Imigra
Generic Name
Sumatriptan
Manufacturer
Square Pharmaceuticals Ltd.
Country
Bangladesh
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Price Details
Current market pricing information
| Variant | Unit Price | Strip Price |
|---|---|---|
| imigra 10 mg tablet | ৳ 5.00 | ৳ 50.00 |
Description
Overview of the medicine
Sumatriptan is a medication primarily used for the acute treatment of migraine attacks, with or without aura, and cluster headaches. It belongs to the triptan class of drugs.
Uses & Indications
Dosage
Adults
For migraine: Take 10 mg orally at the first sign of a migraine attack. If symptoms recur or a satisfactory response is not achieved, a second dose may be taken after at least 2 hours. Do not exceed 2 doses (20 mg total) in 24 hours. The typical oral doses are 25 mg, 50 mg or 100 mg; a 10 mg tablet would be considered a low dose and specific medical advice should be followed.
Elderly
Use with caution due to potential age-related decrease in renal or hepatic function and increased risk of cardiovascular events. Dosage adjustments may be considered based on individual response and tolerability.
Renal_impairment
No specific dose adjustment is generally required, but use with caution in patients with severe renal impairment due to limited experience.
How to Take
Take the tablet orally with water, as soon as migraine symptoms appear. Do not use it for prevention. The tablet should not be crushed, chewed, or split.
Mechanism of Action
Sumatriptan is a selective serotonin (5-HT1B/1D) receptor agonist. It works by causing vasoconstriction of cranial blood vessels, which are thought to be dilated during a migraine attack, and by inhibiting the release of neuropeptides, thereby alleviating migraine symptoms.
Pharmacokinetics
Onset
Oral: Effects typically begin within 30-60 minutes.
Excretion
Primarily renal (60% as inactive metabolite, 20% unchanged). Also excreted in feces.
Half life
Approximately 2-2.5 hours.
Absorption
Rapidly absorbed after oral administration. Bioavailability is about 15% due to first-pass metabolism.
Metabolism
Primarily hepatic, via monoamine oxidase-A (MAO-A) enzyme to an inactive indole acetic acid metabolite.
Side Effects
Contraindications
- •Ischemic heart disease (e.g., angina pectoris, history of myocardial infarction)
- •Cerebrovascular syndromes (e.g., stroke, transient ischemic attack)
- •Peripheral vascular disease
- •Uncontrolled hypertension
- •Severe hepatic impairment
- •Concomitant use with ergotamine-containing medications or other triptans
- •Concomitant use with MAO inhibitors or within 2 weeks of discontinuing MAO inhibitors
- •Hemiplegic or basilar migraine
Drug Interactions
SSRIs/SNRIs
Potential for serotonin syndrome (agitation, hallucinations, rapid heart rate, fever, incoordination, nausea, vomiting, diarrhea). Use with caution, monitor for symptoms.
MAO Inhibitors
Concomitant use is contraindicated, as MAO-A inhibitors reduce sumatriptan clearance, leading to increased plasma levels and risk of toxicity. Do not use within 2 weeks of stopping MAO inhibitors.
Other Triptans
Concomitant use or use within 24 hours of another triptan is contraindicated due to potential for additive cardiovascular effects.
Ergotamine-containing drugs
Concomitant use or use within 24 hours is contraindicated due to additive prolonged vasoconstrictor effects.
Storage
Store below 30°C in a dry place, away from direct light and moisture. Keep out of reach of children.
Overdose
Symptoms of overdose include convulsions, tremor, paralysis, inactivity, ptosis, erythema of the extremities, cyanosis, respiratory depression, and salivation. Management is supportive, monitoring cardiac and respiratory function and managing symptoms for at least 12 hours. There is no specific antidote.
Pregnancy & Lactation
Pregnancy Category C: Animal studies have shown adverse effects on the fetus. Use during pregnancy only if the potential benefit justifies the potential risk to the fetus. Lactation: Sumatriptan is excreted in breast milk. Caution should be exercised when administered to a nursing woman, or consider discarding breast milk for 12 hours after a dose.
Frequently Asked Questions
Common questions about this medicine
Pack Sizes
Shelf Life
Typically 2-3 years from the date of manufacture.
Availability
Pharmacies
Approval Status
Approved by major regulatory bodies
Patent Status
Generic available, original patent expired
WHO Essential Medicine
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Global Brand Names
International brand names for this medicine
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