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  5. Ceftobiprole Medocaril Sodium for Injection
  1. Development Resources

Ceftobiprole Medocaril Sodium for Injection

 

Minimum Inhibitory
Concentrations (mcg/mL)

Disk Diffusiona
(zone diameters in mm)

 Pathogenb

S

I

R

S

I

R

Staphylococcus aureus
(includes methicillin
resistant isolates)

≤ 2

4

≥ 8

≥ 16

14-15

≤ 13

Streptococcus pneumoniae

≤0.5

1

≥2

-

-

-

Streptococcus pyogenesc

≤ 0.5

-

-

≥ 24

-

-

Enterobacteralesd

≤ 0.25

0.5

≥ 1

≥ 23

21-22

≤ 20

Haemophilus influenzae
and parainfluenzae

≤ 0.25

0.5

≥ 1

-

-

-

S = susceptible; I = intermediate; R = resistant
a For disk diffusion, use paper disks impregnated with 5 mcg ceftobiprole.
b Susceptibility interpretive criteria are based on a dose of 667 mg ceftobiprole medocaril sodium every 6 hours on days 1 to 8 and every 8 hours from day 9 for patients with Staphylococcus aureus bacteremia (SAB) and a dose of 667 mg every 8 hours for patients with acute bacterial skin and skin structure infections (ABSSSI) and community acquired bacterial pneumonia (CABP) in adult patients with creatinine clearance > 50 mL/min); 667 mg of ceftobiprole medocaril sodium is equivalent to 500 mg of ceftobiprole.
c The absence of resistant isolates precludes defining any results other than “Susceptible”. Isolates yielding MIC results other than “Susceptible” should be submitted to a reference laboratory for further testing.
d Clinical efficacy was shown for Klebsiella pneumoniae in patients with ABSSSI and for Escherichia coli and Klebsiella pneumoniae in patients with CABP

 
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