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The dose dependency of the pharmacokinetics of dexamethasone and its influence on the endogenous secretion of cortisol has been studied in healthy females. The maximum plasma level occurred between 1. AUC, distribution volume, plasma clearance and c max did not increase in proportion to the dose but only by the factor of about 0. Comparatively high values https://www.healthgrades.com were reached after 3. This may be due to reduced bioavailability of the oral doses. Within the first 12 h after the administration of 0. In the case of administration every second day, the integral reduction within 24 h after the administration of 0. Rent this article via DeepDyve. Br J Clin Pharmacol — J Clin Endocrinol Metab
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Dexamethasone is a type of corticosteroid medication. The long-term use of dexamethasone may result in thrush, bone loss, cataracts, easy bruising, or muscle weakness.
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Ingrid (taken for 1 to 6 years) 19.01.2017
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What is dexamethasone, and how does it work mechanism of action? Dexamethasone is a synthetic man-made corticosteroid. Corticosteroids are naturally-occurring chemicals produced by the adrenal glands located above the kidneys.
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