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Septra
Clinical Pharmacology
Septra
The usual spectrum of antimicrobial activity of SEPTRA includes bacterial pathogens isolated from middle ear exudate and from bronchial secretions {Haemophilus influenzae, including ampicillin- resistant strains, and Streptococcus pneumoniae), and enterotoxigenic strains of Escherichia coli (ETEC) causing bacterial gastroenteritis. Shigella flexneri and Shigella sonnei are also usually susceptible.
REPRESENTATIVE MINIMUM INHIBITORY CONCENTRATION VALUES FOR
ORGANISMS SUSCEPTIBLE TO SEPTRA (MICµg/mL)
| Bacteria | TMP Alone | SMX Alone | TMP/SMX(1:19) | |
| TMP | SMX | |||
| Escherichia coli | 0.05-1.5 | 1.0-245 | 0.05-0.5 | 0.95-9.5 |
| Escherichia coli (enterotoxigenic strains) | 0.015-0.15 | 0.285- > 950 | 0.005-0.15 | 0.095-2.85 |
| Proteus species (indole positive) | 0.5-5.0 . | 7.35-300 | 0.05-1.5 | 0.95-28.5 |
| Bacteria | TMP Alone | SMX Alone | TMP/SMX(1:19) | |
| TMP | SMX | |||
| Morganella morganii | 0.5-5.0 | 7.35-300 | 0.05-1.5 | 0.95-28.5 |
| Proteus mirabilis | 0.5-1.5 | 7.35-30 | 0.05-0.15 | 0.95-2.85 |
| Klebsiella species | 0.15-5.0 | 2.45-245 | 0.05-1.5 | 0.95-28.5 |
| Enterobacter species | 0.15-5.0 | 2.45-245 | 0.05-1.5 | 0.95-28.5 |
| Haemophilus influenzae | 0.15-1.5 | 2.85-95 | 0.015-0.15 | 0.285-2.85 |
| Bacteria | TMP Alone | SMX Alone | TMP/SMX(1:19) | |
| TMP | SMX | |||
| Streptococcus pneumoniae | 0.15-1.5 | 7.35-24.5 | 0.05-0.15 | 0.95-2.85 |
| Shigella flexneri* | < 0.01-0.04 | < 0.16- > 320 | O.002-0.03 | 0.04-0.625 |
| Shigella sonnei* | 0.02-0.08 | 0.625- > 320 | 0.004-0.06 | 0.08-1.25 |
| TMP=trimethoprim SMX=sulfamethoxazole *Rudoy RC, Nelson JD, Haltalin KC. Antimicrobial Agents and Chemotherapy. 1974;5:439-443. |
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Susceptibility Testing
The recommended quantitative disc susceptibility method may be used for estimating the susceptibility of bacteria to SEPTRA.4,5 With this procedure, a report from the laboratory of "Susceptible to trimethoprim and sulfamethoxazole" indicates that the infection is likely to respond to therapy with SEPTRA. If the infection is confined to the urine, a report of "Intermediate susceptibility to trimethoprim and sulfamethoxazole" also indicates that the infection is likely to respond. A report of "Resistant to trimethoprim and sulfamethoxazole" indicates that the infection is unlikely to respond to therapy with SEPTRA.
REFERENCES
1. Kremers P, Duvivier J, Heusghem C. Pharmacokinetic studies of co-trimoxazole in man after single and repeated doses. J Clin Pharmacol. 1974;14:112-117.
2. Kaplan SA, Weinfeld RE, Abruzzo CW, McFaden K, Jack ML, Weissman L. Pharmacokinetic profile of trimethoprim- sulfamethoxazole in man. J Infect Dis. 1973;128(suppl):S547-S555.
3. Varoqaux O, et al. Pharmacokinetics of the trimethoprimsulfamethoxazole combination in the elderly. Br J Clin Pharmacol. 1985; 20: 575-581.
4. Antibiotic susceptibility discs; certification procedure. Federal Register. 1972;37:20527-20529.
5. Bauer AW, Kirby WMM, Sherris JC, Turck M. Antibiotic susceptibility testing by standardized single disk method. Am J Clin Pathol. 1966;45:493-496.
6. Brumfitt W, Pursell R. Trimethoprim-sulfamethoxazole in the treatment of bacteriuria in women. J Infect Dis. 1973;128 (suppl):S657-S663.
7. Marinella MA. Trimethoprim - induced hyperkalemia: An analysis of reported cases. Gerontology 45: 209-212, 1999.
Generic Name: Trimethoprim and Sulfamethoxazole
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