US. FDA approves Zerbaxa to treat pneumonia

US. FDA approves Zerbaxa to treat pneumonia

The U.S. Food and Drug Administration has approved expanded use of Merck & Co Inc’s antibiotic to treat hospital-acquired pneumonia in patients 18 years and older.

The approval is based on the late-stage trial results of Merck’s drug Zerbaxa, which showed to be as effective as another antibacterial drug meropenem. Meropenem is a broad-spectrum antibacterial agent and is also prescribed for treating nosocomial pneumonia (hospital-acquired pneumonia).

Hospital-acquired pneumonia (HAP) occurs in patients at least two to three days after being admitted or in those who are on mechanical breathing machines and have life-threatening lung infections with high mortality rates.

These infections are typically treated using antibiotics, but the growing problem of antibiotic resistance has rendered some of the most commonly prescribed treatments ineffective.

Zerbaxa, which was previously approved for treating complicated urinary tract infections and intra-abdominal infections, was added to Merck’s drug portfolio through its buyout of antibiotics maker Cubist Pharmaceuticals.

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