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BLOOD MAGNESIUM DECREASED side effect

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Avonex Side Effects Report #5663932-2
Physician from UNITED STATES reported AVONEX problem on Feb 27, 2008. Female patient, 49 years of age, was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: blood magnesium decreased, blood potassium decreased, cognitive disorder, fatigue, sinusitis, . AVONEX dosage: unknown. During the same period patient was treated with COZAAR, SINGULAIR, ZOCOR, LYRICA, LEXAPRO, WELLBUTRIN, NASACORT, PROVIGIL. Patient was hospitalized. Patient recovered.

Rebif Side Effects Report #5679567-1
REBIF problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 11, 2008. Female patient, 48 years of age, was diagnosed with off label use and was treated with REBIF. After drug was administered, patient experienced the following problems/side effects: blood magnesium decreased, dehydration, diarrhoea, gastrointestinal infection, headache, hypoaesthesia, nausea, neck pain, vomiting, . REBIF dosage: unknown. Patient was hospitalized. Patient recovered.

Cetuximab Side Effects Report #5684668-8
Consumer or non-health professional from UNITED STATES reported CETUXIMAB problem on May 22, 2007. Male patient, 62 years of age, weighting 147.7 lb, was diagnosed with colorectal cancer and was treated with CETUXIMAB. After drug was administered, patient experienced the following problems/side effects: blood magnesium decreased, hyperkalaemia, renal failure acute, . CETUXIMAB dosage: unknown. During the same period patient was treated with VECTIBIX, HYDROCODONE BITARTRATE. Patient was hospitalized. Patient recovered.

Erbitux Side Effects Report #5684845-6
ERBITUX problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 31, 2007. Male patient, 60 years of age, was diagnosed with colon cancer and was treated with ERBITUX. After drug was administered, patient experienced the following problems/side effects: blood magnesium decreased, . ERBITUX dosage: unknown. Patient recovered.


Erbitux Side Effects Report #5684935-8
Consumer or non-health professional from UNITED STATES reported ERBITUX problem on Jan 08, 2008. Male patient, 76 years of age, weighting 160.9 lb, was diagnosed with lung cancer metastatic and was treated with ERBITUX. After drug was administered, patient experienced the following problems/side effects: blood magnesium decreased, dermatitis acneiform, impaired healing, localised infection, . ERBITUX dosage: unknown. During the same period patient was treated with CEPHALEXIN, AVAPRO, CARBOPLATIN, FLUOROURACIL, TAGAMET, DECADRON, BENADRYL, ALOXI. Patient recovered.

Novoseven Side Effects Report #5613720-8
NOVOSEVEN problem was reported by a Pharmacist from UNITED STATES on Jan 29, 2008. Female patient was diagnosed with factor vii deficiency, hypertension, dyslipidaemia, preoperative care, blood glucose increased and was treated with NOVOSEVEN. After drug was administered, patient experienced the following problems/side effects: blood magnesium decreased, blood potassium decreased, cerebral infarction, convulsion, . NOVOSEVEN dosage: 1.2 MG, SINGLE. During the same period patient was treated with HYDROCHLOROTHIAZIDE, BENAZEPRIL HYDROCHLORIDE, CRESTOR, ASPIRIN, DARVOCET, LEVAQUIN, HUMALOG. Patient died.

Nexavar Side Effects Report #5618650-3
Consumer or non-health professional from UNITED STATES reported NEXAVAR problem on Jan 31, 2008. Female patient, 62 years of age, weighting 149.9 lb, was diagnosed with cervix cancer metastatic and was treated with NEXAVAR. After drug was administered, patient experienced the following problems/side effects: blood magnesium decreased, dehydration, diarrhoea, disorientation, dry skin, haemoglobin decreased, headache, paraesthesia, platelet count decreased, . NEXAVAR dosage: TOTAL DAILY DOSE: 800 MG UNIT DOSE: 200 MG. During the same period patient was treated with TARCEVA, CISPLATIN, HYCAMTIN. Patient was hospitalized. Patient recovered.

Aleve Side Effects Report #5624872-8
ALEVE problem was reported by a Physician from GERMANY on Jan 24, 2008. Female patient, 72 years of age, was diagnosed with osteoarthritis and was treated with ALEVE. After drug was administered, patient experienced the following problems/side effects: blood magnesium decreased, blood potassium decreased, cardiac valve disease, depression, diastolic dysfunction, diverticulum, fluid overload, gastritis, gastrointestinal haemorrhage, . ALEVE dosage: unknown. During the same period patient was treated with NAPROSYN, MOTRIN. Patient was hospitalized. Patient recovered.

Amiodarone Side Effects Report #5625777-9
Consumer or non-health professional from UNITED KINGDOM reported AMIODARONE problem on Jan 31, 2008. Female patient, 65 years of age, was diagnosed with atrial flutter and was treated with AMIODARONE. After drug was administered, patient experienced the following problems/side effects: blood magnesium decreased, bradycardia, electrocardiogram qt prolonged, syncope, torsade de pointes, . AMIODARONE dosage: 200 MG THREE TIMES A DAY FOR A WEEK, THEN TWICE A DAY FOR A WEEK, FOLLOWED BY ONCE DAILY ORAL. During the same period patient was treated with ZOPICLONE, PAROXETINE, MOVICOL, CALCICHEW, RAMIPRIL, LEVOTHYROXINE, CHLORPHENAMINE, FUROSEMIDE. Patient was hospitalized. Patient recovered.


Amiodarone Side Effects Report #5625784-6
AMIODARONE problem was reported by a Consumer or non-health professional from UNITED KINGDOM on Jan 31, 2008. Female patient, 95 years of age, was diagnosed with ventricular tachycardia and was treated with AMIODARONE. After drug was administered, patient experienced the following problems/side effects: blood magnesium decreased, dizziness, hypokalaemia, syncope, tachycardia, torsade de pointes, . AMIODARONE dosage: 200 MG DAILY. During the same period patient was treated with THYROXINE, INDAPAMIDE. Patient recovered.

Avonex Side Effects Report #5631312-1
Physician from UNITED STATES reported AVONEX problem on Feb 01, 2008. Female patient, 49 years of age, was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: blood magnesium decreased, blood potassium decreased, cognitive disorder, fatigue, impaired work ability, sinusitis, . AVONEX dosage: unknown. During the same period patient was treated with COZAAR, SINGULAIR, ZOCOR, LYRICA, LEXAPRO, WELLBUTRIN, NASACORT, PROVIGIL. Patient was hospitalized. Patient recovered.

Novoseven Side Effects Report #5636780-7
NOVOSEVEN problem was reported by a Pharmacist from UNITED STATES on Jan 29, 2008. Female patient was diagnosed with factor vii deficiency, hypertension, dyslipidaemia, preoperative care, blood glucose increased and was treated with NOVOSEVEN. After drug was administered, patient experienced the following problems/side effects: blood magnesium decreased, blood potassium decreased, cerebral infarction, convulsion, hemiparesis, . NOVOSEVEN dosage: 1.2 MG, SINGLE. During the same period patient was treated with HYDROCHLOROTHIAZIDE, BENAZEPRIL HYDROCHLORIDE, CRESTOR, ASPIRIN, DARVOCET, LEVAQUIN, HUMALOG. Patient died.

Seroquel Side Effects Report #5580453-6
Health Professional from UNITED STATES reported SEROQUEL problem on July 23, 2007. Female patient, weighting 285.5 lb, was diagnosed with bipolar disorder, borderline personality disorder and was treated with SEROQUEL. After drug was administered, patient experienced the following problems/side effects: blood magnesium decreased, bronchitis, cardiomegaly, cervical dysplasia, chest pain, contusion, corneal disorder, diabetes mellitus, dysfunctional uterine bleeding, . SEROQUEL dosage: unknown. During the same period patient was treated with FEN PHEN, RISPERDAL, DEPAKOTE, REMERON, EFFEXOR, PROZAC, WELLBUTRIN. Patient recovered.

Revlimid Side Effects Report #5592829-1
REVLIMID problem was reported by a Health Professional from UNITED STATES on Jan 08, 2008. Female patient, 74 years of age, was diagnosed with multiple myeloma and was treated with REVLIMID. After drug was administered, patient experienced the following problems/side effects: blood magnesium decreased, blood potassium decreased, . REVLIMID dosage: 10 MG, 1 IN 1 D, ORAL : 20 MG, 2 IN 1 D, ORAL. Patient died.


Paclitaxel Side Effects Report #5602750-8
Health Professional from UNITED KINGDOM reported PACLITAXEL problem on Jan 23, 2008. Female patient, 61 years of age, was diagnosed with breast cancer and was treated with PACLITAXEL. After drug was administered, patient experienced the following problems/side effects: blood magnesium decreased, haemoglobin decreased, . PACLITAXEL dosage: unknown. During the same period patient was treated with TRASTUZUMAB. Patient was hospitalized. Patient recovered.

Taxol Side Effects Report #5546745-1
TAXOL problem was reported by a Consumer or non-health professional from UNITED STATES on Dec 07, 2007. Female patient, weighting 110.2 lb, was treated with TAXOL. After drug was administered, patient experienced the following problems/side effects: blood magnesium decreased, nausea, . TAXOL dosage: 261 MG. Patient was hospitalized. Patient recovered.

Remicade Side Effects Report #5477931-7
Consumer or non-health professional from UNITED STATES reported REMICADE problem on Sept 24, 2007. Female patient, weighting 130.0 lb, was diagnosed with rheumatoid arthritis and was treated with REMICADE. After drug was administered, patient experienced the following problems/side effects: blood magnesium decreased, gallbladder operation, laboratory test abnormal, . REMICADE dosage: unknown. Patient was hospitalized. Patient recovered.

Gemzar Side Effects Report #5482662-3
GEMZAR problem was reported by a Consumer or non-health professional from FRANCE on Oct 03, 2007. Male patient was diagnosed with lung adenocarcinoma metastatic and was treated with GEMZAR. After drug was administered, patient experienced the following problems/side effects: blood magnesium decreased, renal failure acute, renal tubular disorder, . GEMZAR dosage: 2520 MG, OTHER. During the same period patient was treated with CISPLATIN, KETOPROFEN, INEXIUM, XATRAL, LYTOS, SOPHIDONE, FORLAX, PRIMPERAN. Patient was hospitalized. Patient recovered.

Chantix Side Effects Report #5484667-5
Consumer or non-health professional from UNITED STATES reported CHANTIX problem on Sept 30, 2007. Female patient, weighting 172.0 lb, was treated with CHANTIX. After drug was administered, patient experienced the following problems/side effects: blood magnesium decreased, oral surgery, weight decreased, . CHANTIX dosage: unknown. During the same period patient was treated with GLUCOPHAGE, ACIPHEX, LANTUS, HUMALOG, PRAVACHOL, UNITHROID, METOCLOPRAMIDE, ZETIA. Patient recovered.


Cetuximab Side Effects Report #5492112-9
CETUXIMAB problem was reported by a Health Professional from GERMANY on Oct 15, 2007. Female patient, 56 years of age, was diagnosed with colorectal cancer and was treated with CETUXIMAB. After drug was administered, patient experienced the following problems/side effects: blood magnesium decreased, neutropenia, . CETUXIMAB dosage: unknown. During the same period patient was treated with IRINOTECAN. Patient was hospitalized. Patient recovered.

Vectibix Side Effects Report #5495199-2
Physician from UNITED STATES reported VECTIBIX problem on July 19, 2007. Female patient, weighting 244.3 lb, was diagnosed with colorectal cancer and was treated with VECTIBIX. After drug was administered, patient experienced the following problems/side effects: blood magnesium decreased, paronychia, . VECTIBIX dosage: unknown. During the same period patient was treated with MAGNESIUM SULPHATE. Patient recovered.

Zoloft Side Effects Report #5443782-2
ZOLOFT problem was reported by a Physician from UNITED STATES on Aug 25, 2007. Male patient, weighting 8.18 lb, was diagnosed with depression and was treated with ZOLOFT. After drug was administered, patient experienced the following problems/side effects: blood magnesium decreased, hypocalcaemia, pulmonary hypertension, . ZOLOFT dosage: DAILY DOSE:150MG. Patient recovered.

Seroquel Side Effects Report #5464141-2
Physician from AUSTRALIA reported SEROQUEL problem on Sept 10, 2007. Female patient, 31 years of age, was diagnosed with schizophrenia and was treated with SEROQUEL. After drug was administered, patient experienced the following problems/side effects: blood magnesium decreased, blood potassium decreased, electrocardiogram qt prolonged, tachycardia, . SEROQUEL dosage: unknown. Patient was hospitalized. Patient recovered.

Aspirin Side Effects Report #5411875-1
ASPIRIN problem was reported by a Consumer or non-health professional from UNITED STATES on July 30, 2007. Female patient, 67 years of age, weighting 209.4 lb, was diagnosed with cardiovascular event prophylaxis, vitamin supplementation, lipids increased and was treated with ASPIRIN. After drug was administered, patient experienced the following problems/side effects: blood magnesium decreased, cardiac stress test abnormal, hypertension, palpitations, ventricular tachycardia, . ASPIRIN dosage: TOTAL DAILY DOSE: 162 MG UNIT DOSE: 81 MG. During the same period patient was treated with ONE A DAY, FELDENE, GLUCOVANCE, ZETIA, LOTREL, ATENOLOL, LIPITOR. Patient was hospitalized. Patient recovered.

Lovastatin Side Effects Report #5419370-0
Pharmacist from UNITED STATES reported LOVASTATIN problem on Aug 16, 2007. Female patient, 61 years of age, weighting 106.7 lb, was diagnosed with hyperlipidaemia and was treated with LOVASTATIN. After drug was administered, patient experienced the following problems/side effects: blood magnesium decreased, blood potassium decreased, nausea, rhabdomyolysis, . LOVASTATIN dosage: unknown. Patient was hospitalized. Patient recovered.

Capecitabine Side Effects Report #5419547-4
CAPECITABINE problem was reported by a Physician from UNITED KINGDOM on Aug 08, 2007. Female patient, 61 years of age, weighting 105.8 lb, was diagnosed with breast cancer and was treated with CAPECITABINE. After drug was administered, patient experienced the following problems/side effects: blood magnesium decreased, blood potassium decreased, blood sodium decreased, fatigue, vomiting, . CAPECITABINE dosage: unknown. During the same period patient was treated with EPIRUBICIN. Patient was hospitalized. Patient recovered.

Gemzar Side Effects Report #5427436-4
Consumer or non-health professional from UNITED STATES reported GEMZAR problem on Aug 17, 2007. Female patient, 44 years of age, weighting 183.0 lb, was diagnosed with endometrial cancer and was treated with GEMZAR. After drug was administered, patient experienced the following problems/side effects: blood magnesium decreased, blood potassium decreased, cough, deep vein thrombosis, dyspnoea, face oedema, heart rate increased, hypersensitivity, lung injury, . GEMZAR dosage: unknown. During the same period patient was treated with CARBOPLATIN, FOSAMAX. 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.

Nexavar Side Effects Report #5380301-3
Consumer or non-health professional from UNITED STATES reported NEXAVAR problem on June 29, 2007. Female patient, 62 years of age, weighting 149.9 lb, was diagnosed with cervix cancer metastatic and was treated with NEXAVAR. After drug was administered, patient experienced the following problems/side effects: blood magnesium decreased, dehydration, diarrhoea, disorientation, dry skin, haemoglobin decreased, headache, paraesthesia, platelet count decreased, . NEXAVAR dosage: TOTAL DAILY DOSE: 800 MG UNIT DOSE: 200 MG. During the same period patient was treated with TARCEVA, CISPLATIN, HYCAMTIN. Patient was hospitalized. Patient recovered.

Provigil Side Effects Report #5402423-0
PROVIGIL problem was reported by a Consumer or non-health professional from UNITED STATES on July 16, 2007. Female patient, 38 years of age, weighting 121.0 lb, was diagnosed with narcolepsy and was treated with PROVIGIL. After drug was administered, patient experienced the following problems/side effects: blood magnesium decreased, blood potassium decreased, convulsion, feeling abnormal, syncope, . PROVIGIL dosage: 200 MG BID ORAL. Patient was hospitalized. Patient recovered.

Nexavar Side Effects Report #5380301-3
Consumer or non-health professional from UNITED STATES reported NEXAVAR problem on June 29, 2007. Female patient, 62 years of age, weighting 149.9 lb, was diagnosed with cervix cancer metastatic and was treated with NEXAVAR. After drug was administered, patient experienced the following problems/side effects: blood magnesium decreased, dehydration, diarrhoea, disorientation, dry skin, haemoglobin decreased, headache, paraesthesia, platelet count decreased, . NEXAVAR dosage: TOTAL DAILY DOSE: 800 MG UNIT DOSE: 200 MG. During the same period patient was treated with TARCEVA, CISPLATIN, HYCAMTIN. Patient was hospitalized. Patient recovered.

Provigil Side Effects Report #5402423-0
PROVIGIL problem was reported by a Consumer or non-health professional from UNITED STATES on July 16, 2007. Female patient, 38 years of age, weighting 121.0 lb, was diagnosed with narcolepsy and was treated with PROVIGIL. After drug was administered, patient experienced the following problems/side effects: blood magnesium decreased, blood potassium decreased, convulsion, feeling abnormal, syncope, . PROVIGIL dosage: 200 MG BID ORAL. Patient was hospitalized. Patient recovered.

Cisplatin Side Effects Report #5763786-X
Consumer or non-health professional from UNITED STATES reported CISPLATIN problem on June 04, 2008. Female patient, weighting 104.2 lb, was treated with CISPLATIN. After drug was administered, patient experienced the following problems/side effects: blood magnesium decreased, blood potassium decreased, carbon dioxide decreased, haematocrit decreased, haemoglobin decreased, hydronephrosis, obstruction, platelet count increased, protein urine present, . CISPLATIN dosage: 44 MG. During the same period patient was treated with ERBITUX. Patient was hospitalized. Patient recovered.

Cisplatin Side Effects Report #5765608-X
CISPLATIN problem was reported by a Consumer or non-health professional from UNITED STATES on June 06, 2008. Female patient, weighting 210.8 lb, was treated with CISPLATIN. After drug was administered, patient experienced the following problems/side effects: blood magnesium decreased, . CISPLATIN dosage: 99 MG. During the same period patient was treated with DOXORUBICIN HYDROCHLORIDE, TAXOL, NEULASTA, COMPAZINE, DECADRON. Patient recovered.

Cisplatin Side Effects Report #5767208-4
Consumer or non-health professional from UNITED STATES reported CISPLATIN problem on June 11, 2008. Female patient, weighting 210.8 lb, was treated with CISPLATIN. After drug was administered, patient experienced the following problems/side effects: blood magnesium decreased, . CISPLATIN dosage: 99 MG. During the same period patient was treated with DOXORUBICIN HYDROCHLORIDE, TAXOL, NEULASTA, COMPAZINE, DECADRON. Patient recovered.

Cisplatin Side Effects Report #5767212-6
CISPLATIN problem was reported by a Consumer or non-health professional from UNITED STATES on June 11, 2008. Female patient, weighting 210.8 lb, was treated with CISPLATIN. After drug was administered, patient experienced the following problems/side effects: blood magnesium decreased, . CISPLATIN dosage: 99 MG. During the same period patient was treated with DOXORUBICIN HYDROCHLORIDE, TAXOL, NEULASTA, COMPAZINE, DECADRON. Patient recovered.

Forteo Side Effects Report #5767486-1
Consumer or non-health professional from UNITED STATES reported FORTEO problem on June 09, 2008. Female patient was diagnosed with osteoporosis and was treated with FORTEO. After drug was administered, patient experienced the following problems/side effects: blood magnesium decreased, fall, lower limb fracture, . FORTEO dosage: unknown. Patient was hospitalized. Patient recovered.

Humira Side Effects Report #5771149-6
HUMIRA problem was reported by a Health Professional from UNITED STATES on May 20, 2008. Male patient, weighting 150.1 lb, was diagnosed with crohn's disease, breakthrough pain and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: blood magnesium decreased, hypoaesthesia, muscle contractions involuntary, musculoskeletal stiffness, . HUMIRA dosage: unknown. During the same period patient was treated with VICODIN. Patient recovered.

Cisplatin Side Effects Report #5772081-4
Consumer or non-health professional from UNITED STATES reported CISPLATIN problem on June 12, 2008. Female patient, weighting 210.8 lb, was treated with CISPLATIN. After drug was administered, patient experienced the following problems/side effects: blood magnesium decreased, . CISPLATIN dosage: 99 MG. During the same period patient was treated with DOXORUBICIN HYDROCHLORIDE, TAXOL, NEULASTA, COMPAZINE, DECADRON. Patient recovered.

Cisplatin Side Effects Report #5777104-4
CISPLATIN problem was reported by a Pharmacist from UNITED STATES on June 17, 2008. Male patient, 51 years of age, weighting 184.3 lb, was diagnosed with laryngeal cancer and was treated with CISPLATIN. After drug was administered, patient experienced the following problems/side effects: blood magnesium decreased, lethargy, nausea, . CISPLATIN dosage: 35MG/M2 IV. During the same period patient was treated with FLUCONAZOLE, GABAPENTIN, ONDANSETRON, OXYCODONE, LEVOTHYROXINE. Patient was hospitalized. Patient recovered.

Cisplatin Side Effects Report #5777930-1
Consumer or non-health professional from UNITED STATES reported CISPLATIN problem on June 17, 2008. Female patient, weighting 210.8 lb, was treated with CISPLATIN. After drug was administered, patient experienced the following problems/side effects: blood magnesium decreased, . CISPLATIN dosage: 96 MG. During the same period patient was treated with DOXORUBICIN HYDROCHLORIDE, TAXOL, NEULASTA, DECADRON, COMPAZINE. Patient was hospitalized. Patient recovered.

Geodon Side Effects Report #5785329-7
GEODON problem was reported by a Pharmacist from UNITED STATES on June 20, 2008. Male patient was treated with GEODON. After drug was administered, patient experienced the following problems/side effects: blood magnesium decreased, . GEODON dosage: unknown. Patient recovered.

Byetta Side Effects Report #5829223-1
Consumer or non-health professional from UNITED STATES reported BYETTA problem on Feb 15, 2008. Female patient, 65 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 magnesium decreased, discomfort, fatigue, hypotension, insomnia, iron deficiency, lung infection, nasopharyngitis, nausea, . BYETTA dosage: unknown. During the same period patient was treated with TOPROL, METFORMIN. Patient recovered.

Duragesic Side Effects Report #5730478-2
DURAGESIC problem was reported by a Consumer or non-health professional from UNITED STATES on Apr 25, 2008. Male patient, weighting 197.0 lb, was diagnosed with pain, blood cholesterol, cardiac disorder, dementia alzheimer's type, diabetes mellitus, vitamin supplementation and was treated with DURAGESIC. After drug was administered, patient experienced the following problems/side effects: blood magnesium decreased, decubitus ulcer, pacemaker complication, . DURAGESIC dosage: unknown. During the same period patient was treated with TRICOR, LASIX, LISINOPRIL, ARICEPT, HUMALOG, LANTUS, FOLTX, DIGOXIN. Patient was hospitalized. Patient recovered.

Avonex Side Effects Report #5730864-0
Consumer or non-health professional from UNITED STATES reported AVONEX problem on Apr 24, 2008. Female patient, 63 years of age, was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: blood magnesium decreased, blood potassium decreased, non-cardiac chest pain, . AVONEX dosage: unknown. Patient was hospitalized. Patient recovered.

Tikosyn Side Effects Report #5735785-5
TIKOSYN problem was reported by a Pharmacist from UNITED STATES on May 08, 2008. Male patient, 59 years of age, was treated with TIKOSYN. After drug was administered, patient experienced the following problems/side effects: blood magnesium decreased, cardiac arrest, hypokalaemia, torsade de pointes, . TIKOSYN dosage: unknown. Patient recovered.

Avonex Side Effects Report #5741280-X
Consumer or non-health professional from UNITED STATES reported AVONEX problem on May 05, 2008. Male patient, 56 years of age, was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: blood magnesium decreased, blood potassium decreased, blood sodium decreased, convulsion, . AVONEX dosage: unknown. Patient was hospitalized. Patient recovered.

Digoxin Side Effects Report #5744278-0
DIGOXIN problem was reported by a Consumer or non-health professional from UNITED STATES on May 15, 2008. Female patient, 67 years of age, weighting 210.0 lb, was diagnosed with palpitations and was treated with DIGOXIN. After drug was administered, patient experienced the following problems/side effects: blood magnesium decreased, diarrhoea, hyperhidrosis, hypertension, hypotension, nausea, therapeutic agent toxicity, . DIGOXIN dosage: 0.25MG DAILY PO. During the same period patient was treated with ATENOLOL, PRILOSEC, HYDROCHLOROTHIAZIDE. Patient was hospitalized. Patient recovered.

Bevacizumab Side Effects Report #5747665-X
Physician from UNITED KINGDOM reported BEVACIZUMAB problem on May 08, 2008. Female patient, weighting 121.3 lb, was diagnosed with ovarian epithelial cancer and was treated with BEVACIZUMAB. After drug was administered, patient experienced the following problems/side effects: blood magnesium decreased, dizziness, fatigue, haemoglobin decreased, hypokalaemia, neuropathy peripheral, thrombocytopenia, tinnitus, . BEVACIZUMAB dosage: 412.5 MG, Q3W. During the same period patient was treated with CARBOPLATIN, PACLITAXEL. Patient was hospitalized. Patient recovered.

Bevacizumab Side Effects Report #5751407-1
BEVACIZUMAB problem was reported by a Physician from UNITED KINGDOM on May 14, 2008. Female patient, weighting 121.3 lb, was diagnosed with ovarian epithelial cancer and was treated with BEVACIZUMAB. After drug was administered, patient experienced the following problems/side effects: blood magnesium decreased, fatigue, haemoglobin decreased, hypokalaemia, peripheral sensory neuropathy, thrombocytopenia, . BEVACIZUMAB dosage: 412.5 MG, Q3W. During the same period patient was treated with CARBOPLATIN, PACLITAXEL. Patient was hospitalized. Patient recovered.

Rebif Side Effects Report #5756816-2
Consumer or non-health professional from UNITED STATES reported REBIF problem on May 14, 2008. Female patient, 34 years of age, was diagnosed with multiple sclerosis and was treated with REBIF. After drug was administered, patient experienced the following problems/side effects: blood magnesium decreased, crying, . REBIF dosage: unknown. During the same period patient was treated with ACETAMINOPHEN. Patient was hospitalized. Patient recovered.