Acronac (Aceclofenac)

Adult dose

For adults, the dosage of aceclofenac is 100 mg taken twice daily every 12 hours. For patients with liver impairment, the initial dosage is 100 mg per day. This medication should be taken whole and not chewed or crushed. The dosage may be adjusted according to symptoms. To minimize cardiovascular adverse reactions, it should be administered at the lowest effective dose for the shortest duration.

This medication should be discussed with a doctor or pharmacist before taking if the patient regularly consumes more than three alcoholic drinks per day. Taking this medication or other analgesics may increase the risk of gastrointestinal bleeding. This medication may increase the risk to the cardiovascular and cerebrovascular systems, so patients with risk factors such as heart disease, high blood pressure, diabetes, or smoking should be cautious. The longer the dosage and duration, the greater the risk of cardiovascular disease; therefore, it should be taken for the shortest duration at the lowest effective dose. Serious gastrointestinal adverse reactions such as gastrointestinal bleeding, ulcers, or perforations may occur, so special caution should be exercised for the elderly or those with a history of gastrointestinal diseases. If symptoms of gastrointestinal bleeding or pain appear while taking, consult medical personnel immediately. Patients with active peptic ulcers or bleeding, hypersensitivity to this medication or similar drugs, asthma, or a history of allergies should not take this medication. Patients with heart failure, severe kidney or liver impairment, women in late pregnancy or lactating, and patients with bleeding disorders should also avoid taking this medication. Patients with weak kidney function or heart failure and high blood pressure should be managed carefully according to a doctor's instructions while taking this medication. This medication can cause various side effects, such as dizziness, gastrointestinal disturbances, elevated liver enzyme levels, skin rashes, hematologic abnormalities; if any unusual symptoms appear, they should be reported to healthcare providers immediately. This medication may interact with other drugs, so if the patient is taking digoxin, anticoagulants, diabetes medications, diuretics, etc., it is essential to consult a doctor. Women who are pregnant or planning to become pregnant should avoid taking this medication, and those who are breastfeeding should also refrain from taking it. Safety and efficacy in children and adolescents have not been established; therefore, use is not recommended. Elderly patients have a higher risk of adverse effects such as gastrointestinal bleeding, so special caution is needed during use. In case of overdose, gastrointestinal irritation, decreased blood pressure, respiratory depression, convulsions, etc., may occur, requiring immediate medical attention.

Serious side effects

Hives, severe swelling (edema), tightness in the chest, difficulty breathing, cold sweats, pallor, severe rash with fever, blisters, peeling skin, pain in mouth/eyes mucosa, difficulty breathing or shortness of breath, asthma attacks, cough along with fever-related respiratory abnormalities, yellowing of the skin or eyes (jaundice), profound lethargy, sudden and severe headaches, lightning storm headaches, seizures, confusion, vision abnormalities, paralysis, urination

Mild side effects

• Dizziness
• liver enzyme abnormalities
• itching
• rash
• skin reactions
• anemia
• leukopenia
• thrombocytopenia
• neutropenia
• hemolytic anemia

This medication may be sensitive to air or moisture and should be stored in a sealed container. It is recommended to keep the storage temperature between 1 degree and 30 degrees Celsius at room temperature.

Appearance

White round film-coated tablets

Package unit

30T/bottle, 300T/bottle