FDA mesh warning

July 15, 2011

THE US Food and Drug Administration has warned that that surgical placement of mesh through the vagina to repair pelvic organ prolapse (POP) may expose patients to greater risk than other surgical options. In 2008 the FDA issued a warning about adverse events related to mesh placement, however since then it has seen the number of adverse events increase fivefold. The most common side effects include protruding of tissue, pain, infection and bleeding. As such, the FDA has asked health care providers to recognise, that in most cases POP can be treated successfully without surgery, and that patients continue with routine check-ups and followup care after surgery.

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Pharmacy Daily | FDA mesh warning

FDA mesh warning

Other recent headlines

IPE Colloquium focus on trust

Overwork linked with HC worker brain changes

Designer Brands branches into premium skincare products

SEARCH PHARMACY DAILY

Featured video

Recent issues

INDUSTRY JOB VACANCIES