AZTREONAM

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172
AZTREONAM
CALCUTIONS AREA
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Infant Data


PMA= gestational age plus postnatal age

Results

MEDICAL INFORMATIONS

INDICATIONS

Treatment of neonatal sepsis caused by susceptible gram-negative organisms (e.g. E coli, H influenzae, Klebsiella, Pseudomonas, and Serratia). Generally used in combination with ampicillin (empirical treatment of sepsis) or an aminoglycoside (for synergism against Pseudomonas and Enterobacteriaceae).

ADVERSE EFFECTS

Aztreonam contains 780 mg L-arginine per gram of drug (23.4 mg/kg body weight per dose). Adequate amounts of glucose must be provided to prevent hypoglycemia. Side effects are rare but include eosinophilia, elevation of serum transaminases, and phlebitis at the injection site.

ADMINISTRATION

  • Intravenous: Give IV push over 3 to 5 minutes, or IV infusion over 20 to 60 minutes at a final concentration not to exceed 20 mg/mL.
  • Intramuscular: For IM administration, concentrations range from 66 mg/mL to 333 mg/mL.

MONITORING

Check serum glucose one hour after administration. Measuring serum concentration is not usually necessary. Periodic CBC, AST, ALT.