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BLOOD OSMOLARITY DECREASED side effect

What is BLOOD OSMOLARITY DECREASED ?
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Drugs associated with BLOOD OSMOLARITY DECREASED

AUGMENTIN  BLOPRESS  CACIT  CITALOPRAM  CYCLOSPORINE  DIOVAN  ESCITALOPRAM  FLUDEX  HUMIRA  IBUPROFEN  ISENTRESS  LEVETIRACETAM  MINIRIN  NEORAL  OLANZAPINE  OXCARBAZEPINE  PAROXETINE  PAXIL  RECLAST  REQUIP  SUNITINIB  VALPROATE  VINCRISTINE  WELLBUTRIN  


Minirin Side Effects Report #5662700-5
Consumer or non-health professional from SWITZERLAND reported MINIRIN problem on Mar 05, 2008. Male patient, 58 years of age, was diagnosed with atrial fibrillation, atrial flutter and was treated with MINIRIN. After drug was administered, patient experienced the following problems/side effects: blood osmolarity decreased, hyponatraemia, inappropriate antidiuretic hormone secretion, somnolence, . MINIRIN dosage: unknown. During the same period patient was treated with CORTISONE ACETATE, LEVOTHYROXINE, TESTOSTERONE ENANTHATE, SOTALOL HYDROCHLORIDE, PHENPROCOUMON. Patient recovered.

Humira Side Effects Report #5671439-1
HUMIRA problem was reported by a Consumer or non-health professional from GERMANY on Mar 11, 2008. Male patient, weighting 160.9 lb, was diagnosed with rheumatoid arthritis, hypertension and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: blood osmolarity decreased, bronchitis, cardiac arrest, cardiovascular insufficiency, cholecystitis acute, epistaxis, fluid intake reduced, hypokalaemia, hyponatraemia, . HUMIRA dosage: unknown. During the same period patient was treated with METHOTREXATE, INFLIXIMAB, OLMESARTAN, PREDNISOLONE, BISOPROLOL FUMARATE. Patient was hospitalized. Patient died on 09/26/2007.

Humira Side Effects Report #5677727-7
Consumer or non-health professional from GERMANY reported HUMIRA problem on Mar 19, 2008. Male patient, weighting 160.9 lb, was diagnosed with rheumatoid arthritis, hypertension and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: blood osmolarity decreased, bronchitis, cardiac arrest, cardiovascular insufficiency, cholecystitis acute, epistaxis, fluid intake reduced, hypokalaemia, hyponatraemia, . HUMIRA dosage: unknown. During the same period patient was treated with METHOTREXATE, INFLIXIMAB, OLMESARTAN, PREDNISOLONE, BISOPROLOL FUMARATE. Patient was hospitalized. Patient died on 09/26/2007.

Diovan Side Effects Report #5621763-3
DIOVAN HCT problem was reported by a Health Professional from SWITZERLAND on Feb 01, 2008. Female patient, 70 years of age, was diagnosed with hypertension, hypothyroidism and was treated with DIOVAN HCT. After drug was administered, patient experienced the following problems/side effects: blood osmolarity decreased, fall, hyponatraemia, hypovolaemia, urinary tract infection, urine osmolarity decreased, urine sodium decreased, . DIOVAN HCT dosage: VALS 160 / HCT 12.5 MG/DAY. During the same period patient was treated with GLUCOPHAGE, DIAMICRON, ZOCOR, ELTROXIN, TEMESTA. Patient was hospitalized. Patient recovered.


Sunitinib Side Effects Report #5601245-5
Health Professional from UNITED STATES reported SUNITINIB problem on Jan 22, 2008. Female patient, weighting 119.0 lb, was diagnosed with breast cancer and was treated with SUNITINIB. After drug was administered, patient experienced the following problems/side effects: blood osmolarity decreased, hiatus hernia, hyponatraemia, incorrect dose administered, loss of consciousness, mental status changes, oesophageal disorder, pneumonia aspiration, . SUNITINIB dosage: 12.5MG DAILY ORAL. During the same period patient was treated with LORAZEPAM, OMEPRAZOLE, PROCHLORPERAZINE, NIFEDIPINE, ZOLPIDEM. Patient was hospitalized. Patient recovered.

Cacit Side Effects Report #5577667-8
CACIT D problem was reported by a Consumer or non-health professional from FRANCE on Dec 26, 2007. Female patient, 87 years of age, was diagnosed with sleep disorder, osteoporosis, pain in extremity, epilepsy and was treated with CACIT D. After drug was administered, patient experienced the following problems/side effects: blood osmolarity decreased, cerebral atrophy, computerised tomogram abnormal, epilepsy, fall, fluid intake restriction, glasgow coma scale abnormal, grand mal convulsion, head injury, . CACIT D dosage: unknown. During the same period patient was treated with MOVICOL, DIPROSONE, LACRIGEL, IMOVANE, ACTONEL, DOLIPRANE, DRIPTANE, TRILEPTAL. Patient was hospitalized. Patient recovered.

Ibuprofen Side Effects Report #5506685-0
Consumer or non-health professional from UNITED STATES reported IBUPROFEN problem on Oct 05, 2007. Female patient was diagnosed with analgesia and was treated with IBUPROFEN. After drug was administered, patient experienced the following problems/side effects: blood osmolarity decreased, coma, hyponatraemia, loss of consciousness, . IBUPROFEN dosage: unknown. During the same period patient was treated with DESMOPRESSIN ACETATE. Patient was hospitalized. Patient recovered.

Augmentin Side Effects Report #5514586-7
AUGMENTIN problem was reported by a Consumer or non-health professional from FRANCE on Nov 02, 2007. Female patient, 93 years of age, was diagnosed with bronchopneumopathy, depression, pain and was treated with AUGMENTIN. After drug was administered, patient experienced the following problems/side effects: blood osmolarity decreased, dehydration, diarrhoea, hypoglycaemia, pyrexia, . AUGMENTIN dosage: unknown. During the same period patient was treated with CETORNAN, DEROXAT, LANTUS, ACUPAN, NORMACOL. Patient was hospitalized. Patient recovered.

Blopress Side Effects Report #5498030-4
Health Professional from SWITZERLAND reported BLOPRESS PLUS problem on Oct 15, 2007. Female patient, 73 years of age, was diagnosed with trigeminal neuralgia and was treated with BLOPRESS PLUS. After drug was administered, patient experienced the following problems/side effects: blood osmolarity decreased, confusional state, hyponatraemia, . BLOPRESS PLUS dosage: CANDESARTAN 8 MG / HYDROCHLOROTHIAZIDE 12.5 MG. During the same period patient was treated with TEGRETOL, SINTROM, PANTOPRAZOLE, PONSTAN, ELTROXIN, SYMFONA, SOTALOL. Patient was hospitalized. Patient recovered.


Fludex Side Effects Report #5405903-7
FLUDEX problem was reported by a Consumer or non-health professional from on July 25, 2007. Female patient, 76 years of age, was diagnosed with essential hypertension and was treated with FLUDEX. After drug was administered, patient experienced the following problems/side effects: blood osmolarity decreased, hyponatraemia, inappropriate antidiuretic hormone secretion, urine osmolarity increased, . FLUDEX dosage: unknown. During the same period patient was treated with CARBAMAZEPINE. Patient was hospitalized. Patient recovered.

Vincristine Side Effects Report #5420023-3
Consumer or non-health professional from ITALY reported VINCRISTINE problem on Aug 07, 2007. Female patient, child 12 years of age, was diagnosed with acute lymphocytic leukaemia and was treated with VINCRISTINE. After drug was administered, patient experienced the following problems/side effects: blood osmolarity decreased, cholelithiasis, hepatomegaly, hyponatraemia, pancreatitis acute, . VINCRISTINE dosage: 2.5 MG (1 MG/ML- CYCLICAL); INTRAVENOUS (NO OTHERWISE SPECIFIED). During the same period patient was treated with ASPARAGINASE, PREDNISONE, DAUNORUBICIN, METHYLPREDNISOLONE. Patient was hospitalized. Patient recovered.

Olanzapine Side Effects Report #5399809-X
OLANZAPINE problem was reported by a Physician from BELGIUM on July 19, 2007. Female patient, 72 years of age, weighting 176.4 lb, was diagnosed with dementia alzheimer's type, fungal infection and was treated with OLANZAPINE. After drug was administered, patient experienced the following problems/side effects: blood osmolarity decreased, dehydration, diabetic ketoacidosis, . OLANZAPINE dosage: 5 MG, 3/D. During the same period patient was treated with MESTINON, FLUCONAZOLE. Patient was hospitalized. Patient died.

Olanzapine Side Effects Report #5399809-X
Physician from BELGIUM reported OLANZAPINE problem on July 19, 2007. Female patient, 72 years of age, weighting 176.4 lb, was diagnosed with dementia alzheimer's type, fungal infection and was treated with OLANZAPINE. After drug was administered, patient experienced the following problems/side effects: blood osmolarity decreased, dehydration, diabetic ketoacidosis, . OLANZAPINE dosage: 5 MG, 3/D. During the same period patient was treated with MESTINON, FLUCONAZOLE. Patient was hospitalized. Patient died.

Levetiracetam Side Effects Report #5762147-7
LEVETIRACETAM problem was reported by a Consumer or non-health professional from ITALY on May 19, 2008. Male patient, 76 years of age, was diagnosed with complex partial seizures and was treated with LEVETIRACETAM. After drug was administered, patient experienced the following problems/side effects: blood osmolarity decreased, convulsion, grand mal convulsion, hyponatraemia, . LEVETIRACETAM dosage: 1000 MG 2/D. During the same period patient was treated with AMLODIPINE, LORAZEPAM. Patient was hospitalized. Patient recovered.


Isentress Side Effects Report #5789339-5
Health Professional from UNITED STATES reported ISENTRESS problem on June 16, 2008. Male patient, 58 years of age, was diagnosed with hiv infection and was treated with ISENTRESS. After drug was administered, patient experienced the following problems/side effects: blood osmolarity decreased, dizziness, hyponatraemia, . ISENTRESS dosage: unknown. During the same period patient was treated with VIRACEPT, VIREAD, COMBIVIR. Patient was hospitalized and became disabled. Patient recovered.

Paxil Side Effects Report #5726453-4
PAXIL problem was reported by a Consumer or non-health professional from JAPAN on Apr 24, 2008. Male patient, 79 years of age, was diagnosed with depression and was treated with PAXIL. After drug was administered, patient experienced the following problems/side effects: blood osmolarity decreased, blood sodium decreased, disorientation, inappropriate antidiuretic hormone secretion, malaise, somnolence, . PAXIL dosage: unknown. During the same period patient was treated with SULPIRIDE, AMOXAPINE, MILNACIPRAN HYDROCHLORIDE. Patient recovered.

Paxil Side Effects Report #5742713-5
Health Professional from JAPAN reported PAXIL problem on May 13, 2008. Male patient, 79 years of age, was diagnosed with depression and was treated with PAXIL. After drug was administered, patient experienced the following problems/side effects: blood osmolarity decreased, blood sodium decreased, disorientation, inappropriate antidiuretic hormone secretion, malaise, somnolence, . PAXIL dosage: unknown. During the same period patient was treated with SULPIRIDE, AMOXAPINE, MILNACIPRAN HYDROCHLORIDE. Patient recovered.

Paxil Side Effects Report #5745234-9
PAXIL problem was reported by a Health Professional from JAPAN on May 14, 2008. Male patient, 79 years of age, was diagnosed with depression and was treated with PAXIL. After drug was administered, patient experienced the following problems/side effects: blood osmolarity decreased, blood sodium decreased, disorientation, inappropriate antidiuretic hormone secretion, malaise, somnolence, . PAXIL dosage: unknown. During the same period patient was treated with SULPIRIDE, AMOXAPINE, MILNACIPRAN HYDROCHLORIDE. Patient recovered.

Ibuprofen Side Effects Report #5683448-7
Consumer or non-health professional from UNITED STATES reported IBUPROFEN problem on Oct 05, 2007. Female patient was diagnosed with analgesia and was treated with IBUPROFEN. After drug was administered, patient experienced the following problems/side effects: blood osmolarity decreased, coma, convulsion, hyponatraemia, . IBUPROFEN dosage: unknown. During the same period patient was treated with DESMOPRESSIN ACETATE. Patient was hospitalized. Patient recovered.


Wellbutrin Side Effects Report #5694654-X
WELLBUTRIN problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 28, 2008. Male patient, 34 years of age, was diagnosed with depression and was treated with WELLBUTRIN. After drug was administered, patient experienced the following problems/side effects: blood osmolarity decreased, dehydration, diabetes insipidus, . WELLBUTRIN dosage: 300MG PER DAY. Patient recovered.

Diovan Side Effects Report #5703681-5
Health Professional from SWITZERLAND reported DIOVAN HCT problem on Apr 04, 2008. Female patient, 86 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 osmolarity decreased, confusional state, disorientation, hyponatraemia, inappropriate antidiuretic hormone secretion, moderate mental retardation, syncope, urine osmolarity increased, urine sodium increased, . DIOVAN HCT dosage: unknown. During the same period patient was treated with COAPROVEL, BILOL, ASPIRIN. Patient was hospitalized. Patient recovered.

Escitalopram Side Effects Report #5284365-7
ESCITALOPRAM problem was reported by a Consumer or non-health professional from DENMARK on Mar 13, 2007. Female patient, 76 years of age, was treated with ESCITALOPRAM. After drug was administered, patient experienced the following problems/side effects: blood osmolarity decreased, confusional state, decreased appetite, epistaxis, facial pain, fall, gait disturbance, hyponatraemia, somnolence, . ESCITALOPRAM dosage: 12.5 MG QD; PO. During the same period patient was treated with ATACAND, LORAZEPAM, SIMVASTATIN, SOTALOL HYDROCHLORIDE. Patient recovered.

Valproate Side Effects Report #5664406-5
Consumer or non-health professional from FRANCE reported VALPROATE problem on Mar 06, 2008. Male patient, 22 years of age, was diagnosed with grand mal convulsion and was treated with VALPROATE. After drug was administered, patient experienced the following problems/side effects: abdominal pain, blood osmolarity decreased, hyponatraemia, inappropriate antidiuretic hormone secretion, urine osmolarity increased, vomiting, . VALPROATE dosage: unknown. Patient was hospitalized. Patient recovered.

Neoral Side Effects Report #5624921-7
NEORAL problem was reported by a Physician from JAPAN on Jan 29, 2008. Male patient, 74 years of age, weighting 123.5 lb, was diagnosed with pemphigoid and was treated with NEORAL. After drug was administered, patient experienced the following problems/side effects: blister, blood osmolarity decreased, blood sodium decreased, condition aggravated, disease progression, erythema, hyponatraemia, inappropriate antidiuretic hormone secretion, pemphigoid, . NEORAL dosage: 150 MG/D. During the same period patient was treated with STEROIDS NOS, PREDONINE. Patient was hospitalized. Patient recovered.

Neoral Side Effects Report #5625296-X
Physician from JAPAN reported NEORAL problem on Jan 29, 2008. Male patient, 74 years of age, weighting 123.5 lb, was diagnosed with pemphigoid and was treated with NEORAL. After drug was administered, patient experienced the following problems/side effects: blister, blood osmolarity decreased, blood sodium decreased, disease progression, erythema, hyponatraemia, inappropriate antidiuretic hormone secretion, white blood cell count increased, . NEORAL dosage: 150 MG/D. During the same period patient was treated with STEROIDS NOS, PREDONINE. Patient was hospitalized. Patient recovered.

Paroxetine Side Effects Report #5574960-X
PAROXETINE HYDROCHLORIDE problem was reported by a Consumer or non-health professional from NETHERLANDS on Dec 18, 2007. Female patient, 78 years of age, was diagnosed with depression, hypertension and was treated with PAROXETINE HYDROCHLORIDE. After drug was administered, patient experienced the following problems/side effects: blood creatinine decreased, blood osmolarity decreased, blood potassium decreased, creatinine urine decreased, decreased appetite, headache, hyponatraemia, ill-defined disorder, malaise, . PAROXETINE HYDROCHLORIDE dosage: 20MG PER DAY. During the same period patient was treated with AMILORIDE AND HYDROCHLOROTHIAZIDE, OXAZEPAM, CORTICOSTEROID, NORVASC. Patient was hospitalized. Patient recovered.

Oxcarbazepine Side Effects Report #5512228-8
Physician from GERMANY reported OXCARBAZEPINE problem on Oct 31, 2007. Male patient, 62 years of age, weighting 231.5 lb, was diagnosed with epilepsy and was treated with OXCARBAZEPINE. After drug was administered, patient experienced the following problems/side effects: blood antidiuretic hormone decreased, blood osmolarity decreased, cerebral ischaemia, hypokalaemia, hyponatraemia, traumatic brain injury, . OXCARBAZEPINE dosage: 1800 MG/D. During the same period patient was treated with METOPROLOL SUCCINATE, NEXIUM, AMLODIPINE, NOVALGIN, OXYGESIC, KARVEA, KEPPRA, TOPAMAX. Patient recovered.

Requip Side Effects Report #5409743-4
REQUIP problem was reported by a Physician from JAPAN on Aug 03, 2007. Male patient, 78 years of age, weighting 141.1 lb, was diagnosed with multiple system atrophy, depression, hypertension, benign prostatic hyperplasia, ventricular tachycardia, anxiety disorder and was treated with REQUIP. After drug was administered, patient experienced the following problems/side effects: aspartate aminotransferase increased, blood osmolarity decreased, hyponatraemia, inappropriate antidiuretic hormone secretion, liver disorder, urine sodium normal, . REQUIP dosage: unknown. During the same period patient was treated with LUVOX, MICARDIS, CALBLOCK, ZYRTEC, HARNAL, BETHANECHOL CHLORIDE, PIRMENOL HYDROCHLORIDE, ALPRAZOLAM. Patient was hospitalized. Patient recovered.

Cyclosporine Side Effects Report #5382588-X
Health Professional from UNITED STATES reported CYCLOSPORINE problem on June 27, 2007. Female patient, 27 years of age, was diagnosed with bone marrow transplant and was treated with CYCLOSPORINE. After drug was administered, patient experienced the following problems/side effects: blood lactate dehydrogenase increased, blood osmolarity decreased, blood sodium decreased, epstein-barr virus infection, inappropriate antidiuretic hormone secretion, lymphadenopathy, lymphoproliferative disorder, nausea, pyrexia, . CYCLOSPORINE dosage: 2 MG/KG/DAY. During the same period patient was treated with MYCOPHENOLATE MOFETIL. Patient recovered.

Cyclosporine Side Effects Report #5382588-X
CYCLOSPORINE problem was reported by a Health Professional from UNITED STATES on June 27, 2007. Female patient, 27 years of age, was diagnosed with bone marrow transplant and was treated with CYCLOSPORINE. After drug was administered, patient experienced the following problems/side effects: blood lactate dehydrogenase increased, blood osmolarity decreased, blood sodium decreased, epstein-barr virus infection, inappropriate antidiuretic hormone secretion, lymphadenopathy, lymphoproliferative disorder, nausea, pyrexia, . CYCLOSPORINE dosage: 2 MG/KG/DAY. During the same period patient was treated with MYCOPHENOLATE MOFETIL. Patient recovered.

Citalopram Side Effects Report #5326556-2
Physician from UNITED STATES reported CITALOPRAM HYDROBROMIDE problem on Apr 24, 2007. Male patient, 87 years of age, was diagnosed with depression and was treated with CITALOPRAM HYDROBROMIDE. After drug was administered, patient experienced the following problems/side effects: asthenia, blood osmolarity decreased, cardiomegaly, inappropriate antidiuretic hormone secretion, urine osmolarity increased, weight decreased, . CITALOPRAM HYDROBROMIDE dosage: (20 MG QD). During the same period patient was treated with LOSARTAN POSTASSIUM, OMEPRAZOLE, ALLOPURINOL, CLOPIDOGREL, CARVEDILOL, SIMVASTATIN, ISOSORBIDE MONONITRATE, TIMOLOL MALEATE. Patient was hospitalized. Patient recovered.

Escitalopram Side Effects Report #5442920-5
ESCITALOPRAM problem was reported by a Health Professional from FRANCE on Aug 10, 2007. Male patient, 79 years of age, was diagnosed with hypertension and was treated with ESCITALOPRAM. After drug was administered, patient experienced the following problems/side effects: bedridden, blood chloride decreased, blood osmolarity decreased, blood potassium decreased, confusional state, disorientation, fall, glasgow coma scale abnormal, . ESCITALOPRAM dosage: 10 MG QD PO. During the same period patient was treated with INDAPAMIDE, MOPRAL, PLAVIX, COZAAR, PRAVASTATIN, PROPRANOLOL, ACETAMINOPHEN. Patient was hospitalized. Patient recovered.

Reclast Side Effects Report #5793635-5
Pharmacist from UNITED STATES reported RECLAST problem on June 19, 2008. Female patient, weighting 121.5 lb, was diagnosed with osteoporosis and was treated with RECLAST. After drug was administered, patient experienced the following problems/side effects: arthralgia, bedridden, blood osmolarity decreased, chills, feeling hot, hand deformity, headache, hypocalcaemia, hypokalaemia, . RECLAST dosage: 5 MG, ONCE YEARLY. Patient was hospitalized. Patient recovered.

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