"The European Medicines Agency (EMA) Committee for Medicinal Products for Human Use (CHMP) has recommended approval of dalbavancin 500 mg (Xydalba, Durata Therapeutics) for acute bacterial skin and skin structure infections (ABSSSI) in ad"...
There are no documented reports of serious toxicity in humans resulting from acute ingestion of Selseb. However, acute toxicity studies in animals suggest that ingestion of large amounts could result in potential human toxicity. Evacuation of the stomach contents should be considered in cases of acute oral ingestion.
Contraindicated in persons with known or suspected hypersensitivity to any of the listed ingredients.
Last reviewed on RxList: 9/27/2011
This monograph has been modified to include the generic and brand name in many instances.
Additional Selseb Information
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