Ibuprofen Injection is administered by dilution with 0.9% sodium chloride injection.
Ibuprofen Injection needs to be adjusted according to the patient’s response to the initiation of treatment with this product, the dose and frequency of administration, using the lowest effective dose at the shortest dosing cycle, and to minimize the risk of renal adverse effects, patients need to be adequately hydrated prior to administration.
Ibuprofen Injection should not be diluted to a final use concentration of more than 4 mg/mL, and the diluted solution should be 0.9% sodium chloride injection only, not dextrose injection.
0.1g dose: add 1ml of this product to not less than 100ml of diluted solution.
0.2g dose: add 2ml of the product to not less than 100ml of diluted solution.
0.4g dose: add 4ml of the product to not less than 100ml of diluted solution.
0.8g dose: add 8ml of the product to not less than 200ml of diluent.
For 10mg/kg body weight based dosing dose administration, ensure that the concentration of the product does not exceed 4mg/mL.Before use, the suspended particles and discoloration of the original and diluted solutions should be observed by the naked eye, if milky light, opaque particles, discoloration or other exogenous particles are found, it should not be used.
The diluted injection can remain stable for 24 hours under room temperature conditions (20-25°C) and indoor light conditions. When using Ibuprofen Injection, it should be noted that it needs to be prepared by professionals and used in accordance with the doctor’s instructions, and should not be used blindly on its own.