Ulpower Setsemi Tablet

Adult dose

For children aged 12 and older and adults: Adjust the dosage according to the patient's level of pain and treatment response. It is recommended to start with a dose of 4 tablets, and the subsequent dosing interval should be at least 6 hours apart, but not to exceed 16 tablets per day. Administer the lowest effective dose possible for the shortest duration necessary. Do not use this medication for longer than necessary, and if long-term use is required due to the nature and severity of the disease, regular monitoring should be conducted to determine the continued necessity of this medication. Elderly Administer the usual adult dose. However, in patients aged 75 and older, the elimination half-life of tramadol may be increased by 17% when administered orally, so it should be dosed at least 6 hours apart. Renal impairment patients In patients with moderate renal impairment (creatinine clearance of 10-30 ml/min), extend the dosing interval to 12 hours. In patients with severe renal impairment (creatinine clearance of less than 10 ml/min), administration is not recommended. Tramadol is removed very slowly during blood dialysis and filtration; therefore, it is not necessary to re-administer this medication after dialysis to maintain pain relief. Hepatic impairment patients For patients with moderate hepatic impairment, consider cautiously extending the dosing interval for administration. For patients with severe hepatic impairment, do not administer this medication.

Child dose

For children aged 12 and older and adults: Adjust the dosage according to the patient's level of pain and treatment response. It is recommended to start with a dose of 4 tablets, and the subsequent dosing interval should be at least 6 hours apart, but not to exceed 16 tablets per day.

This medication may put a strain on the liver; therefore, individuals who consume more than three alcoholic beverages per day should consult a doctor or pharmacist before use. If any skin rash or allergic reaction occurs while taking this medication, discontinue use immediately and consult healthcare professionals. The ingredients in this medication may cause seizures, so patients with a history of seizures or those at high risk of seizures should use it cautiously. Patients with impaired respiratory function or those with acute and severe bronchial asthma may find breathing more difficult while taking this medication, and it should be administered under the supervision of a healthcare professional. Taking this medication with alcohol or central nervous system depressants (sleeping pills, sedatives, etc.) can lead to severe drowsiness or respiratory depression, potentially resulting in coma, and should be avoided. Patients with elevated intracranial pressure or head injuries should be cautious as symptoms may worsen with this medication. This medication can lead to physical and psychological dependence; therefore, it is important to avoid long-term use or exceeding the recommended dosage. Patients with impaired liver function must consult their doctor before taking this medication, as there is a risk of liver damage, and it should not be taken with other acetaminophen products. Patients with the genetic trait of being ultra-rapid metabolizers of CYP2D6 should be cautious as the ingredients in this medication may be metabolized quickly in the body, increasing the risk of respiratory depression. It is safe to avoid administering this medication to children under 12 years of age or adolescents under 18 who have had tonsillectomy or adenoidectomy. This medication may cause sleep apnea or hypoxia, so continuous monitoring for the occurrence or worsening of these symptoms is necessary. Electrolyte imbalances such as hyponatremia may occur, and symptom monitoring is particularly needed for elderly patients or those with risk factors. Individuals allergic to the ingredients of this medication or patients with certain central nervous system drug addictions, severe respiratory depression, severe liver or kidney dysfunction, or women who are pregnant or breastfeeding should avoid taking this medication. Drowsiness, dizziness, decreased concentration, and other symptoms may occur during use, so caution is advised when driving or operating machinery. In case of an overdose, serious respiratory depression, seizures, liver damage, etc., can occur; immediate medical attention is required, and emergency care may be necessary. This medication should be stored out of reach of children, and should not be shared with others to prevent misuse.

Serious side effects

Hives, severe swelling, chest tightness, difficulty breathing, cold sweat, pallor, severe rash with high fever, blisters, skin peeling, pain in mucous membranes of mouth/eyes, shortness of breath or difficulty in breathing, asthma attacks, respiratory abnormalities associated with cough and fever, yellowing of skin or eyes (jaundice), extreme lethargy throughout the body, sudden and severe headache, thunderclap headache, seizures, altered consciousness, visual disturbances, paralysis, significant decrease in urine output

Mild side effects

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

This medication should be stored in a sealed container to prevent air and moisture exposure, with a recommended storage temperature of between 1 degree and 30 degrees Celsius. Therefore, it is safe to avoid places that are too hot or too cold, and store it in a cool place away from direct sunlight.

Appearance

Light yellow oval film-coated tablet

Package unit

30 tablets/bottle, 300 tablets/bottle