Ibuprofen 200 mg Tablet (Ibuprofen)

Adult dose

For rheumatoid arthritis, osteoarthritis, ankylosing spondylitis, soft tissue injuries, non-articular rheumatic diseases, acute gout, and psoriatic arthritis, adults can take ibuprofen at a single dose of 200-600 mg, 3-4 times a day orally, with a maximum total daily dose of 3200 mg. For mild to moderate pain and colds, adults can take 200-400 mg, 3-4 times a day orally, adjusting as necessary based on age and symptoms.

Child dose

In the case of juvenile rheumatoid arthritis, children should be orally administered 30-40 mg per day per kg of body weight, divided into 3-4 doses. Children will take a single dosage orally 3-4 times a day, and for those weighing less than 30 kg.

This medication may pose a risk of gastrointestinal bleeding in individuals who regularly consume more than three glasses of alcohol a day, so it should always be discussed with a doctor or pharmacist. This medication can increase the risk of cardiovascular issues such as myocardial infarction and stroke in individuals with existing cardiovascular disease or risk factors, or those who take it for extended periods, so caution is necessary. Adverse cardiovascular reactions may occur while taking this medication, so if symptoms develop, immediate consultation with a doctor is required. Patients with hypertension, congestive heart failure, ischemic heart disease, peripheral artery disease, or cerebrovascular disease should use this medication carefully, particularly avoiding high doses. This medication can cause serious gastrointestinal problems such as gastrointestinal bleeding, ulcers, and perforations, thus elderly patients and those on long-term use should exercise extra caution. Gastrointestinal adverse reactions can sometimes occur suddenly without symptoms, so any unusual symptoms during use should prompt immediate consultation with medical personnel. Individuals with a history of gastrointestinal ulcers or bleeding, severe blood disorders, liver dysfunction, kidney impairment, cardiac failure, or severe hypertension should not take this medication. Individuals allergic to the ingredients of this medication or with a history of asthma, or hypersensitivity to other non-steroidal anti-inflammatory drugs such as aspirin should also avoid its use. In late pregnancy, this medication should not be used due to the risk of premature closure of the ductus arteriosus in the fetus. Patients receiving high-dose methotrexate during chemotherapy should not use this medication. This medication contains lactose; therefore, individuals with certain genetic lactose intolerance should not take it. Do not exceed the recommended dosage, and it is advisable not to take it simultaneously with other non-steroidal anti-inflammatory drugs. This medication can be transmitted through breast milk, raising concerns for serious side effects in infants, so nursing mothers should either discontinue use or stop breastfeeding. Patients with blood disorders, bleeding tendencies, liver or kidney dysfunction, heart disease, hypertension, or a history of hypersensitivity should consult a doctor or pharmacist before taking this medication. Individuals with systemic lupus erythematosus, ulcerative colitis, Crohn's disease, the elderly, pregnant or lactating women should also consult experts before use. Patients taking low-dose aspirin should be cautious, as this medication can reduce the effectiveness of aspirin and increase the risk of gastrointestinal bleeding. There may be interactions when used in conjunction with certain medications (e.g., ACE inhibitors, lithium, diuretics, methotrexate, anticoagulants, selective serotonin reuptake inhibitors), so expert consultation is necessary. If severe allergic reactions, blood disorders, gastrointestinal bleeding, skin rash, liver dysfunction, breathing difficulties, or kidney function decline occur during use, discontinue the medication immediately and consult medical personnel. This medication should be taken for the minimum duration and minimal dosage possible, and regular monitoring is required for long-term use. Fluid retention or edema may occur during use, so patients with heart failure should be particularly cautious. In case of overdose, immediate medical attention is required, and prompt treatment is necessary even if there are no symptoms.

Serious side effects

Hives, severe swelling (angioedema, periorbital swelling, facial swelling), chest tightness, difficulty breathing, asthma attacks, thrombocytopenia, prolonged bleeding time, severe rash with high fever, blisters, skin peeling, oral/ocular mucosal pain, mucocutaneous syndrome (Stevens-Johnson syndrome), toxic epidermal necrolysis (Lyell syndrome), photosensitivity, Drug Reaction with Eosinophilia and Systemic Symptoms (DRESS syndrome), bullous skin eruptions, erythema multiforme, papular rash, skin reddening

Mild side effects

• Nausea
• vomiting
• abdominal pain
• indigestion
• diarrhea
• thirst
• stomatitis
• abdominal bloating
• oral ulcers
• constipation

This medication should be stored in a tightly sealed container to prevent exposure to air or moisture. It is advisable to maintain a storage temperature between 1 and 30 degrees Celsius to preserve the medication's effectiveness and safety for an extended period.

Appearance

Pink round film-coated tablet

Package unit

[For domestic use] 10 tablets/PTP, 1000 tablets/bottle [For export] 1000 tablets (10 tablets/PTP × 100)