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BLOOD ALBUMIN INCREASED side effect

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Humira Side Effects Report #5665339-0
Physician from UNITED STATES reported HUMIRA problem on Dec 05, 2007. Male patient, weighting 200.2 lb, was diagnosed with crohn's disease, gastric ph decreased, vitamin supplementation and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: blood albumin increased, blood bilirubin increased, blood calcium increased, weight increased, . HUMIRA dosage: unknown. During the same period patient was treated with AZATHIOPRINE, ESOMEPRAZOLE MAGNESIUM, ACACOL, DUET STUARTNATAL, DUET STUARTNATAL. Patient recovered.

Omalizumab Side Effects Report #5677797-6
OMALIZUMAB problem was reported by a Physician from SWITZERLAND on Mar 10, 2008. Female patient, weighting 174.2 lb, was diagnosed with asthma and was treated with OMALIZUMAB. After drug was administered, patient experienced the following problems/side effects: blood albumin increased, colon cancer, haematocrit decreased, haemoglobin decreased, platelet count increased, urticaria chronic, . OMALIZUMAB dosage: 300 MG, UNK. During the same period patient was treated with FORMOTEROL, QVAR, SINGULAIR, SYMBICORT. Patient was hospitalized. Patient recovered.

Furosemide Side Effects Report #5680034-X
Physician from CHILE reported FUROSEMIDE problem on Mar 13, 2008. Female patient, 27 years of age, weighting 143.3 lb, was diagnosed with oedema and was treated with FUROSEMIDE. After drug was administered, patient experienced the following problems/side effects: blood albumin increased, blood calcium increased, blood chloride decreased, blood glucose increased, blood potassium decreased, blood sodium decreased, blood uric acid increased, dry skin, electrocardiogram st segment depression, . FUROSEMIDE dosage: 40 20 MG DAILY,. During the same period patient was treated with HERBAL NOS. Patient was hospitalized. Patient recovered.

Simvastatin Side Effects Report #5588244-7
SIMVASTATIN problem was reported by a Consumer or non-health professional from on Dec 24, 2007. Male patient, 24 years of age, was treated with SIMVASTATIN. After drug was administered, patient experienced the following problems/side effects: blood albumin increased, oedema, proteinuria, renal disorder, . SIMVASTATIN dosage: 10MG - QD - PO. During the same period patient was treated with ADALAT, SIROLIMUS, AZITHROMYCIN, FERROUS GLUCONATE, FUROSEMIDE, LANTUS, NOVORAPID. Patient was hospitalized. Patient recovered.


Morphine Side Effects Report #5509149-3
Health Professional from UNITED KINGDOM reported MORPHINE SULPHATE problem on Oct 31, 2007. Female patient, 30 years of age, weighting 158.7 lb, was diagnosed with pain, pruritus, psoriasis and was treated with MORPHINE SULPHATE. After drug was administered, patient experienced the following problems/side effects: blood albumin increased, blood calcium increased, caesarean section, face oedema, heart rate increased, hyperproteinaemia, psoriasis, . MORPHINE SULPHATE dosage: unknown. During the same period patient was treated with CHLORPHENIRAMINE, GENTAMICIN, METRONIDAZOLE, PARACETAMOL, LACTATE COMPOUNDECTION, CYCLOSPORINE, DEXAMETHASONE. Patient recovered.

Morphine Side Effects Report #5530471-9
MORPHINE SULPHATE problem was reported by a Health Professional from UNITED KINGDOM on Nov 21, 2007. Female patient, 30 years of age, weighting 158.7 lb, was diagnosed with pain, pruritus, psoriasis and was treated with MORPHINE SULPHATE. After drug was administered, patient experienced the following problems/side effects: blood albumin increased, blood calcium increased, eyelid oedema, face oedema, heart rate increased, hyperproteinaemia, . MORPHINE SULPHATE dosage: unknown. During the same period patient was treated with CHLORPHENIRAMINE, GENTAMICIN, METRONIDAZOLE, PARACETAMOL, LACTATE COMPOUNDECTION, CYCLOSPORINE, DEXAMETHASONE, ANADIN PARACETAMOL. Patient was hospitalized. Patient recovered.

Diclofenac Side Effects Report #5479256-2
Consumer or non-health professional from JAPAN reported DICLOFENAC problem on Sept 28, 2007. Male patient, 86 years of age, weighting 130.5 lb, was diagnosed with seronegative arthritis and was treated with DICLOFENAC. After drug was administered, patient experienced the following problems/side effects: blood albumin increased, colitis collagenous, colonoscopy, diarrhoea, haemoglobin decreased, hypoproteinaemia, red blood cell count decreased, . DICLOFENAC dosage: unknown. During the same period patient was treated with VALSARTAN, FUROSEMIDE, PREDNISOLONE, LANSOPRAZOLE, MISOPROSTOL, URSODIOL. Patient was hospitalized. Patient recovered.

Omniscan Side Effects Report #5481883-3
OMNISCAN problem was reported by a Physician from UNITED STATES on Sept 26, 2007. Female patient was treated with OMNISCAN. After drug was administered, patient experienced the following problems/side effects: blood albumin increased, nephrogenic systemic fibrosis, . OMNISCAN dosage: BETWEEN 15 AND 20 ML, SINGLE DOSE, IV. During the same period patient was treated with EPOGEN. Patient recovered.

Omniscan Side Effects Report #5481884-5
Physician from UNITED STATES reported OMNISCAN problem on Sept 26, 2007. Female patient was treated with OMNISCAN. After drug was administered, patient experienced the following problems/side effects: blood albumin increased, nephrogenic systemic fibrosis, . OMNISCAN dosage: BETWEEN 15 AND 20 ML, SINGLE DOSE, I.V.. Patient recovered.


Rebif Side Effects Report #5500126-5
REBIF problem was reported by a Physician from FRANCE on Oct 11, 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 albumin increased, blood calcium increased, contusion, fatigue, haematoma, idiopathic thrombocytopenic purpura, injection site reaction, multiple sclerosis relapse, . REBIF dosage: unknown. During the same period patient was treated with VENLAFAXINE, CLONAZEPAM, ZOLPIDEM TARTRATE, ORAL CONTRACEPTIVE. Patient was hospitalized. Patient recovered.

Diclofenac Side Effects Report #5467772-9
Consumer or non-health professional from JAPAN reported DICLOFENAC problem on Sept 18, 2007. Male patient, 86 years of age, was diagnosed with seronegative arthritis and was treated with DICLOFENAC. After drug was administered, patient experienced the following problems/side effects: blood albumin increased, colitis collagenous, diarrhoea, haemoglobin decreased, red blood cell count decreased, . DICLOFENAC dosage: unknown. Patient recovered.

Prednisone Side Effects Report #5395664-2
PREDNISONE problem was reported by a Consumer or non-health professional from on July 17, 2007. Female patient, 37 years of age, was treated with PREDNISONE. After drug was administered, patient experienced the following problems/side effects: blood albumin increased, blood creatinine increased, glomerulonephritis membranoproliferative, graft complication, nephropathy toxic, oedema peripheral, proteinuria, renal disorder, . PREDNISONE dosage: unknown. During the same period patient was treated with BASILIXIMAB, SIROLIMUS, MYCOPHENOLATE MOFETIL. Patient recovered.

Prednisone Side Effects Report #5395664-2
Consumer or non-health professional from reported PREDNISONE problem on July 17, 2007. Female patient, 37 years of age, was treated with PREDNISONE. After drug was administered, patient experienced the following problems/side effects: blood albumin increased, blood creatinine increased, glomerulonephritis membranoproliferative, graft complication, nephropathy toxic, oedema peripheral, proteinuria, renal disorder, . PREDNISONE dosage: unknown. During the same period patient was treated with BASILIXIMAB, SIROLIMUS, MYCOPHENOLATE MOFETIL. Patient recovered.

Tekturna Side Effects Report #5787793-6
TEKTURNA problem was reported by a Physician from UNITED STATES on June 17, 2008. Male patient, weighting 371.9 lb, was diagnosed with hypertension, type 2 diabetes mellitus, venous stasis and was treated with TEKTURNA. After drug was administered, patient experienced the following problems/side effects: blood albumin increased, blood calcium increased, blood creatinine increased, blood potassium increased, blood urea increased, orthostatic hypotension, protein total increased, renal failure acute, weight decreased, . TEKTURNA dosage: 300 MG, QD. During the same period patient was treated with METFORMIN, ATACAND, LASIX, COREG, AVANDARYL, VYTORIN, BYETTA. Patient recovered.


Coreg Side Effects Report #5731499-6
Physician from UNITED STATES reported COREG problem on May 01, 2008. Male patient, 56 years of age, weighting 371.9 lb, was diagnosed with hypertension, venous stasis, type 2 diabetes mellitus and was treated with COREG. After drug was administered, patient experienced the following problems/side effects: blood albumin increased, blood calcium increased, blood creatinine increased, blood potassium increased, blood urea increased, orthostatic hypotension, protein total increased, renal failure acute, weight decreased, . COREG dosage: unknown. During the same period patient was treated with VYTORIN, ATACAND, LASIX, TEKTURNA, METFORMIN, AVANDARYL, BYETTA. Patient recovered.

Ambisome Side Effects Report #5346700-0
AMBISOME problem was reported by a Consumer or non-health professional from JAPAN on May 17, 2007. Female patient, 92 years of age, was diagnosed with meningitis cryptococcal and was treated with AMBISOME. After drug was administered, patient experienced the following problems/side effects: blood albumin increased, cardiac failure, mitral valve incompetence, renal impairment, tricuspid valve incompetence, urinary tract infection, . AMBISOME dosage: 135 MG, UID/QD. During the same period patient was treated with MEROPENEM TRIHYDRATE, MEROPENEM TRIHYDRATE, FIRSTCIN, MUCOSTA, LANSOPRAZOLE, LAC B, MAGMITT, CALONAL. Patient died on 01/27/2007.

Cyclosporine Side Effects Report #5350482-6
Health Professional from FRANCE reported CYCLOSPORINE problem on May 29, 2007. Male patient, 46 years of age, was diagnosed with renal transplant and was treated with CYCLOSPORINE. After drug was administered, patient experienced the following problems/side effects: blood albumin increased, blood creatinine increased, complications of transplanted kidney, dialysis, disease recurrence, focal glomerulosclerosis, proteinuria, . CYCLOSPORINE dosage: 4 MG/DAY. During the same period patient was treated with BASILIXIMAB, MYCOPHENOLATE MOFETIL, PREDNISOLONE, METHYLPREDNISOLONE. Patient was hospitalized. Patient recovered.

Enalapril Side Effects Report #5363463-3
ENALAPRIL MALEATE problem was reported by a Physician from NETHERLANDS on May 31, 2007. Male patient, 43 years of age, was diagnosed with hypertension and was treated with ENALAPRIL MALEATE. After drug was administered, patient experienced the following problems/side effects: blood albumin increased, blood pressure increased, . ENALAPRIL MALEATE dosage: 10 MG BID ORAL. During the same period patient was treated with NIFEDIPINE, HYDROCHLOROTHIAZDE, ATENOLOL. Patient was hospitalized. Patient recovered.

Avandia Side Effects Report #5369525-9
Physician from AUSTRALIA reported AVANDIA problem on June 15, 2007. Male patient, 51 years of age, weighting 229.3 lb, was treated with AVANDIA. After drug was administered, patient experienced the following problems/side effects: blood albumin increased, blood chloride decreased, blood cholesterol increased, blood glucose increased, blood urea increased, dyspnoea, gamma-glutamyltransferase increased, pulmonary oedema, weight increased, . AVANDIA dosage: 8MG PER DAY. During the same period patient was treated with SULFONYLUREA, STATINS, ACE INHIBITOR, ASPIRIN, LIPIDIL, NOTEN, NATRILIX, DIABEX. Patient recovered.


Avandia Side Effects Report #5373533-1
AVANDIA problem was reported by a Physician from UNITED KINGDOM on June 18, 2007. Male patient, 71 years of age, weighting 142.2 lb, was diagnosed with diabetes mellitus non-insulin-dependent and was treated with AVANDIA. After drug was administered, patient experienced the following problems/side effects: blood albumin increased, blood glucose increased, cardiac failure, cardiomegaly, dyspnoea, dyspnoea exertional, electrocardiogram poor r-wave progression, electrocardiogram t wave amplitude decreased, gallop rhythm present, . AVANDIA dosage: unknown. During the same period patient was treated with METFORMIN, SIMVASTATIN, PERINDOPRIL, INSULIN, INDAPAMIDE, ACARBOSE, BENDROFLUAZIDE, BEGRIVAC. Patient was hospitalized and became disabled. Patient recovered.

Veregen Side Effects Report #5331701-9
Consumer or non-health professional from UNITED STATES reported VEREGEN GREEN TEA problem on May 08, 2007. Female patient, 37 years of age, was diagnosed with weight control and was treated with VEREGEN GREEN TEA. After drug was administered, patient experienced the following problems/side effects: blood albumin increased, hepatic necrosis, hepatitis, . VEREGEN GREEN TEA dosage: 128 MG/CAPSULE ORAL 4 MONTHS IN 2005. Patient recovered.

Lapatinib Side Effects Report #5296209-8
LAPATINIB problem was reported by a Physician from CZECH REPUBLIC on Apr 06, 2007. Female patient, 65 years of age, weighting 110.2 lb, was diagnosed with breast cancer metastatic, metastases to bone and was treated with LAPATINIB. After drug was administered, patient experienced the following problems/side effects: blood albumin increased, blood bilirubin increased, blood glucose increased, diarrhoea, fatigue, subileus, vomiting, . LAPATINIB dosage: 1250MG PER DAY. During the same period patient was treated with CAPECITABINE, ZOMETA. Patient was hospitalized. Patient recovered.

Pravastatin Side Effects Report #5313721-3
Consumer or non-health professional from GERMANY reported PRAVASTATIN problem on Apr 13, 2007. Female patient, 49 years of age, was diagnosed with hypercholesterolaemia and was treated with PRAVASTATIN. After drug was administered, patient experienced the following problems/side effects: blood albumin increased, glossodynia, immunoglobulins decreased, laryngeal oedema, myosclerosis, paraesthesia oral, pericardial effusion, sensation of foreign body, transaminases increased, . PRAVASTATIN dosage: unknown. During the same period patient was treated with SORTIS. Patient recovered.

Ventolin Side Effects Report #5256493-3
VENTOLIN problem was reported by a Consumer or non-health professional from GREECE on Feb 23, 2007. Male patient, 24 years of age, was treated with VENTOLIN. After drug was administered, patient experienced the following problems/side effects: blood albumin increased, blood creatine phosphokinase increased, transaminases increased, . VENTOLIN dosage: unknown. During the same period patient was treated with CO Q. Patient recovered.

Amoxicillin Side Effects Report #5680464-6
Pharmacist from UNITED KINGDOM reported AMOXICILLIN problem on Mar 17, 2008. Male patient, 86 years of age, was treated with AMOXICILLIN. After drug was administered, patient experienced the following problems/side effects: alanine aminotransferase increased, blood albumin increased, blood alkaline phosphatase increased, blood cholesterol increased, c-reactive protein increased, haemoglobin decreased, international normalised ratio increased, jaundice, protein total decreased, . AMOXICILLIN dosage: unknown. During the same period patient was treated with ATENOLOL, BENDROFLUAZIDE, URSODIOL, CHLORPHENAMINE, AQUEOUS CREAM, LACTULOSE, PREDNISOLONE. Patient was hospitalized. Patient recovered.

Zyvox Side Effects Report #5577337-6
ZYVOX problem was reported by a Physician from UNITED STATES on Dec 19, 2007. Female patient, 57 years of age, weighting 211.6 lb, was diagnosed with cellulitis, enterococcal infection and was treated with ZYVOX. After drug was administered, patient experienced the following problems/side effects: acidosis, blood albumin increased, blood bicarbonate decreased, blood lactic acid increased, blood ph decreased, dyspnoea, hypoventilation, lactic acidosis, respiratory failure, . ZYVOX dosage: unknown. Patient was hospitalized. Patient died on 10/28/2007.

Exjade Side Effects Report #5474998-7
Physician from UNITED STATES reported EXJADE problem on Sept 25, 2007. Female patient, 46 years of age, was diagnosed with iron overload and was treated with EXJADE. After drug was administered, patient experienced the following problems/side effects: anuria, blood albumin increased, blood creatinine increased, blood potassium increased, blood urea increased, blood urine present, cardiac failure congestive, dialysis, haemoglobin decreased, . EXJADE dosage: 1250 MG, QD. Patient recovered.

Amiodarone Side Effects Report #5488998-4
AMIODARONE problem was reported by a Consumer or non-health professional from ISRAEL on Oct 01, 2007. Female patient, 62 years of age, was diagnosed with atrial fibrillation and was treated with AMIODARONE. After drug was administered, patient experienced the following problems/side effects: atrial fibrillation, blood albumin increased, blood glucose increased, blood osmolarity decreased, blood pressure diastolic increased, chest pain, heart rate increased, heart rate irregular, hyponatraemia, . AMIODARONE dosage: 300 MG (1 IN 1 D). During the same period patient was treated with FAMOTIDINE, LORAZEPAM. Patient was hospitalized. Patient recovered.

Forteo Side Effects Report #5493472-5
Consumer or non-health professional from FRANCE reported FORTEO problem on Oct 10, 2007. Female patient, 76 years of age, was diagnosed with osteoporosis, atrial fibrillation and was treated with FORTEO. After drug was administered, patient experienced the following problems/side effects: albumin urine present, blood albumin increased, . FORTEO dosage: unknown. During the same period patient was treated with PREVISCAN. Patient recovered.

Exjade Side Effects Report #5432978-1
EXJADE problem was reported by a Physician from UNITED STATES on Aug 24, 2007. Female patient, 46 years of age, was diagnosed with iron overload and was treated with EXJADE. After drug was administered, patient experienced the following problems/side effects: anuria, blood albumin increased, blood creatinine increased, blood potassium increased, blood urea increased, blood urine present, cardiac failure congestive, dialysis, haemoglobin decreased, . EXJADE dosage: 1250 MG, QD. Patient recovered.

Amoxicillin Side Effects Report #5743735-0
Consumer or non-health professional from UNITED KINGDOM reported AMOXICILLIN problem on May 06, 2008. Male patient, 86 years of age, was treated with AMOXICILLIN. After drug was administered, patient experienced the following problems/side effects: alanine aminotransferase increased, blood albumin increased, blood alkaline phosphatase increased, blood cholesterol increased, c-reactive protein increased, international normalised ratio increased, jaundice, . AMOXICILLIN dosage: unknown. During the same period patient was treated with ATENOLOL, AQUEOUS CREAM, BENDROFLUOZIDE, CHLORPHENAMINE, LACTULOSE, MENTHOL, PREDNISOLONE, URSODIOL. Patient was hospitalized. Patient recovered.

Acetaminophen Side Effects Report #5713044-4
ACETAMINOPHEN problem was reported by a Consumer or non-health professional from UNITED KINGDOM on Apr 09, 2008. Male patient, 53 years of age, was diagnosed with analgesia and was treated with ACETAMINOPHEN. After drug was administered, patient experienced the following problems/side effects: anion gap increased, blood albumin increased, blood alkaline phosphatase increased, blood chloride increased, blood sodium increased, disorientation, metabolic acidosis, myocardial infarction, . ACETAMINOPHEN dosage: unknown. During the same period patient was treated with DICLOFENAC, AMOXICILLIN, GENTAMICIN, METRONIDAZOLE, LEVOFLOXACIN, VANCOMYCIN, OMEPRAZOLE, METOCLOPRAMIDE. Patient was hospitalized. Patient died.

Indomethacin Side Effects Report #5713773-2
Consumer or non-health professional from UNITED STATES reported INDOMETHACIN problem on Apr 14, 2008. Female patient, 47 years of age, was diagnosed with osteoarthritis and was treated with INDOMETHACIN. After drug was administered, patient experienced the following problems/side effects: autoimmune hepatitis, blood albumin increased, hepatitis acute, international normalised ratio increased, pancytopenia, prothrombin time prolonged, . INDOMETHACIN dosage: 50 MG BID. During the same period patient was treated with METOPROLOL TARTRATE. Patient recovered.

Avandia Side Effects Report #5370783-5
AVANDIA problem was reported by a Physician from AUSTRALIA on June 18, 2007. Male patient, 74 years of age, weighting 66.14 lb, was diagnosed with asthma, left ventricular failure and was treated with AVANDIA. After drug was administered, patient experienced the following problems/side effects: alanine aminotransferase increased, blood albumin increased, blood calcium increased, blood chloride decreased, blood creatinine increased, blood glucose increased, blood potassium increased, blood urea increased, blood uric acid increased, . AVANDIA dosage: 8MG PER DAY. During the same period patient was treated with PANTOPRAZOLE, GOPTEN, CARVEDILOL, SYMBICORT, DAONIL, ASPIRIN, UREMIDE. Patient recovered.

Prograf Side Effects Report #5616236-8
Physician from CANADA reported PROGRAF problem on Jan 25, 2008. Female patient, 58 years of age, was diagnosed with liver transplant and was treated with PROGRAF. After drug was administered, patient experienced the following problems/side effects: abscess, bacterial infection, blood albumin increased, diarrhoea, erythema, escherichia infection, fatigue, inflammation, liver disorder, . PROGRAF dosage: 2 MG, BID, ORAL. During the same period patient was treated with SPIRONOLACTONE, FUROSEMIDE, RIFAMPICIN, URSODIOL. Patient recovered.

Thalomid Side Effects Report #5771373-2
THALOMID problem was reported by a Physician from UNITED STATES on June 02, 2008. Female patient, 53 years of age, was diagnosed with systemic lupus erythematosus and was treated with THALOMID. After drug was administered, patient experienced the following problems/side effects: aspartate aminotransferase increased, bilirubin conjugated increased, blood albumin increased, blood alkaline phosphatase increased, blood bilirubin increased, condition aggravated, hepatotoxicity, protein total increased, . THALOMID dosage: unknown. During the same period patient was treated with PLAQUENIL, PROPRANOL, ALDACTONE, PREVACIDE. Patient recovered.

Exjade Side Effects Report #5792136-8
Physician from UNITED STATES reported EXJADE problem on June 24, 2008. Female patient, weighting 209.0 lb, was diagnosed with iron overload and was treated with EXJADE. After drug was administered, patient experienced the following problems/side effects: aneurysm, aspartate aminotransferase increased, blood albumin increased, blood alkaline phosphatase increased, blood bilirubin increased, blood bilirubin unconjugated increased, blood chloride increased, blood sodium increased, chest pain, . EXJADE dosage: unknown. During the same period patient was treated with MS CONTIN, LORCET, PLAVIX, FOLIC ACID, ADVAIR DISKUS, NORVASC, HYDROCHLOROTHIAZIDE. Patient died on 01/21/2008.

Tysabri Side Effects Report #5717018-9
TYSABRI problem was reported by a Health Professional from UNITED STATES on Apr 09, 2008. Female patient, 60 years of age, weighting 154.8 lb, was diagnosed with multiple sclerosis and was treated with TYSABRI. After drug was administered, patient experienced the following problems/side effects: adrenal adenoma, aspartate aminotransferase increased, blood albumin increased, blood glucose increased, blood potassium increased, blood urea decreased, chest pain, emphysema, gait disturbance, . TYSABRI dosage: 300 MG; QM; IV. During the same period patient was treated with PROVIGIL, SINGULAIR, PRILOSEC, LYRICA, THEOPHYLLINE, LIDOCAINE, CALCIUM. Patient was hospitalized. Patient recovered.

Acetaminophen Side Effects Report #5724317-3
Health Professional from UNITED KINGDOM reported ACETAMINOPHEN problem on Apr 18, 2008. Female patient, 30 years of age, was treated with ACETAMINOPHEN. After drug was administered, patient experienced the following problems/side effects: agitation, base excess, blood albumin increased, blood bicarbonate decreased, blood creatinine increased, blood lactic acid increased, blood potassium increased, blood pressure increased, brain scan abnormal, . ACETAMINOPHEN dosage: unknown. Patient was hospitalized. Patient recovered.

Magnevist Side Effects Report #5333870-3
MAGNEVIST problem was reported by a Health Professional from UNITED STATES on May 10, 2007. Female patient, 77 years of age, weighting 188.0 lb, was diagnosed with nuclear magnetic resonance imaging, pneumonia and was treated with MAGNEVIST. After drug was administered, patient experienced the following problems/side effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood albumin increased, blood glucose increased, haematocrit decreased, haemoglobin decreased, international normalised ratio increased, nephrogenic fibrosing dermopathy, pallor, . MAGNEVIST dosage: 20 ML, 1 DOSE. During the same period patient was treated with COUMADIN, LEVAQUIN, BETA BLOCKING AGENTS. Patient died on 08/10/2005.