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FDA ADVISORY PANEL RECOMMENDS USE OF MERCK'S PRINIVIL(R) FOR HEART FAILURE

 /REPEATING FROM FEB. 18/
 WEST POINT, Pa., Feb. 18 /PRNewswire/ -- An advisory committee of


the Food and Drug Administration today recommended use of Merck's (NYSE: MRK) ACE inhibitor Prinivil(R) (lisinopril) as once-daily adjunctive therapy with diuretics and digitalis for the treatment of heart failure. Since its introduction in 1987, Prinivil has been indicated for the treatment of hypertension.
 In long-term clinical trials, the use of Prinivil in patients with heart failure receiving digitalis and diuretics resulted in greater improvement in exercise capacity, left ventricular systolic performance, signs and symptoms of heart failure and quality of life when compared to placebo.
 Prinivil has been generally well tolerated in patients with heart failure. In these patients, the most frequent clinical adverse experiences are dizziness, dyspnea, chest pain, asthenia, cough, diarrhea, and hypotension.
 Merck is a worldwide, research-intensive health products company that discovers, develops, produces and markets human and animal health products and specialty chemicals.
 NOTE: The recommendation(s) of the Advisory Committee do not indicate final FDA approval.
 /delval/
 -0- 2/18/93 R
 /CONTACT: Gary M. Bruell, 215-652-7485, or, home, 215-368-7328; or Michael Seggev, 215-652-6931, or, home, 215-361-1594, both of Merck/
 (MRK)


CO: Merck & Co., Inc.; U.S. Food and Drug Administration ST: Pennsylvania IN: MTC SU:

CC -- PH016 -- 8888 02/22/93 10:46 EST
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Date:Feb 22, 1993
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