Carbapenems (eg, imipenem, meropenem) and the monobactam antibiotic aztreonam are generally reserved for serious infections caused by. Meropenem – Download as PDF File .pdf), Text File .txt) or read online. antibiotik Meropenem. Copyright: © All Rights Reserved. Download as PDF, TXT or. , Meropenem45, MEM, 10 mcg, 10/SP. , Metronidazole78, MET, 80 mcg, 10/SP. , Mezlocillin46, MZ, 75 mcg, 1/EA.

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Population pharmacokinetic analysis and dosing regimen optimization of meropenem in adult patients. Notable examples of this mode of resistance include methicillin -resistant Staphylococcus aureus MRSA and penicillin-resistant Streptococcus pneumoniae. Dose to be administered every 8 hours. Complicated skin and soft tissue infections. When multiple doses are administered 8-hourly to subjects meeopenem normal renal function, accumulation of meropenem does not occur. Adults and Adolescents Infection Dose to be administered every 8 hours Severe pneumonia including hospital and ventilator-associated pneumonia.

Name of the medicinal product 2.

Infusion For intravenous infusion meropenem vials may be directly constituted with 0. It is expected that ceftazidime-avibactam will be available in the second quarter of In Europe, IV formulations are available.


This information is intended for use by health professionals. This medicinal product contains approximately 4 mEq of sodium per 1 g dose which should be taken into meropenwm by patients on a controlled sodium diet. Meronem IV mg Each vial contains meropenem trihydrate equivalent to mg anhydrous meropenem. KPC – 3 Klebsiella pneumoniae ST clone infection in postoperative abdominal surgery patients in an intensive care setting: Breast-feeding Small amounts of meropenem have been reported to be excreted in human milk.


Morrill1, 2 Jason M. Bactericidal d concentration dependent ; disrupt cell membrane permeability by charge alteration. There are limited safety data available to support the administration of a 2 g dose in adults as an meropenm bolus injection.

Meropenem – Wikipedia

Carbapenemase-producing Klebsiella pneumoniae in Brooklyn, NY: Amikacin b Bactericidal concentration dependent ; protein synthesis inhibition at 30S ribosomal subunit fCmax: Do not freeze the reconstituted solution. At this time, there are a limited selection of treatment options for CRE infections.

Meropensm data have shown that the KPC enzyme may have increased affinity for ertapenem than other carbapenems; therefore, when given together, KPC preferentially deactivates ertapenem, which hinders degradation and improves the activity of the concomitant carbapenem [ 2728 ]. To bookmark a medicine you must sign up and log in.

BNF 69 69 ed. Actual mortality rate for antibioyik of interest not included in referenced study. Line related, 22 It is interesting to note that meropenem, colistin, tigecycline combination was associated with a significant reduction in mortality, even in patients who received inappropriate empiric therapy then this combination as definitive therapy.

Successful treatment with gentamicin and colistin.

β-lactam antibiotic – Wikipedia

In a retrospective cohort study of cases of carbapenem-resistant K pneumoniae bacteriuria, meroprnem with meropenrm in vitro active aminoglycoside was associated with a significantly higher rate of microbiologic clearance compared with either polymyxin B or tigecycline [ 65 ]. Summary of the safety profile In a review of 4, patients with 5, meropenem treatment exposures, meropenem-related adverse reactions most frequently reported were diarrhoea 2. Hepatic function should be closely monitored during treatment with meropenem due to the risk of hepatic toxicity hepatic dysfunction with cholestasis and cytolysis see section 4.

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B No risk in non-human studies. Monotherapy resulted in mortality rates that were not significantly different from those in patients antibitoik with inappropriate therapy with no in vitro active agents In a study that compiled data from several studies, in 44 patients treated with carbapenem monotherapy for infections due to carbapenemase-producing K pneumoniaetreatment efficacy varied based on MIC [ 20 ].

Journal of Anaesthesiology Clinical Pharmacology.

This result may be due to delayed time to active therapy, pharmacologic limitations of available treatment options, and the fact that patients with CRE infections tend to be critically ill. Several observational studies have assessed the efficacy of combination therapy vs monotherapy in the treatment of bloodstream infections due to carbapenemase-producing K pneumoniae mostly KPC producers [ 21 — 2369 ].