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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 821830 of 1,681 matching rows. Filters and search terms remain attached when you move between pages or open the API view.

  1. Projected row 821

    Medicine slug
    lanreotide
    Compared field
    halfLife
    Comparison state
    agree
    Reason codes
    • COMPATIBLE_VALUES_OVERLAP
    Documents examined
    4
    Source count
    4
    Agreement rate
    1
    Recorded readings
    1. 23 to 30 days

      Numeric value
      Not parsed
      Unit
      Not recorded
      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:11da176a-99bc-4ada-8b3f-6bd2b37a6313 (opens source in a new tab)

        Lanreotide label

        Version not recorded · Effective date not recorded

        Lanreotide showed sustained release of lanreotide with a half-life of 23 to 30 days.
      2. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:2892b4c3-0329-4d29-97ff-3b45283bbab1 (opens source in a new tab)

        Lanreotide label

        Version not recorded · Effective date not recorded

        Lanreotide acetate showed sustained release of lanreotide with a half-life of 23 to 30 days.
      3. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:6e4a41fd-a753-4362-87ee-8cc56ed3660d (opens source in a new tab)

        Lanreotide label

        Version not recorded · Effective date not recorded

        SOMATULINE DEPOT showed sustained release of lanreotide with a half-life of 23 to 30 days.
      4. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:eec3c37e-83a7-4195-bccf-cd5973459eef (opens source in a new tab)

        Lanreotide label

        Version not recorded · Effective date not recorded

        Lanreotide acetate showed sustained release of lanreotide with a half-life of 23 to 30 days.
  2. Projected row 822

    Medicine slug
    lansoprazole
    Compared field
    bioavailability
    Comparison state
    agree
    Reason codes
    • COMPATIBLE_VALUES_OVERLAP
    Documents examined
    102
    Source count
    61
    Agreement rate
    1
    Recorded readings
    1. 80%

      Numeric value
      80
      Unit
      %
      Source records
      61

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

      Show all 61 source records
      1. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:9e246e79-2737-4cbb-ad5d-4e76893da3be (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        The absolute bioavailability is over 80%.
      2. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:33fc642c-ad41-410b-9a81-eae456f3fcfb (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        The absolute bioavailability is over 80%.
      3. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:03b7dceb-2128-4324-b068-7f76a2d9887e (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        The absolute bioavailability is over 80%.
      4. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:7d811f01-f0c2-4753-bb36-80b48dabb58c (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Absorption: The absorption of lansoprazole is rapid, with the mean C max occurring approximately 1.7 hours after oral dosing, and the absolute bioavailability is over 80%.
      5. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:6d81faf7-aa59-429c-e053-2a91aa0a8bb2 (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Absorption: The absorption of lansoprazole is rapid, with the mean C max occurring approximately 1.7 hours after oral dosing, and the absolute bioavailability is over 80%.
      6. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:dee80a19-e514-41e6-9153-c959699d97b1 (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        The absolute bioavailability is over 80%.
      7. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:656bc92a-1f95-047d-cd27-724073e63fe6 (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        The absolute bioavailability is over 80%.
      8. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:71ba78cb-7e46-43eb-9425-fa130f537f84 (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        The absolute bioavailability is over 80%.
      9. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:dfdc9aa0-8612-9127-e053-2a95a90ae7c8 (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        The absolute bioavailability is over 80%.
      10. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:9b3869ad-f2f7-4954-b75c-5c23b8951635 (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        The absolute bioavailability is over 80%.
      11. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:a612a237-ec17-49f0-8985-44407608adb5 (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        The absolute bioavailability is over 80%.
      12. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:ce1a4f32-da65-29d3-e053-2995a90a42ee (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        The absolute bioavailability is over 80%.
      13. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:1bbb8f3a-80bf-b881-e063-6294a90ab4f2 (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        The absolute bioavailability is over 80%.
      14. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:960d6601-aec5-4900-a400-385b6687a4bc (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        The absolute bioavailability is over 80%.
      15. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:18b4020f-d7e6-42f8-838d-2b5da152530e (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        The absolute bioavailability is over 80%.
      16. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:ac051296-6fe3-4ab5-a001-cc3e06199a22 (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        The absolute bioavailability is over 80%.
      17. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:427cf924-be17-47dc-8f77-115fa2f3fe17 (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        The absolute bioavailability is over 80%.
      18. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:db42468a-450c-4b12-b2f2-e9a76e976d45 (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        The absolute bioavailability is over 80%.
      19. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:7286d6a5-611b-4993-ab93-4899d599435d (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        The absolute bioavailability is over 80%.
      20. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:22f416bf-00f1-ceb9-e063-6394a90aa1dd (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        The absolute bioavailability is over 80%.
      21. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:b12cca1c-da28-67e2-e053-2a95a90aaf6b (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        The absolute bioavailability is over 80%.
      22. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:136ad992-2e39-dad9-e063-6294a90adcc6 (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        The absolute bioavailability is over 80%.
      23. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:e07c7445-9652-4833-8b17-45c0124c4e5d (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        The absolute bioavailability is over 80%.
      24. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:4c7cc078-09de-f4fc-d111-1248f2261d17 (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        The absolute bioavailability is over 80%.
      25. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:7a79feee-2e21-4cd0-a720-c59643764303 (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        The absolute bioavailability is over 80%.
      26. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:8bbc3af5-faa1-4af1-94e9-9df4aae242ab (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        The absolute bioavailability is over 80%.
      27. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:00a574e0-bd03-deea-9f85-b108f78982ba (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        The absolute bioavailability is over 80%.
      28. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:ae03d05b-0a0f-4bae-bbdc-450b7b5f7a92 (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        The absolute bioavailability is over 80%.
      29. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:9a277b9e-2e13-27c3-e053-2995a90a7ed5 (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        The absolute bioavailability is over 80%.
      30. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:37b221ee-b6a4-76e8-e063-6394a90a7e0b (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        The absolute bioavailability is over 80%.
      31. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:71be1129-8562-476e-9d9b-99a21cbf52ec (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        The absolute bioavailability is over 80%.
      32. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:1c364fc5-eb43-b12f-e063-6294a90a4319 (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        The absolute bioavailability is over 80%.
      33. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:551ae468-1a2d-43d6-a2a8-4e5f26e0f982 (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        The absolute bioavailability is over 80%.
      34. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:12b2e59b-2b7a-4d22-ad9b-9a7d9a5264bd (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        The absolute bioavailability is over 80%.
      35. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:82174fcc-1b0f-2068-7fc4-db335b43b5e2 (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        The absolute bioavailability is over 80%.
      36. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:1dc026b6-b521-4a46-9a74-8c1c140d5329 (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        The absolute bioavailability is over 80%.
      37. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:16dc1e02-4679-4d7f-a65b-6e3706655d35 (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        The absolute bioavailability is over 80%.
      38. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:afcc0f14-8b00-41ac-8e62-4094a15b959c (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        The absolute bioavailability is over 80%.
      39. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:a9dd7e56-1aee-5f0b-e053-2995a90a43bf (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        The absolute bioavailability is over 80%.
      40. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:eea82d0b-6600-4693-a2b8-596a55458f61 (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        The absolute bioavailability is over 80%.
      41. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:e7a3aa37-9c9b-43fe-92be-6e0fdc8d1c92 (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        The absolute bioavailability is over 80%.
      42. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:924c5a35-4804-4e14-a2fc-2b84d186d257 (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        The absolute bioavailability is over 80%.
      43. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:20ff347c-ca18-497b-948d-1145035f2ffc (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        The absolute bioavailability is over 80%.
      44. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:8f0d3f2f-91d9-467a-a841-540664af80f9 (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        The absolute bioavailability is over 80%.
      45. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:c8fa7401-907f-41b6-a2e1-f4bc214f2cdf (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        The absolute bioavailability is over 80%.
      46. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:75691c2d-2265-4153-bc3a-4f7d5d51e250 (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        The absolute bioavailability is over 80%.
      47. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:cc006372-32d3-4539-921a-6bc9ec496b28 (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        The absolute bioavailability is over 80%.
      48. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:e0299cf2-8a8e-499b-a81e-16e844ea3aff (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        The absolute bioavailability is over 80%.
      49. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:495d3ca8-d37d-440a-80ce-9342d9ff281a (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        The absolute bioavailability is over 80%.
      50. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:3e3e63df-e2ad-420b-acb9-28e65ea6fb07 (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Absorption: The absorption of lansoprazole is rapid, with the mean C max occurring approximately 1.7 hours after oral dosing, and the absolute bioavailability is over 80%.
      51. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:44f07613-35be-4673-98f0-4b2467acce9c (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        The absolute bioavailability is over 80%.
      52. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:c77da981-9260-fabd-e053-2a95a90aa71c (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        The absolute bioavailability is over 80%.
      53. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:56cafcf5-ce3d-a312-e063-6294a90a3db1 (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        The absolute bioavailability is over 80%.
      54. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:11344047-7ed4-61e7-e063-6394a90a332d (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        The absolute bioavailability is over 80%.
      55. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:3babf7d9-ad83-4e44-8e5d-f6c11b2d76b6 (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        The absolute bioavailability is over 80%.
      56. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:c9a43df0-efab-4486-860f-92afdb258c8b (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        The absolute bioavailability is over 80%.
      57. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:47a8618c-e768-41bf-9116-634b564405d4 (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        The absolute bioavailability is over 80%.
      58. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:1f2883d8-12db-40b7-9104-22a6690a22a7 (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        The absolute bioavailability is over 80%.
      59. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:6b8dd0e1-cd69-4f9a-887f-e42627b5d78e (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        The absolute bioavailability is over 80%.
      60. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:6b9c60e9-b0d2-4aec-a04b-ccc7a62c822b (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        The absolute bioavailability is over 80%.
      61. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:854e4235-4815-4461-9b9b-d3d783fb775d (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        The absolute bioavailability is over 80%.
  3. Projected row 823

    Medicine slug
    lansoprazole
    Compared field
    halfLife
    Comparison state
    insufficient_context
    Reason codes
    • STRUCTURED_CONTEXT_MISSING
    Documents examined
    102
    Source count
    61
    Agreement rate
    0.95082
    Recorded readings
    1. 1.9 to 2.9 hours

      Numeric value
      1.9
      Unit
      hours
      Source records
      58

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

      Show all 58 source records
      1. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:9e246e79-2737-4cbb-ad5d-4e76893da3be (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Because the mean half-life in the elderly remains between 1.9 to 2.9 hours, repeated once daily dosing does not result in accumulation of lansoprazole.
      2. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:33fc642c-ad41-410b-9a81-eae456f3fcfb (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Because the mean half-life in the elderly remains between 1.9 to 2.9 hours, repeated once daily dosing does not result in accumulation of lansoprazole.
      3. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:03b7dceb-2128-4324-b068-7f76a2d9887e (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Because the mean half-life in the elderly remains between 1.9 to 2.9 hours, repeated once daily dosing does not result in accumulation of lansoprazole.
      4. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:dee80a19-e514-41e6-9153-c959699d97b1 (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Because the mean half-life in the elderly remains between 1.9 to 2.9 hours, repeated once daily dosing does not result in accumulation of lansoprazole.
      5. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:656bc92a-1f95-047d-cd27-724073e63fe6 (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Because the mean half-life in the elderly remains between 1.9 to 2.9 hours, repeated once daily dosing does not result in accumulation of lansoprazole.
      6. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:71ba78cb-7e46-43eb-9425-fa130f537f84 (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Because the mean half-life in the elderly remains between 1.9 to 2.9 hours, repeated once daily dosing does not result in accumulation of lansoprazole.
      7. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:dfdc9aa0-8612-9127-e053-2a95a90ae7c8 (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Because the mean half-life in the elderly remains between 1.9 to 2.9 hours, repeated once daily dosing does not result in accumulation of lansoprazole.
      8. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:9b3869ad-f2f7-4954-b75c-5c23b8951635 (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Because the mean half-life in the elderly remains between 1.9 to 2.9 hours, repeated once daily dosing does not result in accumulation of lansoprazole.
      9. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:a612a237-ec17-49f0-8985-44407608adb5 (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Because the mean half-life in the elderly remains between 1.9 to 2.9 hours, repeated once daily dosing does not result in accumulation of lansoprazole.
      10. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:ce1a4f32-da65-29d3-e053-2995a90a42ee (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Because the mean half-life in the elderly remains between 1.9 to 2.9 hours, repeated once daily dosing does not result in accumulation of lansoprazole.
      11. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:1bbb8f3a-80bf-b881-e063-6294a90ab4f2 (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Because the mean half-life in the elderly remains between 1.9 to 2.9 hours, repeated once daily dosing does not result in accumulation of lansoprazole.
      12. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:960d6601-aec5-4900-a400-385b6687a4bc (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Because the mean half-life in the elderly remains between 1.9 to 2.9 hours, repeated once daily dosing does not result in accumulation of lansoprazole.
      13. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:18b4020f-d7e6-42f8-838d-2b5da152530e (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Because the mean half-life in the elderly remains between 1.9 to 2.9 hours, repeated once daily dosing does not result in accumulation of lansoprazole.
      14. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:ac051296-6fe3-4ab5-a001-cc3e06199a22 (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Because the mean half-life in the elderly remains between 1.9 to 2.9 hours, repeated once daily dosing does not result in accumulation of lansoprazole.
      15. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:427cf924-be17-47dc-8f77-115fa2f3fe17 (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Because the mean half-life in the elderly remains between 1.9 to 2.9 hours, repeated once daily dosing does not result in accumulation of lansoprazole.
      16. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:db42468a-450c-4b12-b2f2-e9a76e976d45 (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Because the mean half-life in the elderly remains between 1.9 to 2.9 hours, repeated once daily dosing does not result in accumulation of lansoprazole.
      17. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:7286d6a5-611b-4993-ab93-4899d599435d (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Because the mean half-life in the elderly remains between 1.9 to 2.9 hours, repeated once daily dosing does not result in accumulation of lansoprazole.
      18. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:22f416bf-00f1-ceb9-e063-6394a90aa1dd (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Because the mean half-life in the elderly remains between 1.9 to 2.9 hours, repeated once daily dosing does not result in accumulation of lansoprazole.
      19. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:b12cca1c-da28-67e2-e053-2a95a90aaf6b (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Because the mean half-life in the elderly remains between 1.9 to 2.9 hours, repeated once daily dosing does not result in accumulation of lansoprazole.
      20. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:136ad992-2e39-dad9-e063-6294a90adcc6 (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Because the mean half-life in the elderly remains between 1.9 to 2.9 hours, repeated once daily dosing does not result in accumulation of lansoprazole.
      21. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:e07c7445-9652-4833-8b17-45c0124c4e5d (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Because the mean half-life in the elderly remains between 1.9 to 2.9 hours, repeated once daily dosing does not result in accumulation of lansoprazole.
      22. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:4c7cc078-09de-f4fc-d111-1248f2261d17 (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Because the mean half-life in the elderly remains between 1.9 to 2.9 hours, repeated once daily dosing does not result in accumulation of lansoprazole.
      23. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:7a79feee-2e21-4cd0-a720-c59643764303 (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Because the mean half-life in the elderly remains between 1.9 to 2.9 hours, repeated once daily dosing does not result in accumulation of lansoprazole.
      24. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:8bbc3af5-faa1-4af1-94e9-9df4aae242ab (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Because the mean half-life in the elderly remains between 1.9 to 2.9 hours, repeated once daily dosing does not result in accumulation of lansoprazole.
      25. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:00a574e0-bd03-deea-9f85-b108f78982ba (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Because the mean half-life in the elderly remains between 1.9 to 2.9 hours, repeated once daily dosing does not result in accumulation of lansoprazole.
      26. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:ae03d05b-0a0f-4bae-bbdc-450b7b5f7a92 (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Because the mean half-life in the elderly remains between 1.9 to 2.9 hours, repeated once daily dosing does not result in accumulation of lansoprazole.
      27. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:9a277b9e-2e13-27c3-e053-2995a90a7ed5 (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Because the mean half-life in the elderly remains between 1.9 to 2.9 hours, repeated once daily dosing does not result in accumulation of lansoprazole.
      28. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:37b221ee-b6a4-76e8-e063-6394a90a7e0b (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Because the mean half-life in the elderly remains between 1.9 to 2.9 hours, repeated once daily dosing does not result in accumulation of lansoprazole.
      29. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:71be1129-8562-476e-9d9b-99a21cbf52ec (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Because the mean half-life in the elderly remains between 1.9 to 2.9 hours, repeated once daily dosing does not result in accumulation of lansoprazole.
      30. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:1c364fc5-eb43-b12f-e063-6294a90a4319 (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Because the mean half-life in the elderly remains between 1.9 to 2.9 hours, repeated once daily dosing does not result in accumulation of lansoprazole.
      31. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:551ae468-1a2d-43d6-a2a8-4e5f26e0f982 (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Because the mean half-life in the elderly remains between 1.9 to 2.9 hours, repeated once daily dosing does not result in accumulation of lansoprazole.
      32. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:12b2e59b-2b7a-4d22-ad9b-9a7d9a5264bd (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Because the mean half-life in the elderly remains between 1.9 to 2.9 hours, repeated once daily dosing does not result in accumulation of lansoprazole.
      33. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:82174fcc-1b0f-2068-7fc4-db335b43b5e2 (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Because the mean half-life in the elderly remains between 1.9 to 2.9 hours, repeated once daily dosing does not result in accumulation of lansoprazole.
      34. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:1dc026b6-b521-4a46-9a74-8c1c140d5329 (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Because the mean half-life in the elderly remains between 1.9 to 2.9 hours, repeated once daily dosing does not result in accumulation of lansoprazole.
      35. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:16dc1e02-4679-4d7f-a65b-6e3706655d35 (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Because the mean half-life in the elderly remains between 1.9 to 2.9 hours, repeated once daily dosing does not result in accumulation of lansoprazole.
      36. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:afcc0f14-8b00-41ac-8e62-4094a15b959c (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Because the mean half-life in the elderly remains between 1.9 to 2.9 hours, repeated once daily dosing does not result in accumulation of lansoprazole.
      37. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:a9dd7e56-1aee-5f0b-e053-2995a90a43bf (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Because the mean half-life in the elderly remains between 1.9 to 2.9 hours, repeated once daily dosing does not result in accumulation of lansoprazole.
      38. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:eea82d0b-6600-4693-a2b8-596a55458f61 (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Because the mean half-life in the elderly remains between 1.9 to 2.9 hours, repeated once daily dosing does not result in accumulation of lansoprazole.
      39. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:e7a3aa37-9c9b-43fe-92be-6e0fdc8d1c92 (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Because the mean half-life in the elderly remains between 1.9 to 2.9 hours, repeated once daily dosing does not result in accumulation of lansoprazole.
      40. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:924c5a35-4804-4e14-a2fc-2b84d186d257 (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Because the mean half-life in the elderly remains between 1.9 to 2.9 hours, repeated once daily dosing does not result in accumulation of lansoprazole.
      41. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:20ff347c-ca18-497b-948d-1145035f2ffc (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Because the mean half-life in the elderly remains between 1.9 to 2.9 hours, repeated once daily dosing does not result in accumulation of lansoprazole.
      42. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:8f0d3f2f-91d9-467a-a841-540664af80f9 (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Because the mean half-life in the elderly remains between 1.9 to 2.9 hours, repeated once daily dosing does not result in accumulation of lansoprazole.
      43. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:c8fa7401-907f-41b6-a2e1-f4bc214f2cdf (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Because the mean half-life in the elderly remains between 1.9 to 2.9 hours, repeated once daily dosing does not result in accumulation of lansoprazole.
      44. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:75691c2d-2265-4153-bc3a-4f7d5d51e250 (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Because the mean half-life in the elderly remains between 1.9 to 2.9 hours, repeated once daily dosing does not result in accumulation of lansoprazole.
      45. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:cc006372-32d3-4539-921a-6bc9ec496b28 (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Because the mean half-life in the elderly remains between 1.9 to 2.9 hours, repeated once daily dosing does not result in accumulation of lansoprazole.
      46. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:e0299cf2-8a8e-499b-a81e-16e844ea3aff (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Because the mean half-life in the elderly remains between 1.9 to 2.9 hours, repeated once daily dosing does not result in accumulation of lansoprazole.
      47. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:495d3ca8-d37d-440a-80ce-9342d9ff281a (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Because the mean half-life in the elderly remains between 1.9 to 2.9 hours, repeated once daily dosing does not result in accumulation of lansoprazole.
      48. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:44f07613-35be-4673-98f0-4b2467acce9c (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Because the mean half-life in the elderly remains between 1.9 to 2.9 hours, repeated once daily dosing does not result in accumulation of lansoprazole.
      49. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:c77da981-9260-fabd-e053-2a95a90aa71c (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Because the mean half-life in the elderly remains between 1.9 to 2.9 hours, repeated once daily dosing does not result in accumulation of lansoprazole.
      50. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:56cafcf5-ce3d-a312-e063-6294a90a3db1 (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Because the mean half-life in the elderly remains between 1.9 to 2.9 hours, repeated once daily dosing does not result in accumulation of lansoprazole.
      51. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:11344047-7ed4-61e7-e063-6394a90a332d (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Because the mean half-life in the elderly remains between 1.9 to 2.9 hours, repeated once daily dosing does not result in accumulation of lansoprazole.
      52. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:3babf7d9-ad83-4e44-8e5d-f6c11b2d76b6 (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Because the mean half-life in the elderly remains between 1.9 to 2.9 hours, repeated once daily dosing does not result in accumulation of lansoprazole.
      53. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:c9a43df0-efab-4486-860f-92afdb258c8b (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Because the mean half-life in the elderly remains between 1.9 to 2.9 hours, repeated once daily dosing does not result in accumulation of lansoprazole.
      54. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:47a8618c-e768-41bf-9116-634b564405d4 (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Because the mean half-life in the elderly remains between 1.9 to 2.9 hours, repeated once daily dosing does not result in accumulation of lansoprazole.
      55. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:1f2883d8-12db-40b7-9104-22a6690a22a7 (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Because the mean half-life in the elderly remains between 1.9 to 2.9 hours, repeated once daily dosing does not result in accumulation of lansoprazole.
      56. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:6b8dd0e1-cd69-4f9a-887f-e42627b5d78e (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Because the mean half-life in the elderly remains between 1.9 to 2.9 hours, repeated once daily dosing does not result in accumulation of lansoprazole.
      57. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:6b9c60e9-b0d2-4aec-a04b-ccc7a62c822b (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Because the mean half-life in the elderly remains between 1.9 to 2.9 hours, repeated once daily dosing does not result in accumulation of lansoprazole.
      58. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:854e4235-4815-4461-9b9b-d3d783fb775d (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Because the mean half-life in the elderly remains between 1.9 to 2.9 hours, repeated once daily dosing does not result in accumulation of lansoprazole.
    2. 2 hours

      Numeric value
      2
      Unit
      hours
      Source records
      3

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

      Show all 3 source records
      1. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:7d811f01-f0c2-4753-bb36-80b48dabb58c (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        The plasma elimination half-life of lansoprazole is less than 2 hours while the acid inhibitory effect lasts more than 24 hours.
      2. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:6d81faf7-aa59-429c-e053-2a91aa0a8bb2 (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        The plasma elimination half-life of lansoprazole is less than 2 hours while the acid inhibitory effect lasts more than 24 hours.
      3. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:3e3e63df-e2ad-420b-acb9-28e65ea6fb07 (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        The plasma elimination half-life of lansoprazole is less than 2 hours while the acid inhibitory effect lasts more than 24 hours.
  4. Projected row 824

    Medicine slug
    lansoprazole
    Compared field
    proteinBinding
    Comparison state
    insufficient_context
    Reason codes
    • STRUCTURED_CONTEXT_MISSING
    Documents examined
    102
    Source count
    61
    Agreement rate
    0.754098
    Recorded readings
    1. 1 to 1.5%

      Numeric value
      1
      Unit
      %
      Source records
      46

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

      Show all 46 source records
      1. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:9e246e79-2737-4cbb-ad5d-4e76893da3be (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Patients with Renal Impairment: In patients with severe renal impairment, plasma protein binding decreased by 1 to 1.5% after administration of 60 mg of lansoprazole.
      2. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:33fc642c-ad41-410b-9a81-eae456f3fcfb (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Patients with Renal Impairment: In patients with severe renal impairment, plasma protein binding decreased by 1 to 1.5% after administration of 60 mg of lansoprazole.
      3. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:03b7dceb-2128-4324-b068-7f76a2d9887e (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Patients with Renal Impairment: In patients with severe renal impairment, plasma protein binding decreased by 1 to 1.5% after administration of 60 mg of lansoprazole.
      4. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:dee80a19-e514-41e6-9153-c959699d97b1 (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Patients with Renal Impairment: In patients with severe renal impairment, plasma protein binding decreased by 1 to 1.5% after administration of 60 mg of lansoprazole.
      5. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:656bc92a-1f95-047d-cd27-724073e63fe6 (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Patients with Renal Impairment: In patients with severe renal impairment, plasma protein binding decreased by 1 to 1.5% after administration of 60 mg of lansoprazole.
      6. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:71ba78cb-7e46-43eb-9425-fa130f537f84 (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Patients with Renal Impairment: In patients with severe renal impairment, plasma protein binding decreased by 1 to 1.5% after administration of 60 mg of lansoprazole.
      7. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:dfdc9aa0-8612-9127-e053-2a95a90ae7c8 (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Patients with Renal Impairment: In patients with severe renal impairment, plasma protein binding decreased by 1 to 1.5% after administration of 60 mg of lansoprazole.
      8. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:9b3869ad-f2f7-4954-b75c-5c23b8951635 (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Patients with Renal Impairment: In patients with severe renal impairment, plasma protein binding decreased by 1 to 1.5% after administration of 60 mg of lansoprazole.
      9. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:ce1a4f32-da65-29d3-e053-2995a90a42ee (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Patients with Renal Impairment: In patients with severe renal impairment, plasma protein binding decreased by 1 to 1.5% after administration of 60 mg of lansoprazole.
      10. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:1bbb8f3a-80bf-b881-e063-6294a90ab4f2 (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Patients with Renal Impairment: In patients with severe renal impairment, plasma protein binding decreased by 1 to 1.5% after administration of 60 mg of lansoprazole.
      11. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:960d6601-aec5-4900-a400-385b6687a4bc (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Patients with Renal Impairment: In patients with severe renal impairment, plasma protein binding decreased by 1 to 1.5% after administration of 60 mg of lansoprazole.
      12. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:18b4020f-d7e6-42f8-838d-2b5da152530e (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Patients with Renal Impairment: In patients with severe renal impairment, plasma protein binding decreased by 1 to 1.5% after administration of 60 mg of lansoprazole.
      13. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:ac051296-6fe3-4ab5-a001-cc3e06199a22 (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Patients with Renal Impairment: In patients with severe renal impairment, plasma protein binding decreased by 1 to 1.5% after administration of 60 mg of lansoprazole.
      14. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:427cf924-be17-47dc-8f77-115fa2f3fe17 (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Patients with Renal Impairment: In patients with severe renal impairment, plasma protein binding decreased by 1 to 1.5% after administration of 60 mg of lansoprazole.
      15. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:7286d6a5-611b-4993-ab93-4899d599435d (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Patients with Renal Impairment: In patients with severe renal impairment, plasma protein binding decreased by 1 to 1.5% after administration of 60 mg of lansoprazole.
      16. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:22f416bf-00f1-ceb9-e063-6394a90aa1dd (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Patients with Renal Impairment: In patients with severe renal impairment, plasma protein binding decreased by 1 to 1.5% after administration of 60 mg of lansoprazole.
      17. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:b12cca1c-da28-67e2-e053-2a95a90aaf6b (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Patients with Renal Impairment: In patients with severe renal impairment, plasma protein binding decreased by 1 to 1.5% after administration of 60 mg of lansoprazole.
      18. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:136ad992-2e39-dad9-e063-6294a90adcc6 (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Patients with Renal Impairment: In patients with severe renal impairment, plasma protein binding decreased by 1 to 1.5% after administration of 60 mg of lansoprazole.
      19. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:e07c7445-9652-4833-8b17-45c0124c4e5d (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Patients with Renal Impairment: In patients with severe renal impairment, plasma protein binding decreased by 1 to 1.5% after administration of 60 mg of lansoprazole.
      20. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:4c7cc078-09de-f4fc-d111-1248f2261d17 (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Patients with Renal Impairment: In patients with severe renal impairment, plasma protein binding decreased by 1 to 1.5% after administration of 60 mg of lansoprazole.
      21. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:7a79feee-2e21-4cd0-a720-c59643764303 (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Patients with Renal Impairment In patients with severe renal impairment, plasma protein binding decreased by 1 to 1.5% after administration of 60 mg of lansoprazole.
      22. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:8bbc3af5-faa1-4af1-94e9-9df4aae242ab (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Patients with Renal Impairment: In patients with severe renal impairment, plasma protein binding decreased by 1 to 1.5% after administration of 60 mg of lansoprazole.
      23. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:9a277b9e-2e13-27c3-e053-2995a90a7ed5 (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Patients with Renal Impairment: In patients with severe renal impairment, plasma protein binding decreased by 1 to 1.5% after administration of 60 mg of lansoprazole.
      24. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:71be1129-8562-476e-9d9b-99a21cbf52ec (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Patients with Renal Impairment: In patients with severe renal impairment, plasma protein binding decreased by 1 to 1.5% after administration of 60 mg of lansoprazole.
      25. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:1c364fc5-eb43-b12f-e063-6294a90a4319 (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Patients with Renal Impairment: In patients with severe renal impairment, plasma protein binding decreased by 1 to 1.5% after administration of 60 mg of lansoprazole.
      26. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:551ae468-1a2d-43d6-a2a8-4e5f26e0f982 (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Patients with Renal Impairment: In patients with severe renal impairment, plasma protein binding decreased by 1 to 1.5% after administration of 60 mg of lansoprazole.
      27. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:12b2e59b-2b7a-4d22-ad9b-9a7d9a5264bd (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Patients with Renal Impairment: In patients with severe renal impairment, plasma protein binding decreased by 1 to 1.5% after administration of 60 mg of lansoprazole.
      28. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:82174fcc-1b0f-2068-7fc4-db335b43b5e2 (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Patients with Renal Impairment: In patients with severe renal impairment, plasma protein binding decreased by 1 to 1.5% after administration of 60 mg of lansoprazole.
      29. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:afcc0f14-8b00-41ac-8e62-4094a15b959c (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Patients with Renal Impairment: In patients with severe renal impairment, plasma protein binding decreased by 1 to 1.5% after administration of 60 mg of lansoprazole.
      30. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:eea82d0b-6600-4693-a2b8-596a55458f61 (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Patients with Renal Impairment In patients with severe renal impairment, plasma protein binding decreased by 1 to 1.5% after administration of 60 mg of lansoprazole.
      31. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:e7a3aa37-9c9b-43fe-92be-6e0fdc8d1c92 (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Patients with Renal Impairment: In patients with severe renal impairment, plasma protein binding decreased by 1 to 1.5% after administration of 60 mg of lansoprazole.
      32. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:924c5a35-4804-4e14-a2fc-2b84d186d257 (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Patients with Renal Impairment : In patients with severe renal impairment, plasma protein binding decreased by 1 to 1.5% after administration of 60 mg of lansoprazole.
      33. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:20ff347c-ca18-497b-948d-1145035f2ffc (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Patients with Renal Impairment In patients with severe renal impairment, plasma protein binding decreased by 1 to 1.5% after administration of 60 mg of lansoprazole.
      34. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:8f0d3f2f-91d9-467a-a841-540664af80f9 (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Patients with Renal Impairment: In patients with severe renal impairment, plasma protein binding decreased by 1 to 1.5% after administration of 60 mg of lansoprazole.
      35. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:c8fa7401-907f-41b6-a2e1-f4bc214f2cdf (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Patients with Renal Impairment In patients with severe renal impairment, plasma protein binding decreased by 1 to 1.5% after administration of 60 mg of lansoprazole.
      36. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:75691c2d-2265-4153-bc3a-4f7d5d51e250 (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Patients with Renal Impairment: In patients with severe renal impairment, plasma protein binding decreased by 1 to 1.5% after administration of 60 mg of lansoprazole.
      37. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:cc006372-32d3-4539-921a-6bc9ec496b28 (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Patients with Renal Impairment: In patients with severe renal impairment, plasma protein binding decreased by 1 to 1.5% after administration of 60 mg of lansoprazole.
      38. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:495d3ca8-d37d-440a-80ce-9342d9ff281a (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Patients with Renal Impairment: In patients with severe renal impairment, plasma protein binding decreased by 1 to 1.5% after administration of 60 mg of lansoprazole.
      39. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:c77da981-9260-fabd-e053-2a95a90aa71c (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Patients with Renal Impairment: In patients with severe renal impairment, plasma protein binding decreased by 1 to 1.5% after administration of 60 mg of lansoprazole.
      40. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:56cafcf5-ce3d-a312-e063-6294a90a3db1 (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Patients with Renal Impairment: In patients with severe renal impairment, plasma protein binding decreased by 1 to 1.5% after administration of 60 mg of lansoprazole.
      41. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:c9a43df0-efab-4486-860f-92afdb258c8b (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Patients with Renal Impairment: In patients with severe renal impairment, plasma protein binding decreased by 1 to 1.5% after administration of 60 mg of lansoprazole.
      42. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:47a8618c-e768-41bf-9116-634b564405d4 (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Patients with Renal Impairment In patients with severe renal impairment, plasma protein binding decreased by 1 to 1.5% after administration of 60 mg of lansoprazole.
      43. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:1f2883d8-12db-40b7-9104-22a6690a22a7 (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Patients with Renal Impairment: In patients with severe renal impairment, plasma protein binding decreased by 1 to 1.5% after administration of 60 mg of lansoprazole.
      44. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:6b8dd0e1-cd69-4f9a-887f-e42627b5d78e (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Patients with Renal Impairment: In patients with severe renal impairment, plasma protein binding decreased by 1 to 1.5% after administration of 60 mg of lansoprazole.
      45. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:6b9c60e9-b0d2-4aec-a04b-ccc7a62c822b (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Patients with Renal Impairment: In patients with severe renal impairment, plasma protein binding decreased by 1 to 1.5% after administration of 60 mg of lansoprazole.
      46. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:854e4235-4815-4461-9b9b-d3d783fb775d (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Patients with Renal Impairment: In patients with severe renal impairment, plasma protein binding decreased by 1 to 1.5% after administration of 60 mg of lansoprazole.
    2. 1.0%

      Numeric value
      1
      Unit
      %
      Source records
      12

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

      Show all 12 source records
      1. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:a612a237-ec17-49f0-8985-44407608adb5 (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Patients with Renal Impairment: In patients with severe renal impairment, plasma protein binding decreased by 1.0% to 1.5% after administration of 60 mg of lansoprazole.
      2. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:db42468a-450c-4b12-b2f2-e9a76e976d45 (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Patients with Renal Impairment: In patients with severe renal impairment, plasma protein binding decreased by 1.0% to 1.5% after administration of 60 mg of lansoprazole.
      3. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:00a574e0-bd03-deea-9f85-b108f78982ba (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Patients with Renal Impairment: In patients with severe renal impairment, plasma protein binding decreased by 1.0% to 1.5% after administration of 60 mg of lansoprazole.
      4. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:ae03d05b-0a0f-4bae-bbdc-450b7b5f7a92 (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Patients with Renal Impairment: In patients with severe renal impairment, plasma protein binding decreased by 1.0% to 1.5% after administration of 60 mg of lansoprazole.
      5. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:37b221ee-b6a4-76e8-e063-6394a90a7e0b (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Patients with Renal Impairment: In patients with severe renal impairment, plasma protein binding decreased by 1.0% to 1.5% after administration of 60 mg of lansoprazole.
      6. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:1dc026b6-b521-4a46-9a74-8c1c140d5329 (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Patients with Renal Impairment: In patients with severe renal impairment, plasma protein binding decreased by 1.0% to 1.5% after administration of 60 mg of lansoprazole.
      7. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:16dc1e02-4679-4d7f-a65b-6e3706655d35 (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Patients with Renal Impairment: In patients with severe renal impairment, plasma protein binding decreased by 1.0% to 1.5% after administration of 60 mg of lansoprazole.
      8. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:a9dd7e56-1aee-5f0b-e053-2995a90a43bf (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Patients with Renal Impairment: In patients with severe renal impairment, plasma protein binding decreased by 1.0% to 1.5% after administration of 60 mg of lansoprazole.
      9. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:e0299cf2-8a8e-499b-a81e-16e844ea3aff (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Patients with Renal Impairment: In patients with severe renal impairment, plasma protein binding decreased by 1.0% to 1.5% after administration of 60 mg of lansoprazole.
      10. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:44f07613-35be-4673-98f0-4b2467acce9c (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Patients with Renal Impairment: In patients with severe renal impairment, plasma protein binding decreased by 1.0% to 1.5% after administration of 60 mg of lansoprazole.
      11. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:11344047-7ed4-61e7-e063-6394a90a332d (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Patients with Renal Impairment: In patients with severe renal impairment, plasma protein binding decreased by 1.0% to 1.5% after administration of 60 mg of lansoprazole.
      12. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:3babf7d9-ad83-4e44-8e5d-f6c11b2d76b6 (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Patients with Renal Impairment: In patients with severe renal impairment, plasma protein binding decreased by 1.0% to 1.5% after administration of 60 mg of lansoprazole.
    3. 1%

      Numeric value
      1
      Unit
      %
      Source records
      3

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

      Show all 3 source records
      1. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:7d811f01-f0c2-4753-bb36-80b48dabb58c (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Renal Impairment: In patients with severe renal impairment, plasma protein binding decreased by 1% to 1.5% after administration of 60 mg of lansoprazole.
      2. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:6d81faf7-aa59-429c-e053-2a91aa0a8bb2 (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Renal Impairment: In patients with severe renal impairment, plasma protein binding decreased by 1% to 1.5% after administration of 60 mg of lansoprazole.
      3. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:3e3e63df-e2ad-420b-acb9-28e65ea6fb07 (opens source in a new tab)

        Lansoprazole label

        Version not recorded · Effective date not recorded

        Renal Impairment: In patients with severe renal impairment, plasma protein binding decreased by 1% to 1.5% after administration of 60 mg of lansoprazole.
  5. Projected row 825

    Medicine slug
    lanthanum-carbonate
    Compared field
    bioavailability
    Comparison state
    agree
    Reason codes
    • COMPATIBLE_VALUES_OVERLAP
    Documents examined
    7
    Source count
    7
    Agreement rate
    1
    Recorded readings
    1. 0.002%

      Numeric value
      0.002
      Unit
      %
      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:22b07167-2b7b-42ba-9ae9-cf58c98a2ab2 (opens source in a new tab)

        Lanthanum Carbonate label

        Version not recorded · Effective date not recorded

        12.3 Pharmacokinetics Absorption and Distribution -Following single-or multiple-dose oral administration of lanthanum carbonate to healthy subjects, the concentration of lanthanum in plasma was very low (bioavailability <0.002%).
      2. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:91556a42-5e16-4f86-bae9-a8cdd6b182a6 (opens source in a new tab)

        Lanthanum Carbonate label

        Version not recorded · Effective date not recorded

        12.3 Pharmacokinetics Absorption and Distribution -Following single- or multiple-dose oral administration of lanthanum carbonate chewable tablets to healthy subjects, the concentration of lanthanum in plasma was very low (bioavailability <0.002%).
      3. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:1d5ff930-1189-4e96-bdfb-9fd9c2c83d1b (opens source in a new tab)

        Lanthanum Carbonate label

        Version not recorded · Effective date not recorded

        12.3 Pharmacokinetics Absorption and Distribution - Following single- or multiple- dose oral administration of lanthanum carbonate to healthy subjects, the concentration of lanthanum in plasma was very low (bioavailability <0.002%).
      4. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:e4b88992-ecb0-455b-b68c-5c4e6d3cf521 (opens source in a new tab)

        Lanthanum Carbonate label

        Version not recorded · Effective date not recorded

        12.3 Pharmacokinetics Absorption and Distribution - Following single- or multiple-dose oral administration of lanthanum carbonate chewable tablets to healthy subjects, the concentration of lanthanum in plasma was very low (bioavailability <0.002%).
      5. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:bb263fe8-2bdf-4dba-807f-194f54a73654 (opens source in a new tab)

        Lanthanum Carbonate label

        Version not recorded · Effective date not recorded

        12.3 Pharmacokinetics Absorption and Distribution - Following single- or multiple-dose oral administration of LANTHANUM CARBONATE to healthy subjects, the concentration of lanthanum in plasma was very low (bioavailability <0.002%).
      6. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:16b0e6f5-4fc9-448c-994a-cb9dd8b03654 (opens source in a new tab)

        Lanthanum Carbonate label

        Version not recorded · Effective date not recorded

        12.3 Pharmacokinetics Absorption and Distribution - Following single- or multiple- dose oral administration of lanthanum carbonate to healthy subjects, the concentration of lanthanum in plasma was very low (bioavailability <0.002%).
      7. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:f10776b2-2c25-4343-aabe-68f302e5cb54 (opens source in a new tab)

        Lanthanum Carbonate label

        Version not recorded · Effective date not recorded

        12.3 Pharmacokinetics Absorption and Distribution - Following single- or multiple-dose oral administration of FOSRENOL to healthy subjects, the concentration of lanthanum in plasma was very low (bioavailability <0.002%).
  6. Projected row 826

    Medicine slug
    lanthanum-carbonate
    Compared field
    halfLife
    Comparison state
    agree
    Reason codes
    • COMPATIBLE_VALUES_OVERLAP
    Documents examined
    7
    Source count
    7
    Agreement rate
    1
    Recorded readings
    1. 53 hours

      Numeric value
      53
      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:22b07167-2b7b-42ba-9ae9-cf58c98a2ab2 (opens source in a new tab)

        Lanthanum Carbonate label

        Version not recorded · Effective date not recorded

        Lanthanum was cleared from plasma of patients undergoing dialysis with an elimination half-life of 53 hours following discontinuation of therapy.
      2. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:91556a42-5e16-4f86-bae9-a8cdd6b182a6 (opens source in a new tab)

        Lanthanum Carbonate label

        Version not recorded · Effective date not recorded

        Lanthanum was cleared from plasma of patients undergoing dialysis with an elimination half-life of 53 hours following discontinuation of therapy.
      3. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:1d5ff930-1189-4e96-bdfb-9fd9c2c83d1b (opens source in a new tab)

        Lanthanum Carbonate label

        Version not recorded · Effective date not recorded

        Lanthanum was cleared from plasma of patients undergoing dialysis with an elimination half-life of 53 hours following discontinuation of therapy.
      4. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:e4b88992-ecb0-455b-b68c-5c4e6d3cf521 (opens source in a new tab)

        Lanthanum Carbonate label

        Version not recorded · Effective date not recorded

        Lanthanum was cleared from plasma of patients undergoing dialysis with an elimination half-life of 53 hours following discontinuation of therapy.
      5. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:bb263fe8-2bdf-4dba-807f-194f54a73654 (opens source in a new tab)

        Lanthanum Carbonate label

        Version not recorded · Effective date not recorded

        Lanthanum was cleared from plasma of patients undergoing dialysis with an elimination half-life of 53 hours following discontinuation of therapy.
      6. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:16b0e6f5-4fc9-448c-994a-cb9dd8b03654 (opens source in a new tab)

        Lanthanum Carbonate label

        Version not recorded · Effective date not recorded

        Lanthanum was cleared from plasma of patients undergoing dialysis with an elimination half-life of 53 hours following discontinuation of therapy.
      7. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:f10776b2-2c25-4343-aabe-68f302e5cb54 (opens source in a new tab)

        Lanthanum Carbonate label

        Version not recorded · Effective date not recorded

        Lanthanum was cleared from plasma of patients undergoing dialysis with an elimination half-life of 53 hours following discontinuation of therapy.
  7. Projected row 827

    Medicine slug
    larotrectinib
    Compared field
    bioavailability
    Comparison state
    agree
    Reason codes
    • COMPATIBLE_VALUES_OVERLAP
    Documents examined
    2
    Source count
    2
    Agreement rate
    1
    Recorded readings
    1. 34%

      Numeric value
      34
      Unit
      %
      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:0c8ca614-58b2-4aa4-83d3-0387a8f782fd (opens source in a new tab)

        Larotrectinib label

        Version not recorded · Effective date not recorded

        Absorption The mean absolute bioavailability of VITRAKVI capsules was 34% (range: 32% to 37%).
      2. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:9525f887-a055-4e33-8e92-898d42828cd1 (opens source in a new tab)

        Larotrectinib label

        Version not recorded · Effective date not recorded

        Absorption The mean absolute bioavailability of VITRAKVI capsules was 34% (range: 32% to 37%).
  8. Projected row 828

    Medicine slug
    larotrectinib
    Compared field
    halfLife
    Comparison state
    agree
    Reason codes
    • COMPATIBLE_VALUES_OVERLAP
    Documents examined
    2
    Source count
    2
    Agreement rate
    1
    Recorded readings
    1. 2.9 hours

      Numeric value
      2.9
      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:0c8ca614-58b2-4aa4-83d3-0387a8f782fd (opens source in a new tab)

        Larotrectinib label

        Version not recorded · Effective date not recorded

        Elimination The mean (CV%) clearance (CL/F) of larotrectinib is 98 (44%) L/h and the half-life is 2.9 hours following oral administration of VITRAKVI in healthy subjects.
      2. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:9525f887-a055-4e33-8e92-898d42828cd1 (opens source in a new tab)

        Larotrectinib label

        Version not recorded · Effective date not recorded

        Elimination The mean (CV%) clearance (CL/F) of larotrectinib is 98 (44%) L/h and the half-life is 2.9 hours following oral administration of VITRAKVI in healthy subjects.
  9. Projected row 829

    Medicine slug
    latanoprost
    Compared field
    tMax
    Comparison state
    agree
    Reason codes
    • COMPATIBLE_VALUES_OVERLAP
    Documents examined
    17
    Source count
    5
    Agreement rate
    1
    Recorded readings
    1. 2 hours

      Numeric value
      2
      Unit
      hours
      Source records
      5

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

      Show all 5 source records
      1. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:34ad5cf6-4df0-4104-bddd-4c7631133ded (opens source in a new tab)

        Latanoprost label

        Version not recorded · Effective date not recorded

        Studies in man indicate that the peak concentration in the aqueous humor is reached about 2 hours after topical administration.
      2. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:463ecfde-5acb-4983-969d-0c0021bfbf48 (opens source in a new tab)

        Latanoprost label

        Version not recorded · Effective date not recorded

        Studies in man indicate that the peak concentration in the aqueous humor is reached about 2 hours after topical administration.
      3. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:5d0b99ad-f05a-44c7-ac61-26b5a533ea8d (opens source in a new tab)

        Latanoprost label

        Version not recorded · Effective date not recorded

        Studies in man indicate that the peak concentration in the aqueous humor is reached about 2 hours after topical administration.
      4. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:a98595b3-9f47-48e0-b18d-550a2095f264 (opens source in a new tab)

        Latanoprost label

        Version not recorded · Effective date not recorded

        Studies in man indicate that the peak concentration in the aqueous humor is reached about 2 hours after topical administration.
      5. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:be74d517-7f73-a74c-e053-2a95a90a3819 (opens source in a new tab)

        Latanoprost label

        Version not recorded · Effective date not recorded

        Studies in man indicate that the peak concentration in the aqueous humor is reached about 2 hours after topical administration.
  10. Projected row 830

    Medicine slug
    leflunomide
    Compared field
    halfLife
    Comparison state
    agree
    Reason codes
    • COMPATIBLE_VALUES_OVERLAP
    Documents examined
    25
    Source count
    25
    Agreement rate
    1
    Recorded readings
    1. 18 to 19 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:c288d1d3-3fbe-4c34-a28a-923d515809b3 (opens source in a new tab)

        Leflunomide label

        Version not recorded · Effective date not recorded

        Due to the very long half-life of teriflunomide (18 to 19 days), a loading dose of 100 mg for 3 days was used in clinical studies to facilitate the rapid attainment of steady-state teriflunomide concentrations.
      2. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:d6f5c510-9ec2-4e2d-b134-25c35bd23fee (opens source in a new tab)

        Leflunomide label

        Version not recorded · Effective date not recorded

        Due to the very long half-life of teriflunomide (18 to 19 days), a loading dose of 100 mg for 3 days was used in clinical studies to facilitate the rapid attainment of steady-state teriflunomide concentrations.
      3. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:af836cd0-da42-772e-e053-2995a90ac103 (opens source in a new tab)

        Leflunomide label

        Version not recorded · Effective date not recorded

        Due to the very long half-life of teriflunomide (18 to 19 days), a loading dose of 100 mg for 3 days was used in clinical studies to facilitate the rapid attainment of steady-state teriflunomide concentrations.
      4. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:753453c5-8a7a-878e-3ce7-1d1edce718a9 (opens source in a new tab)

        Leflunomide label

        Version not recorded · Effective date not recorded

        Due to the very long half-life of teriflunomide (18 to 19 days), a loading dose of 100 mg for 3 days was used in clinical studies to facilitate the rapid attainment of steady-state teriflunomide concentrations.
      5. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:320f63f2-fac3-4aee-aff8-85724e00ef52 (opens source in a new tab)

        Leflunomide label

        Version not recorded · Effective date not recorded

        Due to the very long half-life of teriflunomide (18–19 days), a loading dose of 100 mg for 3 days was used in clinical studies to facilitate the rapid attainment of steady-state teriflunomide concentrations.
      6. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:a48e6ef2-48ad-4fcf-9e67-dbba83ab0b79 (opens source in a new tab)

        Leflunomide label

        Version not recorded · Effective date not recorded

        Due to the very long half-life of teriflunomide (18-19 days), a loading dose of 100 mg for 3 days was used in clinical studies to facilitate the rapid attainment of steady-state teriflunomide concentrations.
      7. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:b9af9870-014f-4c4e-8738-bb04b30b3e85 (opens source in a new tab)

        Leflunomide label

        Version not recorded · Effective date not recorded

        Due to the very long half-life of teriflunomide (18 to 19 days), a loading dose of 100 mg for 3 days was used in clinical studies to facilitate the rapid attainment of steady-state teriflunomide concentrations.
      8. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:acf3efe4-0d70-4718-9c50-789d69ab215d (opens source in a new tab)

        Leflunomide label

        Version not recorded · Effective date not recorded

        Due to the very long half-life of teriflunomide (18 to 19 days), a loading dose of 100 mg for 3 days was used in clinical studies to facilitate the rapid attainment of steady-state teriflunomide concentrations.
      9. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:91712aad-d96c-4ef0-97e7-b31ed18ca6d8 (opens source in a new tab)

        Leflunomide label

        Version not recorded · Effective date not recorded

        Due to the very long half-life of teriflunomide (18 to 19 days), a loading dose of 100 mg for 3 days was used in clinical studies to facilitate the rapid attainment of steady-state teriflunomide concentrations.
      10. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:fa5f71b3-6a56-4616-baf7-4b761023b2a9 (opens source in a new tab)

        Leflunomide label

        Version not recorded · Effective date not recorded

        Due to the very long half-life of teriflunomide (18 to 19 days), a loading dose of 100 mg for 3 days was used in clinical studies to facilitate the rapid attainment of steady-state teriflunomide concentrations.
      11. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:8b365514-c859-ff93-e053-2a95a90ac698 (opens source in a new tab)

        Leflunomide label

        Version not recorded · Effective date not recorded

        Due to the very long half-life of teriflunomide (18 to 19 days), a loading dose of 100 mg for 3 days was used in clinical studies to facilitate the rapid attainment of steady-state teriflunomide concentrations.
      12. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:f6a4107e-b393-45ed-8e5a-70af5bd53826 (opens source in a new tab)

        Leflunomide label

        Version not recorded · Effective date not recorded

        Due to the very long half-life of teriflunomide (18 to 19 days), a loading dose of 100 mg for 3 days was used in clinical studies to facilitate the rapid attainment of steady-state teriflunomide concentrations.
      13. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:c358276a-610e-46da-b81a-95c837af205d (opens source in a new tab)

        Leflunomide label

        Version not recorded · Effective date not recorded

        Due to the very long half-life of teriflunomide (18 to 19 days), a loading dose of 100 mg for 3 days was used in clinical studies to facilitate the rapid attainment of steady-state teriflunomide concentrations.
      14. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:af4079af-c127-476e-a2b3-53b438dc9da4 (opens source in a new tab)

        Leflunomide label

        Version not recorded · Effective date not recorded

        Due to the very long half-life of teriflunomide (18 to 19 days), a loading dose of 100 mg for 3 days was used in clinical studies to facilitate the rapid attainment of steady-state teriflunomide concentrations.
      15. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:0a4f8671-b632-4cc5-8dc9-6b863e62b467 (opens source in a new tab)

        Leflunomide label

        Version not recorded · Effective date not recorded

        Due to the very long half-life of teriflunomide (18 to 19 days), a loading dose of 100 mg for 3 days was used in clinical studies to facilitate the rapid attainment of steady-state teriflunomide concentrations.
      16. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:006b5bf4-97c0-48dc-8e5e-3c6f64d7bdc1 (opens source in a new tab)

        Leflunomide label

        Version not recorded · Effective date not recorded

        Due to the very long half-life of teriflunomide (18 to 19 days), a loading dose of 100 mg for 3 days was used in clinical studies to facilitate the rapid attainment of steady-state teriflunomide concentrations.
      17. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:40dd071a-d07f-452f-bf1a-2a23b9d22ca4 (opens source in a new tab)

        Leflunomide label

        Version not recorded · Effective date not recorded

        Due to the very long half-life of teriflunomide (18 to 19 days), a loading dose of 100 mg for 3 days was used in clinical studies to facilitate the rapid attainment of steady-state teriflunomide concentrations.
      18. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:fc044417-cd9a-42f6-8a3d-a14e7c2f81a2 (opens source in a new tab)

        Leflunomide label

        Version not recorded · Effective date not recorded

        Due to the very long half-life of teriflunomide (18–19 days), a loading dose of 100 mg for 3 days was used in clinical studies to facilitate the rapid attainment of steady-state teriflunomide concentrations.
      19. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:c66cacd1-93f7-483a-a2fc-aad53d5342b0 (opens source in a new tab)

        Leflunomide label

        Version not recorded · Effective date not recorded

        Due to the very long half-life of teriflunomide (18 to 19 days), a loading dose of 100 mg for 3 days was used in clinical studies to facilitate the rapid attainment of steady-state teriflunomide concentrations.
      20. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:2b5c98d0-de59-85f6-e063-6394a90ab67a (opens source in a new tab)

        Leflunomide label

        Version not recorded · Effective date not recorded

        Due to the very long half-life of teriflunomide (18 to 19 days), a loading dose of 100 mg for 3 days was used in clinical studies to facilitate the rapid attainment of steady-state teriflunomide concentrations.
      21. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:d0fb9685-9e54-44e5-b543-1077e1a620c6 (opens source in a new tab)

        Leflunomide label

        Version not recorded · Effective date not recorded

        Due to the very long half-life of teriflunomide (18 to 19 days), a loading dose of 100 mg for 3 days was used in clinical studies to facilitate the rapid attainment of steady-state teriflunomide concentrations.
      22. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:e76d7767-744f-4e52-956d-e59f7a924826 (opens source in a new tab)

        Leflunomide label

        Version not recorded · Effective date not recorded

        Due to the very long half-life of teriflunomide (18 to 19 days), a loading dose of 100 mg for 3 days was used in clinical studies to facilitate the rapid attainment of steady-state teriflunomide concentrations.
      23. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:2b5f387e-b52b-ad80-e063-6394a90a56d5 (opens source in a new tab)

        Leflunomide label

        Version not recorded · Effective date not recorded

        Due to the very long half-life of teriflunomide (18 to 19 days), a loading dose of 100 mg for 3 days was used in clinical studies to facilitate the rapid attainment of steady-state teriflunomide concentrations.
      24. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:e85c4eed-794c-409b-aed5-3c857b14b1fb (opens source in a new tab)

        Leflunomide label

        Version not recorded · Effective date not recorded

        Due to the very long half-life of teriflunomide (18 to 19 days), a loading dose of 100 mg for 3 days was used in clinical studies to facilitate the rapid attainment of steady-state teriflunomide concentrations.
      25. FDA_LABELRetrieved 2026-08-30
        FDA_LABEL:5d48fded-b43b-461a-8488-ca1da5c41a03 (opens source in a new tab)

        Leflunomide label

        Version not recorded · Effective date not recorded

        Due to the very long half-life of teriflunomide (18 to 19 days), a loading dose of 100 mg for 3 days was used in clinical studies to facilitate the rapid attainment of steady-state teriflunomide concentrations.

Access

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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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