"The U.S. Food and Drug Administration today approved a new use for Jakafi (ruxolitinib) to treat patients with polycythemia vera, a chronic type of bone marrow disease. Jakafi is the first drug approved by the FDA for this condition.
The use of Voluven® (hydroxyethyl starch in sodium chloride injection) is contraindicated in the following conditions:
- known hypersensitivity to hydroxyethyl starch [see General WARNINGS and PRECAUTIONS]
- fluid overload (hyperhydration) and especially in cases of pulmonary edema and congestive heart failure
- renal failure with oliguria or anuria not related to hypovolemia
- patients receiving dialysis treatment
- severe hypernatremia or severe hyperchloremia
- intracranial bleeding.
3) Lochbühler H, Galli C, Hagemann H. Hydroxyethyl starch HES 130/0.4 in paediatric surgery: results of an explorative, controlled, multicenter safety study. Crit Care 2003; 7 (Suppl 1):, P107This monograph has been modified to include the generic and brand name in many instances.
Last reviewed on RxList: 2/1/2008
Additional Voluven 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.
Find out what women really need.