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ISTA Pharmaceuticals Receives FDA Approval for BROMDAY™
Date:10/16/2010

UTIONS

  • Sulfite Allergic Reactions
  • Slow or Delayed Healing
  • Potential for cross-sensitivity
  • Increased bleeding of ocular tissues
  • Corneal effects including keratitis
  • Contact Lens Wear

ADVERSE REACTIONS

The most commonly reported adverse reactions in 2-7% of patients were abnormal sensation in the eye, conjunctival hyperemia and eye irritation (including burning/stinging).  

Full prescribing information will be available soon on ISTA Pharmaceuticals' website at http://www.istavision.com.

ABOUT ISTA PHARMACEUTICALS

ISTA Pharmaceuticals, Inc. is the fourth largest and fastest growing branded prescription eye care business in the United States, with an expanding focus on allergy therapeutics. ISTA currently markets five products, including treatments for ocular inflammation and pain associated with cataract surgery, glaucoma, and ocular itching associated with allergic conjunctivitis. The Company's development pipeline contains additional candidates in various stages of development to treat dry eye, ocular inflammation and pain, and nasal allergies. Headquartered in Irvine, California, the Company generated 2009 revenues of $111 million. For additional information about ISTA Pharmaceuticals, please visit the corporate website at www.istavision.com.

FORWARD-LOOKING STATEMENTS

Any statements contained in this press release that refer to future events or other non-historical matters are forward-looking statements.  Without limiting the foregoing, but by way of example, statements contained in this press release related to the expected launch of BROMDAY in 2010, ISTA's anticipated devotion of resources toward the marketing of BROMDAY and BEPREVE, ISTA's intention to discontinue marketing and selling Xibrom in 2011, the potential
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SOURCE ISTA Pharmaceuticals, Inc.
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