Medication info
Migard Tablets 2.5 mg (Propranadiptriptan Succinate Dihydrate)

Migard Tablets 2.5 mg (Propranadiptriptan Succinate Dihydrate)

Prescription medicationTabletOral
Ingredient · strength
Frovatriptan Succinate Monohydrate›3.91mg / 1 tablet
Manufacturer / importer
SK Chemical Co., Ltd.
Appearance
Biconvex white round film-coated tablets
Packaging
6 tablets (6 tablets/PTP packaging x 1), 12 tablets (6 tablets/PTP packaging x 2)
Approval status
Active

MFDS item code 200903830 · Approved 2009.05.29 · Insurance code 644703310

Summary

Main use
Acute treatment of migraine with or without aura
Who takes it
Adults
Adult dose
This medicine should not be taken for the prevention of migraine. If there is no response to treatment after the initial dose of frovatriptan, this medicine should not be taken again for the same attack. ○ Adults (18~65 years) The recommended dose of this medicine is 2.5 milligrams (1 tablet) of frovatriptan. If the migraine recurs after initial relief, another dose may be taken at an interval of at least 2 hours. The total daily dose should not exceed 5 milligrams (2 tablets). ○ Patients with renal impairment No dose adjustment is necessary in patients with renal impairment. ○ Patients with hepatic impairment No dose adjustment is necessary in patients with mild or moderate hepatic impairment. Do not administer to patients with severe hepatic impairment (see section 1. Do not administer to the following patients under Precautions for Use).

Ingredients

Manufacturer
SK Chemical Co., Ltd.

Efficacy & effects

Acute treatment of migraine with or without aura

  • Warning symptoms
  • migraine
View approved original text

This medication is used to treat migraines acutely, whether or not there are warning symptoms. It quickly alleviates headaches caused by migraines, reducing discomfort for the patient. It assists in rapid symptom relief to support a quicker return to daily activities. Therefore, it is used effectively to improve symptoms when a migraine occurs.

How to take

Adult dose

This medicine should not be taken for the prevention of migraine. If there is no response to treatment after the initial dose of frovatriptan, this medicine should not be taken again for the same attack. ○ Adults (18~65 years) The recommended dose of this medicine is 2.5 milligrams (1 tablet) of frovatriptan. If the migraine recurs after initial relief, another dose may be taken at an interval of at least 2 hours. The total daily dose should not exceed 5 milligrams (2 tablets). ○ Patients with renal impairment No dose adjustment is necessary in patients with renal impairment. ○ Patients with hepatic impairment No dose adjustment is necessary in patients with mild or moderate hepatic impairment. Do not administer to patients with severe hepatic impairment (see section 1. Do not administer to the following patients under Precautions for Use).

Precautions

This medication contains the ingredient propranadiptriptan and is used for the treatment of migraine. This medication should not be used in certain patients. For example, it should not be taken by individuals who are allergic to this medication or its components, those with a history of heart disease or vascular issues, patients with severe hypertension, those who have experienced a stroke, and individuals with severe liver dysfunction. Additionally, caution is necessary when used with medications that contain ergotamine or certain migraine treatments as this may pose risks. Side effects such as dizziness, fatigue, headache, paresthesia, and flushing may occur when taking this medication, which are mostly transient and mild, but occasionally severe heart-related issues may arise. Patients, especially those at risk for cardiovascular disease or elderly individuals, should consult a physician before taking this medication, and if chest pain or tightness occurs while taking it, they should immediately discontinue use and seek medical evaluation. This medication is not recommended for pregnant or breastfeeding women, children and adolescents under 18 years of age, or elderly patients over 65 years of age. Dosage must be strictly followed, and in case of overdose, as there is no specific antidote, one should quickly visit a medical institution for appropriate treatment. This medication should be kept out of reach of children and stored in a cool, dry place below 30 degrees Celsius. Finally, this medication may cause drowsiness, so caution is advised when engaging in activities that require alertness, such as driving or operating machinery after taking it.

Side effects

  • Dizziness
  • fatigue
  • paresthesia
  • headache
  • flushing
  • lymphadenopathy
  • dehydration
  • hypocalcemia
  • anxiety
  • insomnia
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  • confusion
  • irritability
  • agitation
  • depression
  • depersonalization
  • abnormal dreams
  • personality disorder
  • drowsiness
  • sensory loss
  • dysgeusia
  • tremor
  • impaired concentration
  • hypersensitivity
  • sedation
  • lightheadedness
  • involuntary muscle contractions
  • forgetfulness
  • muscle tension
  • muscle relaxant effect
  • diminished reflexes
  • activity impairment
  • visual impairment
  • eye pain
  • eye irritation
  • photophobia
  • night blindness
  • tinnitus
  • ear pain
  • ear discomfort
  • ear disorders
  • itching of the ear
  • hyperacusis
  • palpitations
  • tachycardia
  • bradycardia
  • peripheral coldness
  • hypertension
  • throat tension
  • rhinitis
  • sinusitis
  • sore throat
  • epistaxis
  • hiccups
  • excessive breathing
  • throat irritation
  • nausea
  • dry mouth
  • dyspepsia
  • abdominal pain
  • diarrhea
  • dysphagia
  • gastric hyperperistalsis
  • gastric discomfort
  • abdominal distension
  • constipation
  • belching
  • gastroesophageal reflux
  • irritable bowel syndrome
  • cheilitis
  • lip pain
  • esophageal spasm
  • oral mucosal blistering
  • gastric ulcer
  • salivary gland pain
  • stomatitis
  • toothache
  • hyperhidrosis
  • itching
  • erythema
  • hairy
  • purpura
  • urticaria
  • musculoskeletal rigidity
  • musculoskeletal pain
  • limb pain
  • back pain
  • arthralgia
  • polyuria
  • polymyuria
  • nocturia
  • kidney pain
  • chest tightness
  • chest discomfort
  • chest pain
  • heat sensation
  • impaired thermoregulation
  • pain
  • weakness
  • thirst
  • lethargy
  • increased vitality
  • fatigue
  • fever
  • elevated serum bilirubin
  • reduced serum calcium
  • abnormal urinalysis
  • laceration
  • allergic rash
  • dermatitis
  • petechiae
  • skin discoloration
  • facial swelling
  • hives
  • vascular edema
  • anaphylaxis
  • seizures
  • acute myocardial infarction
  • upper abdominal pain
  • chest discomfort
  • oral sensory abnormalities
  • gastric discomfort
  • high sound anxiety
  • myalgia
  • muscle weakness
  • rash
  • chest heaviness
  • nasopharyngitis
  • elevated creatine kinase
  • pelvic inflammatory disease
  • dry mouth
  • throat pain
  • shoulder pain
  • lethargy
  • floaters
  • conjunctival injection
  • altered consciousness
  • weight gain
  • hallucinations

Not everyone experiences these, and they can vary from person to person.

Storage

This medication must be stored in a tightly sealed container to protect it from exposure to air and light. It is important to maintain a storage temperature between 1 degree and 30 degrees Celsius to preserve its efficacy for a longer duration.

Appearance and packaging

Appearance

Biconvex white round film-coated tablets

Package unit

6 tablets (6 tablets/PTP packaging x 1), 12 tablets (6 tablets/PTP packaging x 2)

Same-ingredient medicines

Even with the same ingredient, strength, dosage form and how it is taken can differ.

Even with the same ingredient, the dose and directions can differ by strength and dosage form. Talk to a doctor or pharmacist before switching from a medication you are already taking.

Questions about this medicine

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This drug information is based on data provided by the Korea Ministry of Food and Drug Safety.
Consult a doctor or pharmacist for accurate dosage, administration, and usage instructions.