TRAVASOL 2.75% SULFITE FREE W/ ELECTROLYTES IN DEXTROSE 10% IN PLASTIC CONTAINER
Clinical safety rating: caution
Comprehensive clinical and safety monograph for TRAVASOL 2.75% SULFITE FREE W/ ELECTROLYTES IN DEXTROSE 10% IN PLASTIC CONTAINER (TRAVASOL 2.75% SULFITE FREE W/ ELECTROLYTES IN DEXTROSE 10% IN PLASTIC CONTAINER).
Travasol 2.75% with electrolytes in dextrose 10% is a parenteral nutrition solution. Amino acids provide substrate for protein synthesis, dextrose supplies calories, and electrolytes maintain acid-base balance and osmotic equilibrium.
| Metabolism | Amino acids undergo transamination and deamination in the liver and other tissues; dextrose is metabolized via glycolysis and oxidative phosphorylation; electrolytes are regulated by renal and hormonal mechanisms. |
| Excretion | Renal (primarily as unchanged drug and metabolites). Biliary/fecal excretion is negligible (<5%). |
| Half-life | Not applicable as a single entity; components have variable half-lives. Dextrose has elimination half-life of ~2-4 hours; amino acids have variable half-lives based on individual metabolic rates. |
| Protein binding | Minimal to negligible (<5%); dextrose and amino acids are not significantly protein-bound. |
| Volume of Distribution | Dextrose: ~0.2 L/kg; amino acids: variable, reflects total body water (~0.6 L/kg) but clinical relevance is low due to rapid metabolism. |
| Bioavailability | Intravenous: 100% (only relevant route). Oral administration is not applicable. |
| Onset of Action | Intravenous: immediate upon infusion for dextrose (glucose elevation), amino acids for protein synthesis begins within minutes. |
| Duration of Action | Intravenous: transient effects; dextrose action persists during infusion and for ~1-2 hours post-infusion; amino acids sustain nitrogen balance for hours, requiring continuous infusion. |
Intravenous infusion. Dosage depends on caloric and nitrogen requirements, generally 1-3 L per day in adults providing 4.25 g amino acids and 100 g dextrose per liter.
| Dosage form | INJECTABLE |
| Renal impairment | Contraindicated in patients with severe renal impairment (GFR < 25 mL/min) unless on dialysis. Reduce volume and protein load; monitor electrolytes. |
| Liver impairment | Use with caution in severe hepatic impairment (Child-Pugh class C). Avoid in hepatic encephalopathy. Modified amino acid formulations may be needed. |
| Pediatric use | Individualized based on weight (2-3 g amino acids/kg/day) and glucose infusion rate. Typical starting rate 0.5-1 g amino acids/kg/day, titrate upward. |
| Geriatric use | Monitor renal function and fluid status closely. Start at lower infusion rates. Adjust for comorbidities and polypharmacy. |
| 1st trimester | Consult provider |
| 2nd trimester | Consult provider |
| 3rd trimester | Consult provider |
Clinical note
Comprehensive clinical and safety monograph for TRAVASOL 2.75% SULFITE FREE W/ ELECTROLYTES IN DEXTROSE 10% IN PLASTIC CONTAINER (TRAVASOL 2.75% SULFITE FREE W/ ELECTROLYTES IN DEXTROSE 10% IN PLASTIC CONTAINER).
| Breastfeeding | Excretion into breast milk is minimal; M/P ratio not applicable. Considered safe during lactation when used as directed. |
| Teratogenic Risk | No teratogenic effects reported in animal studies; dextrose and electrolytes are essential nutrients. Inadequate maternal nutrition may pose fetal risk. Use only if clearly needed. |
| Fetal Monitoring |
■ FDA Black Box Warning
NOT FOR INTRAVENOUS INFUSION; FOR USE ONLY AS A COMPONENT OF PARENTERAL NUTRITION. Deaths have occurred in patients receiving aluminum-containing parenteral nutrition products. Premature neonates are at greater risk. Do not administer intravenously at full strength; must be admixed with other nutrients.
| Serious Effects |
Hypersensitivity to any component, severe electrolyte imbalances, anuria, severe hepatic disease, and inborn errors of amino acid metabolism.
| Precautions | Risk of hyperglycemia, electrolyte imbalances, aluminum toxicity, infection due to central line use, and fluid overload. Monitor serum glucose, electrolytes, and renal function. Use with caution in patients with renal impairment, hepatic disease, or metabolic disorders. |
Loading safety data…
| Monitor serum electrolytes, glucose, acid-base balance, fluid status, and renal function. In pregnancy, monitor fetal growth and well-being if prolonged use. |
| Fertility Effects | No known adverse effects on fertility; dextrose and electrolytes are normal metabolic substrates. |