Imipenem/cilastatin

Imipenem/cilastatin
Combination of
Imipenem Carbapenem antibiotic
Cilastatin Dehydropeptidase inhibitor
Clinical data
MedlinePlus a605011
Pregnancy
category
  • US: C (Risk not ruled out)
Legal status
Routes of
administration		 Intravenous
Identifiers
CAS Number 92309-29-0 YesY
ATC code J01DH51
PubChem CID 11954222
ChemSpider 21106325 YesY
ChEMBL CHEMBL296854 YesY
  (verify)

Imipenem/cilastatin (marketed as Primaxin in the USA, and as Cilasafe in India) is an antibiotic useful for the treatment of a number of bacterial infections. It is a broad-spectrum beta-lactam containing equal quantities of imipenem and cilastatin.[1] It is related to the penicillin/cephalosporin family of antibiotics, but is classified as belonging to the carbapenem class.

Imipenem/cilastatin was first sold in 1987.[2] It is on the World Health Organization's List of Essential Medicines, the most important medications needed in a basic health system.[3]

Medical uses

Primaxin is indicated in lower respiratory tract infections, urinary tract infections, intra-abdominal infections, gynecologic infections, bacterial septicemia, bone and joint infections, skin and skin structure infections, endocarditis and polymicrobic infections.[1][4]

Side effects

Common side effects for both forms are:[5]

Major side effects requiring medical attention:[5]

This medicine is passed through breast milk, so its use during pregnancy or breastfeeding should only be done when clearly needed.[4] Primaxin is cleared from the body by the kidneys, so it is important to tell one's doctor about any other drugs being taken that are also cleared through the kidneys (such as other antibiotics), especially for older patients, as kidney function declines with age.[1][4]

Patients who are allergic to penicillin, cephalosporins, and related drugs may react to imipenem.[5] It is important tell one's doctor or pharmacist one's medical history, especially of brain disorders (e.g., seizures, head injury, tumor), kidney disease, liver disease, and stomach/intestinal diseases (e.g., colitis).[1]

Hepatotoxicity

In large clinical trials, imipenem was associated with transient and asymptomatic elevations in serum aminotransferase levels in about 6% of patients given the drug for five to 14 days. More serious hepatic injury from imipenem/cilastatin is rare, but jaundice and liver test abnormalities have been reported in 0.1% of patients in prospective trials of the agent. Several instances of cholestatic jaundice arising during or shortly after therapy have been reported with imipenem-cilastatin and other carbapenems. The latency to onset has been within one to three weeks, and the pattern of enzyme elevations is usually cholestatic. Immunoallergic features can occur, but autoantibodies are rare. The course is usually self-limiting, but at least one case of vanishing bile duct syndrome related to the carbapenems has been reported. Imipenem and other carbapenems have not been linked to cases of acute liver failure.

Mechanism of liver injury

The cause of the mild, transient serum enzyme elevations during imipenem-cilastatin therapy is not known. The cholestatic hepatitis attributed to imipenem-cilastatin and the carbapenems is probably immunoallergic and resembles the rare, clinically apparent liver injury that has been linked to penicillins and cephalosporins.

Outcome and management

The liver injury due to the carbapenems is usually mild and self-limited. Rarely, the carbapenems can cause a clinically apparent acute cholestatic hepatitis that is usually self-limiting and not requiring therapy or intervention. In patients with vanishing bile duct syndrome, corticosteroids are often used but have not been shown to be beneficial and are best avoided. Some patients may benefit from symptomatic therapy of the pruritus associated with cholestasis using antihistamines, ursodiol, or cholestyramine. Little information is available on possible cross-sensitivity to liver injury among the different betalactam antibiotics, but patients with clinically apparent liver injury due to imipenem should probably avoid the other carbapenems.

Interactions

Mechanism of action

Imipenem/cilastatin has the ability to kill a wide variety of bacteria. Imipenem is the active antibiotic agent and works by interfering with their ability to form cell walls, so the bacteria break up and die.

Imipenem is rapidly degraded by the renal enzyme dehydropeptidase if administered alone (making it less effective); the metabolites can cause kidney damage.[7] Imipenem is a broad-spectrum betalactam antibiotic used for severe bacterial infections caused by susceptible organisms. Because imipenem is rapidly inactivated by renal dehydropeptidase I, it is given in combination with cilastatin, a DHP-I inhibitor which increases half-life and tissue penetration of imipenem. Imipenem/cilastatin, like other carbapenems, binds to bacterial penicillin-binding proteins and interferes with bacterial cell wall integrity and synthesis. It has activity against many aerobic and anaerobic Gram-positive and Gram-negative organisms, including Staphylococcus aureus, Streptococcus pyogenes, S. agalactiae, S. viridans- group streptococci, Enterococcus faecalis, Pseudomonas aeruginosa, Escherichia coli, Proteus mirabilis, Bacteroides fragilis and Peptostreptococcus species. Imipenem/cilastatin was approved for use in the United States in 1985. Imipenem/cilastatin is indicated for the treatment of severe or complicated skin, tissue, joint, respiratory tract, intra-abdominal, urinary tract and urogenital infections, but not meningitis (as it does not pass through the blood brain barrier), endocarditis, and sepsis due to susceptible organisms. Its use is generally restricted to severe infections largely in hospitalized patients. The recommended dosage is 250 mg to 1 gram given intravenously every 6 to 8 hours or in intramuscular doses of no more than 1.5 gm daily, usually for five to 14 days. It is commercially available as Primaxin as 250-mg or 500-mg infusion bottles for IV use or 500-mg or 750-mg vials of lyophilized powder for IM injection. The most common side effects of imipenem are diarrhea, nausea, vomiting, skin rash, pruritus, and injection-site reactions.

Pharmacology

Mechanism of action

Imipenem inhibits bacterial cell-wall synthesis by binding to penicillin-binding proteins; cilastatin prevents renal metabolism of imipenem.

Absorption

Bioavailability (IM): imipenem, 60–75%; cilastatin, 95–100%

Distribution

The drug is distributed rapidly and widely to most tissues and fluids, including sputum, pleural fluid, peritoneal fluid, interstitial fluid, bile, aqueous humor, reproductive organs, and bone; highest concentrations occur in pleural fluid, interstitial fluid, peritoneal fluid, and reproductive organs; low concentrations occur in CSF; it crosses the placenta, and enters breast milk

Protein binding

Imipenem, 13–21%; cilastatin, 40%

Metabolism

Imipenem is metabolized in the kidney by dehydropeptidase 1; activity is blocked by cilastatin.

Elimination

Half-life (both drugs): 60 min; prolonged with renal impairment Excretion (both drugs): Urine (~70% as unchanged drug)

Availability and description

Primaxin IV is a combination of imipenem, cilastatin sodium, and sodium bicarbonate which is added as a buffer.[1] Primaxin IM lacks the sodium bicarbonate buffer.[4]

Marketing

Imipenem/cilastatin is marketed by Merck & Co. under the trade names Primaxin, Tienam and Zienam, whereas in India it is marketed as ICL (by Zuventus Healthcare Ltd). The combination is also marketed by Ranbaxy Laboratories and Biocon in India under the brand names Cilanem and Imicelum, respectively, as well as by New Medicon Pharma under the brand name Tinaxin and by Lupin as Lupinem. It is also available under the brand name of Cilapen by Bosch Pharmaceuticals in Pakistan in 250 and 500-mg strengths, and is now the largest-selling generic in the country. It is also marketed by Highnoon Laboratories Ltd. in Pakistan under the trade name Prepenem. Prepenem was launched by Highnoon in May 2007 and was the first generic brand after the research brand Tienam.

References

  1. 1 2 3 4 5 "Primaxin I.V.". RxList. Retrieved January 25, 2013.
  2. ↑ Oxford Handbook of Infectious Diseases and Microbiology. OUP Oxford. 2009. p. 56. ISBN 9780191039621.
  3. ↑ "WHO Model List of EssentialMedicines" (PDF). World Health Organization. October 2013. Retrieved 22 April 2014.
  4. 1 2 3 4 "Primaxin IM". RxList. Retrieved January 25, 2013.
  5. 1 2 3 "Imipenem and Cilastatin Sodium Injection". Medline Plus. Retrieved January 25, 2013.
  6. 1 2 3 4 5 "Primaxin IM-Missed dose". RxList. Retrieved January 25, 2013.
  7. ↑ http://www.accessdata.fda.gov/drugsatfda_docs/label/2008/050587s065,050630s028lbl.pdf


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