"By Megan Brooks
Medscape Medical News
The US Food and Drug Administration (FDA) will require makers of prescription testosterone products to clarify the approved uses of these medications on the product label and add information"...
Patients receiving activated DEFINITY® should be instructed to inform their healthcare provider if they:
- have a congenital heart defect, or recent worsening of heart or lung conditions [see CONTRAINDICATIONS and WARNINGS AND PRECAUTION],
- have had prior reactions to DEFINITY® [see CONTRAINDICATIONS],
- may be pregnant, are trying to become pregnant, or are nursing [see Use In Specific Populations].
Last reviewed on RxList: 11/4/2011
This monograph has been modified to include the generic and brand name in many instances.
Additional Definity 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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