PMID- 20101337 OWN - NLM STAT- PubMed-not-MEDLINE DCOM- 20100623 LR - 20211020 IS - 1998-3611 (Electronic) IS - 0019-5154 (Print) IS - 0019-5154 (Linking) VI - 54 IP - 4 DP - 2009 TI - Efficacy and tolerability of cefditoren pivoxil in uncomplicated skin and skin structure infections in Indian patients. PG - 350-6 LID - 10.4103/0019-5154.57612 [doi] AB - BACKGROUND: Uncomplicated skin and skin structure infections (uSSSI) are commonly encountered community-acquired infections and are typically confined to the superficial layers of the skin. Hence, they seldom lead to the destruction of skin structures. AIMS: To evaluate the efficacy and tolerability of cefditoren pivoxil in uSSSI in Indian patients. METHODS: One hundred and seventy-eight patients diagnosed with uncomplicated SSSI were enrolled in this randomized, comparative, multicentric study. Patients received either cefditoren pivoxil or cefdinir for ten days. Efficacy was assessed both clinically and microbiologically. Safety evaluation consisted of reporting of type, frequency, severity, and causal relationship of adverse events. RESULTS: One hundred and fifty-one patients completed the study. Clinical and bacteriological efficacy of cefditoren pivoxil was comparable to that of cefdinir in the treatment of uSSSI. One hundred and five patients were eligible for per protocol (PP) analysis of bacteriological outcome and clinical efficacy. Clinical cure or improvement was achieved in 98.00% patients treated with cefditoren pivoxil and 98.18% patients treated with cefdinir. In the modified Intent to Treat (mITT) patient population, clinical cure or improvement was recorded in 97.33% patients treated with cefditoren pivoxil and 96.20% patients treated with cefdinir. Microbiological eradication (or presumed eradication) was recorded in 88.00% patients treated with cefditoren pivoxil and 94.55% patients treated with cefdinir. The above differences in the outcome rates between the two drugs were not statistically significant. Six adverse events (AEs) (two in cefditoren group and four in cefdinir group) were reported in this study. CONCLUSION: Cefditoren pivoxil 200 mg b.i.d. was effective and well tolerated in the treatment of uSSSI. FAU - Manaktala, Charu AU - Manaktala C AD - Medical Affairs and Clinical Research, Ranbaxy Laboratories Ltd, 77-B, IFFCO Road, Sector-18, Udyog Vihar Industrial Area, Gurgaon, Haryana, India. charu.manaktala@ranbaxy.com FAU - Singh, Amit Kumar AU - Singh AK FAU - Verma, Manish AU - Verma M FAU - Sachdeva, Asheesh AU - Sachdeva A FAU - Sharma, Himanshu AU - Sharma H FAU - Roy, Arjun AU - Roy A FAU - Jalali, R K AU - Jalali RK FAU - Gowrishankar, R AU - Gowrishankar R FAU - Kumar, A AU - Kumar A FAU - Kumar, A Sainath AU - Kumar AS FAU - Jayaraman, A M AU - Jayaraman AM FAU - Swarnkar, B AU - Swarnkar B FAU - Srinivas, C R AU - Srinivas CR FAU - Nayak, Chitra AU - Nayak C FAU - Duttaroy, D AU - Duttaroy D FAU - Umrigar, D AU - Umrigar D FAU - Jesudanam, Madhuri AU - Jesudanam M FAU - Maheshwari, N AU - Maheshwari N FAU - Shetty, P AU - Shetty P FAU - Singh, R P AU - Singh RP FAU - Ghate, S AU - Ghate S FAU - Sacchidanand, S AU - Sacchidanand S FAU - Tolat, S AU - Tolat S FAU - Bhoira, Salman AU - Bhoira S FAU - Marfatia, Y AU - Marfatia Y LA - eng PT - Journal Article PL - India TA - Indian J Dermatol JT - Indian journal of dermatology JID - 0370750 PMC - PMC2807712 OTO - NOTNLM OT - Cefditoren pivoxil OT - uSSSI OT - uncomplicated skin and skin structure infection COIS- Conflict of Interest: Nil. EDAT- 2010/01/27 06:00 MHDA- 2010/01/27 06:01 PMCR- 2009/10/01 CRDT- 2010/01/27 06:00 PHST- 2010/01/27 06:00 [entrez] PHST- 2010/01/27 06:00 [pubmed] PHST- 2010/01/27 06:01 [medline] PHST- 2009/10/01 00:00 [pmc-release] AID - IJD-54-350 [pii] AID - 10.4103/0019-5154.57612 [doi] PST - ppublish SO - Indian J Dermatol. 2009;54(4):350-6. doi: 10.4103/0019-5154.57612.