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# Rizatriptan
## Overview
Rizatriptan is a selective serotonin (5-HT1B/1D) receptor agonist used for the acute treatment of migraine. It exhibits faster onset compared to sumatriptan and is available as a conventional tablet and an orally disintegrating tablet (ODT).
## Primary Indications
Acute treatment of migraine with or without aura in adults and pediatric patients.
## Adult Dosing
* **Standard Dose:** 5 mg or 10 mg taken at the onset of migraine.
* **Dosing Interval:** If symptoms recur, a second dose may be taken at least 2 hours after the first dose.
* **Maximum Daily Dose:** 30 mg in any 24-hour period.
## Pediatric Dosing (Ages 6 to 17)
* **Weight < 40 kg:** 5 mg single dose.
* **Weight ≥ 40 kg:** 10 mg single dose.
* **Dosing Interval:** If needed, a second dose may be taken at least 2 hours after the first dose.
* **Maximum Dose:** Do not exceed one dose per 24 hours in children; safety/efficacy of multiple doses in pediatric patients is not established.
## Dose Adjustments
* **Patients taking Propranolol:** Reduce dose to 5 mg (maximum 15 mg/24 hours) due to increased rizatriptan plasma concentrations.
* **Hepatic/Renal Impairment:** Use with caution; consider 5 mg dose for mild-to-moderate impairment. Avoid in severe hepatic impairment.
## Contraindications
* History of ischemic heart disease, coronary artery vasospasm (Prinzmetal's angina), or myocardial infarction.
* Uncontrolled hypertension.
* History of stroke or transient ischemic attack (TIA).
* Peripheral vascular disease.
* Ischemic bowel disease.
* Administration within 24 hours of another 5-HT1 agonist or ergotamine-type medication.
* Concomitant use of or within 2 weeks of discontinuing MAO inhibitors.
## Adverse Effects
* **Common:** Paresthesia, dizziness, somnolence, fatigue, and dry mouth.
* **Serious:** Coronary vasospasm/myocardial ischemia, arrhythmias, serotonin syndrome (when combined with serotonergic drugs), and hypertensive crisis.
## Key Drug Interactions
* **MAOIs:** Absolute contraindication; MAO-A inhibition significantly increases rizatriptan exposure.
* **SSRI/SNRIs:** Risk of serotonin syndrome. Monitor for altered mental status and neuromuscular hyperactivity.
* **Propranolol:** Increases rizatriptan bioavailability by ~70%.
## Monitoring
* Monitor cardiovascular status in patients with multiple risk factors (e.g., postmenopausal women, men >40, uncontrolled HTN, hyperlipidemia, smoking).
* Assess for chest pain/pressure or signs of serotonin syndrome.
## Clinical Pearls
* **ODT Formulation:** The orally disintegrating tablet should remain in the blister pack until use. It does not require water but should not be split.
* **Medication Overuse Headache (MOH):** Excessive use (≥10 days/month) can lead to rebound headaches.
* **Efficacy:** If the first dose provides no relief, avoid a second dose for that same attack; verify diagnosis before retreatment.
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*Disclaimer: This information is for educational purposes only. Always consult current clinical practice guidelines, official FDA-approved labeling, or institutional protocols before prescribing or administering medication.*