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BLOOD CHLORIDE INCREASED side effect

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Isoniazid Side Effects Report #5675638-4
Consumer or non-health professional from SPAIN reported ISONIAZID problem on Mar 03, 2008. Female patient, 91 years of age, was diagnosed with joint tuberculosis and was treated with ISONIAZID. After drug was administered, patient experienced the following problems/side effects: blood chloride increased, blood potassium decreased, blood sodium increased, dehydration, gastrointestinal hypomotility, hyperuricaemia, lactic acidosis, pancreatitis acute, sepsis, . ISONIAZID dosage: 250 MG. During the same period patient was treated with PYRAZINAMIDE, RIFAMPICIN, PYRIDOXINE. Patient recovered.

Metformin Side Effects Report #5601946-9
METFORMIN problem was reported by a Physician from UNITED STATES on Jan 07, 2008. Female patient, 69 years of age, was treated with METFORMIN. After drug was administered, patient experienced the following problems/side effects: blood chloride increased, blood potassium increased, blood pressure systolic increased, blood sodium decreased, brain oedema, cerebral infarction, confusional state, haemodialysis, . METFORMIN dosage: unknown. During the same period patient was treated with SERTRALINE, NIFEDIPINE, GLIPIZIDE, GLYBURIDE, MECLIZINE, BACLOFEN, CLONIDINE, METOPROLOL TARTRATE. Patient was hospitalized. Patient died.

Bevacizumab Side Effects Report #5606115-4
Physician from UNITED STATES reported BEVACIZUMAB problem on Jan 22, 2008. Female patient, weighting 186.3 lb, was diagnosed with glioblastoma multiforme, fatigue, headache, insomnia, dyspepsia, hypothyroidism, depression, deep vein thrombosis, prophylaxis and was treated with BEVACIZUMAB. After drug was administered, patient experienced the following problems/side effects: blood chloride increased, . BEVACIZUMAB dosage: 745 MG, Q2W. During the same period patient was treated with PROVIGIL, CODEINE, AMBIEN, PROTONIX, LEVOTHYROXINE, NORTRIPTYLINE, LOVENOX, KEPPRA. Patient was hospitalized. Patient recovered.

Bevacizumab Side Effects Report #5571448-7
BEVACIZUMAB problem was reported by a Physician from UNITED STATES on Dec 17, 2007. Female patient, weighting 186.3 lb, was diagnosed with glioblastoma multiforme, fatigue, headache, insomnia, dyspepsia, hypothyroidism, depression, deep vein thrombosis, prophylaxis and was treated with BEVACIZUMAB. After drug was administered, patient experienced the following problems/side effects: blood chloride increased, . BEVACIZUMAB dosage: 745 MG, Q2W. During the same period patient was treated with PROVIGIL, CODEINE, AMBIEN, PROTONIX, LEVOTHYROXINE, NORTRIPTYLINE, LOVENOX, KEPPRA. Patient was hospitalized. Patient recovered.


Bevacizumab Side Effects Report #5517446-0
Physician from UNITED STATES reported BEVACIZUMAB problem on Nov 06, 2007. Female patient, weighting 186.3 lb, was diagnosed with glioblastoma multiforme, fatigue, headache, insomnia, dyspepsia, hypothyroidism, depression, deep vein thrombosis, prophylaxis and was treated with BEVACIZUMAB. After drug was administered, patient experienced the following problems/side effects: blood chloride increased, . BEVACIZUMAB dosage: 745 MG, Q2W. During the same period patient was treated with PROVIGIL, CODEINE SUL, AMBIEN, PROTONIX, LEVOTHYROXINE, NORTRIPTYLINE, LOVENOX, KEPPRA. Patient was hospitalized. Patient recovered.

Bevacizumab Side Effects Report #5523581-3
BEVACIZUMAB problem was reported by a Physician from UNITED STATES on Nov 15, 2007. Female patient, weighting 186.3 lb, was diagnosed with glioblastoma multiforme, fatigue, headache, insomnia, dyspepsia, hypothyroidism, depression, deep vein thrombosis, prophylaxis and was treated with BEVACIZUMAB. After drug was administered, patient experienced the following problems/side effects: blood chloride increased, nervous system disorder, unresponsive to stimuli, vomiting, . BEVACIZUMAB dosage: 745 MG, Q2W. During the same period patient was treated with PROVIGIL, CODEINE SUL, AMBIEN, PROTONIX, LEVOTHYROXINE, NORTRIPTYLINE, LOVENOX, KEPPRA. Patient was hospitalized. Patient recovered.

Risperdal Side Effects Report #5530826-2
Pharmacist from JAPAN reported RISPERDAL problem on Nov 20, 2007. Female patient, 82 years of age, was treated with RISPERDAL. After drug was administered, patient experienced the following problems/side effects: blood chloride increased, blood pressure increased, dehydration, hypernatraemia, hypocalcaemia, hypokalaemia, muscle twitching, pyrexia, . RISPERDAL dosage: unknown. During the same period patient was treated with SEROQUEL. Patient recovered.

Vfend Side Effects Report #5409939-1
VFEND problem was reported by a Pharmacist from UNITED STATES on Oct 15, 2003. Male patient, 60 years of age, weighting 427.7 lb, was diagnosed with fungal infection and was treated with VFEND. After drug was administered, patient experienced the following problems/side effects: blood chloride increased, blood creatinine increased, blood glucose increased, blood urea increased, infection, lethargy, mental status changes, neurological symptom, . VFEND dosage: DAILY DOSE:1200MG-FREQ:BID. During the same period patient was treated with NOREPINEPHRINE BITARTRATE, POTASSIUM CHLORIDE, METRONIDAZOLE, FUROSEMIDE, METHYLPREDNISOLONE SUCCINATE, HEPARIN, IPRATROPIUM BROMIDE AND SALBUTAMOL SULPHATE, LANSOPRAZOLE. Patient was hospitalized. Patient recovered.

Januvia Side Effects Report #5471295-0
Health Professional from UNITED STATES reported JANUVIA problem on May 03, 2007. Male patient, 68 years of age, was diagnosed with diabetes mellitus and was treated with JANUVIA. After drug was administered, patient experienced the following problems/side effects: blood chloride increased, blood sodium increased, . JANUVIA dosage: 100 MG/DAILY/PO. Patient recovered.


Prograf Side Effects Report #5771682-7
PROGRAF problem was reported by a Physician from JAPAN on June 02, 2008. Male patient, weighting 101.0 lb, was diagnosed with small intestine transplant and was treated with PROGRAF. After drug was administered, patient experienced the following problems/side effects: blood chloride increased, catheter related infection, cytomegalovirus enterocolitis, dehydration, electrolyte imbalance, hyperkalaemia, proctocolitis, renal impairment, . PROGRAF dosage: 4 MG, BID, ORAL. During the same period patient was treated with MEDROL, SULFAMETHOXAZOLE AND TRIMETHOPRIM, VALGANCICLOVIR, RAPAMUNE, FUNGIZONE SYRUP, DIOVAN. Patient was hospitalized. Patient recovered.

Singulair Side Effects Report #5780966-8
Physician from UNITED STATES reported SINGULAIR problem on June 10, 2008. Male patient, 46 years of age, was diagnosed with hypersensitivity and was treated with SINGULAIR. After drug was administered, patient experienced the following problems/side effects: blood chloride increased, bronchitis, chronic sinusitis, diarrhoea, hypotension, tachycardia, vomiting, . SINGULAIR dosage: unknown. During the same period patient was treated with ALLEGRA, ADVAIR DISKUS. Patient recovered.

Melphalan Side Effects Report #5717940-3
MELPHALAN problem was reported by a Consumer or non-health professional from UNITED STATES on Apr 18, 2008. Female patient, 63 years of age, was diagnosed with stem cell transplant, prophylaxis of nausea and vomiting and was treated with MELPHALAN. After drug was administered, patient experienced the following problems/side effects: blood chloride increased, cardiac failure congestive, febrile neutropenia, fluid overload, haematocrit decreased, haemoglobin decreased, mitral valve incompetence, nephropathy toxic, platelet count decreased, . MELPHALAN dosage: 100MGM2 PER DAY. During the same period patient was treated with PALONOSETRON. Patient was hospitalized. Patient recovered.

Memantine Side Effects Report #5350551-0
Consumer or non-health professional from UNITED STATES reported MEMANTINE problem on May 21, 2007. Female patient, 63 years of age, was diagnosed with dementia alzheimer's type, colonoscopy and was treated with MEMANTINE. After drug was administered, patient experienced the following problems/side effects: blood chloride increased, bundle branch block right, carbon dioxide decreased, cerebral atrophy, colorectal cancer, demyelination, disease recurrence, gastrointestinal disorder, . MEMANTINE dosage: unknown. During the same period patient was treated with MEPERIDINE, GALANTAMINE HYDROBROMIDE, LEVOTHYROXINE. Patient recovered.

Advil Side Effects Report #5324888-5
ADVIL problem was reported by a Health Professional from FRANCE on May 11, 2007. Female patient, weighting 16.53 lb, was diagnosed with pyrexia, diarrhoea infectious and was treated with ADVIL. After drug was administered, patient experienced the following problems/side effects: blood chloride increased, blood glucose increased, blood potassium increased, blood sodium increased, dehydration, protein total increased, renal failure, . ADVIL dosage: unknown. During the same period patient was treated with DOLIPRANE, TIORFAN, MOTILIUM. Patient was hospitalized. Patient recovered.


Avastin Side Effects Report #5290171-X
Health Professional from UNITED STATES reported AVASTIN problem on Mar 20, 2007. Female patient, 66 years of age, was diagnosed with colorectal cancer metastatic and was treated with AVASTIN. After drug was administered, patient experienced the following problems/side effects: blood chloride increased, blood potassium decreased, blood urea increased, candidiasis, carbon dioxide decreased, culture stool positive, dehydration, diarrhoea, mucosal inflammation, . AVASTIN dosage: 5 MG/KG, Q2W, INTRAVENOUS. During the same period patient was treated with OXALIPLATIN, CAPECITABINE, AVANDIA, AVALIDE, GLYBURIDE, TOPROL, ASPIRIN, POTASSIUM CHLORIDE. Patient was hospitalized. Patient recovered.

Aredia Side Effects Report #5278209-7
AREDIA problem was reported by a Physician from UNITED STATES on Mar 23, 2007. Female patient, 89 years of age, was diagnosed with breast cancer metastatic, hypertension and was treated with AREDIA. After drug was administered, patient experienced the following problems/side effects: blood chloride increased, blood creatine increased, blood urea increased, dialysis, renal failure, . AREDIA dosage: 60 MG Q 28 DAYS. During the same period patient was treated with ZOMETA, MEGACE, FASLODEX, DYAZIDE. Patient died on 06/25/2003.

Aricept Side Effects Report #5668679-4
Physician from JAPAN reported ARICEPT problem on Mar 06, 2008. Male patient, 74 years of age, weighting 112.4 lb, was diagnosed with dementia alzheimer's type and was treated with ARICEPT. After drug was administered, patient experienced the following problems/side effects: altered state of consciousness, blood chloride increased, blood magnesium increased, blood sodium increased, haemodialysis, renal failure acute, . ARICEPT dosage: 5 MG, 1 IN 1 D, ORAL. During the same period patient was treated with HALOPERIDOL, ASPIRIN, ALLOPURINOL, KNORAMIN, UBRETID, MARILEON, MAGMITT, URSO. Patient was hospitalized. Patient recovered.

Ursodiol Side Effects Report #5647963-4
URSODIOL problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 20, 2008. Female patient, 97 years of age, weighting 95.02 lb, was diagnosed with cholelithiasis and was treated with URSODIOL. After drug was administered, patient experienced the following problems/side effects: anaemia, blood chloride increased, blood sodium increased, dehydration, overdose, urinary tract infection, . URSODIOL dosage: 1200 MG, BID, ORAL; 600 MG, BID, ORAL. Patient was hospitalized. Patient recovered.

Tegretol Side Effects Report #5583840-5
Consumer or non-health professional from FRANCE reported TEGRETOL problem on Jan 02, 2008. Female patient, 41 years of age, was diagnosed with epilepsy and was treated with TEGRETOL. After drug was administered, patient experienced the following problems/side effects: agitation, blood chloride increased, blood glucose decreased, hyperthermia, leukopenia, malaise, neutropenia, petit mal epilepsy, photophobia, . TEGRETOL dosage: unknown. During the same period patient was treated with DEPAKENE, LAMICTAL. Patient was hospitalized. Patient recovered.


Morphine Side Effects Report #5507209-4
MORPHINE problem was reported by a Physician from UNITED STATES on Oct 18, 2007. Male patient, 17 years of age, weighting 130.0 lb, was treated with MORPHINE. After drug was administered, patient experienced the following problems/side effects: alcohol abuse, blood chloride increased, blood glucose decreased, blood potassium increased, contusion, excoriation, ill-defined disorder, . MORPHINE dosage: unknown. During the same period patient was treated with TEMAZEPAM, ALCOHOL. Patient died on 05/28/2007.

Bevacizumab Side Effects Report #5468849-4
Physician from UNITED STATES reported BEVACIZUMAB problem on Sept 13, 2007. Male patient, weighting 185.2 lb, was treated with BEVACIZUMAB. After drug was administered, patient experienced the following problems/side effects: atelectasis, blood chloride increased, blood lactate dehydrogenase increased, blood sodium increased, blood urea increased, disease progression, . BEVACIZUMAB dosage: 1260 MG, Q3W. During the same period patient was treated with ASPIRIN, LASIX, LOPRESSOR, PRAVACHOL, ZESTRIL, GLUCOTROL, NITROSTAT. Patient died on 08/25/2007.

Enalapril Side Effects Report #5473136-4
ENALAPRIL MALEATE problem was reported by a Physician from UNITED KINGDOM on Sept 11, 2007. Female patient, 73 years of age, was treated with ENALAPRIL MALEATE. After drug was administered, patient experienced the following problems/side effects: blood bicarbonate decreased, blood chloride increased, blood creatinine increased, blood potassium increased, blood urea increased, electrocardiogram p wave abnormal, electrocardiogram pr prolongation, fatigue, hyperkalaemia, . ENALAPRIL MALEATE dosage: (40 MG QD ORAL). During the same period patient was treated with METFORMIN, ACETAMINOPHEN, AMITRIPTYLINE HYDROCHLORIDE, ASPIRIN, ATENOLOL, DOXAZOSIN MESYLATE, IBUPROFEN, LEVOTHYROXINE. Patient was hospitalized. Patient recovered.

Amevive Side Effects Report #5766218-0
Physician from UNITED STATES reported AMEVIVE problem on May 19, 2008. Male patient, 46 years of age, weighting 259.9 lb, was diagnosed with psoriasis and was treated with AMEVIVE. After drug was administered, patient experienced the following problems/side effects: atelectasis, blood chloride increased, clostridial infection, deep vein thrombosis, diarrhoea, dyspnoea, haematocrit decreased, haemoglobin decreased, hepatomegaly, . AMEVIVE dosage: 15 MG, WEEKLY, INTRAMUSCULAR. During the same period patient was treated with COUMADIN, LOVENOX. Patient was hospitalized. Patient recovered.

Valtrex Side Effects Report #5740628-X
VALTREX problem was reported by a Physician from JAPAN on May 08, 2008. Male patient, 64 years of age, was diagnosed with herpes simplex and was treated with VALTREX. After drug was administered, patient experienced the following problems/side effects: blood alkaline phosphatase increased, blood chloride increased, blood creatinine increased, blood lactate dehydrogenase increased, blood phosphorus increased, blood urea increased, creatinine renal clearance decreased, delirium, . VALTREX dosage: 500MG TWICE PER DAY. During the same period patient was treated with ITRACONAZOLE, THYRADIN, NORVASC, OMEPRAZOLE, MICARDIS, CALTAN, RENAGEL, DEPAS. Patient was hospitalized. Patient recovered.

Floxacillin Side Effects Report #5754170-3
Physician from NETHERLANDS reported FLOXACILLIN problem on May 07, 2008. Female patient, 52 years of age, was diagnosed with staphylococcal infection, pain and was treated with FLOXACILLIN. After drug was administered, patient experienced the following problems/side effects: blood bicarbonate increased, blood chloride increased, blood lactic acid increased, metabolic acidosis, metastasis, respiratory distress, . FLOXACILLIN dosage: unknown. During the same period patient was treated with ACETAMINOPHEN. Patient recovered.

Minocycline Side Effects Report #5756373-0
MINOCYCLINE problem was reported by a Physician from UNITED STATES on May 18, 2008. Female patient, 18 years of age, was diagnosed with acne and was treated with MINOCYCLINE. After drug was administered, patient experienced the following problems/side effects: asthenia, blood chloride increased, body temperature decreased, chest discomfort, deafness, dyspnoea exertional, facial paresis, fatigue, gait disturbance, . MINOCYCLINE dosage: unknown. During the same period patient was treated with SERTRALINE. Patient was hospitalized. Patient recovered.

Aricept Side Effects Report #5710654-5
Physician from JAPAN reported ARICEPT problem on Mar 31, 2008. Male patient, 74 years of age, weighting 112.4 lb, was diagnosed with dementia alzheimer's type, constipation and was treated with ARICEPT. After drug was administered, patient experienced the following problems/side effects: abnormal behaviour, blood chloride increased, blood creatine phosphokinase increased, blood sodium increased, cerebral atrophy, cognitive disorder, compression fracture, consciousness fluctuating, constipation, . ARICEPT dosage: 2.5 MG, 1 IN 1 D, ORAL. During the same period patient was treated with MAGMITT, ASPIRIN, ALLOPURINOL, KNORAMIN, UBRETID, MARILEON, URSO, MICARDIS. Patient was hospitalized. Patient recovered.

Cubicin Side Effects Report #5712311-8
CUBICIN problem was reported by a Physician from UNITED STATES on Apr 02, 2008. Male patient, 35 years of age, was diagnosed with osteomyelitis and was treated with CUBICIN. After drug was administered, patient experienced the following problems/side effects: bacteraemia, blood chloride increased, blood glucose increased, blood lactic acid decreased, blood sodium decreased, carbon dioxide decreased, cough, decreased appetite, dehydration, . CUBICIN dosage: 4 MG/KG; Q24H; IV. During the same period patient was treated with CLONAZEPAM, SERTRALINE, FERROUS SULPHATE, HYDROMORPHONE, PROCHLORPERAZINE, ASCORBIC ACID. Patient was hospitalized. Patient recovered.

Fluorouracil Side Effects Report #5332915-4
Physician from UNITED STATES reported FLUOROURACIL problem on May 07, 2007. Male patient, 79 years of age, was diagnosed with colorectal cancer metastatic and was treated with FLUOROURACIL. After drug was administered, patient experienced the following problems/side effects: blood calcium decreased, blood chloride increased, blood potassium decreased, dehydration, diarrhoea, haematocrit decreased, haemoglobin decreased, nausea, pyrexia, . FLUOROURACIL dosage: 50. 2857 MG (704 MG, 1 IN 1 2 WK), INTRAVENOUS. During the same period patient was treated with CETUXIMAB, BEVACIZUMAB, LEUCOVORIN CALCIUM, SIMVASTATIN, CALTRATE, MAXIPIME, TOPROL, PROTONIX. Patient was hospitalized. Patient recovered.

Clozapine Side Effects Report #5295772-0
CLOZAPINE problem was reported by a Physician from AUSTRIA on Apr 02, 2007. Male patient was diagnosed with schizophrenia and was treated with CLOZAPINE. After drug was administered, patient experienced the following problems/side effects: blood calcium increased, blood chloride increased, blood cholesterol increased, blood creatinine increased, blood uric acid increased, eosinopenia, mean cell haemoglobin concentration, . CLOZAPINE dosage: 150MG ONCE DAILY. Patient recovered.

Lunesta Side Effects Report #5342406-2
Consumer or non-health professional from UNITED STATES reported LUNESTA problem on Feb 22, 2007. Female patient, 53 years of age, weighting 200.0 lb, was diagnosed with insomnia and was treated with LUNESTA. After drug was administered, patient experienced the following problems/side effects: ammonia increased, blood chloride increased, blood test abnormal, confusional state, learning disorder, memory impairment, . LUNESTA dosage: 3 MG; HS; ORAL. During the same period patient was treated with SYNTHROID, HEPARIN, SILVER, HORMONES AND RELATED, AGENTS, VITAMIN B, MAGNESIUM SULPHATE, VITAMIN E. Patient recovered.

Fluorouracil Side Effects Report #5288088-X
FLUOROURACIL problem was reported by a Physician from UNITED STATES on Mar 14, 2007. Male patient, 79 years of age, was diagnosed with colorectal cancer metastatic and was treated with FLUOROURACIL. After drug was administered, patient experienced the following problems/side effects: blood calcium decreased, blood chloride increased, blood phosphorus decreased, blood potassium decreased, decreased appetite, dehydration, diarrhoea, disease recurrence, haematocrit decreased, . FLUOROURACIL dosage: 50.2857 MG (704 MG, 1 IN 2 WK), INTRAVENOUS. During the same period patient was treated with CETUXIMAB, BEVACIZUMAB, LEUCOVORIN CALCIUM, SIMVASTATIN, CALTRATE, MAXIPIME, TOPROL, PROTONIX. Patient was hospitalized. Patient recovered.

Infergen Side Effects Report #5642248-4
Health Professional from UNITED STATES reported INFERGEN problem on Jan 28, 2008. Male patient, weighting 226.0 lb, was diagnosed with hepatitis c and was treated with INFERGEN. After drug was administered, patient experienced the following problems/side effects: aspartate aminotransferase increased, bilirubin conjugated increased, blood chloride increased, blood creatinine increased, blood glucose increased, blood iron increased, blood triglycerides increased, blood urea increased, blood uric acid increased, . INFERGEN dosage: unknown. During the same period patient was treated with RIBAVIRIN, ASPIRIN, TOPROL, LISINOPRIL, ZOLOFT, PLAVIX. Patient recovered.

Tegretol Side Effects Report #5589270-4
TEGRETOL problem was reported by a Consumer or non-health professional from CANADA on Jan 07, 2008. Female patient, child 4 years of age, weighting 32.19 lb, was diagnosed with epilepsy and was treated with TEGRETOL. After drug was administered, patient experienced the following problems/side effects: blood calcium decreased, blood chloride increased, blood creatinine increased, blood glucose increased, blood phosphorus increased, convulsion, developmental delay, . TEGRETOL dosage: 100 MG, TID. During the same period patient was treated with PREVACID, CARBAMAZEPINE. Patient recovered.

Nipent Side Effects Report #5613734-8
Physician from UNITED STATES reported NIPENT problem on Jan 18, 2008. Male patient, 63 years of age, weighting 231.5 lb, was diagnosed with chronic lymphocytic leukaemia and was treated with NIPENT. After drug was administered, patient experienced the following problems/side effects: blepharitis, blood bicarbonate increased, blood chloride increased, blood creatinine increased, blood culture positive, blood urea increased, bronchospasm, cough, dehydration, . NIPENT dosage: 4 MG/M2 Q12DAYS IV. During the same period patient was treated with RITUXAN, CYTOXAN, GLUCOPHAGE, GLUCOTROL, AVALIDE, TRICOR, NEURONTIN, PROCRIT. Patient was hospitalized. Patient recovered.

Clofarabine Side Effects Report #5553714-4
CLOFARABINE problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 29, 2007. Male patient, weighting 220.5 lb, was diagnosed with myeloid leukaemia and was treated with CLOFARABINE. After drug was administered, patient experienced the following problems/side effects: anxiety, atelectasis, blood chloride increased, bronchoalveolar lavage abnormal, cardiac failure, cold sweat, confusional state, feeling cold, fluid overload, . CLOFARABINE dosage: unknown. During the same period patient was treated with TYLENOL, ATIVAN, LASIX, PANTOPRAZOLE, ATENOLOL, AMLODIPINE, VALSARTAN. Patient recovered.

Revlimid Side Effects Report #5430355-0
Physician from UNITED STATES reported REVLIMID problem on Aug 21, 2007. Female patient, 78 years of age, was diagnosed with multiple myeloma and was treated with REVLIMID. After drug was administered, patient experienced the following problems/side effects: arrhythmia, blood calcium decreased, blood chloride increased, blood sodium decreased, dehydration, gastroenteritis viral, hypokalaemia, influenza, . REVLIMID dosage: 25 MG, 1 IN 1 D, ORAL. During the same period patient was treated with DECADRON, DURAGESIC, LASIX, LOPRESSOR, PROTONIX, NORVASC, COUMADIN, PERCOCET. Patient was hospitalized. Patient recovered.

Valtrex Side Effects Report #5794821-0
VALTREX problem was reported by a Physician from JAPAN on June 26, 2008. Male patient, 83 years of age, weighting 90.39 lb, was diagnosed with herpes zoster, psychomotor seizures, constipation, arteriosclerosis obliterans, hypertension, gastritis and was treated with VALTREX. After drug was administered, patient experienced the following problems/side effects: altered state of consciousness, blood calcium decreased, blood chloride increased, blood creatinine increased, blood potassium decreased, blood sodium decreased, blood urea increased, delirium, dysarthria, . VALTREX dosage: 500MG SEE TEXT. During the same period patient was treated with CLONAZEPAM, SENNOSIDE, GLUFAST, MICARDIS, GASPORT, MUCOSTA. Patient was hospitalized. Patient recovered.

Topiramate Side Effects Report #5731608-9
Physician from FRANCE reported TOPIRAMATE problem on Apr 28, 2008. Female patient, 52 years of age, weighting 123.5 lb, was diagnosed with epilepsy and was treated with TOPIRAMATE. After drug was administered, patient experienced the following problems/side effects: acidosis, blood bicarbonate decreased, blood chloride increased, hyperventilation, hypokalaemia, . TOPIRAMATE dosage: unknown. During the same period patient was treated with CARBAMAZEPINE, LAMOTRIGINE, PHENOBARBITAL. Patient was hospitalized. Patient recovered.

Tysabri Side Effects Report #5741876-5
TYSABRI problem was reported by a Health Professional from UNITED STATES on Apr 29, 2008. Female patient, 38 years of age, weighting 154.3 lb, was diagnosed with multiple sclerosis and was treated with TYSABRI. After drug was administered, patient experienced the following problems/side effects: abdominal pain, asthenia, blood chloride increased, blood urea decreased, cholelithiasis, diarrhoea, dizziness, gastrointestinal disorder, . TYSABRI dosage: 300 MG QM, IV. During the same period patient was treated with TYLENOL, SERTRALINE, ESOMEPRAZOLE MAGNESIUM, ETODOLAC, PREMARIN, PROMETHAZINE. Patient was hospitalized. Patient recovered.

Acetaminophen Side Effects Report #5695489-4
Health Professional from UNITED KINGDOM reported ACETAMINOPHEN problem on Mar 27, 2008. Female patient was diagnosed with pain, intervertebral discitis, sepsis and was treated with ACETAMINOPHEN. After drug was administered, patient experienced the following problems/side effects: abdominal tenderness, acute respiratory distress syndrome, blood chloride increased, depressed level of consciousness, encephalopathy, metabolic acidosis, multi-organ failure, pyroglutamate increased, renal impairment, . ACETAMINOPHEN dosage: unknown. During the same period patient was treated with FLOXACILLIN, CALCIUM CHANNEL BLOCKER, CEFTRIAXONE, GENTAMICIN, GLICLAZIDE, METRONIDAZOLE, TRAMADOL, PYROGLUTAMIC ACID. Patient was hospitalized. Patient recovered.

Ribavirin Side Effects Report #5712269-1
RIBAVIRIN problem was reported by a Health Professional from UNITED STATES on Jan 28, 2008. Male patient, weighting 226.0 lb, was diagnosed with hepatitis c and was treated with RIBAVIRIN. After drug was administered, patient experienced the following problems/side effects: aspartate aminotransferase increased, bilirubin conjugated increased, blood chloride increased, blood cholesterol decreased, blood creatinine increased, blood glucose increased, blood iron increased, blood sodium decreased, blood triglycerides increased, . RIBAVIRIN dosage: (600 MG BID ORAL), (600 MG, BID ORAL). During the same period patient was treated with INFERGEN, ASPIRIN, TOPROL, LISINOPRIL, ZOLOFT, PLAVIX. Patient recovered.

Soma Side Effects Report #5339577-0
Consumer or non-health professional from UNITED STATES reported SOMA problem on May 14, 2007. Female patient, 57 years of age, was treated with SOMA. After drug was administered, patient experienced the following problems/side effects: aggression, apnoea, blood chloride increased, blood glucose increased, blood pressure systolic increased, blood urea increased, convulsion, cyanosis, foaming at mouth, . SOMA dosage: 87 TABLETS (350 MG TABLETS), ORAL. During the same period patient was treated with MOTRIN, BUSPAR, ULTRAM, LORAZEPAM, CLARITIN, NEURONTIN, CELEXA, PHENAZOPYRIDINE. Patient was hospitalized. Patient recovered.

Rosiglitazone Side Effects Report #5308680-3
ROSIGLITAZONE problem was reported by a Physician from UNITED STATES on Apr 20, 2007. Female patient, 87 years of age, weighting 111.3 lb, was diagnosed with dementia alzheimer's type and was treated with ROSIGLITAZONE. After drug was administered, patient experienced the following problems/side effects: aggression, atrial fibrillation, blood chloride increased, cerebral hypoperfusion, dehydration, electrocardiogram poor r-wave progression, electrocardiogram st-t segment abnormal, . ROSIGLITAZONE dosage: 2MG PER DAY. During the same period patient was treated with DONEPEZIL. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5255678-X
Physician from UNITED STATES reported SUTENT problem on Feb 21, 2007. Female patient, weighting 156.1 lb, was diagnosed with metastatic renal cell carcinoma and was treated with SUTENT. After drug was administered, patient experienced the following problems/side effects: arrhythmia, blood calcium abnormal, blood chloride increased, blood copper abnormal, cardiac failure congestive, dehydration, diarrhoea, hyperglycaemia, renal failure chronic, . SUTENT dosage: unknown. During the same period patient was treated with WARFARIN, TRICOR, CLONIDINE, COMPAZINE, LOPERAMIDE, LASIX, METOPROLOL SUCCINATE, ACETYLSALICYLIC ACID SRT. Patient was hospitalized. Patient died on 11/01/2006.