Jexstar Injection (Diclofenac Beta-Dimethylaminoethanol)

Adult administration

As Diclofenac Beta-Dimethylaminoethanol, deep intramuscular injection of 90mg into one upper side of the buttock is administered daily. In severe cases, it can be administered 90mg twice daily, alternating injections between both buttocks. After the initial treatment period, changes may be made to tablets or suppositories. Adjustments should be made based on age, disease, and symptoms. To minimize cardiovascular adverse reactions of this medication, use the minimum effective dose for the shortest duration necessary.

This medication should be discussed with a doctor or pharmacist before taking by individuals who regularly consume three or more alcoholic drinks per day. Using this medication while consuming large amounts of alcohol increases the risk of gastrointestinal bleeding. This medication may increase the risk of cardiovascular disease and may result in serious issues like myocardial infarction or stroke. Individuals with existing cardiovascular diseases or risk factors should be closely monitored for heart-related symptoms while taking this medication. This medication can cause gastrointestinal issues such as bleeding, ulcers, or perforation, with an increased risk particularly in the elderly. If gastrointestinal symptoms occur, it is essential to inform medical personnel immediately and seek treatment. Allergic reactions may occur with this medication, which in severe cases can cause myocardial infarction, so caution is warranted. For ampoules, be careful as glass fragments may be mixed in, particularly for children and the elderly. Products containing benzyl alcohol can cause fatal respiratory issues in premature infants. Individuals with peptic ulcers, severe blood disorders, liver impairment, kidney impairment, hypertension, or heart failure should not take this medication. Patients allergic to aspirin or other non-steroidal anti-inflammatory drugs, or with a history of asthma, should also refrain from use. This medication is not used for pain management before or after coronary artery bypass surgery. It should be avoided during pregnancy, especially in the late stages, as it may pose risks to the fetus. Breastfeeding women should consider discontinuing breastfeeding or the medication, as it may transfer to breast milk and cause adverse reactions in infants. Elderly patients and children should take the minimum dose with caution and remain particularly vigilant for adverse reactions. Regular blood tests and liver and kidney function tests are needed during long-term use of this medication. It is advisable not to combine this medication with other non-steroidal anti-inflammatory drugs, as there may be interactions with certain medications, so it should be reported to a doctor. If symptoms such as headaches, rashes, difficulty breathing, chest pain, indigestion, or bleeding occur during use, immediate consultation with medical personnel is necessary.

Serious side effects

Hives, severe swelling (edema), chest tightness, difficulty breathing, shock symptoms (chest pain, difficulty breathing, drop in blood pressure, swelling, rash, itching), Stevens-Johnson syndrome, Lyell syndrome, photosensitivity, jaundice, liver impairment, acute renal failure, oliguria, hematuria, hives, asthma attacks, severe allergic reactions, severe skin reactions, respiratory issues, liver dysfunction (jaundice), severe swelling or urinary issues, increased blood pressure, Koun

Mild side effects

• Loss of appetite
• nausea
• vomiting
• abdominal pain
• diarrhea
• stomatitis
• thirst
• constipation
• headache
• drowsiness

This medication should be stored in a light-opaque, tightly sealed container and kept at room temperature between 1 and 30 degrees Celsius. This way, you can maintain the medication's effectiveness and prevent deterioration.

Appearance

Brown ampoule injection containing a transparent yellowish solution

Package unit

2ml/ampoule X 50