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EFSA OpenFoodTox 3.0 toxicological reference values distribution — 19748 records, 1007 ADI, 348 UL, 577 ARfD, 18608 "Other" (TDI/TWI/AI/RfD)

EFSA_OpenFoodTox_3_toxref_values_distribution

efsa 580 tok en 2026-07-20

The FLEX_SUM.ToxRefValues sheet in EFSA OpenFoodTox 3.0 (Zenodo record 19388272, DOI 10.5281/zenodo.19388272) contains 19747 data rows across 80 columns (max_row=19748 including the header row). Each row represents a toxicological reference value assigned by EFSA to a substance, derived from a specific dossier assessment. The sheet covers human health hazard characteristics only; animal health reference values (relevant for pet food formulation) are encoded separately in the dossier-level metadata.

Reference value type distribution

The dataset uses five distinct reference value schemas, each tied to a different regulatory question:

Reference ValueSchemaCountShare
ADI (Acceptable Daily Intake)chronic, consumer10075.1%
AOEL (Acceptable Operator Exposure Level)chronic, occupational6073.1%
AAOEL (Acute AOEL)acute, occupational1620.8%
ARfD (Acute Reference Dose)acute, consumer5772.9%
Other Reference Valuesflexible schema (UL/AI/TDI/TWI/AOEC/MTDI/RfD/AAOEC)1860894.2%
Total reference value instances20961106.1%

Note: total counts to 106.1% because individual substances can carry multiple reference values per row (one row may have an ADI plus an Other RefValue descriptor). The 19747 data row total is the number of substance-endpoint combinations; the 20961 reference value instances is the count of populated fields across those rows.

"Other" reference value descriptor distribution (18608 rows)

The Other schema covers 9 distinct descriptor types, with 17980 (96.6%) carrying literal value other:: and no further specification:

DescriptorCountMeaning
other:: (descriptor not specified)1798096.6% of Other rows
UL (Tolerable Upper Intake Level)348upper intake limit for nutrients/vitamins
AI (Adequate Intake)164intake level assumed adequate for groups
TDI (Tolerable Daily Intake)74non-carcinogenic chronic intake limit
TWI (Tolerable Weekly Intake)22weekly intake limit (e.g. heavy metals)
AOEC (Acceptable Operator Exposure Concentration)10air concentration limit for workers
MTDI (Maximum TDI)4group TDI across multiple sources
RfD (Reference Dose, US-EPA-style)4EPA-derived chronic reference
AAOEC (Acute AOEC)2acute air concentration limit

Data quality flag: 17980 of 18608 "Other" rows (96.6%) carry the literal other:: descriptor. EFSA populated the record but did not specify which reference value type applies. This is a major data gap — the bulk of the 19748-row dataset has un-classified reference value semantics. Cross-referencing back to the parent dossier (Document UUIDParent UUIDDOSSIER.Domain.FoodDomain) would be required to recover the actual reference type.

ADI unit distribution (1007 records)

UnitCountShare
mg/kg bw/day96295.5%
mg/kg bw232.3%
µg/kg bw/day151.5%
mg/person/day60.6%
g/person/day10.1%

The dominant unit mg/kg bw/day (milligrams per kilogram body weight per day) is the standard EFSA ADI unit for chronic consumer exposure assessment. The single g/person/day row is unusual — likely a macronutrient (energy/sugar/fat allowance) rather than a chemical hazard threshold.

ADI numerical range

Across 1007 numeric ADI values: minimum 5e-05 mg/kg bw/day (highly potent substance, possibly a mycotoxin or pesticide), maximum 600.0 mg/kg bw/day (a low-toxicity substance, possibly an essential nutrient such as a vitamin C or amino acid). The range spans more than 7 orders of magnitude, reflecting the diversity of substances EFSA evaluates.

ADI Population (intended consumer group)

PopulationCount
consumers (general)1218
adults3
infants3
toddlers1
children1

1218 of 1226 ADI Population records (99.3%) target "consumers" — the general population including infants, children, and adults. Sub-population-specific ADIs (infants only, toddlers only) are rare (7 records total, 0.6%) and used for substances with heightened sensitivity in early-life stages (e.g. nitrates, lead).

Pet food relevance

EFSA's toxicological reference values in this sheet are calibrated for human consumers, not pets. Pet food formulation uses a different derivation path:

  • NOAEL × UF (uncertainty factor) = reference value for target

species. EFSA publishes NOAELs in dossier-level records but the derived pet-specific reference values are not in this dataset.

  • Maximum residue limits / transfer factors for veterinary drug

residues crossing from livestock feed to pet food (rare) are sourced separately under Reg 470/2009.

The 1007 ADI values are nonetheless relevant to pet food safety in two scenarios:

  1. Carry-over contamination — when a feed additive or

contaminant is regulated for humans, the same value is often applied as a default safety threshold for pets.

  1. Cross-validation — pet-specific NOAELs can be compared

against human ADIs to flag substances where the safety margin is unexpectedly tight (e.g. where the human ADI × species conversion factor leaves <10× safety margin for the pet).

Source: toxicology/efsa/OFT3.0_export_repository.xlsx, sheet FLEX_SUM.ToxRefValues (19748 rows × 80 cols). Pet-specific reference value derivation requires parent-dossier join and substance-level NOAEL extraction.

Sources

  • OFT3.0_export_repository.xlsx