Medication info
Pregabalin Tablet 75 mg (Pregabalin)

Pregabalin Tablet 75 mg (Pregabalin)

Prescription medicationTablet경구
Ingredient · strength
Pregabalin›75mg / 1 tablet
Manufacturer / importer
명문제약(주)
Appearance
Light blue oval film-coated tablet
Packaging
30 tablets/bottle
Approval status
Active

MFDS item code 201905644 · Approved 2019.08.09 · Insurance code 649807490

Summary

Main use
Treatment of peripheral and central neuropathic pain, adjunct for epilepsy partial seizures, improvement of fibromyalgia
Who takes it
Adults · Children
Adult dose
This drug is administered orally in divided doses of the total daily dose of pregabalin twice daily, with or without food. 1. Neuropathic Pain 1) Peripheral Neuropathic Pain The starting dose may be 150 mg per day, and can be increased to 300 mg per day after 3 to 7 days. If necessary, the dose can be further increased to a maximum of 600 mg per day at intervals of 7 days. 2) Central Neuropathic Pain The starting dose may be 150 mg per day, and based on individual response and tolerability, the dose can be increased to 300 mg per day after one week. Additionally, the dose can be increased to a target daily dose of 600 mg after another week, if tolerability is not shown at the target dose.
Child dose
Safety and efficacy data are insufficient for children under 12 years of age and adolescents aged 12 to 17 years, so use is not recommended.

Ingredients

Manufacturer
명문제약(주)

Efficacy & effects

Treatment of peripheral and central neuropathic pain, adjunct for epilepsy partial seizures, improvement of fibromyalgia

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

This medication is used to relieve peripheral and central neuropathic pain in adults. It is also effective as an adjunct therapy for partial seizures in epilepsy patients, whether or not there are secondary generalized symptoms. Additionally, it helps in the treatment of fibromyalgia. In other words, this drug is used to treat pain and seizure symptoms associated with various neurological disorders.

How to take

Adult dose

This drug is administered orally in divided doses of the total daily dose of pregabalin twice daily, with or without food. 1. Neuropathic Pain 1) Peripheral Neuropathic Pain The starting dose may be 150 mg per day, and can be increased to 300 mg per day after 3 to 7 days. If necessary, the dose can be further increased to a maximum of 600 mg per day at intervals of 7 days. 2) Central Neuropathic Pain The starting dose may be 150 mg per day, and based on individual response and tolerability, the dose can be increased to 300 mg per day after one week. Additionally, the dose can be increased to a target daily dose of 600 mg after another week, if tolerability is not shown at the target dose.

Child dose

Safety and efficacy data are insufficient for children under 12 years of age and adolescents aged 12 to 17 years, so use is not recommended.

Precautions

This medication may increase the risk of suicidal thoughts or behaviors, so if depression, mood changes, or unusual behavior occurs during treatment, it should be reported to a healthcare provider immediately. Patients with hypersensitivity to this medication or a known allergy to its ingredients should not take it, and those sensitive to certain dyes or lactose should be cautious. Diabetic patients may require adjustment of their blood sugar control medications due to weight gain, so they should consult their doctor. If symptoms of angioedema (swelling around the face or mouth) occur, the medication should be stopped immediately. Elderly patients may experience dizziness, drowsiness, or confusion while taking this medication, so they should exercise caution and avoid dangerous activities during such symptoms. Visual disturbances or changes in vision may occur during treatment, and patients should inform their doctor if these symptoms appear. Discontinuation of use may lead to withdrawal symptoms such as insomnia, headaches, or anxiety, so abrupt cessation should be avoided. Patients with a history of drug abuse may have a higher risk of misuse of this medication, so caution is advised during use, and monitoring for signs of drug misuse is necessary. Patients with impaired kidney function may require dosage adjustments. Patients with severe heart disease should be careful when using this medication, especially those with congestive heart failure. Caution is needed when taking this drug in conjunction with other central nervous system depressants or opioid analgesics, as the risk of respiratory depression may increase. In early pregnancy, there is a risk of congenital malformations to the fetus, so it is advisable to avoid use during pregnancy, and women of childbearing potential should use effective contraception. Lactating women should discuss with their doctor whether to stop breastfeeding or discontinue this medication, as it can be passed into breast milk. Hazardous activities such as driving or operating machinery should be avoided until dizziness or drowsiness has resolved after taking this medication. Severe skin reactions (such as Stevens-Johnson syndrome) may rarely occur, so if any skin abnormalities develop, the medication should be discontinued immediately and medical personnel should be informed. In cases of overdose, symptoms such as drowsiness, confusion, depression, and seizures may occur, so immediate medical attention is required.

Side effects and when to seek care immediately

Serious side effects

Urticaria, angioedema, facial swelling, severe swelling (edema), chest tightness, difficulty breathing, cold sweat, pallor, severe allergic reactions, severe rash with high fever, blisters, skin peeling, pain in the oral/ocular mucosa, severe skin reaction, shortness of breath or difficulty breathing, asthma attacks, respiratory problems with cough + fever, respiratory failure, jaundice (yellowing of skin or eyes), severe systemic symptoms

Mild side effects

  • Dizziness
  • drowsiness
  • confusion
  • disorientation
  • irritability
  • depression
  • euphoria
  • decreased libido
  • insomnia
  • depersonalization
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  • sexual dysesthesia
  • restlessness
  • anxiety
  • mood fluctuations
  • emotional flattening
  • emotional elevation
  • hallucinations
  • abnormal dreams
  • increased libido
  • panic attacks
  • impulsivity
  • apathy
  • ataxia
  • impaired coordination
  • balance disorders
  • memory loss
  • attention deficit
  • cognitive impairment
  • tremor
  • dysarthria
  • sensory abnormalities
  • sensory loss
  • sedation
  • somnolence
  • cognitive dysfunction

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. It is advisable to keep the storage temperature between 1 to 30 degrees Celsius. This storage method will help maintain the drug's efficacy and safety for a longer period.

Appearance and packaging

Appearance

Light blue oval film-coated tablet

Package unit

30 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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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.