Blue Balance Injection

Adult administration

To be used according to physician's prescription, adjusting dosage based on plasma trace element levels. The allowable dosage range for intravenous use is as follows: - Zinc: 2.5 to 4 mg daily - Copper: 0.5 to 1.5 mg daily - Manganese: 0.15 to 0.8 mg daily - Chromium: 10 to 15μg daily - Selenium: 20 to 40μg daily Others: - For patients with stable metabolic enteric fluid loss: 12.2 mg/L (enteric fluid loss amount)

Child administration

Pediatric patients under 5 years old: - Zinc: 100μg per kg of body weight daily - Copper: 20μg per kg of body weight daily - Manganese: 2 to 10μg per kg of body weight daily - Chromium: 0.14 to 0.20μg per kg of body weight daily - Selenium

This drug should not be administered to premature infants and newborns, as it contains benzyl alcohol which can cause fatal respiratory issues in premature infants. This drug should be diluted before direct intravenous injection to prevent the risk of phlebitis. Because it is a hypotonic solution, it should only be used in mixed injection forms and should not be administered alone. If any toxic symptoms appear during administration, the injection should be immediately discontinued. This drug contains aluminum, which can pose a toxicity risk if administered for a prolonged period to patients with impaired renal function or to premature infants. Before administration, the patient's condition and metabolic requirements must be accurately assessed by a physician, and blood levels of trace elements should be regularly monitored to adjust the dosage. Patients with impaired renal or biliary function require special caution, as the trace elements in this drug can accumulate in the body and lead to toxicity. The safety of this drug has not been sufficiently established in pregnant women or women of childbearing potential; it should only be administered when the therapeutic benefits outweigh the risks. In cases of overdose, toxic symptoms of trace elements such as zinc, copper, chromium, and selenium may occur, necessitating immediate treatment and detoxification. This drug must be used strictly under a physician's prescription, and when adding it to non-oral nutritional solutions, aseptic conditions must be maintained and the solution should be checked for discoloration or sediment.

Serious side effects

• Hypotension
• pulmonary edema
• jaundice
• decreased urine output
• severe edema
• coma

Mild side effects

• Sweating
• decreased consciousness
• blurred vision
• tachycardia
• hypothermia
• diarrhea
• vomiting
• hair loss
• nail weakness
• dermatitis

This drug should be stored in a sealed container to prevent exposure to air or moisture. The storage temperature should be kept between 15 to 30 degrees Celsius to maintain the drug’s effectiveness for a longer period.

Appearance

A light blue transparent liquid contained in a colorless and transparent vial.

Package unit

10ml vial X 10