Medication info
Hyperset Tablet

Hyperset Tablet

Prescription medicationTablet경구
Ingredient · strength
Acetaminophen›325mg / 1 tabletTramadol Hydrochloride›37.5mg / 1 tablet
Manufacturer / importer
한화제약(주)
Appearance
Pale yellow oblong film-coated tablet
Packaging
30 tablets/bottle, 100 tablets/bottle, 300 tablets/bottle
Approval status
Active

MFDS item code 200710087 · Notified 2007.09.03 · Insurance code 651600800

Summary

Main use
Relief of moderate to severe acute and chronic pain
Who takes it
Adults · Children
Adult dose
It is recommended to administer 2 tablets as the initial dose, afterward maintaining an interval of at least 6 hours, and not exceeding 8 tablets per day. The lowest effective dose should be used for the shortest duration possible. For elderly patients aged 75 and over, intervals of at least 6 hours are advised. For patients with renal impairment, dosing intervals should be extended to 12 hours for moderate cases, and use is not recommended for severe cases. Liver impairment
Child dose
Children aged 12 and over should receive the same initial dose of 2 tablets, followed by administration at intervals of at least 6 hours, not exceeding 8 tablets per day.

Ingredients

Manufacturer
한화제약(주)

Efficacy & effects

Relief of moderate to severe acute and chronic pain

  • Moderate pain
  • severe pain
  • acute pain
  • chronic pain
View approved original text

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

How to take

Adult dose

It is recommended to administer 2 tablets as the initial dose, afterward maintaining an interval of at least 6 hours, and not exceeding 8 tablets per day. The lowest effective dose should be used for the shortest duration possible. For elderly patients aged 75 and over, intervals of at least 6 hours are advised. For patients with renal impairment, dosing intervals should be extended to 12 hours for moderate cases, and use is not recommended for severe cases. Liver impairment

Child dose

Children aged 12 and over should receive the same initial dose of 2 tablets, followed by administration at intervals of at least 6 hours, not exceeding 8 tablets per day.

Precautions

This medication should be consulted with a doctor or pharmacist before use for those who regularly drink more than three cups of alcohol a day, as taking it with alcohol can increase the risk of liver damage. Rarely, this medication may cause serious skin reactions. If there are any rashes or hypersensitivity reactions, discontinue use immediately and consult a physician. The tramadol component in this medication may increase the risk of seizures; therefore, caution is necessary for patients with a history of seizures or those who are at risk of seizures. Additionally, combining it with specific antidepressants or other narcotic analgesics may further increase the risk of seizures. Rarely, serious allergic reactions may occur during the use of this medication, so if symptoms such as difficulty breathing or hives develop, immediate medical attention should be sought. Patients with acute and severe bronchial asthma are at risk of respiratory depression when using this medication, so it should be administered in a setting with medical personnel present. This medication may cause severe drowsiness, respiratory depression, or coma when taken with alcohol or benzodiazepines, so co-administration should be avoided or used with great caution. Patients with increased intracranial pressure or head injuries are at risk of worsened conditions from this medication, so caution is necessary. This medication can cause psychological and physical dependence, so long-term use should be monitored closely for signs of dependence. Patients with reduced liver function may experience worsened liver damage from this medication, so it's essential to consult with a doctor before using it. Especially patients possessing a gene that rapidly metabolizes this medication may experience strong drug effects, increasing the risk of severe side effects such as respiratory depression. Children under 12 years of age and adolescents under 18 years who have undergone tonsillectomy or adenoidectomy should not be administered this medication, and adolescents between 12 to 18 years should also avoid use unless in special circumstances. This medication may cause sleep apnea or hypoxia, so patients should be continuously monitored for these symptoms, and dosages should be adjusted or stopped if necessary. Hypoatremia may occur during use of this medication, so especially elderly patients or those with risk factors should regularly check serum sodium levels. Patients allergic to the components, those with severe respiratory depression, head injury patients, or those currently taking MAO inhibitors should not use this medication. Women who are pregnant or breastfeeding should consult a physician before use, as it may affect the fetus or newborn. Drowsiness or dizziness may occur during treatment, so caution is needed when driving or operating machinery. In case of overdose, serious respiratory depression, seizures, liver damage, etc., may occur, thus strict adherence to dosage is necessary, and immediate emergency treatment should be sought in doubt. This medication may interact with other analgesics or medications, so if other medications are being taken, healthcare providers should be informed immediately. Elderly patients frequently have reduced function of the liver, kidneys, and heart, as well as concomitant medications, requiring extra caution when using this medication.

Side effects and when to seek care immediately

Serious side effects

Hives, severe swelling (edema), tightness in the chest, difficulty breathing, cold sweat, pallor, severe rash with fever, blisters, peeling skin, pain in oral/ocular mucosa, shortness of breath or difficulty breathing, asthma attacks, cough with fever accompanied by respiratory irregularities, yellowing of the skin or eyes (jaundice), extreme lethargy, sudden and very severe headache, thunderclap headache, seizures, altered consciousness, visual disturbances, paralysis, urination difficulties

Mild side effects

  • Decreased appetite
  • insomnia
  • depression
  • dizziness
  • headache
  • drowsiness
  • nausea
  • vomiting
  • constipation
  • dry mouth
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  • diarrhea
  • indigestion
  • abdominal pain
  • abdominal discomfort
  • flatulence
  • itching
  • sweating
  • rash
  • fatigue
  • flushing
  • hypoglycemia
  • anxiety
  • nervousness
  • emotional instability
  • euphoria
  • decreased libido
  • sleep disturbances
  • confusion
  • disorientation
  • excitability
  • abnormal dreams
  • drug abuse
  • hallucinations
  • withdrawal syndrome
  • migraine
  • drowsiness
  • sensory loss
  • tremors
  • sensory disturbances

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

Storage

This medication should be stored in a sealed container to prevent air or moisture ingress. It is advisable to maintain storage temperatures between 1 and 30 degrees Celsius to safely preserve the medication's effect.

Appearance and packaging

Appearance

Pale yellow oblong film-coated tablet

Package unit

30 tablets/bottle, 100 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.