Drug Guide
Almotriptan Malate
Classification
Therapeutic: Antimigraine Agent
Pharmacological: Selective 5-HT1B/1D Receptor Agonist
FDA Approved Indications
- Acute treatment of migraine attacks with or without aura
Mechanism of Action
Almotriptan binds to serotonin (5-HT) receptors, specifically 5-HT1B and 5-HT1D, causing vasoconstriction of cranial blood vessels and inhibiting the release of pro-inflammatory neuropeptides, thereby alleviating migraine symptoms.
Dosage and Administration
Adult: Initially, 12.5 mg taken orally; if needed, can be repeated after 2 hours. Max dose is 25 mg in 24 hours.
Pediatric: Not approved for use in pediatric patients.
Geriatric: Use with caution due to increased risk of vascular events; start with the lowest dose.
Renal Impairment: Use caution; consider dose adjustment due to reduced clearance.
Hepatic Impairment: Use with caution; dose adjustments may be needed, especially in severe impairment.
Pharmacokinetics
Absorption: Rapid, with peak plasma levels in approximately 1.5-3 hours.
Distribution: Widely distributed, crosses the blood-brain barrier.
Metabolism: Metabolized mainly via monoamine oxidase-A (MAO-A) and conjugation pathways.
Excretion: Excreted primarily in urine (about 60%) and feces.
Half Life: Approximately 3-4 hours.
Contraindications
- History of ischemic heart disease, cerebrovascular syndromes, uncontrolled hypertension, or other significant cardiovascular conditions.
- Use with concomitant ergot-containing drugs or other 5-HT1 agonists within 24 hours.
Precautions
- Use cautiously in patients with risk factors for cardiovascular disease, liver impairment, or a history of stroke.
Adverse Reactions - Common
- Dizziness (Common)
- Tingling or flushing sensation (Common)
- Nausea or somnolence (Common)
Adverse Reactions - Serious
- Serious cardiovascular events (e.g., myocardial infarction, ischemic stroke) (Rare)
- Allergic reactions, including anaphylaxis (Rare)
Drug-Drug Interactions
- Other serotonergic drugs, such as SSRIs, SNRIs, triptans, ergot derivatives, which may increase the risk of serotonin syndrome.
Drug-Food Interactions
N/ADrug-Herb Interactions
N/ANursing Implications
Assessment: Evaluate for cardiovascular risk factors before administering.
Diagnoses:
- Risk for ineffective cerebral perfusion related to vasoconstriction.
Implementation: Administer as prescribed, monitor blood pressure and heart rate, observe for adverse effects.
Evaluation: Assess relief of migraine symptoms within 2 hours of administration.
Patient/Family Teaching
- Instruct patient to take at the first sign of migraine.
- Warn about potential side effects like dizziness, flushing.
- Advise against use with other serotonergic drugs without healthcare provider approval.
- Report chest pain or unusual symptoms immediately.
Special Considerations
Black Box Warnings:
- Serious cardiovascular events have been reported; contraindicated in patients with ischemic cardiac; cerebrovascular disease.
- Potential for medication overuse headache.
Genetic Factors: N/A
Lab Test Interference: N/A
Overdose Management
Signs/Symptoms: Dizziness, nausea, vomiting, chest pain, drowsiness.
Treatment: Supportive care; no specific antagonist. Monitor cardiovascular status.
Storage and Handling
Storage: Store at room temperature, 20°C to 25°C (68°F to 77°F).
Stability: Stable until expiration date when stored properly.