Viewing nowMonit Tablet 350 Milligrams (Moniflumate)
Morniflumate 350mg
Prescription medication
Hawon Pharmaceutical Co., Ltd.

MFDS item code 200900196 · Notified 2009.01.06 · Insurance code 651502670
Relief of pain and inflammation associated with osteoarticular disorders, otorhinolaryngological disorders (e.g., otitis), and respiratory disorders (e.g., tracheitis)
This medication has analgesic and anti-inflammatory effects and is used for respiratory diseases such as laryngitis, tracheitis, bronchitis, ENT diseases such as sinusitis, otitis media, tonsillitis, pharyngitis, and musculoskeletal disorders.
Adults: The initial dose is 350 mg of morniflumate twice daily. Depending on the patient, the dose may be increased to a maximum of 700 mg twice daily. It is advisable to start this medicine at a low dose and increase it to the effective dose. Adjust the dose as appropriate according to age and symptoms.
This medication can cause gastric bleeding if taken by individuals who regularly consume more than three drinks a day, so it is essential to consult a doctor or pharmacist. This medication may affect the cardiovascular system, increasing the risk of serious thrombotic reactions such as myocardial infarction or stroke, especially in those with a history of cardiovascular disease or risk factors. This medication can cause severe gastrointestinal side effects such as gastrointestinal bleeding, ulcers, and perforation, and caution is needed in the elderly or when used over a long period. This medication can cause allergic reactions, and even those who have never been exposed to non-steroidal anti-inflammatory drugs may experience severe allergic reactions such as anaphylaxis. It may mask inflammatory symptoms or reduce pain, potentially delaying the diagnosis of infectious complications. Therefore, it should be used cautiously when an infection is suspected. Patients with a history of peptic ulcers or gastrointestinal bleeding, severe liver, kidney, or heart disease, hypertension, or blood abnormalities should not take this medication, nor should it be administered to pregnant or nursing women, children, or infants. Patients with specific conditions such as blood disorders, liver or kidney function impairment, hypertension, or heart failure, or the elderly should use this medication cautiously and monitor for adverse reactions closely. This medication may cause gastrointestinal side effects such as nausea, vomiting, abdominal pain, diarrhea, and rarely hepatitis, renal failure, skin rashes, and neurological disturbances. Therefore, if any adverse symptoms occur, immediate consultation with a doctor is required. This medication should be administered at the lowest effective dose for the shortest duration, and regular blood tests and liver and kidney function tests should be performed during long-term use. This medication can interact with other non-steroidal anti-inflammatory drugs, anticoagulants, diuretics, lithium, methotrexate, etc., so it is imperative to inform the prescribing physician of any other medications being taken. During pregnancy, especially in the later stages, it may harm the fetus, so women who may become pregnant should consult a doctor before taking it. Elderly patients are more susceptible to adverse reactions, so it is advisable to start with a lower dose and to monitor for adverse symptoms closely during the administration. This medication can cause ulcers if it stays in the esophagus, so it should be taken with plenty of water and not on an empty stomach or just before bedtime. In cases of overdose, emergency treatment such as inducing vomiting or gastric lavage is necessary, and symptoms such as renal failure or hypotension may occur, requiring immediate medical assistance. This medication should be kept out of reach of children and stored in its original container to maintain quality.
Shock symptoms (chest discomfort, coldness, shortness of breath, limb paralysis, low blood pressure, edema, rash, itching), nausea, vomiting, abdominal pain, heartburn, diarrhea, bleeding, peptic ulcer accompanied by perforation, gastrointestinal bleeding (hematemesis, bloody stools, bleeding, diarrhea), esophageal ulcer, loss of appetite, dyspepsia, black stools, aphthous stomatitis, dry mouth, mucosal dryness, bloody diarrhea, changes in appetite, pancreatitis, colitis, abdominal cramps, abdominal distension, discomfort in the stomach area, gastritis, glossitis, esophageal lesions, diaphragm-like small bowel stricture, stomatitis, angular cheilitis, thirst, constipation, strictures with ulcers in the small and large intestine, lower intestinal disorders (nonspecific hemorrhagic colitis, exacerbation of Crohn's disease or ulcerative colitis), neutropenia, decrease in hemoglobin, leukopenia, thrombocytopenia, anemia, aplastic anemia, hemolytic anemia, agranulocytosis, bleeding tendency, platelet dysfunction (prolonged bleeding time), eosinophilia, skin rash, urticaria, bullous pemphigoid, erythema multiforme (exfoliative dermatitis), purpura, allergic purpura, Stevens-Johnson syndrome, Lyell's syndrome, photosensitivity, erythema, itching, eczema, dermatitis, angioedema, polymorphic erythema, flushing, 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, hypercalcemia, hypoalbuminemia, interstitial nephritis, nephrotic syndrome, elevated serum creatinine, elevated BUN, vasculitis, pneumonia, asthma attack, angioedema, anaphylactic systemic reaction including hypotension, rash, urticaria, aseptic meningitis, headache, nausea, vomiting, insomnia, stiffness of the neck, fever, altered consciousness, insomnia, depression, irritability, anxiety, double vision, memory impairment, loss of sense of direction, nightmares, tremors, psychotic reactions, drowsiness, dizziness, nervousness, paralysis, confusion, hallucinations, seizures, clouding of vision, tinnitus, auditory impairment, taste impairment, transient pain, dryness, itching, superficial keratitis, increased blood pressure, decreased blood pressure, palpitations, tachycardia, congestive heart failure, ventricular ectopic beats, myocardial infarction, chest pain, epistaxis, severe asthma attack, pharyngeal edema, interstitial pneumonia, oliguria, hematuria, proteinuria, frequent urination, nocturia, erectile dysfunction, vaginal bleeding, nipple necrosis, rhabdomyolysis, edema, hair loss, generalized weakness, sweating, fever, chest pain, lip swelling
Not everyone experiences these, and they can vary from person to person.
This medication should be stored in a tightly closed container to protect it from air and moisture. It is best to maintain a storage temperature between 1 and 30 degrees Celsius.
Cream-colored oval tablet
30 tablets/bottle, 300 tablets/bottle
Even with the same ingredient, strength, dosage form and how it is taken can differ.
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Even with the same ingredient, the dose and directions can differ by strength and dosage form. Talk to a doctor or pharmacist before switching from a medication you are already taking.
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For anything that needs medical judgment, consult a doctor or pharmacist.
This drug information is based on data provided by the Korea Ministry of Food and Drug Safety.
Consult a doctor or pharmacist for accurate dosage, administration, and usage instructions.