FDA Report: Benzocaine Sprays Associated With Methemoglobinemia

Methemoglobinemia may be associated with benzocaine sprays, according to a U.S. Food and Drug Administration report.

Advertisement

Benzocaine sprays are used to numb the mucous membranes of the mouth and throat in procedures such as transesophageal echocardiogram, endoscopy, bronchoscopy, intubation and feeding tube placements.

Methemoglobinemia is a reduction of oxygen in the blood stream, which in extreme cases can result in death. Signs of methemoglobinemia, including pale-, gray- or blue-colored skin, lips and nail beds; headache; lightheadedness; shortness of breath; fatigue; and rapid heart rate, typically occur within minutes to one or two hours of using benzocaine. 

Since the FDA issued a Public Health Advisory in 2006 about the association of methemoglobinemia with benzocaine sprays, 72 new cases of the condition have been reported. The amount of benzocaine used does not seem to affect the likeliness of contracting methemoglobinemia. 

Although labels of benzocaine sprays are not required to warn about the risk of methemoglobinemia, the FDA is continuing to evaluate their safety.

Read the FDA report on the association of methemoglobinemia with benzocaine sprays.

Read more coverage on anesthesia:

Fentanyl Effective Alternative to Anesthesia for ROP Laser Therapy

University of Michigan Research Examines Anesthetic State Transitions

ASA Responds to Study on Anesthesia Service Contract Compensation

At the Becker's 23rd Annual Spine, Orthopedic and Pain Management-Driven ASC + The Future of Spine Conference, taking place June 11-13 in Chicago, spine surgeons, orthopedic leaders and ASC executives will come together to explore minimally invasive techniques, ASC growth strategies and innovations shaping the future of outpatient spine care. Apply for complimentary registration now.

Advertisement

Next Up in Anesthesia

Advertisement

Comments are closed.