Imipenem/Cilastatin Fresenius Kabi

Imipenem/Cilastatin Fresenius Kabi Uses, Dosage, Side Effects, Food Interaction and all others data.

Imipenem/Cilastatin Fresenius Kabi is an inhibitor of renal dehydropeptidase, an enzyme responsible for both the metabolism of thienamycin beta-lactam antibiotics as well as conversion of leukotriene D4 to leukotriene E4. Since the antibiotic, imipenem, is one such antibiotic that is hydrolyzed by dehydropeptidase, cilastatin is used in combination with imipenem to prevent its metabolism. The first combination product containing both drugs was approved by the FDA in November of 1985 under the trade name Primaxin, marketed by Merck & Co. A newer triple-drug product was approved in July 2019 under the trade name Recarbrio which also contains relebactam.

Imipenem/Cilastatin Fresenius Kabi is a chemical compound which inhibits the human enzyme dehydropeptidase. Renal Dehydropeptidase degrades the antibiotic imipenem. Imipenem/Cilastatin Fresenius Kabi is therefore combined intravenously with imipenem in order to protect it from dehydropeptidase and prolong its antibacterial effect. However, cilastatin in and of itself does not have any antibacterial activity. The increased renal excretion of unchanged imipenem appears to prevent proximal tubular necrosis associated with high doses of imipenem.

Trade Name Imipenem/Cilastatin Fresenius Kabi
Generic Cilastatin
Cilastatin Other Names Cilastatin, Cilastatina, Cilastatine, Cilastatinum
Type
Formula C16H26N2O5S
Weight Average: 358.453
Monoisotopic: 358.156242642
Protein binding

Cilastatin is plasma protein binding is reported to be 35-40%.

Groups Approved, Investigational
Therapeutic Class
Manufacturer
Available Country Hungary, Sweden
Last Updated: September 19, 2023 at 7:00 am
Imipenem/Cilastatin Fresenius Kabi
Imipenem/Cilastatin Fresenius Kabi

Uses

Imipenem/Cilastatin Fresenius Kabi is a renal dehydropeptidase inhibitor used to prevent degradation of imipenem. Both medications are used together to treat a variety of infections.

Imipenem/Cilastatin Fresenius Kabi is indicated, in combination with imipenem with or without relebactam, for the treatment of bacterial infections including respiratory, skin, bone, gynecologic, urinary tract, and intra-abdominal as well as septicemia and endocarditis.

Imipenem/Cilastatin Fresenius Kabi is also used to associated treatment for these conditions: Bloodstream Infections, Bone and Joint Infections, Complicated Intra-Abdominal Infections, Complicated Urinary Tract Infection, Endocarditis caused by staphylococcus aureus, Gynaecological infection, Intra-Abdominal Infections, Lower respiratory tract infection bacterial, Neutropenic Fever, Pyelonephritis, Skin and Subcutaneous Tissue Bacterial Infections, Surgical Site Infections, Uncomplicated Urinary Tract Infections, Hepatic abscess

How Imipenem/Cilastatin Fresenius Kabi works

Imipenem/Cilastatin Fresenius Kabi is a renal dehydropeptidase-I inhibitor. Since the antibiotic, imipenem, is hydrolyzed by dehydropeptidase-I, which resides in the brush border of the renal tubule, cilastatin is administered with imipenem to block the metabolism of imipenem.

Toxicity

In case of overdose with the combination product, including relebactam and imipenem, it is recommended to provide supportive care. Imipenem, cilastatin, and relebactam may be removed via hemodialysis.

Food Interaction

No interactions found.

Volume of Distribution

Imipenem/Cilastatin Fresenius Kabi has a volume of distribution of 14.6-20.1L.

Half Life

The half-life of cilastatin is approximately 1h.

Clearance

Imipenem/Cilastatin Fresenius Kabi has a total clearance of 0.2 L/h/kg and a renal clearance of 0.10-0.16 L/h/kg.

Elimination Route

Imipenem/Cilastatin Fresenius Kabi is reported by official FDA labeling to be 70% excreted in the urine, however published literature has reported values as high as 98%.

Innovators Monograph

You find simplified version here Imipenem/Cilastatin Fresenius Kabi

*** Taking medicines without doctor's advice can cause long-term problems.
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