Eltreset Tablet

Adult dose

Children over 12 and adults: The dosage should be adjusted according to the patient's level of pain and response to treatment. An initial dose of 2 tablets is recommended, thereafter maintaining a minimum interval of 6 hours between doses, ensuring that no more than 8 tablets are taken in one day. The lowest effective dose should be administered for the shortest duration possible. Avoid taking this medication for longer than necessary, and if prolonged treatment is required due to the nature of the disease and severity, regular monitoring should be conducted to reassess the necessity of ongoing treatment. Elderly Administer the usual adult dosage. However, for elderly patients over 75, the half-life of tramadol is prolonged by 17% during oral administration, thus ensure at least 6 hours between doses. Renal impairment For patients with moderate renal impairment (creatinine clearance of 10-30 mL/min), extend the interval to 12 hours. It is not recommended for those with severe renal impairment (creatinine clearance less than 10 mL/min). Tramadal is removed very slowly during hemodialysis and filtration, so there is no need for re-administration after dialysis to maintain its effect. Liver impairment For moderate liver impairment, consider carefully extending the dosing interval.

Child dose

Applicable for children over 12 years and adults; no separate pediatric dosage is specified.

This medication may put a strain on the liver, so individuals who regularly drink more than three glasses of alcohol a day must consult with a doctor or pharmacist before taking this medication. Serious allergic reactions, such as skin rashes or blisters, may occur while taking this medicine. If such symptoms appear, discontinue use immediately and inform medical personnel. The ingredients in this medication can provoke seizures, so caution is required for individuals with a history of seizures or those who are at high risk of seizures. Rarely, this medication may cause severe allergic reactions; symptoms such as difficulty breathing or hives require immediate medical attention. Patients with severe asthma or respiratory issues may find it harder to breathe while taking this medication, and should only take it in an environment with medical personnel nearby or where emergency equipment is available. Taking this medication along with benzodiazepines or alcohol increases the risk of profound drowsiness or respiratory depression, so such combinations should be avoided. For patients with head injuries or elevated intracranial pressure, caution is necessary as this medication may increase brain pressure. The ingredients in this medication can lead to physical or psychological dependence, so careful monitoring for signs of dependence is essential if taken long-term. Patients with compromised liver function must consult a doctor before taking this medication, and dosage adjustments may be necessary. Certain patients with rapid metabolism of this medication may experience stronger effects and side effects than expected, so dosage adjustments and symptom monitoring are necessary. This medication should not be administered to children under 12 or specific pediatric patients after certain surgeries. Caution is also necessary for adolescents over 12 in some cases. This medication may worsen respiratory problems such as sleep apnea, so related symptoms should be regularly monitored for any deterioration. Elderly patients or those at risk of hyponatremia must closely observe changes in serum sodium levels while taking this medication. Before taking this medication, it is essential to adhere to the recommended dosage and avoid using it concurrently with other analgesics. Sudden discontinuation can lead to withdrawal symptoms such as anxiety, insomnia, and tremors; thus, gradually reducing the dosage in consultation with medical personnel is recommended. This medication may interact with various other drugs, so inform a doctor or pharmacist of all other medications currently being taken. Caution is advised when driving or operating machinery, as drowsiness or dizziness may occur. Overdose may lead to severe respiratory depression or liver damage; thus, do not exceed the recommended dosage and seek medical attention for any unusual symptoms.

Serious side effects

Hives, severe swelling (edema), cold sweat, severe allergic reactions, severe rash with high fever, blisters, skin peeling, pain in the mucous membranes of the mouth/eyes, severe skin reactions, difficulty breathing or shortness of breath, asthma attack, respiratory abnormalities with cough and fever, respiratory distress, jaundice, sudden and severe headache, thunderclap headache, seizures, confusion of consciousness, visual disturbances, paralysis, significantly decreased urine output, severe systemic conditions.

Mild side effects

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

Store this medication in a sealed container to prevent exposure to air and moisture, and keep in a cool place below 25 degrees Celsius.

Appearance

Pale yellow rectangular film-coated tablets

Package unit

30 tablets/bottle, 300 tablets/bottle