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J A Settepani

Publications and source records attributed to J A Settepani.

8 recordsLinked to original sources

The hazard of using chloramphenicol in food animals.

To summarize, concern has developed over the extra-label use of chloramphenicol in food-producing animals because a type of blood dyscrasia that is usually fatal to a significant subgroup of the population with an apparent predisposed sensitivity to chloramphenicol has been associated with extremely low levels of exposure to the drug. In a monitoring program, using a method of analysis that is limited as to the type of residues it can detect, USDA has found 4 to 8 animals a year that were slaughtered for use as human food that contained residue levels of chloramphenicol that approach or exceed those concentrations associated in a causal relationship with aplastic anemia in man. Given the preponderance of evidence presented above, the FDA must consider--under its mandate to protect the human health by assuring safe and effective veterinary drugs--a course of action that will preclude the availability and the use of chloramphenicol in food animals.

Anemia, Aplastic↗

Lumi-mestranol and epi-lumi-mestranol.

Treatment of lumi-estrone 3-methyl ether (I) with acetylene gave the C-17-epimeric compounds lumi-mestranol (3-methoxy-17 alpha-ethynyl-13 alpha-estra-1,3,5(10)-trien-17 beta-ol, III ) and epi-lumi-mestranol (3-methoxy-17 beta-ethynyl-13 alpha-estra-1,3,5(10)-trien-17 alpha-ol, IV). The structures of the two isomers were assigned on the basis of their molecular rotations and shift-reagent experiments in the NMR. The irradiation of estrone 3-methyl ether (II) to provide compound I was investigated in two solvent systems. Minor products of these reactions were the seco-steroids VII, VIII and X.

Acetylene↗