Relebactam

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Relebactam is a beta-lactamase inhibitor used in combination with antibiotics to treat certain bacterial infections. It is specifically designed to inhibit the action of beta-lactamase enzymes produced by bacteria, which can degrade beta-lactam antibiotics and render them ineffective.

Mechanism of Action[edit | edit source]

Relebactam works by binding to the active site of beta-lactamase enzymes, thereby preventing these enzymes from breaking down beta-lactam antibiotics. This inhibition allows the antibiotics to retain their antibacterial activity and effectively kill or inhibit the growth of bacteria.

Clinical Use[edit | edit source]

Relebactam is commonly used in combination with imipenem, a broad-spectrum beta-lactam antibiotic. The combination of relebactam and imipenem is marketed under the brand name Recarbrio. This combination is used to treat complicated urinary tract infections (cUTIs), complicated intra-abdominal infections (cIAIs), and hospital-acquired bacterial pneumonia (HABP) and ventilator-associated bacterial pneumonia (VABP).

Pharmacokinetics[edit | edit source]

Relebactam is administered intravenously and has a half-life that allows for dosing every six hours when combined with imipenem. It is primarily excreted unchanged in the urine.

Side Effects[edit | edit source]

Common side effects of relebactam, when used in combination with imipenem, include nausea, diarrhea, headache, and infusion site reactions. Serious side effects may include allergic reactions and seizures, particularly in patients with a history of central nervous system disorders.

Development and Approval[edit | edit source]

Relebactam was developed by Merck & Co. and received approval from the United States Food and Drug Administration (FDA) in 2019 for use in combination with imipenem.

See Also[edit | edit source]

References[edit | edit source]

External Links[edit | edit source]


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Contributors: Prab R. Tumpati, MD