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Public dataset

Recorded source agreement and disagreement

Show whether sources print one normalized reading, have incompatible units, lack structured comparison context, or contain a context-matched numeric difference.

What this does not mean: agree can mean only that sources print the same normalized reading; it is not clinical-context equivalence, independent replication, or proof. differ requires matching structured context and disjoint comparable values. not_comparable and insufficient_context are not disagreement.
Public rows
1,681
Generated
Schema version
source-consensus/2

Coverage

What this run contains

Compared medicine fields
1,681
Agree
1,282
Differ
0
Not comparable
12
Insufficient context
387
Fields represented
5
bioavailability, halfLife, proteinBinding, tMax, volumeOfDistribution

Method

How the rows were made

  1. Deterministic rules normalize recorded pharmacokinetic readings and compare only like-for-like values.
  2. One normalized printed reading may be agree even when clinical context was not extracted; this reports printed-reading agreement only.
  3. Distinct readings may differ only when their units and denominators are comparable and one matching, non-placeholder population/formulation context was structurally extracted. Otherwise they are insufficient_context.
  4. not_comparable preserves incompatible units or denominators instead of guessing. insufficient_context preserves missing or non-matching structured context instead of manufacturing agreement or disagreement.
  5. The agreement rate describes the distribution of recorded source readings; it is not a probability that a value is true.
  6. Every distinct printed reading retains its unit, population context, source count, and complete source records. The API paginates field rows, never child readings or sources.
  7. documentsExamined is every matching single-substance archive document inspected for that medicine. The generator has no document, reading, or source ceiling, so there is no hidden available-versus-retained remainder.

Limits

Read these before using a row

  • Current label parsing does not structurally extract population or formulation context. Distinct otherwise-comparable readings are therefore insufficient_context, never differ; agree may mean printed-reading agreement only. Source records are complete but are not independent-experiment counts.
  • The current deterministic parser does not structurally extract population or formulation context from these sentences. It records that context as unknown and cannot publish distinct same-unit readings as differ.
  • Neither reading is marked wrong. Population, formulation, route, and other unextracted context may explain the printed difference.
  • Only the recorded fields and source documents in this snapshot are compared.
  • A source count is the number of retained source records in the row, not a count of independent experiments.

Provenance

Source examples

abacavir · bioavailability · agree

15 documents examined; 83% (Unknown: population and formulation context were not structurally extracted from this source sentence.)

FDA_LABEL:5676d391-f9a4-44be-9604-954b3d8d0e2b (opens source in a new tab)
The geometric mean absolute bioavailability of the tablet was 83%.

alemtuzumab · volumeOfDistribution · not_comparable

2 documents examined; 0.18 L/kg (Unknown: population and formulation context were not structurally extracted from this source sentence.); 14.1 L (Unknown: population and formulation context were not structurally extracted from this source sentence.)

FDA_LABEL:4f5f7255-7abc-4328-bd1a-ceaf139ef3e0 (opens source in a new tab)
Distribution After the last 30 mg dose, the mean volume of distribution at steady-state was 0.18 L/kg (range 0.1 to 0.4 L/kg).

abiraterone · halfLife · insufficient_context

31 documents examined; 12 ± 5 hours (Unknown: population and formulation context were not structurally extracted from this source sentence.); 18 hours (Unknown: population and formulation context were not structurally extracted from this source sentence.)

FDA_LABEL:c9eb9b46-f847-40a8-802c-a51b40406d5a (opens source in a new tab)
Elimination In patients with metastatic CRPC, the mean terminal half-life of abiraterone in plasma (mean ± SD) is 12 ± 5 hours.

Artifact used for this view: data/source-consensus.ndjson. The reader resolves the current run first and uses the checked-in compatibility run only when a current artifact is absent.

Schema

Fields in the public projection

FieldTypeMeaning
medicineSlugstringStable RNAWiki medicine route key.
fieldstringRecorded pharmacokinetic field being compared.
comparisonStatestringagree (printed-reading agreement), differ (context-matched comparable disjoint values), not_comparable (unit/denominator mismatch), or insufficient_context. Every state remains declared even when its current count is zero.
comparisonReasonsstring[]Deterministic codes explaining the state.
documentsExaminednumberRecorded source documents considered for the field.
sourceCountnumberRecorded source readings represented.
agreementRatenumberShare represented by the leading normalized printed-reading group; not a confidence score or clinical agreement probability.
readingsconsensus-reading[]Complete, untruncated reading groups. Each keeps the printed display, numeric value when parsed, unit, population context, source count, and every source identity, version/effective date or explicit absence, retrieval date, locator, safe link, and excerpt.

Reader

Search and filter the rows

Case-insensitive text search over the public fields named for this dataset.

Exact comparability state.

Exact recorded field key.

Clear

Showing 101110 of 1,681 matching rows. Filters and search terms remain attached when you move between pages or open the API view.

  1. Projected row 101

    Medicine slug
    anidulafungin
    Compared field
    halfLife
    Comparison state
    agree
    Reason codes
    • COMPATIBLE_VALUES_OVERLAP
    Documents examined
    2
    Source count
    2
    Agreement rate
    1
    Recorded readings
    1. 40–50 hours

      Numeric value
      40
      Unit
      hours
      Source records
      2

      Population and context: Unknown: population and formulation context were not structurally extracted from this source sentence.

      Show all 2 source records
      1. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:a88d9010-55fb-4a02-baff-042cd27688ea (opens source in a new tab)

        Anidulafungin label

        Version not recorded · Effective date not recorded

        (10.8) CL [L/h] 0.84 (13.5) 0.94 (24.0) 0.78 (11.3) t 1/2 [h] 43.2 (17.7) 52.0 (11.7) 50.3 (9.7) The clearance of anidulafungin is about 1 L/h and anidulafungin has a terminal elimination half-life of 40–50 hours.
      2. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:d138ab10-1ed9-44be-8d81-49dda1e434ac (opens source in a new tab)

        Anidulafungin label

        Version not recorded · Effective date not recorded

        (10.8) CL [L/h] 0.84 (13.5) 0.94 (24.0) 0.78 (11.3) t 1/2 [h] 43.2 (17.7) 52.0 (11.7) 50.3 (9.7) The clearance of anidulafungin is about 1 L/h and anidulafungin has a terminal elimination half-life of 40–50 hours.
  2. Projected row 102

    Medicine slug
    anidulafungin
    Compared field
    volumeOfDistribution
    Comparison state
    agree
    Reason codes
    • COMPATIBLE_VALUES_OVERLAP
    Documents examined
    2
    Source count
    2
    Agreement rate
    1
    Recorded readings
    1. 30–50 L

      Numeric value
      30
      Unit
      L
      Source records
      2

      Population and context: Unknown: population and formulation context were not structurally extracted from this source sentence.

      Show all 2 source records
      1. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:a88d9010-55fb-4a02-baff-042cd27688ea (opens source in a new tab)

        Anidulafungin label

        Version not recorded · Effective date not recorded

        Distribution The pharmacokinetics of anidulafungin following IV administration are characterized by a short distribution half-life (0.5–1 hour) and a volume of distribution of 30–50 L that is similar to total body fluid volume.
      2. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:d138ab10-1ed9-44be-8d81-49dda1e434ac (opens source in a new tab)

        Anidulafungin label

        Version not recorded · Effective date not recorded

        Distribution The pharmacokinetics of anidulafungin following IV administration are characterized by a short distribution half-life (0.5–1 hour) and a volume of distribution of 30–50 L that is similar to total body fluid volume.
  3. Projected row 103

    Medicine slug
    apixaban
    Compared field
    bioavailability
    Comparison state
    agree
    Reason codes
    • COMPATIBLE_VALUES_OVERLAP
    Documents examined
    11
    Source count
    11
    Agreement rate
    1
    Recorded readings
    1. 50%

      Numeric value
      50
      Unit
      %
      Source records
      11

      Population and context: Unknown: population and formulation context were not structurally extracted from this source sentence.

      Show all 11 source records
      1. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:33a9046a-41cc-46c1-becc-2ff4d7d71538 (opens source in a new tab)

        Apixaban label

        Version not recorded · Effective date not recorded

        Absorption The absolute bioavailability of apixaban is approximately 50% for doses up to 10 mg of ELIQUIS.
      2. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:1523ab32-2c2c-6501-e063-6394a90aa0b3 (opens source in a new tab)

        Apixaban label

        Version not recorded · Effective date not recorded

        Absorption The absolute bioavailability of apixaban is approximately 50% for doses up to 10 mg of ELIQUIS.
      3. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:41a133ef-e461-48ad-8221-b735bdd0ec25 (opens source in a new tab)

        Apixaban label

        Version not recorded · Effective date not recorded

        Absorption The absolute bioavailability of apixaban is approximately 50% for doses up to 10 mg of ELIQUIS.
      4. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:396912c0-9f68-47ed-ba3f-8d9ace755a48 (opens source in a new tab)

        Apixaban label

        Version not recorded · Effective date not recorded

        Absorption The absolute bioavailability of apixaban is approximately 50% for doses up to 10 mg of apixaban tablets.
      5. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:33752f5d-2ca7-45c0-8292-b54742219b97 (opens source in a new tab)

        Apixaban label

        Version not recorded · Effective date not recorded

        Absorption The absolute bioavailability of apixaban is approximately 50% for doses up to 10 mg of ELIQUIS.
      6. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:095a08ac-cf0e-497e-a682-ddef38d6b29c (opens source in a new tab)

        Apixaban label

        Version not recorded · Effective date not recorded

        Absorption The absolute bioavailability of apixaban is approximately 50% for doses up to 10 mg of apixaban.
      7. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:19a60552-374d-4b8b-a8ce-ceae252ea5ba (opens source in a new tab)

        Apixaban label

        Version not recorded · Effective date not recorded

        Absorption The absolute bioavailability of apixaban is approximately 50% for doses up to 10 mg of apixaban.
      8. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:a454cd24-0c6d-46e8-b1e4-197388606175 (opens source in a new tab)

        Apixaban label

        Version not recorded · Effective date not recorded

        Absorption The absolute bioavailability of apixaban is approximately 50% for doses up to 10 mg of ELIQUIS.
      9. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:7be1f4c1-bb2f-4ded-ae9a-515d2a22f93e (opens source in a new tab)

        Apixaban label

        Version not recorded · Effective date not recorded

        Absorption The absolute bioavailability of apixaban is approximately 50% for doses up to 10 mg of ELIQUIS.
      10. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:2f47aa0e-0235-4220-85dd-dfcb8ad0d009 (opens source in a new tab)

        Apixaban label

        Version not recorded · Effective date not recorded

        Absorption The absolute bioavailability of apixaban is approximately 50% for doses up to 10 mg of ELIQUIS.
      11. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:fd383ae7-1e34-44ef-b8f1-ca6906dfbcef (opens source in a new tab)

        Apixaban label

        Version not recorded · Effective date not recorded

        Absorption The absolute bioavailability of apixaban is approximately 50% for doses up to 10 mg of ELIQUIS.
  4. Projected row 104

    Medicine slug
    apixaban
    Compared field
    halfLife
    Comparison state
    agree
    Reason codes
    • COMPATIBLE_VALUES_OVERLAP
    Documents examined
    11
    Source count
    11
    Agreement rate
    1
    Recorded readings
    1. 12 hours

      Numeric value
      12
      Unit
      hours
      Source records
      11

      Population and context: Unknown: population and formulation context were not structurally extracted from this source sentence.

      Show all 11 source records
      1. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:33a9046a-41cc-46c1-becc-2ff4d7d71538 (opens source in a new tab)

        Apixaban label

        Version not recorded · Effective date not recorded

        Apixaban has a total clearance of approximately 3.3 L/hour and an apparent half-life of approximately 12 hours following oral administration.
      2. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:1523ab32-2c2c-6501-e063-6394a90aa0b3 (opens source in a new tab)

        Apixaban label

        Version not recorded · Effective date not recorded

        Apixaban has a total clearance of approximately 3.3 L/hour and an apparent half-life of approximately 12 hours following oral administration.
      3. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:41a133ef-e461-48ad-8221-b735bdd0ec25 (opens source in a new tab)

        Apixaban label

        Version not recorded · Effective date not recorded

        Apixaban has a total clearance of approximately 3.3 L/hour and an apparent half-life of approximately 12 hours following oral administration.
      4. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:396912c0-9f68-47ed-ba3f-8d9ace755a48 (opens source in a new tab)

        Apixaban label

        Version not recorded · Effective date not recorded

        Apixaban has a total clearance of approximately 3.3 L/hour and an apparent half-life of approximately 12 hours following oral administration.
      5. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:33752f5d-2ca7-45c0-8292-b54742219b97 (opens source in a new tab)

        Apixaban label

        Version not recorded · Effective date not recorded

        Apixaban has a total clearance of approximately 3.3 L/hour and an apparent half-life of approximately 12 hours following oral administration.
      6. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:095a08ac-cf0e-497e-a682-ddef38d6b29c (opens source in a new tab)

        Apixaban label

        Version not recorded · Effective date not recorded

        Apixaban has a total clearance of approximately 3.3 L/hour and an apparent half-life of approximately 12 hours following oral administration.
      7. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:19a60552-374d-4b8b-a8ce-ceae252ea5ba (opens source in a new tab)

        Apixaban label

        Version not recorded · Effective date not recorded

        Apixaban has a total clearance of approximately 3.3 L/hour and an apparent half-life of approximately 12 hours following oral administration.
      8. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:a454cd24-0c6d-46e8-b1e4-197388606175 (opens source in a new tab)

        Apixaban label

        Version not recorded · Effective date not recorded

        Apixaban has a total clearance of approximately 3.3 L/hour and an apparent half-life of approximately 12 hours following oral administration.
      9. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:7be1f4c1-bb2f-4ded-ae9a-515d2a22f93e (opens source in a new tab)

        Apixaban label

        Version not recorded · Effective date not recorded

        Apixaban has a total clearance of approximately 3.3 L/hour and an apparent half-life of approximately 12 hours following oral administration.
      10. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:2f47aa0e-0235-4220-85dd-dfcb8ad0d009 (opens source in a new tab)

        Apixaban label

        Version not recorded · Effective date not recorded

        Apixaban has a total clearance of approximately 3.3 L/hour and an apparent half-life of approximately 12 hours following oral administration.
      11. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:fd383ae7-1e34-44ef-b8f1-ca6906dfbcef (opens source in a new tab)

        Apixaban label

        Version not recorded · Effective date not recorded

        Apixaban has a total clearance of approximately 3.3 L/hour and an apparent half-life of approximately 12 hours following oral administration.
  5. Projected row 105

    Medicine slug
    apixaban
    Compared field
    proteinBinding
    Comparison state
    agree
    Reason codes
    • COMPATIBLE_VALUES_OVERLAP
    Documents examined
    11
    Source count
    11
    Agreement rate
    1
    Recorded readings
    1. 87%

      Numeric value
      87
      Unit
      %
      Source records
      11

      Population and context: Unknown: population and formulation context were not structurally extracted from this source sentence.

      Show all 11 source records
      1. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:33a9046a-41cc-46c1-becc-2ff4d7d71538 (opens source in a new tab)

        Apixaban label

        Version not recorded · Effective date not recorded

        Distribution Plasma protein binding in humans is approximately 87%.
      2. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:1523ab32-2c2c-6501-e063-6394a90aa0b3 (opens source in a new tab)

        Apixaban label

        Version not recorded · Effective date not recorded

        Distribution Plasma protein binding in humans is approximately 87%.
      3. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:41a133ef-e461-48ad-8221-b735bdd0ec25 (opens source in a new tab)

        Apixaban label

        Version not recorded · Effective date not recorded

        Distribution Plasma protein binding in humans is approximately 87%.
      4. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:396912c0-9f68-47ed-ba3f-8d9ace755a48 (opens source in a new tab)

        Apixaban label

        Version not recorded · Effective date not recorded

        Distribution Plasma protein binding in humans is approximately 87%.
      5. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:33752f5d-2ca7-45c0-8292-b54742219b97 (opens source in a new tab)

        Apixaban label

        Version not recorded · Effective date not recorded

        Distribution Plasma protein binding in humans is approximately 87%.
      6. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:095a08ac-cf0e-497e-a682-ddef38d6b29c (opens source in a new tab)

        Apixaban label

        Version not recorded · Effective date not recorded

        Distribution Plasma protein binding in humans is approximately 87%.
      7. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:19a60552-374d-4b8b-a8ce-ceae252ea5ba (opens source in a new tab)

        Apixaban label

        Version not recorded · Effective date not recorded

        Distribution Plasma protein binding in humans is approximately 87%.
      8. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:a454cd24-0c6d-46e8-b1e4-197388606175 (opens source in a new tab)

        Apixaban label

        Version not recorded · Effective date not recorded

        Distribution Plasma protein binding in humans is approximately 87%.
      9. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:7be1f4c1-bb2f-4ded-ae9a-515d2a22f93e (opens source in a new tab)

        Apixaban label

        Version not recorded · Effective date not recorded

        Distribution Plasma protein binding in humans is approximately 87%.
      10. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:2f47aa0e-0235-4220-85dd-dfcb8ad0d009 (opens source in a new tab)

        Apixaban label

        Version not recorded · Effective date not recorded

        Distribution Plasma protein binding in humans is approximately 87%.
      11. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:fd383ae7-1e34-44ef-b8f1-ca6906dfbcef (opens source in a new tab)

        Apixaban label

        Version not recorded · Effective date not recorded

        Distribution Plasma protein binding in humans is approximately 87%.
  6. Projected row 106

    Medicine slug
    apixaban
    Compared field
    volumeOfDistribution
    Comparison state
    agree
    Reason codes
    • COMPATIBLE_VALUES_OVERLAP
    Documents examined
    11
    Source count
    11
    Agreement rate
    1
    Recorded readings
    1. 21 liters

      Numeric value
      21
      Unit
      L
      Source records
      11

      Population and context: Unknown: population and formulation context were not structurally extracted from this source sentence.

      Show all 11 source records
      1. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:33a9046a-41cc-46c1-becc-2ff4d7d71538 (opens source in a new tab)

        Apixaban label

        Version not recorded · Effective date not recorded

        The volume of distribution (Vss) is approximately 21 liters.
      2. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:1523ab32-2c2c-6501-e063-6394a90aa0b3 (opens source in a new tab)

        Apixaban label

        Version not recorded · Effective date not recorded

        The volume of distribution (Vss) is approximately 21 liters.
      3. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:41a133ef-e461-48ad-8221-b735bdd0ec25 (opens source in a new tab)

        Apixaban label

        Version not recorded · Effective date not recorded

        The volume of distribution (Vss) is approximately 21 liters.
      4. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:396912c0-9f68-47ed-ba3f-8d9ace755a48 (opens source in a new tab)

        Apixaban label

        Version not recorded · Effective date not recorded

        The volume of distribution (Vss) is approximately 21 liters.
      5. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:33752f5d-2ca7-45c0-8292-b54742219b97 (opens source in a new tab)

        Apixaban label

        Version not recorded · Effective date not recorded

        The volume of distribution (Vss) is approximately 21 liters.
      6. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:095a08ac-cf0e-497e-a682-ddef38d6b29c (opens source in a new tab)

        Apixaban label

        Version not recorded · Effective date not recorded

        The volume of distribution (Vss) is approximately 21 liters.
      7. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:19a60552-374d-4b8b-a8ce-ceae252ea5ba (opens source in a new tab)

        Apixaban label

        Version not recorded · Effective date not recorded

        The volume of distribution (Vss) is approximately 21 liters.
      8. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:a454cd24-0c6d-46e8-b1e4-197388606175 (opens source in a new tab)

        Apixaban label

        Version not recorded · Effective date not recorded

        The volume of distribution (Vss) is approximately 21 liters.
      9. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:7be1f4c1-bb2f-4ded-ae9a-515d2a22f93e (opens source in a new tab)

        Apixaban label

        Version not recorded · Effective date not recorded

        The volume of distribution (Vss) is approximately 21 liters.
      10. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:2f47aa0e-0235-4220-85dd-dfcb8ad0d009 (opens source in a new tab)

        Apixaban label

        Version not recorded · Effective date not recorded

        The volume of distribution (Vss) is approximately 21 liters.
      11. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:fd383ae7-1e34-44ef-b8f1-ca6906dfbcef (opens source in a new tab)

        Apixaban label

        Version not recorded · Effective date not recorded

        The volume of distribution (Vss) is approximately 21 liters.
  7. Projected row 107

    Medicine slug
    apomorphine
    Compared field
    volumeOfDistribution
    Comparison state
    agree
    Reason codes
    • COMPATIBLE_VALUES_OVERLAP
    Documents examined
    2
    Source count
    2
    Agreement rate
    1
    Recorded readings
    1. 218 L

      Numeric value
      218
      Unit
      L
      Source records
      2

      Population and context: Unknown: population and formulation context were not structurally extracted from this source sentence.

      Show all 2 source records
      1. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:aedf70e4-1949-44bc-bf1b-0f282c4f0705 (opens source in a new tab)

        Apomorphine label

        Version not recorded · Effective date not recorded

        Mean (range) apparent volume of distribution was 218 L (123 L to 404 L).
      2. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:f3552b6e-5ae7-4993-aa1a-e399c4a7080a (opens source in a new tab)

        Apomorphine label

        Version not recorded · Effective date not recorded

        Mean (range) apparent volume of distribution was 218 L (123 to 404 L).
  8. Projected row 108

    Medicine slug
    aprepitant
    Compared field
    bioavailability
    Comparison state
    agree
    Reason codes
    • COMPATIBLE_VALUES_OVERLAP
    Documents examined
    8
    Source count
    6
    Agreement rate
    1
    Recorded readings
    1. 60 to 65%

      Numeric value
      60
      Unit
      %
      Source records
      6

      Population and context: Unknown: population and formulation context were not structurally extracted from this source sentence.

      Show all 6 source records
      1. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:f58b8944-93ee-4be1-a238-cc0061ddd93a (opens source in a new tab)

        Aprepitant label

        Version not recorded · Effective date not recorded

        At the dose range of 80 to 125 mg, the mean absolute oral bioavailability of aprepitant is approximately 60 to 65%.
      2. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:d72e0e10-4557-41b0-b65d-d395468cad19 (opens source in a new tab)

        Aprepitant label

        Version not recorded · Effective date not recorded

        At the dose range of 80 to 125 mg, the mean absolute oral bioavailability of aprepitant is approximately 60 to 65%.
      3. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:377c3ecb-fdec-dde4-e063-6294a90a29bd (opens source in a new tab)

        Aprepitant label

        Version not recorded · Effective date not recorded

        At the dose range of 80 to 125 mg, the mean absolute oral bioavailability of aprepitant is approximately 60 to 65%.
      4. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:696f9e80-9cae-403b-de9e-078343ce4713 (opens source in a new tab)

        Aprepitant label

        Version not recorded · Effective date not recorded

        At the dose range of 80 to 125 mg, the mean absolute oral bioavailability of EMEND is approximately 60 to 65%.
      5. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:a78aaa00-a46b-4f9e-a415-2fca9e9a4fb4 (opens source in a new tab)

        Aprepitant label

        Version not recorded · Effective date not recorded

        At the dose range of 80 to 125 mg, the mean absolute oral bioavailability of aprepitant is approximately 60 to 65%.
      6. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:af9b6086-4bf2-472c-8740-4134eaaebace (opens source in a new tab)

        Aprepitant label

        Version not recorded · Effective date not recorded

        At the dose range of 80 to 125 mg, the mean absolute oral bioavailability of aprepitant is approximately 60 to 65%.
  9. Projected row 109

    Medicine slug
    aprepitant
    Compared field
    halfLife
    Comparison state
    insufficient_context
    Reason codes
    • STRUCTURED_CONTEXT_MISSING
    Documents examined
    8
    Source count
    8
    Agreement rate
    0.875
    Recorded readings
    1. 9 to 13 hours

      Numeric value
      9
      Unit
      hours
      Source records
      7

      Population and context: Unknown: population and formulation context were not structurally extracted from this source sentence.

      Show all 7 source records
      1. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:4c218d3a-a508-4abc-9ed8-a6e8e191d1b4 (opens source in a new tab)

        Aprepitant label

        Version not recorded · Effective date not recorded

        The apparent terminal half-life ranged from approximately 9 to 13 hours.
      2. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:f58b8944-93ee-4be1-a238-cc0061ddd93a (opens source in a new tab)

        Aprepitant label

        Version not recorded · Effective date not recorded

        The apparent terminal half-life ranged from approximately 9 to 13 hours.
      3. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:d72e0e10-4557-41b0-b65d-d395468cad19 (opens source in a new tab)

        Aprepitant label

        Version not recorded · Effective date not recorded

        The apparent terminal half-life ranged from approximately 9 to 13 hours.
      4. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:377c3ecb-fdec-dde4-e063-6294a90a29bd (opens source in a new tab)

        Aprepitant label

        Version not recorded · Effective date not recorded

        The apparent terminal halflife ranged from approximately 9 to 13 hours.
      5. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:696f9e80-9cae-403b-de9e-078343ce4713 (opens source in a new tab)

        Aprepitant label

        Version not recorded · Effective date not recorded

        The apparent terminal half-life ranged from approximately 9 to 13 hours.
      6. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:a78aaa00-a46b-4f9e-a415-2fca9e9a4fb4 (opens source in a new tab)

        Aprepitant label

        Version not recorded · Effective date not recorded

        The apparent terminal half-life ranged from approximately 9 to 13 hours.
      7. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:af9b6086-4bf2-472c-8740-4134eaaebace (opens source in a new tab)

        Aprepitant label

        Version not recorded · Effective date not recorded

        The apparent terminal halflife ranged from approximately 9 to 13 hours.
    2. 12 hours

      Numeric value
      12
      Unit
      hours
      Source records
      1

      Population and context: Unknown: population and formulation context were not structurally extracted from this source sentence.

      Show all 1 source records
      1. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:d1b111eb-659a-496b-a86a-8f0fa370f147 (opens source in a new tab)

        Aprepitant label

        Version not recorded · Effective date not recorded

        The mean terminal half-life of aprepitant following administration of APONIVE was 12 hours.
  10. Projected row 110

    Medicine slug
    aprepitant
    Compared field
    volumeOfDistribution
    Comparison state
    insufficient_context
    Reason codes
    • STRUCTURED_CONTEXT_MISSING
    Documents examined
    8
    Source count
    8
    Agreement rate
    0.875
    Recorded readings
    1. 70 L

      Numeric value
      70
      Unit
      L
      Source records
      7

      Population and context: Unknown: population and formulation context were not structurally extracted from this source sentence.

      Show all 7 source records
      1. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:4c218d3a-a508-4abc-9ed8-a6e8e191d1b4 (opens source in a new tab)

        Aprepitant label

        Version not recorded · Effective date not recorded

        The mean apparent volume of distribution at steady state (Vd ss ) was approximately 70 L in humans.
      2. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:f58b8944-93ee-4be1-a238-cc0061ddd93a (opens source in a new tab)

        Aprepitant label

        Version not recorded · Effective date not recorded

        The mean apparent volume of distribution at steady state (Vd ss ) was approximately 70 L in humans.
      3. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:d72e0e10-4557-41b0-b65d-d395468cad19 (opens source in a new tab)

        Aprepitant label

        Version not recorded · Effective date not recorded

        The mean apparent volume of distribution at steady state (Vd ss ) was approximately 70 L in humans.
      4. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:377c3ecb-fdec-dde4-e063-6294a90a29bd (opens source in a new tab)

        Aprepitant label

        Version not recorded · Effective date not recorded

        The mean apparent volume of distribution at steady state (Vd ss ) was approximately 70 L in humans.
      5. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:696f9e80-9cae-403b-de9e-078343ce4713 (opens source in a new tab)

        Aprepitant label

        Version not recorded · Effective date not recorded

        The mean apparent volume of distribution at steady state (Vd ss ) was approximately 70 L in humans.
      6. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:a78aaa00-a46b-4f9e-a415-2fca9e9a4fb4 (opens source in a new tab)

        Aprepitant label

        Version not recorded · Effective date not recorded

        The mean apparent volume of distribution at steady state (Vd ss ) was approximately 70 L in humans.
      7. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:af9b6086-4bf2-472c-8740-4134eaaebace (opens source in a new tab)

        Aprepitant label

        Version not recorded · Effective date not recorded

        The mean apparent volume of distribution at steady state (Vd ss ) was approximately 70 L in humans.
    2. 72 L

      Numeric value
      72
      Unit
      L
      Source records
      1

      Population and context: Unknown: population and formulation context were not structurally extracted from this source sentence.

      Show all 1 source records
      1. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:d1b111eb-659a-496b-a86a-8f0fa370f147 (opens source in a new tab)

        Aprepitant label

        Version not recorded · Effective date not recorded

        The mean volume of distribution following APONVIE administration was approximately 72 L in healthy subjects.

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state
Exact comparability state.Values: agree, differ, not_comparable, insufficient_context
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Exact recorded field key.Values: bioavailability, halfLife, proteinBinding, tMax, volumeOfDistribution
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