Medication info
Proca-van Capsule 25 mg (Pregabalin)

Proca-van Capsule 25 mg (Pregabalin)

Prescription medicationHard capsule경구
Ingredient · strength
Pregabalin›25mg / 1 capsule
Manufacturer / importer
(주)이든파마
Appearance
A hard capsule with a light yellow upper part and white lower part containing a white powder.
Packaging
30 capsules/bottle
Approval status
Active

MFDS item code 202001648 · Approved 2020.03.10 · Insurance code 628901640

Summary

Main use
Treatment of peripheral and central neuropathic pain, adjunctive treatment for partial seizures in epilepsy, improvement of fibromyalgia.
Who takes it
Adults · Children
Adult dose
This medication is taken orally, divided into two doses a day, regardless of food intake. 1. Neuropathic pain - Peripheral neuropathic pain: Start with a daily dose of 150 mg, which can be increased to 300 mg daily after 3 to 7 days. If needed, the dosage can further be increased to a maximum of 600 mg daily, in 7-day intervals. - Central neuropathic pain: Starting dose is 150 mg daily.
Child dose
For children under the age of 12 and adolescents aged 12-17, the adequacy of safety and efficacy data is insufficient, and administration is not recommended.

Ingredients

Manufacturer
(주)이든파마

Efficacy & effects

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

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

This medication is effective in treating pain caused by peripheral and central neuropathy in adults. It is also used as an adjunctive treatment for partial seizures in epilepsy patients, whether there are secondary generalized symptoms or not. Additionally, it helps alleviate the symptoms of fibromyalgia. It is widely utilized in various neurological disorders and contributes to improving the quality of life of patients.

How to take

Adult dose

This medication is taken orally, divided into two doses a day, regardless of food intake. 1. Neuropathic pain - Peripheral neuropathic pain: Start with a daily dose of 150 mg, which can be increased to 300 mg daily after 3 to 7 days. If needed, the dosage can further be increased to a maximum of 600 mg daily, in 7-day intervals. - Central neuropathic pain: Starting dose is 150 mg daily.

Child dose

For children under the age of 12 and adolescents aged 12-17, the adequacy of safety and efficacy data is insufficient, and administration is not recommended.

Precautions

This medication may increase the risk of suicidal thoughts or behavior, so if there are any changes in mood or behavior during use, patients must inform healthcare professionals immediately. Patients with allergies to the ingredients of this medication or certain genetic disorders should not use it. Diabetic patients should be cautious as weight gain may necessitate adjustments in the dosage of blood sugar control medications. If symptoms of angioedema (swelling of the face or around the mouth) occur, use should be discontinued immediately and medical attention sought. Elderly patients should be careful post-administration due to the risk of dizziness or drowsiness leading to falls or injuries. Some patients may experience blurred vision or changes in vision, and if these symptoms occur, they should consult a healthcare professional. Discontinuing this medication suddenly may lead to withdrawal symptoms such as insomnia, headache, and anxiety, so it should be gradually tapered as directed by a healthcare professional. This medication carries a risk of drug abuse, so patients with a history of substance abuse should be particularly vigilant and monitored for abnormal behavior. Patients with impaired kidney function may require dosage adjustments. Patients with severe cardiac conditions should use this medication with caution. When taken with other medications that have central nervous system depressant effects, there may be an increased risk of drowsiness or respiratory depression, so caution is required. In early pregnancy, there may be a risk of congenital malformations in the fetus, so women who are pregnant or planning to become pregnant should consult with healthcare professionals before use and should use effective contraception. Breastfeeding women should discuss with healthcare professionals whether to discontinue breastfeeding or the medication since it can be passed into breast milk. Activities that require concentration, such as driving or operating machinery, should be avoided until dizziness or drowsiness fully resolves. In the case of overdose, symptoms such as confusion, drowsiness, and seizures may occur, and medical attention should be sought immediately; blood dialysis may be required if necessary. Keep this medication out of the reach of children and avoid transferring it to another container. If severe rashes, swelling, or breathing difficulties occur, use should be stopped immediately and healthcare professionals informed.

Side effects and when to seek care immediately

Serious side effects

Hives, severe swelling (edema), angioedema, facial swelling, cold sweat, chest tightness, difficulty breathing, symptoms resembling anaphylaxis, severe rash with fever, blisters, skin peeling, pain in oral/ocular mucosa, Stevens-Johnson syndrome, toxic epidermal necrolysis, mucous membrane syndrome, erythema multiforme, 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
  • rhinopharyngitis
  • increased appetite
  • appetite loss
  • hypoglycemia
  • confusion
  • disorientation
  • irritability
  • depression
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  • euphoria
  • decreased libido
  • insomnia
  • depersonalization
  • hyperesthesia
  • restlessness
  • anxiety
  • mood swings
  • emotional blunting
  • emotional elevation
  • difficulty finding appropriate words
  • hallucinations
  • abnormal dreams
  • increased libido
  • panic attacks
  • lack of impulse control
  • apathy
  • ataxia
  • abnormal coordination
  • equilibrium disorders
  • memory loss
  • attention deficit
  • impaired memory function.

Not everyone experiences these, and they can vary from person to person.

Storage

This medication should be stored in a tightly closed container to prevent exposure to air or moisture, preferably at room temperature between 15℃ and 30℃. Storing it this way helps maintain the medication's effectiveness for a longer period.

Appearance and packaging

Appearance

A hard capsule with a light yellow upper part and white lower part containing a white powder.

Package unit

30 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.