cefOXITIN

Trade name

Cefoxitin (Juno)

Presentation and preparation

For IV administration:

Vial size
(powder volume)
Fluid to add
Volume to add
Resulting concentration
1 g
(0.5 mL)
Water for injections 9.5 mL 100 mg/mL
2 g
(1.1 mL)
Water for injections 18.9 mL  100 mg/mL

Reconstitute to 100 mg/mL for IV administration.

For IM administration:

Vial size
(powder volume)
Fluid to add
Volume to add
Resulting concentration
1 g
(0.5 mL)
Water for injections OR Lidocaine 0.5%* or 1% 2 mL 400 mg/mL
2 g
(1.1 mL)
Water for injections OR Lidocaine  0.5%* or 1%  3.9 mL  400 mg/mL

Reconstitute to 400 mg/mL for IM administration.

Pain at the site of injection is often severe when cefoxitin IM is reconstituted using water for injections.

*Dilute lidocaine 1% with an equal quantity of water or sodium chloride 0.9% to make a 0.5% solution.

IV administration

Give reconstituted solution over at least 3 minutes or further dilute to 40 mg/mL or weaker and infuse over 10 to 60 minutes.

Maximum concentration for peripheral administration: 125 mg/mL.

Can be given as a continuous infusion.

Other routes of administration

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

SC: Not recommended.

Compatible IV fluids

Glucose 5%

Glucose 5% and sodium chloride 0.9%

Glucose 5% and sodium chloride 0.45%

Glucose 10%

Hartmann's

Sodium chloride 0.9%

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

Plasma-Lyte 148

Y-site only:       

Potassium chloride 20 mmol/L

Additional information

IV aminoglycoside antibiotics are inactivated by IV cephalosporins, penicillins and teicoplanin; refer to Glossary and Notes. 

Solution is clear, colourless to pale yellow in colour. Solution may darken upon storage but can still be used.

Protect from light during storage.


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