Penangjeong 350 mg (Moniflumate)

Adult dose

Adults: The initial dose is 350 milligrams of morniflumate twice daily. Depending on the patient, the dose may be increased to a maximum of 700 milligrams twice daily. It is advisable to start this medicine at a low dose and increase it to the effective dose. Adjust the dose appropriately 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, so it is essential to consult a doctor or pharmacist. This medication can increase the risk of cardiovascular disease, so patients with a history of heart disease or stroke or with risk factors should be cautious and closely monitor for any cardiovascular symptoms. Serious gastrointestinal adverse reactions, such as gastrointestinal bleeding, ulcers, and perforations, can occur, so elderly patients or those with a history of gastrointestinal disease should be particularly careful. This medication can cause allergic reactions, especially serious allergic reactions like anaphylaxis, so patients with a history of allergy to non-steroidal anti-inflammatory drugs should not take it. Although it has an anti-inflammatory and analgesic effect, it may delay the diagnosis of infectious complications, so caution should be exercised when infections are suspected. Patients with peptic ulcers, gastrointestinal bleeding, severe blood disorders, liver dysfunction, kidney dysfunction, heart failure, hypertension, hypersensitivity to aspirin or other non-steroidal anti-inflammatory drugs, pregnant or breastfeeding women, children, and infants should not take this medication. Patients with blood disorders, bleeding tendencies, liver or kidney dysfunction, history of hypersensitivity, heart failure, hypertension, autoimmune diseases, asthma, ulcerative colitis, Crohn's disease, esophageal passage disorders, elderly individuals, etc., should be administered this medication with caution, and these patients require close monitoring according to a physician's instructions. During treatment, various adverse reactions such as nausea, vomiting, abdominal pain, diarrhea, gastrointestinal bleeding, skin rash, liver function abnormalities, kidney function decline, hypersensitivity reactions, and neurological symptoms may occur, so if any symptoms appear, immediate consultation with healthcare professionals is necessary. This medication should be used at the minimum effective dose and for the shortest duration possible, and regular blood tests and liver and kidney function tests should be performed during long-term use. When used in conjunction with other non-steroidal anti-inflammatory drugs or certain medications, the risk of adverse effects may increase due to interactions, so consultation with a physician is necessary before simultaneous administration. During pregnancy, especially in late pregnancy, this medication may harm the fetus, so pregnant women should not take it, and women who may become pregnant should also use it with caution. Elderly patients may exhibit adverse reactions more readily, so starting with a low dose and using it cautiously is advised. Medications should be taken with plenty of water, and should not be taken on an empty stomach or just before bedtime, and should be swallowed whole without chewing. In case of overdose, emergency measures such as inducing vomiting and gastric lavage may be required, so it is important to adhere to the prescribed dosage. Store out of reach of children and do not transfer to other containers for safety.

Shock symptoms (chest pain, coldness, shortness of breath, limb paralysis, hypotension, edema, rash, itching), nausea, vomiting, stomach pain, heartburn, diarrhea, bleeding, perforated peptic ulcer, gastrointestinal bleeding (hematemesis, melena, bleeding, diarrhea), esophageal ulcer, loss of appetite, dyspepsia, black stools, aphthous stomatitis, dry mouth, dry mucous membranes, bloody diarrhea, change in appetite, pancreatitis, colitis, abdominal cramps, abdominal bloating, discomfort in the stomach, aphthous gastritis, glossitis, esophageal lesions, diaphragm-related small bowel obstruction, stomatitis, angular cheilitis, thirst, constipation, strictures with ulcers in the small and large intestine, lower gastrointestinal disorders (nonspecific hemorrhagic colitis, exacerbation of Crohn's disease or ulcerative colitis), granulocyte decrease, hemoglobin decrease, leukopenia, thrombocytopenia, anemia, aplastic anemia, hemolytic anemia, agranulocytosis, bleeding tendency, impaired platelet function (prolonged bleeding time), eosinophilia, skin rash, urticaria, bullous pemphigoid, erythema multiforme (exfoliative dermatitis), purpura, allergic purpura, Stevens-Johnson syndrome, Lyell's syndrome, photosensitivity, flushing, itching, eczema, dermatitis, angioedema, polymorphic erythema, erythema, exudative dermatitis, hepatitis, hepatitis accompanied by jaundice, jaundice, liver dysfunction, elevated AST, ALT, ALP, fulminant hepatitis, acute renal failure (interstitial nephritis, renal papillary necrosis, etc.), oliguria, hematuria, proteinuria, nephrotic syndrome, elevated blood creatinine, elevated BUN, vasculitis, pneumonia, asthma attack, angioedema, anaphylactic systemic reaction including hypotension, rash, urticaria, aseptic meningitis, headache, nausea, vomiting, insomnia, stiff neck, fever, altered consciousness, insomnia, depression, irritability, anxiety, diplopia, memory impairment, loss of spatial sense, nightmares, tremors, psychotic reactions, drowsiness, dizziness, neuropathy, paralysis, confusion, hallucinations, convulsions, blurred vision, tinnitus, hearing impairment, taste disturbance, transient pain, dryness, itching, superficial keratitis, elevated blood pressure, decreased blood pressure, palpitations, tachycardia, congestive heart failure, ventricular extrasystole, myocardial infarction, chest pain, epistaxis, severe asthma attack, oropharyngeal edema, interstitial pneumonia, oliguria, hematuria, proteinuria, frequent urination, nocturnal enuresis, erectile dysfunction, vaginal bleeding, nipple necrosis, rhabdomyolysis, edema, hair loss, general malaise, sweating, fever, chest pain, lip edema, heartburn, abdominal pain, gastrointestinal disorders, dyspepsia, nausea, abdominal discomfort, facial edema, vomiting, gastritis, abdominal bloating, diarrhea, constipation, gastric ulcer, stomatitis, abdominal cramps, gastrointestinal bleeding, weight gain, fever, peripheral edema, rash, itching, urticaria, headache, dizziness, wheezing, upper respiratory infection, shortness of breath, palpitations, hypotension, dysuria, urinary incontinence, increased blood creatinine, elevated BUN, hyperglycemia, hypoglycemia, decreased vision, feeling of heaviness, insomnia

This medication is sensitive to air and moisture, so it should be stored in a tightly sealed container. Additionally, it is safest to store it at room temperature between 1°C and 30°C. Avoid excessively hot or cold places.

Appearance

Cream-colored rectangular tablets

Package unit

30 tablets/bottle, 300 tablets/bottle