leukocyte vs leuсocyte

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• The BAL fluid may be analysed for total and differential leukocyte counts, total protein, and lactate dehydrogenase.
• Leukocyte and histamine levels are normal.
• If leukocyte counts exceed 50 x 109/ l after the expected nadir, filgrastim should be discontinued immediately.
• It reduces leukocyte infiltration into the inflamed tissue.
• Decreased serum estradiol and progesterone concentrations have been lon reported in women treated with human leukocyte interferon.
• Decreased serum estradiol and progesterone concentrations have been reported in women treated with human leukocyte interferon.
• Positive dipstick for leukocyte esterase and/or nitrate
• Preclinical data from conventional studies of repeated dose toxicity revealed the expected pharmacological effects including increases in leukocyte count, myeloid hyperplasia in bone marrow, extramedullary haematopoiesis and splenic enlargement.
• Those are the only people who are a match for Nesbit's blood type and human leukocyte antigen.
• However, during the period of administration of filgrastim for PBPC mobilisation, it should be discontinued or its dose should be reduced if the leukocyte counts rise to > 70 x 109/ l.
• Decreased serum estradiol and progesterone concentrations have been reported in women treated with human leukocyte interferon. na
• It is recommended that chemotherapy not be added to treatment with steroids since there is no experience with administration of both steroids and chemotherapy during treatment of the leukocyte activation syndrome due to TRISENOX.
• Leukocyte and histamine levels are normal.
• Leukocyte Activation Syndrome (APL Differentiation Syndrome):
• pharmacological effects including increases in leukocyte count, myeloid hyperplasia in bone marrow, od
• International Units are determined by comparison of the activity of the recombinant interferon alfa-2b with the activity of the international reference preparation of human leukocyte interferon established by the World Health Organisation.
• recombinant interferon alfa-2b with the activity of the international reference preparation of human leukocyte interferon established by the World Health Organisation. na
• Cetuximab has not been studied in patients presenting with one or more of the following laboratory parameters: haemoglobin < 9 g/ dl leukocyte count < 3000/ mm³ absolute neutrophil count < 1500/ mm³ platelet count < 100000/ mm³
• This is a human leukocyte workup.
• If leukocyte counts exceed 50 x 109/ l after the expected nadir, filgrastim should be discontinued immediately.

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