Medication info

Pregabalin Capsule 75 mg

Prescription medicationHard capsuleExpired
Ingredient · strength
Pregabalin›75mg / 1 capsule
Manufacturer / importer
케이엠에스제약(주)
Appearance
Hard capsule with the upper part brownish yellow and the lower part white, containing white powder
Packaging
Domestic - 30 capsules/bottle, Domestic - 60 capsules/bottle
Approval status
Expired

MFDS item code 201908673 · Approved 2019.12.27

This product's status changed to Expired on 2024.12.27. It may no longer be sold, so consult a doctor or pharmacist before taking it.

Summary

Main use
Treatment of peripheral and central neuropathic pain, adjunctive therapy for partial seizures in epilepsy, improvement of fibromyalgia
Who uses it
Adults · Children
Adult dosage
This medication is orally administered in two divided doses per day, regardless of food. 1. Neuropathic pain - Peripheral neuropathic pain: Starting dose is 150 mg per day, can be increased to 300 mg per day within 3 to 7 days, and can be further increased to a maximum of 600 mg per day at 7-day intervals. - Central neuropathic pain: Starting dose is 150 mg per day, can be increased to 300 mg per day after one week.
Children's dosage
For children under 12 years of age and adolescents between 12-17 years, safety and efficacy data are insufficient; therefore, administration is not recommended.

Ingredients

Manufacturer
케이엠에스제약(주)

Efficacy & effects

Treatment of peripheral and central neuropathic pain, adjunctive therapy for partial seizures in epilepsy, improvement of fibromyalgia

  • Peripheral neuropathic pain
  • central neuropathic pain
  • epilepsy
  • secondary generalized symptoms
  • partial seizures
  • fibromyalgia
View approved original text

This medication is used to treat peripheral and central neuropathic pain in adults and is used as an adjunctive therapy for partial seizures with or without secondary generalized symptoms in epilepsy patients. It is also effective in treating fibromyalgia. This medication helps with various neurological disorders and pain management.

Dosage and Administration

Adult dosage

This medication is orally administered in two divided doses per day, regardless of food. 1. Neuropathic pain - Peripheral neuropathic pain: Starting dose is 150 mg per day, can be increased to 300 mg per day within 3 to 7 days, and can be further increased to a maximum of 600 mg per day at 7-day intervals. - Central neuropathic pain: Starting dose is 150 mg per day, can be increased to 300 mg per day after one week.

Children's dosage

For children under 12 years of age and adolescents between 12-17 years, safety and efficacy data are insufficient; therefore, administration is not recommended.

Precautions

This medication may increase the risk of suicidal thoughts or behavior; therefore, if mood changes or unusual behavior occur during treatment, consult a doctor immediately. This medication should not be used if there is an allergy to any of the ingredients contained. Patients with certain genetic problems such as lactose intolerance should not take this medication. Diabetic patients may need to adjust the dosage of blood sugar control medications due to weight gain. If serious allergic reactions such as angioedema occur, discontinue the medication immediately and inform medical personnel. Elderly patients are at higher risk of injury due to dizziness or drowsiness from taking this medication. This medication may cause temporary blurred vision or changes in eyesight; if these symptoms occur, consult a doctor. Discontinuation of this medication should be gradual to avoid withdrawal symptoms such as insomnia, headache, and anxiety; do so under medical supervision. Patients with a history of drug abuse are at higher risk for misuse or dependence on this medication, and caution is required during use. Patients with impaired kidney function may require dosage adjustments. Patients with heart disease should use caution when taking this medication. Caution is advised when used in combination with opioid analgesics as it may increase central nervous system depressant effects. This medication poses a risk of respiratory depression; consult a doctor if there are respiratory disorders or kidney problems. During early pregnancy, there may be a risk of fetal malformation; therefore, women who are pregnant or planning to become pregnant should consult a physician and use effective contraception. During breastfeeding, this medication may be transmitted through breast milk, so consult medical personnel regarding the nursing status and medication use. It is advisable to avoid activities that require caution such as driving or operating machinery until dizziness or drowsiness has resolved after taking this medication. If severe rashes or swelling occur, discontinue the medication immediately and inform medical personnel. In case of overdose, symptoms such as drowsiness, confusion, and seizures may occur; seek emergency treatment immediately. This medication should be kept out of the reach of children, and it is safe not to transfer it to another container.

Side effects and when to seek care immediately

Serious side effects

Hives, severe swelling (including 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, pain in oral/ocular mucosa, severe allergic reactions, severe dermatological adverse reactions, breathing difficulties, jaundice (yellowing of the skin or eyes), profound lethargy, liver dysfunction (jaundice), sudden and severe headaches, lightning-like pain

Mild side effects

  • Dizziness
  • drowsiness
  • confusion
  • disorientation
  • irritability
  • depression
  • euphoria
  • decreased libido
  • insomnia
  • depersonalization
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  • sexual dysfunction
  • restlessness
  • anxiety
  • mood swings
  • emotional lability
  • difficulty finding appropriate words
  • hallucinations
  • abnormal dreams
  • increased libido
  • panic attacks
  • impulsivity
  • numbness
  • ataxia
  • motor coordination abnormalities
  • balance disorders
  • amnesia
  • attention disorders
  • memory impairment
  • tremor
  • dysarthria
  • 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 prevent air or moisture from entering. It is best to maintain a storage temperature between 15 degrees and 30 degrees Celsius (room temperature).

Appearance and packaging

Appearance

Hard capsule with the upper part brownish yellow and the lower part white, containing white powder

Package unit

Domestic - 30 capsules/bottle, Domestic - 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.