Sblue 5 weeks

Adult administration

Use according to a doctor’s prescription, adjusting dosage based on plasma trace element levels. For patients receiving metabolically stable non-oral nutrition IV: - Zinc: 2.5-4 mg daily - Copper: 0.5-1.5 mg daily - Manganese: 0.15-0.8 mg daily - Chromium: 10-15 μg daily - Selenium: 20-40 μg daily For acute burn patients: 4.5-6 mg daily For deficiencies due to prolonged non-oral nutrition IV.

Child administration

Pediatric patients - Under 5 years: Daily per kg body weight - Zinc: 100 μg - Copper: 20 μg - Manganese: 2-10 μg - Chromium: 0.14-0.20 μg - Selenium: 3 μg Others - General

This medication should not be administered to premature infants or neonates. It contains benzyl alcohol, which can cause life-threatening respiratory issues in these patients. Administering this medication via direct intravenous injection without dilution may result in venous thrombophlebitis, so it must be diluted before use. Additionally, since it is a hypotonic solution, it should only be used for mixed injections. If any toxic symptoms appear during administration of any ingredient, usage should be immediately discontinued. Special caution is required for patients with impaired kidney function or premature infants due to the risk of aluminum toxicity. The zinc, copper, manganese, chromium, and selenium included in this medication are in small amounts, so toxicity is not usually observed at normal doses; however, the patient's condition and metabolic needs must be accurately assessed by the physician prior to administration. Patients with renal failure may accumulate zinc in the body, and patients with biliary obstruction may be at risk for accumulation of copper and manganese, necessitating caution. Chromium is mainly excreted through the kidneys and can affect blood sugar control in diabetic patients; therefore, the treatment of diabetes must be confirmed. For patients with kidney or gastrointestinal dysfunction, dosage adjustments for selenium are necessary, and for patients receiving blood transfusions, the effects of the transfusion should be considered. The safety of this medication during pregnancy has not been established, so it should only be administered to pregnant women or those who could become pregnant if the therapeutic benefit outweighs the risks. In cases of overdose, toxic symptoms related to each component such as zinc, copper, chromium, and selenium may occur, and immediate medical attention should be sought. This medication should not be used without a doctor's prescription, and when mixing it with non-oral nutritional solutions, it should be prepared in a sterile environment. Before administration, ensure that the solution has not changed color or contains any foreign matter and store it in a dry place out of reach of children.

Serious side effects

• Hypotension
• pulmonary edema
• jaundice
• decreased urine output
• peripheral edema
• and coma.

Mild side effects

Sweating, decreased consciousness, blurred vision, tachycardia, hypothermia, diarrhea, vomiting, hair loss, nail weakness, dermatitis, dental damage, gastrointestinal disturbances, irritability, depression, metallic taste, garlic smell during sweating or respiration, fatigue, behavioral changes, glare, nausea, ulcers, and coma.

This medication should be stored in a sealed container to prevent air and moisture from entering, and it is safe to store at room temperature between 15 to 30 degrees Celsius. Storing it this way maintains the drug's effectiveness and prevents degradation.

Appearance

A colorless or pale blue transparent liquid without odor, contained in a colorless transparent vial for injection.

Package unit

(10mL/vial)*10