Is Keflex (cephalexin) a broad-spectrum antibiotic?

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Is Keflex a Broad-Spectrum Antibiotic?

No, Keflex (cephalexin) is not a broad-spectrum antibiotic—it is a narrow-spectrum first-generation cephalosporin with limited activity primarily against gram-positive organisms and select gram-negative bacteria, but notably lacks coverage against important pathogens like Haemophilus influenzae and Pseudomonas aeruginosa. 1, 2

Antimicrobial Spectrum of Cephalexin

Cephalexin's spectrum includes:

  • Gram-positive coverage: Effective against methicillin-sensitive Staphylococcus aureus (MSSA) and Streptococcus species, making it useful for streptococcal and staphylococcal skin infections with cure rates of 90% or higher 3

  • Limited gram-negative coverage: Active against some common urinary tract pathogens and certain Enterobacteriaceae, but this is significantly restricted compared to broader-spectrum agents 4

  • Critical gaps in coverage: Notably ineffective against Haemophilus influenzae, with failure rates of 50% in H. influenzae otitis media 2, 5. Also lacks activity against Pseudomonas aeruginosa, anaerobes (requiring combination with metronidazole when anaerobic coverage is needed), and extended-spectrum beta-lactamase (ESBL)-producing organisms 6

Comparison to Broad-Spectrum Agents

The evidence clearly distinguishes cephalexin from broad-spectrum antibiotics:

  • Narrow-spectrum designation: Clinical guidelines specifically classify cephalexin alongside cefadroxil as "narrow-spectrum cephalosporins," in contrast to "broad-spectrum cephalosporins" like cefixime, cefuroxime, cefdinir, and cefpodoxime 7

  • Preferred for narrow coverage: Guidelines recommend narrow-spectrum cephalosporins like cephalexin over broad-spectrum alternatives specifically because of their narrower antimicrobial spectrum and lower risk of selecting for antibiotic-resistant flora 7

  • Contrast with true broad-spectrum agents: Broad-spectrum antibiotics listed in guidelines include piperacillin-tazobactam (with anti-Pseudomonas and anaerobic coverage), carbapenems (active against ESBL-producing pathogens and anaerobes), and fourth-generation cephalosporins like cefepime (effective against AmpC-producing organisms) 6

Clinical Implications

  • Appropriate uses: Cephalexin is effective for uncomplicated skin and soft tissue infections caused by streptococci and staphylococci, urinary tract infections caused by susceptible organisms, and streptococcal pharyngitis in penicillin-allergic patients 6, 7, 4, 3

  • Inappropriate uses: Should not be relied upon for respiratory infections where H. influenzae is suspected (particularly in pediatric populations), infections requiring anaerobic coverage, or any infection where Pseudomonas or ESBL-producing organisms are concerns 2, 5

  • Resistance considerations: The narrow spectrum is actually advantageous in appropriate clinical scenarios, as it minimizes disruption of normal flora and reduces selection pressure for resistant organisms compared to broad-spectrum alternatives 7

References

Research

The pharmacology of cephalexin.

Postgraduate medical journal, 1983

Research

Cephalexin in the therapy of infections of the urinary tract.

Postgraduate medical journal, 1983

Research

Cephalexin in lower respiratory tract infections.

Postgraduate medical journal, 1983

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Cefixime vs Cefuroxime for Bacterial Pharyngitis

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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