BLOOD SODIUM DECREASED side effect
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Drugs associated with BLOOD SODIUM DECREASED
ABILIFY ABRAXANE ACETADOTE ACIPHEX ACYCLOVIR ADENOSCAN ADRIAMYCIN ADVAIR ADVIL ALBYL ALDACTONE ALLERX ALPRAZOLAM ALTACE AMARYL AMBISOME AMEVIVE AMITIZA AMITRIPTYLINE APROVEL AREDIA ARICEPT ARIMIDEX ARTIST ASCORBIC ASPIRIN AUGMENTIN AVANDIA AVAPRO AVASTIN AVELOX AVONEX BENICAR BETAPACE BETASERON BEVACIZUMAB BISOPROLOL BLOPRESS BONIVA BUSPAR BYETTA BYSTOLIC CAPECITABINE CARBAMAZEPINE CARBOPLATIN CELEXA CEPHALEXIN CETUXIMAB CHANTIX CIPRO CISPLATIN CITALOPRAM CLAFORAN CLINDAMYCIN CLOFARABINE CLOZARIL COREG COROPRES CRESTOR CYCLOPHOSPHAMIDE CYCLOSPORINE CYMBALTA CYTARABINE CYTOXAN DALTEPARIN DARVOCET DASATINIB DDAVP DECITABINE DEPAKENE DESMOPRESSIN DEXAMETHASONE DIASTAT DIGOXIN DILTIAZEM DIOVAN DOCETAXEL DOXORUBICIN DULCOLAX EFFEXOR ENALAPRIL ENBREL ENTOCORT ERAXIS ERLOTINIB ERLOTINIBLET) ESCITALOPRAM ESIDRIX ETHYOL EXJADE FACTIVE FENTANYL FLEET FLUDARA FLUOROURACIL FORTEO FOSAMAX FOSINOPRIL FOSRENOL FUROSEMIDE GABAPENTIN GEMCITABINE GLEEVEC GLUCOPHAGE HUMATE HUMATROPE HUMIRA HYCAMTIN HYDROCHLOROTHIAZ HYDROCORTONE HYZAAR IBUPROFEN IDURSULFASE INNOHEP INSPRA INTRON INVEGA IRINOTECAN ISENTRESS JANTOVEN JANUVIA KEFLEX KEPPRA KETEK LAMICTAL LANTUS LEUCOVORIN LEVAQUIN LEXAPRO LIPITOR LISINOPRIL LISTERINE LORAZEPAM LOVENOX LYRICA MABTHERA MELPHALAN METFORMIN METHYLCELLULOSE METOPROLOL MICARDIS MODURETIC MOPRAL MORPHINE MOVIPREP MYLOTARG NAMENDA NATALIZUMAB NATEGLINIDE NEORAL NEUPRO NEVIRAPINE NEXAVAR NIFEDIPINE NORVASC OMEPRAZOLE OVIDE OXCARBAZEPINE PACERONE PANITUMUMAB PAROXETINE PAXIL PEGASYS PEMETREXED PENICILLIN PENTASA PERCOCET PHOSPHOSODA PLAVIX PREDNISOLONE PREDNISONE PROCARDIA PROCRIT PROGRAF PROTONIX PROVIGIL PROZAC PSEUDOEPHEDRINE QUESTRAN RABEPRAZOLE REBIF RECLAST REGLAN REMERON REMICADE RENAGEL RETEPLASE REVLIMID RISPERDAL RISPERIDONE RITUXAN RYTHMOL SERETIDE SEROQUEL SIMVASTATIN SORAFENIB STAVUDINE SUTENT SYMBICORT SYMLIN TARCEVA TAXOTERE TEGRETOL TEKTURNA TEMODAL TEMODAR TEMOZOLOMIDE TERAZOSIN THALIDOMIDE THEOPHYLLINE THYROGEN TIOTROPIUM TOPAMAX TOPOTECAN TOPROL TRAMADOL TRIAMTERENE TRILEPTAL TRITTICO TRUVADA VALTREX VAPRISOL VASOTEC VELCADE VESANOID VFEND VIAGRA VINCRISTINE WINRHO XOPENEX XYZALL ZETIA ZIDOVUDINE ZOCOR ZOLOFT ZYPREXA ZYVOXFosamax Side Effects Report #5648973-3
Physician from UNITED STATES reported FOSAMAX problem on Feb 28, 2008. Female patient, 90 years of age, was diagnosed with osteoporosis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: blood sodium decreased, hip fracture, tooth disorder, . FOSAMAX dosage: unknown. During the same period patient was treated with SYNTHROID, REMERON, PAXIL, ZANTAC, BOOST, TYLENOL. Patient was hospitalized and became disabled. Patient recovered.
Invega Side Effects Report #5653619-4
INVEGA problem was reported by a Physician from UNITED STATES on Feb 28, 2008. Male patient, 72 years of age, was diagnosed with schizophrenia and was treated with INVEGA. After drug was administered, patient experienced the following problems/side effects: blood sodium decreased, . INVEGA dosage: unknown. During the same period patient was treated with RISPERDAL. Patient was hospitalized. Patient recovered.
Citalopram Side Effects Report #5657960-0
Consumer or non-health professional from UNITED KINGDOM reported CITALOPRAM HYDROBROMIDE problem on Feb 21, 2008. Female patient, 43 years of age, was diagnosed with depression and was treated with CITALOPRAM HYDROBROMIDE. After drug was administered, patient experienced the following problems/side effects: blood sodium decreased, . CITALOPRAM HYDROBROMIDE dosage: 20 MG ORAL; 40 MG ORAL. During the same period patient was treated with CITALOPRAM HYDROBROMIDE, ASCORBIC ACID, CARBAMAZEPINE, DANTROLENE, LANSOPRAZOLE, METOCLOPRAMIDE, PROPANTHELINE, PYRIDOXINE. Patient recovered.
Moviprep Side Effects Report #5660246-1
MOVIPREP problem was reported by a Consumer or non-health professional from UNITED KINGDOM on Mar 04, 2008. Female patient, 76 years of age, was treated with MOVIPREP. After drug was administered, patient experienced the following problems/side effects: blood sodium decreased, confusional state, convulsion, . MOVIPREP dosage: unknown. During the same period patient was treated with ATENOLOL, ATORVASTATIN CALCIUM, BENDROFLUMETHIAZIDE, METFORMIN, RAMIPRIL. Patient was hospitalized. Patient recovered.
Abraxane Side Effects Report #5664768-9
Physician from UNITED STATES reported ABRAXANE problem on Feb 26, 2008. Female patient, 61 years of age, weighting 187.0 lb, was diagnosed with breast cancer metastatic and was treated with ABRAXANE. After drug was administered, patient experienced the following problems/side effects: blood sodium decreased, colitis ischaemic, endotoxic shock, metastases to lung, neutropenia, pneumonia, renal failure acute, septic shock, . ABRAXANE dosage: LAST DOSE (200 MG) PRIOR TO SAE ON 05-FEB-2008 (CYCLE 5) (WEEKLY, 3WKS ON THEN 1 WK. OFF), INTRAVENO. During the same period patient was treated with KYTRIL, DECADRON, TOPROL, ACIPHEX, LASIX, GABAPENTIN, CYMBALTA, ZAROXOLYN. Patient was hospitalized. Patient recovered.
Sutent Side Effects Report #5664820-8
SUTENT problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 04, 2008. Female patient, weighting 112.0 lb, was diagnosed with glioblastoma and was treated with SUTENT. After drug was administered, patient experienced the following problems/side effects: blood sodium decreased, cerebral haemorrhage, fall, loss of consciousness, neoplasm progression, platelet count decreased, white blood cell count decreased, . SUTENT dosage: unknown. During the same period patient was treated with BACTRIM DS, CALCIUM WITH VITAMIN D, COMPAZINE, LIPITOR, RITALIN, LEVOTHYROXINE. Patient was hospitalized. Patient recovered.
Benicar Side Effects Report #5672743-3
Consumer or non-health professional from UNITED STATES reported BENICAR problem on Mar 06, 2008. Male patient, 65 years of age, weighting 200.0 lb, was diagnosed with hypertension and was treated with BENICAR. After drug was administered, patient experienced the following problems/side effects: blood sodium decreased, muscle spasms, . BENICAR dosage: 20 MG (20 MG, QD), PER ORAL; 20 MG (20 MG, QD), PER ORAL. During the same period patient was treated with BENICAR HCT, TOPROL, COUMADIN. Patient recovered.
Lyrica Side Effects Report #5677494-7
LYRICA problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 12, 2008. Male patient, 48 years of age, weighting 149.9 lb, was diagnosed with neuropathy peripheral, hepatitis c and was treated with LYRICA. After drug was administered, patient experienced the following problems/side effects: blood sodium decreased, candidiasis, dry mouth, haemoglobin decreased, mental status changes, oral pain, overdose, unresponsive to stimuli, . LYRICA dosage: unknown. During the same period patient was treated with RIBAVIRIN. Patient was hospitalized. Patient recovered.
Citalopram Side Effects Report #5678051-9
Consumer or non-health professional from UNITED KINGDOM reported CITALOPRAM HYDROBROMIDE problem on Mar 13, 2008. Female patient, 43 years of age, was diagnosed with depression and was treated with CITALOPRAM HYDROBROMIDE. After drug was administered, patient experienced the following problems/side effects: blood sodium decreased, . CITALOPRAM HYDROBROMIDE dosage: 20 MG ORAL : 40 MG ORAL. During the same period patient was treated with CITALOPRAM HYDROBROMIDE, ASCORBIC ACID, CARBAMAZEPINE, DANTROLENE, LANSOPRAZOLE, METOCLOPRAMIDE, PROPANTHELINE, PYRIDOXINE. Patient recovered.
Rebif Side Effects Report #5679577-4
REBIF problem was reported by a Health Professional from UNITED STATES on Mar 11, 2008. Female patient, 61 years of age, weighting 210.0 lb, was diagnosed with multiple sclerosis and was treated with REBIF. After drug was administered, patient experienced the following problems/side effects: blood sodium decreased, clostridial infection, muscle spasms, urinary tract infection, . REBIF dosage: unknown. During the same period patient was treated with PROVIGIL, BACLOFEN, FLEXERIL, DARVOCET, DITROPAN, DETROL, PROZAC. Patient was hospitalized. Patient recovered.
Paroxetine Side Effects Report #5679859-6
Consumer or non-health professional from ITALY reported PAROXETINE problem on Mar 10, 2008. Female patient, 84 years of age, was diagnosed with depression and was treated with PAROXETINE. After drug was administered, patient experienced the following problems/side effects: blood sodium decreased, hepatic encephalopathy, hepatic failure, hepatitis acute, hyperammonaemia, renal failure, white blood cell count increased, . PAROXETINE dosage: 10 MG / PER DAY. During the same period patient was treated with VERAPAMIL, TICLOPIDINE, SPIRONOLACTONE, NIMODIPINE. Patient was hospitalized. Patient recovered.
Nateglinide Side Effects Report #5611241-X
NATEGLINIDE problem was reported by a Physician from SPAIN on Jan 23, 2008. Male patient, 88 years of age, weighting 130.1 lb, was diagnosed with glucose tolerance impaired, cardiovascular disorder and was treated with NATEGLINIDE. After drug was administered, patient experienced the following problems/side effects: blood sodium decreased, electrolyte imbalance, . NATEGLINIDE dosage: unknown. During the same period patient was treated with VALSARTAN. Patient was hospitalized. Patient recovered.
Vfend Side Effects Report #5611393-1
Physician from JAPAN reported VFEND problem on Jan 21, 2008. Female patient, weighting 88.18 lb, was diagnosed with candidiasis, sepsis and was treated with VFEND. After drug was administered, patient experienced the following problems/side effects: blood sodium decreased, hypoglycaemia, renal failure, respiratory failure, sepsis, . VFEND dosage: unknown. During the same period patient was treated with BIAPENEM, NITROGLYCERIN. Patient died on 12/28/2007.
Sutent Side Effects Report #5633478-6
SUTENT problem was reported by a Health Professional from UNITED STATES on Feb 09, 2008. Male patient, 69 years of age, weighting 189.6 lb, was diagnosed with renal cancer metastatic and was treated with SUTENT. After drug was administered, patient experienced the following problems/side effects: blood sodium decreased, nephritis interstitial, renal failure acute, . SUTENT dosage: unknown. During the same period patient was treated with IRON SULPHATETHIAMIN COMPOUND, TAMSULOSIN, PROTONIX, ASCORBIC ACID, VICODIN, MARINOL, HERBAL PREPARATION. Patient was hospitalized. Patient recovered.
Desmopressin Side Effects Report #5634219-9
Pharmacist from UNITED STATES reported DESMOPRESSIN ACETATE problem on Feb 21, 2008. Female patient, weighting 88.18 lb, was diagnosed with hypernatraemia and was treated with DESMOPRESSIN ACETATE. After drug was administered, patient experienced the following problems/side effects: blood sodium decreased, convulsion, incorrect dose administered, . DESMOPRESSIN ACETATE dosage: unknown. Patient was hospitalized. Patient recovered.
Diovan Side Effects Report #5634983-9
DIOVAN HCT problem was reported by a Physician from TAIWAN, PROVINCE OF CHINA on Feb 14, 2008. Male patient, 56 years of age, was diagnosed with hypertension and was treated with DIOVAN HCT. After drug was administered, patient experienced the following problems/side effects: blood sodium decreased, dehydration, dizziness, dyspnoea, hypoaesthesia, nausea, vomiting, . DIOVAN HCT dosage: 80/12.5 MG/DAY. During the same period patient was treated with ACCUPRIL. Patient was hospitalized. Patient recovered.
Moduretic Side Effects Report #5637674-3
Health Professional from UNITED KINGDOM reported MODURETIC problem on Feb 21, 2008. Female patient, 94 years of age, was diagnosed with hypertension, glaucoma and was treated with MODURETIC. After drug was administered, patient experienced the following problems/side effects: blood sodium decreased, . MODURETIC dosage: unknown. During the same period patient was treated with FELODIPINE, LATANOPROST, LEVOBUNOLOL HYDROCHLORIDE, POLYETHYLENE GLYCOL, ACETAMINOPHEN. Patient was hospitalized. Patient recovered.
Avonex Side Effects Report #5645904-7
AVONEX problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 15, 2008. Female patient, 65 years of age, weighting 145.0 lb, was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: blood sodium decreased, depression, hypertension, pain, . AVONEX dosage: unknown. Patient was hospitalized. Patient recovered.
Lorazepam Side Effects Report #5647962-2
Consumer or non-health professional from UNITED STATES reported LORAZEPAM problem on Feb 20, 2008. Female patient, weighting 149.9 lb, was diagnosed with anxiety and was treated with LORAZEPAM. After drug was administered, patient experienced the following problems/side effects: blood sodium decreased, blood sodium increased, breast swelling, cerebrovascular accident, constipation, convulsion, deafness, electroencephalogram abnormal, . LORAZEPAM dosage: 1-2MG, TID-QID. During the same period patient was treated with VITAMINS, CALCIUM. Patient recovered.
Thyrogen Side Effects Report #5648092-6
THYROGEN problem was reported by a Physician from ARGENTINA on Feb 20, 2008. Female patient, 40 years of age, weighting 167.6 lb, was diagnosed with diagnostic procedure and was treated with THYROGEN. After drug was administered, patient experienced the following problems/side effects: blood sodium decreased, blood urea abnormal, hyperkalaemia, nausea, vomiting, . THYROGEN dosage: unknown. During the same period patient was treated with CALCIUM CARBONATE, VITAMIN B12, CALCITRIOL, ERYTHROPOIETIN, IRON. Patient was hospitalized. Patient recovered.
Humate Side Effects Report #5650210-0
Consumer or non-health professional from CANADA reported HUMATE problem on Feb 19, 2008. Female patient, 58 years of age, weighting 187.0 lb, was diagnosed with von willebrand's disease and was treated with HUMATE. After drug was administered, patient experienced the following problems/side effects: blood sodium decreased, dyspnoea, fluid retention, hypersensitivity, insomnia, localised oedema, oedema peripheral, pruritus, rales, . HUMATE dosage: unknown. During the same period patient was treated with DICLOFENAC, CIPRO, FLUTICASONE, CLONAZEPAM, DOMPERIDONE, ESOMEPRAZOLE MAGNESIUM, CITALOPRAM, BUPROPION. Patient recovered.
Seroquel Side Effects Report #5581749-4
SEROQUEL problem was reported by a Health Professional from UNITED STATES on Apr 06, 2007. Female patient, weighting 190.5 lb, was diagnosed with psychotic disorder, schizophrenia, paranoid type, insomnia and was treated with SEROQUEL. After drug was administered, patient experienced the following problems/side effects: blood sodium decreased, chest pain, colonoscopy, convulsion, diabetes mellitus, headache, schizophrenia, paranoid type, suicidal ideation, . SEROQUEL dosage: unknown. During the same period patient was treated with RISPERDAL. Patient was hospitalized. Patient recovered.
Vfend Side Effects Report #5588030-8
Physician from JAPAN reported VFEND problem on Dec 28, 2007. Female patient, 80 years of age, was treated with VFEND. After drug was administered, patient experienced the following problems/side effects: blood sodium decreased, hypoglycaemia, pneumonia fungal, renal failure, . VFEND dosage: DAILY DOSE:400MG. During the same period patient was treated with BIAPENEM. Patient died on 12/28/2007.
Blopress Side Effects Report #5588517-8
BLOPRESS PLUS problem was reported by a Health Professional from SWITZERLAND on Jan 02, 2008. Female patient, 72 years of age, was diagnosed with essential hypertension, hypercholesterolaemia and was treated with BLOPRESS PLUS. After drug was administered, patient experienced the following problems/side effects: blood sodium decreased, confusional state, inappropriate antidiuretic hormone secretion, vomiting, . BLOPRESS PLUS dosage: unknown. During the same period patient was treated with PRAVASTATIN. Patient was hospitalized. Patient recovered.
Humira Side Effects Report #5598667-8
Consumer or non-health professional from UNITED KINGDOM reported HUMIRA problem on Jan 14, 2008. Female patient, weighting 145.5 lb, was diagnosed with rheumatoid arthritis and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: blood sodium decreased, . HUMIRA dosage: unknown. During the same period patient was treated with FOLIC ACID, CYANOCOBALAMIN, METHOTREXATE. Patient was hospitalized. Patient recovered.
Aprovel Side Effects Report #5599673-X
APROVEL problem was reported by a Health Professional from UNITED KINGDOM on Jan 14, 2008. Male patient, 74 years of age, was treated with APROVEL. After drug was administered, patient experienced the following problems/side effects: blood sodium decreased, neuropathy peripheral, . APROVEL dosage: unknown. During the same period patient was treated with ASPIRIN, BENDROFLUMETHIAZIDE, DOXAZOSIN, LISINOPRIL, MIXTARD, QUININE, SIMVASTATIN, TILDIEM. Patient was hospitalized and became disabled. Patient recovered.
Theophylline Side Effects Report #5602032-4
Pharmacist from UNITED STATES reported THEOPHYLLINE problem on Jan 22, 2008. Female patient, 71 years of age, weighting 125.7 lb, was diagnosed with chronic obstructive pulmonary disease and was treated with THEOPHYLLINE. After drug was administered, patient experienced the following problems/side effects: blood sodium decreased, cardio-respiratory arrest, haematemesis, haemoglobin abnormal, hypotension, leukocytosis, mental status changes, sepsis, . THEOPHYLLINE dosage: 200MG BID PO. Patient was hospitalized. Patient died on 01/19/2008.
Nateglinide Side Effects Report #5602160-3
NATEGLINIDE problem was reported by a Physician from SPAIN on Jan 16, 2008. Male patient, 88 years of age, weighting 130.1 lb, was diagnosed with glucose tolerance impaired, cardiovascular disorder and was treated with NATEGLINIDE. After drug was administered, patient experienced the following problems/side effects: blood sodium decreased, electrolyte imbalance, . NATEGLINIDE dosage: unknown. During the same period patient was treated with VALSARTAN. Patient was hospitalized. Patient recovered.
Remicade Side Effects Report #5602271-2
Health Professional from SWEDEN reported REMICADE problem on Jan 18, 2008. Female patient, 61 years of age, was diagnosed with rheumatoid arthritis, hypertension and was treated with REMICADE. After drug was administered, patient experienced the following problems/side effects: blood sodium decreased, pneumonia, . REMICADE dosage: unknown. During the same period patient was treated with NORMORIX, NAPROXEN, CITODON, LASIX, FOLACIN, METHOTREXATE. Patient was hospitalized. Patient recovered.
Revlimid Side Effects Report #5646053-4
REVLIMID problem was reported by a Health Professional from UNITED STATES on Dec 12, 2007. Female patient, 66 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 sodium decreased, syncope, . REVLIMID dosage: 25 MG, DAILY AS DIRECTED, ORAL. Patient was hospitalized. Patient recovered.
Pemetrexed Side Effects Report #5545769-8
Physician from JAPAN reported PEMETREXED problem on Dec 03, 2007. Male patient, weighting 114.0 lb, was diagnosed with pleural mesothelioma malignant, prophylaxis, diabetes mellitus, cancer pain and was treated with PEMETREXED. After drug was administered, patient experienced the following problems/side effects: blood sodium decreased, disseminated intravascular coagulation, neutrophil count decreased, pneumonia, sepsis, thrombocytopenia, . PEMETREXED dosage: 700 MG, OTHER. During the same period patient was treated with PARAPLATIN, PANVITAN, CYANOCOBALAMIN, DECADRON, NASEA, NOVOLIN R, OXYCONTIN, LOXONIN. Patient was hospitalized. Patient died on 10/20/2007.
Aricept Side Effects Report #5565814-3
ARICEPT problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 30, 2007. Female patient, 92 years of age, was diagnosed with dementia and was treated with ARICEPT. After drug was administered, patient experienced the following problems/side effects: blood sodium decreased, candidiasis, cardiac failure congestive, cardiomegaly, decubitus ulcer, fracture, haematocrit decreased, platelet count increased, pneumonia aspiration, . ARICEPT dosage: 5 MG, 1 IN 1 D, ORAL. During the same period patient was treated with SEROQUEL, NAMENDA, RIMERON, NITROFURANTOIN, METFORMIN, DIGOXIN, LISINOPRIL, FUROSEMIDE. Patient was hospitalized. Patient recovered.
Risperidone Side Effects Report #5570678-8
Physician from UNITED KINGDOM reported RISPERIDONE problem on Dec 17, 2007. Male patient, 45 years of age, was diagnosed with schizophrenia, agitation, nicotine dependence, extrapyramidal disorder, constipation and was treated with RISPERIDONE. After drug was administered, patient experienced the following problems/side effects: blood sodium decreased, . RISPERIDONE dosage: unknown. During the same period patient was treated with LORAZEPAM, NICOTINE, PROCYLIDINE, SENNA. Patient was hospitalized. Patient recovered.
Avandia Side Effects Report #5574924-6
AVANDIA problem was reported by a Consumer or non-health professional from UNITED STATES on Dec 21, 2007. Female patient, 84 years of age, was treated with AVANDIA. After drug was administered, patient experienced the following problems/side effects: blood sodium decreased, cerebral infarction, cerebrovascular accident, convulsion, hemiparesis, lacunar infarction, malaise, myocardial infarction, oedema peripheral, . AVANDIA dosage: unknown. Patient was hospitalized. Patient died on 06/30/2007.
Neoral Side Effects Report #5577657-5
Physician from JAPAN reported NEORAL problem on Dec 25, 2007. Female patient was diagnosed with pemphigoid and was treated with NEORAL. After drug was administered, patient experienced the following problems/side effects: blood sodium decreased, disease progression, hyponatraemia, inappropriate antidiuretic hormone secretion, . NEORAL dosage: 100 MG/D. During the same period patient was treated with STEROIDS NOS. Patient recovered.
Viagra Side Effects Report #5587410-4
VIAGRA problem was reported by a Physician from UNITED STATES on Aug 24, 2007. Male patient, 65 years of age, weighting 190.0 lb, was diagnosed with erectile dysfunction and was treated with VIAGRA. After drug was administered, patient experienced the following problems/side effects: blood sodium decreased, syncope, . VIAGRA dosage: 100 MG. During the same period patient was treated with ANTIHYPERTENSIVES, AVAPRO, LIPITOR, WARFARIN. Patient recovered.
Effexor Side Effects Report #5587890-4
Health Professional from UNITED STATES reported EFFEXOR problem on June 21, 2007. Female patient, 71 years of age, weighting 140.1 lb, was diagnosed with depression and was treated with EFFEXOR. After drug was administered, patient experienced the following problems/side effects: blood sodium decreased, . EFFEXOR dosage: 37.5 MG 1 X PER 1 DAY, ^TITRATED^, 112.5 MG, 150 MG 1 X PER 1 DAY, ORAL. During the same period patient was treated with TRILEPTAL, NORVASC, INDERAL, LISINOPRIL, ATIVAN. Patient was hospitalized. Patient recovered.
Esidrix Side Effects Report #5507274-4
ESIDRIX problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 29, 2007. Female patient, 78 years of age, weighting 146.0 lb, was treated with ESIDRIX. After drug was administered, patient experienced the following problems/side effects: blood sodium decreased, fatigue, . ESIDRIX dosage: 25 MG, QD. Patient was hospitalized. Patient recovered.
Pemetrexed Side Effects Report #5511610-2
Physician from JAPAN reported PEMETREXED problem on Nov 01, 2007. Male patient, weighting 114.0 lb, was diagnosed with pleural mesothelioma malignant and was treated with PEMETREXED. After drug was administered, patient experienced the following problems/side effects: blood sodium decreased, bone marrow failure, sepsis, . PEMETREXED dosage: unknown. During the same period patient was treated with PARAPLATIN, FOLIC ACID, VITAMIN B. Patient died on 10/27/2007.
Tiotropium Side Effects Report #5512078-2
TIOTROPIUM problem was reported by a Consumer or non-health professional from on Nov 05, 2007. Female patient, 55 years of age, was diagnosed with chronic obstructive pulmonary disease and was treated with TIOTROPIUM. After drug was administered, patient experienced the following problems/side effects: blood sodium decreased, chronic obstructive pulmonary disease, condition aggravated, gastric ulcer, haemoglobin increased, oedema peripheral, pharyngolaryngeal pain, platelet count increased, upper respiratory tract infection, . TIOTROPIUM dosage: unknown. Patient was hospitalized. Patient recovered.
Coreg Side Effects Report #5515131-2
Consumer or non-health professional from UNITED STATES reported COREG problem on Jan 12, 2007. Female patient was diagnosed with hypertension and was treated with COREG. After drug was administered, patient experienced the following problems/side effects: blood sodium decreased, . COREG dosage: 12.5MG TWICE PER DAY. Patient recovered.
Pemetrexed Side Effects Report #5518073-1
PEMETREXED problem was reported by a Physician from JAPAN on Nov 06, 2007. Male patient, weighting 132.6 lb, was diagnosed with pleural mesothelioma malignant, nausea and was treated with PEMETREXED. After drug was administered, patient experienced the following problems/side effects: blood sodium decreased, . PEMETREXED dosage: 800 MG, OTHER. During the same period patient was treated with CISPLATIN, PANVITAN, METHYCOBAL, METOCLOPRAMIDE, LIORESAL, POLARAMINE. Patient was hospitalized. Patient recovered.
Betaseron Side Effects Report #5523918-5
Consumer or non-health professional from UNITED STATES reported BETASERON problem on Nov 14, 2007. Female patient, 52 years of age, was diagnosed with secondary progressive multiple sclerosis, hypertension and was treated with BETASERON. After drug was administered, patient experienced the following problems/side effects: blood sodium decreased, dehydration, electrolyte imbalance, feeling hot, hypertension, . BETASERON dosage: unknown. During the same period patient was treated with ANTIHYPERTENSIVES. Patient was hospitalized. Patient recovered.
Micardis Side Effects Report #5528631-6
MICARDIS HCT problem was reported by a Physician from UNITED STATES on July 30, 2007. Male patient was treated with MICARDIS HCT. After drug was administered, patient experienced the following problems/side effects: blood sodium decreased, . MICARDIS HCT dosage: unknown. Patient was hospitalized. Patient recovered.
Mopral Side Effects Report #5529583-5
Physician from BELGIUM reported MOPRAL problem on Nov 22, 2007. Female patient, weighting 106.5 lb, was treated with MOPRAL. After drug was administered, patient experienced the following problems/side effects: blood sodium decreased, confusional state, fatigue, gastrointestinal candidiasis, hypersensitivity, pain, photosensitivity reaction, urticaria, . MOPRAL dosage: unknown. During the same period patient was treated with ESTROGEL, PREDNISOLONE. Patient recovered.
Celexa Side Effects Report #5529929-8
CELEXA problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 20, 2007. Female patient, 53 years of age, was diagnosed with depression, pain and was treated with CELEXA. After drug was administered, patient experienced the following problems/side effects: blood sodium decreased, confusional state, fall, hip fracture, visual disturbance, . CELEXA dosage: 40 MG QD PO. During the same period patient was treated with MORPHINE, ULTRACET, PERCOCET, TRAZODONE, SEROQUEL, RESTORIL, KLONOPIN. Patient was hospitalized. Patient recovered.
Temozolomide Side Effects Report #5533883-2
Physician from SPAIN reported TEMOZOLOMIDE problem on Nov 15, 2007. Female patient, 51 years of age, was diagnosed with glioblastoma multiforme and was treated with TEMOZOLOMIDE. After drug was administered, patient experienced the following problems/side effects: blood sodium decreased, dry skin, febrile neutropenia, lymphopenia, mucosal inflammation, white blood cell count decreased, . TEMOZOLOMIDE dosage: 110 MG;. During the same period patient was treated with URSOBILANE, OMEPRAZOLE, ZOLPIDEM TARTRATE, LEXATIN, FORTECORTIN, KEPPRA, PENTAMIDINE ISETHIONATE. Patient was hospitalized. Patient recovered.
Januvia Side Effects Report #5534857-8
JANUVIA problem was reported by a Physician from UNITED STATES on Sept 28, 2007. Male patient, 82 years of age, was diagnosed with diabetes mellitus and was treated with JANUVIA. After drug was administered, patient experienced the following problems/side effects: blood sodium decreased, . JANUVIA dosage: 100 MG/DAILY/PO. During the same period patient was treated with ACTOS. Patient recovered.
Trileptal Side Effects Report #5474447-9
Physician from UNITED STATES reported TRILEPTAL problem on Sept 24, 2007. Female patient, 27 years of age, weighting 120.0 lb, was diagnosed with convulsion and was treated with TRILEPTAL. After drug was administered, patient experienced the following problems/side effects: blood sodium decreased, grand mal convulsion, normal newborn, pre-eclampsia, tremor, weight decreased, . TRILEPTAL dosage: 300 MG, BID. Patient was hospitalized. Patient recovered.
Chantix Side Effects Report #5477492-2
CHANTIX problem was reported by a Consumer or non-health professional from UNITED STATES on Sept 23, 2007. Female patient, weighting 115.1 lb, was diagnosed with hypertension and was treated with CHANTIX. After drug was administered, patient experienced the following problems/side effects: blood sodium decreased, nausea, somnolence, . CHANTIX dosage: unknown. During the same period patient was treated with TOPROL, HYDROCHLOROTHIAZIDE, LIBRIUM, VITAMINS, DARVOCET, HYDROCODONE. Patient recovered.
Avapro Side Effects Report #5478146-9
Consumer or non-health professional from UNITED STATES reported AVAPRO problem on Jan 03, 2007. Female patient, 64 years of age, was treated with AVAPRO. After drug was administered, patient experienced the following problems/side effects: blood sodium decreased, . AVAPRO dosage: unknown. During the same period patient was treated with NORVASC, TOPROL, VASOTEC, ZETIA. Patient recovered.