Diprofen Syrup (Dexibuprofen)

Adult dose

Specific details regarding the adult dosage have not been provided.

Child dose

For children over 6 months of age, administer a single dose of 0.4–0.6mL/kg (5–7mg/kg of dexibuprofen) at intervals of 4–6 hours as needed, not exceeding a maximum of 4 doses per day (28mg/kg).

This medication may pose a risk of gastrointestinal bleeding in individuals who consume more than three glasses of alcohol regularly, and it is essential to consult a doctor or pharmacist. This medication can increase the risk of cardiovascular diseases, so patients with a history or risk factors for heart disease or stroke should be particularly cautious and monitor for cardiovascular symptoms under medical supervision. It can cause serious gastrointestinal issues such as gastrointestinal bleeding, ulcers, and perforation, so patients with a history of gastrointestinal disorders should use it cautiously and seek treatment immediately if abnormal symptoms occur. Patients with peptic ulcer, severe blood disorders, liver impairment, kidney impairment, heart failure, hypertension, and those allergic to any component of this medication should not use it. Individuals with a history of asthma or allergic reactions due to aspirin or non-steroidal anti-inflammatory drugs may also be at risk when taking this medication. Regular blood tests, liver function tests, and kidney function tests are necessary while using this medication, and if abnormalities are detected, discontinuation or dosage adjustment is required. Pregnant women, especially in the later stages of pregnancy, should avoid using this medication as it may harm the fetus, and breastfeeding women should be cautious as it may cause abnormal reactions in infants. Children and the elderly may experience side effects more readily, so the minimum effective dose should be used cautiously. There may be interactions with other non-steroidal anti-inflammatory drugs, anticoagulants, diuretics, antihypertensives, etc., so it is crucial to consult a doctor or pharmacist regarding any concurrently taken medications. If symptoms such as shock, severe skin rash, difficulty breathing, blood pressure changes, kidney function abnormalities, or liver function abnormalities occur while taking this medication, discontinue use immediately and consult medical personnel. This medication should be used at the lowest effective dose for the shortest duration necessary, and regular monitoring is required during long-term use. Store out of reach of children and avoid transferring to another container.

Serious side effects

• Hives
• severe swelling (edema)
• difficulty breathing
• asthma attacks
• Stevens-Johnson syndrome
• toxic epidermal necrolysis
• severe allergic reactions
• severe skin reactions
• jaundice
• liver abnormalities

Mild side effects

• Nausea
• vomiting
• abdominal pain
• dyspepsia
• diarrhea
• gastric discomfort
• thirst
• stomatitis
• abdominal bloating
• constipation

Drug interactions

Do not take this medication in combination with other non-steroidal anti-inflammatory drugs, aspirin, or high doses of methotrexate. Also, consult with a doctor or pharmacist when taking it with glucocorticoids, digoxin, phenytoin, probenecid, sulfinpyrazone, sulfonylureas, diuretics, antihypertensives, ACE inhibitors, furosemide, lithium, low doses of methotrexate, and coumarin anticoagulants (such as warfarin), and low-dose aspirin.

Food interactions

Caution is advised when taking this medication with alcohol.

This medication is sensitive to light, so it should be stored in a tightly closed container that does not allow light to enter. Additionally, it is important to maintain its effectiveness by storing it at room temperature between 15 degrees and 25 degrees.

Appearance

A white to pale yellow opaque syrup formulation in a distinctive scented white bottle

Package unit

500mL/bottle × 1