Menu

• Ask a Health Expert about BLOOD SODIUM INCREASED
• Post Your Side Effect related to BLOOD SODIUM INCREASED
• BLOOD SODIUM INCREASED and FDA Warnings
• BLOOD SODIUM INCREASED in Patients Wiki
• Report BLOOD SODIUM INCREASED in Drug Side Effect Survey

BLOOD SODIUM INCREASED side effect

What is BLOOD SODIUM INCREASED ?

A Health Expert wants to answer your question. Please provide details below.

Type your question here

 letters left

Citalopram Side Effects Report #5663646-9
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 increased, . CITALOPRAM HYDROBROMIDE dosage: 20 MG;ORAL. During the same period patient was treated with CITALOPRAM HYDROBROMIDE, ASCORBIC ACID, CARBAMAZEPINE, DANTROLENE, LANSOPRAZOLE, METOCLOPRAMIDE, PROPANTHELINE, PYRIDOXINE. Patient recovered.

Heparin Side Effects Report #5672074-1
HEPARIN problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 19, 2008. Male patient, weighting 150.0 lb, was diagnosed with vascular graft and was treated with HEPARIN. After drug was administered, patient experienced the following problems/side effects: blood sodium increased, gait disturbance, heart rate increased, nosocomial infection, platelet count decreased, pneumonia, pulmonary thrombosis, . HEPARIN dosage: unknown. Patient died on 02/21/2008.

Infliximab Side Effects Report #5684386-6
Pharmacist from UNITED STATES reported INFLIXIMAB problem on Mar 19, 2008. Female patient, weighting 257.0 lb, was diagnosed with crohn's disease and was treated with INFLIXIMAB. After drug was administered, patient experienced the following problems/side effects: blood sodium increased, crohn's disease, disease progression, escherichia urinary tract infection, gastritis, helicobacter pylori identification test positive, hypertension, ileus, pitting oedema, . INFLIXIMAB dosage: unknown. During the same period patient was treated with HUMIRA, PENTESA, PREVACID, PREDNISONE. Patient was hospitalized. Patient recovered.

Temodal Side Effects Report #5619278-1
TEMODAL problem was reported by a Physician from JAPAN on Feb 01, 2008. Female patient, 74 years of age, weighting 94.80 lb, was diagnosed with anaplastic astrocytoma and was treated with TEMODAL. After drug was administered, patient experienced the following problems/side effects: blood sodium increased, cardiac failure acute, platelet count decreased, protein total decreased, shock, . TEMODAL dosage: 75 MG/M2;QD;PO. During the same period patient was treated with GLYCEOL, KYTRIL, ZONISAMIDE, FAMOTIDINE, PREDONINE, EFFORTIL, MEYLON, CATABON. Patient died on 02/10/2007.


Finibax Side Effects Report #5622006-7
Physician from JAPAN reported FINIBAX problem on Feb 06, 2008. Male patient, weighting 97.00 lb, was diagnosed with pneumonia, prophylaxis, diabetes mellitus and was treated with FINIBAX. After drug was administered, patient experienced the following problems/side effects: blood sodium increased, blood urea increased, diabetes mellitus, disease progression, . FINIBAX dosage: unknown. During the same period patient was treated with AVELOX, AUGMENTIN, MAGMITT, GLIMICRON. Patient died on 09/28/2007.

Citalopram Side Effects Report #5645255-0
CITALOPRAM HYDROBROMIDE problem was reported by a Health Professional from UNITED KINGDOM on Feb 22, 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 increased, . CITALOPRAM HYDROBROMIDE dosage: unknown. During the same period patient was treated with CITALOPRAM HYDROBROMIDE. Patient recovered.

Desmopressin Side Effects Report #5598603-4
Consumer or non-health professional from UNITED STATES reported DESMOPRESSIN ACETATE problem on Feb 21, 2007. Male patient, 20 years of age, was diagnosed with diabetes insipidus and was treated with DESMOPRESSIN ACETATE. After drug was administered, patient experienced the following problems/side effects: blood sodium increased, urine output decreased, urine output increased, . DESMOPRESSIN ACETATE dosage: unknown. During the same period patient was treated with DESMOPRESSIN ACETATE, DESMOPRESSIN ACETATE, DESMOPRESSIN ACETATE, VALIUM, PHENOBARBITAL, CLARITIN, TYLENOL, MILK OF MAGNESIA. Patient recovered.

Tiotropium Side Effects Report #5599040-9
TIOTROPIUM problem was reported by a Consumer or non-health professional from on Jan 16, 2008. Female patient, 68 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 increased, colitis, gastrointestinal inflammation, . TIOTROPIUM dosage: unknown. Patient was hospitalized. Patient recovered.

Aricept Side Effects Report #5565004-4
Pharmacist from UNITED STATES reported ARICEPT problem on Dec 03, 2007. Male patient, 83 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 increased, collapse of lung, heart rate abnormal, . ARICEPT dosage: unknown. Patient was hospitalized. Patient recovered.


Temozolomide Side Effects Report #5481970-X
TEMOZOLOMIDE problem was reported by a Physician from UNITED STATES on Sept 27, 2007. Male patient, 61 years of age, weighting 194.0 lb, was diagnosed with glioblastoma multiforme, muscular weakness and was treated with TEMOZOLOMIDE. After drug was administered, patient experienced the following problems/side effects: blood sodium increased, blood urea increased, cellulitis, depression, diabetes mellitus, hyperglycaemia, hypoalbuminaemia, hyponatraemia, . TEMOZOLOMIDE dosage: unknown. During the same period patient was treated with BOTOX. Patient was hospitalized. Patient recovered.

Hypertonic Side Effects Report #5491577-6
Pharmacist from UNITED STATES reported HYPERTONIC SALINE problem on Oct 18, 2007. Female patient, 52 years of age, was diagnosed with intracranial pressure increased and was treated with HYPERTONIC SALINE. After drug was administered, patient experienced the following problems/side effects: blood sodium increased, hyporeflexia, ill-defined disorder, refusal of treatment by relative, . HYPERTONIC SALINE dosage: 5% 150 ML. During the same period patient was treated with APAP, ASPIRIN, INSULIN, LANSOPRAZOLE. Patient recovered.

Vaprisol Side Effects Report #5508889-X
VAPRISOL problem was reported by a Pharmacist from UNITED STATES on Sept 11, 2007. Female patient, 56 years of age, was diagnosed with hyponatraemia and was treated with VAPRISOL. After drug was administered, patient experienced the following problems/side effects: blood sodium increased, hypotension, . VAPRISOL dosage: 20 MG, IV BOLUS ; 20 MG, IV DRIP. During the same period patient was treated with PROTON PUMP INHIBITORS. Patient recovered.

Vaprisol Side Effects Report #5508899-2
Consumer or non-health professional from UNITED STATES reported VAPRISOL problem on July 03, 2007. Female patient was treated with VAPRISOL. After drug was administered, patient experienced the following problems/side effects: blood sodium increased, . VAPRISOL dosage: 20 MG. Patient recovered.

Vaprisol Side Effects Report #5508901-8
VAPRISOL problem was reported by a Physician from UNITED STATES on July 17, 2007. Male patient was treated with VAPRISOL. After drug was administered, patient experienced the following problems/side effects: blood sodium increased, . VAPRISOL dosage: 20 MG. Patient recovered.


Vaprisol Side Effects Report #5508903-1
Pharmacist from UNITED STATES reported VAPRISOL problem on July 05, 2007. Female patient was treated with VAPRISOL. After drug was administered, patient experienced the following problems/side effects: blood sodium increased, . VAPRISOL dosage: 20 MG, IV BOLUS. During the same period patient was treated with DEMECLOCYCLINE. Patient recovered.

Temodal Side Effects Report #5445962-9
TEMODAL problem was reported by a Physician from JAPAN on Aug 30, 2007. Female patient, 74 years of age, weighting 94.80 lb, was diagnosed with anaplastic astrocytoma and was treated with TEMODAL. After drug was administered, patient experienced the following problems/side effects: blood sodium increased, cardiac failure acute, dyspnoea, platelet count decreased, shock, . TEMODAL dosage: 75 MG/M2;QD;PO. During the same period patient was treated with GLYCEOL, KYTRIL, EXCEGRAM, FAMOTIDINE, PREDONINE, EFFORTIL, MEYLON, CATABON. Patient died on 02/10/2007.

Furosemide Side Effects Report #5455146-6
Physician from UNITED KINGDOM reported FUROSEMIDE problem on Sept 03, 2007. Male patient, 64 years of age, was diagnosed with polyuria, renin-angiotensin system inhibition, hypomania and was treated with FUROSEMIDE. After drug was administered, patient experienced the following problems/side effects: blood sodium increased, confusional state, haemodialysis, mood swings, nephrogenic diabetes insipidus, respiratory failure, sepsis, . FUROSEMIDE dosage: unknown. During the same period patient was treated with RAMIPRIL, LITHIUM CARBONATE, AMILORIDE. Patient was hospitalized. Patient recovered.

Sertraline Side Effects Report #5407006-4
SERTRALINE problem was reported by a Consumer or non-health professional from UNITED KINGDOM on July 17, 2007. Female patient, 65 years of age, was diagnosed with depression and was treated with SERTRALINE. After drug was administered, patient experienced the following problems/side effects: blood sodium increased, hypertension, somnolence, . SERTRALINE dosage: 25 MG. During the same period patient was treated with PROVIGIL, DANTROLENE, LANSOPRAZOLE, RAMIPRIL, SINEMET. Patient recovered.

Sertraline Side Effects Report #5408356-8
Health Professional from UNITED KINGDOM reported SERTRALINE problem on July 17, 2007. Female patient, 65 years of age, was diagnosed with depression and was treated with SERTRALINE. After drug was administered, patient experienced the following problems/side effects: blood sodium increased, hypertension, somnolence, . SERTRALINE dosage: 25 MG. During the same period patient was treated with PROVIGIL, DANTROLENE, LANSOPRAZOLE, RAMIPRIL, SINEMET. Patient recovered.


Lithium Side Effects Report #5409757-4
LITHIUM CARBONATE problem was reported by a Consumer or non-health professional from UNITED KINGDOM on July 31, 2007. Female patient, 36 years of age, was diagnosed with schizophrenia, epilepsy and was treated with LITHIUM CARBONATE. After drug was administered, patient experienced the following problems/side effects: blood sodium increased, cellulitis, convulsion, diabetes insipidus, mental status changes, red blood cell count decreased, status epilepticus, therapeutic agent toxicity, . LITHIUM CARBONATE dosage: unknown. During the same period patient was treated with CLOZARIL, EPILIM. Patient was hospitalized. Patient recovered.

Vaprisol Side Effects Report #5454244-0
Physician from UNITED STATES reported VAPRISOL problem on Apr 09, 2007. Female patient, 91 years of age, was diagnosed with hyponatraemia and was treated with VAPRISOL. After drug was administered, patient experienced the following problems/side effects: blood sodium increased, . VAPRISOL dosage: 20 MG, TOTAL DOSE, PARENTERAL. During the same period patient was treated with LEVAQUIN. Patient recovered.

Vaprisol Side Effects Report #5454245-2
VAPRISOL problem was reported by a Consumer or non-health professional from UNITED STATES on May 31, 2007. Female patient was treated with VAPRISOL. After drug was administered, patient experienced the following problems/side effects: blood sodium increased, . VAPRISOL dosage: 20 MG. Patient recovered.

Avandamet Side Effects Report #5390078-3
Consumer or non-health professional from UNITED STATES reported AVANDAMET problem on July 11, 2007. Female patient, 72 years of age, was treated with AVANDAMET. After drug was administered, patient experienced the following problems/side effects: blood sodium increased, carbon dioxide decreased, lactic acidosis, . AVANDAMET dosage: unknown. During the same period patient was treated with LIPITOR, LISINOPRIL, VERAPAMIL, FAMOTIDINE, VITAMIN. Patient recovered.

Sertraline Side Effects Report #5399723-X
SERTRALINE problem was reported by a Health Professional from UNITED KINGDOM on July 18, 2007. Female patient, 65 years of age, was diagnosed with depression, depressed level of consciousness and was treated with SERTRALINE. After drug was administered, patient experienced the following problems/side effects: blood sodium increased, hypertension, somnolence, . SERTRALINE dosage: unknown. During the same period patient was treated with MODAFINIL, DANTROLENE, LANSOPRAZOLE, RAMIPRIL, SINEMET. Patient recovered.

Sertraline Side Effects Report #5401334-4
Consumer or non-health professional from UNITED STATES reported SERTRALINE problem on July 17, 2007. Female patient, 65 years of age, was diagnosed with depression, depressed level of consciousness and was treated with SERTRALINE. After drug was administered, patient experienced the following problems/side effects: blood sodium increased, hypertension, somnolence, . SERTRALINE dosage: 25 MG, QD. During the same period patient was treated with MODAFINIL, DANTROLENE, LANSOPRAZOLE, RAMIPRIL, SINEMET. Patient recovered.

Sertraline Side Effects Report #5402021-9
SERTRALINE problem was reported by a Health Professional from UNITED KINGDOM on July 16, 2007. Female patient, 65 years of age, was diagnosed with depression and was treated with SERTRALINE. After drug was administered, patient experienced the following problems/side effects: blood sodium increased, hypertension, somnolence, . SERTRALINE dosage: 25MG;QD. During the same period patient was treated with PROVIGIL, LANSOPRAZOLE, RAMIPRIL, SINEMET, DANTROLENE. Patient recovered.

Avandamet Side Effects Report #5390078-3
Consumer or non-health professional from UNITED STATES reported AVANDAMET problem on July 11, 2007. Female patient, 72 years of age, was treated with AVANDAMET. After drug was administered, patient experienced the following problems/side effects: blood sodium increased, carbon dioxide decreased, lactic acidosis, . AVANDAMET dosage: unknown. During the same period patient was treated with LIPITOR, LISINOPRIL, VERAPAMIL, FAMOTIDINE, VITAMIN. Patient recovered.

Sertraline Side Effects Report #5399723-X
SERTRALINE problem was reported by a Health Professional from UNITED KINGDOM on July 18, 2007. Female patient, 65 years of age, was diagnosed with depression, depressed level of consciousness and was treated with SERTRALINE. After drug was administered, patient experienced the following problems/side effects: blood sodium increased, hypertension, somnolence, . SERTRALINE dosage: unknown. During the same period patient was treated with MODAFINIL, DANTROLENE, LANSOPRAZOLE, RAMIPRIL, SINEMET. Patient recovered.

Sertraline Side Effects Report #5401334-4
Consumer or non-health professional from UNITED STATES reported SERTRALINE problem on July 17, 2007. Female patient, 65 years of age, was diagnosed with depression, depressed level of consciousness and was treated with SERTRALINE. After drug was administered, patient experienced the following problems/side effects: blood sodium increased, hypertension, somnolence, . SERTRALINE dosage: 25 MG, QD. During the same period patient was treated with MODAFINIL, DANTROLENE, LANSOPRAZOLE, RAMIPRIL, SINEMET. Patient recovered.

Sertraline Side Effects Report #5402021-9
SERTRALINE problem was reported by a Health Professional from UNITED KINGDOM on July 16, 2007. Female patient, 65 years of age, was diagnosed with depression and was treated with SERTRALINE. After drug was administered, patient experienced the following problems/side effects: blood sodium increased, hypertension, somnolence, . SERTRALINE dosage: 25MG;QD. During the same period patient was treated with PROVIGIL, LANSOPRAZOLE, RAMIPRIL, SINEMET, DANTROLENE. Patient recovered.

Humira Side Effects Report #5763755-X
Consumer or non-health professional from BRAZIL reported HUMIRA problem on June 04, 2008. Female patient, weighting 165.3 lb, was diagnosed with rheumatoid arthritis, hypertension and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: blood sodium increased, haematochezia, pneumonia, pulmonary embolism, renal failure, . HUMIRA dosage: unknown. Patient was hospitalized. Patient recovered.

Aleve Side Effects Report #5779126-6
ALEVE problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 28, 2008. Female patient, 77 years of age, weighting 125.7 lb, was diagnosed with arthralgia and was treated with ALEVE. After drug was administered, patient experienced the following problems/side effects: blood sodium increased, . ALEVE dosage: TOTAL DAILY DOSE: 440 MG UNIT DOSE: 220 MG. During the same period patient was treated with FOSAMAX, CADUET, ASPIRIN. Patient recovered.

Citalopram Side Effects Report #5692860-1
Consumer or non-health professional from reported CITALOPRAM HYDROBROMIDE problem on Mar 15, 2008. Female patient, 43 years of age, weighting 99.21 lb, was diagnosed with depression and was treated with CITALOPRAM HYDROBROMIDE. After drug was administered, patient experienced the following problems/side effects: blood sodium increased, . CITALOPRAM HYDROBROMIDE dosage: 20MG; PO. During the same period patient was treated with CITALOPRAM HYDROBROMIDE, ASCORBIC ACID, CARBAMAZEPINE, DANTROLENE, LANSOPRAZOLE, METOCLOPRAMIDE, PROPANTHELINE, PYRIDOXINE. Patient recovered.

Citalopram Side Effects Report #5700851-7
CITALOPRAM HYDROBROMIDE problem was reported by a Health Professional from UNITED KINGDOM 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 increased, . CITALOPRAM HYDROBROMIDE dosage: 20 MG; PO. During the same period patient was treated with TOLTERODINE TARTRATE, METOCLOPRAMIDE, ASCORBIC ACID, TIZANIDINE, TRIMETHOPRIM, LANSOPRAZOLE, SENNA, PYRIDOXINE. Patient was hospitalized. Patient recovered.

Humira Side Effects Report #5703310-0
Consumer or non-health professional from BRAZIL reported HUMIRA problem on Apr 04, 2008. Female patient, weighting 165.3 lb, was diagnosed with rheumatoid arthritis, hypertension and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: blood sodium increased, haematochezia, pneumonia, pulmonary embolism, renal failure, . HUMIRA dosage: unknown. Patient was hospitalized. Patient recovered.

Humira Side Effects Report #5721848-7
HUMIRA problem was reported by a Consumer or non-health professional from BRAZIL on Apr 22, 2008. Female patient, weighting 165.3 lb, was diagnosed with rheumatoid arthritis, hypertension and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: blood sodium increased, haematochezia, pneumonia, pulmonary embolism, renal failure, . HUMIRA dosage: unknown. Patient was hospitalized. Patient recovered.

Trileptal Side Effects Report #5352541-0
Health Professional from SPAIN reported TRILEPTAL problem on May 30, 2007. Male patient, 54 years of age, was diagnosed with psychotic disorder, lipid metabolism disorder and was treated with TRILEPTAL. After drug was administered, patient experienced the following problems/side effects: blood sodium increased, . TRILEPTAL dosage: 1200 MG/DAY. During the same period patient was treated with SEROQUEL, RISPERDAL, GEMFIBROZILO. Patient recovered.

Micardis Side Effects Report #5317243-5
MICARDIS HCT problem was reported by a Physician from AUSTRALIA on Mar 06, 2007. Female patient, 75 years of age, was treated with MICARDIS HCT. After drug was administered, patient experienced the following problems/side effects: blood sodium increased, dehydration, . MICARDIS HCT dosage: unknown. Patient was hospitalized. Patient recovered.

Carbamazepine Side Effects Report #5320878-7
Consumer or non-health professional from JAPAN reported CARBAMAZEPINE problem on Apr 17, 2007. Male patient, 46 years of age, was diagnosed with agitation and was treated with CARBAMAZEPINE. After drug was administered, patient experienced the following problems/side effects: blood sodium increased, cerebral disorder, diabetes insipidus, stupor, . CARBAMAZEPINE dosage: 600MG, QD, ORAL. During the same period patient was treated with LITHIUM CARBONATE, PROMETHAZINE HYDROCHLORIDE, FLUNITRAZEPAM, NIMETAZEPAM, OXATOMIDE. Patient was hospitalized. Patient recovered.

Ddavp Side Effects Report #5333354-2
DDAVP problem was reported by a Consumer or non-health professional from UNITED STATES on May 16, 2007. Female patient, weighting 180.8 lb, was diagnosed with diabetes insipidus, growth hormone deficiency and was treated with DDAVP. After drug was administered, patient experienced the following problems/side effects: blood sodium increased, fluid retention, migraine, oliguria, vital capacity decreased, . DDAVP dosage: unknown. During the same period patient was treated with DILANTIN, GROWTH HORMONE. Patient was hospitalized. Patient recovered.

Carbamazepine Side Effects Report #5297315-4
Physician from JAPAN reported CARBAMAZEPINE problem on Mar 28, 2007. Male patient, 46 years of age, was diagnosed with schizophrenia and was treated with CARBAMAZEPINE. After drug was administered, patient experienced the following problems/side effects: blood sodium increased, central nervous system lesion, csf test abnormal, diabetes insipidus, . CARBAMAZEPINE dosage: 600 MG DAILY. During the same period patient was treated with PROMETHAZINE, LITHIUM CARBONATE, NIMETAZEPAM, OXATOMIDE, LISPERIDONE, BULOTIZOLAM. Patient was hospitalized. Patient recovered.

Micardis Side Effects Report #5264164-2
MICARDIS HCT problem was reported by a Physician from AUSTRALIA on Mar 06, 2007. Female patient, 75 years of age, was treated with MICARDIS HCT. After drug was administered, patient experienced the following problems/side effects: blood sodium increased, dehydration, . MICARDIS HCT dosage: unknown. Patient was hospitalized. Patient recovered.

Baclofen Side Effects Report #5678847-3
Consumer or non-health professional from TAIWAN, PROVINCE OF CHINA reported BACLOFEN problem on Feb 19, 2008. Female patient, 70 years of age, was diagnosed with myalgia and was treated with BACLOFEN. After drug was administered, patient experienced the following problems/side effects: blood pressure increased, blood sodium increased, cerebral atrophy, confusional state, haemoglobin decreased, leukoaraiosis, overdose, somnolence, . BACLOFEN dosage: 5 MG; 3 TIMES A DAY ORAL, 5 MG; ORAL; 3 TIMES A DAY. Patient was hospitalized. Patient recovered.

Dexamethasone Side Effects Report #5680026-0
DEXAMETHASONE problem was reported by a Physician from UNITED STATES on Mar 25, 2008. Male patient, 59 years of age, weighting 171.0 lb, was diagnosed with brain oedema, neoplasm and was treated with DEXAMETHASONE. After drug was administered, patient experienced the following problems/side effects: alopecia, blood sodium increased, cognitive disorder, cushingoid, deep vein thrombosis, hyperglycaemic hyperosmolar nonketotic syndrome, hypertonia, muscular weakness, pneumonia aspiration, . DEXAMETHASONE dosage: 4 MG TID PO. Patient was hospitalized. Patient recovered.

Temodal Side Effects Report #5683547-X
Physician from JAPAN reported TEMODAL problem on Mar 24, 2008. Female patient, 74 years of age, weighting 94.80 lb, was diagnosed with anaplastic astrocytoma and was treated with TEMODAL. After drug was administered, patient experienced the following problems/side effects: blood pressure decreased, blood sodium increased, cardiac failure acute, dyspnoea, platelet count decreased, protein total decreased, shock, . TEMODAL dosage: 75 MG/M2; QD; PO. During the same period patient was treated with GLYCEOL, KYTRIL, ZONISAMIDE, FAMOTIDINE, PREDONINE, EFFORTIL, MEYLON, CATABON. Patient died on 02/10/2007.

Lorazepam Side Effects Report #5647962-2
LORAZEPAM problem was reported by a Consumer or non-health professional from UNITED STATES 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.

Vaprisol Side Effects Report #5627034-3
Consumer or non-health professional from UNITED STATES reported VAPRISOL problem on Oct 05, 2007. Female patient, 56 years of age, was diagnosed with hyponatraemia and was treated with VAPRISOL. After drug was administered, patient experienced the following problems/side effects: anaemia, blood sodium increased, hypotension, urinary tract infection, . VAPRISOL dosage: 20 MG, IV BOLUS. During the same period patient was treated with PROTON PUMP INHIBITORS. Patient was hospitalized. Patient recovered.

Xopenex Side Effects Report #5553546-7
XOPENEX problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 29, 2007. Female patient, 87 years of age, was diagnosed with bronchitis chronic, chronic obstructive pulmonary disease, pneumonia and was treated with XOPENEX. After drug was administered, patient experienced the following problems/side effects: blood potassium decreased, blood sodium increased, cerebrovascular accident, escherichia infection, feeling cold, lung infiltration, respiratory disorder, staphylococcal infection, tremor, . XOPENEX dosage: 1.25 MG/3ML; BID; INHALATION. During the same period patient was treated with ALUPENT, WARFARIN, TOPROL, PREDNISONE, LEXAPRO, TYLENOL. Patient was hospitalized. Patient recovered.

Lithium Side Effects Report #5504588-9
Consumer or non-health professional from reported LITHIUM CARBONATE problem on Oct 25, 2007. Male patient, 64 years of age, was diagnosed with hypomania, infection, nephrogenic diabetes insipidus and was treated with LITHIUM CARBONATE. After drug was administered, patient experienced the following problems/side effects: blood creatinine increased, blood sodium increased, blood urea increased, body temperature increased, confusional state, nephrogenic diabetes insipidus, polyuria, respiratory failure, sepsis, . LITHIUM CARBONATE dosage: unknown. During the same period patient was treated with FUROSEMIDE, AMILORIDE HYDROCHLORIDE, RAMIPRIL, ANTIBIOTICS, DDAVP. Patient was hospitalized. Patient recovered.

Mylotarg Side Effects Report #5511713-2
MYLOTARG problem was reported by a Physician from JAPAN on Nov 01, 2007. Male patient, weighting 145.5 lb, was diagnosed with acute myeloid leukaemia, prophylaxis, pyrexia, insomnia and was treated with MYLOTARG. After drug was administered, patient experienced the following problems/side effects: anaemia, blood sodium increased, diarrhoea, gastrointestinal infection, neutrophil count decreased, petechiae, platelet count decreased, venoocclusive liver disease, white blood cell count decreased, . MYLOTARG dosage: unknown. During the same period patient was treated with ADALAT, DIFLUCAN, PN TWIN, ZANTAC, ZYVOX, SILECE. Patient was hospitalized. Patient recovered.

Ambisome Side Effects Report #5479420-2
Pharmacist from UNITED STATES reported AMBISOME problem on Oct 03, 2007. Female patient, 57 years of age, weighting 454.2 lb, was diagnosed with systemic candida and was treated with AMBISOME. After drug was administered, patient experienced the following problems/side effects: blood electrolytes abnormal, blood sodium increased, diabetes insipidus, hypokalaemia, . AMBISOME dosage: 600 MG DAILY IV BOLUS. Patient was hospitalized and became disabled. Patient recovered.