BLOOD PH INCREASED side effect
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Drugs associated with BLOOD PH INCREASED
AMIODARONE AMITRIPTLINE AMITRIPTYLINE AMLODIPINE AMOXICILLIN ARSENIC BACLOFEN BENZOCAINE BEVACIZUMAB CARBAMAZEPINE CILOSTAZOL CLOFARABINE CLOZAPINE CYCLOPHOSPHAMIDE DECITABINE DOTAREM ESIDRIX FUROSEMIDE GEMZAR LIDOCAINE LORTAB MYOZYME OSMITROLECTION PREDNISONE PROPYLTHIOURACIL RITALIN SALBUTAMOL THALIDOMIDE THALOMID TOPAMAX VENTOLIN VOLTAREN WARFARIN WINRHO ZEVALINLidocaine Side Effects Report #5664135-8
Consumer or non-health professional from UNITED STATES reported LIDOCAINE problem on Mar 06, 2008. Male patient, 62 years of age, was diagnosed with anaesthesia and was treated with LIDOCAINE. After drug was administered, patient experienced the following problems/side effects: blood ph increased, cyanosis central, methaemoglobinaemia, oxygen saturation decreased, po2 increased, post procedural complication, . LIDOCAINE dosage: unknown. During the same period patient was treated with HURRICANE, CEFALEXIN, AMITRIPTYLINE, AMLODIPINE, ENOXAPARIN, GABAPENTIN, PANTOPRAZOLE, OXYCODONE. Patient was hospitalized. Patient recovered.
Prednisone Side Effects Report #5625282-X
PREDNISONE problem was reported by a Physician from BRAZIL on Jan 30, 2008. Male patient, 49 years of age, was diagnosed with idiopathic thrombocytopenic purpura and was treated with PREDNISONE. After drug was administered, patient experienced the following problems/side effects: blood ph increased, blood thyroid stimulating hormone decreased, cushingoid, haemoglobin decreased, herpes virus infection, nocardiosis, pulmonary cavitation, respiratory failure, thyroiditis, . PREDNISONE dosage: 1 MG/KG, QD. Patient died.
Cyclophosphamide Side Effects Report #5635129-3
Consumer or non-health professional from UNITED STATES reported CYCLOPHOSPHAMIDE problem on Feb 21, 2008. Male patient, weighting 209.4 lb, was treated with CYCLOPHOSPHAMIDE. After drug was administered, patient experienced the following problems/side effects: blood ph increased, febrile neutropenia, haemorrhage, hypotension, nervous system disorder, pco2 decreased, pneumonia, pulmonary embolism, . CYCLOPHOSPHAMIDE dosage: 1220 MG. During the same period patient was treated with DOXORUBICIN HYDROCHLORIDE, PREDNISONE, RITUXIMAB, VINCRISTINE SULPHATE. Patient was hospitalized. Patient recovered.
Myozyme Side Effects Report #5567550-6
MYOZYME problem was reported by a Physician from AUSTRALIA on Dec 05, 2007. Female patient, 47 years of age, weighting 121.3 lb, was diagnosed with glycogen storage disease type ii and was treated with MYOZYME. After drug was administered, patient experienced the following problems/side effects: blood ph increased, bronchiectasis, dyspnoea, pco2 decreased, pneumothorax, po2 increased, pulmonary fibrosis, respiratory failure, . MYOZYME dosage: 20 MG/KG Q2WKS IV. During the same period patient was treated with ALPHA, ESOMEPRAZOLE, CITALOPRAM HYDROBROMIDE, OXYBUTYNIN CHLORIDE, ACETAMINOPHEN. Patient was hospitalized. Patient recovered.
Dotarem Side Effects Report #5481023-0
Health Professional from JAPAN reported DOTAREM problem on Sept 04, 2007. Male patient, 77 years of age, weighting 53.00 lb, was diagnosed with nuclear magnetic resonance imaging and was treated with DOTAREM. After drug was administered, patient experienced the following problems/side effects: blood ph increased, cardiac arrest, hypotension, loss of consciousness, respiratory arrest, . DOTAREM dosage: 10, ML MILLILITRE (S), 1, 1 TOTAL INTRAVENOUS (NOT OTHERWISE SPECIFIED). During the same period patient was treated with WARFARIN, LANSOPRAZOLE, ALLOPURINOL, GLEEVEC, GASTROM, LASIX, ALDACTONE. Patient recovered.
Voltaren Side Effects Report #5404812-7
VOLTAREN problem was reported by a Consumer or non-health professional from FRANCE on July 30, 2007. Female patient, 73 years of age, weighting 244.7 lb, was diagnosed with osteoarthritis and was treated with VOLTAREN. After drug was administered, patient experienced the following problems/side effects: blood ph increased, bronchoalveolar lavage, cyanosis, eosinophilia, haematocrit decreased, haemoglobin decreased, hypoxia, interstitial lung disease, knee arthroplasty, . VOLTAREN dosage: unknown. During the same period patient was treated with FELDENE, TRAMADOL, MODURETIC, STILNOX, ALDACTONE, EFFERALGAN CODEINE. Patient was hospitalized. Patient recovered.
Topamax Side Effects Report #5409515-0
Consumer or non-health professional from UNITED STATES reported TOPAMAX problem on Aug 08, 2007. Female patient, weighting 155.0 lb, was diagnosed with affective disorder and was treated with TOPAMAX. After drug was administered, patient experienced the following problems/side effects: blood ph increased, economic problem, nephrolithiasis, . TOPAMAX dosage: 200 MG DAILY PO. Patient recovered.
Cyclophosphamide Side Effects Report #5777971-4
CYCLOPHOSPHAMIDE problem was reported by a Consumer or non-health professional from UNITED STATES on June 17, 2008. Male patient, weighting 202.8 lb, was treated with CYCLOPHOSPHAMIDE. After drug was administered, patient experienced the following problems/side effects: blood ph increased, cerebral ischaemia, convulsion, encephalitis, feeling abnormal, haemorrhagic cerebral infarction, hypertensive encephalopathy, nausea, nystagmus, . CYCLOPHOSPHAMIDE dosage: 7020MG. During the same period patient was treated with DACTINOMYCIN, IRINOTECAN, MESNA, VINCRISTINE SULPHATE. Patient was hospitalized. Patient died on 04/10/2008.
Amiodarone Side Effects Report #5739677-7
Consumer or non-health professional from JAPAN reported AMIODARONE problem on Apr 08, 2008. Male patient, 44 years of age, was diagnosed with congestive cardiomyopathy and was treated with AMIODARONE. After drug was administered, patient experienced the following problems/side effects: blood ph increased, body mass index increased, cardiac failure, cardiomegaly, cholestasis, dyspnoea exertional, hepatic congestion, hypothyroidism, hypoxia, . AMIODARONE dosage: 400 MG; X1, 200 MG; DAILY. Patient died.
Voltaren Side Effects Report #5368175-8
VOLTAREN problem was reported by a Consumer or non-health professional from FRANCE on June 15, 2007. Female patient, 73 years of age, weighting 244.7 lb, was diagnosed with osteoarthritis and was treated with VOLTAREN. After drug was administered, patient experienced the following problems/side effects: blood ph increased, bronchoalveolar lavage, cyanosis, eosinophilia, haematocrit decreased, haemoglobin decreased, hypoxia, interstitial lung disease, knee arthroplasty, . VOLTAREN dosage: unknown. During the same period patient was treated with FELDENE. Patient was hospitalized. Patient recovered.
Cilostazol Side Effects Report #5337028-3
Consumer or non-health professional from JAPAN reported CILOSTAZOL problem on May 10, 2007. Male patient, 73 years of age, was diagnosed with carotid artery stenosis and was treated with CILOSTAZOL. After drug was administered, patient experienced the following problems/side effects: blood ph increased, heart rate increased, interstitial lung disease, palpitations, . CILOSTAZOL dosage: 200 MG ORAL. During the same period patient was treated with ALLOPURTNOL, AMLODIPINE BESYLATE, ASPIRIN. Patient was hospitalized. Patient recovered.
Amitriptline Side Effects Report #5315335-8
AMITRIPTLINE problem was reported by a Health Professional from UNITED STATES on Apr 16, 2007. Male patient, 50 years of age, was treated with AMITRIPTLINE. After drug was administered, patient experienced the following problems/side effects: blood ph increased, blood sodium increased, brugada syndrome, coma, convulsion, electrocardiogram qrs complex prolonged, overdose, pulse absent, . AMITRIPTLINE dosage: unknown. During the same period patient was treated with LORAZEPAM, OXCARBAZEPINE, SERTRALINE, HYDROXYZINE. Patient was hospitalized. Patient recovered.
Lortab Side Effects Report #5174116-9
Health Professional from UNITED STATES reported LORTAB problem on Nov 22, 2006. Female patient, 56 years of age, was diagnosed with breakthrough pain, depression and was treated with LORTAB. After drug was administered, patient experienced the following problems/side effects: blood ph increased, cardiac disorder, cardiac failure congestive, cardiomegaly, delirium, delusion, electrocardiogram st-t change, hallucination, lethargy, . LORTAB dosage: unknown. During the same period patient was treated with FENTANYL CITRATE, FENTANYL CITRATE, OXYCONTIN, LEXAPRO, ACETAMINOPHEN, FLEXERIL, SEROQUEL, ALBUTEROL. Patient was hospitalized. Patient recovered.
Amiodarone Side Effects Report #5262367-4
AMIODARONE problem was reported by a Consumer or non-health professional from JAPAN on Feb 22, 2007. Male patient, 44 years of age, was diagnosed with congestive cardiomyopathy and was treated with AMIODARONE. After drug was administered, patient experienced the following problems/side effects: blood ph increased, body mass index increased, cardiac failure, cholestasis, hypothyroidism, interstitial lung disease, myocardial fibrosis, no therapeutic response, pulmonary fibrosis, . AMIODARONE dosage: 400 MG QD. Patient was hospitalized. Patient died.
Amlodipine Side Effects Report #5656239-0
Physician from NETHERLANDS reported AMLODIPINE BESYLATE problem on Feb 25, 2008. Female patient, 47 years of age, was treated with AMLODIPINE BESYLATE. After drug was administered, patient experienced the following problems/side effects: blood glucose increased, blood ph increased, blood potassium decreased, heart rate decreased, intentional overdose, poisoning, suicide attempt, . AMLODIPINE BESYLATE dosage: 200 MG; X 1; PO. During the same period patient was treated with LORAZEPAM. Patient was hospitalized. Patient recovered.
Myozyme Side Effects Report #5603318-X
MYOZYME problem was reported by a Physician from AUSTRALIA on Jan 08, 2008. Female patient, 47 years of age, weighting 121.3 lb, was diagnosed with glycogen storage disease type ii and was treated with MYOZYME. After drug was administered, patient experienced the following problems/side effects: acquired diaphragmatic eventration, blood ph increased, bronchiectasis, lung injury, pleural fibrosis, pneumothorax, respiratory failure, urinary tract infection, . MYOZYME dosage: 20 MG/KG, Q2W, INTRAVENOUS. During the same period patient was treated with ESOMEPRAZOLE, CITALOPRAM HYDROBROMIDE, OXYBUTYNIN CHLORIDE, ACETAMINOPHEN. Patient was hospitalized. Patient recovered.
Prednisone Side Effects Report #5605992-0
Physician from BRAZIL reported PREDNISONE problem on Jan 14, 2008. Male patient, 49 years of age, was diagnosed with idiopathic thrombocytopenic purpura and was treated with PREDNISONE. After drug was administered, patient experienced the following problems/side effects: anorexia, blood ph increased, blood thyroid stimulating hormone decreased, chest x-ray abnormal, cushingoid, haemoglobin decreased, herpes virus infection, malaise, nocardiosis, . PREDNISONE dosage: 1 MG/KG, QD. Patient died.
Amitriptyline Side Effects Report #5614689-2
AMITRIPTYLINE problem was reported by a Physician from UNITED STATES on Jan 21, 2008. Male patient, 50 years of age, was diagnosed with intentional overdose and was treated with AMITRIPTYLINE. After drug was administered, patient experienced the following problems/side effects: blood magnesium increased, blood ph increased, blood sodium increased, brugada syndrome, coma, convulsion, overdose, pulse absent, tachycardia, . AMITRIPTYLINE dosage: unknown. Patient was hospitalized. Patient recovered.
Gemzar Side Effects Report #5557901-0
Consumer or non-health professional from UNITED STATES reported GEMZAR problem on Dec 06, 2007. Male patient, 79 years of age, weighting 150.0 lb, was diagnosed with small intestine carcinoma and was treated with GEMZAR. After drug was administered, patient experienced the following problems/side effects: azotaemia, blood ph increased, brain natriuretic peptide abnormal, bullous lung disease, cardio-respiratory arrest, chronic obstructive pulmonary disease, cor pulmonale, decreased appetite, . GEMZAR dosage: 1000 MG/M2, UNK. During the same period patient was treated with VANCOMYCIN, ZOSYN. Patient was hospitalized. Patient died on 10/06/2007.
Ventolin Side Effects Report #5569669-2
VENTOLIN problem was reported by a Consumer or non-health professional from FRANCE on Dec 10, 2007. Female patient, 83 years of age, was diagnosed with chronic obstructive pulmonary disease, insomnia and was treated with VENTOLIN. After drug was administered, patient experienced the following problems/side effects: alkalosis, blood ph increased, chest x-ray abnormal, cognitive disorder, dyspnoea, fall, haemoconcentration, heart rate increased, . VENTOLIN dosage: unknown. During the same period patient was treated with LASILIX, PULMICORT, ATROVENT, BRICANYL, IMOVANE, HEXAQUINE, SPECIAFOLDINE. Patient was hospitalized. Patient recovered.
Amlodipine Side Effects Report #5576105-9
Physician from NETHERLANDS reported AMLODIPINE problem on Dec 11, 2007. Female patient, 47 years of age, was treated with AMLODIPINE. After drug was administered, patient experienced the following problems/side effects: blood creatinine abnormal, blood ph increased, bradycardia, hyperglycaemia, hypotension, respiratory rate increased, . AMLODIPINE dosage: 5 MG X 40 TABLETS, ORAL. During the same period patient was treated with LORAZEPAM. Patient was hospitalized. Patient recovered.
Thalidomide Side Effects Report #5521641-4
THALIDOMIDE problem was reported by a Consumer or non-health professional from UNITED KINGDOM on Nov 09, 2007. Female patient, 56 years of age, was diagnosed with multiple myeloma and was treated with THALIDOMIDE. After drug was administered, patient experienced the following problems/side effects: asthma, blood ph increased, condition aggravated, . THALIDOMIDE dosage: 400 MG, 8 IN 1 D, ORAL. Patient was hospitalized. Patient recovered.
Thalomid Side Effects Report #5485954-7
Physician from UNITED KINGDOM reported THALOMID problem on Oct 03, 2007. Female patient, 56 years of age, was diagnosed with multiple myeloma and was treated with THALOMID. After drug was administered, patient experienced the following problems/side effects: asthma, blood ph increased, condition aggravated, . THALOMID dosage: 400 MG, 8 IN 1 D, ORAL. Patient was hospitalized. Patient recovered.
Baclofen Side Effects Report #5448236-5
BACLOFEN problem was reported by a Health Professional from UNITED STATES on Sept 03, 2007. Male patient, 48 years of age, weighting 176.4 lb, was treated with BACLOFEN. After drug was administered, patient experienced the following problems/side effects: apnoea, blood ph increased, blood pressure increased, depression, electroencephalogram abnormal, faecal incontinence, grand mal convulsion, intentional overdose, . BACLOFEN dosage: unknown. Patient was hospitalized. Patient recovered.
Winrho Side Effects Report #5467650-5
Pharmacist from UNITED STATES reported WINRHO SDF problem on Aug 31, 2007. Female patient, weighting 26.46 lb, was diagnosed with idiopathic thrombocytopenic purpura and was treated with WINRHO SDF. After drug was administered, patient experienced the following problems/side effects: blood glucose increased, blood ph increased, intravascular haemolysis, tongue blistering, white blood cell count increased, . WINRHO SDF dosage: unknown. During the same period patient was treated with BENADRYL, ZOFRAN, DECADRON, POTASSIUM CHLORIDE. Patient was hospitalized. Patient recovered.
Amitriptyline Side Effects Report #5444067-0
AMITRIPTYLINE problem was reported by a Physician from UNITED STATES on Aug 21, 2007. Male patient, 50 years of age, was diagnosed with overdose and was treated with AMITRIPTYLINE. After drug was administered, patient experienced the following problems/side effects: blood magnesium decreased, blood ph increased, blood potassium decreased, blood sodium increased, coma, convulsion, electrocardiogram abnormal, electrocardiogram qrs complex prolonged, overdose, . AMITRIPTYLINE dosage: unknown. During the same period patient was treated with OXCARBAZEPINE, LORAZEPAM, SERTRALINE, HYDROXYZINE. Patient was hospitalized. Patient recovered.
Propylthiouracil Side Effects Report #5379374-3
Consumer or non-health professional from UNITED STATES reported PROPYLTHIOURACIL problem on June 19, 2007. Female patient, 23 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: aortic valve incompetence, blood ph increased, blood thyroid stimulating hormone decreased, caesarean section, cardiac murmur, cardiomegaly, chest x-ray abnormal, ejection fraction decreased, . PROPYLTHIOURACIL dosage: 100 MG;TID;PO. Patient was hospitalized. Patient recovered.
Propylthiouracil Side Effects Report #5379374-3
PROPYLTHIOURACIL problem was reported by a Consumer or non-health professional from UNITED STATES on June 19, 2007. Female patient, 23 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: aortic valve incompetence, blood ph increased, blood thyroid stimulating hormone decreased, caesarean section, cardiac murmur, cardiomegaly, chest x-ray abnormal, ejection fraction decreased, . PROPYLTHIOURACIL dosage: 100 MG;TID;PO. Patient was hospitalized. Patient recovered.
Amoxicillin Side Effects Report #5748889-8
Consumer or non-health professional from SPAIN reported AMOXICILLIN TRIHYDRATE problem on May 07, 2008. Female patient was treated with AMOXICILLIN TRIHYDRATE. After drug was administered, patient experienced the following problems/side effects: apgar score low, blood ph increased, cardiomegaly, hypotension, neonatal hypoxia, neonatal respiratory distress syndrome, persistent foetal circulation, . AMOXICILLIN TRIHYDRATE dosage: unknown. Patient was hospitalized. Patient recovered.
Decitabine Side Effects Report #5717278-4
DECITABINE problem was reported by a Physician from AUSTRALIA on Apr 15, 2008. Male patient, 77 years of age, was diagnosed with acute myeloid leukaemia and was treated with DECITABINE. After drug was administered, patient experienced the following problems/side effects: anorexia, blood ph increased, body temperature increased, cholelithiasis, fatigue, hepatic cyst, liver disorder, liver function test abnormal, malaise, . DECITABINE dosage: 10 MG/M2, IN 5 DAY, INTRAVENOUS. During the same period patient was treated with ASPIRIN, MINAX, ACIMAX, NATURAL B VITAMINS, PROFLOXIN, AMOXYCILLIN, MAXOLON. Patient was hospitalized. Patient recovered.
Amiodarone Side Effects Report #5305008-X
Health Professional from UNITED STATES reported AMIODARONE problem on Apr 05, 2007. Female patient, 73 years of age, was diagnosed with non-hodgkin's lymphoma and was treated with AMIODARONE. After drug was administered, patient experienced the following problems/side effects: acute respiratory distress syndrome, blood ph increased, cardiopulmonary failure, deep vein thrombosis, enterococcal infection, lung infection pseudomonal, multi-organ failure, pneumomediastinum, pneumothorax, . AMIODARONE dosage: 300 MG, BID. During the same period patient was treated with CYCLOPHOSPHAMIDE, SIMVASTATIN, ATENOLOL, WARFARIN, RITUXIMAB, DOXORUBICIN, VINCRISTINE, PREDNISONE. Patient died.
Warfarin Side Effects Report #5314303-X
WARFARIN problem was reported by a Consumer or non-health professional from UNITED STATES on Apr 11, 2007. Female patient, 73 years of age, was diagnosed with atrial fibrillation, non-hodgkin's lymphoma and was treated with WARFARIN. After drug was administered, patient experienced the following problems/side effects: acute respiratory distress syndrome, blood ph increased, computerised tomogram abnormal, deep vein thrombosis, enterococcal infection, lung infection pseudomonal, multi-organ failure, pco2 decreased, pulmonary toxicity, . WARFARIN dosage: 1.5MG, QD, ORAL. During the same period patient was treated with AMIODARONE, CYCLOPHOSPHAMIDE, SIMVASTATIN, ATENOLOL. Patient was hospitalized and became disabled. Patient died.
Clozapine Side Effects Report #5273372-6
Physician from NEW ZEALAND reported CLOZAPINE problem on Mar 09, 2007. Female patient, 60 years of age, was diagnosed with schizoaffective disorder and was treated with CLOZAPINE. After drug was administered, patient experienced the following problems/side effects: blood glucose decreased, blood ph increased, polyserositis, . CLOZAPINE dosage: 250 MG QDAY. During the same period patient was treated with VALPROATE, VENLAFAXINE, LEVOTHYROXINE. Patient was hospitalized. Patient recovered.
Propylthiouracil Side Effects Report #5635698-3
PROPYLTHIOURACIL problem was reported by a Consumer or non-health professional from TURKEY 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.
Bevacizumab Side Effects Report #5567154-5
Health Professional from UNITED STATES reported BEVACIZUMAB problem on Dec 13, 2007. Female patient, weighting 169.0 lb, was diagnosed with breast cancer metastatic and was treated with BEVACIZUMAB. After drug was administered, patient experienced the following problems/side effects: alpha haemolytic streptococcal infection, atelectasis, blood ph increased, mental status changes, pneumonia, pulmonary embolism, renal disorder, sputum discoloured, . BEVACIZUMAB dosage: 1550 MG, Q3W. During the same period patient was treated with ABRAXANE. Patient died on 12/04/2007.
Myozyme Side Effects Report #5510571-X
MYOZYME problem was reported by a Physician from UNITED STATES on Oct 23, 2007. Female patient, weighting 29.98 lb, was diagnosed with glycogen storage disease type ii and was treated with MYOZYME. After drug was administered, patient experienced the following problems/side effects: acinetobacter infection, bacteria urine identified, blood ph increased, blood pressure diastolic decreased, diarrhoea, enterococcal infection, escherichia infection, heart rate increased, hydronephrosis, . MYOZYME dosage: 20 MG/KG Q2WKS IV. During the same period patient was treated with ALPHA, PREVACID, ENALAPRIL MALEATE, DIGOXIN, MIRALAX, LASIX. Patient was hospitalized. Patient recovered.
Carbamazepine Side Effects Report #5524806-0
Consumer or non-health professional from SPAIN reported CARBAMAZEPINE problem on Nov 02, 2007. Male patient, 74 years of age, was treated with CARBAMAZEPINE. After drug was administered, patient experienced the following problems/side effects: arrhythmia, atrial fibrillation, blood ph increased, cholestasis, confusional state, cryptogenic organising pneumonia, cytolytic hepatitis, eosinophilia, hallucination, visual, . CARBAMAZEPINE dosage: unknown. Patient was hospitalized. Patient recovered.
Zevalin Side Effects Report #5524876-X
ZEVALIN problem was reported by a Physician from FRANCE on Nov 06, 2007. Male patient, 60 years of age, was diagnosed with bone marrow conditioning regimen and was treated with ZEVALIN. After drug was administered, patient experienced the following problems/side effects: amyotrophy, blood culture positive, blood ph increased, blood potassium decreased, blood pressure increased, dysaesthesia, electrocardiogram abnormal, encephalopathy, eschar, . ZEVALIN dosage: unknown. During the same period patient was treated with MABTHERA, CARMUSTINE, ETOPOSIDE, ARACYTINE, MELPHALAN, PROZAC, MOPRAL. Patient was hospitalized. Patient recovered.
Clofarabine Side Effects Report #5481591-9
Physician from UNITED STATES reported CLOFARABINE problem on Sept 20, 2007. Male patient, 67 years of age, weighting 189.6 lb, was diagnosed with acute myeloid leukaemia and was treated with CLOFARABINE. After drug was administered, patient experienced the following problems/side effects: adrenal adenoma, atelectasis, blood ph increased, deep vein thrombosis, depressed level of consciousness, hypovolaemia, lymphadenopathy, lymphadenopathy mediastinal, . CLOFARABINE dosage: 30 MG/M2 IV. During the same period patient was treated with ACETAMINOPHEN, LOVENOX, TOBRAMYCIN, VANCOMYCIN, DOUBUTAMINE, ALBUMIN, NOREPINEPHRINE, MEROPENEM. Patient was hospitalized. Patient recovered.
Ritalin Side Effects Report #5425823-1
RITALIN problem was reported by a Consumer or non-health professional from SWEDEN on Aug 16, 2007. Female patient, 16 years of age, was treated with RITALIN. After drug was administered, patient experienced the following problems/side effects: agitation, anxiety, blood ph increased, blood potassium decreased, blood pressure increased, heart rate increased, pco2 decreased, . RITALIN dosage: 940 MG, ONCE/SINGLE. Patient recovered.
Ritalin Side Effects Report #5427141-4
Consumer or non-health professional from SWEDEN reported RITALIN problem on Aug 16, 2007. Female patient, 16 years of age, was treated with RITALIN. After drug was administered, patient experienced the following problems/side effects: agitation, anxiety, blood ph increased, blood potassium decreased, blood pressure increased, heart rate increased, pco2 decreased, . RITALIN dosage: 940 MG, ONCE/SINGLE. Patient recovered.
Salbutamol Side Effects Report #5380574-7
SALBUTAMOL problem was reported by a Consumer or non-health professional from UNITED KINGDOM on June 20, 2007. Female patient, 28 years of age, was diagnosed with asthma and was treated with SALBUTAMOL. After drug was administered, patient experienced the following problems/side effects: abdominal pain, abdominal rigidity, blood ph increased, carbon dioxide increased, hyperlactacidaemia, . SALBUTAMOL dosage: 5 MG. Patient was hospitalized. Patient recovered.
Salbutamol Side Effects Report #5380574-7
Consumer or non-health professional from UNITED KINGDOM reported SALBUTAMOL problem on June 20, 2007. Female patient, 28 years of age, was diagnosed with asthma and was treated with SALBUTAMOL. After drug was administered, patient experienced the following problems/side effects: abdominal pain, abdominal rigidity, blood ph increased, carbon dioxide increased, hyperlactacidaemia, . SALBUTAMOL dosage: 5 MG. Patient was hospitalized. Patient recovered.
Furosemide Side Effects Report #5739216-0
FUROSEMIDE problem was reported by a Consumer or non-health professional from FRANCE on May 13, 2008. Male patient, 61 years of age, was treated with FUROSEMIDE. After drug was administered, patient experienced the following problems/side effects: asterixis, blood bicarbonate increased, blood ph increased, depressed level of consciousness, diaphragmatic disorder, encephalopathy, hypercapnia, hypoventilation, lung infiltration, . FUROSEMIDE dosage: unknown. During the same period patient was treated with ESIDRIX, LASILIX, ZOCOR, NEO MERCAZOLE, XATRAL, TRIATEC, DIFFU K, IPRATROPIUM BROMIDE. Patient was hospitalized. Patient recovered.
Arsenic Side Effects Report #5692772-3
Consumer or non-health professional from FRANCE reported ARSENIC TRIOXIDE problem on Mar 19, 2008. Male patient, 57 years of age, weighting 152.1 lb, was diagnosed with acute myeloid leukaemia and was treated with ARSENIC TRIOXIDE. After drug was administered, patient experienced the following problems/side effects: apallic syndrome, aplasia, blood ph increased, blood pressure systolic increased, brain herniation, cerebral haemorrhage, cholestasis, coma, erythema, . ARSENIC TRIOXIDE dosage: 11 MG DAYS 1-5 OF 12 DAY CYCLE QD INTRAVENOUS. During the same period patient was treated with IDARUBICINE, ARACYTINE, PLITICAN, NEXIUM. Patient was hospitalized. Patient died on 11/04/2007.
Esidrix Side Effects Report #5710926-4
ESIDRIX problem was reported by a Consumer or non-health professional from FRANCE on Apr 14, 2008. Male patient, 61 years of age, was treated with ESIDRIX. After drug was administered, patient experienced the following problems/side effects: asterixis, blood bicarbonate increased, blood ph increased, depressed level of consciousness, diaphragmatic disorder, encephalopathy, hypercapnia, hypoventilation, lung infiltration, . ESIDRIX dosage: unknown. During the same period patient was treated with LASILIX, ZOCOR, NEO MERCAZOLE, XATRAL, TRIATEC, DIFFU K, IPRATROPIUM BROMIDE. Patient was hospitalized. Patient recovered.
Benzocaine Side Effects Report #5366291-8
Pharmacist from UNITED STATES reported BENZOCAINE SPRAY problem on June 19, 2007. Male patient, 72 years of age, was diagnosed with echocardiogram and was treated with BENZOCAINE SPRAY. After drug was administered, patient experienced the following problems/side effects: base excess increased, blood methaemoglobin present, blood ph increased, cyanosis, pco2 decreased, po2 increased, post procedural complication, . BENZOCAINE SPRAY dosage: unknown. Patient recovered.
Osmitrolection Side Effects Report #5287763-0
OSMITROLECTION IN VIAFLEX PLASTIC CONTAINER problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 30, 2007. Male patient, 41 years of age, was diagnosed with intra-cerebral aneurysm operation and was treated with OSMITROLECTION IN VIAFLEX PLASTIC CONTAINER. After drug was administered, patient experienced the following problems/side effects: amnesia, blood ph decreased, blood ph increased, cardiac arrest, haemolysis, hyperkalaemia, ventricular fibrillation, . OSMITROLECTION IN VIAFLEX PLASTIC CONTAINER dosage: unknown. Patient recovered.
Clozapine Side Effects Report #5264776-6
Health Professional from NEW ZEALAND reported CLOZAPINE problem on Mar 01, 2007. Female patient, 60 years of age, was diagnosed with schizoaffective disorder, depression and was treated with CLOZAPINE. After drug was administered, patient experienced the following problems/side effects: blood glucose increased, blood lactate dehydrogenase increased, blood ph increased, cough, influenza like illness, monocyte percentage increased, neutrophil percentage decreased, oxygen saturation decreased, pericardial effusion, . CLOZAPINE dosage: 250 MG/DAY. During the same period patient was treated with VALPROATE, VENLAFAXINE, LEVOTHYROXINE. Patient was hospitalized. Patient recovered.