BLOOD CALCIUM DECREASED side effect
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Drugs associated with BLOOD CALCIUM DECREASED
ACLASTA ADRIBLASTINE ALBYL ALIMTA AMEVIVE AMITIZA AMLODIPINE AMOXICILLIN AMPHOTERICIN ARANESP ARIMIDEX AUGMENTIN AVANDIA AVONEX BETASERON BEVACIZUMAB BONIVA BRISERIN BYETTA CALCITRIOL CALCIUM CAMPATH CAP CAPREOMYCIN CARBOPLATIN CEFTRIAXONE CETUXIMAB CHAMPIX CHANTIX CISPLATIN CITALOPRAM CLOFARABINE CLOZARIL CYCLOSPORINE CYMBALTA CYTARABINE DACARBAZINE DACLIZUMAB DACOGEN DECITABINE DEPAS DIAMOX DIANEAL DICLOFENAC DIOVAN DITROPAN DOBUTAMINE DOXIL ENBREL ERBITUX ERLOTINIB ERLOTINIBLET) ESCITALOPRAM ETHYOL EVISTA EXJADE FENTANYL FLUOROURACIL FORTEO FOSAMAX GEMZAR HUMALOG HUMIRA HYDROXYZINE INTRON LANSOPRAZOLE LASIX LIPITOR LORAZEPAM LYRICA MEMANTINE METHERGINE METHOTREXATE METOPROLOL MICONAZOLE MILK MIMPARA NAPROXEN NEORAL NEXAVAR NEXIUM NITROFURANTOIN NOLVADEX NUTROPIN OMNISCAN ORLISTAT OROCAL ORTHO OSMOPREP OXALIPLATIN PAROXETINE PAXIL PEMETREXED PHOSBLOCK PHOSPHOSODA PROCRIT PROGRAF REBIF RECLAST RENAGEL REVLIMID RIBASPHERE RIBAVIRIN SENSIPAR SEVOFLURANE SORAFENIB SUTENT SYMBICORT TAXOTERE TEGRETOL TEKTURNA TEMODAR TEMOZOLOMIDE TENOFOVIR THALIDOMIDE THALOMID TIKOSYN TOPROL TRANQIPAM TRILEPTAL TRISENOX TRUVADA TYSABRI VALSARTAN VALTREX VELCADE VISICOL WARFARIN ZEMPLAR ZOLEDRONATE ZOLEDRONIC ZOMETA ZYPREXACisplatin Side Effects Report #5670684-9
Consumer or non-health professional from UNITED STATES reported CISPLATIN problem on Mar 17, 2008. Male patient, weighting 134.3 lb, was treated with CISPLATIN. After drug was administered, patient experienced the following problems/side effects: blood calcium decreased, blood glucose decreased, blood magnesium decreased, blood potassium decreased, blood sodium decreased, dehydration, haemoglobin decreased, hypotension, nausea, . CISPLATIN dosage: 130 MG. During the same period patient was treated with TAXOTERE. Patient was hospitalized. Patient recovered.
Pemetrexed Side Effects Report #5680500-7
PEMETREXED problem was reported by a Physician from JAPAN on Mar 14, 2008. Male patient, weighting 142.9 lb, was diagnosed with pleural mesothelioma malignant, nausea, constipation and was treated with PEMETREXED. After drug was administered, patient experienced the following problems/side effects: blood calcium decreased, blood creatinine increased, blood magnesium decreased, blood sodium decreased, dyspnoea, pleural effusion, . PEMETREXED dosage: 830 MG, OTHER. During the same period patient was treated with CISPLATIN, PANVITAN, CYANOCOBALAMIN, METOCLOPRAMIDE, POLARAMINE, MAGLAX, GLYCERIN. Patient was hospitalized. Patient recovered.
Naproxen Side Effects Report #5684714-1
Physician from NETHERLANDS reported NAPROXEN problem on Oct 27, 1980. Female patient, 64 years of age, was diagnosed with rheumatoid arthritis and was treated with NAPROXEN. After drug was administered, patient experienced the following problems/side effects: blood calcium decreased, confusional state, malaise, nausea, paraproteinaemia, renal failure acute, scleroderma, . NAPROXEN dosage: unknown. Patient was hospitalized. Patient recovered.
Avonex Side Effects Report #5616209-5
AVONEX problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 22, 2008. Female patient, 45 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 calcium decreased, colonic polyp, constipation, . AVONEX dosage: unknown. Patient was hospitalized. Patient recovered.
Tysabri Side Effects Report #5624748-6
Health Professional from UNITED STATES reported TYSABRI problem on Jan 30, 2008. Female patient, 34 years of age, weighting 300.0 lb, was diagnosed with multiple sclerosis and was treated with TYSABRI. After drug was administered, patient experienced the following problems/side effects: blood calcium decreased, blood glucose decreased, blood potassium decreased, convulsion, fatigue, hypersensitivity, influenza like illness, infusion site reaction, lung disorder, . TYSABRI dosage: 300 MG QM IV. Patient was hospitalized. Patient recovered.
Tysabri Side Effects Report #5628907-8
TYSABRI problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 05, 2008. Female patient, 34 years of age, weighting 300.0 lb, was diagnosed with multiple sclerosis and was treated with TYSABRI. After drug was administered, patient experienced the following problems/side effects: blood calcium decreased, blood glucose decreased, chest discomfort, convulsion, dyspnoea, erythema, fatigue, flushing, hypersensitivity, . TYSABRI dosage: 300 MG; QM; IV. Patient was hospitalized. Patient recovered.
Reclast Side Effects Report #5630408-8
Physician from UNITED STATES reported RECLAST problem on Feb 11, 2008. Female patient was treated with RECLAST. After drug was administered, patient experienced the following problems/side effects: blood calcium decreased, hypocalcaemia, . RECLAST dosage: 5 MG, UNK. Patient was hospitalized. Patient recovered.
Orlistat Side Effects Report #5633420-8
ORLISTAT problem was reported by a Consumer or non-health professional from UNITED KINGDOM on Feb 12, 2008. Female patient, 41 years of age, weighting 207.2 lb, was diagnosed with obesity, schizophrenia and was treated with ORLISTAT. After drug was administered, patient experienced the following problems/side effects: blood calcium decreased, blood potassium decreased, magnesium deficiency, pneumonia, vitamin d deficiency, . ORLISTAT dosage: unknown. During the same period patient was treated with ZAPONEX, AMITRIPTYLINE, AMOXICLAV. Patient was hospitalized. Patient recovered.
Ditropan Side Effects Report #5633579-2
Consumer or non-health professional from UNITED STATES reported DITROPAN problem on Feb 18, 2008. Female patient, 65 years of age, weighting 125.7 lb, was treated with DITROPAN. After drug was administered, patient experienced the following problems/side effects: blood calcium decreased, hypocalcaemia, paraesthesia, . DITROPAN dosage: 5 MG, QD. During the same period patient was treated with VITAMIN, CALCIUM W, RECLAST. Patient was hospitalized. Patient recovered.
Calcium Side Effects Report #5636346-9
CALCIUM problem was reported by a Consumer or non-health professional from BRAZIL on Feb 18, 2008. Male patient, 69 years of age, weighting 160.9 lb, was diagnosed with parathyroidectomy, memory impairment, diabetes mellitus and was treated with CALCIUM. After drug was administered, patient experienced the following problems/side effects: blood calcium decreased, feeling abnormal, gait disturbance, memory impairment, musculoskeletal stiffness, pain in extremity, . CALCIUM dosage: 500 MG, BID. During the same period patient was treated with HYDERGINE, DAONIL, METFORMIN, VITAMIN D. Patient was hospitalized. Patient recovered.
Gemzar Side Effects Report #5638165-6
Physician from JAPAN reported GEMZAR problem on Feb 14, 2008. Male patient, weighting 138.9 lb, was diagnosed with pancreatic carcinoma, prophylaxis and was treated with GEMZAR. After drug was administered, patient experienced the following problems/side effects: blood calcium decreased, cardiac failure congestive, haemoglobin decreased, neutrophil count decreased, white blood cell count decreased, . GEMZAR dosage: 1000 MG, OTHER. During the same period patient was treated with BERIZYM, GASMOTIN, URSO, GASTER D, LAC B, LEUCON, CEPHARANTHIN, NEUPOGEN. Patient recovered.
Dianeal Side Effects Report #5643114-0
DIANEAL problem was reported by a Health Professional from UNITED STATES on Feb 19, 2008. Female patient, 38 years of age, was diagnosed with peritoneal dialysis and was treated with DIANEAL. After drug was administered, patient experienced the following problems/side effects: blood calcium decreased, blood potassium decreased, muscle spasms, . DIANEAL dosage: unknown. During the same period patient was treated with ANTIHYPERTENSIVES. Patient was hospitalized. Patient recovered.
Reclast Side Effects Report #5585244-8
Physician from UNITED STATES reported RECLAST problem on Dec 18, 2007. Female patient, 73 years of age, weighting 129.0 lb, was diagnosed with osteoporosis and was treated with RECLAST. After drug was administered, patient experienced the following problems/side effects: blood calcium decreased, chills, myalgia, pyrexia, syncope, . RECLAST dosage: 5 MG IV YEARLY. During the same period patient was treated with VYTORIN, PRILOSEC, ASPIRIN, CALCIUM GLUCONATE. Patient was hospitalized. Patient recovered.
Trileptal Side Effects Report #5599711-4
TRILEPTAL problem was reported by a Consumer or non-health professional from FRANCE on Jan 17, 2008. Female patient, 44 years of age, weighting 174.2 lb, was diagnosed with neuralgia, rheumatoid arthritis, adrenal insufficiency and was treated with TRILEPTAL. After drug was administered, patient experienced the following problems/side effects: blood calcium decreased, blood parathyroid hormone increased, blood phosphorus decreased, hyperparathyroidism secondary, hypocalcaemia, muscle spasms, urine calcium increased, vitamin d decreased, . TRILEPTAL dosage: 120 MG, BID. During the same period patient was treated with PROPOFAN, LAROXYL, LIDOCAINE, METHOTREXATE, LEDERFOLIN, CORTANCYL, HYDROCORTISONE, FLUDROCORTISONE ACETATE. Patient recovered.
Gemzar Side Effects Report #5605905-1
Physician from JAPAN reported GEMZAR problem on Jan 16, 2008. Male patient, weighting 138.9 lb, was diagnosed with pancreatic carcinoma, prophylaxis and was treated with GEMZAR. After drug was administered, patient experienced the following problems/side effects: blood calcium decreased, cardiac failure congestive, haemoglobin decreased, neutrophil count decreased, oedema, pleural effusion, white blood cell count decreased, . GEMZAR dosage: 1000 MG, OTHER. During the same period patient was treated with BERIZYM, GASMOTIN, URSO, GASTER D, LAC B, LEUCON, CEPHARANTHIN, NEUPOGEN. Patient recovered.
Paroxetine Side Effects Report #5612174-5
PAROXETINE problem was reported by a Consumer or non-health professional from TAIWAN, PROVINCE OF CHINA on Nov 03, 2006. Male patient, 57 years of age, was diagnosed with depression and was treated with PAROXETINE. After drug was administered, patient experienced the following problems/side effects: blood calcium decreased, blood chloride decreased, blood magnesium decreased, blood pressure systolic increased, delirium, electrolyte imbalance, hypokalaemia, hyponatraemia, hypophosphataemia, . PAROXETINE dosage: 20 MG; 60 MG. Patient was hospitalized. Patient recovered.
Dacarbazine Side Effects Report #5613644-6
Consumer or non-health professional from UNITED STATES reported DACARBAZINE problem on Jan 16, 2008. Male patient, 63 years of age, was diagnosed with metastatic malignant melanoma and was treated with DACARBAZINE. After drug was administered, patient experienced the following problems/side effects: blood calcium decreased, cystitis haemorrhagic, metastases to central nervous system, . DACARBAZINE dosage: 600MG/M2; 700MG/M2; 850 MG/. Patient was hospitalized. Patient died.
Sevoflurane Side Effects Report #5534181-3
SEVOFLURANE problem was reported by a Consumer or non-health professional from UNITED KINGDOM on Nov 28, 2007. Male patient, 14 years of age, weighting 198.4 lb, was treated with SEVOFLURANE. After drug was administered, patient experienced the following problems/side effects: blood calcium decreased, blood phosphorus increased, blood potassium abnormal, cardiac arrest, creatinine renal clearance decreased, metabolic acidosis, rhabdomyolysis, . SEVOFLURANE dosage: unknown. During the same period patient was treated with SUPRANE, PROPOFOL, FENTANYL, DICLOFENAC, PARACETAMOL, MORPHINE, ONDANSETRON. Patient died on 09/08/2007.
Reclast Side Effects Report #5541533-4
Physician from UNITED STATES reported RECLAST problem on Dec 03, 2007. Female patient, 87 years of age, weighting 86.98 lb, was diagnosed with osteoporosis and was treated with RECLAST. After drug was administered, patient experienced the following problems/side effects: blood calcium decreased, blood potassium decreased, muscle contracture, paraesthesia, . RECLAST dosage: unknown. During the same period patient was treated with SINGULAIR, ADVAIR DISKUS, PULMICORT, TOPAMAX, PREDNISONE. Patient was hospitalized. Patient recovered.
Avonex Side Effects Report #5550576-6
AVONEX problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 30, 2007. Male patient, 54 years of age, weighting 245.0 lb, was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: blood calcium decreased, blood parathyroid hormone decreased, nephrolithiasis, phrenic nerve paralysis, procedural complication, . AVONEX dosage: unknown. Patient was hospitalized. Patient recovered.
Reclast Side Effects Report #5556887-2
Physician from UNITED STATES reported RECLAST problem on Dec 11, 2007. Female patient, 56 years of age, weighting 86.98 lb, was diagnosed with osteoporosis and was treated with RECLAST. After drug was administered, patient experienced the following problems/side effects: blood calcium decreased, blood potassium decreased, muscle contracture, paraesthesia, . RECLAST dosage: unknown. During the same period patient was treated with SINGULAIR, ADVAIR DISKUS, PULMICORT, TOPAMAX, PREDNISONE. Patient was hospitalized. Patient recovered.
Reclast Side Effects Report #5571465-7
RECLAST problem was reported by a Physician from FRANCE on Dec 17, 2007. Male patient, 70 years of age, was diagnosed with osteitis deformans and was treated with RECLAST. After drug was administered, patient experienced the following problems/side effects: blood calcium decreased, blood phosphorus decreased, osteomalacia, urine phosphate increased, . RECLAST dosage: 5 MG, ONCE/SINGLE. During the same period patient was treated with CALCIUM, VITAMIN D. Patient was hospitalized. Patient recovered.
Sevoflurane Side Effects Report #5571545-6
Consumer or non-health professional from UNITED KINGDOM reported SEVOFLURANE problem on Dec 14, 2007. Male patient, 14 years of age, weighting 198.4 lb, was treated with SEVOFLURANE. After drug was administered, patient experienced the following problems/side effects: blood calcium decreased, blood phosphorus increased, blood potassium abnormal, cardiac arrest, creatinine renal clearance decreased, metabolic acidosis, rhabdomyolysis, . SEVOFLURANE dosage: unknown. During the same period patient was treated with SUPRANE, PROPOFOL, FENTANYL, DICLOFENAC, ACETAMINOPHEN, MORPHINE, ONDANSETRON. Patient died on 09/08/2007.
Sevoflurane Side Effects Report #5571549-3
SEVOFLURANE problem was reported by a Consumer or non-health professional from UNITED KINGDOM on Dec 14, 2007. Male patient, 14 years of age, weighting 198.4 lb, was treated with SEVOFLURANE. After drug was administered, patient experienced the following problems/side effects: blood calcium decreased, blood phosphorus increased, blood potassium abnormal, cardiac arrest, creatinine renal clearance decreased, metabolic acidosis, rhabdomyolysis, . SEVOFLURANE dosage: unknown. During the same period patient was treated with SUPRANE, PROPOFOL, FENTANYL, DICLOFENAC, ACETAMINOPHEN, MORPHINE, ONDANSETRON. Patient died on 09/08/2007.
Sevoflurane Side Effects Report #5571584-5
Consumer or non-health professional from UNITED KINGDOM reported SEVOFLURANE problem on Dec 14, 2007. Male patient, 14 years of age, weighting 198.4 lb, was treated with SEVOFLURANE. After drug was administered, patient experienced the following problems/side effects: blood calcium decreased, blood phosphorus increased, blood potassium abnormal, cardiac arrest, creatinine renal clearance decreased, metabolic acidosis, rhabdomyolysis, . SEVOFLURANE dosage: unknown. During the same period patient was treated with SUPRANE, PROPOFOL, FENTANYL, DICLOFENAC, ACETAMINOPHEN, MORPHINE, ONDANSETRON. Patient died on 09/08/2007.
Amlodipine Side Effects Report #5572036-9
AMLODIPINE BESYLATE problem was reported by a Consumer or non-health professional from UNITED STATES on Dec 05, 2007. Male patient, 81 years of age, weighting 177.0 lb, was diagnosed with hypertension and was treated with AMLODIPINE BESYLATE. After drug was administered, patient experienced the following problems/side effects: blood calcium decreased, blood potassium decreased, blood pressure inadequately controlled, constipation, diplopia, fatigue, heart rate irregular, insomnia, myalgia, . AMLODIPINE BESYLATE dosage: 2.5 MG; AS NEEDED; ORAL, 2.5 MG; DAILY; ORAL. During the same period patient was treated with AMLODIPINE BESYLATE, ATENOLOL, HYDROCHLOROTHIAZIDE, CENTRUM SILVER, VITAMIN B6, VITAMIN E. Patient was hospitalized. Patient recovered.
Diamox Side Effects Report #5573920-2
Consumer or non-health professional from UNITED STATES reported DIAMOX problem 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.
Avonex Side Effects Report #5580368-3
AVONEX problem was reported by a Consumer or non-health professional from UNITED STATES on Dec 12, 2007. Female patient, 45 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 calcium decreased, constipation, . AVONEX dosage: unknown. Patient was hospitalized. Patient recovered.
Carboplatin Side Effects Report #5507425-1
Health Professional from UNITED STATES reported CARBOPLATIN problem on Nov 05, 2007. Male patient, 62 years of age, weighting 185.2 lb, was diagnosed with non-small cell lung cancer and was treated with CARBOPLATIN. After drug was administered, patient experienced the following problems/side effects: blood calcium decreased, diarrhoea, fall, hypotension, hypovolaemia, intracranial aneurysm, neutrophil count decreased, platelet count decreased, syncope, . CARBOPLATIN dosage: unknown. During the same period patient was treated with DOCETAXEL, AMBIEN, ATIVAN, CELEXA, COMPAZINE, DECADRON, DOCUSATE, SENNA. Patient was hospitalized. Patient recovered.
Sevoflurane Side Effects Report #5512667-5
SEVOFLURANE problem was reported by a Consumer or non-health professional from UNITED KINGDOM on Oct 31, 2007. Male patient, 14 years of age, weighting 198.4 lb, was treated with SEVOFLURANE. After drug was administered, patient experienced the following problems/side effects: blood calcium decreased, blood phosphorus increased, blood potassium abnormal, cardiac arrest, creatinine renal clearance decreased, metabolic acidosis, rhabdomyolysis, . SEVOFLURANE dosage: unknown. During the same period patient was treated with SUPRANE, PROPOFOL, FENTANYL, DICLOFENAC, PARACETAMOL, MORPHINE, ONDANSETRON. Patient died on 09/08/2007.
Toprol Side Effects Report #5519086-6
Consumer or non-health professional from UNITED STATES reported TOPROL problem on Nov 09, 2007. Female patient, 50 years of age, was diagnosed with hypertension and was treated with TOPROL. After drug was administered, patient experienced the following problems/side effects: blood calcium decreased, blood sodium decreased, dehydration, dizziness, eye disorder, gastric ulcer, platelet count decreased, visual disturbance, . TOPROL dosage: unknown. Patient was hospitalized. Patient recovered.
Fosamax Side Effects Report #5521015-6
FOSAMAX problem was reported by a Physician from JAPAN on Nov 06, 2007. Female patient, 77 years of age, weighting 110.2 lb, was diagnosed with osteoporosis, hypothyroidism, depression and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: blood calcium decreased, left ventricular failure, . FOSAMAX dosage: unknown. During the same period patient was treated with ENALAPRIL MALEATE, CHOLECALCIFEROL AND VITAMIN A, THYRADIN, ASPARA, LUVOX. Patient was hospitalized. Patient recovered.
Miconazole Side Effects Report #5521795-X
Physician from UNITED KINGDOM reported MICONAZOLE problem on Nov 09, 2007. Female patient, 84 years of age, was diagnosed with parkinson's disease and was treated with MICONAZOLE. After drug was administered, patient experienced the following problems/side effects: blood calcium decreased, confusional state, international normalised ratio increased, somnolence, . MICONAZOLE dosage: unknown. During the same period patient was treated with NITROFURANTOIN, VITAMIN D, WARFARIN, LAMOTRIGINE, CALCIUM, COLECALCIFEROL. Patient recovered.
Betaseron Side Effects Report #5522643-4
BETASERON problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 19, 2007. Female patient, 56 years of age, weighting 206.0 lb, was diagnosed with relapsing-remitting multiple sclerosis, depression, arthritis and was treated with BETASERON. After drug was administered, patient experienced the following problems/side effects: blood calcium decreased, blood iron decreased, blood potassium decreased, coeliac disease, contusion, dyspnoea, fatigue, haemoglobin decreased, hypoproteinaemia, . BETASERON dosage: unknown. During the same period patient was treated with ZOLOFT, CELEBREX, ALEVE. Patient recovered.
Avandia Side Effects Report #5524502-X
Consumer or non-health professional from UNITED STATES reported AVANDIA problem on Nov 19, 2007. Male patient, 67 years of age, was diagnosed with multiple myeloma and was treated with AVANDIA. After drug was administered, patient experienced the following problems/side effects: blood calcium decreased, blood potassium decreased, catheter related infection, convulsion, urinary tract infection, . AVANDIA dosage: 4 MG, UNK. During the same period patient was treated with NOVOLOG, ZOMETA, REVLIMID. Patient was hospitalized. Patient recovered.
Amlodipine Side Effects Report #5525400-8
AMLODIPINE BESYLATE problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 05, 2007. Male patient, 81 years of age, was diagnosed with hypertension and was treated with AMLODIPINE BESYLATE. After drug was administered, patient experienced the following problems/side effects: blood calcium decreased, blood potassium decreased, blood pressure inadequately controlled, constipation, diplopia, dizziness, fatigue, headache, heart rate increased, . AMLODIPINE BESYLATE dosage: 2.5 MG; AS NEEDED; ORAL; 2.5 MG; DAILY; ORAL. During the same period patient was treated with AMLODIPINE BESYLATE, ATENOLOL, HYDROCHLOROTHIAZIDE, CENTRUM SILVER, VITAMIN B6, VITAMIN E. Patient was hospitalized. Patient recovered.
Nitrofurantoin Side Effects Report #5528187-8
Consumer or non-health professional from UNITED KINGDOM reported NITROFURANTOIN problem on Nov 09, 2007. Female patient, 84 years of age, was treated with NITROFURANTOIN. After drug was administered, patient experienced the following problems/side effects: blood calcium decreased, confusional state, international normalised ratio increased, somnolence, . NITROFURANTOIN dosage: unknown. During the same period patient was treated with WARFARIN, MICONAZOLE, ERGOCALCIFEROL. Patient recovered.
Warfarin Side Effects Report #5528519-0
WARFARIN problem was reported by a Consumer or non-health professional from UNITED KINGDOM on Nov 12, 2007. Female patient, 84 years of age, was treated with WARFARIN. After drug was administered, patient experienced the following problems/side effects: blood calcium decreased, confusional state, international normalised ratio increased, somnolence, . WARFARIN dosage: 3 MG;ORAL. During the same period patient was treated with NITROFURANTOIN, MICONAZOLE, VITAMIN D, CALCIUM, COLECALCIFEROL, LAMOTRIGINE, VITAMIN D. Patient recovered.
Nitrofurantoin Side Effects Report #5528554-2
Health Professional from UNITED KINGDOM reported NITROFURANTOIN MACROCRYSTALS problem on Nov 09, 2007. Female patient, 84 years of age, was treated with NITROFURANTOIN MACROCRYSTALS. After drug was administered, patient experienced the following problems/side effects: blood calcium decreased, confusional state, international normalised ratio increased, somnolence, . NITROFURANTOIN MACROCRYSTALS dosage: unknown. During the same period patient was treated with MICONAZOLE, ERGOCALCIFEROL, WARFARIN, CALCIUM, COLECALCIFEROL, LAMOTRIGINE. Patient recovered.
Fentanyl Side Effects Report #5528847-9
FENTANYL TRANSDERMAL SYSTEM problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 20, 2007. Female patient, weighting 252.0 lb, was diagnosed with arthritis, pain and was treated with FENTANYL TRANSDERMAL SYSTEM. After drug was administered, patient experienced the following problems/side effects: blood calcium decreased, blood test abnormal, eating disorder, inadequate analgesia, somnolence, weight decreased, . FENTANYL TRANSDERMAL SYSTEM dosage: unknown. During the same period patient was treated with OXYCODONE. Patient was hospitalized. Patient recovered.
Warfarin Side Effects Report #5530396-9
Health Professional from UNITED KINGDOM reported WARFARIN problem on Nov 12, 2007. Female patient, 84 years of age, was treated with WARFARIN. After drug was administered, patient experienced the following problems/side effects: blood calcium decreased, confusional state, international normalised ratio increased, somnolence, . WARFARIN dosage: 3 MG; ORAL. During the same period patient was treated with NITROFURANTOIN, MICONAZOLE, ERGOCALCIFEROL, CALCIUM, COLECALCIFEROL, LAMOTRIGINE. Patient recovered.
Avonex Side Effects Report #5421742-5
AVONEX problem was reported by a Consumer or non-health professional from UNITED STATES on Aug 10, 2007. Female patient, 42 years of age, weighting 165.0 lb, was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: blood calcium decreased, coronary artery occlusion, depression, electrocardiogram abnormal, hypoaesthesia, suicidal ideation, . AVONEX dosage: unknown. During the same period patient was treated with ZANAFLEX. Patient was hospitalized. Patient recovered.
Fosamax Side Effects Report #5482446-6
Physician from UNITED STATES reported FOSAMAX problem on Oct 05, 2007. Female patient, 65 years of age, was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: blood calcium decreased, blood magnesium decreased, bone disorder, . FOSAMAX dosage: unknown. Patient was hospitalized. Patient recovered.
Rebif Side Effects Report #5483877-0
REBIF problem was reported by a Physician from FRANCE on Sept 24, 2007. Female patient, 36 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 calcium decreased, contusion, fatigue, idiopathic thrombocytopenic purpura, injection site reaction, multiple sclerosis relapse, pregnancy, premature separation of placenta, . REBIF dosage: unknown. During the same period patient was treated with VENLAFAXINE, CLONAZEPAM, ZOLPIDEM, ORAL CONTRACEPTIVE NOS. Patient was hospitalized. Patient recovered.
Betaseron Side Effects Report #5485925-0
Consumer or non-health professional from UNITED STATES reported BETASERON problem on Oct 02, 2007. Female patient, 56 years of age, weighting 206.0 lb, was diagnosed with relapsing-remitting multiple sclerosis, depression, arthritis and was treated with BETASERON. After drug was administered, patient experienced the following problems/side effects: blood calcium decreased, blood iron decreased, blood potassium decreased, coeliac disease, contusion, dyspnoea, fatigue, haemoglobin decreased, hypoproteinaemia, . BETASERON dosage: unknown. During the same period patient was treated with ZOLOFT, CELEBREX, ALEVE. Patient recovered.
Albyl Side Effects Report #5486319-4
ALBYL problem was reported by a Consumer or non-health professional from NORWAY on Oct 09, 2007. Female patient, 83 years of age, was diagnosed with pain and was treated with ALBYL. After drug was administered, patient experienced the following problems/side effects: blood calcium decreased, blood creatine phosphokinase increased, blood sodium decreased, brain natriuretic peptide increased, c-reactive protein increased, chest pain, duodenal ulcer, endoscopy gastrointestinal, gastrointestinal haemorrhage, . ALBYL dosage: unknown. During the same period patient was treated with FOSAMAX, IMDUR, SAROTEX, SOBRIL, DICLOFENAC. Patient was hospitalized. Patient recovered.
Fosamax Side Effects Report #5490845-1
Physician from JAPAN reported FOSAMAX problem on Oct 12, 2007. Female patient, 77 years of age, was diagnosed with osteoporosis, hypothyroidism and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: blood calcium decreased, cardiac failure acute, . FOSAMAX dosage: unknown. During the same period patient was treated with RENIVACE, CHOLECALCIFEROL AND VITAMIN A, THYRADIN, ASPARA. Patient was hospitalized. Patient recovered.
Amlodipine Side Effects Report #5495487-X
AMLODIPINE BESYLATE problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 15, 2007. Male patient, 81 years of age, was diagnosed with hypertension and was treated with AMLODIPINE BESYLATE. After drug was administered, patient experienced the following problems/side effects: blood calcium decreased, blood potassium decreased, blood pressure inadequately controlled, constipation, diplopia, dizziness, fatigue, headache, heart rate irregular, . AMLODIPINE BESYLATE dosage: 2.5 MG;DAILY;ORAL. During the same period patient was treated with ATENOLOL, HYDROCHLOROTHIAZIDE. Patient was hospitalized. Patient recovered.
Tekturna Side Effects Report #5497363-5
Physician from UNITED STATES reported TEKTURNA problem on Oct 22, 2007. Male patient, 62 years of age, weighting 210.0 lb, was diagnosed with hypertension, oedema and was treated with TEKTURNA. After drug was administered, patient experienced the following problems/side effects: blood calcium decreased, blood creatinine increased, blood urea increased, bradycardia, cardiac arrest, cardiomyopathy, dyspnoea, hypotension, hypoxia, . TEKTURNA dosage: 300 MG, QD. During the same period patient was treated with EXFORGE, LASIX. Patient was hospitalized. Patient died on 09/26/2007.
Omniscan Side Effects Report #5498473-9
OMNISCAN problem was reported by a Physician from UNITED STATES on Oct 15, 2007. Male patient, 76 years of age, was treated with OMNISCAN. After drug was administered, patient experienced the following problems/side effects: blood calcium decreased, blood parathyroid hormone increased, haemodialysis, liver transplant, mobility decreased, nephrogenic systemic fibrosis, refusal of treatment by patient, renal failure acute, . OMNISCAN dosage: A TOTAL OF 49 ML WAS ADMINISTERED FOR THE MRI AND MRA., SINGLE DOSE, I.V.; A TOTAL OF 49 ML WAS ADMI. During the same period patient was treated with DARBEPOETIN ALFA, METOPROLOL TARTRATE, HYDROMORPHONE, PANTOPRAZOLE. Patient recovered.
Reclast Side Effects Report #5500991-1
Physician from FRANCE reported RECLAST problem on Oct 18, 2007. Male patient, 70 years of age, was diagnosed with osteitis deformans and was treated with RECLAST. After drug was administered, patient experienced the following problems/side effects: blood calcium decreased, blood phosphorus decreased, osteomalacia, . RECLAST dosage: 5 MG, ONCE/SINGLE. During the same period patient was treated with CALCIUM, VITAMIN D. Patient recovered.