Medical Pharmacology Chapter 35 Antibacterial Drugs
Third Generation Cephalosporins in More Detail
Cefotaxime Therapeutic Uses (Continued)
In perforated appendicitis, diverticulitis with abscess, or secondary peritonitis without severe sepsis or high ESBL risk, cefotaxime plus metronidazole is an effective combination which targets Enterobacterales and anaerobes respectively.
SBP is typically on monomicrobial infection due to enteric-type bacteria such as Escherichia coli, Klebsiella pneumoniae, and Enterococcus faecalis.
Guidelines for Spontaneous Bacterial Peritonitis (SBP) and other intra‑abdominal infections identify cefotaxime as a standard third‑generation cephalosporin option, especially in community‑acquired settings.6,7,8,9
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Skin and soft‑tissue infections8,10
Cefotaxime can be used for moderate to severe cellulitis or soft‑tissue infections when streptococci and some staphylococci are implicated, particularly if a Gram‑negative component is suspected post‑surgery or in diabetics.
For pure MSSA infections, narrower agents such as cefazolin are preferred, but cefotaxime is useful when broader coverage is needed while cultures are pending.
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Bone and Joint Infections8,10
In osteomyelitis or septic arthritis caused by susceptible streptococci or Gram‑negative bacilli, cefotaxime achieves therapeutic bone and synovial levels and is often part of combination therapy.
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Cefuroxime is commonly selected when polymicrobial infections or Gram‑negative coverage are concerns, with targeted agents added for staphylococci or anaerobes as indicated.
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Gynecologic and Pelvic Infections8,10,11,12,13
Cefotaxime has been used in pelvic inflammatory disease and postpartum endometritis to cover Gram‑negative rods and streptococci.
Other more current regimens based on ceftriaxone is often recommended, as describe in references 12,13 and in the table below.
Cefuroxime was often combined with metronidazole and doxycycline (or azithromycin) targeting anaerobes and Chlamydia trachomatis.
Such multi‑drug approaches take into account the polymicrobial character of upper genital tract infections.
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February, 2026
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