Aztreonam

Trade name

Azactam

Presentation and preparation

For IV administration:

Vial size
(powder volume)
Fluid to add
Volume to add
Resulting concentration
1 g
(1.2 mL)
Water for injections 9.1 mL  100 mg/mL

Reconstitute to 100 mg/mL for IV administration. 

Shake vial vigorously until powder is dissolved. There is approximately 0.3 mL overage in the vial. Reconstituted solution must be used or diluted further immediately.

A slight pink tint may develop on standing without affecting potency.

For IM administration:

Vial size
(powder volume)
Fluid to add
Volume to add
Resulting concentration
1 g
(1.2 mL)
Water for injections 2.6 mL  270 mg/mL

Reconstitute to 270 mg/mL or weaker for IM administration. 

Shake vigorously until powder is dissolved. A slight pink tint may develop on standing without affecting potency.

IV administration

Give reconstituted solution over 3 5 minutes.

Maximum concentration if necessary: 149 mg/mL.

Intermittent infusion: dilute to 20 mg/mL or weaker give over 20 60 minutes.

Other routes of administration

IV administration is the preferred route for doses greater than 1 g.

IM: Suitable. Give reconstituted solution by deep IM injection into a large muscle mass.

SC: Not recommended.

Compatible IV fluids

Sodium chloride 0.9%

Aztreonam 20 mg/mL or weaker:

Glucose 5%

Glucose 5% and sodium chloride 0.45%

Glucose 5% and sodium chloride 0.9%

Glucose 10%

Hartmann’s

Ringer’s

Y-site only and aztreonam 20 mg/mL or weaker:

Potassium chloride 20 mmol/L

Additional information

Reconstituted solution should be clear and colourless to pale yellow or slight pink. 

IV: reconstituted solution should be used immediately. Discard any unused vial contents.

IM: reconstituted solution is stable for 48 hours.


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