Furijex Injection (Diclofenac Sodium)

Adult dosage

(Oral) Initial dose of diclofenac sodium is 100-150mg per day, and in alleviated cases or for long-term treatment, 75-100mg per day should be administered in 2-3 divided doses. (Injection) For diclofenac sodium, inject 75mg (1 ampoule) deep intramuscularly into one side of the upper buttock once daily. In severe cases, 75mg (1 ampoule) can be administered twice daily alternating between both buttocks.

Children's dosage

Administer orally divided into 2-3 doses of 0.5-3mg per kg of body weight per day. Adjust the dosage appropriately based on age, disease, and symptoms.

This medication may pose a risk of gastrointestinal bleeding if taken by individuals who regularly consume more than three glasses of alcohol daily, so it must be discussed with a physician or pharmacist. This medication can increase the risk of cardiovascular diseases, so patients with a history of heart disease or stroke or risk factors should be especially cautious. It 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 use it carefully. Severe allergic reactions can cause symptoms similar to a myocardial infarction, so if abnormal symptoms such as chest pain occur, notify medical personnel immediately. In the case of ampoule injections, there is a risk of glass fragment contamination, so caution is needed during use, especially for children and the elderly. This medication should not be used in certain patients with peptic ulcer, severe liver impairment, kidney impairment, hypertension, heart failure, or drug hypersensitivity. Patients with a history of peptic ulcer or impairment of liver or kidney function, elderly individuals, and children should use this medication with caution, and those with a history of allergies or asthma should also be careful. During the use of this medication, blood pressure, liver function, kidney function, etc., should be regularly checked, and if abnormal symptoms occur, consult medical personnel immediately. Taking other non-steroidal anti-inflammatory drugs together may increase the risk of side effects, so co-administration should be avoided. It should be avoided during pregnancy, especially in late pregnancy, as it may pose a risk to the fetus, and breastfeeding should be stopped or the medication should be discontinued in cases of breastfeeding. In cases of overdose, symptoms such as hypotension, renal failure, seizures, gastrointestinal disturbances, and respiratory depression may occur, and immediate medical attention should be sought.

Serious side effects

• Hives
• severe swelling (edema)
• chest tightness
• difficulty breathing
• cold sweat
• paleness
• serious cardiovascular thrombotic events
• myocardial infarction
• stroke
• gastrointestinal bleeding

Mild side effects

• Hives
• rash
• itching
• increased blood pressure
• decreased blood pressure
• palpitations
• tachycardia
• swelling
• frequent urination
• nocturia

This medication should be stored in a sealed container and kept at room temperature between 1 to 30 degrees Celsius. Proper storage will maintain the efficacy of the medication and prevent deterioration.

Appearance

A brown ampoule containing a colorless or pale yellow transparent solution

Package unit

2ml x 50 ampoules