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62 results

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Page 1
Clinical Trial to Reconfirm the Efficacy and Safety of Cefetamet Pivoxil Treatment in Sinusitis Patients: A Double-Blind, Randomized, Parallel Designed, Multicenter, Active Comparator Study (CASIS Study).
Park CS, Cho JH, Lee HM, Kim KS, Kim JK, Kim DY, Baek BJ, Kim HJ, Kim YD, Hwang CS, Kim ST, Cho SH, Kim YM, Lee SH, Jeong JH, In SM, Kim BG. Park CS, et al. Ear Nose Throat J. 2023 Feb;102(2):101-109. doi: 10.1177/01455613211036236. Epub 2021 Aug 24. Ear Nose Throat J. 2023. PMID: 34427151 Free article. Clinical Trial.
RESULTS: Treatment with cefetamet pivoxil for 2 weeks showed 82.4% clinical cure and improvement rates in patients with acute bacterial rhinosinusitis compared to 84.68% in those taking cefdinir for 2 weeks, showing that cefetamet pivoxil administered twice a day for 2 wee …
RESULTS: Treatment with cefetamet pivoxil for 2 weeks showed 82.4% clinical cure and improvement rates in patients with acute bacterial rhin …
Comparison of cefdinir and penicillin for the treatment of streptococcal pharyngitis. Cefdinir Pharyngitis Study Group.
Nemeth MA, McCarty J, Gooch WM 3rd, Henry D, Keyserling CH, Tack KJ. Nemeth MA, et al. Clin Ther. 1999 Nov;21(11):1873-81. doi: 10.1016/s0149-2918(00)86735-1. Clin Ther. 1999. PMID: 10890259 Clinical Trial.
The eradication rates 4 to 9 days after completion of therapy were 91.4% in the cefdinir QD group, 91.7% in the cefdinir BID group, and 83.4% in the penicillin group (P = 0.02 for cefdinir QD vs penicillin, P = 0.01 for cefdinir BID vs penicillin, P = …
The eradication rates 4 to 9 days after completion of therapy were 91.4% in the cefdinir QD group, 91.7% in the cefdinir BID g …
[Pharmacokinetic and clinical studies of cefdinir in the pediatric field. Pediatric Study Group of Cefdinir].
Fujii R, Yoshioka H, Fujita K, Sakata H, Nire H, Iseki K, Murono K, Takahashi Y, Wagatsuma Y, Fukushima N, et al. Fujii R, et al. Jpn J Antibiot. 1991 Oct;44(10):1168-91. Jpn J Antibiot. 1991. PMID: 1762172 Clinical Trial. Japanese.
We studied pharmacokinetics and clinical effects of 5% and 10% fine granules of cefdinir (FK 482, CFDN), a new oral cephalosporin, in the pediatric field and the following results were obtained. 1. ...
We studied pharmacokinetics and clinical effects of 5% and 10% fine granules of cefdinir (FK 482, CFDN), a new oral cephalosporin, in …
Five-day twice daily cefdinir therapy for acute otitis media: microbiologic and clinical efficacy.
Block SL, Hedrick JA, Kratzer J, Nemeth MA, Tack KJ. Block SL, et al. Pediatr Infect Dis J. 2000 Dec;19(12 Suppl):S153-8. doi: 10.1097/00006454-200012001-00004. Pediatr Infect Dis J. 2000. PMID: 11144397 Clinical Trial.
OBJECTIVE: To examine the microbiologic and clinical efficacy of a 5-day course of cefdinir in the treatment of tympanocentesis-documented acute otitis media (AOM). DESIGN: Open label noncomparative trial. ...Cefdinir should be considered a suitable second line anti …
OBJECTIVE: To examine the microbiologic and clinical efficacy of a 5-day course of cefdinir in the treatment of tympanocentesis-docum …
[Clinical efficacy and bacteriological studies of clarithromycin and cefdinir against group A beta-hemolytic streptococcal tonsillopharyngitis].
Nishimura T, Sugita K, Taniguchi K, Uemura T, Harada Y, Kino M, Morikawa Y. Nishimura T, et al. Jpn J Antibiot. 2003 Aug;56(4):281-8. Jpn J Antibiot. 2003. PMID: 14567252 Clinical Trial. Japanese.
The clinical efficacy and safety of clarithromycin (CAM) and cefdinir (CFDN) were evaluated in 65 pediatric outpatients with group A beta-hemolytic streptococcal tonsillopharyngitis. ...
The clinical efficacy and safety of clarithromycin (CAM) and cefdinir (CFDN) were evaluated in 65 pediatric outpatients with group A …
Comparison of cefdinir and penicillin for the treatment of pediatric streptococcal pharyngitis.
Nemeth MA, Gooch WM 3rd, Hedrick J, Slosberg E, Keyserling CH, Tack KJ. Nemeth MA, et al. Clin Ther. 1999 Sep;21(9):1525-32. doi: 10.1016/s0149-2918(00)80007-7. Clin Ther. 1999. PMID: 10509847 Clinical Trial.

The eradication rates of S pyogenes, determined 4 to 9 days after completion of therapy, were 94.3% in the cefdinir QD group, 94.3% in the cefdinir BID group, and 70.0% in the penicillin V group (95% confidence interval [CI] 17.6%-30.9%, P < 0.001 for cefdinir

…
The eradication rates of S pyogenes, determined 4 to 9 days after completion of therapy, were 94.3% in the cefdinir QD group, 94.3% i …
Efficacy and safety of cefdinir in the treatment of maxillary sinusitis.
Steurer M, Schenk P. Steurer M, et al. Eur Arch Otorhinolaryngol. 2000;257(3):140-8. doi: 10.1007/s004050050211. Eur Arch Otorhinolaryngol. 2000. PMID: 10839487 Clinical Trial.
In this investigator-blinded multicenter phase III clinical study, 569 patients were randomly assigned to one of three treatment regimens: one daily dose of cefdinir 600 mg (OD), cefdinir 300 mg every 12 h (BD), and amox/clav 500/125 mg every 8 h. ...Present finding …
In this investigator-blinded multicenter phase III clinical study, 569 patients were randomly assigned to one of three treatment regimens: o …
[Bacteriological, pharmacokinetic and clinical studies of 5% and 10% granules of cefdinir in the pediatric field].
Toyonaga Y, Hatakeyama K, Yamori K, Sakaguchi N, Nakano K, Yamazaki M, Sugita M, Hori M. Toyonaga Y, et al. Jpn J Antibiot. 1992 Jan;45(1):48-73. Jpn J Antibiot. 1992. PMID: 1495196 Clinical Trial. Japanese.
Bacteriological, pharmacokinetic and clinical studies on cefdinir (CFDN, FK482), a new oral cephalosporin, 5% and 10% granules, were performed in the field of pediatrics. ...
Bacteriological, pharmacokinetic and clinical studies on cefdinir (CFDN, FK482), a new oral cephalosporin, 5% and 10% granules, were …
[Pharmacokinetics and clinical effects of cefdinir 10% fine granules in pediatrics].
Motohiro T, Handa S, Yamada S, Oki S, Tsumura N, Yoshinaga Y, Sasaki H, Aramaki M, Oda K, Kawakami A, et al. Motohiro T, et al. Jpn J Antibiot. 1992 Jan;45(1):74-86. Jpn J Antibiot. 1992. PMID: 1495197 Clinical Trial. Japanese.
Cefdinir (CFDN), a newly developed oral cephalosporin in a 10% fine granular form, was administered to 8 children and concentrations of the drug in plasma and urine and urinary recovery rates of the drug were determined. ...
Cefdinir (CFDN), a newly developed oral cephalosporin in a 10% fine granular form, was administered to 8 children and concentrations …
Comparison of cefdinir and cefaclor in treatment of community-acquired pneumonia.
Drehobl M, Bianchi P, Keyserling CH, Tack KJ, Griffin TJ. Drehobl M, et al. Antimicrob Agents Chemother. 1997 Jul;41(7):1579-83. doi: 10.1128/AAC.41.7.1579. Antimicrob Agents Chemother. 1997. PMID: 9210689 Free PMC article. Clinical Trial.
Six hundred ninety patients were enrolled in a multicenter, randomized, double-blind trial comparing the efficacy and safety of cefdinir with those of cefaclor in the treatment of community-acquired pneumonia. Patients received either 10 days of treatment with cefdinir …
Six hundred ninety patients were enrolled in a multicenter, randomized, double-blind trial comparing the efficacy and safety of cefdinir …
62 results