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Humira Side Effects Report #5558583-4
Consumer or non-health professional from UNITED STATES reported HUMIRA problem on Oct 16, 2007. Male patient, weighting 333.8 lb, was diagnosed with psoriatic arthropathy, type 2 diabetes mellitus, arthralgia, heart rate increased, blood cholesterol increased and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: cardiac output decreased, feeling abnormal, heart rate increased, hyperhidrosis, hypoaesthesia, myocardial infarction, pain, paraesthesia, stress, . HUMIRA dosage: unknown. During the same period patient was treated with GLIBOMET, TRAMADOL, LISINOPRIL, INEGY. Patient recovered.

Arava Side Effects Report #5510483-1
ARAVA problem was reported by a Physician from GERMANY on Nov 02, 2007. Male patient, 69 years of age, was treated with ARAVA. After drug was administered, patient experienced the following problems/side effects: cardiac output decreased, vital capacity decreased, . ARAVA dosage: unknown. Patient recovered.

Fuzeon Side Effects Report #5473211-4
Physician from BRAZIL reported FUZEON problem on Sept 19, 2007. Male patient, 42 years of age, weighting 154.3 lb, was treated with FUZEON. After drug was administered, patient experienced the following problems/side effects: cardiac output decreased, confusional state, myocarditis, . FUZEON dosage: unknown. During the same period patient was treated with TENOFOVIR DISOPROXIL FUMARATE, TENOFOVIR DISOPROXIL FUMARATE, DARUNAVIR, ABACAVIR, LAMIVUDINE. Patient was hospitalized. Patient recovered.

Arava Side Effects Report #5482329-1
ARAVA problem was reported by a Consumer or non-health professional from GERMANY on Oct 04, 2007. Male patient, 69 years of age, was treated with ARAVA. After drug was administered, patient experienced the following problems/side effects: cardiac output decreased, vital capacity decreased, . ARAVA dosage: unknown. Patient recovered.


Filgrastim Side Effects Report #5443267-3
Health Professional from UNITED KINGDOM reported FILGRASTIM problem on Aug 24, 2007. Male patient, 78 years of age, was diagnosed with myelodysplastic syndrome and was treated with FILGRASTIM. After drug was administered, patient experienced the following problems/side effects: cardiac output decreased, lactic acidosis, . FILGRASTIM dosage: unknown. During the same period patient was treated with ATENOLOL, CLOPIDOGREL, ISOSORBIDE MONONITRATE, OMEPRAZOLE, ASPIRIN. Patient died.

Nifedipine Side Effects Report #5409655-6
NIFEDIPINE problem was reported by a Pharmacist from UNITED STATES on Aug 08, 2007. Male patient, 70 years of age, was treated with NIFEDIPINE. After drug was administered, patient experienced the following problems/side effects: cardiac output decreased, condition aggravated, dyspnoea, pulmonary hypertension, . NIFEDIPINE dosage: 30MG EVERY DAY PO. Patient was hospitalized. Patient recovered.

Clozaril Side Effects Report #5410824-X
Physician from CANADA reported CLOZARIL problem on Aug 07, 2007. Male patient, 21 years of age, was diagnosed with schizophrenia and was treated with CLOZARIL. After drug was administered, patient experienced the following problems/side effects: cardiac output decreased, dialysis, hypotension, intubation, myocarditis, pneumonia streptococcal, renal failure acute, respiratory distress, shock, . CLOZARIL dosage: unknown. During the same period patient was treated with OLANZAPINE. Patient was hospitalized. Patient recovered.

Extraneal Side Effects Report #5398056-5
EXTRANEAL problem was reported by a Consumer or non-health professional from NETHERLANDS on July 18, 2007. Male patient, weighting 240.3 lb, was diagnosed with peritoneal dialysis and was treated with EXTRANEAL. After drug was administered, patient experienced the following problems/side effects: cardiac output decreased, fluid overload, hypertension, . EXTRANEAL dosage: unknown. During the same period patient was treated with PHYSIOSOL IN PLASTIC CONTAINER, NUTRINEAL, GAMBROSOL. Patient recovered.

Extraneal Side Effects Report #5398056-5
Consumer or non-health professional from NETHERLANDS reported EXTRANEAL problem on July 18, 2007. Male patient, weighting 240.3 lb, was diagnosed with peritoneal dialysis and was treated with EXTRANEAL. After drug was administered, patient experienced the following problems/side effects: cardiac output decreased, fluid overload, hypertension, . EXTRANEAL dosage: unknown. During the same period patient was treated with PHYSIOSOL IN PLASTIC CONTAINER, NUTRINEAL, GAMBROSOL. Patient recovered.


Rebif Side Effects Report #5766030-2
REBIF problem was reported by a Consumer or non-health professional from CANADA on May 21, 2008. Male patient, 50 years of age, was diagnosed with multiple sclerosis and was treated with REBIF. After drug was administered, patient experienced the following problems/side effects: cardiac output decreased, coronary artery occlusion, myocardial infarction, . REBIF dosage: unknown. During the same period patient was treated with RAMIPRIL, DIGOXIN, ASPIRIN, SPIRONOLACTONE, FUROSEMIDE, ATORVASTATIN, CARVEDILOL. Patient was hospitalized. Patient recovered.

Novantrone Side Effects Report #5734583-6
Consumer or non-health professional from UNITED STATES reported NOVANTRONE problem on Apr 29, 2008. Female patient, 34 years of age, was diagnosed with multiple sclerosis and was treated with NOVANTRONE. After drug was administered, patient experienced the following problems/side effects: cardiac output decreased, . NOVANTRONE dosage: unknown. Patient recovered.

Extraneal Side Effects Report #5341651-X
EXTRANEAL problem was reported by a Consumer or non-health professional from NETHERLANDS on May 30, 2007. Male patient, weighting 240.3 lb, was diagnosed with peritoneal dialysis and was treated with EXTRANEAL. After drug was administered, patient experienced the following problems/side effects: cardiac output decreased, fluid overload, hypertension, . EXTRANEAL dosage: unknown. During the same period patient was treated with PHYSIOSOL IN PLASTIC CONTAINER, NUTRINEAL, GAMBROSOL. Patient recovered.

Zelnorm Side Effects Report #5316465-7
Consumer or non-health professional from UNITED STATES reported ZELNORM problem on Apr 25, 2007. Female patient, 67 years of age, was diagnosed with constipation, diabetes mellitus, hypercholesterolaemia and was treated with ZELNORM. After drug was administered, patient experienced the following problems/side effects: cardiac output decreased, . ZELNORM dosage: 6 MG, BID. During the same period patient was treated with GLYBURIDE, ZETIA. Patient recovered.

Coumadin Side Effects Report #5321079-9
COUMADIN problem was reported by a Consumer or non-health professional from UNITED STATES on May 08, 2007. Male patient, 92 years of age, was diagnosed with ejection fraction decreased, discomfort and was treated with COUMADIN. After drug was administered, patient experienced the following problems/side effects: cardiac output decreased, cardiogenic shock, . COUMADIN dosage: WARFARIN 1MG ALSO MENTIONED. During the same period patient was treated with MORPHINE, PHENERGAN, ATIVAN. Patient died on 12/13/2006.


Avonex Side Effects Report #5322119-3
Consumer or non-health professional from UNITED STATES reported AVONEX problem on Apr 23, 2007. Male patient, 66 years of age, was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: cardiac output decreased, ejection fraction decreased, . AVONEX dosage: unknown. During the same period patient was treated with NOVANTRONE. Patient recovered.

Coumadin Side Effects Report #5322158-2
COUMADIN problem was reported by a Consumer or non-health professional from UNITED STATES on May 08, 2007. Male patient, 92 years of age, was diagnosed with ejection fraction decreased, discomfort and was treated with COUMADIN. After drug was administered, patient experienced the following problems/side effects: cardiac output decreased, cardiogenic shock, . COUMADIN dosage: WARFARIN 1MG ALSO MENTIONED. During the same period patient was treated with MORPHINE, PHENERGAN, ATIVAN. Patient died on 12/13/2006.

Visipaque Side Effects Report #5324494-2
Health Professional from INDIA reported VISIPAQUE problem on Apr 28, 2007. Male patient, 55 years of age, weighting 165.3 lb, was diagnosed with atrioventricular block and was treated with VISIPAQUE. After drug was administered, patient experienced the following problems/side effects: cardiac output decreased, chills, left ventricular dysfunction, renal failure acute, . VISIPAQUE dosage: 100 ML, SINGLE DOSE, I.V.. Patient died.

Avonex Side Effects Report #5233343-2
AVONEX problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 24, 2007. Female patient, 47 years of age, weighting 245.0 lb, was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: cardiac output decreased, deep vein thrombosis, fall, hypertension, influenza like illness, muscle spasms, . AVONEX dosage: unknown. During the same period patient was treated with ADVIL, AMBIEN. Patient was hospitalized. Patient recovered.

Extraneal Side Effects Report #5294694-9
Consumer or non-health professional from NETHERLANDS reported EXTRANEAL problem on Apr 10, 2007. Male patient, weighting 240.3 lb, was diagnosed with peritoneal dialysis and was treated with EXTRANEAL. After drug was administered, patient experienced the following problems/side effects: cardiac output decreased, fluid overload, hypertension, . EXTRANEAL dosage: unknown. During the same period patient was treated with NUTRINEAL, GAMBROSOL. Patient recovered.


Zelnorm Side Effects Report #5304148-9
ZELNORM problem was reported by a Consumer or non-health professional from UNITED STATES on Apr 12, 2007. Female patient was diagnosed with constipation and was treated with ZELNORM. After drug was administered, patient experienced the following problems/side effects: cardiac output decreased, . ZELNORM dosage: 6 MG, BID. Patient recovered.

Melphalan Side Effects Report #5675905-4
Pharmacist from FRANCE reported MELPHALAN problem on Mar 19, 2008. Female patient was diagnosed with bone marrow transplant and was treated with MELPHALAN. After drug was administered, patient experienced the following problems/side effects: blood pressure decreased, cardiac output decreased, cardiogenic shock, . MELPHALAN dosage: 350MG PER DAY. During the same period patient was treated with ZOPHREN, DEXAMETHASONE, GENTAMICIN, BACTRIM, FUNGIZONE, VALACYCLOVIR, TOPALGIC, MOPRAL. Patient was hospitalized. Patient recovered.

Melphalan Side Effects Report #5675906-6
MELPHALAN problem was reported by a Pharmacist from FRANCE on Mar 19, 2008. Female patient was diagnosed with bone marrow transplant and was treated with MELPHALAN. After drug was administered, patient experienced the following problems/side effects: blood pressure decreased, cardiac output decreased, cardiogenic shock, . MELPHALAN dosage: 400MG PER DAY. During the same period patient was treated with ZOPHREN, DEXAMETHASONE, BACTRIM, FUNGIZONE, VALACYCLOVIR, MOPRAL, HEPARIN, FOLINATE DE CALCIUM. Patient was hospitalized. Patient recovered.

Melphalan Side Effects Report #5621975-9
Pharmacist from FRANCE reported MELPHALAN problem on Jan 31, 2008. Female patient was diagnosed with bone marrow transplant and was treated with MELPHALAN. After drug was administered, patient experienced the following problems/side effects: blood pressure decreased, cardiac output decreased, cardiogenic shock, . MELPHALAN dosage: 350MG PER DAY. Patient was hospitalized. Patient recovered.

Melphalan Side Effects Report #5621976-0
MELPHALAN problem was reported by a Pharmacist from FRANCE on Jan 31, 2008. Female patient was diagnosed with bone marrow transplant and was treated with MELPHALAN. After drug was administered, patient experienced the following problems/side effects: blood pressure decreased, cardiac output decreased, cardiogenic shock, . MELPHALAN dosage: 400MG PER DAY. Patient was hospitalized. Patient recovered.

Melphalan Side Effects Report #5621977-2
Pharmacist from FRANCE reported MELPHALAN problem on Jan 31, 2008. Female patient was diagnosed with bone marrow transplant and was treated with MELPHALAN. After drug was administered, patient experienced the following problems/side effects: blood pressure decreased, cardiac output decreased, cardiogenic shock, . MELPHALAN dosage: 480MG PER DAY. Patient was hospitalized. Patient recovered.

Melphalan Side Effects Report #5630584-7
MELPHALAN problem was reported by a Pharmacist from FRANCE on Feb 18, 2008. Female patient was diagnosed with bone marrow transplant and was treated with MELPHALAN. After drug was administered, patient experienced the following problems/side effects: blood pressure decreased, cardiac output decreased, cardiogenic shock, . MELPHALAN dosage: 350MG PER DAY. During the same period patient was treated with ZOPHREN, DEXAMETHASONE, GENTAMICIN, BACTRIM, FUNGIZONE, VALACYCLOVIR, TOPALGIC, MOPRAL. Patient was hospitalized. Patient recovered.

Zovirax Side Effects Report #5759788-X
Consumer or non-health professional from FRANCE reported ZOVIRAX problem on May 29, 2008. Female patient, 17 years of age, was diagnosed with delirium, convulsion, neuroleptic malignant syndrome and was treated with ZOVIRAX. After drug was administered, patient experienced the following problems/side effects: arrhythmia, cardiac output decreased, convulsion, electroencephalogram abnormal, encephalopathy, respiratory distress, . ZOVIRAX dosage: unknown. During the same period patient was treated with ZYPREXA, TERCIAN, DEPAKENE, RIVOTRIL, TRANXENE, ATARAX. Patient was hospitalized. Patient died on 01/01/2006.

Rivotril Side Effects Report #5774213-0
RIVOTRIL problem was reported by a Physician from FRANCE on June 03, 2008. Female patient, 17 years of age, was diagnosed with delusion, neuroleptic malignant syndrome, convulsion and was treated with RIVOTRIL. After drug was administered, patient experienced the following problems/side effects: arrhythmia, cardiac output decreased, convulsion, respiratory distress, . RIVOTRIL dosage: unknown. During the same period patient was treated with ZOVIRAX, ATARAX, TRANXENE, DEPAKENE, TERCIAN, ZYPREXA. Patient died on 03/01/2006.

Corgard Side Effects Report #5718047-1
Consumer or non-health professional from UNITED STATES reported CORGARD problem on Apr 21, 2008. Female patient was treated with CORGARD. After drug was administered, patient experienced the following problems/side effects: bradycardia, cardiac output decreased, cardiogenic shock, dialysis, ejection fraction decreased, epilepsy, heart rate increased, hepatic failure, . CORGARD dosage: 80 MG, QD. During the same period patient was treated with CORDARONE, ATORVASTATIN CALCIUM, PREVISCAN, CARDENSIEL. Patient was hospitalized. Patient recovered.

Zetia Side Effects Report #5367267-7
ZETIA problem was reported by a Physician from AUSTRALIA on June 19, 2007. Male patient, 50 years of age, weighting 176.4 lb, was diagnosed with hypertension, coronary artery disease, ischaemia, left ventricular failure and was treated with ZETIA. After drug was administered, patient experienced the following problems/side effects: anaemia, cardiac output decreased, chronic hepatic failure, hepatic enzyme increased, hepatitis acute, hepatomegaly, ischaemia, renal failure, . ZETIA dosage: unknown. During the same period patient was treated with CLOPIDOGREL BISULPHATE, LIPITOR, COVERSYL, CARVEDILOL, LASIX. Patient was hospitalized. Patient died.

Dobutamine Side Effects Report #5314521-0
Health Professional from UNITED STATES reported DOBUTAMINE problem on May 01, 2007. Male patient, 61 years of age, was treated with DOBUTAMINE. After drug was administered, patient experienced the following problems/side effects: blood pressure decreased, cardiac output decreased, oxygen saturation decreased, . DOBUTAMINE dosage: 1250MG/250ML IV DRIP. Patient recovered.

Flolan Side Effects Report #5294616-0
FLOLAN problem was reported by a Physician from JAPAN on Apr 10, 2007. Female patient, 18 years of age, weighting 158.7 lb, was diagnosed with pulmonary hypertension and was treated with FLOLAN. After drug was administered, patient experienced the following problems/side effects: cardiac index decreased, cardiac output decreased, cardiogenic shock, . FLOLAN dosage: unknown. During the same period patient was treated with DOBUTAMINE, FUROSEMIDE, DIGOXIN. Patient was hospitalized and became disabled. Patient died on 05/10/2006.

Cymbalta Side Effects Report #5340064-4
Consumer or non-health professional from UNITED STATES reported CYMBALTA problem on Nov 13, 2006. Male patient, 70 years of age, was diagnosed with depression and was treated with CYMBALTA. After drug was administered, patient experienced the following problems/side effects: cardiac failure congestive, cardiac output decreased, dyspnoea, . CYMBALTA dosage: 20 MG, 3/D. During the same period patient was treated with MELATONIN, COREG, LISINOPRIL, FUROSEMIDE, SPIRONOLACTONE, FLUOXETINE. Patient was hospitalized. Patient recovered.

Desoxyn Side Effects Report #5678386-X
DESOXYN problem was reported by a Physician from UNITED STATES on Mar 09, 2008. Female patient, 42 years of age, was treated with DESOXYN. After drug was administered, patient experienced the following problems/side effects: arterial spasm, blood pressure increased, cardiac output decreased, mitral valve incompetence, palpitations, peripheral coldness, poor peripheral circulation, procedural hypotension, . DESOXYN dosage: unknown. Patient was hospitalized. Patient recovered.

Hydrochlorothiaz Side Effects Report #5683443-8
Consumer or non-health professional from reported HYDROCHLOROTHIAZIDE problem on Mar 13, 2008. Female patient, 70 years of age, was diagnosed with hypertension and was treated with HYDROCHLOROTHIAZIDE. After drug was administered, patient experienced the following problems/side effects: agitation, back pain, cardiac output decreased, chills, confusional state, cyanosis, dizziness, dyspnoea, faecal incontinence, . HYDROCHLOROTHIAZIDE dosage: 12.5MG X 1 DOSE. During the same period patient was treated with BISOPROLOL FUMARATE, ACETYLSALICYLIC ACID SRT. Patient was hospitalized. Patient recovered.

Zidovudine Side Effects Report #5569740-5
ZIDOVUDINE problem was reported by a Consumer or non-health professional from NETHERLANDS on Dec 04, 2007. Male patient was diagnosed with prophylaxis against hiv infection, hiv test positive, premature rupture of membranes and was treated with ZIDOVUDINE. After drug was administered, patient experienced the following problems/side effects: atrioventricular block complete, blood lactic acid increased, cardiac output decreased, congestive cardiomyopathy, no therapeutic response, premature baby, . ZIDOVUDINE dosage: 4 MG/KG / PER DAY. During the same period patient was treated with LAMIVUDINE, LOPINAVIR AND RITONAVIR. Patient recovered.

Tracleer Side Effects Report #5578455-9
Physician from UNITED STATES reported TRACLEER problem on Dec 18, 2007. Female patient, 49 years of age, was diagnosed with pulmonary hypertension and was treated with TRACLEER. After drug was administered, patient experienced the following problems/side effects: blood pressure decreased, body temperature increased, cardiac output decreased, dyspnoea, eye swelling, headache, international normalised ratio increased, lactic acidosis, lethargy, . TRACLEER dosage: 62.5 MG, BID, ORAL. During the same period patient was treated with REVATIO. Patient was hospitalized. Patient recovered.

Velcade Side Effects Report #5449557-2
VELCADE problem was reported by a Physician from UNITED STATES on Aug 27, 2007. Female patient, 52 years of age, weighting 176.4 lb, was diagnosed with non-small cell lung cancer and was treated with VELCADE. After drug was administered, patient experienced the following problems/side effects: acute respiratory distress syndrome, atrial fibrillation, cardiac output decreased, cardio-respiratory arrest, oliguria, pneumonitis, post procedural complication, pulmonary hypertension, respiratory failure, . VELCADE dosage: 0.30 MG/M2. During the same period patient was treated with TAXOL, CARBOPLATIN, CONJUGATED ESTROGENS, FLUOXETINE, NIFEDIPINE, OMEPRAZOLE, RISPERIDONE, TERBINAFINE. Patient was hospitalized. Patient died on 01/10/2005.

Amlodipine Side Effects Report #5414975-5
Health Professional from TAIWAN, PROVINCE OF CHINA reported AMLODIPINE MALEATE problem on July 05, 2007. Female patient, 40 years of age, was treated with AMLODIPINE MALEATE. After drug was administered, patient experienced the following problems/side effects: abdominal pain, bradycardia, cardiac output decreased, diastolic dysfunction, electrocardiogram qt prolonged, gastrointestinal sounds abnormal, hypotension, intentional overdose, . AMLODIPINE MALEATE dosage: 5 MG, QD, ORAL. During the same period patient was treated with GLIPIZIDE, RANITIDINE, SALINE. Patient was hospitalized. Patient recovered.

Hydrochlorothiaz Side Effects Report #5386294-7
HYDROCHLOROTHIAZIDE problem was reported by a Health Professional from BELGIUM on July 03, 2007. Female patient, 70 years of age, was diagnosed with hypertension and was treated with HYDROCHLOROTHIAZIDE. After drug was administered, patient experienced the following problems/side effects: agitation, back pain, cardiac output decreased, chills, confusional state, cyanosis, dizziness, dyspnoea, faecal incontinence, . HYDROCHLOROTHIAZIDE dosage: 12.5 MG/DAY. During the same period patient was treated with BISOPROLOL. Patient recovered.

Amlodipine Side Effects Report #5398225-4
Consumer or non-health professional from reported AMLODIPINE problem on July 19, 2007. Female patient, 40 years of age, was diagnosed with hypertension, diabetes mellitus, duodenal ulcer and was treated with AMLODIPINE. After drug was administered, patient experienced the following problems/side effects: abdominal tenderness, bradycardia, cardiac output decreased, gastrointestinal sounds abnormal, hypotension, loss of consciousness, mental status changes, nausea, nodal rhythm, . AMLODIPINE dosage: 30 MG X 1 DOSE. During the same period patient was treated with GLIPIZIDE, RANITIDINE. Patient was hospitalized. Patient recovered.

Hydrochlorothiaz Side Effects Report #5386294-7
HYDROCHLOROTHIAZIDE problem was reported by a Health Professional from BELGIUM on July 03, 2007. Female patient, 70 years of age, was diagnosed with hypertension and was treated with HYDROCHLOROTHIAZIDE. After drug was administered, patient experienced the following problems/side effects: agitation, back pain, cardiac output decreased, chills, confusional state, cyanosis, dizziness, dyspnoea, faecal incontinence, . HYDROCHLOROTHIAZIDE dosage: 12.5 MG/DAY. During the same period patient was treated with BISOPROLOL. Patient recovered.

Amlodipine Side Effects Report #5398225-4
Consumer or non-health professional from reported AMLODIPINE problem on July 19, 2007. Female patient, 40 years of age, was diagnosed with hypertension, diabetes mellitus, duodenal ulcer and was treated with AMLODIPINE. After drug was administered, patient experienced the following problems/side effects: abdominal tenderness, bradycardia, cardiac output decreased, gastrointestinal sounds abnormal, hypotension, loss of consciousness, mental status changes, nausea, nodal rhythm, . AMLODIPINE dosage: 30 MG X 1 DOSE. During the same period patient was treated with GLIPIZIDE, RANITIDINE. Patient was hospitalized. Patient recovered.

Baclofen Side Effects Report #5719068-5
BACLOFEN problem was reported by a Physician from NETHERLANDS on Apr 07, 2008. Male patient, 53 years of age, was diagnosed with muscle spasticity and was treated with BACLOFEN. After drug was administered, patient experienced the following problems/side effects: bradycardia, cardiac failure, cardiac output decreased, conduction disorder, delirium, fall, hallucination, hypertension, hyperventilation, . BACLOFEN dosage: 5MG, ORAL. Patient recovered.

Zetia Side Effects Report #5356405-8
Physician from AUSTRALIA reported ZETIA problem on June 05, 2007. Male patient, 50 years of age, weighting 176.4 lb, was diagnosed with hypertension, coronary artery disease, ischaemia, left ventricular failure and was treated with ZETIA. After drug was administered, patient experienced the following problems/side effects: anaemia, cardiac disorder, cardiac output decreased, chronic hepatic failure, hepatic enzyme increased, hepatitis acute, hepatomegaly, ischaemia, . ZETIA dosage: unknown. During the same period patient was treated with CLOPIDOGREL BISULPHATE, LIPITOR, COVERSYL, CARVEDILOL, LASIX. Patient was hospitalized. Patient died.

Sutent Side Effects Report #5273575-0
SUTENT problem was reported by a Pharmacist from UNITED STATES on Mar 21, 2007. Female patient, weighting 196.7 lb, was treated with SUTENT. After drug was administered, patient experienced the following problems/side effects: asthenia, cardiac arrest, cardiac output decreased, cardiogenic shock, chest pain, coronary artery disease, fatigue, sinus bradycardia, . SUTENT dosage: 12.5MG DAILY PO. Patient died on 02/26/2007.

Nitrofurantoin Side Effects Report #5284081-1
Consumer or non-health professional from UNITED STATES reported NITROFURANTOIN problem on Mar 15, 2007. Male patient, 87 years of age, was treated with NITROFURANTOIN. After drug was administered, patient experienced the following problems/side effects: abasia, asthenia, cardiac output decreased, dyspnoea, dyspnoea exertional, heart rate decreased, oedema peripheral, . NITROFURANTOIN dosage: unknown. During the same period patient was treated with ISOSORBIDE, METAPROTERENOL. Patient was hospitalized. Patient recovered.