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DIASTOLIC DYSFUNCTION side effect

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Bevacizumab Side Effects Report #5629396-X
Consumer or non-health professional from UNITED STATES reported BEVACIZUMAB problem on Feb 15, 2008. Male patient, weighting 160.3 lb, was treated with BEVACIZUMAB. After drug was administered, patient experienced the following problems/side effects: diastolic dysfunction, left ventricular dysfunction, . BEVACIZUMAB dosage: 762 MG. During the same period patient was treated with CAMPTOSAR, ELOXATIN, DILTIAZEM. Patient recovered.

Myozyme Side Effects Report #5567346-5
MYOZYME problem was reported by a Physician from SAUDI ARABIA on Dec 11, 2007. Male patient, child 1 years of age, weighting 13.23 lb, was diagnosed with glycogen storage disease type ii and was treated with MYOZYME. After drug was administered, patient experienced the following problems/side effects: diastolic dysfunction, infection, respiratory failure, . MYOZYME dosage: 20 MG/KG Q2WKS IV. During the same period patient was treated with VANCOMYCIN, CEFTAZIDIME. Patient was hospitalized and became disabled. Patient recovered.

Myozyme Side Effects Report #5513552-5
Physician from SAUDI ARABIA reported MYOZYME problem on Oct 25, 2007. Male patient, child 1 years of age, weighting 13.23 lb, was diagnosed with glycogen storage disease type ii and was treated with MYOZYME. After drug was administered, patient experienced the following problems/side effects: diastolic dysfunction, infection, respiratory failure, . MYOZYME dosage: 20 MG/KG Q2WKS IV. During the same period patient was treated with VANCOMYCIN, CEFTAZIDIME. Patient was hospitalized and became disabled. Patient recovered.

Cetuximab Side Effects Report #5518115-3
CETUXIMAB problem was reported by a Health Professional from UNITED STATES on Nov 13, 2007. Female patient, 37 years of age, weighting 134.5 lb, was diagnosed with breast cancer metastatic and was treated with CETUXIMAB. After drug was administered, patient experienced the following problems/side effects: diastolic dysfunction, pericardial effusion, . CETUXIMAB dosage: 432MG 8 WEEK IV. During the same period patient was treated with CARBOPLATIN. Patient was hospitalized. Patient recovered.


Revlimid Side Effects Report #5489553-2
Pharmacist from UNITED STATES reported REVLIMID problem on Oct 16, 2007. Male patient, weighting 323.0 lb, was diagnosed with multiple myeloma and was treated with REVLIMID. After drug was administered, patient experienced the following problems/side effects: diastolic dysfunction, oedema, pain, weight decreased, . REVLIMID dosage: 25MG DAILY PO. During the same period patient was treated with DEXAMETHASONE. Patient was hospitalized. Patient recovered.

Myozyme Side Effects Report #5501335-1
MYOZYME problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 15, 2007. Female patient, 62 years of age, weighting 170.9 lb, was diagnosed with glycogen storage disease type ii and was treated with MYOZYME. After drug was administered, patient experienced the following problems/side effects: diastolic dysfunction, hypotension, . MYOZYME dosage: 20 MG/KG Q2WKS IV. Patient was hospitalized. Patient recovered.

Loratadine Side Effects Report #5429315-5
Physician from ISRAEL reported LORATADINE problem on Oct 12, 2005. Female patient, 73 years of age, was diagnosed with hypersensitivity, ventricular tachycardia and was treated with LORATADINE. After drug was administered, patient experienced the following problems/side effects: diastolic dysfunction, left ventricular hypertrophy, sinus bradycardia, torsade de pointes, ventricular extrasystoles, . LORATADINE dosage: 10 MG, DAILY. During the same period patient was treated with AMIODARONE, CILAZAPRIL, PRAVASTATIN, WARFARIN. Patient was hospitalized. Patient recovered.

Lyrica Side Effects Report #5775833-X
LYRICA problem was reported by a Physician from UNITED STATES on June 05, 2008. Female patient, weighting 153.0 lb, was diagnosed with complex regional pain syndrome, neuropathy peripheral and was treated with LYRICA. After drug was administered, patient experienced the following problems/side effects: diastolic dysfunction, pain in extremity, pulmonary hypertension, weight increased, . LYRICA dosage: unknown. During the same period patient was treated with VALIUM, ZOLOFT, ZYRTEC, CATAPRES, HYDROXYZINE, PRILOSEC. Patient recovered.

Cyclosporine Side Effects Report #5792702-X
Physician from UNITED STATES reported CYCLOSPORINE problem on June 12, 2008. Male patient, 66 years of age, was diagnosed with heart transplant and was treated with CYCLOSPORINE. After drug was administered, patient experienced the following problems/side effects: diastolic dysfunction, dysstasia, gait disturbance, haemodialysis, muscle necrosis, myopathy toxic, pneumonia, respiratory distress, . CYCLOSPORINE dosage: 150MG DAILY. During the same period patient was treated with METHYLPREDNISOLONE, PROPOFOL, COLCHICINE, SIMVASTATIN. Patient was hospitalized. Patient died.


Actos Side Effects Report #5737978-X
ACTOS problem was reported by a Health Professional from UNITED KINGDOM on May 02, 2008. Male patient, 55 years of age, was diagnosed with diabetes mellitus and was treated with ACTOS. After drug was administered, patient experienced the following problems/side effects: diastolic dysfunction, pericardial drainage, pericardial effusion, . ACTOS dosage: 15 MG (1 IN 1 D) PER ORAL. During the same period patient was treated with ASPIRIN, GLICLAZIDE, OMEPRAZOLE, SALBUTAMOL. Patient recovered.

Tracleer Side Effects Report #5701378-9
Health Professional from BELGIUM reported TRACLEER problem on Mar 25, 2008. Male patient, child 2 years of age, weighting 22.05 lb, was diagnosed with pulmonary hypertension and was treated with TRACLEER. After drug was administered, patient experienced the following problems/side effects: diastolic dysfunction, supraventricular tachycardia, . TRACLEER dosage: 31.25 MG, ORAL. Patient died on 03/04/2008.

Bevacizumab Side Effects Report #5722546-6
BEVACIZUMAB problem was reported by a Consumer or non-health professional from UNITED KINGDOM on Apr 16, 2008. Female patient, weighting 198.4 lb, was diagnosed with breast cancer metastatic and was treated with BEVACIZUMAB. After drug was administered, patient experienced the following problems/side effects: diastolic dysfunction, pulmonary hypertension, . BEVACIZUMAB dosage: 1350 MG, Q3W. During the same period patient was treated with PARACETAMOL, NEXIUM, DIABEX, SIMVASTATIN, TELFAST, BRUFEN. Patient was hospitalized. Patient recovered.

Loratadine Side Effects Report #5374131-6
Health Professional from ISRAEL reported LORATADINE problem on June 13, 2007. Female patient, 73 years of age, was diagnosed with hypersensitivity, atrial fibrillation and was treated with LORATADINE. After drug was administered, patient experienced the following problems/side effects: diastolic dysfunction, electrocardiogram qt prolonged, syncope, torsade de pointes, ventricular hypertrophy, . LORATADINE dosage: 10 MG, QD. During the same period patient was treated with CILAZAPRIL, PRAVASTATIN, WARFARIN. Patient recovered.

Orencia Side Effects Report #5655435-6
ORENCIA problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 28, 2008. Female patient, 52 years of age, weighting 134.5 lb, was diagnosed with rheumatoid arthritis and was treated with ORENCIA. After drug was administered, patient experienced the following problems/side effects: blood pressure increased, diastolic dysfunction, . ORENCIA dosage: unknown. During the same period patient was treated with METHOTREXATE, FOLIC ACID, FOSAMAX. Patient recovered.


Nelarabine Side Effects Report #5664482-X
Physician from ITALY reported NELARABINE problem on Mar 05, 2008. Female patient, 43 years of age, weighting 114.6 lb, was diagnosed with neoplasm malignant, hypertension and was treated with NELARABINE. After drug was administered, patient experienced the following problems/side effects: blood pressure diastolic increased, diastolic dysfunction, dyspnoea, hypertension, oliguria, tachycardia, . NELARABINE dosage: 1500MG PER DAY. During the same period patient was treated with ENALAPRIL MALEATE. Patient recovered.

Avandamet Side Effects Report #5594809-9
AVANDAMET problem was reported by a Consumer or non-health professional from FRANCE on Jan 10, 2008. Male patient, 62 years of age, weighting 224.9 lb, was treated with AVANDAMET. After drug was administered, patient experienced the following problems/side effects: cardiac failure, diastolic dysfunction, hypoglycaemia, left ventricular hypertrophy, oedema peripheral, pulmonary congestion, . AVANDAMET dosage: unknown. During the same period patient was treated with HYZAAR, DAONIL, LIPANTHYL, ALDALIX. Patient was hospitalized. Patient recovered.

Nelarabine Side Effects Report #5532090-7
Physician from ITALY reported NELARABINE problem on Nov 30, 2007. Female patient, 43 years of age, weighting 114.6 lb, was diagnosed with hypertension and was treated with NELARABINE. After drug was administered, patient experienced the following problems/side effects: blood pressure diastolic increased, diastolic dysfunction, dyspnoea, hypertension, oliguria, tachycardia, . NELARABINE dosage: 1500MG PER DAY. During the same period patient was treated with ENALAPRIL. Patient recovered.

Novantrone Side Effects Report #5578562-0
NOVANTRONE problem was reported by a Consumer or non-health professional from FRANCE on Dec 11, 2007. Male patient, 76 years of age, was diagnosed with metastases to bone, prostate cancer and was treated with NOVANTRONE. After drug was administered, patient experienced the following problems/side effects: cardiac failure, diastolic dysfunction, left ventricular failure, pleural effusion, . NOVANTRONE dosage: 20 MG, 1 CYCLE, INTRAVENOUS. Patient was hospitalized. Patient recovered.

Erbitux Side Effects Report #5529307-1
Consumer or non-health professional from UNITED STATES reported ERBITUX problem on Nov 20, 2007. Female patient, 68 years of age, weighting 130.1 lb, was diagnosed with non-small cell lung cancer and was treated with ERBITUX. After drug was administered, patient experienced the following problems/side effects: anorexia, diastolic dysfunction, dyspnoea, fatigue, hypoxia, left ventricular dysfunction, pulmonary oedema, sinus tachycardia, . ERBITUX dosage: unknown. During the same period patient was treated with PACLITAXEL, CARBOPLATIN, BEVACIZUMAB, COREG, LASIX. Patient was hospitalized. Patient recovered.


Bevacizumab Side Effects Report #5468934-7
BEVACIZUMAB problem was reported by a Physician from UNITED STATES on Sept 14, 2007. Female patient, weighting 156.0 lb, was diagnosed with colon cancer metastatic, mitral valve prolapse and was treated with BEVACIZUMAB. After drug was administered, patient experienced the following problems/side effects: aortic arteriosclerosis, diastolic dysfunction, ischaemic stroke, mitral valve sclerosis, tricuspid valve sclerosis, . BEVACIZUMAB dosage: 5 MG/KG, Q2W. During the same period patient was treated with CORGARD, LORTAB, ACIPHEX, EFFEXOR, SYNTHROID, ZOCOR, MOBIC. Patient was hospitalized. Patient died on 07/04/2007.

Rebif Side Effects Report #5403318-9
Health Professional from UNITED STATES reported REBIF problem on July 16, 2007. Female patient, 54 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 failure congestive, diastolic dysfunction, fatigue, hepatitis b, hypersomnia, lethargy, weight increased, . REBIF dosage: unknown. During the same period patient was treated with PLAVIX, CLONIDINE, ASPIRIN. Patient recovered.

Rebif Side Effects Report #5403318-9
REBIF problem was reported by a Health Professional from UNITED STATES on July 16, 2007. Female patient, 54 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 failure congestive, diastolic dysfunction, fatigue, hepatitis b, hypersomnia, lethargy, weight increased, . REBIF dosage: unknown. During the same period patient was treated with PLAVIX, CLONIDINE, ASPIRIN. Patient recovered.

Cytarabine Side Effects Report #5772086-3
Consumer or non-health professional from UNITED STATES reported CYTARABINE problem on June 12, 2008. Female patient, weighting 136.5 lb, was treated with CYTARABINE. After drug was administered, patient experienced the following problems/side effects: bone marrow failure, diastolic dysfunction, electrocardiogram qt prolonged, febrile neutropenia, septic shock, streptococcal sepsis, . CYTARABINE dosage: 13190 MG. During the same period patient was treated with MYLOTARG, MITOXANTRONE HYDROCHLORIDE. Patient was hospitalized. Patient recovered.

Tracleer Side Effects Report #5746755-5
TRACLEER problem was reported by a Health Professional from BELGIUM on May 07, 2008. Male patient, child 2 years of age, weighting 22.05 lb, was diagnosed with pulmonary arterial hypertension and was treated with TRACLEER. After drug was administered, patient experienced the following problems/side effects: cardiac failure, diastolic dysfunction, supraventricular tachycardia, . TRACLEER dosage: 31.25 MG, ORAL. During the same period patient was treated with SILDENAFILLET. Patient died on 03/04/2008.

Lisinopril Side Effects Report #5749955-3
Pharmacist from UNITED STATES reported LISINOPRIL problem on May 21, 2008. Male patient, 57 years of age, weighting 227.0 lb, was diagnosed with hypertension and was treated with LISINOPRIL. After drug was administered, patient experienced the following problems/side effects: blood pressure increased, diastolic dysfunction, left ventricular hypertrophy, syncope, . LISINOPRIL dosage: 20 MG EVERY DAY PO. Patient was hospitalized. Patient recovered.

Wellbutrin Side Effects Report #5753897-7
WELLBUTRIN problem was reported by a Physician from BELGIUM on May 23, 2008. Female patient, 72 years of age, weighting 271.2 lb, was diagnosed with depression and was treated with WELLBUTRIN. After drug was administered, patient experienced the following problems/side effects: atrial fibrillation, diastolic dysfunction, . WELLBUTRIN dosage: 150MG PER DAY. During the same period patient was treated with CARDIOASPIRINE, XANAX, EMCONCOR, LASIX, PIROXICAM, LIPITOR, RISPERDAL, LORAZEPAM. Patient was hospitalized. Patient recovered.

Candesartan Side Effects Report #5302180-2
Health Professional from JAPAN reported CANDESARTAN problem on Apr 10, 2007. Male patient, 28 years of age, weighting 165.3 lb, was diagnosed with hypertension and was treated with CANDESARTAN. After drug was administered, patient experienced the following problems/side effects: chest pain, diastolic dysfunction, dyspnoea, hypertension, mitral valve incompetence, renin increased, tricuspid valve incompetence, ventricular hypertrophy, . CANDESARTAN dosage: unknown. During the same period patient was treated with LERCANIDIPINE, HYDROCHLOROTHIAZIDE, URAPIDIL, RILMENIDINE. Patient was hospitalized. Patient recovered.

Actos Side Effects Report #5542053-3
ACTOS problem was reported by a Consumer or non-health professional from JAPAN on Nov 21, 2007. Female patient, 66 years of age, was diagnosed with type 2 diabetes mellitus and was treated with ACTOS. After drug was administered, patient experienced the following problems/side effects: brain natriuretic peptide increased, cardiac failure, diastolic dysfunction, dyspnoea, hypercapnia, hypoxia, oxygen saturation decreased, pco2 increased, . ACTOS dosage: 30 MG (15 MG, 2 IN 1 D) PER ORAL. During the same period patient was treated with AMLODIPINE BESYLATE, AMARYL, PRAVASTATIN, AROMASIN. Patient was hospitalized. Patient recovered.

Aromasin Side Effects Report #5574708-9
Health Professional from UNITED STATES reported AROMASIN problem on Dec 21, 2007. Female patient, weighting 181.0 lb, was diagnosed with breast cancer and was treated with AROMASIN. After drug was administered, patient experienced the following problems/side effects: cardiac failure congestive, condition aggravated, diastolic dysfunction, hypercalcaemia, . AROMASIN dosage: 25 MG ONCE PER DAY ORAL. During the same period patient was treated with ATACAND, LISINOPRIL, HYDROCHLOROTHIAZIDE, CLONIDINE, ATENOLOL, ASPIRIN. Patient was hospitalized. Patient recovered.

Cyclophosphamide Side Effects Report #5479442-1
CYCLOPHOSPHAMIDE problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 03, 2007. Female patient, weighting 129.0 lb, was treated with CYCLOPHOSPHAMIDE. After drug was administered, patient experienced the following problems/side effects: atrial flutter, blood creatinine abnormal, diastolic dysfunction, dyspnoea, febrile neutropenia, haemodialysis, haemoglobin abnormal, herpes simplex serology positive, hypotension, . CYCLOPHOSPHAMIDE dosage: 1155 MG. During the same period patient was treated with DOXIL, HEPARIN LOCK, LORAZEPAM, LUCENTIS, NORVASC, PRILOSEC, PROCRIT, PROPOXYPHENE. Patient was hospitalized. Patient recovered.

Clonidine Side Effects Report #5481771-2
Consumer or non-health professional from UNITED STATES reported CLONIDINE problem on Sept 25, 2007. Female patient, weighting 37.00 lb, was diagnosed with agitation and was treated with CLONIDINE. After drug was administered, patient experienced the following problems/side effects: cardiac arrest, chest x-ray abnormal, diastolic dysfunction, echocardiogram abnormal, heart rate increased, pulse absent, sedation, sinus bradycardia, ventricular dysfunction, . CLONIDINE dosage: 0.3 MG OVER 9 HR PERIOD, ORAL. During the same period patient was treated with ZANTAC, LACTULOSE, LIORSEAL. Patient recovered.

Sudafed Side Effects Report #5482007-9
SUDAFED S problem was reported by a Consumer or non-health professional from UNITED STATES on Sept 19, 2007. Female patient, 41 years of age, weighting 180.0 lb, was diagnosed with cough, contraception and was treated with SUDAFED S. After drug was administered, patient experienced the following problems/side effects: aphasia, cerebral infarction, diastolic dysfunction, hypertension, lacunar infarction, mitral valve incompetence, tricuspid valve incompetence, . SUDAFED S dosage: unknown. During the same period patient was treated with ORTHO EVRA, DIMETAPP, ROBITUSSIN, MIGRANAL, PENICILLIN, ORAL CONTRACEPTIVE NOS, DEPO PROVERA. Patient was hospitalized. Patient recovered.

Exubera Side Effects Report #5456932-9
Physician from UNITED STATES reported EXUBERA problem on Sept 06, 2007. Female patient, 71 years of age, was diagnosed with diabetes mellitus and was treated with EXUBERA. After drug was administered, patient experienced the following problems/side effects: abdominal pain upper, chest pain, diastolic dysfunction, dyspnoea, hyperhidrosis, nausea, vomiting, . EXUBERA dosage: unknown. During the same period patient was treated with INSULIN DETEMIR, NOVOLOG, NPH INSULIN. Patient was hospitalized. Patient recovered.

Novantrone Side Effects Report #5398333-8
NOVANTRONE problem was reported by a Consumer or non-health professional from UNITED STATES on July 11, 2007. Female patient, 56 years of age, weighting 210.0 lb, was diagnosed with multiple sclerosis and was treated with NOVANTRONE. After drug was administered, patient experienced the following problems/side effects: cardiac stress test abnormal, coronary artery occlusion, diastolic dysfunction, dyspnoea, . NOVANTRONE dosage: unknown. During the same period patient was treated with REBIF, BACLOFEN, PROVIGIL, IMURAN. Patient recovered.

Diprivan Side Effects Report #5401147-3
Health Professional from UNITED STATES reported DIPRIVAN problem on July 20, 2007. Male patient, 66 years of age, was diagnosed with sedation, polymyositis and was treated with DIPRIVAN. After drug was administered, patient experienced the following problems/side effects: blood pressure systolic increased, blood uric acid increased, diastolic dysfunction, gouty tophus, haemodialysis, mitochondrial toxicity, myopathy toxic, oliguria, . DIPRIVAN dosage: unknown. During the same period patient was treated with SIMVASTATIN, COLCHICUM JTL LIQ, CYCLOSPORINE, METHYLPREDNISOLONE, PREDNISONE, MYCOPHENOLATE, INSULIN. Patient was hospitalized and became disabled. Patient died.

Novantrone Side Effects Report #5398333-8
NOVANTRONE problem was reported by a Consumer or non-health professional from UNITED STATES on July 11, 2007. Female patient, 56 years of age, weighting 210.0 lb, was diagnosed with multiple sclerosis and was treated with NOVANTRONE. After drug was administered, patient experienced the following problems/side effects: cardiac stress test abnormal, coronary artery occlusion, diastolic dysfunction, dyspnoea, . NOVANTRONE dosage: unknown. During the same period patient was treated with REBIF, BACLOFEN, PROVIGIL, IMURAN. Patient recovered.

Diprivan Side Effects Report #5401147-3
Health Professional from UNITED STATES reported DIPRIVAN problem on July 20, 2007. Male patient, 66 years of age, was diagnosed with sedation, polymyositis and was treated with DIPRIVAN. After drug was administered, patient experienced the following problems/side effects: blood pressure systolic increased, blood uric acid increased, diastolic dysfunction, gouty tophus, haemodialysis, mitochondrial toxicity, myopathy toxic, oliguria, . DIPRIVAN dosage: unknown. During the same period patient was treated with SIMVASTATIN, COLCHICUM JTL LIQ, CYCLOSPORINE, METHYLPREDNISOLONE, PREDNISONE, MYCOPHENOLATE, INSULIN. Patient was hospitalized and became disabled. Patient died.

Methadone Side Effects Report #5787810-3
METHADONE problem was reported by a Pharmacist from UNITED STATES on June 24, 2008. Male patient, 49 years of age, was diagnosed with agitation, anxiety and was treated with METHADONE. After drug was administered, patient experienced the following problems/side effects: agitation, cardiac arrest, diastolic dysfunction, electrocardiogram qt prolonged, fluid overload, hypoxia, treatment noncompliance, ventricular tachycardia, . METHADONE dosage: 50 MG TWICE DAILY PO. During the same period patient was treated with HALOPERIDOL, THIAMINE, CHLORDIAZEPOXIDE, LORAZEPAM, ONDANSETRON, ACETAMINOPHEN. Patient was hospitalized. Patient recovered.

Femara Side Effects Report #5345369-9
Consumer or non-health professional from UNITED STATES reported FEMARA problem on May 25, 2007. Female patient, 61 years of age, weighting 199.0 lb, was diagnosed with breast cancer and was treated with FEMARA. After drug was administered, patient experienced the following problems/side effects: arthralgia, cardiac flutter, diastolic dysfunction, electrocardiogram ambulatory, gait disturbance, heart rate irregular, joint injury, palpitations, pulmonary valve incompetence, . FEMARA dosage: unknown. Patient recovered.

Femara Side Effects Report #5363778-9
FEMARA problem was reported by a Consumer or non-health professional from UNITED STATES on June 12, 2007. Female patient, 61 years of age, weighting 199.0 lb, was diagnosed with breast cancer and was treated with FEMARA. After drug was administered, patient experienced the following problems/side effects: arthralgia, cardiac flutter, diastolic dysfunction, electrocardiogram ambulatory, gait disturbance, heart rate irregular, joint injury, osteoarthritis, pain in extremity, . FEMARA dosage: 2.5 MG, QD. During the same period patient was treated with VITAMIN CAP, GLUCOSAMINE, VITAMIN B CAP, ASPIRIN. Patient recovered.

Femara Side Effects Report #5364393-3
Consumer or non-health professional from UNITED STATES reported FEMARA problem on June 12, 2007. Female patient, 61 years of age, weighting 199.0 lb, was diagnosed with breast cancer and was treated with FEMARA. After drug was administered, patient experienced the following problems/side effects: arthralgia, cardiac flutter, diastolic dysfunction, electrocardiogram ambulatory, gait disturbance, heart rate irregular, joint injury, osteoarthritis, pain in extremity, . FEMARA dosage: 2.5 MG, QD. During the same period patient was treated with VITAMIN CAP, GLUCOSAMINE, VITAMIN B CAP, ASPIRIN. Patient recovered.

Duraclon Side Effects Report #5264404-X
DURACLON problem was reported by a Physician from UNITED STATES on Feb 26, 2007. Female patient, child 5 years of age, weighting 37.04 lb, was diagnosed with restlessness and was treated with DURACLON. After drug was administered, patient experienced the following problems/side effects: blood pressure decreased, cardiac arrest, diastolic dysfunction, overdose, pulse absent, sinus bradycardia, . DURACLON dosage: 0.1 MG; PRN; GT. During the same period patient was treated with SEVOFLURANE, NITROUS OXIDE W, RANITIDINE, LACTULOSE, BACLOFEN. Patient was hospitalized. Patient recovered.

Thalomid Side Effects Report #5274715-X
Physician from UNITED STATES reported THALOMID problem on Mar 13, 2007. Male patient, 58 years of age, was diagnosed with multiple myeloma and was treated with THALOMID. After drug was administered, patient experienced the following problems/side effects: cardiac disorder, condition aggravated, diastolic dysfunction, fluid overload, hypertrophic cardiomyopathy, neuropathy peripheral, non-obstructive cardiomyopathy, . THALOMID dosage: 200MG - 100MG - 50 MG, DAILY, ORAL. During the same period patient was treated with DEXAMETHASONE, VELCADE. Patient recovered.