Minovey Injection 2mL (Diclofenac β-Dimethylaminoethanol)

Adult administration

Administer Diclofenac beta-dimethylaminoethanol by deep injection into the upper outer quadrant of one buttock at a dose of 90mg per day. In severe cases, it can be administered at 90mg twice a day, alternating sides for each injection. After the initial treatment phase, switch to oral tablets or suppositories. Adjust doses according to age, condition, and symptoms. To minimize cardiovascular adverse reactions associated with this medication, use the minimum effective dose for the shortest duration.

This medication may pose a risk of gastrointestinal bleeding if taken by individuals who regularly consume more than three alcoholic beverages daily; it is necessary to consult a doctor or pharmacist. Those with cardiovascular diseases or risk factors should note that the risk of cardiovascular complications such as myocardial infarction and stroke may increase while taking this medicine. This medication can cause serious gastrointestinal adverse reactions, such as gastrointestinal bleeding, ulcers, and perforations, so elderly patients and those with a history of gastrointestinal diseases should exercise particular caution. Severe allergic reactions may lead to serious heart problems accompanied by chest pain, so if any allergic symptoms appear, immediate consultation with a medical professional is advised. Injectable forms in ampoule may contain glass particles, requiring careful handling during use, particularly when given to children or the elderly. Patients with peptic ulcers, severe blood disorders, hepatic dysfunction, renal dysfunction, severe hypertension, significant cardiac dysfunction, and those allergic to components of this medication should not take it. Individuals who have had allergic reactions to asthma, aspirin, or other non-steroidal anti-inflammatory drugs should also avoid this medication. This drug should be used cautiously for certain patients, including those with a history of peptic ulcers, hepatic dysfunction, renal dysfunction, hypertension, cardiac dysfunction, asthma, the elderly, and children, and the possibility of allergic reactions should also be considered. During treatment, rare side effects may include shock, gastrointestinal bleeding, blood disorders, serious skin reactions, hepatic dysfunction, renal impairment, and neuropsychiatric symptoms; thus, if any adverse effects are observed, discontinue use and consult a physician immediately. This medication should be used at the lowest effective dose for the shortest duration possible. Long-term use may necessitate regular blood tests and evaluations of hepatic and renal function. Patients with hypertension, heart failure, or impaired renal or hepatic function require special caution while using this medication and should regularly check their blood pressure and renal function. During pregnancy, especially in the third trimester, this medication may pose risks to the fetus; therefore, pregnant individuals should avoid its use, and breastfeeding mothers should either cease breastfeeding or stop taking the medication due to concerns about adverse effects on infants. This medication may interact with other non-steroidal anti-inflammatory drugs, aspirin, lithium, warfarin, methotrexate, etc., so it is essential to consult a healthcare professional when taken concomitantly. Elderly patients and children may experience adverse effects more readily, so the minimum effective dose should be used, and changes in symptoms should be closely monitored.

Serious side effects

Urticaria, severe swelling (edema), chest tightness, difficulty breathing, cold sweat, pallor, severe allergic reactions, high fever accompanied by severe rashes, blisters, skin desquamation, oral/ocular mucosal pain, severe skin adverse effects, shortness of breath or breathing difficulties, asthma attacks, respiratory difficulties accompanied by cough and fever, breathing problems, yellowing of the skin or eyes (jaundice), extreme lethargy, hepatic abnormalities (jaundice), sudden and

Mild side effects

• Loss of appetite
• nausea
• vomiting
• abdominal pain
• diarrhea
• stomatitis
• thirst
• constipation
• granulocytopenia
• thrombocytopenia

This medication should be stored in a tightly sealed container that blocks light, maintaining a storage temperature between 1°C and 30°C at room temperature. Proper storage helps maintain the efficacy of the drug.

Appearance

Brown ampoule containing a colorless to pale yellow transparent solution

Package unit

2mL/ampoule × 50