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BLOOD MAGNESIUM INCREASED side effect

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Cap Side Effects Report #5670994-5
Consumer or non-health professional from UNITED STATES reported CAP VORINOSTAT UNK problem on Feb 25, 2008. Male patient, 64 years of age, weighting 264.0 lb, was diagnosed with acute myeloid leukaemia and was treated with CAP VORINOSTAT UNK. After drug was administered, patient experienced the following problems/side effects: blood magnesium increased, disease progression, gastrooesophageal reflux disease, haematemesis, haemoglobin decreased, hypokalaemia, thrombocytopenia, . CAP VORINOSTAT UNK dosage: 400 MG/DAILY/PO. During the same period patient was treated with INJ DECITABINE UNK, DIFLUCAN, EUCERIN CREME, EXJADE, HYDREA, IMODIUM. Patient was hospitalized and became disabled. Patient recovered.

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.

Lithium Side Effects Report #5575494-9
Physician from UNITED STATES reported LITHIUM CARBONATE problem on Dec 11, 2007. Female patient, 67 years of age, weighting 165.3 lb, was diagnosed with bipolar disorder and was treated with LITHIUM CARBONATE. After drug was administered, patient experienced the following problems/side effects: blood magnesium increased, hypercalcaemia, hyperparathyroidism, hypertension, osteoarthritis, osteoporosis, renal failure chronic, urinary tract infection, . LITHIUM CARBONATE dosage: 300 MG, BID,. During the same period patient was treated with CELECOXIB, ESTRADIOL, AMITRIPTYLINE, RABEPRAZOLE, VERAPAMIL EXTENDED RELEASE, ATORVASTATIN CALCIUM, LEVOTHYROXINE, ASCORBIC ACID. Patient recovered.

Lithium Side Effects Report #5575502-5
LITHIUM CARBONATE problem was reported by a Physician from UNITED STATES on Dec 11, 2007. Male patient, 63 years of age, weighting 260.1 lb, was diagnosed with bipolar disorder and was treated with LITHIUM CARBONATE. After drug was administered, patient experienced the following problems/side effects: blood magnesium increased, hypercalcaemia, hyperparathyroidism, obesity, prostatic specific antigen increased, renal cyst, renal failure chronic, . LITHIUM CARBONATE dosage: 450 MG, QD,. During the same period patient was treated with VALSARTAN, BUPROPION, IMIPRAMINE, ABLUTEROL. Patient recovered.


Concerta Side Effects Report #5507962-X
Physician from PHILIPPINES reported CONCERTA problem on Oct 26, 2007. Male patient, child 7 years of age, was diagnosed with attention deficit/hyperactivity disorder and was treated with CONCERTA. After drug was administered, patient experienced the following problems/side effects: blood magnesium increased, . CONCERTA dosage: unknown. Patient recovered.

Advil Side Effects Report #5520649-2
ADVIL LIQUI problem was reported by a Health Professional from FRANCE on Nov 13, 2007. Male patient was diagnosed with headache and was treated with ADVIL LIQUI. After drug was administered, patient experienced the following problems/side effects: blood magnesium increased, blood phosphorus increased, haematuria, proteinuria, pyrexia, . ADVIL LIQUI dosage: 200 MG TWICE A DAY. During the same period patient was treated with PERFALGAN, CEBUTID, EFFERALGAN, APRANAX. Patient was hospitalized. Patient recovered.

Advil Side Effects Report #5521557-3
Health Professional from FRANCE reported ADVIL LIQUI problem on Nov 13, 2007. Male patient was diagnosed with headache and was treated with ADVIL LIQUI. After drug was administered, patient experienced the following problems/side effects: blood magnesium increased, blood phosphorus increased, haematuria, proteinuria, pyrexia, renal disorder, . ADVIL LIQUI dosage: 200 MG TWICE A DAY. During the same period patient was treated with PERFALGAN, CEBUTID, EFFERALGAN, APRANAX. Patient was hospitalized. Patient recovered.

Bactroban Side Effects Report #5522183-2
BACTROBAN problem was reported by a Health Professional from UNITED STATES on Nov 15, 2007. Male patient, 39 years of age, was treated with BACTROBAN. After drug was administered, patient experienced the following problems/side effects: blood magnesium increased, blood potassium increased, metabolic disorder, mineral metabolism disorder, prothrombin time prolonged, . BACTROBAN dosage: unknown. During the same period patient was treated with COUMADIN, DEPAKOTE, LASIX, LEXAPRO, DONNATAL, VANCOMYCIN, VALTREX, FLAGYL. Patient was hospitalized. Patient recovered.

Lithium Side Effects Report #5404749-3
Physician from UNITED STATES reported LITHIUM SALT problem on July 20, 2007. Female patient, 28 years of age, was diagnosed with psychotic disorder and was treated with LITHIUM SALT. After drug was administered, patient experienced the following problems/side effects: blood magnesium increased, chest pain, confusional state, dehydration, delirium, disturbance in attention, haemodialysis, . LITHIUM SALT dosage: unknown. During the same period patient was treated with FLUCONAZOLE, FLUOXETINE, PREDNISONE, LEVOTHYROXINE. Patient was hospitalized. Patient recovered.


Avonex Side Effects Report #5760433-8
AVONEX problem was reported by a Consumer or non-health professional from UNITED STATES on May 22, 2008. Male patient, weighting 3.50 lb, was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: blood magnesium increased, caesarean section, jaundice neonatal, premature baby, small for dates baby, . AVONEX dosage: unknown. Patient was hospitalized. Patient recovered.

Velcade Side Effects Report #5788444-7
Health Professional from UNITED STATES reported VELCADE problem on June 12, 2008. Male patient, 52 years of age, weighting 209.4 lb, was diagnosed with prostate cancer and was treated with VELCADE. After drug was administered, patient experienced the following problems/side effects: blood magnesium increased, myocardial ischaemia, rhabdomyolysis, supraventricular tachycardia, . VELCADE dosage: 1.6 MG/M2, INTRAVENOUS. During the same period patient was treated with TAXOTERE, VYTORIN, DIOVAN, ASPIRIN, COLACE, PROSCAR, DETROL, PREDNISONE. Patient was hospitalized. Patient recovered.

Nexium Side Effects Report #5312659-5
NEXIUM problem was reported by a Pharmacist from UNITED STATES on Feb 09, 2007. Female patient, 52 years of age, was treated with NEXIUM. After drug was administered, patient experienced the following problems/side effects: blood magnesium increased, . NEXIUM dosage: unknown. Patient recovered.

Magnesium Side Effects Report #5313675-X
Health Professional from UNITED STATES reported MAGNESIUM SULPHATE problem on Apr 30, 2007. Female patient was treated with MAGNESIUM SULPHATE. After drug was administered, patient experienced the following problems/side effects: blood magnesium increased, incorrect dose administered, . MAGNESIUM SULPHATE dosage: unknown. Patient recovered.

Digoxin Side Effects Report #5258758-8
DIGOXIN problem was reported by a Pharmacist from UNITED STATES on Mar 06, 2007. Female patient, 62 years of age, weighting 173.0 lb, was diagnosed with cardiac failure congestive and was treated with DIGOXIN. After drug was administered, patient experienced the following problems/side effects: blood magnesium increased, fatigue, international normalised ratio increased, mental status changes, road traffic accident, . DIGOXIN dosage: 0.25MG DAILY PO. Patient was hospitalized. Patient recovered.


Phillips Side Effects Report #5276695-X
Health Professional from UNITED STATES reported PHILLIPS LIQUID GELS problem on Mar 15, 2007. Female patient, 32 years of age, weighting 160.9 lb, was diagnosed with constipation and was treated with PHILLIPS LIQUID GELS. After drug was administered, patient experienced the following problems/side effects: blood magnesium increased, blood potassium increased, . PHILLIPS LIQUID GELS dosage: UNIT DOSE: 100 MG. During the same period patient was treated with EFFEXOR, NEPHRO, MECLIZINE, VYTORIN, LISINOPRIL, RENAGEL, ZEMPLAR. Patient recovered.

Phillips Side Effects Report #5278353-4
PHILLIPS LIQUID GELS problem was reported by a Health Professional from UNITED STATES on Mar 15, 2007. Female patient, 32 years of age, weighting 160.9 lb, was diagnosed with constipation and was treated with PHILLIPS LIQUID GELS. After drug was administered, patient experienced the following problems/side effects: blood magnesium increased, blood potassium increased, . PHILLIPS LIQUID GELS dosage: UNIT DOSE: 100 MG. During the same period patient was treated with EFFEXOR, NEPHRO, MECLIZINE, VYTORIN, LISINOPRIL, RENAGEL, ZEMPLAR. Patient recovered.

Cap Side Effects Report #5663718-9
Consumer or non-health professional from UNITED STATES reported CAP VORINOSTAT UNK problem on Feb 25, 2008. Male patient, 64 years of age, weighting 264.0 lb, was diagnosed with acute myeloid leukaemia and was treated with CAP VORINOSTAT UNK. After drug was administered, patient experienced the following problems/side effects: acute myeloid leukaemia, blood magnesium increased, condition aggravated, gastrooesophageal reflux disease, haematemesis, hypokalaemia, nausea, vomiting, . CAP VORINOSTAT UNK dosage: 400 MG/DAILY/PO. During the same period patient was treated with INJ DECITABINE UNK, DIFLUCAN, EUCERIN CREME, EXJADE, HYDREA, IMODIUM. Patient was hospitalized and became disabled. Patient recovered.

Diamox Side Effects Report #5573920-2
DIAMOX problem was reported by a Consumer or non-health professional from UNITED STATES on Dec 05, 2007. Male patient, child 12 years of age, was diagnosed with asthma and was treated with DIAMOX. After drug was administered, patient experienced the following problems/side effects: blood calcium decreased, blood magnesium increased, bronchial secretion retention, cardiogenic shock, disseminated intravascular coagulation, duodenal ulcer haemorrhage, erosive duodenitis, gastritis, gastrointestinal necrosis, . DIAMOX dosage: unknown. During the same period patient was treated with ALBUTEROL SULPHATE, FENTANYL, IBUPROFEN, LASIX, PROVENTIL, TERBUTALINE SULPHATE, ATROVENT. Patient was hospitalized. Patient died on 04/12/1997.

Trisenox Side Effects Report #5515367-0
Physician from UNITED STATES reported TRISENOX problem on Oct 25, 2007. Female patient, weighting 142.0 lb, was diagnosed with multiple myeloma and was treated with TRISENOX. After drug was administered, patient experienced the following problems/side effects: bacteraemia, blood magnesium increased, coronary artery disease, enterococcal infection, febrile neutropenia, haematocrit decreased, haemoglobin decreased, heart rate increased, hypotension, . TRISENOX dosage: 0.25 MG/KG UNK INTRAVENOUS. During the same period patient was treated with HYDROMORPHONE, LOPERAMIDE, HEPARIN, CHLORIDE, LANOLIN, LORAZEPAM, MORPHINE, OMEPRAZOLE. Patient was hospitalized. Patient recovered.


Myozyme Side Effects Report #5532913-1
MYOZYME problem was reported by a Physician from UNITED STATES on Nov 14, 2007. Female patient, child 3 years of age, weighting 30.20 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 calcium increased, blood magnesium increased, bone density decreased, brain natriuretic peptide increased, cardiac disorder, cardiomegaly, condition aggravated, culture urine positive, diarrhoea, . MYOZYME dosage: 20 MG/KG Q2WKS IV. During the same period patient was treated with ALPHA, DIGOXIN, ENALAPRIL. Patient was hospitalized. Patient recovered.

Velcade Side Effects Report #5776524-1
Health Professional from UNITED STATES reported VELCADE problem on June 04, 2008. Male patient, 52 years of age, weighting 209.4 lb, was diagnosed with prostate cancer and was treated with VELCADE. After drug was administered, patient experienced the following problems/side effects: blood creatine phosphokinase increased, blood magnesium increased, dizziness, electrolyte imbalance, hyperhidrosis, myocardial ischaemia, palpitations, respiratory rate increased, rhabdomyolysis, . VELCADE dosage: 1.6 MG/M2, INTRAVENOUS. During the same period patient was treated with TAXOTERE, VYTORIN, DIOVAN, ASPIRIN, COLACE, PROSCAR, DETROL, PREDNISONE. Patient was hospitalized. Patient recovered.

Cap Side Effects Report #5792715-8
CAP VORINOSTAT UNK problem was reported by a Consumer or non-health professional from UNITED STATES on June 09, 2008. Male patient, 64 years of age, weighting 264.0 lb, was diagnosed with acute myeloid leukaemia and was treated with CAP VORINOSTAT UNK. After drug was administered, patient experienced the following problems/side effects: acute myeloid leukaemia, blood magnesium increased, blood phosphorus decreased, disease progression, haematemesis, haemoglobin decreased, hypokalaemia, nausea, thrombocytopenia, . CAP VORINOSTAT UNK dosage: 400 MG/DAILY/PO. During the same period patient was treated with INJ DECITABINE UNK, DIFLUCAN, EUCERIN CREME, EXJADE, HYDREA, IMODIUM. Patient was hospitalized and became disabled. Patient died.

Velcade Side Effects Report #5757187-8
Health Professional from UNITED STATES reported VELCADE problem on May 20, 2008. Male patient, 52 years of age, weighting 209.4 lb, was diagnosed with prostate cancer and was treated with VELCADE. After drug was administered, patient experienced the following problems/side effects: blood creatine phosphokinase increased, blood magnesium increased, chest pain, dizziness, electrocardiogram abnormal, hyperhidrosis, myocardial ischaemia, palpitations, presyncope, . VELCADE dosage: 1.6 MG/M2, INTRAVENOUS. During the same period patient was treated with TAXOTERE, VYTORIN, DIOVAN, ASPIRIN, COLACE, PROSCAR, DETROL, PREDNISONE. Patient was hospitalized. Patient recovered.

Indomethacin Side Effects Report #5331086-8
INDOMETHACIN problem was reported by a Pharmacist from UNITED STATES on May 18, 2007. Male patient, 80 years of age, weighting 202.4 lb, was diagnosed with cardiac failure congestive, gout and was treated with INDOMETHACIN. After drug was administered, patient experienced the following problems/side effects: blood creatinine increased, blood magnesium increased, blood phosphorus increased, blood potassium increased, blood urea increased, brain natriuretic peptide increased, creatinine urine increased, gout, troponin t increased, . INDOMETHACIN dosage: 50 MG TID PO (DURATION: { 14 DAYS). During the same period patient was treated with LISINOPRIL. Patient was hospitalized. Patient recovered.

Zometa Side Effects Report #5298084-4
Pharmacist from UNITED STATES reported ZOMETA problem on Apr 03, 2007. Male patient, 53 years of age, was diagnosed with multiple myeloma and was treated with ZOMETA. After drug was administered, patient experienced the following problems/side effects: blood creatinine increased, blood magnesium increased, blood potassium decreased, hypercalcaemia, . ZOMETA dosage: 4 MG MONTHLY. During the same period patient was treated with BORTEZOMIB, DOXIL. Patient recovered.

Benicar Side Effects Report #5283718-0
BENICAR HCT problem was reported by a Physician from UNITED STATES on Mar 13, 2007. Male patient, 54 years of age, weighting 178.0 lb, was diagnosed with hypertension and was treated with BENICAR HCT. After drug was administered, patient experienced the following problems/side effects: asthenia, blood magnesium increased, cardiac murmur, dizziness, hyperhidrosis, hypertension, loss of consciousness, syncope, ventricular hypertrophy, . BENICAR HCT dosage: 20.125 MG QD PO. Patient was hospitalized. Patient recovered.

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.

Cisplatin Side Effects Report #5408289-7
CISPLATIN problem was reported by a Consumer or non-health professional from UNITED STATES on Aug 06, 2007. Female patient, weighting 145.0 lb, was treated with CISPLATIN. After drug was administered, patient experienced the following problems/side effects: arteriosclerosis, blood glucose increased, blood magnesium increased, blood phosphorus increased, blood sodium decreased, haemoglobin decreased, hydronephrosis, hyperphagia, lung neoplasm, . CISPLATIN dosage: 88 MG. During the same period patient was treated with DOXORUBICIN HYDROCHLORIDE, TAXOL. Patient was hospitalized. Patient recovered.

Myozyme Side Effects Report #5416400-7
Physician from UNITED STATES reported MYOZYME problem 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.

Myozyme Side Effects Report #5796381-7
MYOZYME problem was reported by a Physician from UNITED STATES on June 18, 2008. Male patient, weighting 11.90 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: atelectasis, band neutrophil percentage decreased, blood magnesium increased, faeces discoloured, grunting, hypertrophic cardiomyopathy, irritability, lymphocyte percentage increased, metapneumovirus infection, . MYOZYME dosage: 20 MG/KG, Q2W, INTRAVENOUS. During the same period patient was treated with OXYGEN. Patient was hospitalized. Patient recovered.

Cap Side Effects Report #5801773-3
Consumer or non-health professional from UNITED STATES reported CAP VORINOSTAT UNK problem on June 09, 2008. Male patient, 64 years of age, weighting 264.0 lb, was diagnosed with acute myeloid leukaemia and was treated with CAP VORINOSTAT UNK. After drug was administered, patient experienced the following problems/side effects: acute myeloid leukaemia, blood calcium decreased, blood magnesium increased, blood phosphorus decreased, blood urea increased, disease progression, haematemesis, hypokalaemia, nausea, . CAP VORINOSTAT UNK dosage: 400 MG/DAILY/PO. During the same period patient was treated with INJ DECITABINE UNK, DIFLUCAN, EUCERIN CREME, EXJADE, HYDREA, IMODIUM. Patient was hospitalized and became disabled. Patient died.

Prednisone Side Effects Report #5353632-0
PREDNISONE problem was reported by a Pharmacist from UNITED STATES on June 08, 2007. Male patient, 48 years of age, weighting 287.0 lb, was diagnosed with nephrotic syndrome and was treated with PREDNISONE. After drug was administered, patient experienced the following problems/side effects: blood chloride decreased, blood creatinine increased, blood magnesium increased, blood phosphorus increased, blood pressure decreased, blood sodium decreased, blood urea increased, body temperature decreased, depressed level of consciousness, . PREDNISONE dosage: 40MG DAILY PO. Patient was hospitalized. Patient recovered.

Neurontin Side Effects Report #5331532-X
Physician from UNITED STATES reported NEURONTIN problem on May 15, 2007. Female patient, weighting 223.1 lb, was treated with NEURONTIN. After drug was administered, patient experienced the following problems/side effects: anaemia, blood creatinine increased, blood magnesium increased, blood urea increased, convulsion, hyperkalaemia, hypocalcaemia, hypotension, muscle twitching, . NEURONTIN dosage: unknown. During the same period patient was treated with CELEBREX, DURAGESIC, EFFEXOR, VASOTEC, TOPROL, LORTAB, PAMELOR, ESTRATEST. Patient recovered.

Gabapentin Side Effects Report #5305024-8
GABAPENTIN problem was reported by a Physician from UNITED STATES on Apr 11, 2007. Female patient, weighting 223.1 lb, was treated with GABAPENTIN. After drug was administered, patient experienced the following problems/side effects: anaemia, blood creatinine increased, blood magnesium increased, blood urea increased, convulsion, hyperkalaemia, hypocalcaemia, hypotension, muscle twitching, . GABAPENTIN dosage: unknown. During the same period patient was treated with CELEBREX, DURAGESIC, EFFEXOR, VASOTEC, TOPROL, LORTAB, PAMELOR, ESTRATEST. Patient recovered.

Thalomid Side Effects Report #5307769-2
Physician from UNITED STATES reported THALOMID problem on Apr 11, 2007. Male patient, 20 years of age, was diagnosed with acute graft versus host disease in skin and was treated with THALOMID. After drug was administered, patient experienced the following problems/side effects: acute graft versus host disease in liver, blood glucose increased, blood magnesium increased, blood pressure increased, blood sodium decreased, blood urea increased, discomfort, enterococcal infection, fluid intake reduced, . THALOMID dosage: 400-800 MG, ORAL. During the same period patient was treated with DECADRON, ACTIGALL, ARANESP, PROCARDIA, COLACE, SENOKOT, LACTULOSE, VERSED. Patient was hospitalized. Patient died on 02/15/2003.

Cymbalta Side Effects Report #5253464-8
CYMBALTA problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 19, 2007. Female patient, 55 years of age, weighting 166.0 lb, was diagnosed with neuropathy and was treated with CYMBALTA. After drug was administered, patient experienced the following problems/side effects: blood albumin decreased, blood alkaline phosphatase increased, blood magnesium increased, rash pruritic, . CYMBALTA dosage: 60 MG, DAILY (1/D). During the same period patient was treated with LIPITOR, METFORMIN, ACTOS, AMARYL. Patient recovered.