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. 2014 May 5;3(2):174–192. doi: 10.3390/antibiotics3020174

Table 2.

Antimicrobial management of acute uncomplicated cystitis a.

Antimicrobial Dosing and Duration Efficacy
First-Line Agents
Nitrofurantoin monohydrate/macrocrystal b 100 mg twice daily × 5 days (with meals)
  • Clinical efficacy of 5–7 day regimen: 93% (84%–95%)

  • 3–day regimen appears less effective vs. longer regimens

  • Minimal in vitro resistance

Trimethoprim-sulfamethoxazole c 160/800 mg twice-daily × 3 days
  • Clinical efficacy of 3-day TMP-SMX regimen: 93% (90%–100%)

  • Avoid if resistance >20% or exposure in prior 3–6 months

Fosfomycin trometamol 3 g sachet in a single dose
  • Appears to be less effective vs. TMP-SMX or fluoroquinolones

  • Minimal in vitro resistance, but most labs do not test

Pivmecillinam 400 mg twice daily × 3–7 days
  • Clinical efficacy of 3–7 day regimens: 73% (55%–82%)

  • Minimal in vitro resistance

  • Unavailable in some countries

Second-Line Agents
Fluoroquinolone:
Ciprofloxacin c
Levofloxacin c
250 mg twice daily × 3 days
250 mg or 500 mg once daily × 3 days
  • Clinical efficacy 90% (85%–98%)

  • High prevalence of in vitro resistance in some regions of the world

β-lactamb:(e.g., amoxicillin-clavulanate, cefdinir, cefaclor, and cefpodoxime-proxetil) 3–7 days
  • Clinical efficacy of 3–5 day regimens: 89% (79%–98%)

  • Less effective thanTMP-SMX and fluoroquinolones

  • Prevalence of E. coli resistance is variable

Adapted from ref. [2]. a Efficacy data and antimicrobial recommendations based on IDSA guidelines [13]; b Pregnancy category B—no clear risk to fetus based on animal and/or human studies; c Pregnancy category C—animal studies have shown an adverse effect on the fetus; use only if potential benefit justifies the potential risk to the fetus.