Drug Guide
Sumatriptan
Classification
Therapeutic: Antimigraine agent
Pharmacological: Serotonin receptor agonist (triptan)
FDA Approved Indications
- Migraine attacks with or without aura
- Cluster headaches
Mechanism of Action
Selective agonist for 5-HT1B/1D receptors, leading to vasoconstriction of intracranial blood vessels, inhibition of inflammatory neuropeptide release, and interruption of migraine pain pathways.
Dosage and Administration
Adult: Typically 25-100 mg orally at symptom onset; may repeat in 2-hour intervals, not exceeding 200 mg/day.
Pediatric: Use not established; consult specific pediatric guidelines or specialist.
Geriatric: Start at lower end of dosing range, monitor for cardiovascular effects.
Renal Impairment: Use with caution; dose adjustment may be necessary.
Hepatic Impairment: Starting dose should be reduced; hepatic function should be monitored.
Pharmacokinetics
Absorption: Rapid, peak plasma levels within 2-3 hours after oral dose.
Distribution: Widely distributed; crosses the blood-brain barrier.
Metabolism: Primarily hepatic via monoamine oxidase A (MAO-A), and also by other pathways.
Excretion: Renal (mainly as metabolites), fecal.
Half Life: Approx. 2 hours.
Contraindications
- Coronary artery disease, history of stroke or TIA, uncontrolled hypertension, basilar or hemiplegic migraine, ischemic heart disease.
Precautions
- Use with caution in patients with liver disease, hypertension, or risk factors for cardiovascular disease. Not recommended during pregnancy unless benefits outweigh risks.
Adverse Reactions - Common
- Sensations of tingling, warmth, flushing (Common)
- Dizziness, drowsiness (Common)
Adverse Reactions - Serious
- Coronary vasospasm leading to myocardial infarction (Rare)
- Serotonin syndrome (when combined with serotonergic agents) (Rare)
- Allergic reactions including anaphylaxis (Rare)
Drug-Drug Interactions
- SSRIs, SNRIs, MAO inhibitors (risk of serotonin syndrome)
- Other vasoconstrictive agents
Drug-Food Interactions
N/ADrug-Herb Interactions
N/ANursing Implications
Assessment: Monitor cardiovascular status before and after administration, especially in at-risk populations.
Diagnoses:
- Risk for ineffective tissue perfusion related to vasospasm.
- Pain related to migraine.
Implementation: Administer at onset of migraine symptoms, ensure patient understands dosing limits.
Evaluation: Assess relief of migraine symptoms within 2 hours, monitor for adverse effects.
Patient/Family Teaching
- Instruct to take at first sign of migraine for best effectiveness.
- Avoid activities requiring alertness immediately after taking.
- Report chest pain, severe dizziness, or allergic reactions immediately.
Special Considerations
Black Box Warnings:
- Cardiovascular risk: avoid in patients with ischemic heart disease or risk factors for cardiovascular disease.
Genetic Factors: None specifically tied to genetic factors but consider CYP2D6 metabolism for some formulations.
Lab Test Interference: None known.
Overdose Management
Signs/Symptoms: Severe hypertension, coronary vasospasm, CNS disturbances.
Treatment: Supportive care; no specific antidote exists, manage symptoms and provide cardiovascular support as needed.
Storage and Handling
Storage: Store at room temperature away from moisture and light.
Stability: Stable for 2-3 years if properly stored.