 28, 2010 by a Male patient taking Furosemide (View Usage) (Dosage: 80 Mg Every Day Po) was diagnosed with cardiac failure congestive and. Location: UNITED STATES , 66 years of age, weighting 288.8 lb, After Furosemide was administered, patient had the following side effects: dehydration, dizziness (What is dizziness?), renal injury. Patient was hospitalized.

6880843-5 | Colitis, Mesenteric Occlusion
on Jul 15, 2010 Male patient from CANADA , 73 years of age, was treated with Furosemide (View Usage). Patient experienced the following unwanted or unexpected effects: colitis, mesenteric occlusion. Furosemide dosage: Dose As Used: Unk. During the same period patient was treated with ACETYLSALICYLIC ACID SRT (Dose As Used: Unk) (View Acetylsalicylic Acid Srt Review and Acetylsalicylic Acid Srt Label ), AMIODARONE HCL (Dose As Used: Unk) (View Amiodarone Hcl Review and Amiodarone Hcl Label ), ACE INHIBITOR NOS (View Ace Inhibitor Nos Review and Ace Inhibitor Nos Label ), ANTI ASTHMATICS (View Anti-asthmatics Review and Anti-asthmatics Label ), FERROUS GLUCONATE (View Ferrous Gluconate Review and Ferrous Gluconate Label ), CHOLESTEROL AND TRIGLYCERIDE REDUCERS (View Cholesterol- And Triglyceride Reducers Review and Cholesterol- And Triglyceride Reducers Label ), LEVOTHYROXINE SODIUM (View Levothyroxine Sodium Review and Levothyroxine Sodium Label ), WARFARIN SODIUM (View Warfarin Sodium Review and Warfarin Sodium Label ).

6879295-0 | Colitis, Mesenteric Occlusion
on Jul 15, 2010 Male patient from CANADA , 73 years of age, was treated with Furosemide (View Usage). Patient had the following side effects: colitis, mesenteric occlusion. Furosemide dosage: Dose As Used: Unk. During the same period patient was treated with ACETYLSALICYLIC ACID SRT (Dose As Used: Unk) (View Acetylsalicylic Acid Srt Review and Acetylsalicylic Acid Srt Label ), AMIODARONE HCL (Dose As Used: Unk) (View Amiodarone Hcl Review and Amiodarone Hcl Label ), ACE INHIBITOR NOS (View Ace Inhibitor Nos Review and Ace Inhibitor Nos Label ), ANTI ASTHMATICS (View Anti-asthmatics Review and Anti-asthmatics Label ), FERROUS GLUCONATE (View Ferrous Gluconate Review and Ferrous Gluconate Label ), CHOLESTEROL AND TRIGLYCERIDE REDUCERS (View Cholesterol- And Triglyceride Reducers Review and Cholesterol- And Triglyceride Reducers Label ), LEVOTHYROXINE SODIUM (View Levothyroxine Sodium Review and Levothyroxine Sodium Label ), WARFARIN (View Warfarin Review and Warfarin Label ).

6878504-1 | Arthralgia
Patient was taking Furosemide (View Usage). After Furosemide was administered, patient had the following side effects: arthralgia on Jul 26, 2010 from UNITED KINGDOM Additional patient health information: Female patient , 82 years of age, weighting 191.8 lb, . Furosemide dosage: .

6867834-5 | Product Quality Issue
Adverse event was reported on Jul 22, 2010 by a Male patient taking Furosemide (View Usage) (Dosage: 1 Tablet Daily) was diagnosed with oedema and. Location: UNITED STATES , 80 years of age, weighting 136.0 lb, Patient experienced the following unwanted or unexpected effects: product quality issue.

6867759-5 | Depression, Sinus Bradycardia
on Jul 19, 2010 Female patient from , 73 years of age, weighting 88.18 lb, was diagnosed with depression (What is depression?) and was treated with Furosemide (View Usage). Patient had the following side effects: depression (What is depression?), sinus bradycardia. Furosemide dosage: . During the same period patient was treated with SERTRALINE HCL (50 Mg) (View Sertraline Hcl Review and Sertraline Hcl Label ), LITHIUM CARBONATE (400 Mg) (View Lithium Carbonate Review and Lithium Carbonate Label ), LAMOTRIGINE (50 Mg) (View Lamotrigine Review and Lamotrigine Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), WARFARIN SODIUM (View Warfarin Sodium Review and Warfarin Sodium Label ), ISOSORBIDE (View Isosorbide Review and Isosorbide Label ), ENALAPRIL MALEATE (View Enalapril Maleate Review and Enalapril Maleate Label ), BISOPROLOL (View Bisoprolol Review and Bisoprolol Label ). Patient was hospitalized.

6865044-9 | Decreased Appetite, Eosinophil Percentage Increased, Granulomatous Liver Disease, Haemoglobin Decreased, Hypercalcaemia, Weight Decreased
on Jul 06, 2010 Male patient from SPAIN , 62 years of age, was diagnosed with blood calcium increased, hyperuricaemia and was treated with Furosemide (View Usage). After Furosemide was administered, patient had the following side effects: decreased appetite, eosinophil percentage increased, granulomatous liver disease, haemoglobin decreased, hypercalcaemia, weight decreased. Furosemide dosage: . During the same period patient was treated with ALLOPURINOL (View Allopurinol Review and Allopurinol Label ).

6860207-0 | Cardiac Arrest
Patient was taking Furosemide (View Usage). Patient experienced the following unwanted or unexpected effects: cardiac arrest (What is cardiac arrest?) on Jul 06, 2010 from CANADA Additional patient health information: Female patient , weighting 212.1 lb, . Furosemide dosage: . During the same period patient was treated with OXALIPLATIN (View Oxaliplatin Review and Oxaliplatin Label ), FOLINIC ACID (View Folinic Acid Review and Folinic Acid Label ), FLUOROURACIL (View Fluorouracil Review and Fluorouracil Label ), BEVACIZUMAB (View Bevacizumab Review and Bevacizumab Label ).

6843823-1 | Fall, Hypovolaemia, Polyuria
Adverse event was reported on Jul 14, 2010 by a Male patient taking Furosemide (View Usage) (Dosage: 60 Mg Bid Po) was diagnosed with cardiac failure congestive and. Location: UNITED STATES , 82 years of age, weighting 182.1 lb, Patient had the following side effects: fall (What is fall?), hypovolaemia, polyuria. Patient was hospitalized.

6843546-9 | Renal Failure Acute
on Jun 24, 2010 Male patient from GERMANY , 82 years of age, was treated with Furosemide (View Usage). After Furosemide was administered, patient had the following side effects: renal failure acute. Furosemide dosage: 80 Mg, Intravenous. During the same period patient was treated with VANCOMYCIN (VANCOMYCIN) (VANCOMYCIN) (View Vancomycin (vancomycin) (vancomycin) Review and Vancomycin (vancomycin) (vancomycin) Label ), GENTAMYCIN (GENTAMICIN) (GENTAMICIN) (View Gentamycin (gentamicin) (gentamicin) Review and Gentamycin (gentamicin) (gentamicin) Label ), ACTRAPID HUMAN (INSULIN HUMAN) (INSULIN HUMAN) (View Actrapid Human (insulin Human) (insulin Human) Review and Actrapid Human (insulin Human) (insulin Human) Label ), NEBILET (NEBIVOLOL HYDROCHLORIDE) (NEBIVOLOL HYDROCHLORIDE) (View Nebilet (nebivolol Hydrochloride) (nebivolol Hydrochloride) Review and Nebilet (nebivolol Hydrochloride) (nebivolol Hydrochloride) Label ), THEOPHYLLINE (View Theophylline Review and Theophylline Label ).

6828120-2 | Cerebrovascular Accident, Dehydration, Renal Failure
on Jul 08, 2010 Female patient from UNITED STATES , 84 years of age, weighting 200.0 lb, was diagnosed with cardiac failure congestive and was treated with Furosemide (View Usage). Patient experienced the following unwanted or unexpected effects: cerebrovascular accident, dehydration, renal failure. Furosemide dosage: 40 Mg 2 Times Daily Po. Patient was hospitalized.

6822211-8 | Blood Glucose Increased
Patient was taking Furosemide (View Usage). Patient had the following side effects: blood glucose increased on Jul 07, 2010 from UNITED STATES Additional patient health information: Female patient , 53 years of age, weighting 256.0 lb, was diagnosed with oedema peripheral, pericardial effusion and. Furosemide dosage: 40 Mg 1 @ Day Po.