Geonil Rodin 200 mg (Unmodified Etodolac)

Adult dose

Acute symptoms: Adults: Administer 200-400 mg of etodolac orally per dose, 3-4 times daily (every 6-8 hours). Chronic symptoms: The initial dose is 800-1200 mg daily, taken orally in 2-4 divided doses. The maintenance dose is 600-1200 mg daily, taken orally in 2-4 divided doses. Do not exceed 1200 mg per day. Adjust the dose as appropriate according to age and symptoms.

Individuals who regularly consume more than three glasses of alcohol per day should consult a doctor or pharmacist before taking this medication. Regular drinkers taking this medication may be at risk of gastrointestinal bleeding. This medication may increase the risk of cardiovascular diseases; therefore, individuals with a history of heart disease or stroke, or those with risk factors, should be especially cautious. If any heart-related symptoms occur during treatment, medical attention should be sought immediately, and patients must be aware of such symptoms in advance. It can affect gastrointestinal health and may lead to serious problems such as gastrointestinal bleeding, ulcers, and perforation. The risk may be greater for elderly individuals or those taking the medication for extended periods, necessitating close observation of gastrointestinal symptoms. Individuals with a history of peptic ulcers or gastrointestinal bleeding, or those allergic to this medication or non-steroidal anti-inflammatory drugs (NSAIDs), should not take this medication. Moreover, individuals with a history of allergic reactions such as asthma, rhinitis, or hives should exercise caution as serious allergic reactions may occur with this drug. Individuals with impaired kidney or liver function must consult a doctor before taking this medication and should have their kidney and liver functions regularly checked during treatment. Those with hypotension, heart failure, or fluid retention may also experience side effects when using this drug and should be cautious. Taking this medication may lead to various side effects such as nausea, diarrhea, abdominal pain, liver function abnormalities, skin rash, headache, dizziness, and blood pressure changes; any abnormal symptoms should be discussed with a doctor immediately. Before taking this medication, the potential interactions with other drugs must be checked, especially if taken alongside antihypertensives, diuretics, anticoagulants, or chemotherapeutics. This medication should be avoided during pregnancy, especially in the last trimester, and should only be used in minimal doses for a short duration after mid-pregnancy as it may affect fetal kidney function. Breastfeeding women should consult a doctor before taking this medication as it may be excreted in breast milk and could affect the infant; breastfeeding may need to be discontinued if necessary. The safety and efficacy in children have not been established, and the elderly should be particularly cautious regarding dosage adjustments and monitoring for side effects. In case of overdose, gastrointestinal bleeding, drowsiness, dizziness, vomiting, and in severe cases, respiratory depression or coma may occur, necessitating immediate suitable treatment at a hospital. This medication should be stored out of reach of children, and transferring it to another container may compromise its quality, so care should be taken.

gastrointestinal bleeding, ulcer, perforation, nausea, diarrhea, upper abdominal pain, loss of appetite, hepatitis, jaundice, belching, elevated liver enzymes, heartburn, indigestion, bloating, abdominal pain, gastrointestinal cramps, abdominal gas accumulation, constipation, gastritis, bloody stool, thirst, dry mouth, ulcerative stomatitis, melena, vomiting, esophagitis with stricture or pyloric muscle spasm, colitis, ischemic or ulcerative colitis, colonic ulcer, membranous colitis, pancreatitis, headache, dizziness, drowsiness, insomnia, nervousness, anxiety, depression, weakness, fatigue, lethargy, somnolence, paralysis, coma, sensory disturbance, confusion, pruritus, rash, angioedema, sweating, urticaria, vesicular rash, subcutaneous vasculitis with purpura, Stevens-Johnson syndrome, hyperpigmentation, erythema multiforme, hair loss, skin desquamation, maculopapular rash, photosensitivity, nipple necrosis, chills, fever, fatigue, weakness, malaise, allergic reaction, anaphylactic reaction, infectious disease, dysuria, frequent urination, renal failure, renal impairment, renal papillary necrosis, cystitis, hematuria, leukorrhea, kidney stones, interstitial nephritis, irregular uterine bleeding, blurred vision, lifespan, tinnitus, photophobia, transient visual disturbance, conjunctivitis, hearing loss, taste disturbance, hypotension, hypertension, congestive heart failure, flushing, tachycardia, palpitations, syncope, vasculitis, petechiae, anemia, thrombocytopenia, prolonged bleeding time, agranulocytosis, hemolytic anemia, leukopenia, neutropenia, pancytopenia, arrhythmia, myocardial infarction, fluid retention, cerebrovascular accident, asthma, bronchitis, dyspnea, pharyngitis, rhinitis, sinusitis, phlebitis, edema, increased serum creatinine, weight change, hyperglycemia, drowsiness, phenomenon, external heart pain, upper abdominal pain, respiratory depression, coma

This medication should be stored in a sealed container to prevent air or moisture from entering. This will help maintain the integrity and effectiveness of the drug.

Appearance

Brown oval film-coated tablet

Package unit

30 tablets/bottle, 100 tablets/bottle, 1000 tablets/bottle