Medication info
Pregatine Capsule 50 Milligram (Pregabalin)

Pregatine Capsule 50 Milligram (Pregabalin)

Prescription medicationHard capsule경구
Ingredient · strength
Pregabalin›50mg / 1 capsule
Manufacturer / importer
하나제약(주)
Appearance
A hard capsule with a dark blue body and white cap that contains a white or pale yellow powder.
Packaging
For domestic use - 30 capsules/bottle, For domestic use - 100 capsules/bottle
Approval status
Active

MFDS item code 201900612 · Approved 2019.01.23 · Insurance code 657806380

Summary

Main use
Treatment of peripheral and central neuropathic pain, adjunctive therapy for partial seizures, improvement of fibromyalgia.
Who takes it
Adults · Children
Adult dose
This medication is administered orally in two divided doses regardless of food intake. 1. Neuropathic pain - Peripheral neuropathic pain: Starting dose of 150 mg once daily can be administered with a possible increase to 300 mg after 3 to 7 days, and if necessary, can be titrated to a maximum of 600 mg once daily at 7-day intervals. - Central neuropathic pain: Starting dose of 150 mg once daily may be increased to 300 mg after a week.
Child dose
The safety and efficacy of this medication have not been sufficiently established for children under 12 years of age and adolescents aged 12-17, therefore it is not recommended for them.

Ingredients

Manufacturer
하나제약(주)

Efficacy & effects

Treatment of peripheral and central neuropathic pain, adjunctive therapy for partial seizures, improvement of fibromyalgia.

  • Peripheral neuropathic pain
  • central neuropathic pain
  • partial seizures
  • fibromyalgia
View approved original text

This medication is used for the treatment of peripheral and central neuropathic pain in adults. It is also used as an adjunctive therapy for partial seizures in epilepsy patients, applicable regardless of the presence of secondary generalized symptoms. Additionally, it helps relieve symptoms in fibromyalgia patients. In summary, it is used for alleviating neuropathic pain, adjunctive therapy for partial seizures, and treatment of fibromyalgia.

How to take

Adult dose

This medication is administered orally in two divided doses regardless of food intake. 1. Neuropathic pain - Peripheral neuropathic pain: Starting dose of 150 mg once daily can be administered with a possible increase to 300 mg after 3 to 7 days, and if necessary, can be titrated to a maximum of 600 mg once daily at 7-day intervals. - Central neuropathic pain: Starting dose of 150 mg once daily may be increased to 300 mg after a week.

Child dose

The safety and efficacy of this medication have not been sufficiently established for children under 12 years of age and adolescents aged 12-17, therefore it is not recommended for them.

Precautions

This medication is used as an anticonvulsant, and it may increase the risk of suicidal thoughts or behavior; therefore, if symptoms of depression or mood changes occur during treatment, consultation with a healthcare professional should be sought immediately. Patients with allergies to this drug's components or genetic lactose-related disorders should not take this medication. Diabetic patients may need to adjust their blood sugar control medications due to weight gain, and if angioedema symptoms occur, the medication should be discontinued immediately. Elderly patients should be cautious of the risk of falls due to dizziness or drowsiness, and visual impairments or changes in vision may occur. When discontinuing this medication, withdrawal symptoms such as insomnia, headaches, nausea, and anxiety may arise, so consultation with a healthcare professional is necessary. Patients with a history of drug abuse should be carefully monitored due to the potential for abuse with this medication. Patients with heart diseases or impaired kidney function should consult with a healthcare professional before taking this medication as dose adjustments may be necessary. Concomitant use of this drug and opioid analgesics can enhance central nervous system depression, posing risks such as respiratory depression, so caution is warranted. In early pregnancy, there may be a risk of fetal malformations; therefore, pregnant women are advised against taking this medication, and women of childbearing age should use effective contraceptive methods. Lactating women should consult with their healthcare provider about whether to discontinue breastfeeding due to the potential effects on the baby, as this medication may pass into breast milk. This medication may cause dizziness and drowsiness; therefore, caution is necessary when driving or operating dangerous machinery. In cases of overdose, confusion, drowsiness, depression, seizures, etc., may occur, requiring immediate medical attention. Store out of reach of children and do not transfer to another container for safety. If serious allergic reactions such as skin rashes, fever, or breathing difficulties occur during use, stop taking the medication immediately and visit a hospital.

Side effects and when to seek care immediately

Serious side effects

  • Hives
  • severe swelling (edema)
  • angioedema
  • facial swelling
  • symptoms of angioedema
  • chest tightness
  • difficulty breathing
  • respiratory distress
  • respiratory depression
  • anaphylactic-like symptoms
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  • cold sweat
  • pallor
  • severe rash with fever
  • blisters
  • skin peeling
  • pain in oral/ocular mucosa
  • Stevens-Johnson syndrome
  • toxic epidermal necrolysis
  • mucocutaneous syndrome
  • severe allergic reactions
  • severe skin adverse reactions
  • severe edema
  • jaundice
  • liver dysfunction

Mild side effects

Dizziness, drowsiness, confusion, loss of direction sense, irritability, depression, happiness, decreased libido, insomnia, depersonalization, sexual hypersensitivity, restlessness, anxiety, mood swings, emotional dullness, emotional elevation, difficulty finding appropriate terminology, hallucinations, abnormal dreams, increased libido, panic attacks, loss of restraint, apathy, ataxia, abnormal coordination, balance disorder, amnesia, attention disorder, memory disorder, tremors, dysarthria, sensory disturbances, sensory loss

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

Storage

This medication may be sensitive to air or moisture, so it should be stored in a tightly sealed container. Additionally, for maintaining the drug's efficacy, it is advisable to keep it at room temperature between 15 to 30 degrees Celsius.

Appearance and packaging

Appearance

A hard capsule with a dark blue body and white cap that contains a white or pale yellow powder.

Package unit

For domestic use - 30 capsules/bottle, For domestic use - 100 capsules/bottle

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.