Medication info
Lyrica 75 mg (Pregabalin)

Lyrica 75 mg (Pregabalin)

Prescription medicationTablet경구
Ingredient · strength
Pregabalin›75mg / 1 tablet
Manufacturer / importer
위더스제약(주)
Appearance
Pale green oval tablet
Packaging
30 tablets/bottle, 100 tablets/bottle
Approval status
Active

MFDS item code 202002264 · Approved 2020.03.31 · Insurance code 660703410

Summary

Main use
Treatment of peripheral and central neuropathic pain and seizures (partial seizures), relief of fibromyalgia
Who takes it
Adults · Children
Adult dose
This medication is Pregabalin and is taken orally, divided into two doses daily, regardless of food. 1. Neuropathic Pain 1) Peripheral Neuropathic Pain The initial dose is 150 mg per day, which may be increased to 300 mg per day after 3 to 7 days. If necessary, it can be increased to a maximum of 600 mg per day at 7-day intervals. 2) Central Neuropathic Pain The initial dose is 150 mg per day, and after one week, it may be increased to a maximum of 300 mg per day, based on the patient's response and tolerance. An additional increase to the target daily dose of 600 mg may occur after another week.
Child dose
Administration is not recommended for children under 12 years old and adolescents aged 12-17, due to insufficient safety and efficacy data.

Ingredients

Manufacturer
위더스제약(주)

Efficacy & effects

Treatment of peripheral and central neuropathic pain and seizures (partial seizures), relief of fibromyalgia

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

This medicine is used for alleviating peripheral and central neuropathic pain in adults. It also serves as an adjunct treatment for partial seizures in epilepsy patients, with or without secondary general symptoms. Additionally, it helps relieve pain caused by fibromyalgia. In other words, this medication is used to treat various neurological disorders and pain conditions.

How to take

Adult dose

This medication is Pregabalin and is taken orally, divided into two doses daily, regardless of food. 1. Neuropathic Pain 1) Peripheral Neuropathic Pain The initial dose is 150 mg per day, which may be increased to 300 mg per day after 3 to 7 days. If necessary, it can be increased to a maximum of 600 mg per day at 7-day intervals. 2) Central Neuropathic Pain The initial dose is 150 mg per day, and after one week, it may be increased to a maximum of 300 mg per day, based on the patient's response and tolerance. An additional increase to the target daily dose of 600 mg may occur after another week.

Child dose

Administration is not recommended for children under 12 years old and adolescents aged 12-17, due to insufficient safety and efficacy data.

Precautions

This medication may increase the risk of suicidal thoughts and behaviors, so you should consult your doctor immediately if you notice any changes in mood or behavior during treatment. Patients who are allergic to pregabalin or any components of this medication should not take it. Patients with diabetes may experience changes in blood sugar control due to weight gain, and adjustments in the dosage of diabetic medication may be needed. If you experience symptoms of angioedema, such as swelling of the face or around the mouth, stop taking the drug immediately and consult your healthcare provider. Elderly patients may experience increased dizziness or drowsiness, so special caution should be taken during initial treatment, and it is advisable to avoid driving or operating hazardous machinery. Some patients may experience blurred vision or vision changes; if these symptoms occur, the medication should be stopped or a doctor consulted. Discontinuation of medication may result in withdrawal symptoms such as insomnia, headache, and anxiety, so do not stop suddenly and consult your healthcare provider. As there is a risk of drug abuse, special caution should be exercised by patients with a history of substance abuse or mental illness, and any unusual behavior should be reported immediately. Patients with impaired renal function may need dose adjustments, so it should be taken according to a doctor's instructions. Patients with severe heart disease should be cautious as there is a risk of congestive heart failure. Care should be taken when combining this medication with opioid analgesics, as it may increase the risk of central nervous system depression. Patients with respiratory or neurological diseases or elderly patients may require dose adjustments due to the risk of severe respiratory depression. Pregnant women should not use this medication in the early stages of pregnancy as it may affect the fetus, and women of childbearing age should use effective contraception. While breastfeeding, this medication may be passed into breast milk, so it is advisable to discuss whether to discontinue breastfeeding or the medication with your doctor. This medication can cause dizziness and drowsiness, so you should check your condition before driving or operating hazardous machinery. Rarely, severe skin reactions may occur, so if you notice any unusual symptoms such as skin rash or swelling, stop taking the medication immediately and consult your healthcare provider. In case of overdose, symptoms such as confusion, drowsiness, and depression may occur, and you should visit a medical institution immediately; treatment such as hemodialysis may be required if necessary. Special caution is needed for children, elderly patients, and those with impaired renal function in terms of storage and use, and it should be kept out of reach of children.

Side effects and when to seek care immediately

Serious side effects

Rash, severe swelling (angioedema, facial swelling, swelling around the mouth and upper airway), chest tightness, difficulty breathing, cold sweat, pallor, severe rash with high fever, blisters, skin peeling, oral/ocular mucosal pain, severe skin adverse reactions (Stevens-Johnson syndrome, toxic epidermal necrolysis), shortness of breath or difficulty breathing, asthma attacks, respiratory abnormalities with cough and fever, jaundice (yellowing of the skin or eyes)

Mild side effects

  • Dizziness
  • drowsiness
  • confusion
  • disorientation
  • irritability
  • depression
  • euphoria
  • decreased libido
  • insomnia
  • depersonalization
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  • altered sexual sensation
  • restlessness
  • agitation
  • mood swings
  • emotional flatness
  • emotional lability
  • difficulty finding appropriate terms
  • hallucinations
  • abnormal dreams
  • increased libido
  • panic attacks
  • impulsivity
  • indifference
  • ataxia
  • motor coordination issues
  • balance disturbances
  • amnesia
  • attention disorders
  • memory disturbances
  • 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 sealed container to protect it from air and moisture, and it is best to store it at room temperature between 1 degree and 30 degrees Celsius. By storing it this way, the efficacy of the medication can be maintained for a longer period.

Appearance and packaging

Appearance

Pale green oval tablet

Package unit

30 tablets/bottle, 100 tablets/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.