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Dietary Supplement Analysis (NIH data)

products_fda_reports

Read-only

FDA recalls and adverse event reports (CAERS) for one supplement, from openFDA. Give a product name, barcode, DSLD ID, or brand and name. Recalls are listed only when they carry the barcode or the brand and every product-name word; adverse event reports are counted with their most common reactions. Reports do not show that a product caused an event.

Input Schema

TableJSON Schema
NameRequiredDescriptionDefault
upcNoUPC-A or EAN barcode digits as printed on the bottle, e.g. "031604026974" (spaces and dashes are ignored)
nameNoProduct name as printed, used with "brand" when the product is not in DSLD
brandNoBrand (with "name", or to narrow "query")
queryNoProduct as the user named it; resolved to a DSLD label
dsld_idNoDSLD label ID, e.g. from /v1/products/search

Schema Changelog

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