July 6, 2015
Recommended Topic Related To:

Zymaxid

"The U.S. Food and Drug Administration today approved the Argus II Retinal Prosthesis System, the first implanted device to treat adult patients with advanced retinitis pigmentosa (RP). The device, which includes a small video camera, transmitter "...

Zymaxid

PATIENT INFORMATION

Avoiding Contamination Of The Product

Patients should be instructed to avoid contaminating the applicator tip with material from the eye, fingers, or other source.

Avoidance Of Contact Lens Wear

Patients should be advised not to wear contact lenses if they have signs and symptoms of bacterial conjunctivitis.

Last reviewed on RxList: 6/4/2015
This monograph has been modified to include the generic and brand name in many instances.

Report Problems to the Food and Drug Administration

 

You are encouraged to report negative side effects of prescription drugs to the FDA. Visit the FDA MedWatch website or call 1-800-FDA-1088.


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