A story built from the name vasopressin itself - so the mechanism of action, key side effects, and the way Step 1 actually tests it stick on the first read.

Which adverse effect is most classically associated with excessive V2-mediated action of vasopressin?
Vasopressin (ADH) acts on two receptor subtypes with distinct effects. V1 receptors on vascular smooth muscle cause vasoconstriction, making vasopressin useful in vasodilatory shock and esophageal variceal bleeding. V2 receptors in the collecting duct increase aquaporin-2 insertion, concentrating urine — this is the basis for treating central diabetes insipidus. Excess V2 activity leads to water retention, hyponatremia, and water intoxication.
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