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# Rizatriptan
## Overview
Rizatriptan is a selective serotonin 5-HT1B/1D receptor agonist used for the acute treatment of migraine headaches with or without aura. It is available as standard tablets and orally disintegrating tablets (ODT).
## Primary Indications
Acute treatment of migraine headaches.
## Adult Dosing
* **Standard Dose:** 5 mg or 10 mg at the onset of migraine.
* **Maximum Dose:** 30 mg in a 24-hour period.
* **Repeat Dosing:** If symptoms persist or recur, dose may be repeated after a minimum of 2 hours. Do not exceed 30 mg in 24 hours.
## Pediatric Dosing
* **Children 6–17 years (weight-based):**
* **Weight < 40 kg:** 5 mg as a single dose.
* **Weight ≥ 40 kg:** 10 mg as a single dose.
* **Maximum:** Dosing is limited to one dose per 24 hours in pediatric patients. Safety/efficacy of repeat dosing in children has not been established.
## Dose Adjustments
* **Propranolol:** Patients taking propranolol should use a reduced dose of 5 mg (max 15 mg/24 hours) due to increased rizatriptan plasma concentrations.
* **Renal/Hepatic Impairment:** Use with caution in mild-to-moderate impairment. Not recommended in severe impairment.
## 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.
* Hemiplegic or basilar migraine.
* Administration within 24 hours of another 5-HT1 agonist or ergotamine-type medication.
* MAO-A inhibitor use or within 2 weeks of MAO-A inhibitor discontinuation.
## Adverse Effects
* **Common:** Paresthesia, somnolence, dizziness, fatigue.
* **Serious:** Coronary vasospasm/myocardial ischemia, arrhythmias, serotonin syndrome (especially with SSRIs/SNRIs), and hypertensive crisis.
## Key Drug Interactions
* **MAO inhibitors:** Potentiate rizatriptan levels; strictly contraindicated.
* **Propranolol:** Increases rizatriptan bioavailability via inhibition of metabolism.
* **Serotonergic agents (SSRIs, SNRIs, TCAs):** Potential risk of serotonin syndrome; monitor clinical status.
## Monitoring
* **Cardiac:** Baseline assessment of cardiovascular risk factors in patients with significant risk profiles. Monitor for signs of ischemia (chest pain, shortness of breath) after first dose.
* **Neurologic:** Monitor for excessive use leading to medication-overuse headache.
## Clinical Pearls
* **ODT Administration:** The ODT formulation should be placed on the tongue and allowed to dissolve; no water is required. Do not split ODT tablets.
* **Consistency:** Efficacy has not been established for the treatment of cluster headaches or chronic daily headaches.
* **Education:** Patients should be advised that relief should occur within 2 hours; if no relief occurs, the diagnosis of migraine should be re-evaluated.
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*Disclaimer: This information is for educational purposes only. Clinical guidelines and local protocols vary. Always verify current prescribing information, contraindications, and drug interactions via a reliable primary reference (e.g., Lexicomp, UpToDate, or package insert) before prescribing or administering medication.*