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AUREOMYCIN IN GRANULOMA INGUINALE

LYNDON M. HILL, M.D.; LOUIS T. WRIGHT, M.D.; AARON PRIGOT, M.D.; MYRA A. LOGAN, M.D.

JAMA. 1949;141(15):1047-1050. doi:10.1001/jama.1949.02910150013005.

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Duggar¹ and associates of the Lederle Laboratories Division, American Cyanamid Company, introduced aureomycin, a new and versatile antibiotic which is derived from a strain of streptomyces. It has shown a wide range of activity against many infections, and the literature is beginning to contain many reports of the different diseases in human beings against which it is useful.

It was first employed in the treatment of human beings while we were carrying on a study of lymphogranuloma venereum² which was started in January 1948. During that study it occurred to one of us (L. T. W.) that it might be effective in the treatment of granuloma inguinale, and it was accordingly used in 3 cases which were described in our previous report.³ We were both surprised and pleased over the rapid and favorable results obtained with amazingly small doses of the drug, and we decided to continue

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Country-Specific Mortality and Growth Failure in Infancy and Yound Children and Association With Material Stature

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HILL LM, WRIGHT LT, PRIGOT A, LOGAN MA. AUREOMYCIN IN GRANULOMA INGUINALE. JAMA. 1949;141(15):1047-1050. doi:10.1001/jama.1949.02910150013005.

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