T.Mazzei, A.Novelli pdf - Sipps

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Oxacillin Dose/response relationship for brand and generic drugs in a model of thigh infection in neutropenic mice Gauzit R & Lakdhari M, Med Mal Infect. 2012; Moet GJ et al., Diagn Microbiol Infect Dis, 2009
Generic vancomycin products fail in vivo despite being pharmaceutical equivalents of the innovator Omar Vesga, Maria Agudelo, Beatriz E. Salazar, Carlos A. Rodriguez, and Andres F. Zuluaga Except for one product exhibiting slightly greater concentration, vancomycin generics were undistinguishable from the innovator based on concentration and potency, protein binding, in vitro antibacterial effect determined by minimal inhibitory or bactericidal concentrations and serum pharmacokinetics. Antimicrobial Agents and Chemotherapy, 2010, Vol. 54, No. 8, p. 3271–3279
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Page 3 and 4: FARMACO GENERICO / EQUIVALENTE •
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Page 7 and 8: Concentration Pharmacokinetic of ch
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Page 15 and 16: Canada France Germany Italy Japan S
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Page 20 and 21: Mean amoxicillin concentration-time
Page 22 and 23: Generic versus non-generic formulat
Page 24 and 25: Antibiotici generici / equivalenti
Page 26 and 27: Tetracycline Average plasma levels
Page 28 and 29: Vancomycin 500 mg Susceptibility pr
Page 30 and 31: Teicoplanin (400mgx2 day1, 400mg/di
Page 32 and 33: Piperacillin/tazobactam General pro
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Page 40 and 41: Amoxicillin Dissolution behaviour o
Page 42 and 43: Amoxicillin Dissolution behaviour o
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