recarbrio
merck sharp & dohme b.v. - imipenem monohydrate, cilastatin sodium, relebactam monohydrate - gram-negative bacterial infections - carbapenems, antibacterials for systemic use, - recarbrio is indicated for:- treatment of hospital-acquired pneumonia (hap), including ventilator associated pneumonia (vap), in adults (see sections 4.4 and 5.1).- treatment of bacteraemia that occurs in association with, or is suspected to be associated with hap or vap, in adults.- treatment of infections due to aerobic gram-negative organisms in adults with limited treatment options (see sections 4.2, 4.4, and 5.1).consideration should be given to official guidance on the appropriate use of antibacterial agents.
recarbrio- imipenem anhydrous, cilastatin, and relebactam anhydrous injection, powder, for solution
merck sharp & dohme llc - imipenem anhydrous (unii: q20im7he75) (imipenem anhydrous - unii:q20im7he75), cilastatin (unii: 141a6amn38) (cilastatin - unii:141a6amn38), relebactam anhydrous (unii: 1oqf7tt3pf) (relebactam anhydrous - unii:1oqf7tt3pf) - recarbrio™ is indicated for the treatment of patients 18 years of age and older with hospital-acquired bacterial pneumonia and ventilator-associated bacterial pneumonia, caused by the following susceptible gram-negative microorganisms: acinetobacter calcoaceticus-baumannii complex, enterobacter cloacae , escherichia coli , haemophilus influenzae , klebsiella aerogenes, klebsiella oxytoca, klebsiella pneumoniae, pseudomonas aeruginosa, and serratia marcescens. recarbrio is indicated in patients 18 years of age and older who have limited or no alternative treatment options, for the treatment of complicated urinary tract infections (cuti), including pyelonephritis, caused by the following susceptible gram-negative microorganisms: enterobacter cloacae , escherichia coli , klebsiella aerogenes, klebsiella pneumoniae, and pseudomonas aeruginosa . approval of this indication is based on limited clinical safety and efficacy data for recarbrio [see clinical studies (14.2)] . recarbrio is indicated in patients
imipenem/cilastatine fresenius kabi 500 mg - 500 mg inf. sol. (pwdr.) i.v. vial
fresenius kabi sa-nv - cilastatin sodium 530 mg - eq. cilastatin 500 mg; imipenem monohydrate 530 mg - eq. imipenem 500 mg - powder for solution for infusion - imipenem and enzyme inhibitor
imipenem and cilastatin sodium injection powder for solution
cardinal health - imipenem (unii: 71otz9ze0a) (imipenem anhydrous - unii:q20im7he75) - imipenem anhydrous 500 mg
taro-imipenem-cilastatin powder for solution
sun pharma canada inc - imipenem; cilastatin (cilastatin sodium) - powder for solution - 250mg; 250mg - imipenem 250mg; cilastatin (cilastatin sodium) 250mg - carbapenems
taro-imipenem-cilastatin powder for solution
sun pharma canada inc - imipenem; cilastatin (cilastatin sodium) - powder for solution - 500mg; 500mg - imipenem 500mg; cilastatin (cilastatin sodium) 500mg - carbapenems
imipenem/cilastatin 250 mg/250 mg powder for solution for infusion
fresenius kabi deutschland gmbh - imipenem; cilastatin - powder for solution for infusion - 250 mg/250 milligram(s) - imipenem and enzyme inhibitor
imipenem/cilastatin 500 mg/500 mg powder for solution for infusion
fresenius kabi deutschland gmbh - imipenem; cilastatin - powder for solution for infusion - 500 mg/500 milligram(s) - imipenem and enzyme inhibitor
hovid imipenem + cilastatin for injection 250mg/250mg
hovid berhad - imipenem monohydrate; cilastatin sodium -
hovid imipenem + cilastatin for injection 500mg/500mg
hovid berhad - imipenem monohydrate; cilastatin sodium -