Indications & Uses
JUNIMIN is used as part of the intravenous nutrition of preterm and term newborns, infants and children. It is intended to meet the basal requirements for trace elements. This medication is a solution of glucose and electrolytes (mineral salts).
Dosage Reference
Reference Information Only
Dosages shown are general references from official sources. Always consult your doctor or pharmacist for personalized dosing.
Adults:
Patients with baseline or moderately increased requirements: 1 ampoule (10 ml) of JUNIMIN/day Patients with significantly increased TE requirements: 2 ampoules (20 ml) of JUNIMIN/day Diluted in an infusion solution of 50 ml 0.9% NaCl or 50 ml 5 % of glucose for 10ml or 100 ml 0.9% NaCl or 100 ml 5 % of glucose for 20ml added to PN mixtures After dilution, the physico chemical stability of the diluted solution has been demonstrated for 48 hours at 25°C protected from light.
Side Effects
Elimination of manganese, copper and zinc, leading to accumulation and overdose. Copper overdose must be considered in the presence of nausea, vomiting, gastralgia.
Cautions & Contraindications
Warnings & Precautions
Monitoring: Continuous monitoring of blood glucose, electrolyte levels, kidney function, and liver function is essential to prevent complications like hyperglycemia, metabolic disturbances, or organ dysfunction.