Effectiveness and tolerability of cephalexin and clavulanic acid fixed dose combination, amoxicillin and clavulanic acid fixed dose combination, and azithromycin in patients with pharyngitis in India: a real-world retrospective study from electronic medical records (PHARYSPOR) - Summary - MDSpire

Effectiveness and tolerability of cephalexin and clavulanic acid fixed dose combination, amoxicillin and clavulanic acid fixed dose combination, and azithromycin in patients with pharyngitis in India: a real-world retrospective study from electronic medical records (PHARYSPOR)

  • By

  • Subramanyam Sarof

  • Nikita Kariappa Somana

  • Ravindra Channagiri S

  • Ramesh Chinthalapalli Venkataram

  • Jyothi Sharma R

  • Sabhapathi SV

  • Ramakrishnaiah Peddi

  • Sadanandam K

  • Nitin Rai Vohra

  • Lokesh Kumar Bhama

  • Mahendrakumar Shah

  • Vijay Chile

  • Ameeta Gunderia

  • Farad Momin

  • Anit Banerjee

  • Saumitra Kumar

  • Sandeep Rungta

  • Ashik Ikbal

  • Sunil Singhvi

  • Annamalai Natarajan

  • Monjori Mitra

  • Vijay Kadam

  • Shruti Dharmadhikari

  • Chintan Khandhedia

  • Gaurav Puppalwar

  • Neeraj Markandeywar

  • Amey Mane

  • Suyog Mehta

  • July 9, 2026

  • 0 min

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Objective:

To assess the effectiveness and tolerability of cephalexin-clavulanate compared to co-amoxiclav and azithromycin in adult patients with acute bacterial pharyngitis.

Approach:
  • Study Design: Retrospective, multicenter, comparative observational study analyzing electronic medical records of adults with clinically suspected acute bacterial pharyngitis.
  • Patient Selection: Included adults treated with study medications between November 2022 and March 2023, excluding those with incomplete records, hospitalizations, or requiring parenteral antibiotics.
  • Outcomes: Primary outcomes included clinical cure rates by Day 10; secondary outcomes included time to clinical improvement and adverse events.
Key Findings:
  • 752 patients analyzed: cephalexin-CV (n = 285), co-amoxiclav (n = 245), azithromycin (n = 222).
  • Overall clinical cure rates and time to improvement were similar across all groups.
  • Cephalexin-CV showed earlier clinical improvement by Day 2 (27% vs. 18% for co-amoxiclav, p = 0.035; 15% for azithromycin, p = 0.003) and Day 3 (58% vs. 47% for co-amoxiclav, p = 0.022; 48% for azithromycin, p = 0.071).
  • NSAID requirements were similar for cephalexin-CV and co-amoxiclav (46% each) but higher for azithromycin (57%, p = 0.020).
  • Adverse events were minimal across all groups.
Interpretation:

No statistically significant differences in overall clinical outcomes or tolerability among the three treatment groups, but cephalexin-CV was associated with earlier symptom improvement and lower NSAID use.

Limitations:
  • Retrospective design may introduce bias.
  • Data limited to a specific geographic region in India.
Conclusion:

Cephalexin-CV may offer early symptomatic relief and reduced NSAID requirements, making it a potential option for treating pharyngitis.

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