Zn2+
What it isEssential trace element with NMDA, GPR39, and GABA-A effects; deficiency replacement and Wilson disease.
Why this oneIn Wilson disease it induces intestinal metallothionein, blocking copper absorption without chelation.
What limits itChronic excess causes copper deficiency with anemia and myeloneuropathy; it also reduces quinolone and tetracycline absorption.
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| FDA dosing | Population | Start | Target | Max |
|---|---|---|---|---|
| Zinc source in parenteral nutrition (oral/enteral not possible, insufficient, or contraindicated) | Adults | 3 mg/day IV (in PN admixture) | 3 mg/day; higher daily dose may be needed (monitored) with small-bowel fluid loss, excess stool, or ileostomy output | Individualized |
| Zinc source in parenteral nutrition | Peds ≥10 kg | 50 mcg/kg/day IV | 50 mcg/kg/day | 3 mg/day |
| Zinc source in parenteral nutrition | Peds 5 to <10 kg | 100 mcg/kg/day IV | 100 mcg/kg/day | Individualized |
| Zinc source in parenteral nutrition | Term neonates 3 to <5 kg | 250 mcg/kg/day IV (higher needs first 3 months of life) | 250 mcg/kg/day | Individualized |
| Zinc source in parenteral nutrition | Preterm neonates <3 kg | 400 mcg/kg/day IV | 400 mcg/kg/day | Individualized |
Renal Undefined
Hepatic Undefined
Individualize by clinical condition, nutritional requirements, and oral/enteral zinc intake
Pregnancy Recommended doses in PN not expected to cause major birth defects or adverse maternal/fetal outcomes; zinc deficiency itself is associated with adverse pregnancy outcomes
Lactation Zinc present in human milk; recommended doses not expected to harm a breastfed infant
NO BOXED WARNINGS
Principal riskChronic excess causes COPPER deficiency with anemia and myeloneuropathy
