Moniflu Tablet 350 mg (Moniflumate)

Adult dose

Adults: The initial dose is moniflumate 350 milligrams 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 drug at a low dose and increase it to the effective dose. Adjust the dose as appropriate according to age and symptoms.

Patients who regularly consume more than three glasses of alcohol per day should consult a physician or pharmacist before taking this medication, as it increases the risk of gastrointestinal bleeding when taken with alcohol. This medication may affect the cardiovascular system and increase the risk of myocardial infarction and stroke. Individuals with cardiovascular diseases or risk factors should exercise additional caution and consult a doctor regarding cardiovascular symptoms during treatment. This medication can cause serious gastrointestinal adverse reactions such as gastrointestinal bleeding, ulcers, and perforation. Older adults or individuals with a history of gastrointestinal diseases are at greater risk, and symptoms should be carefully monitored while taking this medication. Allergic reactions may occur even if there has been no prior exposure to this or similar medications. If sudden rashes, difficulty breathing, or other symptoms arise, discontinue use and consult medical personnel immediately. This medication can mask symptoms related to inflammation, delaying the diagnosis of infectious complications. Therefore, it should be used cautiously in conjunction with antibiotics when an infection is suspected. Do not administer this drug to individuals with peptic ulcers, gastrointestinal bleeding, severe liver or kidney dysfunction, severe heart failure, high blood pressure, those with specific allergy histories, pregnant or breastfeeding women, or children and infants. Those with blood disorders, bleeding tendencies, liver or kidney disease, a history of hypersensitivity, decreased cardiac function, and elderly individuals should use caution when taking this medication, and regular monitoring may be necessary. During administration, side effects such as nausea, vomiting, abdominal pain, diarrhea, skin rash, liver dysfunction, and kidney dysfunction may occur, so consult a doctor immediately if these symptoms arise. Interactions may occur when this medication is taken with other anti-inflammatory analgesics or certain medications, so inform medical personnel if other medications are being used. Pregnant women should exercise caution, especially in the late stages of pregnancy, as it may harm the fetus, and should avoid use. Elderly patients may experience side effects more easily, so it is advisable to start with the minimum dose and monitor their condition closely. When taking this medication, it is important to take it with sufficient water and after meals to help reduce gastrointestinal discomfort. Avoid chewing or taking it on an empty stomach. In case of overdose, emergency measures such as inducing vomiting, gastric lavage, and drug absorption may be necessary, so adhere to the prescribed dosage and contact medical personnel immediately if abnormal symptoms occur. Store this medication out of reach of children in a safe place and it is important to avoid transferring it to another container to maintain the quality of the drug.

• Shock symptoms
• nausea
• vomiting
• abdominal pain
• heartburn
• diarrhea
• peptic ulcer
• gastrointestinal bleeding
• hematemesis
• melena

This medication may be sensitive to air or moisture, so it should be stored in a tightly sealed container. Additionally, it should be stored at room temperature between 1 degree and 30 degrees Celsius.

Appearance

Cream-colored oblong tablet

Package unit

10 tablets/bottle, 30 tablets/bottle, 100 tablets/bottle, 300 tablets/bottle