Medication info
Larakacapsule 150 mg (Pregabalin)

Larakacapsule 150 mg (Pregabalin)

Prescription medicationHard capsule경구
Ingredient · strength
Pregabalin›150mg / 1 capsule
Manufacturer / importer
(주)유영제약
Appearance
A hard capsule with a white upper part and a white lower part containing a white powder that is white or light yellow in color.
Packaging
Domestic use - 30 capsules/bottle, Domestic use - 60 capsules/bottle, Export use - 100 capsules/bottle, Export use - 30 capsules/PTP, Export use - 100 capsules/PTP
Approval status
Active

MFDS item code 201109024 · Approved 2011.10.24 · Insurance code 648203500

Summary

Main use
Treatment of peripheral and central neuropathic pain, as an adjunctive therapy for partial seizures, improvement of fibromyalgia.
Who takes it
Adults · Children
Adult dose
This medication should be administered orally as Pregabalin, divided into two doses per day regardless of meals. 1. Neuropathic pain - Peripheral neuropathic pain: An initial dose of 150 mg per day may be administered, and can be increased to 300 mg per day after 3 to 7 days, if necessary, further increments can be made to a maximum of 600 mg per day at 7-day intervals. - Central neuropathic pain: Initial dose of 150 mg per day.
Child dose
The safety and efficacy data are insufficient for children under 12 years of age and adolescents aged 12 to 17 years, thus administration is not recommended.

Ingredients

Manufacturer
(주)유영제약

Efficacy & effects

Treatment of peripheral and central neuropathic pain, as an 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 to treat peripheral and central neuropathic pain in adults. It is also used as an adjunct treatment for partial seizures in epilepsy patients with or without secondary generalization. Additionally, it is effective in alleviating the symptoms of fibromyalgia. In summary, this medication is used for neuropathic pain, partial seizures, and fibromyalgia.

How to take

Adult dose

This medication should be administered orally as Pregabalin, divided into two doses per day regardless of meals. 1. Neuropathic pain - Peripheral neuropathic pain: An initial dose of 150 mg per day may be administered, and can be increased to 300 mg per day after 3 to 7 days, if necessary, further increments can be made to a maximum of 600 mg per day at 7-day intervals. - Central neuropathic pain: Initial dose of 150 mg per day.

Child dose

The safety and efficacy data are insufficient for children under 12 years of age and adolescents aged 12 to 17 years, thus administration is not recommended.

Precautions

This medication may increase the risk of suicidal thoughts or behaviors, and any changes in mood or unusual behavior should be reported to a doctor immediately while taking it. Individuals with hypersensitivity to this medication or certain genetic disorders, such as lactose intolerance, should not take it. Diabetic patients should discuss dosage adjustments with their doctor due to potential weight gain affecting blood sugar control. If symptoms of angioedema appear, the medication should be stopped immediately and healthcare personnel should be notified. Elderly individuals should be cautious due to the risk of falls from dizziness or drowsiness, especially during the initial stages of treatment. Transient blurring of vision or changes in eyesight may occur, so consult a physician if unusual symptoms arise. Abrupt discontinuation of this medication can cause withdrawal symptoms such as insomnia, headache, and anxiety, so it should be tapered off gradually under medical guidance. Patients with a history of substance abuse may require special attention due to the potential for misuse or dependence on this medication. Patients with impaired kidney function should have their dosage adjusted, and patients with heart failure should also use this medication cautiously. When combined with opioid analgesics, there is an increased risk of central nervous system depression, thus caution is needed. Patients with compromised respiratory function or elderly patients have a risk of severe respiratory depression and should take this medication under the direction of healthcare personnel. During early pregnancy, there is a risk of fetal malformations, so women who are pregnant or planning to become pregnant should consult a physician and use effective contraception. For breastfeeding women, this medication may be passed into breast milk, hence they should discuss with their physician whether to discontinue breastfeeding or the medication. Tasks requiring concentration, such as driving or operating machinery, should be avoided until dizziness or drowsiness completely resolves. If serious allergic reactions such as skin rashes, fever, or difficulty in breathing occur while taking this medication, treatment should be stopped immediately and the hospital should be visited. In case of overdose, confusion, drowsiness, and depression may occur, so immediate medical attention should be sought.

Side effects and when to seek care immediately

Serious side effects

Hives, severe swelling (edema), chest tightness, difficulty breathing, cold sweats, pallor, severe rash with high fever, blisters, peeling skin, pain in oral/eye mucous membranes, shortness of breath or difficulty breathing, asthmatic attacks, respiratory issues with coughing and fever, jaundice (yellowing of skin or eyes), extreme lethargy, sudden and very severe headaches, lightning headaches, seizures, confusion of consciousness, visual disturbances, paralysis, urination.

Mild side effects

  • Dizziness
  • drowsiness
  • confusion
  • loss of direction
  • irritability
  • depression
  • euphoria
  • decreased libido
  • insomnia
  • depersonalization
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  • sexual hypersensitivity
  • restlessness
  • anxiety
  • mood swings
  • emotional blunting
  • emotional elevation
  • difficulty finding appropriate terms
  • hallucinations
  • abnormal dreams
  • increased libido
  • panic attacks
  • loss of impulse control
  • apathy
  • ataxia
  • motor coordination issues
  • balance disorders
  • memory loss
  • attention disorders
  • memory impairment
  • tremors
  • speech disturbances
  • sensory abnormalities
  • 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 must be stored in a tightly sealed container. The storage temperature should be maintained between 15 degrees and 30 degrees Celsius.

Appearance and packaging

Appearance

A hard capsule with a white upper part and a white lower part containing a white powder that is white or light yellow in color.

Package unit

Domestic use - 30 capsules/bottle, Domestic use - 60 capsules/bottle, Export use - 100 capsules/bottle, Export use - 30 capsules/PTP, Export use - 100 capsules/PTP

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.