Safety and tolerability of linezolid

被引:148
作者
French, G [1 ]
机构
[1] Guys & St Thomas Hosp, Dept Infect, London SE1 7EH, England
[2] Univ London Kings Coll, London SE1 7EH, England
关键词
D O I
10.1093/jac/dkg253
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Clinical trials have shown that linezolid (600 mg twice daily in adults) is safe and generally well tolerated for up to 28 days. Drug-related adverse events, which are typically mild to moderate in intensity and of limited duration, include diarrhoea, nausea and headache in adults, and diarrhoea, loose stools and vomiting in children. Clostridium difficile-related complications with linezolid are uncommon. Linezolid is a weak, reversible monoamine oxidase inhibitor: foods containing high concentrations of tyramine should be avoided, and linezolid should be used with caution in patients taking adrenergic or serotonergic agents or in those with uncontrolled hypertension. In the majority of patients, linezolid has minimal adverse effects on blood chemistry or haematology. There have been case reports of reversible thrombocytopenia, anaemia and neutropenia associated with linezolid therapy. In Phase III studies, 2.4% of patients treated with linezolid and 1.5% of patients treated with comparator drugs developed reversible thrombocytopenia (P = 0.066), but there was no evidence of an increased risk of agranulocytosis, aplastic anaemia or other irreversible blood dyscrasias. Reduced platelet counts were associated with linezolid treatment for greater than or equal to2 weeks; complete blood counts should be monitored weekly in patients receiving linezolid for more than 14 days and treatment should be discontinued if there is evidence of myelosuppression.
引用
收藏
页码:45 / 53
页数:9
相关论文
共 49 条
[1]   In vitro activity of linezolid, quinupristin-dalfopristin, vancomycin, teicoplanin, moxifloxacin and mupirocin against methicillin-resistant Staphylococcus aureus: comparative evaluation by the E test and a broth microdilution method [J].
Abb, J .
DIAGNOSTIC MICROBIOLOGY AND INFECTIOUS DISEASE, 2002, 43 (04) :319-321
[2]  
Abena PA, 2001, JAMA-J AM MED ASSOC, V286, P1973, DOI 10.1001/jama.286.16.1973
[3]   Linezolid, a novel oxazolidinone antibiotic: Assessment of monoamine oxidase inhibition using presser response to oral tyramine [J].
Antal, EJ ;
Hendershot, PE ;
Batts, DH ;
Sheu, WP ;
Hopkins, NK ;
Donaldson, KM .
JOURNAL OF CLINICAL PHARMACOLOGY, 2001, 41 (05) :552-562
[4]  
Arellano FM, 2001, JAMA-J AM MED ASSOC, V286, P1973
[5]   Thrombocytopenia associated with linezolid therapy [J].
Attassi, K ;
Hershberger, E ;
Alam, R ;
Zervos, MJ .
CLINICAL INFECTIOUS DISEASES, 2002, 34 (05) :695-698
[6]   A multicenter evaluation of linezolid antimicrobial activity in North America [J].
Ballow, CH ;
Jones, RN ;
Biedenbach, DJ .
DIAGNOSTIC MICROBIOLOGY AND INFECTIOUS DISEASE, 2002, 43 (01) :75-83
[7]  
Barbachyn MR, 1998, ADV EXP MED BIOL, V456, P219
[8]   Linezolid for the treatment of multidrug-resistant, gram-positive infections: Experience from a compassionate-use program [J].
Birmingham, MC ;
Rayner, CR ;
Meagher, AK ;
Flavin, SM ;
Batts, DH ;
Schentag, JJ .
CLINICAL INFECTIOUS DISEASES, 2003, 36 (02) :159-168
[9]   Synthesis and antibacterial activity of U-100592 and U-100766, two oxazolidinone antibacterial agents for the potential treatment of multidrug-resistant Gram-positive bacterial infections [J].
Brickner, SJ ;
Hutchinson, DK ;
Barbachyn, MR ;
Manninen, PR ;
Ulanowicz, DA ;
Garmon, SA ;
Grega, KC ;
Hendges, SK ;
Toops, DS ;
Ford, CW ;
Zurenko, GE .
JOURNAL OF MEDICINAL CHEMISTRY, 1996, 39 (03) :673-679
[10]  
BRIER ME, 1999, 38 INT C ANT AG CHEM, P17