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BLOOD ALBUMIN DECREASED side effect

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Prograf Side Effects Report #5580096-4
Physician from JAPAN reported PROGRAF problem on Dec 14, 2007. Male patient, 38 years of age, weighting 108.0 lb, was diagnosed with lung transplant and was treated with PROGRAF. After drug was administered, patient experienced the following problems/side effects: blood albumin decreased, blood lactate dehydrogenase increased, diarrhoea, eosinophil count increased, lymphoproliferative disorder, opportunistic infection, osteomyelitis, pneumonia, . PROGRAF dosage: unknown. Patient was hospitalized. Patient recovered.

Cytarabine Side Effects Report #5646675-0
CYTARABINE problem was reported by a Physician from VENEZUELA on Feb 26, 2008. Female patient, 21 years of age, weighting 238.1 lb, was diagnosed with chronic myeloid leukaemia and was treated with CYTARABINE. After drug was administered, patient experienced the following problems/side effects: blood albumin decreased, blood creatinine increased, blood urea increased, glomerular filtration rate decreased, nephrotic syndrome, oedema, weight increased, . CYTARABINE dosage: unknown. During the same period patient was treated with IDARUBICIN, ALBUMIN, FILGRASTIM, PREDNISONE. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5646984-5
Physician from JAPAN reported ARIXTRA problem on Feb 26, 2008. Female patient, 48 years of age, weighting 88.41 lb, was diagnosed with thrombosis prophylaxis, infection prophylaxis, insomnia, pruritus, gastritis, systemic lupus erythematosus and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: blood albumin decreased, blood alkaline phosphatase increased, blood creatinine increased, blood iron decreased, blood urea increased, fibrin d dimer increased, gamma-glutamyltransferase increased, haematocrit decreased, haemoglobin decreased, . ARIXTRA dosage: 1.5MG PER DAY. During the same period patient was treated with LACTEC, RASENAZOLIN, MYSLEE, CLARITIN REDI, RIVOTRIL, PROMAC, GASTER D, PREDNISOLONE. Patient recovered.

Tramadol Side Effects Report #5650175-1
TRAMADOL problem was reported by a Physician from FRANCE on Feb 18, 2008. Male patient, 33 years of age, was treated with TRAMADOL. After drug was administered, patient experienced the following problems/side effects: blood albumin decreased, blood bicarbonate decreased, blood creatine phosphokinase increased, blood glucose increased, blood lactic acid decreased, body temperature decreased, bundle branch block right, cardiac arrest, cardiogenic shock, . TRAMADOL dosage: unknown. During the same period patient was treated with HYDROXYZINE, GABAPENTIN, CLONAZEPAM. Patient was hospitalized. Patient recovered.


Temozolomide Side Effects Report #5663906-1
Physician from UNITED KINGDOM reported TEMOZOLOMIDE problem on Mar 06, 2008. Female patient, 78 years of age, weighting 145.3 lb, was diagnosed with glioblastoma, swelling and was treated with TEMOZOLOMIDE. After drug was administered, patient experienced the following problems/side effects: blood albumin decreased, blood creatinine decreased, hyperglycaemia, lymphocyte count decreased, monocyte count decreased, platelet count decreased, pneumonia aspiration, urinary tract infection, . TEMOZOLOMIDE dosage: unknown. During the same period patient was treated with DEXAMETHASONE, PHENYTOIN, PARACETAMOL, DOMPERIDONE. Patient was hospitalized. Patient died on 01/29/2008.

Tasmar Side Effects Report #5671426-3
TASMAR problem was reported by a Pharmacist from CANADA on Mar 03, 2008. Male patient, 90 years of age, was diagnosed with parkinson's disease and was treated with TASMAR. After drug was administered, patient experienced the following problems/side effects: blood albumin decreased, blood creatinine increased, blood urea increased, dyspnoea, hallucination, oedema peripheral, . TASMAR dosage: 300 MG; QD; PO. During the same period patient was treated with SINEMET CR, BROMOCRIPTINE MESYLATE, DOCUSATE, DOMPERIDONE. Patient was hospitalized. Patient recovered.

Didanosine Side Effects Report #5673167-5
Health Professional from UNITED STATES reported DIDANOSINE problem on Mar 14, 2008. Female patient, 49 years of age, was diagnosed with hiv infection and was treated with DIDANOSINE. After drug was administered, patient experienced the following problems/side effects: blood albumin decreased, cardiac murmur, cardiac tamponade, cardiomegaly, congestive cardiomyopathy, pericardial effusion, pleural effusion, respiratory distress, respiratory rate increased, . DIDANOSINE dosage: unknown. During the same period patient was treated with PREZISTA, TRUVADA, RITONAVIR, ROSUVASTATIN CALCIUM, LISINOPRIL, BUPROPION, PROZAC. Patient was hospitalized. Patient recovered.

Tramadol Side Effects Report #5678700-5
TRAMADOL problem was reported by a Physician from FRANCE on Mar 10, 2008. Male patient, 33 years of age, was treated with TRAMADOL. After drug was administered, patient experienced the following problems/side effects: blood albumin decreased, blood bicarbonate decreased, blood glucose increased, blood lactic acid increased, body temperature decreased, bundle branch block right, cardiac arrest, cerebral disorder, chest x-ray abnormal, . TRAMADOL dosage: unknown. During the same period patient was treated with HYDROXYZINE, GABAPENTIN, CLONAZEPAM. Patient was hospitalized. Patient recovered.

Levemir Side Effects Report #5684424-0
Physician from JAPAN reported LEVEMIR problem on Mar 24, 2008. Female patient, 65 years of age, was diagnosed with insulin-requiring type 2 diabetes mellitus and was treated with LEVEMIR. After drug was administered, patient experienced the following problems/side effects: blood albumin decreased, cardiac arrest, glycosylated haemoglobin increased, hyperglycaemia, hyperkalaemia, hypoglycaemia, nasopharyngitis, nephropathy, respiratory arrest, . LEVEMIR dosage: unknown. During the same period patient was treated with NOVORAPID CHU FLEXPEN, NOVOLIN N, MIGLITOL, CRESTOR. Patient died on 03/05/2008.


Amevive Side Effects Report #5691286-4
AMEVIVE IM problem was reported by a Physician from UNITED STATES on Mar 13, 2008. Female patient, 44 years of age, weighting 214.1 lb, was diagnosed with psoriasis and was treated with AMEVIVE IM. After drug was administered, patient experienced the following problems/side effects: blood albumin decreased, blood pressure decreased, chills, electrocardiogram st segment abnormal, electrocardiogram t wave abnormal, escherichia sepsis, gastroenteritis radiation, haematocrit decreased, haemoglobin decreased, . AMEVIVE IM dosage: 15 MG, WEEKLY, INTRAMUSCULAR. Patient was hospitalized. Patient recovered.

Cosmegen Side Effects Report #5615734-0
Consumer or non-health professional from UNITED STATES reported COSMEGEN problem on Jan 22, 2008. Male patient, 40 years of age, was diagnosed with germ cell cancer and was treated with COSMEGEN. After drug was administered, patient experienced the following problems/side effects: blood albumin decreased, blood bicarbonate decreased, blood bilirubin increased, blood calcium decreased, blood chloride increased, blood creatine increased, blood phosphorus decreased, blood potassium decreased, febrile neutropenia, . COSMEGEN dosage: 2 MG; Q2W; IV. During the same period patient was treated with CISPLATIN, ETOPOSIDE, METHOTREXATE, DEXTROSE WITH POTASSIUM BICARBONATE AND S, FILGRASTIM, FOLINIC ACID. Patient died on 06/20/1999.

Arsenic Side Effects Report #5621670-6
ARSENIC TRIOXIDE problem was reported by a Physician from UNITED STATES on Jan 22, 2008. Female patient, 82 years of age, weighting 202.0 lb, was diagnosed with acute myeloid leukaemia and was treated with ARSENIC TRIOXIDE. After drug was administered, patient experienced the following problems/side effects: blood albumin decreased, chest pain, condition aggravated, confusional state, delirium, dyspnoea, fluid overload, fungal infection, . ARSENIC TRIOXIDE dosage: 18.5 MG QD INTRAVENOUS. During the same period patient was treated with CYTARABINE, CARTIA XT, BIOTENE, CEFEPIME, CYCLOBENZAPRINE, DILTIAZAEM, ESOMEPRAZOLE MAGNESIUM, GABAPENTIN. Patient died on 01/24/2008.

Temozolomide Side Effects Report #5625275-2
Physician from UNITED KINGDOM reported TEMOZOLOMIDE problem on Feb 01, 2008. Female patient, 78 years of age, weighting 145.3 lb, was diagnosed with glioblastoma, swelling and was treated with TEMOZOLOMIDE. After drug was administered, patient experienced the following problems/side effects: blood albumin decreased, blood creatinine decreased, c-reactive protein increased, hyperglycaemia, lymphocyte count decreased, monocyte count decreased, platelet count decreased, protein total decreased, urinary tract infection, . TEMOZOLOMIDE dosage: unknown. During the same period patient was treated with DEXAMETHASONE, PHENYTOIN, ACETAMINOPHEN, DOMPERIDONE. Patient was hospitalized. Patient died on 01/29/2008.

Hydroxyzine Side Effects Report #5628883-8
HYDROXYZINE HYDROCHLORIDE problem was reported by a Consumer or non-health professional from FRANCE on Feb 05, 2008. Male patient, 33 years of age, was treated with HYDROXYZINE HYDROCHLORIDE. After drug was administered, patient experienced the following problems/side effects: blood albumin decreased, blood bicarbonate decreased, blood creatine phosphokinase increased, blood creatinine increased, blood glucose increased, blood lactic acid increased, body temperature decreased, bundle branch block right, cardiac arrest, . HYDROXYZINE HYDROCHLORIDE dosage: unknown. During the same period patient was treated with GABAPENTIN, TRAMADOL, CLONAZEPAM. Patient was hospitalized. Patient recovered.


Arixtra Side Effects Report #5629666-5
Physician from JAPAN reported ARIXTRA problem on Feb 08, 2008. Female patient, 48 years of age, weighting 88.41 lb, was diagnosed with thrombosis prophylaxis, infection prophylaxis, insomnia, pruritus, gastritis, systemic lupus erythematosus and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: blood albumin decreased, blood alkaline phosphatase increased, blood creatinine increased, blood iron decreased, blood urea increased, fibrin d dimer increased, gamma-glutamyltransferase increased, haematocrit decreased, haemoglobin decreased, . ARIXTRA dosage: 1.5MG PER DAY. During the same period patient was treated with LACTEC, RASENAZOLIN, MYSLEE, CLARITIN REDI, RIVOTRIL, PROMAC, GASTER D, PREDNISOLONE. Patient recovered.

Enbrel Side Effects Report #5634611-2
ENBREL problem was reported by a Health Professional from BRAZIL on Feb 12, 2008. Female patient, 59 years of age, weighting 88.18 lb, was diagnosed with psoriatic arthropathy and was treated with ENBREL. After drug was administered, patient experienced the following problems/side effects: blood albumin decreased, blood calcium decreased, blood creatinine increased, blood pressure decreased, blood urea increased, dehydration, malnutrition, protein total decreased, sepsis, . ENBREL dosage: unknown. Patient was hospitalized. Patient died on 01/25/2008.

Propylthiouracil Side Effects Report #5635698-3
Consumer or non-health professional from TURKEY reported PROPYLTHIOURACIL problem on Feb 11, 2008. Female patient, 43 years of age, was diagnosed with basedow's disease and was treated with PROPYLTHIOURACIL. After drug was administered, patient experienced the following problems/side effects: blood albumin decreased, blood immunoglobulin e increased, blood ph increased, breath sounds abnormal, eosinophil percentage increased, haemoglobin decreased, neutrophil percentage decreased, no therapeutic response, percussion test abnormal, . PROPYLTHIOURACIL dosage: unknown. Patient was hospitalized. Patient recovered.

Acyclovir Side Effects Report #5635889-1
ACYCLOVIR problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 06, 2008. Female patient, 77 years of age, was diagnosed with herpes zoster and was treated with ACYCLOVIR. After drug was administered, patient experienced the following problems/side effects: blood albumin decreased, blood creatine increased, blood glucose increased, blood sodium decreased, coma, haemodialysis, haemoglobin decreased, neurotoxicity, pneumonia aspiration, . ACYCLOVIR dosage: 800 MG; ORAL; TWICE A DAY, 800 MG; TWICE A DAY, ORAL. During the same period patient was treated with NIFEDIPINE ER, FLUOXETINE, OMEPRAZOLE, ERYTHROPOIETIN, IRON. Patient was hospitalized. Patient recovered.

Mylotarg Side Effects Report #5636498-0
Physician from JAPAN reported MYLOTARG problem on Feb 13, 2008. Male patient, weighting 112.4 lb, was diagnosed with acute myeloid leukaemia recurrent, prophylaxis and was treated with MYLOTARG. After drug was administered, patient experienced the following problems/side effects: blood albumin decreased, blood lactate dehydrogenase increased, blood uric acid increased, disease progression, febrile neutropenia, hyperchloraemia, hyperkalaemia, hypernatraemia, hypoproteinaemia, . MYLOTARG dosage: unknown. During the same period patient was treated with FAMOTIDINE, ZYLORIC, LASIX, ITRIZOLE. Patient was hospitalized. Patient recovered.


Memantine Side Effects Report #5642287-3
MEMANTINE problem was reported by a Consumer or non-health professional from JAPAN on July 24, 2007. Male patient, 90 years of age, was diagnosed with dementia alzheimer's type and was treated with MEMANTINE. After drug was administered, patient experienced the following problems/side effects: blood albumin decreased, chest pain, cholecystitis, cholelithiasis, depressed mood, disease recurrence, heart rate increased, pyrexia, . MEMANTINE dosage: unknown. During the same period patient was treated with DONEPEZIL, AMBROXOL HYDROCHLORIDE, SIENNA LEAF, RANITIDINE HYDROCHLORIDE, TEPRENONE, URSODESOXYCHOLIC ACID. Patient was hospitalized. Patient recovered.

Panitumumab Side Effects Report #5645658-4
Physician from AUSTRALIA reported PANITUMUMAB problem on Feb 19, 2008. Male patient, weighting 127.2 lb, was diagnosed with squamous cell carcinoma and was treated with PANITUMUMAB. After drug was administered, patient experienced the following problems/side effects: blood albumin decreased, blood alkaline phosphatase increased, blood bilirubin increased, blood calcium decreased, blood chloride decreased, blood cortisol increased, blood creatinine increased, blood magnesium decreased, blood potassium decreased, . PANITUMUMAB dosage: unknown. During the same period patient was treated with CISPLATIN, FLUOROURACIL, EMEND, PANTOPRAZOLE, LACTULOSE, DOCUSATE, METOCLOPRAMIDE, TEMAZEPAM. Patient was hospitalized. Patient recovered.

Revlimid Side Effects Report #5647932-4
REVLIMID problem was reported by a Physician from UNITED STATES on Feb 21, 2008. Female patient, 75 years of age, weighting 126.0 lb, was diagnosed with myeloproliferative disorder and was treated with REVLIMID. After drug was administered, patient experienced the following problems/side effects: blood albumin decreased, blood calcium decreased, presyncope, protein total decreased, thrombocythaemia, . REVLIMID dosage: unknown. During the same period patient was treated with PREDNISONE, HYDREA, TRIAMTERENE, PREMARIN, CALCIUM, VITAMIN, PROTONIX, MEGACE. Patient was hospitalized. Patient recovered.

Cytarabine Side Effects Report #5585285-0
Consumer or non-health professional from UNITED STATES reported CYTARABINE problem on Jan 04, 2008. Male patient, weighting 175.3 lb, was treated with CYTARABINE. After drug was administered, patient experienced the following problems/side effects: blood albumin decreased, blood count abnormal, caecitis, deep vein thrombosis, flatulence, iliac artery thrombosis, pelvic venous thrombosis, small intestinal obstruction, . CYTARABINE dosage: 1330 MG. During the same period patient was treated with DAUNORUBICIN, ETOPOSIDE. Patient was hospitalized. Patient recovered.

Dilantin Side Effects Report #5596484-6
DILANTIN problem was reported by a Physician from UNITED STATES on Jan 09, 2008. Female patient, weighting 172.0 lb, was diagnosed with epilepsy and was treated with DILANTIN. After drug was administered, patient experienced the following problems/side effects: blood albumin decreased, bone pain, convulsion, gait disturbance, hypocalcaemia, nephrotic syndrome, osteoporosis, therapeutic agent toxicity, . DILANTIN dosage: unknown. During the same period patient was treated with PHENOBARBITAL. Patient recovered.

Diclofenac Side Effects Report #5597122-9
Health Professional from CROATIA (local name: Hrvatska) reported DICLOFENAC problem on Jan 11, 2008. Female patient, 53 years of age, weighting 183.0 lb, was diagnosed with myalgia and was treated with DICLOFENAC. After drug was administered, patient experienced the following problems/side effects: blood albumin decreased, blood creatinine increased, nephrotic syndrome, pallor, protein total decreased, proteinuria, red blood cell sedimentation rate increased, red blood cells urine positive, . DICLOFENAC dosage: unknown. Patient was hospitalized. Patient recovered.

Humalog Side Effects Report #5597696-8
HUMALOG problem was reported by a Consumer or non-health professional from JAPAN on Jan 11, 2008. Female patient was treated with HUMALOG. After drug was administered, patient experienced the following problems/side effects: blood albumin decreased, diabetes mellitus inadequate control, eye disorder, gallbladder polyp, glycosylated haemoglobin increased, hypoglycaemia, injection site calcification, injection site induration, insomnia, . HUMALOG dosage: unknown. Patient was hospitalized. Patient recovered.

Tarceva Side Effects Report #5598681-2
Physician from GREECE reported TARCEVA problem on Jan 02, 2008. Male patient, 72 years of age, was diagnosed with lung neoplasm malignant and was treated with TARCEVA. After drug was administered, patient experienced the following problems/side effects: blood albumin decreased, blood potassium decreased, diarrhoea, pigmentation disorder, . TARCEVA dosage: unknown. Patient recovered.

Diltiazem Side Effects Report #5599171-3
DILTIAZEM HYDROCHLORIDE problem was reported by a Pharmacist from UNITED STATES on Oct 10, 2007. Male patient, 78 years of age, was diagnosed with atrial fibrillation and was treated with DILTIAZEM HYDROCHLORIDE. After drug was administered, patient experienced the following problems/side effects: blood albumin decreased, cardiac failure congestive, pulmonary oedema, troponin i increased, . DILTIAZEM HYDROCHLORIDE dosage: 25 MG/5ML INTRAVENOUS (NOT OTHERWISE SPECIFIED). During the same period patient was treated with DIGOXIN, AMIODARONE. Patient recovered.

Azasan Side Effects Report #5599270-6
Physician from UNITED STATES reported AZASAN problem on Jan 02, 2008. Male patient, 71 years of age, was treated with AZASAN. After drug was administered, patient experienced the following problems/side effects: blood albumin decreased, condition aggravated, crohn's disease, cryptogenic organising pneumonia, dyspnoea, inflammation, lenticular opacities, leukocytosis, . AZASAN dosage: 100 MG; QD;. During the same period patient was treated with PREDNISONE. Patient was hospitalized. Patient recovered.

Neoral Side Effects Report #5599570-X
NEORAL problem was reported by a Consumer or non-health professional from JAPAN on Jan 16, 2008. Male patient, 60 years of age, was diagnosed with aplastic anaemia and was treated with NEORAL. After drug was administered, patient experienced the following problems/side effects: blood albumin decreased, focal glomerulosclerosis, low density lipoprotein apheresis, oedema, proteinuria, . NEORAL dosage: unknown. During the same period patient was treated with PREDNISOLONE. Patient was hospitalized. Patient recovered.

Cyclophosphamide Side Effects Report #5609082-2
Consumer or non-health professional from UNITED STATES reported CYCLOPHOSPHAMIDE problem on Jan 30, 2008. Male patient, weighting 139.1 lb, was treated with CYCLOPHOSPHAMIDE. After drug was administered, patient experienced the following problems/side effects: blood albumin decreased, laboratory test abnormal, . CYCLOPHOSPHAMIDE dosage: 3725 MG. During the same period patient was treated with ETOPOSIDE, LEUCOVORIN CALCIUM, METHOTREXATE, BACTRIM, FLUCONAZOLE. Patient was hospitalized. Patient recovered.

Tenofovir Side Effects Report #5534340-X
TENOFOVIR DISOPROXIL FUMARATE problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 26, 2007. Female patient, 38 years of age, weighting 105.8 lb, was diagnosed with hiv infection and was treated with TENOFOVIR DISOPROXIL FUMARATE. After drug was administered, patient experienced the following problems/side effects: blood albumin decreased, . TENOFOVIR DISOPROXIL FUMARATE dosage: unknown. During the same period patient was treated with TENOFOVIR DISOPROXIL FUMARATE. Patient recovered.

Neoral Side Effects Report #5557966-6
Consumer or non-health professional from JAPAN reported NEORAL problem on Dec 05, 2007. Male patient, 60 years of age, was diagnosed with aplastic anaemia and was treated with NEORAL. After drug was administered, patient experienced the following problems/side effects: blood albumin decreased, focal glomerulosclerosis, low density lipoprotein apheresis, oedema, proteinuria, . NEORAL dosage: unknown. During the same period patient was treated with PREDNISOLONE. Patient was hospitalized. Patient recovered.

Aranesp Side Effects Report #5562776-X
ARANESP problem was reported by a Consumer or non-health professional from POLAND on Dec 06, 2007. Female patient, weighting 191.8 lb, was diagnosed with dialysis and was treated with ARANESP. After drug was administered, patient experienced the following problems/side effects: blood albumin decreased, caesarean section, labile blood pressure, premature labour, therapeutic response decreased, . ARANESP dosage: unknown. During the same period patient was treated with FOLIC ACID, CALCIUM, ASCORBIC ACID, VITAMIN D, METHYLDOPA, LABETALOL HYDROCHLORIDE. Patient was hospitalized. Patient recovered.

Amiodarone Side Effects Report #5565066-4
Health Professional from FRANCE reported AMIODARONE problem on Dec 12, 2007. Male patient, 65 years of age, was diagnosed with cardiac failure congestive and was treated with AMIODARONE. After drug was administered, patient experienced the following problems/side effects: blood albumin decreased, blood chloride decreased, blood creatinine increased, blood glucose increased, blood potassium increased, blood sodium decreased, blood urea increased, brain natriuretic peptide increased, cardiac failure congestive, . AMIODARONE dosage: unknown. During the same period patient was treated with SIMVASTATIN, DOBUTAMINE, ALBUTEROL, BUMETANIDE, CALCIUM ACETATE, DOCUSATE, EPOETIN ALFA, FERROUS SULPHATE. Patient was hospitalized. Patient recovered.

Temodal Side Effects Report #5568677-5
TEMODAL problem was reported by a Physician from JAPAN on Mar 30, 2007. Male patient, 63 years of age, weighting 121.3 lb, was diagnosed with glioblastoma multiforme and was treated with TEMODAL. After drug was administered, patient experienced the following problems/side effects: blood albumin decreased, liver disorder, nausea, platelet count decreased, sepsis, vomiting, . TEMODAL dosage: 150 MG/M2;QD;PO. During the same period patient was treated with RINDERON, ZANTAC, TAGAMET, AMLODIN. Patient was hospitalized. Patient recovered.

Erlotinib Side Effects Report #5572355-6
Physician from ISRAEL reported ERLOTINIB problem on Dec 04, 2007. Male patient, 83 years of age, was diagnosed with non-small cell lung cancer stage iv and was treated with ERLOTINIB. After drug was administered, patient experienced the following problems/side effects: blood albumin decreased, blood alkaline phosphatase increased, blood bilirubin increased, blood lactate dehydrogenase increased, dyspnoea, pleural effusion, protein total decreased, . ERLOTINIB dosage: (50 MG, QD), ORAL. Patient was hospitalized. Patient recovered.

Tegretol Side Effects Report #5573281-9
TEGRETOL problem was reported by a Pharmacist from JAPAN on Dec 18, 2007. Female patient, 59 years of age, was diagnosed with bipolar i disorder and was treated with TEGRETOL. After drug was administered, patient experienced the following problems/side effects: blood albumin decreased, blood amylase decreased, blood cholinesterase decreased, blood creatine phosphokinase increased, blood lactate dehydrogenase increased, c-reactive protein increased, cardiac murmur, endocarditis, gamma-glutamyltransferase increased, . TEGRETOL dosage: 100 MG, QD. During the same period patient was treated with SEPAZON, LITHIUM CARBONATE, CHLORPROMAZINE, THYRADIN, AKINETON. Patient was hospitalized. Patient recovered.

Cyclosporine Side Effects Report #5574063-4
Consumer or non-health professional from TURKEY reported CYCLOSPORINE problem on Dec 11, 2007. Female patient, 52 years of age, was diagnosed with glomerulonephritis membranoproliferative and was treated with CYCLOSPORINE. After drug was administered, patient experienced the following problems/side effects: blood albumin decreased, blood cholesterol increased, haematocrit decreased, haemoglobin decreased, kaposi's sarcoma, white blood cell count decreased, . CYCLOSPORINE dosage: unknown. During the same period patient was treated with AZATHIOPRINE, MYCOPHENOLATE MOFETIL, PREDNISONE, RAMIPRIL, LOSARTAN POTASSIUM, ACETYLSALICYLIC ACID SRT, SIMVASTATIN. Patient was hospitalized. Patient recovered.

Emtricitabine Side Effects Report #5574736-3
EMTRICITABINE problem was reported by a Health Professional from UNITED STATES on Dec 21, 2007. Female patient, 28 years of age, weighting 121.3 lb, was diagnosed with hiv infection and was treated with EMTRICITABINE. After drug was administered, patient experienced the following problems/side effects: blood albumin decreased, blood potassium decreased, haematocrit decreased, haemoglobin decreased, malaria, postpartum haemorrhage, pyrexia, . EMTRICITABINE dosage: 200 MG QD PO. During the same period patient was treated with DIDANOSINE, ATAZANAVIR SULPHATE, TRUVADA, ZIDOVUDINE, NEVIRAPINE, FERROUS SULPHATE. Patient was hospitalized. Patient recovered.

Simvastatin Side Effects Report #5576089-3
Health Professional from UNITED KINGDOM reported SIMVASTATIN problem on Dec 12, 2007. Male patient, 24 years of age, was treated with SIMVASTATIN. After drug was administered, patient experienced the following problems/side effects: blood albumin decreased, nephrotic syndrome, renal failure chronic, . SIMVASTATIN dosage: 10 MG, QD, ORAL. During the same period patient was treated with ADALAT, SIROLIMUS, AZITHROMYCIN, FERROUS GLUCONATE, FUROSEMIDE, LANTUS, NOVORAPID. Patient was hospitalized. Patient recovered.

Tarceva Side Effects Report #5578146-4
TARCEVA problem was reported by a Physician from GREECE on Dec 18, 2007. Male patient was diagnosed with lung neoplasm malignant and was treated with TARCEVA. After drug was administered, patient experienced the following problems/side effects: blood albumin decreased, blood potassium decreased, diarrhoea, pigmentation disorder, . TARCEVA dosage: unknown. Patient recovered.

Ambisome Side Effects Report #5578659-5
Physician from JAPAN reported AMBISOME problem on Dec 10, 2007. Male patient, 80 years of age, was diagnosed with post procedural infection and was treated with AMBISOME. After drug was administered, patient experienced the following problems/side effects: blood albumin decreased, cholecystitis acute, hypokalaemia, platelet count decreased, platelet count increased, protein total decreased, white blood cell count decreased, wound infection staphylococcal, . AMBISOME dosage: 100 MG, UID/QD, IV NOS. Patient recovered.

Prograf Side Effects Report #5580096-4
PROGRAF problem was reported by a Physician from JAPAN on Dec 14, 2007. Male patient, 38 years of age, weighting 108.0 lb, was diagnosed with lung transplant and was treated with PROGRAF. After drug was administered, patient experienced the following problems/side effects: blood albumin decreased, blood lactate dehydrogenase increased, diarrhoea, eosinophil count increased, foreign body trauma, lymphoproliferative disorder, nausea, opportunistic infection, . PROGRAF dosage: unknown. Patient was hospitalized. Patient recovered.

Azathioprine Side Effects Report #5505976-7
Health Professional from IRELAND reported AZATHIOPRINE problem on Nov 02, 2007. Male patient, 21 years of age, was diagnosed with psoriatic arthropathy and was treated with AZATHIOPRINE. After drug was administered, patient experienced the following problems/side effects: blood albumin decreased, blood creatinine increased, cardiac amyloidosis, cardiac failure, cellulitis, dialysis, glomerular filtration rate decreased, hypertension, lobar pneumonia, . AZATHIOPRINE dosage: unknown. During the same period patient was treated with METHOTREXATE, PREDNISOLONE, DICLOFENAC, CYCLOSPORINE. Patient died on 11/01/2004.

Erlotinib Side Effects Report #5509047-5
ERLOTINIB problem was reported by a Physician from DENMARK on Oct 19, 2007. Male patient, 67 years of age, was diagnosed with gastrointestinal carcinoma, gastric cancer, pain, nausea, weight control and was treated with ERLOTINIB. After drug was administered, patient experienced the following problems/side effects: blood albumin decreased, blood alkaline phosphatase increased, diarrhoea, feeling abnormal, haemoglobin decreased, skin disorder, . ERLOTINIB dosage: 150 MG, QD, ORAL. During the same period patient was treated with BEVACIZUMAB, FENTANYL, ACETAMINOPHEN, MORPHINE, IMODIUM, PREDNISONE, SUPPLEMENT NOS, GABAPENTIN. Patient died on 09/10/2007.

Clofarabine Side Effects Report #5512601-8
Health Professional from UNITED KINGDOM reported CLOFARABINE problem on Oct 24, 2007. Female patient, 61 years of age, was diagnosed with acute myeloid leukaemia and was treated with CLOFARABINE. After drug was administered, patient experienced the following problems/side effects: blood albumin decreased, blood bicarbonate decreased, blood calcium decreased, blood potassium decreased, neutropenic sepsis, renal failure acute, . CLOFARABINE dosage: unknown. During the same period patient was treated with DAUNORUBICIN. Patient recovered.

Gemzar Side Effects Report #5520491-2
GEMZAR problem was reported by a Physician from JAPAN on Nov 06, 2007. Female patient, weighting 106.9 lb, was diagnosed with gallbladder cancer stage iv and was treated with GEMZAR. After drug was administered, patient experienced the following problems/side effects: blood albumin decreased, haemoglobin decreased, hepatic function abnormal, malignant neoplasm progression, neutrophil count decreased, platelet count decreased, po2 decreased, white blood cell count decreased, . GEMZAR dosage: 1400 MG, OTHER. Patient was hospitalized. Patient recovered.

Voltaren Side Effects Report #5526866-X
Physician from JAPAN reported VOLTAREN problem on Nov 21, 2007. Male patient, 52 years of age, was diagnosed with spinal cord injury cervical and was treated with VOLTAREN. After drug was administered, patient experienced the following problems/side effects: blood albumin decreased, blood creatinine decreased, nephrotic syndrome, oedema peripheral, protein total decreased, protein urine present, renal impairment, . VOLTAREN dosage: 50 MG, UNK. During the same period patient was treated with LORCAM, TERNELIN, CYANOCOBALAMIN, SOLON. Patient was hospitalized. Patient recovered.

Lisinopril Side Effects Report #5533556-6
LISINOPRIL problem was reported by a Physician from UNITED STATES on Nov 16, 2007. Male patient, 52 years of age, was diagnosed with oedema and was treated with LISINOPRIL. After drug was administered, patient experienced the following problems/side effects: blood albumin decreased, dyspnoea, haemodialysis, renal disorder, renal failure, . LISINOPRIL dosage: (10 MG QD). During the same period patient was treated with FUROSEMIDE. Patient recovered.

Sandimmune Side Effects Report #5474076-7
Pharmacist from GERMANY reported SANDIMMUNE problem on Sept 25, 2007. Male patient was diagnosed with heart transplant and was treated with SANDIMMUNE. After drug was administered, patient experienced the following problems/side effects: blood albumin decreased, cachexia, dialysis, red blood cell count decreased, renal impairment, white blood cell count decreased, . SANDIMMUNE dosage: 250 MG DAILY. Patient was hospitalized. Patient recovered.