Medication info
Nerica Capsule 75mg (Pregabalin)

Nerica Capsule 75mg (Pregabalin)

Prescription medicationHard capsule경구
Ingredient · strength
Pregabalin›75mg / 1 capsule
Manufacturer / importer
동아에스티(주)
Appearance
This medicine is a hard capsule with a reddish-brown upper part and a white lower part containing white powder that appears white or light yellow.
Packaging
30 capsules/bottle, 300 capsules/bottle
Approval status
Active

MFDS item code 201109231 · Approved 2011.10.27 · Insurance code 642506710

Summary

Main use
Relief of peripheral and central neuropathic pain, adjunctive treatment for partial seizures, treatment of fibromyalgia
Who takes it
Adults · Children
Adult dose
This medication, which contains pregabalin, is to be orally administered divided into two doses per day without regard to food. 1. Neuropathic Pain 1) Peripheral Neuropathic Pain - Starting dose: 150 mg per day - After 3 to 7 days, may increase to 300 mg per day - If necessary, may continue to increase every 7 days up to a maximum of 600 mg per day. 2) Central Neuropathic Pain - Starting dose: 150 mg per day.
Child dose
There is insufficient safety and efficacy data for children under 12 years of age and adolescents aged 12 to 17 years; therefore, administration is not recommended.

Ingredients

Manufacturer
동아에스티(주)

Efficacy & effects

Relief of peripheral and central neuropathic pain, adjunctive treatment for partial seizures, treatment of fibromyalgia

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

This medication is used for the treatment of peripheral and central neuropathic pain in adults. It also serves as an adjunct to help control partial seizures in patients with epilepsy. In particular, it is effective in alleviating symptoms of fibromyalgia. It is widely used to improve symptoms related to pain and neurological disorders.

How to take

Adult dose

This medication, which contains pregabalin, is to be orally administered divided into two doses per day without regard to food. 1. Neuropathic Pain 1) Peripheral Neuropathic Pain - Starting dose: 150 mg per day - After 3 to 7 days, may increase to 300 mg per day - If necessary, may continue to increase every 7 days up to a maximum of 600 mg per day. 2) Central Neuropathic Pain - Starting dose: 150 mg per day.

Child dose

There is insufficient safety and efficacy data for children under 12 years of age and adolescents aged 12 to 17 years; therefore, administration is not recommended.

Precautions

This drug may increase the risk of suicidal thoughts or behaviors; therefore, if depressive symptoms or mood changes occur during treatment, it is important to consult medical personnel immediately. Patients with hypersensitivity to this drug or genetic issues such as lactose intolerance should not take it. Diabetic patients should be careful as weight gain may necessitate dose adjustments of blood sugar control medications. If severe allergic reactions such as angioedema occur, the medication should be discontinued immediately, and medical personnel notified. Elderly patients may be at increased risk of falls due to dizziness or drowsiness, so caution is especially advised during the initial phase of treatment. Blurred vision or changes in vision may occur; if these symptoms appear, advice from medical personnel should be sought. Sudden discontinuation of this medication may cause withdrawal symptoms such as insomnia, headache, and anxiety, so the dose should be gradually reduced according to medical advice. Patients with a history of substance abuse may be at risk of misuse of this medication and should be monitored closely while taking it. Patients with impaired kidney function may require dose adjustments. Patients with heart disease should consult medical personnel before taking this medication. When taken with opioid analgesics, the central nervous system depressant effects may be increased; thus, caution is required when used in combination. Patients with impaired respiratory function or elderly patients may have a higher risk of severe respiratory depression and may require dose adjustments. During early pregnancy, there is a risk of fetal malformations; therefore, women who are pregnant or planning to become pregnant should consult with medical personnel before taking this medication and use effective contraception. Nursing mothers should consult with medical personnel about whether to take this medication since it may be passed into breast milk. This medication can cause dizziness and drowsiness; therefore, patients should avoid dangerous activities such as driving or operating machinery after taking it. Severe skin responses such as Stevens-Johnson syndrome may rarely occur; if skin abnormalities develop, the medication should be stopped immediately and medical personnel notified. In case of overdose, confusion, drowsiness, and seizures may occur, and blood dialysis may be required if necessary. This medicine must be kept out of the reach of children and should not be transferred to other containers for safety.

Side effects and when to seek care immediately

Serious side effects

Hives, severe swelling (edema), chest tightness, difficulty breathing, cold sweat, pallor, angioedema, symptoms of angioedema (facial, oral, and upper airway swelling), loss of consciousness, confusion, mental disorders, visual disturbances, paralysis, decreased urination, renal failure, edema, generalized edema, suicidal thoughts and behaviors, severe rash with fever, blisters, skin peeling, pain in mouth/eyes mucosa, Stevens-Johnson syndrome, toxic epidermal necrolysis

Mild side effects

  • Dizziness
  • drowsiness
  • confusion
  • disorientation
  • irritability
  • depression
  • euphoria
  • decreased libido
  • insomnia
  • depersonalization
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  • sexual dysesthesia
  • restlessness
  • anxiety
  • mood swings
  • emotional blunting
  • emotional elevation
  • difficulty finding appropriate words
  • hallucinations
  • abnormal dreams
  • increased libido
  • panic attacks
  • impulsivity
  • apathy
  • ataxia
  • coordination disturbances
  • balance disorders
  • amnesia
  • attention deficits
  • memory impairment
  • tremors
  • speech disorders
  • 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 exposure to air or moisture. The ideal storage temperature is between 1 degree and 30 degrees Celsius.

Appearance and packaging

Appearance

This medicine is a hard capsule with a reddish-brown upper part and a white lower part containing white powder that appears white or light yellow.

Package unit

30 capsules/bottle, 300 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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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.