_____ is an allosteric activator of the Ca2+ sensing (CaSR) receptor on the Parathyroid Gland
_____ is a drug that inhibits glucocorticoid biosynthesis via inhibition of the enzyme 11-hydroxylase
_____ may be used in the treatment of primary or secondary hyperparathyroidism by increasing the sensitivity of calcium-sensing receptors to extracellular calcium.
What type(s) of diabetes may be treated with sulfonylureas and meglitinides? _____
_____, with hard exudates surrounding the blood vessels is a rare adverse effect seen with thiazolidinediones
The azole _____ inhibits the adrenal enzyme 17,20-desmolase
_____ inhibits the synthesis of glucocorticoids by inhibiting steroid 11-hydroxylase reversibly.
One mechanism by which metformin decreases gluconeogenesis is via _____ of the enzyme AMP-activated protein kinase (AMPK)
_____-acting insulins should not be given intravenously or intramuscularly.
_____, a synthetic analogue of α-MSH, is FDA-approved for the treatment of erythropoietic protoporphyria.
Hypothalamic and Pituitary Hormones
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Thyroid Drugs and Antithyroid Agents
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Insulin and Oral Hypoglycemic Agents
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Adrenocorticosteroids
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Sex Hormones: Estrogens and Progestins
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Androgens and Anabolic Steroids
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Hormonal Contraceptives
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Drugs Affecting Calcium Metabolism
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Drugs for Osteoporosis
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Pharmacological Management of Obesity
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