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BLOOD CHLORIDE DECREASED side effect

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Orfidal Side Effects Report #5656229-8
Health Professional from SPAIN reported ORFIDAL problem on Feb 20, 2008. Female patient, 69 years of age, was diagnosed with insomnia, influenza, pain and was treated with ORFIDAL. After drug was administered, patient experienced the following problems/side effects: blood chloride decreased, disorientation, hyponatraemia, . ORFIDAL dosage: (1 MG QD ORAL). During the same period patient was treated with FRENADOL, NEURONTIN, ENALAPRIL MALEATE, PARACETAMOL. Patient died on 01/01/2008.

Pletal Side Effects Report #5619215-X
PLETAL problem was reported by a Consumer or non-health professional from JAPAN on Jan 22, 2008. Male patient, 68 years of age, was diagnosed with cerebral infarction, depression and was treated with PLETAL. After drug was administered, patient experienced the following problems/side effects: blood chloride decreased, blood pressure increased, blood pressure systolic increased, blood sodium decreased, bronchitis, cervical vertebral fracture, dyspnoea, electrolyte imbalance, epilepsy, . PLETAL dosage: 100 MG, BID; MG;ORAL, 81 MG QD. During the same period patient was treated with ZOLPIDEM TARTRATE, GLYCERIN, PURSENNID, PAXIL, DEYSREL. Patient was hospitalized. Patient recovered.

Omeprazole Side Effects Report #5643043-2
Physician from GUATEMALA reported OMEPRAZOLE problem on Feb 19, 2008. Female patient, 85 years of age, was diagnosed with hypertension and was treated with OMEPRAZOLE. After drug was administered, patient experienced the following problems/side effects: blood chloride decreased, blood pressure inadequately controlled, dizziness, electrocardiogram abnormal, haemoglobin decreased, headache, hypomagnesaemia, hyponatraemia, normochromic normocytic anaemia, . OMEPRAZOLE dosage: 20 MG/DAY. During the same period patient was treated with DIOVAN HCT, DILTIAZEM, ASPIRIN. Patient was hospitalized. Patient recovered.

Diovan Side Effects Report #5579127-7
DIOVAN problem was reported by a Pharmacist from JAPAN on Dec 26, 2007. Male patient, 82 years of age, was diagnosed with hypertension and was treated with DIOVAN. After drug was administered, patient experienced the following problems/side effects: blood chloride decreased, blood sodium decreased, hyponatraemia, . DIOVAN dosage: 40 MG/DAY. During the same period patient was treated with ARICEPT, TAKEPRON, AMLODIN, DEPAS, FLORINEF. Patient recovered.


Duloxetine Side Effects Report #5587324-X
Physician from PORTUGAL reported DULOXETINE HYDROCHLORIDE problem on Jan 02, 2008. Female patient, 72 years of age, was diagnosed with depression and was treated with DULOXETINE HYDROCHLORIDE. After drug was administered, patient experienced the following problems/side effects: blood chloride decreased, dehydration, hypokalaemia, hyponatraemia, . DULOXETINE HYDROCHLORIDE dosage: unknown. Patient was hospitalized. Patient recovered.

Desmopressin Side Effects Report #5598619-8
DESMOPRESSIN ACETATE problem was reported by a Consumer or non-health professional from UNITED STATES on Sept 05, 2007. Male patient, 68 years of age, was diagnosed with benign prostatic hyperplasia, off label use, hypertension, blood cholesterol increased, diabetes mellitus and was treated with DESMOPRESSIN ACETATE. After drug was administered, patient experienced the following problems/side effects: blood chloride decreased, blood sodium decreased, diarrhoea, fatigue, nausea, . DESMOPRESSIN ACETATE dosage: unknown. During the same period patient was treated with DESMOPRESSIN ACETATE, DESMOPRESSIN ACETATE, DESMOPRESSIN ACETATE, ALTACE, TENORMIN, LIPITOR, STARLIX. Patient recovered.

Carbamazepine Side Effects Report #5607497-X
Consumer or non-health professional from SPAIN reported CARBAMAZEPINE problem on Jan 18, 2008. Female patient was diagnosed with complex partial seizures and was treated with CARBAMAZEPINE. After drug was administered, patient experienced the following problems/side effects: blood chloride decreased, inappropriate antidiuretic hormone secretion, leukocytosis, neutrophilia, syncope, . CARBAMAZEPINE dosage: 400MG, BID, ORAL. During the same period patient was treated with LAMOTRIGINE, PHENOBARBITAL, KEPPRA, ALPRAZOLAM, VENLAFAXINE, MIRTAZAPINE. Patient was hospitalized. Patient recovered.

Zidovudine Side Effects Report #5609691-0
ZIDOVUDINE problem was reported by a Physician from SOUTH AFRICA on Jan 24, 2008. Male patient, weighting 19.84 lb, was diagnosed with hiv infection and was treated with ZIDOVUDINE. After drug was administered, patient experienced the following problems/side effects: blood chloride decreased, blood sodium decreased, dehydration, gastroenteritis, haemoglobin decreased, lactic acidosis, myocarditis, neutropenia, pneumonia, . ZIDOVUDINE dosage: 105MG TWICE PER DAY. During the same period patient was treated with LAMIVUDINE, KALETRA. Patient was hospitalized. Patient recovered.

Byetta Side Effects Report #5652547-8
Physician from UNITED STATES reported BYETTA problem on Nov 07, 2007. Female patient, 55 years of age, was diagnosed with type 2 diabetes mellitus and was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: blood chloride decreased, blood sodium decreased, dizziness, feeling abnormal, inappropriate antidiuretic hormone secretion, pollakiuria, rash, thirst, weight decreased, . BYETTA dosage: unknown. During the same period patient was treated with EXENATIDE, HORMONES NOS, CLARITIN. Patient recovered.


Bevacizumab Side Effects Report #5536094-X
BEVACIZUMAB problem was reported by a Consumer or non-health professional from UNITED KINGDOM on Nov 23, 2007. Male patient, weighting 116.8 lb, was diagnosed with non-small cell lung cancer and was treated with BEVACIZUMAB. After drug was administered, patient experienced the following problems/side effects: blood chloride decreased, blood potassium decreased, blood sodium decreased, diarrhoea, platelet count decreased, white blood cell count decreased, . BEVACIZUMAB dosage: 800 MG, Q3W. During the same period patient was treated with PREDNISOLONE, VINORELBINE, CISPLATIN, DEXAVENT, SYNCUMAR, CODEINE SUL, THIOCODIN, LANSOPRAZOLE. Patient was hospitalized. Patient died on 10/19/2007.

Diovan Side Effects Report #5556882-3
Consumer or non-health professional from reported DIOVAN HCT problem on Dec 03, 2007. Female patient, 74 years of age, was diagnosed with hypertension and was treated with DIOVAN HCT. After drug was administered, patient experienced the following problems/side effects: blood chloride decreased, blood potassium decreased, blood sodium decreased, dehydration, protein total decreased, . DIOVAN HCT dosage: unknown. During the same period patient was treated with TRIMEBUTINE, RABEPRAZOLE, AROPAX, EUTIROX, PLAVIX, SENNOSIDE, NITROGLYCERIN. Patient was hospitalized. Patient recovered.

Diovan Side Effects Report #5508403-9
DIOVAN problem was reported by a Pharmacist from JAPAN on Oct 30, 2007. Male patient, 82 years of age, was diagnosed with hypertension and was treated with DIOVAN. After drug was administered, patient experienced the following problems/side effects: blood chloride decreased, blood sodium decreased, hyponatraemia, . DIOVAN dosage: 40 MG/DAY. During the same period patient was treated with ARICEPT, TAKEPRON, AMLODIN, DEPAS. Patient recovered.

Hyzaar Side Effects Report #5521020-X
Pharmacist from JAPAN reported HYZAAR problem on Nov 13, 2007. Male patient, 70 years of age, was diagnosed with hypertension and was treated with HYZAAR. After drug was administered, patient experienced the following problems/side effects: blood chloride decreased, blood potassium decreased, hyponatraemia, . HYZAAR dosage: unknown. Patient was hospitalized. Patient recovered.

Diovan Side Effects Report #5524531-6
DIOVAN problem was reported by a Pharmacist from JAPAN on Nov 15, 2007. Male patient, 82 years of age, was diagnosed with hypertension and was treated with DIOVAN. After drug was administered, patient experienced the following problems/side effects: blood chloride decreased, blood sodium decreased, hyponatraemia, . DIOVAN dosage: 40 MG/DAY. During the same period patient was treated with ARICEPT, TAKEPRON, AMLODIN, DEPAS. Patient recovered.


Humalog Side Effects Report #5529505-7
Consumer or non-health professional from UNITED STATES reported HUMALOG problem on Nov 20, 2007. Male patient, weighting 256.0 lb, was diagnosed with diabetes mellitus and was treated with HUMALOG. After drug was administered, patient experienced the following problems/side effects: blood chloride decreased, blood glucose decreased, blood glucose increased, convulsion, hyperglycaemia, injection site haemorrhage, neuropathy peripheral, . HUMALOG dosage: unknown. During the same period patient was treated with LANTUS, DOXAZOSIN MESYLATE, DIOVAN, DOSTINEX, LEVITRA, CYANOCOBALAMIN. Patient recovered.

Olmesartan Side Effects Report #5533874-1
OLMESARTAN MEDOXOMIL problem was reported by a Consumer or non-health professional from JAPAN on Nov 20, 2007. Female patient, 66 years of age, was diagnosed with hypertension and was treated with OLMESARTAN MEDOXOMIL. After drug was administered, patient experienced the following problems/side effects: blood chloride decreased, inappropriate antidiuretic hormone secretion, . OLMESARTAN MEDOXOMIL dosage: 20 MG (20 MG, 1 IN 1 D), PER ORAL. Patient recovered.

Lipitor Side Effects Report #5549941-2
Physician from UNITED STATES reported LIPITOR problem on Apr 11, 2007. Male patient was treated with LIPITOR. After drug was administered, patient experienced the following problems/side effects: blood chloride decreased, blood cholesterol increased, blood creatine phosphokinase increased, blood glucose increased, blood triglycerides increased, blood urea increased, eosinophil count increased, high density lipoprotein decreased, low density lipoprotein increased, . LIPITOR dosage: 40 MG (40 MG, 1 IN 1 D). During the same period patient was treated with ZETIA. Patient recovered.

Diovan Side Effects Report #5476576-2
DIOVAN problem was reported by a Pharmacist from JAPAN on Sept 26, 2007. Male patient, 82 years of age, was diagnosed with hypertension and was treated with DIOVAN. After drug was administered, patient experienced the following problems/side effects: blood chloride decreased, blood sodium decreased, hyponatraemia, . DIOVAN dosage: 40 MG/DAY. During the same period patient was treated with ARICEPT, LANSOPRAZOLE, AMLODIPINE, DEPAS. Patient recovered.

Erlotinib Side Effects Report #5481997-8
Health Professional from UNITED STATES reported ERLOTINIB problem on Sept 10, 2007. Female patient, 71 years of age, weighting 166.9 lb, was diagnosed with oesophageal carcinoma and was treated with ERLOTINIB. After drug was administered, patient experienced the following problems/side effects: blood chloride decreased, blood glucose increased, blood sodium decreased, diarrhoea, haemoglobin decreased, heart rate increased, leukopenia, mucosal inflammation, neutrophil count decreased, . ERLOTINIB dosage: 100 MG. During the same period patient was treated with BEVACIZUMAB, PACLITAXEL, CARBOPLATIN, FLUOROURACIL, ACIPHEX, IMITREX, NAPROXEN. Patient was hospitalized. Patient recovered.


Velcade Side Effects Report #5484426-3
VELCADE problem was reported by a Physician from JAPAN on Oct 01, 2007. Female patient, 62 years of age, weighting 94.80 lb, was diagnosed with multiple myeloma and was treated with VELCADE. After drug was administered, patient experienced the following problems/side effects: blood chloride decreased, hyponatraemia, platelet count decreased, . VELCADE dosage: 1.30 MG/M2, INTRAVENOUS. During the same period patient was treated with DEXAMETHASONE, OMEPRAL, ITRIZOLE, BAKTAR, ALLOPURINOL, PLATELETS. Patient recovered.

Ambisome Side Effects Report #5484787-5
Consumer or non-health professional from JAPAN reported AMBISOME problem on Sept 26, 2007. Male patient, 90 years of age, was diagnosed with meningitis cryptococcal and was treated with AMBISOME. After drug was administered, patient experienced the following problems/side effects: blood chloride decreased, blood sodium decreased, dehydration, hypoalbuminaemia, hypokalaemia, oedema, pneumonia, urine output increased, . AMBISOME dosage: 150 MG, UID/QD, IV DRIP. During the same period patient was treated with UNASYN, PRODIF, FIRSTCIN, DIFLUCAN. Patient recovered.

Temodal Side Effects Report #5494424-1
TEMODAL problem was reported by a Physician from JAPAN on Oct 18, 2007. Male patient, 48 years of age, weighting 105.8 lb, was diagnosed with oligodendroglioma and was treated with TEMODAL. After drug was administered, patient experienced the following problems/side effects: blood chloride decreased, blood glucose increased, blood sodium decreased, disseminated intravascular coagulation, neoplasm progression, pneumonia, white blood cell count decreased, . TEMODAL dosage: PO, 200 MG/M2; QD; PO, 200 MG/M2; QD; PO, 200 MG/M2; QD; PO. During the same period patient was treated with BAKTAR, ZOFRAN, PRIMPERAN, LENDORMIN D, EXCEGRAN. Patient died on 03/06/2007.

Zometa Side Effects Report #5502095-0
Health Professional from UNITED STATES reported ZOMETA problem on Mar 20, 2007. Male patient, 92 years of age, was diagnosed with prostate cancer metastatic and was treated with ZOMETA. After drug was administered, patient experienced the following problems/side effects: blood chloride decreased, blood creatinine increased, blood glucose increased, blood magnesium increased, blood phosphorus increased, blood potassium increased, blood urea increased, carbon dioxide increased, creatinine renal clearance decreased, . ZOMETA dosage: 2 MG, INFUSION; 3 MG, INFUSION; 2 MG; 3 MG; 2 MG, INFUSION. During the same period patient was treated with ASPIRIN, COREG, ISOSORBIDE, FUROSEMIDE. Patient recovered.

Tegretol Side Effects Report #5447187-X
TEGRETOL problem was reported by a Physician from JAPAN on Sept 05, 2007. Female patient, 45 years of age, weighting 97.00 lb, was diagnosed with affective disorder and was treated with TEGRETOL. After drug was administered, patient experienced the following problems/side effects: blood chloride decreased, blood creatinine increased, blood glucose increased, blood pressure decreased, convulsion, depressed level of consciousness, dyskinesia, . TEGRETOL dosage: 5000 MG, ONCE/SINGLE. During the same period patient was treated with DEPAS, LEXOTAN, CONSTAN, ZOLPIDEM, PAXIL. Patient was hospitalized. Patient recovered.

Symlin Side Effects Report #5463587-6
Physician from UNITED STATES reported SYMLIN problem on Aug 31, 2007. Male patient, 51 years of age, weighting 186.0 lb, was diagnosed with type 1 diabetes mellitus and was treated with SYMLIN. After drug was administered, patient experienced the following problems/side effects: blood chloride decreased, blood ph decreased, blood sodium decreased, confusional state, diabetic ketoacidosis, dyspnoea, hypoglycaemia, lobar pneumonia, . SYMLIN dosage: unknown. During the same period patient was treated with LANTUS, HUMALOG, METHOTREXATE, WELCHOL, ALTACE, LEVOXYL. Patient was hospitalized. Patient recovered.

Moviprep Side Effects Report #5472414-2
MOVIPREP problem was reported by a Health Professional from UNITED STATES on Sept 21, 2007. Female patient, 66 years of age, weighting 139.0 lb, was diagnosed with colonoscopy and was treated with MOVIPREP. After drug was administered, patient experienced the following problems/side effects: blood chloride decreased, blood potassium decreased, blood sodium decreased, convulsion, electrolyte imbalance, vomiting, water intoxication, . MOVIPREP dosage: unknown. During the same period patient was treated with ACETYLSALICYLIC ACID, PRENATAL VITAMINS, CALCIUM CITRATE, BONIVA. Patient was hospitalized and became disabled. Patient recovered.

Tigecycline Side Effects Report #5410066-8
Physician from UNITED STATES reported TIGECYCLINE problem on July 30, 2007. Male patient, weighting 167.2 lb, was diagnosed with diabetic foot infection, coronary artery disease, hypercholesterolaemia, diabetes mellitus, implantable defibrillator insertion, hypertension and was treated with TIGECYCLINE. After drug was administered, patient experienced the following problems/side effects: blood chloride decreased, blood glucose increased, carbon dioxide increased, dehydration, prothrombin time prolonged, renal failure acute, streptococcal bacteraemia, . TIGECYCLINE dosage: unknown. During the same period patient was treated with DILTIAZEM, DIGITEK, FUROSEMIDE, VYTORIN, BUMETANIDE, GLYCOPYRROLATE, COUMADIN, METOPROLOL SUCCINATE. Patient was hospitalized. Patient recovered.

Myozyme Side Effects Report #5416400-7
MYOZYME problem was reported by a Physician from UNITED STATES on July 31, 2007. Male patient was diagnosed with glycogen storage disease type ii and was treated with MYOZYME. After drug was administered, patient experienced the following problems/side effects: blood chloride decreased, blood glucose increased, blood magnesium increased, blood ph decreased, blood potassium increased, blood sodium decreased, cardio-respiratory arrest, pneumonia aspiration, respiratory failure, . MYOZYME dosage: 20 MG/KG Q2WKS IV. During the same period patient was treated with UNASYN, ARGININ, HYDROCORTISONE, EPINEPHRINE. Patient was hospitalized. Patient died on 07/19/2007.

Tegretol Side Effects Report #5427483-2
Physician from JAPAN reported TEGRETOL problem on Aug 21, 2007. Female patient, 45 years of age, weighting 97.00 lb, was diagnosed with affective disorder and was treated with TEGRETOL. After drug was administered, patient experienced the following problems/side effects: blood chloride decreased, blood creatinine increased, blood glucose increased, blood pressure decreased, convulsion, depressed level of consciousness, dyskinesia, . TEGRETOL dosage: 5000 MG, ONCE/SINGLE. During the same period patient was treated with DEPAS, LEXOTAN, CONSTAN, ZOLPIDEM, PAXIL. Patient was hospitalized. Patient recovered.

Tegretol Side Effects Report #5427786-1
TEGRETOL problem was reported by a Physician from JAPAN on Aug 21, 2007. Female patient, 45 years of age, weighting 97.00 lb, was diagnosed with affective disorder and was treated with TEGRETOL. After drug was administered, patient experienced the following problems/side effects: blood chloride decreased, blood creatinine increased, blood glucose increased, blood pressure decreased, convulsion, depressed level of consciousness, dyskinesia, . TEGRETOL dosage: 5000 MG, ONCE/SINGLE. During the same period patient was treated with DEPAS, LEXOTAN, CONSTAN, ZOLPIDEM, PAXIL. Patient was hospitalized. Patient recovered.

Ambisome Side Effects Report #5392773-9
Physician from JAPAN reported AMBISOME problem on July 03, 2007. Male patient, 15 years of age, was diagnosed with fungal sepsis and was treated with AMBISOME. After drug was administered, patient experienced the following problems/side effects: blood chloride decreased, blood potassium decreased, blood sodium decreased, condition aggravated, hypokalaemia, leukaemia, . AMBISOME dosage: unknown. During the same period patient was treated with MEROPEN, VANCOMYCIN HYDROCHLORIDE, BICARBONATE, ZOVIRAX, OMEGACIN, LASIX. Patient recovered.

Sutent Side Effects Report #5392803-4
SUTENT problem was reported by a Consumer or non-health professional from UNITED STATES on July 09, 2007. Male patient, weighting 154.1 lb, was diagnosed with prostate cancer and was treated with SUTENT. After drug was administered, patient experienced the following problems/side effects: blood chloride decreased, blood potassium decreased, blood sodium decreased, disease progression, platelet count increased, pneumonia, . SUTENT dosage: unknown. During the same period patient was treated with RESTORIL, PREVACID, LIPITOR, LORTAB, XANAX, VITAMIN CAP, ROXICODONE, ZITHROMAX. Patient was hospitalized. Patient recovered.

Fabrazyme Side Effects Report #5394844-X
Physician from UNITED STATES reported FABRAZYME problem on July 10, 2007. Male patient, 34 years of age, was diagnosed with fabry's disease and was treated with FABRAZYME. After drug was administered, patient experienced the following problems/side effects: blood chloride decreased, blood pressure decreased, blood sodium increased, cerebrovascular accident, diabetic ketoacidosis, heart rate decreased, hyperglycaemia, mental status changes, metabolic encephalopathy, . FABRAZYME dosage: 70 MG Q2WKS IV. During the same period patient was treated with LANTUS, NOVOLOG, PLAVIX, LOPRESSOR, PRILOSEC, REGLAN, ZOCOR, LISINOPRIL. Patient was hospitalized. Patient recovered.

Fluphenazine Side Effects Report #5402060-8
FLUPHENAZINE DECANOATE problem was reported by a Health Professional from UNITED STATES on July 17, 2007. Male patient, 44 years of age, was diagnosed with schizophrenia and was treated with FLUPHENAZINE DECANOATE. After drug was administered, patient experienced the following problems/side effects: blood chloride decreased, bradypnoea, brain oedema, cardiac arrest, coma, disorientation, fatigue, hyperglycaemia, . FLUPHENAZINE DECANOATE dosage: 25MG/IM/TWICE MONTHLY. During the same period patient was treated with HALOPERIDOL LACTATE. Patient was hospitalized. Patient died.

Erlotiniblet) Side Effects Report #5404265-9
Health Professional from UNITED STATES reported ERLOTINIBLET) problem on July 16, 2007. Female patient, 71 years of age, weighting 181.0 lb, was diagnosed with oesophageal carcinoma and was treated with ERLOTINIBLET). After drug was administered, patient experienced the following problems/side effects: blood chloride decreased, blood glucose increased, blood sodium decreased, diarrhoea, leukopenia, mucosal inflammation, neutrophil count decreased, protein total decreased, pyrexia, . ERLOTINIBLET) dosage: 100 MG. During the same period patient was treated with BEVACIZUMAB, PACLITAXEL, CARBOPLATIN. Patient was hospitalized. Patient recovered.

Trileptal Side Effects Report #5421741-3
TRILEPTAL problem was reported by a Physician from UNITED STATES on May 16, 2006. Male patient, child 1 years of age, was diagnosed with epilepsy and was treated with TRILEPTAL. After drug was administered, patient experienced the following problems/side effects: blood chloride decreased, blood cortisol increased, carbon dioxide decreased, convulsion, hyponatraemia, . TRILEPTAL dosage: unknown. Patient recovered.

Ambisome Side Effects Report #5392773-9
Physician from JAPAN reported AMBISOME problem on July 03, 2007. Male patient, 15 years of age, was diagnosed with fungal sepsis and was treated with AMBISOME. After drug was administered, patient experienced the following problems/side effects: blood chloride decreased, blood potassium decreased, blood sodium decreased, condition aggravated, hypokalaemia, leukaemia, . AMBISOME dosage: unknown. During the same period patient was treated with MEROPEN, VANCOMYCIN HYDROCHLORIDE, BICARBONATE, ZOVIRAX, OMEGACIN, LASIX. Patient recovered.

Sutent Side Effects Report #5392803-4
SUTENT problem was reported by a Consumer or non-health professional from UNITED STATES on July 09, 2007. Male patient, weighting 154.1 lb, was diagnosed with prostate cancer and was treated with SUTENT. After drug was administered, patient experienced the following problems/side effects: blood chloride decreased, blood potassium decreased, blood sodium decreased, disease progression, platelet count increased, pneumonia, . SUTENT dosage: unknown. During the same period patient was treated with RESTORIL, PREVACID, LIPITOR, LORTAB, XANAX, VITAMIN CAP, ROXICODONE, ZITHROMAX. Patient was hospitalized. Patient recovered.

Fabrazyme Side Effects Report #5394844-X
Physician from UNITED STATES reported FABRAZYME problem on July 10, 2007. Male patient, 34 years of age, was diagnosed with fabry's disease and was treated with FABRAZYME. After drug was administered, patient experienced the following problems/side effects: blood chloride decreased, blood pressure decreased, blood sodium increased, cerebrovascular accident, diabetic ketoacidosis, heart rate decreased, hyperglycaemia, mental status changes, metabolic encephalopathy, . FABRAZYME dosage: 70 MG Q2WKS IV. During the same period patient was treated with LANTUS, NOVOLOG, PLAVIX, LOPRESSOR, PRILOSEC, REGLAN, ZOCOR, LISINOPRIL. Patient was hospitalized. Patient recovered.

Fluphenazine Side Effects Report #5402060-8
FLUPHENAZINE DECANOATE problem was reported by a Health Professional from UNITED STATES on July 17, 2007. Male patient, 44 years of age, was diagnosed with schizophrenia and was treated with FLUPHENAZINE DECANOATE. After drug was administered, patient experienced the following problems/side effects: blood chloride decreased, bradypnoea, brain oedema, cardiac arrest, coma, disorientation, fatigue, hyperglycaemia, . FLUPHENAZINE DECANOATE dosage: 25MG/IM/TWICE MONTHLY. During the same period patient was treated with HALOPERIDOL LACTATE. Patient was hospitalized. Patient died.

Erlotiniblet) Side Effects Report #5404265-9
Health Professional from UNITED STATES reported ERLOTINIBLET) problem on July 16, 2007. Female patient, 71 years of age, weighting 181.0 lb, was diagnosed with oesophageal carcinoma and was treated with ERLOTINIBLET). After drug was administered, patient experienced the following problems/side effects: blood chloride decreased, blood glucose increased, blood sodium decreased, diarrhoea, leukopenia, mucosal inflammation, neutrophil count decreased, protein total decreased, pyrexia, . ERLOTINIBLET) dosage: 100 MG. During the same period patient was treated with BEVACIZUMAB, PACLITAXEL, CARBOPLATIN. Patient was hospitalized. Patient recovered.

Trileptal Side Effects Report #5421741-3
TRILEPTAL problem was reported by a Physician from UNITED STATES on May 16, 2006. Male patient, child 1 years of age, was diagnosed with epilepsy and was treated with TRILEPTAL. After drug was administered, patient experienced the following problems/side effects: blood chloride decreased, blood cortisol increased, carbon dioxide decreased, convulsion, hyponatraemia, . TRILEPTAL dosage: unknown. Patient recovered.

Lapatinib Side Effects Report #5757088-5
Physician from ISRAEL reported LAPATINIB problem on May 27, 2008. Female patient, 53 years of age, weighting 130.1 lb, was diagnosed with breast cancer metastatic, hypertension and was treated with LAPATINIB. After drug was administered, patient experienced the following problems/side effects: blood chloride decreased, dizziness, hyponatraemia, nausea, neuropathy peripheral, vomiting, . LAPATINIB dosage: 1250MG PER DAY. During the same period patient was treated with XELODA, NORMITEN, LORIVAN. Patient was hospitalized. Patient recovered.

Zyvox Side Effects Report #5767555-6
ZYVOX problem was reported by a Pharmacist from JAPAN on June 03, 2008. Female patient, 80 years of age, was diagnosed with staphylococcal infection and was treated with ZYVOX. After drug was administered, patient experienced the following problems/side effects: blood chloride decreased, blood potassium decreased, hyponatraemia, thrombocytopenia, . ZYVOX dosage: unknown. During the same period patient was treated with HABEKACIN, VANCOMYCIN, MUCOSTA, NU LOTAN, LASIX, FAMOTIDINE, ALSIODOL, MOBIC. Patient was hospitalized. Patient recovered.

Avonex Side Effects Report #5775391-X
Pharmacist from UNITED KINGDOM reported AVONEX problem on May 28, 2008. Female patient, 66 years of age, weighting 125.7 lb, was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: blood chloride decreased, breast cancer female, condition aggravated, multiple sclerosis, . AVONEX dosage: unknown. During the same period patient was treated with BACLOFEN. Patient was hospitalized. Patient recovered.

Carboplatin Side Effects Report #5793090-5
CARBOPLATIN problem was reported by a Consumer or non-health professional from UNITED STATES on June 26, 2008. Female patient, weighting 108.6 lb, was treated with CARBOPLATIN. After drug was administered, patient experienced the following problems/side effects: blood chloride decreased, blood glucose increased, blood urea increased, hypokalaemia, hyponatraemia, nausea, platelet count decreased, protein urine present, urinary sediment abnormal, . CARBOPLATIN dosage: 590 MG. During the same period patient was treated with TAXOL. Patient was hospitalized. Patient recovered.

Zyvox Side Effects Report #5735665-5
Pharmacist from JAPAN reported ZYVOX problem on May 02, 2008. Female patient, 80 years of age, was treated with ZYVOX. After drug was administered, patient experienced the following problems/side effects: blood chloride decreased, blood potassium increased, blood sodium increased, . ZYVOX dosage: DAILY DOSE:1200MG. During the same period patient was treated with HABEKACIN, VANCOMYCIN. Patient recovered.

Zyvox Side Effects Report #5748460-8
ZYVOX problem was reported by a Pharmacist from JAPAN on May 13, 2008. Female patient, 80 years of age, was treated with ZYVOX. After drug was administered, patient experienced the following problems/side effects: blood chloride decreased, blood potassium decreased, blood sodium decreased, . ZYVOX dosage: DAILY DOSE:1200MG. During the same period patient was treated with HABEKACIN, VANCOMYCIN. Patient recovered.

Cisplatin Side Effects Report #5750711-0
Consumer or non-health professional from UNITED STATES reported CISPLATIN problem on May 23, 2008. Female patient, weighting 130.1 lb, was treated with CISPLATIN. After drug was administered, patient experienced the following problems/side effects: blood chloride decreased, blood urea increased, dehydration, electrocardiogram st-t change, heart rate decreased, hypovolaemia, nausea, oral intake reduced, syncope, . CISPLATIN dosage: 83 MG. During the same period patient was treated with DOXORUBICIN HYDROCHLORIDE, TAXOL, AMLODIPINE, ATENLOL. Patient was hospitalized. Patient recovered.

Zometa Side Effects Report #5751619-7
ZOMETA problem was reported by a Pharmacist from JAPAN on May 19, 2008. Female patient was diagnosed with metastases to bone, breast cancer, hypertension and was treated with ZOMETA. After drug was administered, patient experienced the following problems/side effects: blood chloride decreased, blood creatine phosphokinase increased, body temperature decreased, cyanosis, depressed level of consciousness, echocardiogram abnormal, haematocrit decreased, hypertension, hypoaesthesia, . ZOMETA dosage: 4 MG, UNK. During the same period patient was treated with AROMASIN, NIVADIL. Patient was hospitalized. Patient recovered.

Zyvox Side Effects Report #5754431-8
Pharmacist from JAPAN reported ZYVOX problem on May 20, 2008. Female patient, 80 years of age, was diagnosed with nephropathy, staphylococcal infection and was treated with ZYVOX. After drug was administered, patient experienced the following problems/side effects: blood chloride decreased, blood potassium decreased, blood sodium decreased, . ZYVOX dosage: DAILY DOSE:1200MG. During the same period patient was treated with HABEKACIN, VANCOMYCIN, MUCOSTA, NU LOTAN, LASIX. Patient was hospitalized. Patient recovered.