TABLE 1.
Drug(s) | Projected daily dosage (g)a | Maximum concn tested (g/liter)b | pHc |
---|---|---|---|
Aztreonam | 8 | 100* | 4.8 |
Piperacillin | 16 | 128* | 5.7 |
Piperacillin + tazobactam | 16 | 128* | 6.2 |
Azlocillin | 20 | 128* | 7.3 |
Mezlocillin | 20 | 128* | 5.7 |
Ceftazidime | 6 | 120 | 7.4 |
Cefepime | 6 | 50 | 4.5 |
Cefpirome | 4 | 32 | 7.3 |
Imipenem + cilastatin | 4 | 8 | 7.8 |
Meropenem | 6 | 64* | 8.2 |
Faropenem | 64 | 6.8 |
That is, the highest recommended dosage for severe, life-threatening infection and/or cystic fibrosis, based on the official registration information (Belgian package inserts for all, except for imipenem [U.S. package insert data]); for faropenem, for which no pertinent registration data are available, the values of meropenem were used.
Corresponding to the maximum daily dose in a volume of 48 ml (used for intensive care patients) for ceftazidime. For all other drugs, lower concentrations had to be used for the reasons indicated. Symbols: *, higher concentrations caused unacceptable viscosity; , higher concentrations caused a marked change of color after a few hours at 37°C; , limit of solubility (precipitation observed at >10 g/liter).
Value observed after dissolution of the product (supplied as for hospital-based usage, except for azlocillin, mezlocillin, and faropenem) at the concentration indicated without adjustment.