"The U.S. Food and Drug Administration today expanded the approved use of Xgeva (denosumab) to treat adults and some adolescents with giant cell tumor of the bone (GCTB), a rare and usually non-cancerous tumor.
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- Clinician Information:
Survanta Patient Information including How Should I Take
In this Article
- What is beractant (Survanta)?
- What are the possible side effects of beractant (Survanta)?
- What is the most important information I should know about beractant (Survanta)?
- What should I discuss with my health care provider before my child receives beractant (Survanta)?
- How is beractant given (Survanta)?
- What happens if my child misses a dose (Survanta)?
- What happens if my child receives an overdose (Survanta)?
- What should be avoided after my child receives beractant (Survanta)?
- What other drugs will affect beractant (Survanta)?
- Where can I get more information?
What should I discuss with my health care provider before my child receives beractant (Survanta)?
Your child will require special care in the hospital during treatment for RDS. Talk with your doctor about any special instructions for handling the infant and watching for side effects while beractant is given.
How is beractant given (Survanta)?
Beractant is given within minutes or hours after the infant is born. The medication must be given in a neonatal intensive care unit (NICU), a specialized setting for premature babies or newborns who need special care.
This medication is given through an endotracheal (en-doe-TRAY-kee-al) tube. This is a flexible plastic tube placed in the infant's mouth and passed down into the airway. A doctor will insert the tube using a scope to see the inside of the airway while guiding the tube into place.
Beractant is usually given every 6 hours.
To make sure this medication is helping your child's condition and is not causing any harmful effects, your child's lung function will need to be tested often. This will help your doctor determine how long to continue treatment with beractant. Your child may also need blood tests.
Additional Survanta Information
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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