2001
DOI: 10.1006/rtph.2001.1460
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Postmarketing Surveillance of New Food Ingredients: Results from the Program with the Fat Replacer Olestra

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Cited by 17 publications
(10 citation statements)
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“…[25][26][27] The first attempt at such monitoring (for phytosterol enriched foods) found that people who buy the product eat less than was anticipated and that no serious adverse effects have been reported to manufacturers' consumer care lines. 19 27 Data were gathered at the household level only, however, so users were not characterised and it was not possible specifically to estimate exposure.…”
Section: Discussionmentioning
confidence: 99%
“…[25][26][27] The first attempt at such monitoring (for phytosterol enriched foods) found that people who buy the product eat less than was anticipated and that no serious adverse effects have been reported to manufacturers' consumer care lines. 19 27 Data were gathered at the household level only, however, so users were not characterised and it was not possible specifically to estimate exposure.…”
Section: Discussionmentioning
confidence: 99%
“…PMM is currently not an obligatory requirement for all new foods, but in the past legislative authorities have requested PMM programs as part of the approval of certain new food ingredients (Van Puijenbroek et al, 2007). For example, the US Food and Drug Administration (FDA) demanded a post-market monitoring program after the introduction of Aspartame (artificial sweetener) and the fat substitute Olestra (Allgood et al, 2001). The European Commission called for PMM after the introduction of a cholesterol lowering vegetable oil spread (Amanor-Boadu, 2004).…”
Section: Developing Satiety Enhancing Food Productsmentioning
confidence: 99%
“…A number of studies have proposed methods for the Post-Market Monitoring of novel foods (Butchko et all 1994, Allgood et al 2001, Simojoki et al 2005, Welch et al 2011and Willems et al 2013. Below the methodologies have been split by those for intake assessments and those for causality assessment of adverse events for reporting.…”
Section: Monitoring Of Novel Foodsmentioning
confidence: 99%
“…This could include information on: patient demographics, levels of consumption, the severity and duration of the reaction and if medical assistance e.g. a hospital visit was required (Hepburn et al 2006, Allgood et al 2001and Wal et al 2003. Once the information on the adverse event had been gathered, the data could be sent for internal and external review, by trained medical professionals e.g.…”
mentioning
confidence: 99%