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# Rizatriptan
## Overview
Rizatriptan is a selective serotonin (5-HT$_{1B/1D}$) receptor agonist used for the acute treatment of migraine. It is available as oral tablets and orally disintegrating tablets (ODT).
## Primary Indications
Acute treatment of migraine attacks with or without aura in adults and pediatric patients (aged 6 to 17 years).
## Adult Dosing
* **Initial Dose:** 5 mg or 10 mg.
* **Administration:** If the migraine returns or the initial response is inadequate, a second dose may be administered at least 2 hours after the first.
* **Maximum Dose:** 30 mg in a 24-hour period.
## Pediatric Dosing
* **Aged 6 to 17 years (weight < 40 kg):** 5 mg single dose.
* **Aged 6 to 17 years (weight ≥ 40 kg):** 10 mg single dose.
* **Note:** Efficacy and safety of a second dose in pediatric patients have not been established; local institutional protocols regarding repeat dosing vary.
## Dose Adjustments
* **Hepatic Impairment:** Mild to moderate impairment requires no initial adjustment, but caution is advised. Not recommended in severe impairment.
* **Renal Impairment:** No dose adjustment necessary.
* **Concomitant Propranolol:** Use 5 mg dose. Propranolol increases rizatriptan plasma concentrations; the maximum daily dose is 15 mg (three 5 mg doses) in 24 hours.
## Contraindications
* History of ischemic heart disease, coronary artery vasospasm (Prinzmetal's angina), or myocardial infarction.
* History of stroke or transient ischemic attack (TIA).
* Peripheral vascular disease or ischemic bowel disease.
* Uncontrolled hypertension.
* Administration within 24 hours of another 5-HT$_1$ agonist or ergotamine-type medication.
* Use within 2 weeks of discontinuing a monoamine oxidase (MAO) inhibitor.
## Adverse Effects
* **Common:** Paresthesia, dizziness, somnolence, fatigue, and pain/tightness in the chest, neck, or throat ("triptan sensations").
* **Severe:** Coronary artery vasospasm, arrhythmias, myocardial infarction, serotonin syndrome, and hypertension.
## Key Drug Interactions
* **MAO Inhibitors:** Risk of severe increase in rizatriptan plasma concentrations.
* **Propranolol:** Increases rizatriptan levels (requires dose reduction).
* **Serotonergic Drugs (SSRIs/SNRIs):** Increased risk of serotonin syndrome.
* **Ergot-containing drugs:** Additive risk of vasospastic effects.
## Monitoring
* Monitor blood pressure periodically in patients with controlled hypertension.
* Assess for cardiovascular symptoms (chest pain, shortness of breath) during the first administration.
* Monitor for signs of serotonin syndrome if used with other serotonergic agents.
## Clinical Pearls
* **ODT formulation:** ODTs should be placed on the tongue and allowed to dissolve; no liquid is required. Do not use if you have phenylketonuria (contains phenylalanine).
* **Timing:** Administer as soon as possible after migraine onset; efficacy is optimal when taken early in the headache phase.
* **Overuse:** Limit use to prevent medication-overuse headache (MOH). Frequency should generally not exceed 10 days per month.
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*Disclaimer: This information is for educational purposes and does not replace professional clinical judgment. Always verify current prescribing information, institutional guidelines, and patient-specific factors before prescribing or administering medication.*