Medication info
Lureka OD Tablet 50 mg (Pregabalin)

Lureka OD Tablet 50 mg (Pregabalin)

Prescription medicationOrally disintegrating Tablet
Ingredient · strength
Pregabalin›50mg / 1 tablet
Manufacturer / importer
(주)휴온스생명과학
Appearance
Yellow round orally disintegrating tablet
Packaging
30 tablets/PTP [10 tablets/PTP x 3], 100 tablets/PTP [10 tablets/PTP x 10]
Approval status
Active

MFDS item code 202600534 · Approved 2026.02.24

Summary

Main use
Relief of peripheral and central neuropathic pain, adjunctive treatment for partial seizures in epilepsy, improvement of fibromyalgia
Who uses it
Adults · Children
Adult dosage
This medication is taken orally twice a day, regardless of meals, and should be placed on the tongue and swallowed without water once it disintegrates. 1. Neuropathic pain 1) Peripheral neuropathic pain: Initiate with a dose of 150 mg daily, which can be increased to 300 mg over 3 to 7 days, and if needed, further increase to a maximum of 600 mg over intervals of 7 days. 2) Central neuropathic pain: Initiate with a dose of 150 mg daily.
Children's dosage
Administration is not recommended due to insufficient safety and efficacy data in children under 12 years of age and adolescents aged 12 to 17.

Ingredients

Manufacturer
(주)휴온스생명과학

Efficacy & effects

Relief of peripheral and central neuropathic pain, adjunctive treatment for partial seizures in epilepsy, improvement of fibromyalgia

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

This medication is effective for the treatment of peripheral and central neuropathic pain in adults. It is also used as an adjunct to control partial seizures in patients with epilepsy. Additionally, it helps in alleviating symptoms of fibromyalgia. It is used to improve symptoms of various neurological disorders.

Dosage and Administration

Adult dosage

This medication is taken orally twice a day, regardless of meals, and should be placed on the tongue and swallowed without water once it disintegrates. 1. Neuropathic pain 1) Peripheral neuropathic pain: Initiate with a dose of 150 mg daily, which can be increased to 300 mg over 3 to 7 days, and if needed, further increase to a maximum of 600 mg over intervals of 7 days. 2) Central neuropathic pain: Initiate with a dose of 150 mg daily.

Children's dosage

Administration is not recommended due to insufficient safety and efficacy data in children under 12 years of age and adolescents aged 12 to 17.

Precautions

This medication may increase the risk of suicidal thoughts or behaviors, so you should consult your healthcare provider immediately if you notice any mood changes or behavioral abnormalities during treatment. Patients allergic to pregabalin or any components of this medication should not take it. Diabetic patients may experience weight gain when taking this medication, which may require adjustment of their blood sugar control medication. If symptoms of angioedema, such as swelling of the face or around the mouth, occur, stop taking immediately and inform your healthcare provider. Elderly patients may experience dizziness, drowsiness, or confusion when taking this medication and should take precautions, avoiding dangerous activities until they acclimate to the effects of the new medication. Transient blurred vision or changes in vision may occur, and these symptoms can improve after discontinuing the medication. There is insufficient research on the safety and efficacy of this medication if other antiepileptic drugs are discontinued before its use, so careful consideration is warranted. Abrupt discontinuation of the medication may lead to withdrawal symptoms such as insomnia, headache, nausea, and anxiety, so it is safe to taper off the medication gradually in consultation with your healthcare provider. Patients with a history of substance abuse may have an increased risk of misuse with this medication, so it should be administered carefully, and signs of substance abuse should be closely monitored. Patients with impaired kidney function may require dose adjustments of this medication. Patients with heart disease, especially those with congestive heart failure, require careful monitoring while taking this medication. When taken with opioid analgesics, respiratory depression may increase due to enhanced central nervous system depressant effects, warranting caution. In early pregnancy, there may be a risk of congenital malformations for the fetus; therefore, pregnant women should avoid taking this medication as much as possible, and women of childbearing age should use effective contraception. Breastfeeding women should discuss the use of this medication with their healthcare providers, as it may be excreted in breast milk. This medication may cause dizziness and drowsiness, so it is advisable to avoid driving or operating hazardous machinery after taking it. Severe skin reactions may rarely occur, so if any skin abnormalities develop, discontinue the medication immediately and inform your healthcare provider. Overdose may result in drowsiness, confusion, depression, seizures, and treatment such as blood dialysis may be required if necessary. Children and elderly individuals should store this medication in a safe place out of reach of children.

Side effects and when to seek care immediately

Serious side effects

Hives, severe swelling (edema), chest tightness, difficulty breathing, cold sweat, severe allergic reactions, high fever coupled with severe rash, blisters, skin peeling, pain in mucous membranes of the mouth/eyes, severe abnormal skin reactions, shortness of breath or difficulty breathing, asthma attacks, breathing difficulties associated with cough and fever, yellowing of the skin or eyes (jaundice), profound lethargy, liver abnormalities, sudden and severe headaches, thunderclap headache

Mild side effects

  • Dizziness
  • drowsiness
  • confusion
  • disturbances in spatial orientation
  • irritability
  • depression
  • euphoria
  • decreased libido
  • insomnia
  • depersonalization
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  • sexual hyperesthesia
  • restlessness
  • anxiety
  • mood swings
  • emotional blunting
  • emotional elevation
  • hallucinations
  • abnormal dreams
  • increased libido
  • panic attacks
  • impulsivity
  • apathy
  • ataxia
  • motor coordination disturbances
  • balance disorders
  • amnesia
  • attention deficit
  • memory impairment
  • tremors
  • dysarthria
  • sensory abnormalities
  • sensory loss
  • sedation
  • cognitive impairment
  • ocular tremors

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

Storage

This medication may be sensitive to air and moisture, so it should be stored in a tightly sealed container. It is best to maintain room temperature between 1 degree and 30 degrees Celsius. Proper storage will ensure the safety and effectiveness of the medication.

Appearance and packaging

Appearance

Yellow round orally disintegrating tablet

Package unit

30 tablets/PTP [10 tablets/PTP x 3], 100 tablets/PTP [10 tablets/PTP x 10]

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.