Elephant Formulary

© 2003-17 Susan K. Mikota DVM and Donald C. Plumb, Pharm.D. Published by
Elephant Care International
www.elephantcare.org

Disclaimer: the information on this page is used entirely at the reader's discretion, and is made available on the express condition that no liability, expressed or implied, is accepted by the authors or publisher for the accuracy, content, or use thereof.

Cefoxitin Sodium

Elephant specific information, if available, is in blue.

For general information on the cephalosporins including adverse effects, contraindications, over­dosage, drug interactions, and monitoring parameters, refer to the monograph: Cephalosporins, General Information.

 

Chemistry – Actually a cephamycin, cefoxitin sodium is a semisynthetic antibiotic that is derived from cephamycin C which is produced by Streptomyces lactamdurans. It occurs as a white to off-white, somewhat hygroscopic powder or granules with a slight characteristic odor. It is very soluble in water and slightly soluble in alcohol. Each gram of cefoxitin sodium contains 2.3 mEq of sodium.

 

Storage/Stability/Compatibility – Cefoxitin sodium powder for injection should be stored at temperatures less than 30°C and should not be exposed to temperatures greater than 50°C. The frozen solution for injection should be stored at temperatures no higher than -20°C.

 

After reconstitution, the solution is stable for 24 hours when kept at room temperature and from 48 hours to 1 week if refrigerated. If after reconstitution the solution is immediately frozen in the original container, the preparation is stable up to 30 weeks when stored at -20°C. Stability is dependent on the diluent used and the reader should refer to the package insert or other specialized references for more information. The powder or reconstituted solution may darken, but this apparently does not affect the potency of the product.

 

All commonly used IV fluids and the following drugs are reportedly compatible with cefoxitin: amikacin sulfate, cimetidine HCl, gentamicin sulfate, kanamycin sulfate, mannitol, metronidazole, mutivitamin infusion concentrate, sodium bicarbonate, tobramycin sulfate and vitamin B-complex with C. Compatibility is dependent upon factors such as pH, concentration, temperature and diluents used. It is suggested to consult specialized references for more specific information (e.g., Handbook on Injectable Drugs by Trissel; see bibliography).

 

Pharmacology/Spectrum of Activity – Although not a true cephalosporin, cefoxitin is usually classified as a 2nd generation agent. Cefoxitin has activity against gram positive cocci, but less so on a per weight basis than the 1st generation agents. Unlike the first generation agents, it has good activity against many strains of E. coliKlebsiella and Proteus that may be resistant to the first generation agents. In human medicine, cefoxitin’s activity against many strains of Bacteroides fragilis has placed it in a significant therapeutic role. While Bacteroides fragilis has been isolated from anerobic infections in veterinary patients, it may not be as significant a pathogen in veterinary species as in humans.

 

Because 2nd generation cephalosporins exhibit specific activities against bacteria, a 30-micrograms cefoxitin disk should be used when performing Kirby-Bauer disk susceptibility tests for this antibiotic

 

Uses/Indications – In the United States, there are no cefoxitin products approved for veterinary species, but it has been used clinically in several species when an injectable second generation cephalosporin may be indicated.

 

Pharmacokinetics (specific) – Cefoxitin is not appreciably absorbed after oral administration and must be given parenterally to achieve therapeutic serum levels. The absorbed drug is primarily excreted unchanged by the kidneys into the urine via both tubular secretion and glomerular filtration. In humans, approximately 2% of a dose is metabolized to descarbamylcefoxitin, which is inactive. Elimination half-lives may be significantly prolonged in patients with severely dimin­ished renal function.

 

In horses, the apparent volume of distribution at steady state is 110 ml/kg, total body clearance of 4.32 ml/min/kg with a serum elimination half-life of 49 minutes.

 

In calves, the volume of distribution is 318 ml/kg, and has a terminal elimination half-life of 67 minutes after IV dosing, and 81 minutes after IM administration. Cefoxitin is approximately 50% bound to calf plasma proteins. Probenecid (40 mg/kg) has been demonstrated to significantly prolong elimination half-lives.

 

Doses –

Horses:

For susceptible infections:

a)   Foals: 20 mg/kg IV q4-6h (Caprile and Short 1987)

 

Dosage Forms/Preparations/FDA Approval Status –

 

Veterinary-Approved Products: None

 

Human-Approved Products:

Cefoxitin Sodium  Powder for Injection 1 g (of cefoxitin), 2 g, 10 g

Mefoxin®  (Merck); (Rx)

 

Cefoxitin Sodium in Dextrose 5% (Frozen) 1 g (20 mg/ml), 2 g (40 mg/ml)

Mefoxin® (Merck); (Rx)