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• W1979803702 abstract "I write to correct factual errors in the correspondence of Eric Brunner and Erik Millstone (July 3, p 71)1Brunner E Millstone E Health risks of genetically modified foods..Lancet. 1999; 354: 71Summary Full Text Full Text PDF PubMed Scopus (3) Google Scholar regarding trial data on Monsanto's recombinant bovine somatotropin. They state “official regulatory authorities accepted the manufacturer's unpublished analysis”. In both the European Union and the USA, regulatory authorities did their own analysis of the mastitis data from Monsanto research trials in addition to the analyses by Monsanto Company. These analyses were in agreement and are a matter of public record.2Committee for Veterinary Medicinal Products. Final scientific report of the Committee for Veterinary Medicinal Products on the application for marketing authorization submitted by the Monsanto companyfor SOMATECH. 37th meeting of CVMP. Jan 27, 1993. Brussels, Belgium: CVMP, 1993.Google Scholar, 3US Food and Drug Administration's Freedom of Information Summary. POSILAC (sterile sometribove zinc suspension) for increasing milk production in lactating dairy cows. The Agricultural Group of Monsanto Company. FDA Ctr Vet Med, Rockville, MDMay 29 1996Google Scholar They further state, “We previously identified the shortcomings in this analysis, and did our own, but were unable to publish it because the company concerned withheld consent. Here the peer-review process was compromised”. In fact, the peer-review process revealed that Brunner and Millstone were attempting to publish results from trials they did not conduct. These results were fully published in the peer-review journal, Dairy Sdence by the scientists who actually did the trials.4White TC Madsen KS Hintz RL et al.Clinical mastitis in cows treated with Sometribove (recombinant bovine somatotropin) and its relationship to milk yield..J Dairy Scr. 1994; 77: 2249-2260Summary Full Text PDF PubMed Scopus (27) Google Scholar After approval of bovine somatotropin in the USA, a postapproval monitoring programme assessed mastitis incidence in the US dairy industry through three separate approaches, including adverse experience reports, incidence of discarded milk due to antibiotic contamination, and actual mastitis incidence in commercial dairy herds. The results from these studies were presented in two public hearings chaired by the Centre for Veterinary Medicine Advisory Committee. The results showed that mastitis incidence in herds treated with bovine somatotropin was easily made manageable and did not pose a risk to human health. The bottom line is that the incidence of mastitis in herds treated with bovine somatotropin has been evaluated in many peer-reviewed publications, by independent regulatory authorities, and in public hearings. The claim by Brunner and Millstone that “the peer-review process was compromised” simply has no merit." @default.
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• W1979803702 date "1999-08-01" @default.
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• W1979803702 title "Debate continues on recombinant bovine somatotropin" @default.
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• W1979803702 doi "https://doi.org/10.1016/s0140-6736(05)77667-4" @default.
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