Hansol Nafroxen Soft Capsule

Adult dose

1. Rheumatoid arthritis, osteoarthritis, ankylosing spondylitis: Take 250 mg to 500 mg of Nafroxen orally twice daily (every 12 hours). 2. Acute gout: Take an initial dose of 750 mg of Nafroxen orally and follow up with 250 mg orally every 8 hours until the attack resolves. 3. Muscular disorders, postoperative pain, pain after tooth extraction, dysmenorrhea, tendinitis, bursitis: Initial dose of 500 mg of Nafroxen orally, followed by 250 mg every 6 to 8 hours. Do not exceed a total daily dose of 1,250 mg. 4. Migraine: Take an initial dose of 750 mg of Nafroxen orally. If needed, additional doses of 250 mg to 500 mg may be taken on the same day, administering the additional dose 30 minutes after the initial dose. Do not exceed a total daily dose of 1,250 mg. Adjust according to age and symptoms.

This medication may cause gastrointestinal bleeding if taken by individuals who regularly consume more than three glasses of alcohol daily, and medical consultation should be sought. This drug may affect the cardiovascular system, significantly increasing the risk of severe thrombotic events such as myocardial infarction or stroke, so individuals with a history of cardiovascular disease or risk factors should exercise greater caution. This medication may cause serious adverse reactions such as ulcers, bleeding, or perforation in the gastrointestinal tract, so older adults or those with a history of gastrointestinal diseases should be monitored closely during use. Individuals with peptic ulcers, severe blood disorders, severe liver, heart, or kidney dysfunction, hypertension, and allergies to this drug's ingredients or non-steroidal anti-inflammatory drugs should not use this medication. Patients with a history of peptic ulcers, blood disorders, bleeding tendencies, liver or kidney disease, hypertension, asthma, autoimmune diseases, etc. should use this drug cautiously. This medication can cause various side effects such as hypersensitivity, gastrointestinal bleeding, blood disorders, liver dysfunction, kidney impairment, neurological abnormalities, and skin rashes, so if symptoms occur, use should be discontinued immediately, and consultation with a physician is necessary. This drug may have an increased risk of side effects when taken with other non-steroidal anti-inflammatory drugs or certain medications, so caution is advised when used in combination. During pregnancy, especially in the late stages, this medication should be avoided as it may harm the fetus, and careful use is required during the early or mid stages of pregnancy. This drug may pass into breast milk and affect newborns, so it is advisable not to use it while breastfeeding. It is preferable not to use this medication in infants under the age of 2 as safety has not been established, and it should be administered cautiously at minimal doses in children and the elderly. This medication may affect blood test results, so it should be disclosed before testing, and in case of overdose, appropriate medical treatment should be sought immediately. Keep this medication out of the reach of children and do not transfer it to other containers for safety.

Serious side effects

Hives, severe swelling, chest tightness, difficulty breathing, cold sweat, pallor, severe rash with fever, blisters, mucosal pain in mouth/eyes, shortness of breath or difficulty breathing, asthma attacks, respiratory abnormalities accompanied by cough and fever, yellowing of skin or eyes (jaundice), extreme fatigue, sudden and severe headache, thunderclap headache, seizures, confusion, visual disturbances, paralysis, decreased urine output,

Mild side effects

• Nausea
• stomach pain
• abdominal pain
• vomiting
• loss of appetite
• dyspepsia
• heartburn
• diarrhea
• constipation
• stomatitis

Drug interactions

Do not take this medication with other non-steroidal anti-inflammatory drugs or Nafroxen derivatives. Avoid concurrent use with hydantoin antiepileptics, sulfonamides, sulfonylurea-based hypoglycemics, propranolol and other beta-blockers, ACE inhibitors (such as captopril), loop and thiazide diuretics, probenecid, aspirin, lithium, methotrexate, coumarin anticoagulants (such as warfarin), zidovudine, and quinolone antibiotics (such as enoxacin).

This drug is sensitive to air and moisture, so it must be stored in a tightly sealed container. It is advisable to keep it at room temperature between 1 degree and 30 degrees.

Appearance

Transparent teal oval soft capsule containing a colorless transparent liquid

Package unit

10 capsules/PTP