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BLOOD UREA ABNORMAL side effect

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Lithium Side Effects Report #5423097-9
Physician from INDIA reported LITHIUM CARBONATE problem on Aug 07, 2007. Female patient, 16 years of age, was treated with LITHIUM CARBONATE. After drug was administered, patient experienced the following problems/side effects: blood urea abnormal, blood urea increased, catatonia, decreased appetite, dehydration, diet refusal, hyperreflexia, immobile, mutism, . LITHIUM CARBONATE dosage: 1200 MG, QD. Patient was hospitalized. Patient recovered.

Velcade Side Effects Report #5615699-1
VELCADE problem was reported by a Physician from JAPAN on Jan 22, 2008. Male patient, 77 years of age, weighting 143.3 lb, was diagnosed with multiple myeloma and was treated with VELCADE. After drug was administered, patient experienced the following problems/side effects: blood creatinine increased, blood urea abnormal, disease progression, dyspnoea, metabolic acidosis, oedema, tumour lysis syndrome, weight increased, . VELCADE dosage: 1.60 MG, INTRAVENOUS. During the same period patient was treated with DEXAMETHASONE, FAMOTIDINE, SELBEX, BAKTAR, ALLOPURINOL, METHYCOBAL. Patient died on 08/03/2007.

Thyrogen Side Effects Report #5648092-6
Physician from ARGENTINA reported THYROGEN problem 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.

Tekturna Side Effects Report #5641668-1
TEKTURNA problem was reported by a Physician from UNITED STATES on Nov 19, 2007. Male patient, 57 years of age, weighting 201.9 lb, was diagnosed with hypertension and was treated with TEKTURNA. After drug was administered, patient experienced the following problems/side effects: blood creatinine abnormal, blood urea abnormal, joint swelling, pain, . TEKTURNA dosage: 300 MG, QD, ORAL. During the same period patient was treated with ATACAND, LIPITOR, COVERA, LANOXIN. Patient recovered.


Seroquel Side Effects Report #5460295-2
Physician from UNITED STATES reported SEROQUEL problem on June 20, 2007. Male patient, 33 years of age, was diagnosed with bipolar disorder and was treated with SEROQUEL. After drug was administered, patient experienced the following problems/side effects: blood creatine abnormal, blood urea abnormal, . SEROQUEL dosage: unknown. Patient recovered.

Fosrenol Side Effects Report #5460946-2
FOSRENOL problem was reported by a Physician from UNITED STATES on June 19, 2007. Female patient, 60 years of age, weighting 244.9 lb, was diagnosed with hyperphosphataemia and was treated with FOSRENOL. After drug was administered, patient experienced the following problems/side effects: blood calcium abnormal, blood urea abnormal, swollen tongue, urea renal clearance decreased, . FOSRENOL dosage: 1000 MG TID, ORAL; 250 MG WITH MEALS. During the same period patient was treated with PHOSLO, TOPROL, DONNATAL L, LOMOTIL, OXYCODONE, LEVOXYL, CYCLOBENZAPRINE. Patient recovered.

Cozaar Side Effects Report #5370582-4
Physician from CANADA reported COZAAR problem on June 21, 2007. Female patient, 80 years of age, was diagnosed with hypertension and was treated with COZAAR. After drug was administered, patient experienced the following problems/side effects: blood creatinine increased, blood urea abnormal, dementia, . COZAAR dosage: unknown. Patient recovered.

Zoloft Side Effects Report #5381495-6
ZOLOFT problem was reported by a Health Professional from UNITED STATES on Feb 06, 2007. Female patient, 47 years of age, weighting 115.1 lb, was diagnosed with myelodysplastic syndrome and was treated with ZOLOFT. After drug was administered, patient experienced the following problems/side effects: blood creatinine abnormal, blood urea abnormal, pancreatitis, . ZOLOFT dosage: 100 MG (100 MG, 1 IN 1 D);. During the same period patient was treated with AZACITIDINE, QUINAPRIL AND HYDROCHLOROTHIAZIDE, PRAVASTATIN, NISOLDIPINE, LORATADINE, ACCURETIC. Patient was hospitalized. Patient recovered.

Humira Side Effects Report #5614087-1
Consumer or non-health professional from BRAZIL reported HUMIRA problem on Jan 31, 2008. Female patient, weighting 85.98 lb, was diagnosed with rheumatoid arthritis, pain and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: anaemia, blood creatinine abnormal, blood urea abnormal, c-reactive protein increased, rheumatoid factor increased, scar, sepsis, streptococcal identification test positive, . HUMIRA dosage: unknown. During the same period patient was treated with PREDNISONE, TRAMADOL. Patient was hospitalized. Patient died on 01/07/2008.


Boniva Side Effects Report #5570872-6
BONIVA problem was reported by a Consumer or non-health professional from UNITED STATES on Dec 14, 2007. Female patient, 91 years of age, was diagnosed with osteoporosis and was treated with BONIVA. After drug was administered, patient experienced the following problems/side effects: anaemia, blood creatinine abnormal, blood urea abnormal, diarrhoea, fall, nausea, urinary tract infection, vomiting, . BONIVA dosage: unknown. During the same period patient was treated with VITAMIN D, CALCIUM, GABAPENTIN, DICLOFENAC, VITAMINS NOS, ARICEPT. Patient was hospitalized. Patient recovered.

Letrozole Side Effects Report #5491492-8
Health Professional from UNITED STATES reported LETROZOLE problem on Oct 11, 2007. Female patient, 66 years of age, weighting 238.0 lb, was diagnosed with breast cancer metastatic and was treated with LETROZOLE. After drug was administered, patient experienced the following problems/side effects: blood creatinine abnormal, blood disorder, blood urea abnormal, dehydration, diarrhoea, dysphagia, epistaxis, exercise tolerance decreased, myalgia, . LETROZOLE dosage: 2.5 MG, QD. During the same period patient was treated with LUNESTA, ADVIL LIQUI, TARCEVA, LEVOTHYROXINE, SYNTHROID, CARDURA, IMODIUM, ACCUPRIL. Patient was hospitalized. Patient recovered.

Boniva Side Effects Report #5690219-4
BONIVA problem was reported by a Physician from UNITED STATES on Mar 24, 2008. Female patient, 91 years of age, was diagnosed with osteoporosis and was treated with BONIVA. After drug was administered, patient experienced the following problems/side effects: anaemia, blood creatinine abnormal, blood urea abnormal, diarrhoea, fall, nausea, urinary tract infection, vomiting, . BONIVA dosage: unknown. During the same period patient was treated with VITAMIN D, CALCIUM, GABAPENTIN, DICLOFENAC, VITAMINS NOS, ARICEPT. Patient was hospitalized. Patient recovered.

Warfarin Side Effects Report #5359384-2
Physician from UNITED KINGDOM reported WARFARIN problem on June 11, 2007. Female patient, 72 years of age, was treated with WARFARIN. After drug was administered, patient experienced the following problems/side effects: arrhythmia, blood electrolytes abnormal, blood urea abnormal, cardiac failure congestive, confusional state, decreased appetite, hypoventilation, international normalised ratio increased, malaise, . WARFARIN dosage: unknown. During the same period patient was treated with VERAPAMIL, DIGOXIN, METOLAZONE. Patient was hospitalized. Patient died on 07/13/2006.

Zevalin Side Effects Report #5371776-4
ZEVALIN problem was reported by a Health Professional from TAIWAN, PROVINCE OF CHINA on May 22, 2007. Female patient, 82 years of age, was diagnosed with b-cell lymphoma and was treated with ZEVALIN. After drug was administered, patient experienced the following problems/side effects: abscess oral, blood urea abnormal, headache, metastatic neoplasm, oedema peripheral, pyrexia, white blood cell count decreased, . ZEVALIN dosage: unknown. During the same period patient was treated with RITUXIMAB. Patient was hospitalized. Patient recovered.


Humalog Side Effects Report #5383089-5
Consumer or non-health professional from UNITED STATES reported HUMALOG problem on Jan 23, 2007. Male patient, 51 years of age, was diagnosed with diabetes mellitus and was treated with HUMALOG. After drug was administered, patient experienced the following problems/side effects: blood cholesterol, blood creatine abnormal, blood urea abnormal, cataract, hypertension, muscle spasms, neuropathy peripheral, renal disorder, . HUMALOG dosage: unknown. During the same period patient was treated with LANTUS, CRESTOR, AMBIEN. Patient was hospitalized. Patient recovered.