Medication info

Boryeong Pregabalin Capsule 150 mg

Prescription medication경구Expired
Ingredient · strength
Pregabalin›150mg / 1 capsule
Manufacturer / importer
(주)보령
Appearance
A hard capsule of white color with white or light yellow powder inside.
Packaging
30 capsules/bottle, 100 capsules/bottle
Approval status
Expired

MFDS item code 202001636 · Approved 2020.03.10

This product's status changed to Expired on 2025.03.10. It may no longer be sold, so consult a doctor or pharmacist before taking it.

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 pregabalin and is taken orally, divided into total daily doses administered twice a day, irrespective of food. 1. Neuropathic pain 1) Peripheral neuropathic pain: Starting dose may be 150 mg per day, with possible titration to a maximum of 600 mg per day after 3 to 7 days. 2) Central neuropathic pain: Starting dose of 150 mg per day, increase to 300 mg per day after 1 week, and then up to 600 mg per day thereafter.
Child dose
Safety and efficacy data are insufficient for children under 12 and adolescents aged 12-17, therefore use is not recommended.

Ingredients

Manufacturer
(주)보령

Efficacy & effects

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

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

This medication is used to relieve peripheral and central neuropathic pain in adults. It is also suitable as an adjunctive therapy to control partial seizures in patients with epilepsy. Additionally, it helps alleviate symptoms of fibromyalgia. Overall, this medication is effective in improving symptoms associated with various nerve-related disorders.

How to take

Adult dose

This medication is pregabalin and is taken orally, divided into total daily doses administered twice a day, irrespective of food. 1. Neuropathic pain 1) Peripheral neuropathic pain: Starting dose may be 150 mg per day, with possible titration to a maximum of 600 mg per day after 3 to 7 days. 2) Central neuropathic pain: Starting dose of 150 mg per day, increase to 300 mg per day after 1 week, and then up to 600 mg per day thereafter.

Child dose

Safety and efficacy data are insufficient for children under 12 and adolescents aged 12-17, therefore use is not recommended.

Precautions

This medication is used as an anticonvulsant, and there is an increased risk of developing mental health issues such as suicidal thoughts or behavior, and depression during treatment. Therefore, patients taking this medication should immediately inform their healthcare provider of any changes in mood or behavior. This medication should not be administered to patients with hypersensitivity to its ingredients or those with certain genetic lactose intolerance. Diabetic patients may experience weight gain from this medication, which may require adjustment of their blood sugar control medications. Allergic reactions such as angioedema may occur, so if swelling of the face or around the mouth occurs, medication should be discontinued immediately. Elderly patients may experience increased dizziness or drowsiness when taking this medication and should be cautious about falling; neurological symptoms such as loss of consciousness or confusion may also be observed. Visual disturbances such as blurred vision may occur, and these symptoms may improve after discontinuation of the medication. There is insufficient information on the cessation of other anticonvulsants before using this medication alone, and caution is advised. Abrupt withdrawal may result in withdrawal symptoms such as insomnia, headaches, nausea, and anxiety, so gradual reduction as per doctor's instructions is necessary. Patients with a history of substance abuse should be closely monitored due to a higher risk of misuse of this medication. Patients with decreased renal function may require dose adjustments, and there have been cases where renal function improved after discontinuing or reducing the dose of this medication. Careful administration is needed for patients with heart disease, especially those with congestive heart failure. Combining this medication with other drugs that have central nervous system depressant effects may increase the risk of respiratory depression, thus caution is required. While taking this medication, caution should be observed when driving or operating hazardous machinery, as dizziness or drowsiness may occur. In early pregnancy, there may be a risk of congenital malformations to the fetus; thus, women who are pregnant or planning to become pregnant should consult a healthcare provider before taking this medication and use effective contraception. Lactating women should decide carefully whether to discontinue breastfeeding or the medication, as this drug may pass into breast milk and affect the baby. In cases of overdose, symptoms may include drowsiness, confusion, depression, and seizures; professional treatment, including possible dialysis, may be required. This medication should be stored in a safe place out of reach of children, and it should not be transferred to other containers. Various side effects may occur with this medication, so it is important to consult a healthcare provider immediately if any unusual symptoms appear.

Side effects and when to seek care immediately

Serious side effects

  • Hives
  • severe swelling (edema)
  • angioedema
  • chest tightness
  • difficulty breathing
  • cold sweat
  • pallor
  • severe rash with high fever
  • blisters
  • mucosal pain in the mouth/eyes
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  • severe skin reactions
  • difficulty breathing
  • asthma attack
  • respiratory issues with cough and fever
  • jaundice (skin or eyes turning yellow)
  • extreme lethargy
  • liver abnormalities (jaundice)
  • sudden and severe headaches
  • lightning-like pain

Mild side effects

  • Dizziness
  • drowsiness
  • confusion
  • loss of sense of direction
  • irritability
  • depression
  • euphoria
  • decreased libido
  • insomnia
  • depersonalization
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  • altered sexual sensation
  • restlessness
  • anxiety
  • mood swings
  • emotional lability
  • difficulty finding appropriate terms
  • hallucinations
  • abnormal dreams
  • increased libido
  • panic attacks
  • impulsivity
  • numbness
  • ataxia
  • abnormal motor coordination
  • balance disorders
  • memory loss
  • attention deficit
  • memory impairment
  • tremors
  • speech disturbances
  • sensory disturbances
  • sensory loss

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

Storage

This medication should be stored in a tightly closed container to prevent air and moisture from entering. The storage temperature should be between 15 and 30 degrees Celsius, avoiding excessively hot or cold places.

Appearance and packaging

Appearance

A hard capsule of white color with white or light yellow powder inside.

Package unit

30 capsules/bottle, 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.