Literature DB >> 9179528

Clarithromycin. A review of its efficacy in the treatment of respiratory tract infections in immunocompetent patients.

H D Langtry1, R N Brogden.   

Abstract

Clarithromycin is a broad spectrum macrolide antibacterial agent active in vitro and effective in vivo against the major pathogens responsible for respiratory tract infections in immunocompetent patients. It is highly active in vitro against pathogens causing atypical pneumonia (Chlamydia pneumoniae, Mycoplasma pneumoniae and Legionella spp.) and has similar activity to other macrolides against Staphylococcus aureus. Streptococcus pyogenes, Moraxella catarrhalis and Streptococcus pneumoniae. Haemophilus influenzae is susceptible or intermediately susceptible to clarithromycin alone, but activity is enhanced when the parent drug and metabolite are combined in vitro. Absorption of clarithromycin is unaffected by food. More than half of an oral dose is systemically available as the parent drug and the active 14-hydroxy metabolite. Pharmacokinetics are nonlinear, with plasma concentrations increasing in more than proportion to the dosage. First-pass metabolism results in the rapid appearance of the active metabolite 14-hydroxy-clarithromycin in plasma. Clarithromycin and its active metabolite are found in greater concentrations in the tissues and fluids of the respiratory tract than in plasma. Dosage adjustments are required for patients with severe renal failure, but not for elderly patients or those with hepatic impairment. Drug interactions related to the cytochrome P450 system may occur with clarithromycin use. In addition to the standard immediate-release formulation for administration twice daily, a modified-release formulation of clarithromycin is now available for use once daily. In dosages of 500 to 1000 mg/day for 5 to 14 days, clarithromycin was as effective in the treatment of community-acquired upper and lower respiratory tract infections in hospital and community settings as beta-lactam agents (with or without a beta-lactamase inhibitor), cephalosporins and most other macrolides. Clarithromycin was similar in efficacy to azithromycin in comparative studies and is as effective as and better tolerated than erythromycin. Adverse events are primarily gastrointestinal in nature, but result in fewer withdrawals from therapy than are seen with erythromycin. Clarithromycin provides similar clinical and bacteriological efficacy to that seen with beta-lactam agents, cephalosporins and other macrolides. It offers a cost-saving alternative to intravenous erythromycin use in US hospitals and is available in both once-daily and twice-daily formulations. The spectrum of activity of clarithromycin against common and emerging respiratory tract pathogens may make it suitable for use in the community as empirical therapy of respiratory tract infections in both children and adults.

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Year:  1997        PMID: 9179528     DOI: 10.2165/00003495-199753060-00006

Source DB:  PubMed          Journal:  Drugs        ISSN: 0012-6667            Impact factor:   9.546


  137 in total

1.  Clinical efficacy and tolerance of two new macrolides, clarithromycin and josamycin, in the treatment of patients with acute exacerbations of chronic bronchitis.

Authors:  F Fraschini
Journal:  J Int Med Res       Date:  1990 Mar-Apr       Impact factor: 1.671

2.  Reduced serum levels of clarithromycin in patients treated with multidrug regimens including rifampin or rifabutin for Mycobacterium avium-M. intracellulare infection.

Authors:  R J Wallace; B A Brown; D E Griffith; W Girard; K Tanaka
Journal:  J Infect Dis       Date:  1995-03       Impact factor: 5.226

3.  Clarithromycin versus cefaclor for the treatment of mild-to-moderate acute bacterial bronchitis.

Authors:  R Wettengel; N Vetter; F A Waardenburg
Journal:  J Antimicrob Chemother       Date:  1993-06       Impact factor: 5.790

4.  Clarithromycin pharmacokinetics in healthy young and elderly volunteers.

Authors:  S Y Chu; D S Wilson; D R Guay; C Craft
Journal:  J Clin Pharmacol       Date:  1992-11       Impact factor: 3.126

5.  Susceptibility surveillance of U.S. respiratory pathogen isolates to newer macrolide and azalide antibiotics.

Authors:  S Brown; A L Barry; P Burton
Journal:  Int J Antimicrob Agents       Date:  1996-05       Impact factor: 5.283

6.  Clarithromycin-carbamazepine interaction in a clinical setting.

Authors:  N K O'Connor; J Fris
Journal:  J Am Board Fam Pract       Date:  1994 Nov-Dec

7.  Pharmacokinetics of a clarithromycin suspension in infants and children.

Authors:  V N Gan; S Y Chu; H T Kusmiesz; J C Craft
Journal:  Antimicrob Agents Chemother       Date:  1992-11       Impact factor: 5.191

8.  Comparative study of clarithromycin and ampicillin in the treatment of patients with acute bacterial exacerbations of chronic bronchitis.

Authors:  R T Bachand
Journal:  J Antimicrob Chemother       Date:  1991-02       Impact factor: 5.790

9.  Immunomodulatory effects of three macrolides, midecamycin acetate, josamycin, and clarithromycin, on human T-lymphocyte function in vitro.

Authors:  K Morikawa; F Oseko; S Morikawa; K Iwamoto
Journal:  Antimicrob Agents Chemother       Date:  1994-11       Impact factor: 5.191

10.  Effect of clarithromycin on sputum production and its rheological properties in chronic respiratory tract infections.

Authors:  J Tamaoki; K Takeyama; E Tagaya; K Konno
Journal:  Antimicrob Agents Chemother       Date:  1995-08       Impact factor: 5.191

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  9 in total

1.  Lack of effect of zafirlukast on the pharmacokinetics of azithromycin, clarithromycin, and 14-hydroxyclarithromycin in healthy volunteers.

Authors:  K W Garey; C A Peloquin; P G Godo; A N Nafziger; G W Amsden
Journal:  Antimicrob Agents Chemother       Date:  1999-05       Impact factor: 5.191

Review 2.  Review of macrolides and ketolides: focus on respiratory tract infections.

Authors:  G G Zhanel; M Dueck; D J Hoban; L M Vercaigne; J M Embil; A S Gin; J A Karlowsky
Journal:  Drugs       Date:  2001       Impact factor: 9.546

3.  A survey of the quality of generic clarithromycin products from 18 countries.

Authors:  C H Nightingale
Journal:  Clin Drug Investig       Date:  2005       Impact factor: 2.859

Review 4.  Comparative tolerability of erythromycin and newer macrolide antibacterials in paediatric patients.

Authors:  N Principi; S Esposito
Journal:  Drug Saf       Date:  1999-01       Impact factor: 5.606

Review 5.  Clinical pharmacokinetics of clarithromycin.

Authors:  K A Rodvold
Journal:  Clin Pharmacokinet       Date:  1999-11       Impact factor: 6.447

Review 6.  Community-acquired pneumonia in the elderly: a practical guide to treatment.

Authors:  D Lieberman; D Lieberman
Journal:  Drugs Aging       Date:  2000-08       Impact factor: 3.923

7.  Pharmacokinetic interaction between amprenavir and clarithromycin in healthy male volunteers.

Authors:  D F Brophy; D S Israel; A Pastor; C Gillotin; G E Chittick; W T Symonds; Y Lou; B M Sadler; R E Polk
Journal:  Antimicrob Agents Chemother       Date:  2000-04       Impact factor: 5.191

8.  Broader and safer clinically-relevant activities of pentadecanoic acid compared to omega-3: Evaluation of an emerging essential fatty acid across twelve primary human cell-based disease systems.

Authors:  Stephanie K Venn-Watson; Camden N Butterworth
Journal:  PLoS One       Date:  2022-05-26       Impact factor: 3.752

9.  Modeling the autoinhibition of clarithromycin metabolism during repeated oral administration.

Authors:  Khaled Abduljalil; Martina Kinzig; Jürgen Bulitta; Stefan Horkovics-Kovats; Fritz Sörgel; Michael Rodamer; Uwe Fuhr
Journal:  Antimicrob Agents Chemother       Date:  2009-05-04       Impact factor: 5.191

  9 in total

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