Medication info
Jayartset Tablets

Jayartset Tablets

Prescription medicationTablet경구
Ingredient · strength
Tramadol Hydrochloride›37.5mg / 1 tabletAcetaminophen›325mg / 1 tablet
Manufacturer / importer
(주)라이트팜텍
Appearance
Pale yellow oblong film-coated tablets
Packaging
30 tablets/bottle, 300 tablets/bottle
Approval status
Active

MFDS item code 201902554 · Approved 2019.04.24

Summary

Main use
Relief of moderate to severe acute and chronic pain
Who takes it
Adults · Children
Adult dose
Children aged 12 and over and adults: Adjust the dosage according to the patient's level of pain and response to treatment. Start with an initial dose of 2 tablets, with a minimum interval of 6 hours between doses. Do not exceed 8 tablets in a day. Use the lowest effective dosage for the shortest duration possible, and do not use for longer than necessary. Elderly patients over 75 years of age should be administered at least 6 hours apart.
Child dose
Children aged 12 and over: Adjust the dosage according to the patient's level of pain and response to treatment. Start with an initial dose of 2 tablets, with a minimum interval of 6 hours between doses. Do not exceed 8 tablets in a day.

Ingredients

Manufacturer
(주)라이트팜텍

Efficacy & effects

Relief of moderate to severe acute and chronic pain

  • Acute pain
  • chronic pain
View approved original text

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

How to take

Adult dose

Children aged 12 and over and adults: Adjust the dosage according to the patient's level of pain and response to treatment. Start with an initial dose of 2 tablets, with a minimum interval of 6 hours between doses. Do not exceed 8 tablets in a day. Use the lowest effective dosage for the shortest duration possible, and do not use for longer than necessary. Elderly patients over 75 years of age should be administered at least 6 hours apart.

Child dose

Children aged 12 and over: Adjust the dosage according to the patient's level of pain and response to treatment. Start with an initial dose of 2 tablets, with a minimum interval of 6 hours between doses. Do not exceed 8 tablets in a day.

Precautions

This medication should be used with caution in individuals who regularly consume more than three alcoholic beverages a day; consultation with a physician or pharmacist is imperative prior to use. This is because co-administration with alcohol may cause liver damage. This drug can rarely cause severe skin reactions, and if skin rashes or hypersensitivity reactions occur, the medication should be stopped immediately and a physician should be consulted. One of the ingredients in this medication may induce seizures, so patients with a history of seizures or those at high risk for seizures should be cautious when using this product. The risk of seizures may be increased, especially when taken with certain antidepressants or other central nervous system medications. Life-threatening allergic reactions can occur, although rarely, during the use of this medication. Patients should be informed to notify medical personnel immediately if they experience symptoms such as difficulty breathing or hives. Patients with severe respiratory diseases may risk respiratory suppression with this medication; if necessary, it should be administered in a location equipped for cardiopulmonary resuscitation. This medication may cause severe drowsiness or respiratory suppression when taken with central nervous system depressants like alcohol or benzodiazepines, so extreme caution is needed for concomitant use. Patients with head injuries or elevated intracranial pressure should be cautious, as respiratory suppression and increased intracranial pressure may worsen symptoms when taking this medication. This drug has the potential to cause psychological and physical dependence, so regular monitoring for potential dependence is important during long-term use. Patients with impaired liver function should consult a physician before use, particularly due to the risk of liver damage from an ingredient in this medication. Individuals with certain genetic traits may metabolize this drug rapidly, increasing the risk of respiratory suppression. Such patients should consider dosage adjustments or alternative medications. Children under 12 years old and adolescents under 18 years old who have undergone tonsillectomy or adenoidectomy should not be administered this medication; adolescents between 12 and 18 years old should use it cautiously. This medication may cause sleep apnea and hypoxemia; continuous monitoring for worsening symptoms is required during treatment, and dosage should be reduced or discontinued as necessary. Elderly patients or those at risk of hyponatremia should be carefully monitored for signs during treatment with this drug. This medication may interact with specific drugs, so patients taking other medications should inform their physician; particular caution is advised for concomitant use with antidepressants, antibiotics, antifungals, and anticoagulants. Women who are pregnant or may become pregnant should consult a physician regarding the impact of this medication on the fetus, and breastfeeding mothers should avoid this medication as it can transfer into breast milk and affect the baby. This drug can cause drowsiness or dizziness, so caution is advised during driving or operating hazardous machinery. In cases of overdose, serious respiratory suppression, seizures, liver damage, and other severe effects may occur, so do not exceed the recommended dosage, and if an overdose is suspected, contact medical services immediately. This medication should be stored in a safe place out of the reach of children and precautions should be taken to prevent misuse.

Side effects and when to seek care immediately

Serious side effects

Hives, severe swelling (edema), chest tightness, difficulty breathing, cold sweat, paleness, severe rash with fever, blisters, skin peeling, pain in mouth/eyes, shortness of breath or breathing difficulty, asthma attacks, respiratory abnormalities accompanied by cough and fever, jaundice (yellowing of skin or eyes), extreme lethargy, sudden severe headache, thunderclap headache, seizures, confusion, visual disturbances, paralysis, and altered urinary output.

Mild side effects

  • Decreased appetite
  • insomnia
  • depression
  • dizziness
  • headache
  • drowsiness
  • nausea
  • vomiting
  • constipation
  • dry mouth
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  • diarrhea
  • indigestion
  • abdominal pain
  • discomfort
  • flatulence
  • pruritus
  • sweating
  • rash
  • fatigue
  • flushing
  • hypoglycemia
  • anxiety
  • irritability
  • emotional instability
  • euphoria
  • decreased libido
  • sleep disturbances
  • confusion
  • disorientation
  • agitation
  • abnormal dreams
  • drug abuse
  • hallucinations
  • withdrawal syndrome
  • migraines
  • drowsiness
  • sensory impairment
  • tremors
  • and sensitivity.

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

Storage

This medication should be stored in a sealed container to prevent exposure to air or humidity. Additionally, avoid storing in excessively hot or cold locations; it is best to store it at room temperature, between 1 and 30 degrees Celsius.

Appearance and packaging

Appearance

Pale yellow oblong film-coated tablets

Package unit

30 tablets/bottle, 300 tablets/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.