Ultraset Semi Tablet

Adult dose

Children over 12 years and adults: Dosage should be adjusted according to the severity of the patient's pain and treatment response. An initial dose of 4 tablets is recommended, thereafter the interval between doses should be at least 6 hours, and not exceed 16 tablets per day. The lowest effective dose should be given for the shortest duration. Avoid taking this medication longer than necessary, and if prolonged use is required due to the nature and severity of the disease, regular monitoring should be conducted to assess the need for continued treatment with this medication. In the elderly: Administer the usual adult dosage. However, in patients aged 75 years and older, the elimination half-life of tramadol may increase by 17% when taken orally, so intervals of at least 6 hours should be maintained between doses. In patients with renal impairment: For patients with moderate renal impairment (creatinine clearance of 10-30 ml/min), extend the dosing interval to 12 hours. Administration is not recommended for patients with severe renal impairment (creatinine clearance less than 10 ml/min). Tramadol is removed very slowly during hemodialysis and filtration, so there is no need for redosing after dialysis to maintain analgesic effects. In patients with hepatic impairment: For patients with moderate liver impairment, consider carefully extending the dosing interval. Do not administer this medication in patients with severe liver impairment.

Child dose

Children over 12 years and adults: Dosage should be adjusted according to the severity of the patient's pain and treatment response. An initial dose of 4 tablets is recommended, thereafter the interval between doses should be at least 6 hours, and not exceed 16 tablets per day.

This medication can put a strain on the liver, so those who consume more than a certain amount of alcohol daily should consult a doctor or pharmacist before taking it. This medication can rarely cause serious skin allergy reactions, so if a rash or hypersensitivity occurs, discontinue use immediately and inform a healthcare provider. One of the ingredients in this medication can increase the risk of seizures, so caution is needed for those with a history of seizures or taking related medications. Patients with severe acute bronchial asthma may experience difficulty breathing when taking this medication, so it must be administered under the supervision of a healthcare professional. Taking this medication with central nervous system depressants can result in severe drowsiness or respiratory depression, thus it is essential to use the lowest effective dose for a short duration when used in combination. Patients with increased intracranial pressure or those with head injuries should be cautious as symptoms may worsen with this medication. This medication can lead to dependence, so those taking it long-term should adjust the dosage or take drug holidays according to a doctor's instructions. Patients with impaired liver function must consult a doctor before taking this medication and should be careful not to take it with other acetaminophen products. Patients with specific genotypes may metabolize this medication faster, increasing the risk of respiratory depression, thus special management from a physician is necessary in such cases. This medication should not be administered to children under 12 years of age or to adolescents under 18 who have undergone certain surgeries, and it should be used cautiously in adolescents aged 12 to 18. This medication can exacerbate sleep apnea or hypoxia, so if related symptoms occur, consider dosage adjustment or discontinuation. Patients at risk for hyponatremia need to monitor symptoms during the use of this medication. Patients with biliary diseases or a history of gallbladder surgery should be closely monitored for the possibility of pancreatitis. Patients who are allergic to any of the components, have central nervous system drug dependency, severe respiratory depression, brain injury, or are taking MAO inhibitors should not use this medication. Pregnant or breastfeeding women should consult with a healthcare provider before taking this medication as it can affect the fetus or newborn. This medication may cause drowsiness or dizziness, so caution is needed when driving or operating machinery. Overdose can lead to severe respiratory depression, seizures, and liver damage, so dosage should be strictly followed and healthcare facilities should be visited immediately if suspected. This medication should be stored in a safe place out of the reach of children, and care should be taken to prevent drug abuse and misuse.

Serious side effects

Hives, severe swelling (edema), chest tightness, difficulty breathing, cold sweat, paleness, severe rash with high fever, blisters, skin peeling, pain in mouth/eye mucous membranes, shortness of breath or difficulty breathing, asthma attacks, respiratory abnormalities with coughing and fever, yellowing of skin or eyes (jaundice), extreme lethargy, sudden and severe headaches, thunderclap headaches, seizures, confusion, vision disturbances, paralysis, urination changes

Mild side effects

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

This medication should be stored in a tightly sealed container to prevent air ingress and kept at room temperature between 1 degree and 30 degrees Celsius. Storing it this way helps maintain its effectiveness for a longer period.

Appearance

Light yellow rectangular film-coated tablets

Package unit

50 tablets/box[(10 tablets/PTP×5)], 100 tablets/bottle