Medication info
Pregalin Capsule 75 mg (Pregabalin)

Pregalin Capsule 75 mg (Pregabalin)

Prescription medicationHard capsule경구
Ingredient · strength
Pregabalin›75mg / 1 capsule
Manufacturer / importer
고려제약(주)
Appearance
A reddish-brown, hard capsule containing a white powder that is white or light yellow in color
Packaging
Domestic Use: 30 capsules/bottle Export Use: 28 capsules (7 capsules/PTP×4)
Approval status
Active

MFDS item code 201109238 · Approved 2011.10.27 · Insurance code 642802410

Summary

Main use
Treatment of peripheral and central neuropathic pain, adjunctive therapy for epilepsy partial seizures, and relief of fibromyalgia
Who takes it
Adults · Children
Adult dose
This medication is administered orally, divided into two doses per day, regardless of food. 1. Neuropathic Pain - Peripheral Neuropathic Pain: The starting dose is 150 mg per day, and it may be increased to 300 mg per day after 3 to 7 days; if necessary, it can be escalated to a maximum of 600 mg at 7-day intervals. - Central Neuropathic Pain: The starting dose is 150 mg per day; after one week, 300 mg may be prescribed.
Child dose
Safety and efficacy data are insufficient for children under 12 years of age and adolescents aged 12 to 17 years, so administration is not recommended.

Ingredients

Manufacturer
고려제약(주)

Efficacy & effects

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

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

This medication is effective for the treatment of peripheral and central neuropathic pain in adults. It is also used as an adjunct for patients with epilepsy to help control partial seizures. It is utilized for alleviating pain in fibromyalgia patients. In other words, it is used for peripheral and central neuralgia, adjunctive treatment for epilepsy, and improvement of fibromyalgia.

How to take

Adult dose

This medication is administered orally, divided into two doses per day, regardless of food. 1. Neuropathic Pain - Peripheral Neuropathic Pain: The starting dose is 150 mg per day, and it may be increased to 300 mg per day after 3 to 7 days; if necessary, it can be escalated to a maximum of 600 mg at 7-day intervals. - Central Neuropathic Pain: The starting dose is 150 mg per day; after one week, 300 mg may be prescribed.

Child dose

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

Precautions

This medication may increase the risk of suicidal thoughts or behavior; if symptoms of depression, mood changes, or abnormal behavior occur during treatment, immediately inform healthcare professionals. Do not take this medication if you have an allergy to any of its components. Patients with specific genetic issues such as lactose intolerance should also refrain from using this drug. Diabetic patients may experience weight gain due to this medication, which may require an adjustment in their blood glucose control drugs. In case of severe allergic reactions such as angioedema, discontinue the medication immediately and consult with healthcare professionals. Elderly patients may experience increased dizziness or drowsiness while taking this medication; hence, they should be cautious and avoid hazardous activities until they are accustomed to the medication. Some patients may experience blurred vision or changes in vision; it is important to notify healthcare professionals if these symptoms arise. If this medication is suddenly discontinued, withdrawal symptoms such as insomnia, headaches, and anxiety may occur; therefore, it should be tapered off gradually under the guidance of a healthcare professional. Patients with a history of drug abuse may have an increased risk of misuse with this medication; extra caution should be taken and they should be closely monitored for signs of misuse or dependence. Patients with impaired kidney function may require dose adjustments of this medication. Patients with severe heart diseases should exercise caution while using this medication, especially those with congestive heart failure who should use it with caution. Concurrent use of this medication with opioid analgesics may increase central nervous system depression; therefore, caution is advised. Patients with respiratory diseases, kidney impairment, elderly individuals, etc. are at risk for severe respiratory depression, and should discuss with healthcare professionals before using this medication. In early pregnancy, the use of this medication may affect the fetus, so it is advisable for pregnant women to avoid it, and women of childbearing age should use effective contraception. Breastfeeding women should be aware that this medication can be transmitted through breast milk, and should consult healthcare professionals about stopping breastfeeding or the medication. When engaging in hazardous activities such as driving or operating machinery, caution should be taken as dizziness or drowsiness may occur after taking this medication. If severe skin reactions such as rashes, blisters, or intense itching occur while using this medication, it should be discontinued immediately and the healthcare professional should be informed. In the case of overdose, symptoms may include confusion, drowsiness, and depression, and appropriate treatment such as hemodialysis may be required.

Side effects and when to seek care immediately

Serious side effects

Hives, severe swelling (edema), chest tightness, difficulty breathing, cold sweat, pallor, severe rash with fever, blisters, skin peeling, pain in oral/ocular mucous membranes, shortness of breath or difficulty breathing, asthma attack, respiratory abnormalities accompanied by cough and fever, jaundice (yellowing of the skin or eyes), profound lethargy, sudden and severe headaches, thunderclap headaches, seizures, altered consciousness, visual disturbances, paralysis, urination changes

Mild side effects

  • Dizziness
  • drowsiness
  • confusion
  • spatial disorientation
  • irritability
  • depression
  • euphoria
  • decreased libido
  • insomnia
  • depersonalization
Show 23 more
  • sexual paresthesia
  • agitation
  • anxiety
  • mood swings
  • emotional blunting
  • emotional elevation
  • difficulty finding appropriate words
  • hallucinations
  • abnormal dreams
  • increased libido
  • panic attacks
  • disinhibition
  • apathy
  • ataxia
  • motor coordination issues
  • balance disorders
  • amnesia
  • attention deficits
  • memory disturbances
  • tremors
  • 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 closed container to protect it from air and moisture. It is best to store the medication at room temperature, which should not be too hot or too cold, ideally between 15 to 30 degrees Celsius.

Appearance and packaging

Appearance

A reddish-brown, hard capsule containing a white powder that is white or light yellow in color

Package unit

Domestic Use: 30 capsules/bottle Export Use: 28 capsules (7 capsules/PTP×4)

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

No questions yet.

For anything that needs medical judgment, consult a doctor or pharmacist.

Related searches

Search tags

Suggested searches

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.