Nomigran
Sumatriptan ·Ambee Pharmaceuticals Ltd.·Tablet
Administration
- Single-dose of 10 mg of nasal spray.
- The maximum dose in a 24 hour period: 30 mg; separate doses by at least one hour or as directed by the physician.
Effects
Rare side effects: Anxiety, burning sensation, discomfort of the nasal cavity and throat, general feeling of illness or tiredness & vision changes.
Indications
Limitations of Use:
- Use only if a clear diagnosis of migraine headache has been established.
- Not indicated for the prophylactic therapy of migraine attacks.
- Not indicated for the treatment of cluster headache.
Pharmacology
Precautions
- Myocardial ischemia/infarction and Prinzmetal’s angina: Perform cardiac evaluation in patients with multiple cardiovascular risk factors
- Arrhythmias: Discontinue Sumatriptan if occurs
- Chest/throat/neck/jaw pain, tightness, pressure, or heaviness: Generally, not associated with Myocardial Ischemia; evaluate for coronary artery disease in patients at high risk
- Cerebral hemorrhage, subarachnoid hemorrhage, and stroke: Discontinue Sumatriptan if occurs
- Gastrointestinal ischemia and reactions, peripheral vasospastic reactions: Discontinue Sumatriptan if occurs
- Medication overuse headache: Detoxification may be necessary
- Serotonin syndrome: Discontinue Sumatriptan if occurs
- Increase in blood pressure: Hypertensive crisis can occur
- Hypersensitivity reactions: Angioedema and anaphylaxis can occur
- Seizures: Use with caution in patients with epilepsy or a lowered seizure threshold
- Local irritation: Burning and abnormal taste can occur
Therapeutic
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