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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 651660 of 1,681 matching rows. Filters and search terms remain attached when you move between pages or open the API view.

  1. Projected row 651

    Medicine slug
    fosaprepitant-dimeglumine
    Compared field
    halfLife
    Comparison state
    agree
    Reason codes
    • COMPATIBLE_VALUES_OVERLAP
    Documents examined
    27
    Source count
    27
    Agreement rate
    1
    Recorded readings
    1. 9 to 13 hours

      Numeric value
      9
      Unit
      hours
      Source records
      27

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

      Show all 27 source records
      1. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:d624667d-ee3b-3501-53fe-da453352042d (opens source in a new tab)

        Fosaprepitant Dimeglumine label

        Version not recorded · Effective date not recorded

        The apparent terminal half-liferanged from approximately 9 to 13 hours.
      2. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:ffee61d1-c1c6-4224-871c-ab7ff6cd01e5 (opens source in a new tab)

        Fosaprepitant Dimeglumine 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:5bb41bcb-c775-4447-9bd0-d4c55ad110ea (opens source in a new tab)

        Fosaprepitant Dimeglumine 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:df341f63-0fef-4411-a89b-6df6b9e792be (opens source in a new tab)

        Fosaprepitant Dimeglumine label

        Version not recorded · Effective date not recorded

        The apparent terminal half-life ranged from approximately 9 to 13 hours.
      5. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:bf207918-100d-4917-88b0-3433c0e72249 (opens source in a new tab)

        Fosaprepitant Dimeglumine 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:2d30d839-bb88-46ce-a9ed-66fe32a12a7a (opens source in a new tab)

        Fosaprepitant Dimeglumine 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:46edae30-d50c-4112-9941-954b13ed5eda (opens source in a new tab)

        Fosaprepitant Dimeglumine label

        Version not recorded · Effective date not recorded

        The apparent terminal half-life ranged from approximately 9 to 13 hours.
      8. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:21b08b87-70e3-4233-9531-dd6d84eab5d0 (opens source in a new tab)

        Fosaprepitant Dimeglumine label

        Version not recorded · Effective date not recorded

        The apparent terminal half-life ranged from approximately 9 to 13 hours.
      9. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:1cc7d482-5d45-4621-9ffc-cd3f7c54614d (opens source in a new tab)

        Fosaprepitant Dimeglumine label

        Version not recorded · Effective date not recorded

        The apparent terminal half-life ranged from approximately 9 to 13 hours.
      10. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:9b6d5ea3-2f7a-4501-9a4a-6fa1a7c2d50a (opens source in a new tab)

        Fosaprepitant Dimeglumine label

        Version not recorded · Effective date not recorded

        The apparent terminal half-life ranged from approximately 9 to 13 hours.
      11. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:3ed3e0a9-a0a8-4555-9f73-2043e79e3398 (opens source in a new tab)

        Fosaprepitant Dimeglumine label

        Version not recorded · Effective date not recorded

        The apparent terminal half-life ranged from approximately 9 to 13 hours.
      12. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:1a7d2f44-b578-4d99-a4ff-f267626064d0 (opens source in a new tab)

        Fosaprepitant Dimeglumine label

        Version not recorded · Effective date not recorded

        The apparent terminal half-life ranged from approximately 9 to 13 hours.
      13. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:3f942e4c-e26a-4155-9e14-344b2970b189 (opens source in a new tab)

        Fosaprepitant Dimeglumine label

        Version not recorded · Effective date not recorded

        The apparent terminal half-life ranged from approximately 9 to 13 hours.
      14. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:18a60093-cec8-1b8c-e063-6394a90a8902 (opens source in a new tab)

        Fosaprepitant Dimeglumine label

        Version not recorded · Effective date not recorded

        The apparent terminal half-life ranged from approximately 9 to 13 hours.
      15. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:7afe33d8-5416-465a-b98b-f4eedc327a94 (opens source in a new tab)

        Fosaprepitant Dimeglumine label

        Version not recorded · Effective date not recorded

        The apparent terminal half-life ranged from approximately 9 to 13 hours.
      16. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:a7343abe-b2b0-4e5a-907b-532a8e16dfcb (opens source in a new tab)

        Fosaprepitant Dimeglumine label

        Version not recorded · Effective date not recorded

        The apparent terminal half-life ranged from approximately 9 to 13 hours.
      17. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:9dbd4c29-d894-4839-9b22-a2f65c8c8ad1 (opens source in a new tab)

        Fosaprepitant Dimeglumine label

        Version not recorded · Effective date not recorded

        The apparent terminal half-life ranged from approximately 9 to 13 hours.
      18. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:8d66803a-6811-4c29-9c57-e16acfa87f21 (opens source in a new tab)

        Fosaprepitant Dimeglumine label

        Version not recorded · Effective date not recorded

        The apparent terminal half-life ranged from approximately 9 to 13 hours.
      19. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:19919480-960b-4741-9611-c133d68512f5 (opens source in a new tab)

        Fosaprepitant Dimeglumine label

        Version not recorded · Effective date not recorded

        The apparent terminal half-life ranged from approximately 9 to 13 hours.
      20. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:7375ab3f-a6fc-4601-9415-07b4f681cdef (opens source in a new tab)

        Fosaprepitant Dimeglumine label

        Version not recorded · Effective date not recorded

        The apparent terminal half-life ranged from approximately 9 to 13 hours.
      21. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:679c195a-cf59-4ca5-aa05-fa35d08ddb5c (opens source in a new tab)

        Fosaprepitant Dimeglumine label

        Version not recorded · Effective date not recorded

        The apparent terminal half-life ranged from approximately 9 to 13 hours.
      22. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:a41b7c3a-1376-43a7-b5b9-6ba2eba1e169 (opens source in a new tab)

        Fosaprepitant Dimeglumine label

        Version not recorded · Effective date not recorded

        The apparent terminal half-life ranged from approximately 9 to 13 hours.
      23. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:557a48d5-0e1f-f3d5-d3bc-db422d19c399 (opens source in a new tab)

        Fosaprepitant Dimeglumine label

        Version not recorded · Effective date not recorded

        The apparent terminal half-life ranged from approximately 9 to 13 hours.
      24. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:f34c931c-78b9-90c1-3fa5-bb34a227f2ad (opens source in a new tab)

        Fosaprepitant Dimeglumine label

        Version not recorded · Effective date not recorded

        The apparent terminal half-liferanged from approximately 9 to 13 hours.
      25. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:ad89825f-aa31-469f-9685-159a4524dfdc (opens source in a new tab)

        Fosaprepitant Dimeglumine label

        Version not recorded · Effective date not recorded

        The apparent terminal half-life ranged from approximately 9 to 13 hours.
      26. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:7dbdf8f5-6936-4143-b52d-96774b799a7d (opens source in a new tab)

        Fosaprepitant Dimeglumine label

        Version not recorded · Effective date not recorded

        The apparent terminal half-life ranged from approximately 9 to 13 hours.
      27. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:1e6b36b2-3c8b-4ac4-827e-d6f00d999032 (opens source in a new tab)

        Fosaprepitant Dimeglumine label

        Version not recorded · Effective date not recorded

        The apparent terminal half-life ranged from approximately 9 to 13 hours.
  2. Projected row 652

    Medicine slug
    fosaprepitant-dimeglumine
    Compared field
    volumeOfDistribution
    Comparison state
    agree
    Reason codes
    • COMPATIBLE_VALUES_OVERLAP
    Documents examined
    27
    Source count
    27
    Agreement rate
    1
    Recorded readings
    1. 70 L

      Numeric value
      70
      Unit
      L
      Source records
      27

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

      Show all 27 source records
      1. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:d624667d-ee3b-3501-53fe-da453352042d (opens source in a new tab)

        Fosaprepitant Dimeglumine 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:ffee61d1-c1c6-4224-871c-ab7ff6cd01e5 (opens source in a new tab)

        Fosaprepitant Dimeglumine 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:5bb41bcb-c775-4447-9bd0-d4c55ad110ea (opens source in a new tab)

        Fosaprepitant Dimeglumine 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:df341f63-0fef-4411-a89b-6df6b9e792be (opens source in a new tab)

        Fosaprepitant Dimeglumine 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:bf207918-100d-4917-88b0-3433c0e72249 (opens source in a new tab)

        Fosaprepitant Dimeglumine 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:2d30d839-bb88-46ce-a9ed-66fe32a12a7a (opens source in a new tab)

        Fosaprepitant Dimeglumine 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:46edae30-d50c-4112-9941-954b13ed5eda (opens source in a new tab)

        Fosaprepitant Dimeglumine 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.
      8. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:21b08b87-70e3-4233-9531-dd6d84eab5d0 (opens source in a new tab)

        Fosaprepitant Dimeglumine 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.
      9. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:1cc7d482-5d45-4621-9ffc-cd3f7c54614d (opens source in a new tab)

        Fosaprepitant Dimeglumine 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.
      10. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:9b6d5ea3-2f7a-4501-9a4a-6fa1a7c2d50a (opens source in a new tab)

        Fosaprepitant Dimeglumine 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.
      11. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:3ed3e0a9-a0a8-4555-9f73-2043e79e3398 (opens source in a new tab)

        Fosaprepitant Dimeglumine 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.
      12. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:1a7d2f44-b578-4d99-a4ff-f267626064d0 (opens source in a new tab)

        Fosaprepitant Dimeglumine 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.
      13. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:3f942e4c-e26a-4155-9e14-344b2970b189 (opens source in a new tab)

        Fosaprepitant Dimeglumine 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.
      14. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:18a60093-cec8-1b8c-e063-6394a90a8902 (opens source in a new tab)

        Fosaprepitant Dimeglumine 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.
      15. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:7afe33d8-5416-465a-b98b-f4eedc327a94 (opens source in a new tab)

        Fosaprepitant Dimeglumine 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.
      16. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:a7343abe-b2b0-4e5a-907b-532a8e16dfcb (opens source in a new tab)

        Fosaprepitant Dimeglumine 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.
      17. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:9dbd4c29-d894-4839-9b22-a2f65c8c8ad1 (opens source in a new tab)

        Fosaprepitant Dimeglumine 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.
      18. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:8d66803a-6811-4c29-9c57-e16acfa87f21 (opens source in a new tab)

        Fosaprepitant Dimeglumine 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.
      19. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:19919480-960b-4741-9611-c133d68512f5 (opens source in a new tab)

        Fosaprepitant Dimeglumine 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.
      20. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:7375ab3f-a6fc-4601-9415-07b4f681cdef (opens source in a new tab)

        Fosaprepitant Dimeglumine 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.
      21. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:679c195a-cf59-4ca5-aa05-fa35d08ddb5c (opens source in a new tab)

        Fosaprepitant Dimeglumine 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.
      22. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:a41b7c3a-1376-43a7-b5b9-6ba2eba1e169 (opens source in a new tab)

        Fosaprepitant Dimeglumine label

        Version not recorded · Effective date not recorded

        The mean apparent volume of distribution at steady state (Vdss) was approximately 70 L in humans.
      23. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:557a48d5-0e1f-f3d5-d3bc-db422d19c399 (opens source in a new tab)

        Fosaprepitant Dimeglumine label

        Version not recorded · Effective date not recorded

        The mean apparent volume of distribution at steady state (Vdss) was approximately 70 L in humans.
      24. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:f34c931c-78b9-90c1-3fa5-bb34a227f2ad (opens source in a new tab)

        Fosaprepitant Dimeglumine 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.Aprepitant crossesthe blood brainbarrier in humans[see Clinical Pharmacology ( 12.1 )].
      25. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:ad89825f-aa31-469f-9685-159a4524dfdc (opens source in a new tab)

        Fosaprepitant Dimeglumine 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.
      26. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:7dbdf8f5-6936-4143-b52d-96774b799a7d (opens source in a new tab)

        Fosaprepitant Dimeglumine 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.
      27. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:1e6b36b2-3c8b-4ac4-827e-d6f00d999032 (opens source in a new tab)

        Fosaprepitant Dimeglumine 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. Projected row 653

    Medicine slug
    foscarnet
    Compared field
    halfLife
    Comparison state
    agree
    Reason codes
    • COMPATIBLE_VALUES_OVERLAP
    Documents examined
    10
    Source count
    10
    Agreement rate
    1
    Recorded readings
    1. 87.5 ± 41.8 hours

      Numeric value
      87.5
      Unit
      hours
      Source records
      10

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

      Show all 10 source records
      1. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:b612e6f1-584f-4188-b96e-1a9adfcfe75c (opens source in a new tab)

        Foscarnet label

        Version not recorded · Effective date not recorded

        The foscarnet terminal half-life determined by urinary excretion was 87.5 ± 41.8 hours, possibly due to release of foscarnet from bone.
      2. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:90e3da4e-3b1f-428b-99ca-e4bed1c80028 (opens source in a new tab)

        Foscarnet label

        Version not recorded · Effective date not recorded

        The foscarnet terminal half-life determined by urinary excretion was 87.5 ± 41.8 hours, possibly due to release of foscarnet from bone.
      3. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:b03cbb8e-f555-4ed3-854e-dd962604f144 (opens source in a new tab)

        Foscarnet label

        Version not recorded · Effective date not recorded

        The foscarnet terminal half-life determined by urinary excretion was 87.5 ± 41.8 hours, possibly due to release of foscarnet from bone.
      4. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:8a7caffd-9d8a-4d45-ad48-70d511a89c29 (opens source in a new tab)

        Foscarnet label

        Version not recorded · Effective date not recorded

        The foscarnet terminal half-life determined by urinary excretion was 87.5 ± 41.8 hours, possibly due to release of foscarnet from bone.
      5. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:d4048736-389f-48d8-aadd-6bc76d604ddb (opens source in a new tab)

        Foscarnet label

        Version not recorded · Effective date not recorded

        The foscarnet terminal half-life determined by urinary excretion was 87.5 ± 41.8 hours, possibly due to release of foscarnet from bone.
      6. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:6ec3bb2a-fb40-4d4a-bc1b-feea80cc1a95 (opens source in a new tab)

        Foscarnet label

        Version not recorded · Effective date not recorded

        The foscarnet terminal half-life determined by urinary excretion was 87.5 ± 41.8 hours, possibly due to release of foscarnet from bone.
      7. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:a09299d5-9c55-4cef-aed0-3a6a45532289 (opens source in a new tab)

        Foscarnet label

        Version not recorded · Effective date not recorded

        The foscarnet terminal half-life determined by urinary excretion was 87.5 ± 41.8 hours, possibly due to release of foscarnet from bone.
      8. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:d2b4ce68-5a81-4b14-8914-21bc38f01008 (opens source in a new tab)

        Foscarnet label

        Version not recorded · Effective date not recorded

        The foscarnet terminal half-life determined by urinary excretion was 87.5 ± 41.8 hours, possibly due to release of foscarnet from bone.
      9. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:335f7deb-a045-43cb-b319-d7b73bfda73c (opens source in a new tab)

        Foscarnet label

        Version not recorded · Effective date not recorded

        The foscarnet terminal half-life determined by urinary excretion was 87.5 ± 41.8 hours, possibly due to release of foscarnet from bone.
      10. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:2f49c1bc-0828-4e5c-a3c0-81e997213b0e (opens source in a new tab)

        Foscarnet label

        Version not recorded · Effective date not recorded

        The foscarnet terminal half-life determined by urinary excretion was 87.5 ± 41.8 hours, possibly due to release of foscarnet from bone.
  4. Projected row 654

    Medicine slug
    fosfomycin
    Compared field
    bioavailability
    Comparison state
    agree
    Reason codes
    • COMPATIBLE_VALUES_OVERLAP
    Documents examined
    9
    Source count
    8
    Agreement rate
    1
    Recorded readings
    1. 37%

      Numeric value
      37
      Unit
      %
      Source records
      8

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

      Show all 8 source records
      1. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:d101b5d8-bffc-4ee6-b93b-4589fcb8750d (opens source in a new tab)

        Fosfomycin label

        Version not recorded · Effective date not recorded

        Absolute oral bioavailability under fasting conditions is 37%.
      2. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:aacd04a4-f2d5-45a2-b9e7-0e92244a5880 (opens source in a new tab)

        Fosfomycin label

        Version not recorded · Effective date not recorded

        Absolute oral bioavailability under fasting conditions is 37%.
      3. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:3fa61bd4-fc55-0987-e063-6394a90abce2 (opens source in a new tab)

        Fosfomycin label

        Version not recorded · Effective date not recorded

        Absolute oral bioavailability under fasting conditions is 37%.
      4. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:f8ec4771-3f8d-473a-a1d0-e42038f61a42 (opens source in a new tab)

        Fosfomycin label

        Version not recorded · Effective date not recorded

        Absolute oral bioavailability under fasting conditions is 37%.
      5. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:48e352bc-52ea-4778-905a-60ef38a5c18a (opens source in a new tab)

        Fosfomycin label

        Version not recorded · Effective date not recorded

        Absolute oral bioavailability under fasting conditions is 37%.
      6. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:f44b79d0-a789-46cb-ab70-7eb33a7debaf (opens source in a new tab)

        Fosfomycin label

        Version not recorded · Effective date not recorded

        Absolute oral bioavailability under fasting conditions is 37%.
      7. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:6b9167a9-80e9-44e1-a609-c3eb78960acf (opens source in a new tab)

        Fosfomycin label

        Version not recorded · Effective date not recorded

        Absolute oral bioavailability under fasting conditions is 37%.
      8. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:4f206750-8126-99a3-e063-6294a90ade4c (opens source in a new tab)

        Fosfomycin label

        Version not recorded · Effective date not recorded

        Absolute oral bioavailability under fasting conditions is 37%.
  5. Projected row 655

    Medicine slug
    fosinopril
    Compared field
    halfLife
    Comparison state
    agree
    Reason codes
    • COMPATIBLE_VALUES_OVERLAP
    Documents examined
    10
    Source count
    10
    Agreement rate
    1
    Recorded readings
    1. 11 to 13 hours

      Numeric value
      11
      Unit
      hours
      Source records
      10

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

      Show all 10 source records
      1. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:ff1323cc-7ad8-488d-94a7-a11555db78a7 (opens source in a new tab)

        Fosinopril label

        Version not recorded · Effective date not recorded

        The terminal elimination half-life of fosinoprilat in pediatric patients was 11 to 13 hours, also similar to that observed in adults.
      2. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:880e5bf4-ced8-4765-a5c2-2361fd06ed9c (opens source in a new tab)

        Fosinopril label

        Version not recorded · Effective date not recorded

        The terminal elimination half-life of fosinoprilat in pediatric patients was 11 to 13 hours, also similar to that observed in adults.
      3. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:736fe52f-69fb-48b2-b1c5-f06531878538 (opens source in a new tab)

        Fosinopril label

        Version not recorded · Effective date not recorded

        The terminal elimination half-life of fosinoprilat in pediatric patients was 11 to 13 hours, also similar to that observed in adults.
      4. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:0a66f606-5e6f-473d-8a1e-9ef316adb2e2 (opens source in a new tab)

        Fosinopril label

        Version not recorded · Effective date not recorded

        The terminal elimination half-life of fosinoprilat in pediatric patients was 11 to 13 hours, also similar to that observed in adults.
      5. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:ee78de8e-22f4-4c3b-a721-e9464d704eda (opens source in a new tab)

        Fosinopril label

        Version not recorded · Effective date not recorded

        The terminal elimination half-life of fosinoprilat in pediatric patients was 11 to 13 hours, also similar to that observed in adults.
      6. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:fc38f1bb-f175-4a81-8ed9-c8701efdea35 (opens source in a new tab)

        Fosinopril label

        Version not recorded · Effective date not recorded

        The terminal elimination half-life of fosinoprilat in pediatric patients was 11 to 13 hours, also similar to that observed in adults.
      7. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:6562a532-b502-4515-88df-591d71293b56 (opens source in a new tab)

        Fosinopril label

        Version not recorded · Effective date not recorded

        The terminal elimination half-life of fosinoprilat in pediatric patients was 11 to 13 hours, also similar to that observed in adults.
      8. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:aee04f17-8ee9-42f5-861f-b6ba17220ca4 (opens source in a new tab)

        Fosinopril label

        Version not recorded · Effective date not recorded

        The terminal elimination half-life of fosinoprilat in pediatric patients was 11 to 13 hours, also similar to that observed in adults.
      9. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:e2ff3171-a17a-456a-9272-ca1682b01d19 (opens source in a new tab)

        Fosinopril label

        Version not recorded · Effective date not recorded

        The terminal elimination half-life of fosinoprilat in pediatric patients was 11 to 13 hours, also similar to that observed in adults.
      10. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:46e3e4e8-c611-4d4f-ad57-050b4c01fcd8 (opens source in a new tab)

        Fosinopril label

        Version not recorded · Effective date not recorded

        The terminal elimination half-life of fosinoprilat in pediatric patients was 11 to 13 hours, also similar to that observed in adults.
  6. Projected row 656

    Medicine slug
    fosinopril
    Compared field
    tMax
    Comparison state
    agree
    Reason codes
    • COMPATIBLE_VALUES_OVERLAP
    Documents examined
    10
    Source count
    10
    Agreement rate
    1
    Recorded readings
    1. 3 hours

      Numeric value
      3
      Unit
      hours
      Source records
      10

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

      Show all 10 source records
      1. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:ff1323cc-7ad8-488d-94a7-a11555db78a7 (opens source in a new tab)

        Fosinopril label

        Version not recorded · Effective date not recorded

        Times to peak concentrations are independent of dose and are achieved in approximately 3 hours.
      2. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:880e5bf4-ced8-4765-a5c2-2361fd06ed9c (opens source in a new tab)

        Fosinopril label

        Version not recorded · Effective date not recorded

        Times to peak concentrations are independent of dose and are achieved in approximately 3 hours.
      3. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:736fe52f-69fb-48b2-b1c5-f06531878538 (opens source in a new tab)

        Fosinopril label

        Version not recorded · Effective date not recorded

        Times to peak concentrations are independent of dose and are achieved in approximately 3 hours.
      4. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:0a66f606-5e6f-473d-8a1e-9ef316adb2e2 (opens source in a new tab)

        Fosinopril label

        Version not recorded · Effective date not recorded

        Times to peak concentrations are independent of dose and are achieved in approximately 3 hours.
      5. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:ee78de8e-22f4-4c3b-a721-e9464d704eda (opens source in a new tab)

        Fosinopril label

        Version not recorded · Effective date not recorded

        Times to peak concentrations are independent of dose and are achieved in approximately 3 hours.
      6. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:fc38f1bb-f175-4a81-8ed9-c8701efdea35 (opens source in a new tab)

        Fosinopril label

        Version not recorded · Effective date not recorded

        Times to peak concentrations are independent of dose and are achieved in approximately 3 hours.
      7. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:6562a532-b502-4515-88df-591d71293b56 (opens source in a new tab)

        Fosinopril label

        Version not recorded · Effective date not recorded

        Times to peak concentrations are independent of dose and are achieved in approximately 3 hours.
      8. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:aee04f17-8ee9-42f5-861f-b6ba17220ca4 (opens source in a new tab)

        Fosinopril label

        Version not recorded · Effective date not recorded

        Times to peak concentrations are independent of dose and are achieved in approximately 3 hours.
      9. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:e2ff3171-a17a-456a-9272-ca1682b01d19 (opens source in a new tab)

        Fosinopril label

        Version not recorded · Effective date not recorded

        Times to peak concentrations are independent of dose and are achieved in approximately 3 hours.
      10. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:46e3e4e8-c611-4d4f-ad57-050b4c01fcd8 (opens source in a new tab)

        Fosinopril label

        Version not recorded · Effective date not recorded

        Times to peak concentrations are independent of dose and are achieved in approximately 3 hours.
  7. Projected row 657

    Medicine slug
    fosphenytoin
    Compared field
    halfLife
    Comparison state
    insufficient_context
    Reason codes
    • STRUCTURED_CONTEXT_MISSING
    Documents examined
    10
    Source count
    10
    Agreement rate
    0.9
    Recorded readings
    1. 12.0 to 28.9 hr

      Numeric value
      12
      Unit
      hours
      Source records
      9

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

      Show all 9 source records
      1. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:d4c36fad-0ba2-4cd4-9c5e-dcf843f38a5a (opens source in a new tab)

        Fosphenytoin label

        Version not recorded · Effective date not recorded

        Elimination : Mean total phenytoin half-life values (12.0 to 28.9 hr) following CEREBYX administration at these doses are similar to those after equal doses of parenteral Dilantin and tend to be greater at higher plasma phenytoin concentrations.
      2. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:bb38bc6a-99c7-4cda-b3f0-37f629d060cf (opens source in a new tab)

        Fosphenytoin label

        Version not recorded · Effective date not recorded

        Elimination: Mean total phenytoin half-life values (12.0 to 28.9 hr) following fosphenytoin sodium administration at these doses are similar to those after equal doses of parenteral Dilantin and tend to be greater at higher plasma phenytoin concentrations.
      3. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:b60c9c82-e5c7-4e05-98c7-5bbba4af04b2 (opens source in a new tab)

        Fosphenytoin label

        Version not recorded · Effective date not recorded

        Elimination : Mean total phenytoin half-life values (12.0 to 28.9 hr) following fosphenytoin sodium injection administration at these doses are similar to those after equal doses of parenteral phenytoin sodium and tend to be greater at higher plasma phenytoin concentrations.
      4. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:de5a6711-4abb-4c3d-a18b-266b094ace11 (opens source in a new tab)

        Fosphenytoin label

        Version not recorded · Effective date not recorded

        Elimination : Mean total phenytoin half-life values (12.0 to 28.9 hr) following CEREBYX administration at these doses are similar to those after equal doses of parenteral Dilantin and tend to be greater at higher plasma phenytoin concentrations.
      5. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:519a44e3-8a93-456c-b71c-894513810d45 (opens source in a new tab)

        Fosphenytoin label

        Version not recorded · Effective date not recorded

        Elimination : Mean total phenytoin half-life values (12.0 to 28.9 hr) following fosphenytoin sodium injection administration at these doses are similar to those after equal doses of parenteral Dilantin and tend to be greater at higher plasma phenytoin concentrations.
      6. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:a0def32c-e693-43e5-9509-0cef9642441c (opens source in a new tab)

        Fosphenytoin label

        Version not recorded · Effective date not recorded

        Elimination: Mean total phenytoin half-life values (12.0 to 28.9 hr) following fosphenytoin sodium administration at these doses are similar to those after equal doses of parenteral Dilantin and tend to be greater at higher plasma phenytoin concentrations.
      7. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:49b08648-6a83-42c7-ae7b-80c29f2534fc (opens source in a new tab)

        Fosphenytoin label

        Version not recorded · Effective date not recorded

        Elimination: Mean total phenytoin half-life values (12.0 to 28.9 hr) following fosphenytoin sodium administration at these doses are similar to those after equal doses of parenteral Dilantin and tend to be greater at higher plasma phenytoin concentrations.
      8. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:c92df63b-5140-4213-8d43-8327ff6230b7 (opens source in a new tab)

        Fosphenytoin label

        Version not recorded · Effective date not recorded

        Elimination: Mean total phenytoin half-life values (12.0 to 28.9 hr) following Fosphenytoin Sodium Injection administration at these doses are similar to those after equal doses of parenteral Dilantin and tend to be greater at higher plasma phenytoin concentrations.
      9. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:e1dab8ad-cbf6-4273-92fa-02629de2abde (opens source in a new tab)

        Fosphenytoin label

        Version not recorded · Effective date not recorded

        Elimination: Mean total phenytoin half-life values (12.0 to 28.9 hr) following fosphenytoin sodium administration at these doses are similar to those after equal doses of parenteral Dilantin and tend to be greater at higher plasma phenytoin concentrations.
    2. 12 to 28.9 hr

      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:87ff8a91-5b37-401c-b75c-dc6efd348761 (opens source in a new tab)

        Fosphenytoin label

        Version not recorded · Effective date not recorded

        Mean total phenytoin half-life values (12 to 28.9 hr) following fosphenytoin injection administration at these doses are similar to those after equal doses of parenteral phenytoin sodium and tend to be greater at higher plasma phenytoin concentrations.
  8. Projected row 658

    Medicine slug
    frovatriptan
    Compared field
    halfLife
    Comparison state
    agree
    Reason codes
    • COMPATIBLE_VALUES_OVERLAP
    Documents examined
    4
    Source count
    4
    Agreement rate
    1
    Recorded readings
    1. 26 hours

      Numeric value
      26
      Unit
      hours
      Source records
      4

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

      Show all 4 source records
      1. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:d303af88-e0c1-4fb2-ba8e-83b7e6d163cd (opens source in a new tab)

        Frovatriptan label

        Version not recorded · Effective date not recorded

        The mean terminal elimination half-life of frovatriptan in both males and females is approximately 26 hours.
      2. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:92c91060-c06e-4a8a-b586-a3fb25c33433 (opens source in a new tab)

        Frovatriptan label

        Version not recorded · Effective date not recorded

        The mean terminal elimination half-life of frovatriptan in both males and females is approximately 26 hours.
      3. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:94b996dc-ddc4-41ce-9a9f-3d91cb187473 (opens source in a new tab)

        Frovatriptan label

        Version not recorded · Effective date not recorded

        The mean terminal elimination half-life of frovatriptan in both males and females is approximately 26 hours.
      4. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:03a58215-dba7-4f63-8b98-d74d054a574a (opens source in a new tab)

        Frovatriptan label

        Version not recorded · Effective date not recorded

        The mean terminal elimination half-life of frovatriptan in both males and females is approximately 26 hours.
  9. Projected row 659

    Medicine slug
    fulvestrant
    Compared field
    halfLife
    Comparison state
    agree
    Reason codes
    • COMPATIBLE_VALUES_OVERLAP
    Documents examined
    25
    Source count
    25
    Agreement rate
    1
    Recorded readings
    1. 40 days

      Numeric value
      Not parsed
      Unit
      Not recorded
      Source records
      25

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

      Show all 25 source records
      1. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:477098a1-cd37-48ad-b17f-aef610cb0f57 (opens source in a new tab)

        Fulvestrant label

        Version not recorded · Effective date not recorded

        After an intramuscular injection of 250 mg, the clearance (Mean ± SD) was 690 ± 226 mL/min with an apparent half-life about 40 days.
      2. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:57352662-d2fa-4dce-828f-4c51e46e0b4d (opens source in a new tab)

        Fulvestrant label

        Version not recorded · Effective date not recorded

        After an intramuscular injection of 250 mg, the clearance (Mean ± SD) was 690 ± 226 mL/min with an apparent half-life about 40 days.
      3. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:a51aa693-b433-4b2d-a71b-9ba029b10ce3 (opens source in a new tab)

        Fulvestrant label

        Version not recorded · Effective date not recorded

        After an intramuscular injection of 250 mg, the clearance (Mean ± SD) was 690 ± 226 mL/min with an apparent half-life about 40 days.
      4. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:0f05b699-c440-42c1-9557-46759a10ab17 (opens source in a new tab)

        Fulvestrant label

        Version not recorded · Effective date not recorded

        After an intramuscular injection of 250 mg, the clearance (Mean ± SD) was 690 ± 226 mL/min with an apparent half-life about 40 days.
      5. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:e20d8ca3-8837-4003-8b01-1ebec342062a (opens source in a new tab)

        Fulvestrant label

        Version not recorded · Effective date not recorded

        After an intramuscular injection of 250 mg, the clearance (Mean ± SD) was 690 ± 226 mL/min with an apparent half-life about 40 days.
      6. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:99cf8b69-4c23-4886-80e9-b23e348b5bd7 (opens source in a new tab)

        Fulvestrant label

        Version not recorded · Effective date not recorded

        After an intramuscular injection of 250 mg, the clearance (Mean ± SD) was 690 ± 226 mL/min with an apparent half-life about 40 days.
      7. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:b02915fe-6c44-48c1-aaeb-997ddc59a595 (opens source in a new tab)

        Fulvestrant label

        Version not recorded · Effective date not recorded

        After an intramuscular injection of 250 mg, the clearance (Mean ± SD) was 690 ± 226 mL/min with an apparent half-life about 40 days.
      8. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:994edf79-20a5-4e3a-bb35-c4fe3e65acba (opens source in a new tab)

        Fulvestrant label

        Version not recorded · Effective date not recorded

        After an intramuscular injection of 250 mg, the clearance (Mean ± SD) was 690 ± 226 mL/min with an apparent half-life about 40 days.
      9. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:306c283b-9abe-4985-856b-1957f1f3af8b (opens source in a new tab)

        Fulvestrant label

        Version not recorded · Effective date not recorded

        After an intramuscular injection of 250 mg, the clearance (Mean ± SD) was 690 ± 226 mL/min with an apparent half-life about 40 days.
      10. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:46086fe7-190d-4963-97bc-1fe22d36e6d2 (opens source in a new tab)

        Fulvestrant label

        Version not recorded · Effective date not recorded

        After an intramuscular injection of 250 mg, the clearance (Mean ± SD) was 690 ± 226 mL/min with an apparent half-life about 40 days.
      11. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:f36f19ad-f044-4dba-80b6-d074ddffcd86 (opens source in a new tab)

        Fulvestrant label

        Version not recorded · Effective date not recorded

        After an intramuscular injection of 250 mg, the clearance (Mean ± SD) was 690 ± 226 mL/min with an apparent half-life about 40 days.
      12. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:67566681-19b5-89df-2030-25df5b0cf641 (opens source in a new tab)

        Fulvestrant label

        Version not recorded · Effective date not recorded

        After an intramuscular injection of 250 mg, the clearance (Mean ± SD) was 690 ± 226 mL/min with an apparent half-life about 40 days.
      13. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:f44cffcc-8f5e-4a4c-a36e-ab946ce86266 (opens source in a new tab)

        Fulvestrant label

        Version not recorded · Effective date not recorded

        After an intramuscular injection of 250 mg, the clearance (Mean ± SD) was 690 ± 226 mL/min with an apparent half-life about 40 days.
      14. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:fabe9bd8-ac23-4df1-a89a-223d5cd38914 (opens source in a new tab)

        Fulvestrant label

        Version not recorded · Effective date not recorded

        After an intramuscular injection of 250 mg, the clearance (Mean ± SD) was 690 ± 226 mL/min with an apparent half-life about 40 days.
      15. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:80b6dfe6-449d-4e2f-af90-bfbf9b04163b (opens source in a new tab)

        Fulvestrant label

        Version not recorded · Effective date not recorded

        After an intramuscular injection of 250 mg, the clearance (Mean ± SD) was 690 ± 226 mL/min with an apparent half-life about 40 days.
      16. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:83d7a440-e904-4e36-afb5-cb02b1c919f7 (opens source in a new tab)

        Fulvestrant label

        Version not recorded · Effective date not recorded

        After an intramuscular injection of 250 mg, the clearance (Mean ± SD) was 690 ± 226 mL/min with an apparent half-life about 40 days.
      17. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:840cd7c0-9f33-f74e-f136-de7fe899bfb4 (opens source in a new tab)

        Fulvestrant label

        Version not recorded · Effective date not recorded

        After an intramuscular injection of 250 mg, the clearance (Mean ± SD) was 690 ± 226 mL/min with an apparent half-life about 40 days.
      18. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:7a03f714-b109-4256-80a6-78c82127d624 (opens source in a new tab)

        Fulvestrant label

        Version not recorded · Effective date not recorded

        After an intramuscular injection of 250 mg, the clearance (Mean ± SD) was 690 ± 226 mL/min with an apparent half-life about 40 days.
      19. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:8ed06e0e-c17b-4c71-8d03-888bcde4a638 (opens source in a new tab)

        Fulvestrant label

        Version not recorded · Effective date not recorded

        After an intramuscular injection of 250 mg, the clearance (Mean ± SD) was 690 ± 226 mL/min with an apparent half-life about 40 days.
      20. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:2fc17ba3-83c7-a2b4-8a75-6a0cb1e07682 (opens source in a new tab)

        Fulvestrant label

        Version not recorded · Effective date not recorded

        After an intramuscular injection of 250 mg, the clearance (Mean ± SD) was 690 ± 226 mL/min with an apparent half-life about 40 days.
      21. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:d5ae9e07-73b0-4063-a9e4-0ffc5614c2b8 (opens source in a new tab)

        Fulvestrant label

        Version not recorded · Effective date not recorded

        After an intramuscular injection of 250 mg, the clearance (Mean ± SD) was 690 ± 226 mL/min with an apparent half-life about 40 days.
      22. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:b471eb51-488e-5312-e053-2a95a90a8116 (opens source in a new tab)

        Fulvestrant label

        Version not recorded · Effective date not recorded

        After an intramuscular injection of 250 mg, the clearance (Mean ± SD) was 690 ± 226 mL/min with an apparent half-life about 40 days.
      23. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:bc7b4eac-3b63-53d2-e053-2995a90ad5e7 (opens source in a new tab)

        Fulvestrant label

        Version not recorded · Effective date not recorded

        After an intramuscular injection of 250 mg, the clearance (Mean ± SD) was 690 ± 226 mL/min with an apparent half-life about 40 days.
      24. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:015fafb6-23f7-4566-9c23-386eee7b035d (opens source in a new tab)

        Fulvestrant label

        Version not recorded · Effective date not recorded

        After an intramuscular injection of 250 mg, the clearance (Mean ± SD) was 690 ± 226 mL/min with an apparent half-life about 40 days.
      25. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:141f439e-078c-4a59-acff-ebf7685f55b8 (opens source in a new tab)

        Fulvestrant label

        Version not recorded · Effective date not recorded

        After an intramuscular injection of 250 mg, the clearance (Mean ± SD) was 690 ± 226 mL/min with an apparent half-life about 40 days.
  10. Projected row 660

    Medicine slug
    fulvestrant
    Compared field
    volumeOfDistribution
    Comparison state
    insufficient_context
    Reason codes
    • STRUCTURED_CONTEXT_MISSING
    Documents examined
    25
    Source count
    25
    Agreement rate
    0.92
    Recorded readings
    1. 3 to 5 L/kg

      Numeric value
      3
      Unit
      L/kg
      Source records
      23

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

      Show all 23 source records
      1. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:477098a1-cd37-48ad-b17f-aef610cb0f57 (opens source in a new tab)

        Fulvestrant label

        Version not recorded · Effective date not recorded

        e given on Day 15 Single dose 25.1 (35.3) 16.3 (25.9) 11400 (33.4) Multiple dose steady state Month 3 28.0 (27.9) 12.2 (21.7) 13100 (23.4) Distribution: The apparent volume of distribution at steady state is approximately 3 to 5 L/kg.
      2. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:57352662-d2fa-4dce-828f-4c51e46e0b4d (opens source in a new tab)

        Fulvestrant label

        Version not recorded · Effective date not recorded

        Month 3 Distribution: The apparent volume of distribution at steady state is approximately 3 to 5 L/kg.
      3. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:0f05b699-c440-42c1-9557-46759a10ab17 (opens source in a new tab)

        Fulvestrant label

        Version not recorded · Effective date not recorded

        ng.hr/mL) 500 mg + AD 1 Single dose 25.1 (35.3) 16.3 (25.9) 11400 (33.4) Multiple dose steady state 2 28.0 (27.9) 12.2 (21.7) 13100 (23.4) Distribution: The apparent volume of distribution at steady state is approximately 3 to 5 L/kg.
      4. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:e20d8ca3-8837-4003-8b01-1ebec342062a (opens source in a new tab)

        Fulvestrant label

        Version not recorded · Effective date not recorded

        Month 3 Distribution: The apparent volume of distribution at steady state is approximately 3 to 5 L/kg.
      5. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:99cf8b69-4c23-4886-80e9-b23e348b5bd7 (opens source in a new tab)

        Fulvestrant label

        Version not recorded · Effective date not recorded

        6.3 (25.9) 11400 (33.4) Multiple dose steady state 2 28 (27.9) 12.2 (21.7) 13100 (23.4) 1 Additional 500 mg dose given on Day 15 2 Month 3 Distribution: The apparent volume of distribution at steady state is approximately 3 to 5 L/kg.
      6. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:b02915fe-6c44-48c1-aaeb-997ddc59a595 (opens source in a new tab)

        Fulvestrant label

        Version not recorded · Effective date not recorded

        Month 3 Distribution: The apparent volume of distribution at steady state is approximately 3 to 5 L/kg.
      7. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:994edf79-20a5-4e3a-bb35-c4fe3e65acba (opens source in a new tab)

        Fulvestrant label

        Version not recorded · Effective date not recorded

        3 (25.9) 11400 (33.4) Multiple dose steady state 2 28.0 (27.9) 12.2 (21.7) 13100 (23.4) 1 Additional 500 mg dose given on Day 15 2 Month 3 Distribution: The apparent volume of distribution at steady state is approximately 3 to 5 L/kg.
      8. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:306c283b-9abe-4985-856b-1957f1f3af8b (opens source in a new tab)

        Fulvestrant label

        Version not recorded · Effective date not recorded

        e given on Day 15 Single dose 25.1 (35.3) 16.3 (25.9) 11,400 (33.4) Multiple dose steady state Month 3 28 (27.9) 12.2 (21.7) 13,100 (23.4) Distribution: The apparent volume of distribution at steady state is approximately 3 to 5 L/kg.
      9. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:46086fe7-190d-4963-97bc-1fe22d36e6d2 (opens source in a new tab)

        Fulvestrant label

        Version not recorded · Effective date not recorded

        Month 3 C max (ng/mL) C min (ng/mL) AUC (ng.hr/mL) 500 mg + AD 1 Single dose 25.1 (35.3) 16.3 (25.9) 11400 (33.4) Multiple dose steady state 2 28.0 (27.9) 12.2 (21.7) 13100 (23.4) Distribution The apparent volume of distribution at steady state is approximately 3 to 5 L/kg.
      10. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:67566681-19b5-89df-2030-25df5b0cf641 (opens source in a new tab)

        Fulvestrant label

        Version not recorded · Effective date not recorded

        ng.hr/mL) 500 mg + AD * Single dose 25.1 (35.3) 16.3 (25.9) 11400 (33.4) Multiple dose steady state † 28.0 (27.9) 12.2 (21.7) 13100 (23.4) Distribution: The apparent volume of distribution at steady state is approximately 3 to 5 L/kg.
      11. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:f44cffcc-8f5e-4a4c-a36e-ab946ce86266 (opens source in a new tab)

        Fulvestrant label

        Version not recorded · Effective date not recorded

        Month 3 C max (ng/mL) C min (ng/mL) AUC (ng.hr/mL) 500 mg + AD 1 Single dose 25.1 (35.3) 16.3 (25.9) 11400 (33.4) Multiple dose steady state 2 28.0 (27.9) 12.2 (21.7) 13100 (23.4) Distribution The apparent volume of distribution at steady state is approximately 3 to 5 L/kg.
      12. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:fabe9bd8-ac23-4df1-a89a-223d5cd38914 (opens source in a new tab)

        Fulvestrant label

        Version not recorded · Effective date not recorded

        Month 3 C max (ng/mL) C min (ng/mL) AUC (ng.hr/mL) 500 mg + AD 1 Single dose 25.1 (35.3) 16.3 (25.9) 11400 (33.4) Multiple dose steady state 2 28.0 (27.9) 12.2 (21.7) 13100 (23.4) Distribution: The apparent volume of distribution at steady state is approximately 3 to 5 L/kg.
      13. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:80b6dfe6-449d-4e2f-af90-bfbf9b04163b (opens source in a new tab)

        Fulvestrant label

        Version not recorded · Effective date not recorded

        ng.hr/mL) 500 mg + AD 1 Single dose 25.1 (35.3) 16.3 (25.9) 11400 (33.4) Multiple dose steady state 2 28.0 (27.9) 12.2 (21.7) 13100 (23.4) Distribution: The apparent volume of distribution at steady state is approximately 3 to 5 L/kg.
      14. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:83d7a440-e904-4e36-afb5-cb02b1c919f7 (opens source in a new tab)

        Fulvestrant label

        Version not recorded · Effective date not recorded

        e given on Day 15 Single dose 25.1 (35.3) 16.3 (25.9) 11400 (33.4) Multiple dose steady state Month 3 28.0 (27.9) 12.2 (21.7) 13100 (23.4) Distribution: The apparent volume of distribution at steady state is approximately 3 to 5 L/kg.
      15. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:840cd7c0-9f33-f74e-f136-de7fe899bfb4 (opens source in a new tab)

        Fulvestrant label

        Version not recorded · Effective date not recorded

        ng.hr/mL) 500 mg + AD * Single dose 25.1 (35.3) 16.3 (25.9) 11400 (33.4) Multiple dose steady state † 28.0 (27.9) 12.2 (21.7) 13100 (23.4) Distribution: The apparent volume of distribution at steady state is approximately 3 to 5 L/kg.
      16. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:7a03f714-b109-4256-80a6-78c82127d624 (opens source in a new tab)

        Fulvestrant label

        Version not recorded · Effective date not recorded

        dose given on Day 15 Single dose 25.1 (35.3) 16.3 (25.9) 11400 (33.4) Multiple dose steady state Month 3 28 (27.9) 12.2 (21.7) 13100 (23.4) Distribution The apparent volume of distribution at steady state is approximately 3 to 5 L/kg.
      17. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:8ed06e0e-c17b-4c71-8d03-888bcde4a638 (opens source in a new tab)

        Fulvestrant label

        Version not recorded · Effective date not recorded

        Month 3 C max (ng/mL) C min (ng/mL) AUC (ng.hr/mL) 500 mg + AD 1 Single dose 25.1 (35.3) 16.3 (25.9) 11400 (33.4) Multiple dose steady state 2 28.0 (27.9) 12.2 (21.7) 13100 (23.4) Distribution The apparent volume of distribution at steady state is approximately 3 to 5 L/kg.
      18. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:2fc17ba3-83c7-a2b4-8a75-6a0cb1e07682 (opens source in a new tab)

        Fulvestrant label

        Version not recorded · Effective date not recorded

        3 (25.9) 11400 (33.4) Multiple dose steady state 2 28.0 (27.9) 12.2 (21.7) 13100 (23.4) 1 Additional 500 mg dose given on Day 15 2 Month 3 Distribution: The apparent volume of distribution at steady state is approximately 3 to 5 L/kg.
      19. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:d5ae9e07-73b0-4063-a9e4-0ffc5614c2b8 (opens source in a new tab)

        Fulvestrant label

        Version not recorded · Effective date not recorded

        ng.hr/mL) 500 mg + AD 1 Single dose 25.1 (35.3) 16.3 (25.9) 11400 (33.4) Multiple dose steady state 2 28.0 (27.9) 12.2 (21.7) 13100 (23.4) Distribution: The apparent volume of distribution at steady state is approximately 3 to 5 L/kg.
      20. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:b471eb51-488e-5312-e053-2a95a90a8116 (opens source in a new tab)

        Fulvestrant label

        Version not recorded · Effective date not recorded

        e given on Day 15 Single dose 25.1 (35.3) 16.3 (25.9) 11400 (33.4) Multiple dose steady state Month 3 28.0 (27.9) 12.2 (21.7) 13100 (23.4) Distribution: The apparent volume of distribution at steady state is approximately 3 to 5 L/kg.
      21. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:bc7b4eac-3b63-53d2-e053-2995a90ad5e7 (opens source in a new tab)

        Fulvestrant label

        Version not recorded · Effective date not recorded

        Month 3 Distribution: The apparent volume of distribution at steady-state is approximately 3 to 5 L/kg.
      22. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:015fafb6-23f7-4566-9c23-386eee7b035d (opens source in a new tab)

        Fulvestrant label

        Version not recorded · Effective date not recorded

        (ng.hr/mL) 500 mg + AD 1 Single dose 25.1 (35.3) 16.3 (25.9) 11400 (33.4) Multiple dose steady state 2 28.0 (27.9) 12.2 (21.7) 13100 (23.4) Distribution The apparent volume of distribution at steady state is approximately 3 to 5 L/kg.
      23. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:141f439e-078c-4a59-acff-ebf7685f55b8 (opens source in a new tab)

        Fulvestrant label

        Version not recorded · Effective date not recorded

        16.3 (25.9) 11400 (33.4) Multiple dose steady state † 28 (27.9) 12.2 (21.7) 13100 (23.4) * Additional 500 mg dose given on Day 15 † Month 3 Distribution The apparent volume of distribution at steady state is approximately 3 to 5 L/kg.
    2. 3 L/kg

      Numeric value
      3
      Unit
      L/kg
      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:a51aa693-b433-4b2d-a71b-9ba029b10ce3 (opens source in a new tab)

        Fulvestrant label

        Version not recorded · Effective date not recorded

        Month 3 Distribution: The apparent volume of distribution at steady-state is approximately 3 L/kg to 5 L/kg.
      2. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:f36f19ad-f044-4dba-80b6-d074ddffcd86 (opens source in a new tab)

        Fulvestrant label

        Version not recorded · Effective date not recorded

        Month 3 Distribution: The apparent volume of distribution at steady-state is approximately 3 L/kg to 5 L/kg.

Access

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GET /api/datasets/source-consensus?limit=10&offset=650

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