Medication info
Lyrica Capsule 75mg (Pregabalin)

Lyrica Capsule 75mg (Pregabalin)

Prescription medicationHard capsule경구
Ingredient · strength
Pregabalin›75mg / 1 capsule
Manufacturer / importer
한국휴텍스제약(주)
Appearance
A hard capsule with a light brown upper part and a white lower part containing a white powder that is white to pale yellow in color.
Packaging
30 capsules/bottle, 60 capsules/bottle
Approval status
Active

MFDS item code 201600253 · Approved 2016.01.14 · Insurance code 649102940

Summary

Main use
Treatment of peripheral and central neuropathic pain, adjunctive treatment for partial seizures, improvement of fibromyalgia.
Who takes it
Adults · Children
Adult dose
This medication is taken orally, divided into two doses per day regardless of food. 1. Neuropathic Pain - Peripheral neuropathic pain: Starting dose of 150 mg once daily can be increased to 300 mg after 3 to 7 days, and if necessary, can be increased to a maximum of 600 mg at 7-day intervals. - Central neuropathic pain: Starting dose of 150 mg once daily can be increased to 300 mg after one week.
Child dose
Administration is not recommended as there is insufficient safety and efficacy data for children under 12 years and adolescents aged 12 to 17.

Ingredients

Manufacturer
한국휴텍스제약(주)

Efficacy & effects

Treatment of peripheral and central neuropathic pain, adjunctive treatment 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 treatment for partial seizures in epilepsy. It is effective in treating fibromyalgia. Therefore, it helps improve symptoms of neuropathic pain, seizures, and myalgia.

How to take

Adult dose

This medication is taken orally, divided into two doses per day regardless of food. 1. Neuropathic Pain - Peripheral neuropathic pain: Starting dose of 150 mg once daily can be increased to 300 mg after 3 to 7 days, and if necessary, can be increased to a maximum of 600 mg at 7-day intervals. - Central neuropathic pain: Starting dose of 150 mg once daily can be increased to 300 mg after one week.

Child dose

Administration is not recommended as there is insufficient safety and efficacy data for children under 12 years and adolescents aged 12 to 17.

Precautions

This medication may increase the risk of suicidal thoughts or behavior, so if there are changes in mood or symptoms of depression during use, consult a doctor immediately. Individuals allergic to pregabalin or any of its components should not take this medicine. Patients with lactose intolerance or specific genetic metabolic disorders should also avoid this medication. Diabetic patients should be cautious as weight gain may require adjustment of blood sugar control medications. If severe allergic reactions such as angioedema occur, stop taking and inform healthcare providers immediately. Elderly individuals may experience dizziness, drowsiness, or confusion after taking this medication, so they should use it with caution. Some patients may experience blurred vision or changes in eyesight, so inform a doctor if any of these symptoms occur. Suddenly stopping this medication may lead to withdrawal symptoms such as insomnia, headache, nausea, and anxiety, so dosage should be gradually reduced according to medical advice. Patients with a history of drug abuse should be cautious as this medication may have a high risk of abuse; report any unusual behavior immediately. Patients with impaired renal function may require dosage adjustments. Patients with heart disease should also exercise caution when taking this medication. Concomitant use with other CNS depressants or alcohol may increase the risk of drowsiness or respiratory depression; caution is advised. During early pregnancy, there may be a risk of fetal malformations, so pregnant women should avoid this medication, and women of childbearing age should use effective contraception. Breastfeeding women should discuss with their doctor whether to stop breastfeeding or discontinue this medication as it can be passed into breast milk. Avoid driving or operating hazardous machinery while taking this medication for safety. Severe skin reactions may occur, and if symptoms such as rashes or blisters occur, stop taking this medication immediately. In case of overdose, symptoms like drowsiness, confusion, and seizures may appear, requiring immediate medical attention. Children, elderly patients, and those with impaired renal function should exercise particular caution when taking this medication. This medication should be kept out of the reach of children and caution should be taken not to transfer it to other containers as it may change the quality.

Side effects and when to seek care immediately

Serious side effects

Hives, severe swelling (edema), chest tightness, difficulty breathing, cold sweats, paleness, severe rash with fever, blisters, skin peeling, pain in the mucous membranes of the mouth/eyes, shortness of breath or trouble breathing, asthma attack, respiratory problems accompanying cough and fever, yellowing of skin or eyes (jaundice), severe lethargy, sudden and severe headaches, thunderclap headache, seizures, confusion of consciousness, visual disturbances, paralysis, urination problems.

Mild side effects

  • Dizziness
  • drowsiness
  • confusion
  • impaired sense of direction
  • irritability
  • depression
  • euphoria
  • decreased libido
  • insomnia
  • depersonalization
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  • hyperesthesia
  • restlessness
  • anxiety
  • mood swings
  • emotional lability
  • difficulty finding appropriate words
  • hallucinations
  • abnormal dreams
  • increased libido
  • panic attacks
  • impulsivity
  • apathy
  • ataxia
  • impaired coordination
  • equilibrium disturbance
  • amnesia
  • attention deficits
  • impaired memory
  • tremors
  • speech disturbances
  • sensory disturbances
  • decreased sensation

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 sealed container. It is recommended to maintain a storage temperature between 15 degrees and 30 degrees Celsius. This helps maintain the medication's efficacy and safety for a longer time.

Appearance and packaging

Appearance

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

Package unit

30 capsules/bottle, 60 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.