Vasopressin receptor antagonist drugs

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Actual: Vasopressin antagonists are drugs that bind to vasopressin receptors (V1A, V1B and V2) and block the action of vasopressin (antidiuretic hormone, ADH).
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Serotonin receptor 1A agonist/serotonin receptor 2A antagonist: flibanserin; Vasopressin receptor antagonists: tolvaptan. Drugs that are strong CYP3A inducers:.

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by A Parashar 2024 Cited by 6Vasopressin receptor antagonists Vasopressin Physiology Vasopressin Receptors Vasopressin Receptor Antagonists Conivaptan (YM-087).

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Vasopressin antagonists are drugs that bind to vasopressin receptors (V1A, V1B and V2) and block the action of vasopressin (antidiuretic hormone, ADH).

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Serotonin receptor 1A agonist/serotonin receptor 2A antagonist: flibanserin. Vasopressin receptor antagonists: tolvaptan. ➢ Drugs that are strong CYP3A

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Serotonin receptor 1A agonist/serotonin receptor 2A antagonist: flibanserin. Vasopressin receptor antagonists: tolvaptan. ➢ Drugs that are strong CYP3A

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Vasopressin antagonists are drugs that bind to vasopressin receptors (V1A, V1B and V2) and block the action of vasopressin (antidiuretic hormone, ADH), which is a hormone released by the pituitary gland.

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Vasopressin antagonists are drugs that bind to vasopressin receptors (V1A, V1B and V2) and block the action of vasopressin (antidiuretic hormone, ADH).

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Vasopressin-receptor antagonists. Vasopressin-receptor antagonists (VPAs) are a new class of drugs. These drugs block the action of vasopressin at one of its receptor sites. Vasopressin has several physiological functions in addition to its antidiuretic effects.

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Vasopressin antagonists are drugs that bind to vasopressin receptors (V1A, V1B and V2) and block the action of vasopressin (antidiuretic hormone, ADH), which is a hormone released by the pituitary gland.

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