sumatriptan succinate(redirected from Apo-Sumatriptan)
Apo-Sumatriptan (CA), Co Sumatriptan (CA), Dom-Sumatriptan (CA), Gen-Sumatriptan (CA), Imigran (UK), Imitrex, Novo-Sumatriptan (CA), PHL-Sumatriptan (CA), PMS-Sumatriptan (CA), Ratio-Sumatriptan (CA), Riva-Sumatriptan (CA), Sandoz Sumatriptan (CA), Sumavel DosePro
Pharmacologic class: Selective 5-hydroxytryptamine1 (5-HT1) agonist
Therapeutic class: Vascular headache suppressant
Pregnancy risk category C
Selectively activates vascular 5-HT1 receptor sites, causing vasoconstriction in intracranial arteries
Injection: 6 mg/0.5-ml prefilled syringes, 0.6 mg/0.5-ml single-dose vials; 6 mg/0.5-ml prefilled, single-dose, needle-free subcutaneous delivery system; 4- and 6-mg STATdose system containing two prefilled single-dose syringe cartridges and one STATdose Pen; 4-and 6-mg kits containing two prefilled single-dose syringe cartridges and one autoinjector pen
Nasal spray: 5 mg in 100-mcl unit dose spray device (package of six), 20 mg in 100-mcl unit dose spray device (package of six)
Tablets: 25 mg, 50 mg, 100 mg
⊘Indications and dosages
➣ Acute migraine, cluster headaches
Adults: Initially, 25 mg P.O.; if response inadequate after 2 hours, may give up to 100 mg P.O. If migraine recurs, repeat dose q 2 hours, not to exceed 200 mg/day. Or 6 mg subcutaneously, repeated as needed after 1 hour, not to exceed 12 mg in 24 hours. If P.O. therapy will follow subcutaneous injection, additional P.O. sumatriptan may be given q 2 hours, not to exceed 100 mg/day. Or a single dose of 5, 10, or 20 mg intranasally in one nostril, repeated p.r.n. in 2 hours, not to exceed 40 mg in 24 hours.
• Hepatic impairment
• Hypersensitivity to drug
• Hemiplegic or basilar migraine headache
• Ischemic cardiac, cerebrovascular, or peripheral vascular disease (such as a history of myocardial infarction, stroke, angina, or ischemic bowel)
• Uncontrolled hypertension
• Severe hepatic impairment
• MAO inhibitor use within past 14 days
• Use of other 5-HT1 agonists, ergotamine-containing drugs, or ergot-type products within past 24 hours
Use cautiously in:
• patients with cardiovascular risk factors (hypertension, hypercholesterolemia, smoking, obesity, diabetes, family history of cardiovascular disease, men over age 40, menopausal women)
• elderly patients
• women of childbearing age
• pregnant or breastfeeding patients
• children younger than age 18 (safety not established).
• Be aware that parenteral form is for subcutaneous use only.
• Be aware that an autoinjection device is available for use with the 4- and 6-mg prefilled syringe cartridges to facilitate patient self-administration using the 4- or 6-mg dose. For patients receiving doses other than 4 or 6 mg, only the 6-mg single-dose vial dosage form should be used.
☞ If patient has risk factors for coronary artery disease, know that first dose should be given in medical setting with emergency equipment at hand.
☞ Don't give within 14 days of MAO inhibitors.
☞ Don't administer within 24 hours of other 5-HT1 agonists, ergotamine-containing drugs, or ergot-type products.
CNS: headache, malaise, dizziness, drowsiness, fatigue, vertigo, anxiety, tight feeling in head, numbness
CV: angina, chest pressure or tightness, transient hypertension, ECG changes, coronary vasospasm, myocardial infarction
EENT: vision changes, nasal sinus discomfort, throat discomfort
GI: abdominal discomfort, dysphagia
Musculoskeletal: jaw discomfort, muscle cramps, myalgia, neck pain or stiffness
Skin: flushing; tingling; warm, cool or, burning sensation
Other: injection site reaction, feeling of heaviness or tightness
Drug-drug.Dihydroergotamine, ergotamine, methysergide: increased risk of vasospastic reaction
Lithium, MAO inhibitors, selective serotonin reuptake inhibitors: weakness, hyperreflexia, incoordination
Drug-herbs.Horehound: enhanced serotonergic effects
☞ Monitor cardiovascular status closely. Be aware that drug may cause serious and possibly fatal cardiac disorders.
• Watch for neurologic and vision changes. Institute safety measures as needed to prevent injury.
• Monitor patient's response to drug. Assess need for repeat doses.
• Watch for injection site reaction, which should subside within 1 hour.
• Instruct patient to take as soon as possible after migraine onset.
☞ Teach patient to recognize and immediately report serious cardiovascular reactions.
• Explain proper drug use. Tell patient it doesn't prevent migraine.
• With subcutaneous use, instruct patient to follow directions in the patient leaflet carefully before injecting drug and to inject dose subcutaneously using spring-loaded injector system or needle-free subcutaneous delivery system included in package. If headache recurs after dose, tell him he may take a second dose, but should wait at least 1 hour after initial dose and shouldn't exceed two 6-mg injections in a 24-hour period. Instruct him to report injection site reaction that doesn't subside within 1 hour.
• With oral use, tell patient he may take a second dose 2 hours after first dose if migraine recurs. Tell him he may repeat oral doses every 2 hours as needed, up to 200 mg in a 24-hour period.
• With intranasal use, tell patient to spray 5, 10, or 20 mg into one nostril, as prescribed. Tell him he may repeat dose after 2 hours but shouldn't exceed 40 mg in a 24-hour period.
• Advise patient not to use drug for more than four episodes per month.
• Caution patient to avoid driving and other hazardous activities until he knows how drug affects concentration and alertness.
• As appropriate, review all other significant and life-threatening adverse reactions and interactions, especially those related to the drugs and herbs mentioned above.
sumatriptan succinateImitrex® Neurology An agent used for migraines Pros ↓ Headaches, clinical disability, nausea, photophobia Contraindications CAD, uncontrolled HTN, Prinzmetal's angina, concurrent MAOI therapy Adverse events Angina, stroke, TIAs, HTN, ischemic bowel disease. See Migraine. Cf Losartan.
sumatriptan succinate (soo´mətrip´-tan suk´sənāt´),
drug class: serotonin agonist;
action: selective agonist for the vascular 5-hydroxytryptamine (5-HT-1) (serotonin) receptor in cranial arteries, causing vasodilation with little or no effect on peripheral pressure;
use: treatment of migraine headaches.