Medication info
Protriptyline Tablet 2.5 mg (Protriptyline Succinate Dihydrate)

Protriptyline Tablet 2.5 mg (Protriptyline Succinate Dihydrate)

Prescription medicationTabletOral
Ingredient · strength
Frovatriptan Succinate Monohydrate›3.91mg / 1 tablet
Manufacturer / importer
Myeongin Pharmaceutical Co., Ltd.
Appearance
Biconvex white round film-coated tablet
Packaging
20 tablets/box [(10 tablets/PTP x 2)]
Approval status
Active

MFDS item code 202501584 · Approved 2025.06.26 · Insurance code 651905400

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 therapeutic response after the initial dose of frovatriptan, this medicine should not be administered 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, the dose may be repeated after 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 Precautions for Use, 1. Patients Who Should Not Take This Medicine).

Ingredients

Manufacturer
Myeongin Pharmaceutical Co., Ltd.

Efficacy & effects

Acute treatment of migraine with or without aura

  • Aura symptoms
  • migraine
View approved original text

This medication is used to rapidly relieve acute symptoms of migraine, with or without aura. It helps to reduce the discomfort associated with migraine headaches, improving the patient's daily life.

How to take

Adult dose

This medicine should not be taken for the prevention of migraine. If there is no therapeutic response after the initial dose of frovatriptan, this medicine should not be administered 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, the dose may be repeated after 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 Precautions for Use, 1. Patients Who Should Not Take This Medicine).

Precautions

This medication may not be suitable for certain patients. For example, it should not be administered to patients allergic to this drug or its components, patients with cardiovascular diseases or vascular problems, patients with severe hypertension, patients who have previously experienced a stroke or transient ischemic attack, patients with severe liver dysfunction, and patients taking certain medications. Various side effects such as dizziness, fatigue, headache, and sensory disturbances may occur while taking this medication, but most are temporary and mild to moderate. However, serious heart-related issues may arise infrequently, hence caution is required. This medication should only be used for patients diagnosed specifically with migraine, and prior to use, an assessment by a physician is necessary if non-migraine headaches or neurological conditions are suspected. Additionally, it should be used with caution in patients at high risk for cardiovascular diseases or in the elderly. This medicine may interact with other specific drugs, so if taking ergotamine derivatives or serotonin-related drugs, it must be separated by more than 24 hours. Care should be taken not to exceed the recommended dosage when taking the medication, as long-term or excessive use can worsen headaches. Women who are pregnant or breastfeeding, children and adolescents, and the elderly should avoid use unless absolutely necessary, as safety has not been adequately established for these groups. In cases of overdose, there is no specific antidote, so immediate medical attention is required for appropriate treatment and monitoring. Finally, drowsiness or dizziness may occur after taking this medication, so caution is advised when driving or operating hazardous machinery.

Side effects

  • Dizziness
  • fatigue
  • paresthesia
  • headache
  • flushing
  • lymphadenopathy
  • dehydration
  • hypocalcemia
  • anxiety
  • insomnia
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  • confusion
  • irritability
  • restlessness
  • depression
  • depersonalization
  • abnormal dreams
  • personality disorders
  • drowsiness
  • sensory disturbances
  • sensory loss
  • taste abnormalities
  • tremors
  • concentration difficulties
  • somnolence
  • hypersensitivity
  • sedation
  • vertigo
  • involuntary muscle contractions
  • forgetfulness
  • hypertonia
  • muscle hypotonia
  • decreased reflexes
  • activity impairment
  • visual disturbances
  • eye pain
  • eye irritation
  • photophobia
  • night blindness
  • tinnitus
  • ear pain
  • ear discomfort
  • ear disorders
  • ear itching
  • hyperacusis
  • palpitations
  • tachycardia
  • bradycardia
  • peripheral coldness
  • hypertension
  • throat tension
  • rhinitis
  • sinusitis
  • sore throat
  • nosebleed
  • hiccups
  • hyperventilation
  • 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
  • pruritus
  • erythema
  • piloerection
  • purpura
  • urticaria
  • musculoskeletal stiffness
  • musculoskeletal pain
  • limb pain
  • low back pain
  • arthralgia
  • frequent urination
  • polyuria
  • nocturia
  • renal pain
  • chest tenderness
  • chest discomfort
  • chest pain
  • heat sensation
  • impaired thermoregulation
  • pain
  • weakness
  • thirst
  • lethargy
  • increased vitality
  • malaise
  • fever
  • increased serum bilirubin
  • decreased serum calcium
  • abnormal urinalysis
  • abrasion
  • allergic rash
  • dermatitis
  • petechiae
  • skin discoloration
  • facial swelling
  • urticaria
  • angioedema
  • anaphylaxis
  • seizures
  • acute myocardial infarction
  • upper abdominal pain
  • chest discomfort
  • oral sensory abnormalities
  • upper gastric discomfort
  • high anxiety
  • myalgia
  • myasthenia
  • rash
  • chest tightness
  • nasopharyngitis
  • elevated creatine kinase
  • pelvic inflammation
  • dry mouth
  • throat pain
  • shoulder pain
  • lethargy
  • floaters
  • eye congestion
  • decreased consciousness
  • weight gain
  • hallucinations

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

Storage

This medication may be sensitive to air and moisture, so it must be stored in a tightly sealed container. Additionally, it should be kept at a temperature between 1 degree and 30 degrees Celsius, at room temperature. Proper storage will help maintain the effectiveness of the medication for a longer time.

Appearance and packaging

Appearance

Biconvex white round film-coated tablet

Package unit

20 tablets/box [(10 tablets/PTP 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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For anything that needs medical judgment, consult a doctor or pharmacist.

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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.