ALBUMIN GLOBULIN RATIO DECREASED side effect
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Drugs associated with ALBUMIN GLOBULIN RATIO DECREASED
AREDIA DIOVAN HUMIRA LIALDA RECLAST RISEDRONATE SULFACETAMIDE VALTREXReclast Side Effects Report #5600424-0
Consumer or non-health professional from UNITED STATES reported RECLAST problem on Jan 15, 2008. Male patient, 64 years of age, weighting 189.6 lb, was diagnosed with arrhythmia and was treated with RECLAST. After drug was administered, patient experienced the following problems/side effects: albumin globulin ratio decreased, atrial fibrillation, blood bilirubin increased, blood chloride increased, fatigue, feeling abnormal, hypocalcaemia, muscle spasms, oedema peripheral, . RECLAST dosage: unknown. During the same period patient was treated with RYTHMOL, VITAMIN CAP, COUMADIN. Patient was hospitalized. Patient recovered.
Sulfacetamide Side Effects Report #5503732-7
SULFACETAMIDE problem was reported by a Physician from UNITED STATES on Oct 17, 2007. Female patient, 72 years of age, weighting 123.5 lb, was diagnosed with conjunctivitis allergic and was treated with SULFACETAMIDE. After drug was administered, patient experienced the following problems/side effects: albumin globulin ratio decreased, blood albumin decreased, blood glucose increased, blood pressure increased, blood urea increased, blood urea nitrogen/creatinine ratio increased, cellulitis orbital, conjunctivitis, facial pain, . SULFACETAMIDE dosage: unknown. During the same period patient was treated with ERYTHROMYCIN, NATTOKINASE, RED YEAST RICE, VITAMIN E, ASCORBIC ACID, MOTRIN, ASPIRIN, CALCIUM. Patient was hospitalized. Patient recovered.
Reclast Side Effects Report #5505170-X
Consumer or non-health professional from UNITED STATES reported RECLAST problem on Oct 25, 2007. Male patient, 64 years of age, weighting 189.6 lb, was treated with RECLAST. After drug was administered, patient experienced the following problems/side effects: albumin globulin ratio decreased, atrial fibrillation, blood bilirubin increased, blood chloride increased, fatigue, feeling abnormal, hypocalcaemia, muscle spasms, oedema peripheral, . RECLAST dosage: unknown. During the same period patient was treated with RYTHMOL, VITAMIN CAP, COUMADIN. Patient was hospitalized. Patient recovered.
Risedronate Side Effects Report #5485938-9
RISEDRONATE problem was reported by a Physician from JAPAN on Sept 27, 2007. Female patient, 80 years of age, was diagnosed with osteoporosis and was treated with RISEDRONATE. After drug was administered, patient experienced the following problems/side effects: albumin globulin ratio decreased, alpha globulin increased, blood albumin decreased, blood cholinesterase decreased, immunoglobulins increased, monocyte count increased, neutrophil count increased, osteomyelitis, pain in jaw, . RISEDRONATE dosage: 2.5 MG DAILY, ORAL. During the same period patient was treated with CANDESARTAN CILEXETIL, PRAVASTATIN, NILZIPIN, SIGMART. Patient was hospitalized. Patient recovered.
Valtrex Side Effects Report #5403984-8
Physician from JAPAN reported VALTREX problem on July 27, 2007. Female patient, 87 years of age, weighting 94.80 lb, was diagnosed with facial palsy, hypothyroidism, hypertension, insomnia, gastritis and was treated with VALTREX. After drug was administered, patient experienced the following problems/side effects: albumin globulin ratio decreased, basophil count increased, blood albumin decreased, blood alkaline phosphatase increased, blood calcium increased, blood cholinesterase decreased, blood creatinine increased, blood lactate dehydrogenase increased, blood phosphorus, . VALTREX dosage: 500MG PER DAY. During the same period patient was treated with THYRADIN, ENALAPRIL MALEATE, OLMESARTAN MEDOXOMIL, ATELEC, NITRAZEPAM, METHYCOBAL, SELBEX, ALFAROL. Patient was hospitalized. Patient recovered.
Valtrex Side Effects Report #5386580-0
VALTREX problem was reported by a Physician from JAPAN on July 09, 2007. Female patient, 87 years of age, weighting 94.80 lb, was diagnosed with facial palsy, hypothyroidism, hypertension, insomnia, gastritis and was treated with VALTREX. After drug was administered, patient experienced the following problems/side effects: albumin globulin ratio decreased, basophil count increased, blood albumin decreased, blood alkaline phosphatase increased, blood calcium increased, blood cholinesterase decreased, blood creatinine increased, blood lactate dehydrogenase increased, blood phosphorus, . VALTREX dosage: 500MG PER DAY. During the same period patient was treated with THYRADIN, RENIVACE, OLMESARTAN MEDOXOMIL, ATELEC, NITRAZEPAM, CYANOCOBALAMIN, SELBEX, ALFAROL. Patient was hospitalized. Patient recovered.
Valtrex Side Effects Report #5386580-0
Physician from JAPAN reported VALTREX problem on July 09, 2007. Female patient, 87 years of age, weighting 94.80 lb, was diagnosed with facial palsy, hypothyroidism, hypertension, insomnia, gastritis and was treated with VALTREX. After drug was administered, patient experienced the following problems/side effects: albumin globulin ratio decreased, basophil count increased, blood albumin decreased, blood alkaline phosphatase increased, blood calcium increased, blood cholinesterase decreased, blood creatinine increased, blood lactate dehydrogenase increased, blood phosphorus, . VALTREX dosage: 500MG PER DAY. During the same period patient was treated with THYRADIN, RENIVACE, OLMESARTAN MEDOXOMIL, ATELEC, NITRAZEPAM, CYANOCOBALAMIN, SELBEX, ALFAROL. Patient was hospitalized. Patient recovered.
Humira Side Effects Report #5760265-0
HUMIRA problem was reported by a Consumer or non-health professional from UNITED STATES on May 29, 2008. Female patient, weighting 210.2 lb, was diagnosed with rheumatoid arthritis, blood pressure, diabetes mellitus, gastrooesophageal reflux disease, fibromyalgia, hypersensitivity, vitamin supplementation, anxiety and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: albumin globulin ratio decreased, blood chloride decreased, blood urea nitrogen/creatinine ratio increased, injection site irritation, injection site pain, intervertebral disc protrusion, mean platelet volume decreased, white blood cell count increased, . HUMIRA dosage: unknown. During the same period patient was treated with ATENOLOL, INSULIN GLARGINE, ESOMEPRAZOLE MAGNESIUM, PREGABALIN, MONTELUKAST, FOLIC ACID, LORAZEPAM. Patient was hospitalized. Patient recovered.
Lialda Side Effects Report #5637738-4
Physician from UNITED STATES reported LIALDA problem on Feb 05, 2008. Female patient, 46 years of age, was diagnosed with colitis ulcerative and was treated with LIALDA. After drug was administered, patient experienced the following problems/side effects: alanine aminotransferase increased, albumin globulin ratio decreased, aspartate aminotransferase increased, bilirubin conjugated increased, blood alkaline phosphatase increased, blood glucose increased, chromaturia, gallbladder disorder, hepatic enzyme increased, . LIALDA dosage: unknown. Patient recovered.
Diovan Side Effects Report #5399181-5
DIOVAN problem was reported by a Pharmacist from JAPAN on June 27, 2007. Male patient, 68 years of age, weighting 105.8 lb, was diagnosed with hypertension and was treated with DIOVAN. After drug was administered, patient experienced the following problems/side effects: alanine aminotransferase increased, albumin globulin ratio decreased, aspartate aminotransferase increased, blood albumin decreased, blood chloride increased, blood creatine phosphokinase increased, blood creatinine increased, blood lactate dehydrogenase increased, blood sodium increased, . DIOVAN dosage: 80 MG, BID. During the same period patient was treated with AMIODARONE. Patient recovered.
Diovan Side Effects Report #5399181-5
Pharmacist from JAPAN reported DIOVAN problem on June 27, 2007. Male patient, 68 years of age, weighting 105.8 lb, was diagnosed with hypertension and was treated with DIOVAN. After drug was administered, patient experienced the following problems/side effects: alanine aminotransferase increased, albumin globulin ratio decreased, aspartate aminotransferase increased, blood albumin decreased, blood chloride increased, blood creatine phosphokinase increased, blood creatinine increased, blood lactate dehydrogenase increased, blood sodium increased, . DIOVAN dosage: 80 MG, BID. During the same period patient was treated with AMIODARONE. Patient recovered.
Aredia Side Effects Report #5287706-X
AREDIA problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 26, 2007. Female patient, 70 years of age, was diagnosed with osteoporosis and was treated with AREDIA. After drug was administered, patient experienced the following problems/side effects: activated partial thromboplastin time prolonged, albumin globulin ratio decreased, biopsy kidney abnormal, blood albumin decreased, blood calcium decreased, blood creatinine increased, blood glucose increased, blood urea increased, cachexia, . AREDIA dosage: 45MG QMOS. During the same period patient was treated with PREDNISONE, ATENOLOL, LISINOPRIL, NORVASC, ASPIRIN, MAGNESIUM OXIDE, LASIX. Patient was hospitalized. Patient recovered.
Aredia Side Effects Report #5297576-1
Physician from UNITED STATES reported AREDIA problem on Apr 03, 2007. Female patient, 70 years of age, was diagnosed with osteoporosis and was treated with AREDIA. After drug was administered, patient experienced the following problems/side effects: activated partial thromboplastin time prolonged, albumin globulin ratio decreased, anorexia, biopsy kidney abnormal, blood albumin decreased, blood calcium decreased, blood creatinine increased, blood glucose increased, blood urea increased, . AREDIA dosage: 45MG QMOS. During the same period patient was treated with PREDNISONE, ATENOLOL, LISINOPRIL, NORVASC, ASPIRIN, MAGNESIUM OXIDE, LASIX. Patient was hospitalized. Patient recovered.