Literature DB >> 2107639

Stability of famotidine in a 3-in-1 total nutrient admixture.

B F Shea1, P F Souney.   

Abstract

The stability of famotidine in a 3-in-1 total nutrient admixture stored at room temperature (24 degrees C) was evaluated over 24 hours. Famotidine injection was diluted to a theoretical concentration of 20 mg/L in a total nutrient admixture containing 5% amino acid injection, 25% dextrose injection, and 2.25% intravenous fat emulsion. Admixtures were prepared in 2-L ethylene-vinyl acetate bags using conventional techniques and stored at room temperature. At 0, 4, 8, 12, and 24 hours, the admixtures were visually inspected for color change, creaming, or phase separation, and samples were obtained for assay with a stability-indicating method of HPLC, using samples obtained at time zero as controls. Two-way analysis of variance was used for data evaluation. There was no evidence of color change, creaming, or phase separation before quantitative analysis was performed, nor was there significant change in observed famotidine concentration over 24 hours. Based upon our data, famotidine intravenous solution 20 mg/L in the solution tested is stable at room temperature for 24 hours.

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Year:  1990        PMID: 2107639     DOI: 10.1177/106002809002400302

Source DB:  PubMed          Journal:  DICP        ISSN: 1042-9611


  2 in total

1.  Y-site compatibility of medications with parenteral nutrition.

Authors:  Christine A Robinson; Jaclyn E Lee
Journal:  J Pediatr Pharmacol Ther       Date:  2007-01

2.  Y-site compatibility of medications with parenteral nutrition.

Authors:  Christine A Robinson; Jaclyn E Sawyer
Journal:  J Pediatr Pharmacol Ther       Date:  2009-01
  2 in total

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