Medication info
Atrapent Semi Tablet

Atrapent Semi Tablet

Prescription medicationTablet경구
Ingredient · strength
Tramadol Hydrochloride›18.75mg / 1 tabletAcetaminophen›162.5mg / 1 tablet
Manufacturer / importer
한국프라임제약(주)
Appearance
Pale yellow rectangular film-coated tablet
Packaging
(Domestic use) 30 tablets/bottle, 300 tablets/bottle (Export use) 50 tablets (10 tablets/PTP×5)
Approval status
Active

MFDS item code 200805737 · Notified 2008.05.22 · Insurance code 663602840

Summary

Main use
Relief of moderate to severe acute and chronic pain
Who takes it
Adults · Children
Adult dose
For children over 12 years and adults: The dosage should be adjusted according to the severity of the patient's pain and treatment response. A starting dose of 4 tablets is recommended, followed by a dosing interval of at least 6 hours or more, but should not exceed 16 tablets per day. The lowest effective dose should be administered for the shortest duration possible. This medication should not be taken for longer than necessary, and if long-term administration is required due to the nature and severity of the disease, regular monitoring should be performed to determine the continuation of this medication.
Child dose
For children over 12 years and adults: The dosage should be adjusted according to the severity of the patient's pain and treatment response. A starting dose of 4 tablets is recommended, followed by a dosing interval of at least 6 hours or more per day.

Ingredients

Manufacturer
한국프라임제약(주)

Efficacy & effects

Relief of moderate to severe acute and chronic pain

  • Acute pain
  • chronic pain
View approved original text

This medication is used to relieve moderate to severe acute and chronic pain.

How to take

Adult dose

For children over 12 years and adults: The dosage should be adjusted according to the severity of the patient's pain and treatment response. A starting dose of 4 tablets is recommended, followed by a dosing interval of at least 6 hours or more, but should not exceed 16 tablets per day. The lowest effective dose should be administered for the shortest duration possible. This medication should not be taken for longer than necessary, and if long-term administration is required due to the nature and severity of the disease, regular monitoring should be performed to determine the continuation of this medication.

Child dose

For children over 12 years and adults: The dosage should be adjusted according to the severity of the patient's pain and treatment response. A starting dose of 4 tablets is recommended, followed by a dosing interval of at least 6 hours or more per day.

Precautions

This medication may cause liver damage, thus individuals who consume large amounts of alcohol daily should consult a doctor or pharmacist before taking it. If any abnormal symptoms such as rashes or blisters appear on the skin after taking this medication, it should be discontinued immediately, and a doctor should be consulted. Due to the risk of seizures, patients with a history of seizures or at high risk for seizures should use this medication with caution. This medication can rarely cause severe allergic reactions; if signs of hypersensitivity occur, immediate medical attention should be sought. Patients with acute bronchial asthma are at greater risk of respiratory distress when using this medication, so it should only be administered in special environments. Taking this medication in conjunction with alcohol or central nervous system depressants may lead to severe drowsiness or respiratory depression, and caution is required. Patients with head injuries or brain disorders may experience problems such as increased intracranial pressure while taking this medication, and should use it with caution. This medication may cause physical and psychological dependence, and therefore should be taken under a doctor's guidance if used for extended periods. Patients with compromised liver function must consult a doctor before taking this medication and should be careful not to exceed the recommended dosage. Patients with specific genotypes may metabolize this medication rapidly, increasing the risk of respiratory depression, so caution is required. This medication should not be used in children under the age of 12 or specific pediatric patients after certain surgeries, and adolescents over 12 should be administered it carefully. Patients with sleep apnea or at risk for hypoxemia should continuously monitor for symptom deterioration while taking this medication. This medication may induce hyponatremia, so elderly individuals or those with risk factors should verify serum sodium levels during administration. Patients with allergies to this medication's ingredients or those taking certain drugs should not take it, and it is also contraindicated in patients with severe respiratory depression. Pregnant or breastfeeding women should consult a doctor before using this medication, as it may affect the fetus or newborn. Caution is required, as drowsiness or dizziness may occur while driving or operating machinery. Overdose may result in severe respiratory depression, seizures, liver damage, etc., so the prescribed dose must be adhered to strictly. Care should be taken not to take other analgesics or medications containing acetaminophen concurrently during the course of this medication. Abrupt cessation of use may result in withdrawal symptoms, so dosages should be tapered off gradually according to a doctor's instructions. Since this medication interacts with many other drugs, if you are taking other medications, you must inform your doctor or pharmacist, especially if taking antidepressants or anticonvulsants.

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 high fever, blisters, skin peeling, pain in oral/ocular mucous membranes, shortness of breath or difficulty breathing, asthma attacks, respiratory issues accompanied by cough and fever, jaundice (yellowing of the skin or eyes), extreme lethargy, sudden and severe headache, thunderclap headache, seizures, confusion of consciousness, visual disturbances, paralysis, urination.

Mild side effects

  • Loss of appetite
  • insomnia
  • depression
  • dizziness
  • headache
  • drowsiness
  • nausea
  • vomiting
  • constipation
  • dry mouth
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  • diarrhea
  • dyspepsia
  • abdominal pain
  • abdominal discomfort
  • flatulence
  • pruritus
  • sweating
  • rash
  • fatigue
  • flushing
  • anxiety
  • irritability
  • emotional instability
  • euphoria
  • decreased libido
  • sleep disturbances
  • confusion
  • spatial disorientation
  • excitement
  • abnormal dreams
  • drug abuse
  • hallucinations
  • withdrawal syndrome
  • migraine
  • somnolence
  • sensory impairment
  • tremors
  • paraesthesia
  • attention.

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 and moisture from entering, and it is best kept at room temperature between 1 degree and 30 degrees Celsius.

Appearance and packaging

Appearance

Pale yellow rectangular film-coated tablet

Package unit

(Domestic use) 30 tablets/bottle, 300 tablets/bottle (Export use) 50 tablets (10 tablets/PTP×5)

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.

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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.