Superset Tablet

Adult dose

Children over 12 years and adults: The dosage should be adjusted based on the degree of pain and therapeutic response. It is recommended to administer an initial dose of 2 tablets, and the interval between doses should be at least 6 hours, with a daily limit not to exceed 8 tablets. Administer the lowest effective dose for the shortest duration possible. Avoid taking this medication longer than necessary, and if prolonged use is required due to the characteristics and severity of the illness, regular monitoring should be conducted to confirm the need for continued use of this medication.

Child dose

Children over 12 years and adults: The dosage should be adjusted based on the degree of pain and therapeutic response. It is recommended to administer an initial dose of 2 tablets, and the interval between doses should be at least 6 hours, with a daily limit not to exceed 8 tablets.

This medication may cause liver damage if taken by individuals who regularly consume more than three glasses of alcohol per day; consultation with a doctor or pharmacist is essential. If a rash or hypersensitivity reaction occurs during the use of this medication, discontinue use immediately and inform healthcare personnel. The tramadol component of this medication may increase the risk of seizures, so individuals with a history of seizures or who are at high risk should use it cautiously. Although rare, acute allergic reactions may occur when taking this medication; if unusual symptoms arise, immediate consultation with healthcare personnel is necessary. Patients with acute and severe bronchial asthma may experience difficulty breathing while taking this medication, and it should be administered in a facility equipped for emergencies. Caution is required when combining this medication with alcohol or central nervous system depressants, as it may result in severe drowsiness, respiratory depression, or coma. Patients with head injuries or elevated intracranial pressure may worsen symptoms due to respiratory depression and increased intracranial pressure while taking this medication. This medication may cause dependence similar to morphine; therefore, caution is needed with long-term use. Excessive doses of acetaminophen can lead to liver damage, so the total daily dosage should not exceed 4,000 mg. Patients with compromised liver function should consult a doctor before using this medication. Some patients, including ultrafast metabolizers of the enzyme CYP2D6, may experience increased effects of this medication, elevating the risk of respiratory depression. This medication should not be administered to children under 12 years old or adolescents under 18 who have undergone tonsillectomy or adenoidectomy. This medication may exacerbate sleep apnea or hypoxia; therefore, dosage should be reduced or discontinued if relevant symptoms are present. Elderly patients or those at risk of hyponatremia should be closely monitored for symptoms of hyponatremia while taking this medication. Do not administer this medication to individuals with allergies to its components, severe respiratory depression, head injuries, or those taking MAO inhibitors. The risk of seizures or respiratory depression increases when used in combination with narcotic analgesics or central nervous system depressants, so healthcare professionals must be consulted. If unusual symptoms or side effects occur while taking this medication, promptly inform healthcare personnel and seek appropriate measures. Pregnant or breastfeeding women should be cautious as this medication may impact the fetus or newborn. Drowsiness or dizziness may occur; it is advisable to avoid activities such as driving or operating machinery. In case of overdose, serious respiratory depression, seizures, and liver damage may occur, so adherence to prescribed dosages is crucial, and emergency services should be contacted immediately if needed. Keep this medication out of reach of children to prevent accidental ingestion.

Serious side effects

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

Mild side effects

• Decreased appetite
• insomnia
• depression
• dizziness
• headache
• drowsiness
• nausea
• vomiting
• constipation
• dry mouth

Store this medication in a tightly closed container to prevent air and moisture from entering. Additionally, it is recommended to keep it at a temperature between 1°C and 30°C, avoiding extremes of heat or cold.

Appearance

Pale yellow, rectangular film-coated tablets

Package unit

For domestic use: 30 tablets/bottle, 300 tablets/bottle For export: 10 tablets (10 tablets/PTP*1), 100 tablets (10 tablets/PTP*10)