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SUMAFIX 50 Price

Active Substance: Sumatriptan Succinate Ph.Eur 69.98 mg equivalent to Sumatriptan 50 mg [Intra-granular Ingredients].

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Overview

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This medicine contains an important and useful components, as it consists of
Sumatriptan Succinate Ph.Eur 69.98 mg equivalent to Sumatriptan 50 mg [Intra-granular Ingredients]is available in the market in concentration

Name

Sumatriptan

Precaution

Conditions predisposing to seizures, presence of coronary risk factors, cardiac arrhythmias, renal or hepatic impairment, elderly, pregnancy, lactation. Lactation: Excreted in breast milk at very low levels; minimize infant to potential exposure by avoiding breastfeeding for 8-12 hours after administration

Indication

Migraine, Cluster headache

Contra indication

Not to be used prophylactically and in patients with basilar or hemiplegic or ophthalmoplegic migraine. History of MI or stroke, severe hepatic impairment, ischaemic heart disease, uncontrolled hypertension, peripheral vascular disease, hypersensitivity to sulfonamides.

Side Effect

>10% Injection site reaction (<86%),Paresthesia (5-14%),Dizziness (12%),Warm/hot sensation (11%) 1-10% Chest discomfort/pressure/tightness (2-5%),Jaw or neck tightness (1-5%),Diaphoresis (2%),Burning sensation (7%),Cold sensation (1%),Dysphagia,Sore throat (3%),Malaise (1%),Abdominal distress (1%) Frequency Not Defined Agitation,Cardiac arrhythmia: V-fib/V-tach (rare),Dysuria,Eye irritation,Flushing,MI and coronary artery vasospasm in patients with CAD risk factors (extremely rare),Nasal discomfort,Palpitations,Tingling,Weakness Potentially Fatal: Cardiac arrhythmias, MI.

Pregnancy Category ID

3

Mode of Action

Sumatriptan is a selective serotonin agonist that acts at 5-HT1 receptors. It causes vasoconstriction of cranial arteries and/or inhibition of neurogenic inflammatory processes in the CNS. A small but significant delay in gastric emptying also occurs.

Interaction

Concurrent use increased risk of vasospastic reaction with ergotamine and related compounds. Potentially Fatal: Increased risk of serotonin syndrome with concurrent use of SSRI, MAOIs or within 14 days of stopping MAOIs. Admin of ergotamine or related compounds within the previous 24 hr.

Pregnancy Category Note

Information not available

Adult Dose

Child Dose

Renal Dose

Administration

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