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Provided 1 December 2007. Macrolide-Inducible Url to Clindamycin and the D-Test archived 2016-01-07; Loved 2012-06-16. Owls mothers' soy. Fifth ed. New Nineveh, NY: Springer; 2017.
Tidsskr Nor Laegeforen. 1972 May 30;92(15):1065-6. [Clindamycin ( Dalacin " Upjohn"). A modified lincomycin preparation]. [Article in Norwegian]. Holten E.
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EUCASTbreakpoints for Gram-positive anaerobes are listed below. these breakpoints are based on use dalacin 600 systemic infections.Streptococci - Serious respiratory tract infections; serious skin and skin structure infections; septicaemia.
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The following side effects have been reported by at least 1% of people taking this medication.Long term studies in animals have dalacin 600 been performed with clindamycin to evaluate carcinogenic potential.
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Data sources include IBM Watson Micromedex updated 10 Aug 2020 Cerner Multum updated 3 Aug 2020 Wolters Kluwer updated 10 Aug 2020 andothers.46 Clindamycin may prolong the dalacin 600 mg capsules of neuromuscular-blocking drugs, such as succinylcholine and vecuronium. Its similarity to the mechanism of action of macrolides and chloramphenicol means they should not be given simultaneously, as this causes antagonism 19 and possible cross-resistance.
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Biologically inactive clindamycin phosphate is converted to active clindamycin. By the end dalacin 600 short-term intravenous infusion, peak serum levels of active clindamycin are reached.Clindamycin has a predominately bacteriostatic action.
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Clindamycin is indicated in the dalacin 600 mg tab of serious infections caused by susceptible anaerobic bacteria. Clindamycin is also indicated in the treatment of serious infections due to susceptible strains of streptococci, pneumococci, and staphylococci.Westblom TU, Belshe RB.
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