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Preparation. Administration. Evidence.

IV Dilution &
Medication Reference

Search 255 medications, read preserved historical references, and inspect separately reviewed preparation statements. Full monograph updates remain pending.

Version 6.4Release date 2026-11-04For healthcare professionals
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Medication reference

Etomidate

Monograph awaiting updateThis monograph will be updated in the future.

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No original site article was mapped to this record. The available historical structured fields and official-source links are retained.

Historical first look: uses, mechanism, dosing context, and administration

Recovered v5.1 source content; historical, awaiting current review.

Id
etomidate
Source IDH51-89BBFC3D4C4314900DB7E7C1
Generic name
Etomidate
Source IDH51-175C92265DF6A73B6C87E4BC
Class
Sedation, analgesia, and anesthesia
Source IDH51-2AD638D1D9BEB47A34A9AF02
Subclass
General anesthetic
Source IDH51-6DAAB476BE6E22EB9F1A1AC1
Primary uses
  1. Induction for rapid-sequence intubation
    Source IDH51-DF8811522710C7146D2AA031
Mechanism
Enhances GABA-A receptor-mediated inhibition and produces hypnosis.
Source IDH51-34A2206256F31DA14BB61C87
Mechanism level
drug_specific
Source IDH51-6D10F2FBB71F469F366E85CB
Basic dosing orientation
Adult / Pediatric | Adult commonly 0.2 to 0.3 mg/kg; pediatric weight based | Adult commonly 0.2 to 0.3 mg/kg; pediatric weight based | Patient- and indication-specific | See current package insert | IV push
Source IDH51-CEBE4E28FECF51F8032019AC
Administration orientation
Over 30 to 60 seconds; 2 mg/mL; Over 30 to 60 seconds
Source IDH51-A5A0866376797C9C713B90D3
Renal and population orientation
Separate renal reference: Open Renal Dosing Master (opens in a new tab)The existing monograph contains a renal or nephrotoxicity signal; verify exact adjustment and monitoring in the current label.
Source IDH51-070724A5E0FFAC53F82F2B8A
Key safety orientation
  1. Apnea, hypotension, myoclonus, nausea/vomiting, and adrenal suppression.
    Source IDH51-A34C03EEE6C4727AE82C04EF
Coverage path
structured_local_snapshot
Source IDH51-219CEFA789998BAD246851A7
Coverage path label
Structured GlobalRPh route snapshot
Source IDH51-76ACAFA7C92F430408F4F466
Review note
First-look orientation only. Verify indication, patient population, weight basis, organ function, exact IV product, dose, concentration, compatibility, rate, and current labeling before use.
Source IDH51-85F9ADF92B26BE8DD75C30B2
Search text
Etomidate Sedation, analgesia, and anesthesia General anesthetic Induction for rapid-sequence intubation Enhances GABA-A receptor-mediated inhibition and produces hypnosis. Adult / Pediatric | Adult commonly 0.2 to 0.3 mg/kg; pediatric weight based | Adult commonly 0.2 to 0.3 mg/kg; pediatric weight based | Patient- and indication-specific | See current package insert | IV push Over 30 to 60 seconds; 2 mg/mL; Over 30 to 60 seconds The existing monograph contains a renal or nephrotoxicity signal; verify exact adjustment and monitoring in the current label. Apnea, hypotension, myoclonus, nausea/vomiting, and adrenal suppression. Structured GlobalRPh route snapshot
Source IDH51-ED18D5F34EEC68C32DAEB6EE
Official access mode
search
Source IDH51-E539DAF552C4974E1C98FEEF
Official search query
Etomidate
Source IDH51-63726A540D8847C3AD4E50D2
Official access reason
A source-backed DailyMed search is available; select and confirm the exact IV product.
Source IDH51-F7CA895EB9A1A3DCE0A5EA5C
Product identifiers and clinical review status

This monograph will be updated in the future. Historical material is available where present in the original sources; full current exact-product and claim-level review remains pending.

Exact formulation, concentration, container, manufacturer, regulatory identifiers, and a reproducible label snapshot have not all been reconciled.

What remains to be completed
  • Retrievable exact-product SPL XML with version, revision, retrieval date and reproducible hash
  • Clinically reviewed, individually identified statements with two exact source mappings
  • Exact formulation, strength, container, manufacturer/labeler, application and NDC reconciliation
  • Renal-function methods and dialysis/CRRT modality review where applicable
  • Mechanism provenance, clinical source disagreements and full medication-specific safety reconciliation

Supplemental historical fields

Restored-data provenance and review notes

Source release: 2026-08-31. Current clinical review is incomplete. Original uses of current, verified, or normalized describe the historical source. They do not inherit the status of separately reviewed statements. Product formulations and source dates can differ.

Current review annotations for historical renal, dialysis, mechanism, and product fieldsSeparate renal reference: Open Renal Dosing Master (opens in a new tab)
Renal
Status
not_locally_normalized
Original classification
renal_review_flagged
Entries
    General note
    Preserve the source-specific renal-function basis. An indexed CrCl table is not interchangeable with unindexed CrCl or eGFR. Generic advice to check a method does not identify the equation for a dose row.
    Dialysis
    Status
    no_local_structured_regimen
    Entries
      General note
      Named modality alone does not establish applicability. CRRT subtype, effluent rate, residual renal function, timing and interruptions require review. Historical absence is not evidence that no guidance exists.
      Mechanisms
      • Source kind
        first_look
        Local pointer
        /mechanism
        Original level
        drug_specific
        Provenance classification
        historical_drug_specific_uncorroborated
        Label derived verified
        false
        Independently corroborated
        false
        Exact label section
        Not recorded
        Original source note
        Not recorded
        Review status
        historical_unverified
        Note
        Drug-specific wording in the old file is not proof of independent corroboration or an exact label locator. Consult separately published current mechanism claims where present.
      Future update
      Status
      pending_review
      Message
      This monograph will be updated in the future as current exact-product and claim-level review is completed.
      Source unavailable
      false
      Reason
      The historical content is restored; comprehensive contemporary verification remains incomplete.

      No separate structured rows were bundled for preparation, continuous infusion, dialysis, CRRT. Historical article content and source links may cover these topics.

      Historical IV-push guidance

      Recovered v5.1 source content; historical, awaiting current review.

      PopulationDose scopeConcentrationRateStatusNotes
      Source IDH51-A36726970C94375433201AFB
      Adult / Pediatric
      Source IDH51-5A74F8C64FD1DCC77CED80B5
      		Adult commonly 0.2 to 0.3 mg/kg; pediatric weight based
      Source IDH51-57ACC2011552C199A20FAE63
      		2 mg/mL
      Source IDH51-DAE5495B85C86D3AA5EBCE71
      		Over 30 to 60 seconds
      Source IDH51-B6AEED9F3C8957655E41678D
      		Use only when ordered and supported by current labeling or institutional policy
      Source IDH51-FCE31AB28A142A1F2DDF085E
      		Provides no analgesia. Myoclonus is common; transient adrenal suppression should be considered in context.
      Source IDH51-E4AC6D16A8958366D57D6701

      Historical indication and population dosing

      Recovered tables and source-separated snapshots; full clinical revalidation remains pending.

      Existing dose and route snapshots

      RoutePopulationIndicationDoseIntervalDurationAdministrationSource levelNotes
      Source IDH51-CE2F2C6E0F9F59A4EC73FA13
      IV push
      Source IDH51-BCC56E3FDA7E95C337B5DDA8
      		Adult / Pediatric
      Source IDH51-F050A1E3A582DBCF0E66BEC3
      		Adult commonly 0.2 to 0.3 mg/kg; pediatric weight based
      Source IDH51-4B3F4B09D25A9DAEAF38E286
      		Adult commonly 0.2 to 0.3 mg/kg; pediatric weight based
      Source IDH51-5783FC42688583F89E0C155A
      		Patient- and indication-specific
      Source IDH51-15CCF4311A49CE6534F8FC27
      		See current package insert
      Source IDH51-0EA913193C594CDB71676532
      		Over 30 to 60 seconds
      Source IDH51-EFBA23E1CF5C86FD8FEA1D73
      		Existing GlobalRPh IV push snapshot
      Source IDH51-256E3C01E458FACB865D7A34
      		Use only when ordered and supported by current labeling or institutional policy Provides no analgesia. Myoclonus is common; transient adrenal suppression should be considered in context.
      Source IDH51-5768772D5C3120D821A1CBEE

      Historical renal-function guidance

      Recovered v5.1 source content; historical, awaiting current review.

      Separate renal reference: Open Renal Dosing Master (opens in a new tab)
      Classification
      renal_review_flagged
      Source IDH51-BA791C6166BB02930BB0F6D4
      Summary
      The existing monograph contains a renal or nephrotoxicity signal; verify exact adjustment and monitoring in the current label.
      Source IDH51-CFCA4114313913021AF855FC
      Method note
      Use the renal function estimate and body-size convention specified by the selected label or institutional protocol. Do not interchange Cockcroft-Gault CrCl, indexed eGFR, and de-indexed eGFR without confirming the dosing source.
      Source IDH51-BE62B2D52F7B5DCE8BDF7FE4

      Historical Common IV uses

      Recovered v5.1 source content; historical, awaiting current review.

      1. Induction for rapid-sequence intubation
        Source IDH51-B38BC49A094930D1A0FBDD0F

      Historical Warnings and safeguards

      Recovered v5.1 source content; historical, awaiting current review.

      1. Apnea, hypotension, myoclonus, nausea/vomiting, and adrenal suppression.
        Source IDH51-3DAFECFB3B42583DCDE887B0

      Historical Monitoring

      Recovered v5.1 source content; historical, awaiting current review.

      1. Continuous ECG, blood pressure, oxygenation, and ventilation
        Source IDH51-BD16DEF33686FA65B93C9BC7
      Other recovered source fields and original editorial metadata

      Original status words such as current, verified, or normalized describe the historical source release. They do not change the clinical review status of this release.

      Catalog source fields

      Id
      etomidate
      Source IDH51-8F85D16C73C3B9FE4C3EFB0D
      Generic name
      Etomidate
      Source IDH51-0E1860B71120A30B9CF295E3
      Brand names
      1. Amidate
        Source IDH51-3A6704B23A79FC0A54D297C3
      Class
      Sedation, analgesia, and anesthesia
      Source IDH51-EC897F81C83C864F28A7D897
      Subclass
      General anesthetic
      Source IDH51-E5599A970F613A618806BA6D
      Summary
      Rapid-onset induction agent used as a single bolus only with immediate airway and ventilation capability.
      Source IDH51-5726F0D7E1454E286958FE71
      Populations
      1. Adult
        Source IDH51-4F19D6CF32E2E57A457A307E
      2. Pediatric
        Source IDH51-C012D62605A953A8938D9396
      Evidence tier
      IV push safety normalization - verify stocked product
      Source IDH51-5A8BCDFCE6D2A721D9AC64CF
      High alert
      true
      Source IDH51-C5EBE631F04BD19A3C5C9870
      Hazardous
      false
      Source IDH51-3D7563AFCF87F88F452D4503
      Status
      Active
      Source IDH51-C2A46598ED3C3C3A8F882959
      Reviewed
      2026-08-29
      Source IDH51-9CB2CDBB41266FF2B40C1F6E
      Version added
      1.2
      Source IDH51-FE2B9D6402725FB5C878A471
      Sources
      LabelUrlKind
      Source IDH51-6309195ED2EC309DF8B30D96
      DailyMed label search
      Source IDH51-A6EABB3CB1143407ED31B417
      		https://dailymed.nlm.nih.gov/dailymed/search.cfm?query=Etomidate (opens in a new tab)
      Source IDH51-18B8A4B328C0C1A003165A84
      		Primary
      Source IDH51-A86C8BA89A58B47A6DC0FCF7
      Source IDH51-6C557B3225484BE8E47FBC43
      GlobalRPh legacy IV dilution monograph
      Source IDH51-A7001D3DEAC9340E9C805965
      		legacy:auto
      Source IDH51-B2B469D77AA601B7189F2C84
      		Legacy
      Source IDH51-D6C7ACA16BDA494CFC7C6254
      Clinical release verification
      Audit version
      3.4
      Source IDH51-E0FC2A381597840BBCE79ACF
      Audited on
      2026-08-30
      Source IDH51-8DCAB6E1A3F3A8D4CFD5E42A
      Level
      amber
      Source IDH51-29B11A5048464950B018B85C
      Release gate
      trusted_professional_source_present_exact_label_unconfirmed
      Source IDH51-BAF7AB60A8D502CA8AF0C9AE
      Exact current label candidate
      false
      Source IDH51-3C916B271BF92535249917CC
      Numeric support ratio
      0
      Source IDH51-847BFDDA7FD18B8E95EADC43
      Reference url count
      1
      Source IDH51-EC22ECE62893431E7B7DA4ED
      Broken reference count
      0
      Source IDH51-4D8ADC79219DC55C56CE04AD
      Point of use confirmation required
      true
      Source IDH51-AAAAAC02FD6EBE71F5AD75E4
      Note
      Do not treat this record as a fully current product-specific monograph until the exact IV formulation and current sources are confirmed.
      Source IDH51-D72DCFCE06A4AD13C80195BF

      Dosing source fields

      Id
      etomidate
      Source IDH51-C60E3A773BC8BAD9FA0D513B
      Generic name
      Etomidate
      Source IDH51-5E602D1231C1F39ECC543AB6
      Coverage status
      direct_official_label_access_plus_local_snapshot
      Source IDH51-16CD075E7D84393A1A81923A
      Package insert
      Query name
      Etomidate
      Source IDH51-78C3AC718B203D2034835E27
      Product and route must match
      true
      Source IDH51-CB0516ADD0830D505DD6FDA1
      Live current label enabled
      false
      Source IDH51-E1404832C09941172B5A9029
      Source priority
      Reviewed local summary when available, then a verified DailyMed label or product search when available, followed by professional references and institutional policy.
      Source IDH51-8C6CBD335792E0466D4834B2
      Direct official label access enabled
      true
      Source IDH51-7B23A058C3F1DA5AD3BFB06F
      Outbound server request required
      false
      Source IDH51-6A708BC6C6AA468F032D8610
      Local summary status
      not_bundled
      Source IDH51-D641A792CC3568CC410B60B2
      Clinical review
      Locally normalized
      false
      Source IDH51-1C562C33D4E50861BEC73C1E
      Reviewed
      2026-08-29
      Source IDH51-58E67BDAE172D93411D9C5A7
      Status
      Direct official package-insert access enabled; indication-specific local normalization pending.
      Source IDH51-3ABE672C2F2F04E4302ED408
      Clinical release verification
      Audit version
      3.4
      Source IDH51-517D70E1EA81D12B034491A8
      Audited on
      2026-08-30
      Source IDH51-9D304889DDADECB9D27C763C
      Level
      amber
      Source IDH51-1AF5572E07DE279E7AB16895
      Release gate
      trusted_professional_source_present_exact_label_unconfirmed
      Source IDH51-A5BBF4C6DF445A84D33F1CB0
      Exact current label candidate
      false
      Source IDH51-0FAC9FB990D2A1D09BCD833E
      Numeric support ratio
      0
      Source IDH51-E7100855F5CFF30226E61B96
      Reference url count
      1
      Source IDH51-B32E7762ADEB0FC9667C5B38
      Broken reference count
      0
      Source IDH51-9DAD5276250C03AE3E10B138
      Point of use confirmation required
      true
      Source IDH51-FDA149C858DDD593869C0BAA
      Note
      Do not treat this record as a fully current product-specific monograph until the exact IV formulation and current sources are confirmed.
      Source IDH51-B462E8E142F7C91F72410091
      Historical preparation assessment

      Recovered v5.1 source content; historical, awaiting current review.

      Id
      etomidate
      Source IDH51-7BB87ED415651AF3FCF43D33
      Name
      Etomidate
      Source IDH51-21C9BC65BF781B825CA7810A
      Brands
      Amidate
      Source IDH51-0EF37EB7F5C63204847CF7B3
      Therapeutic class
      Sedation, analgesia, and anesthesia
      Source IDH51-460853CC4AD4286920053B8A
      Review version
      3.1
      Source IDH51-C8193E084A720E0FCE53717B
      Review date
      2026-08-30
      Source IDH51-EADBA2825BA3FEDAC4E2A2A5
      Release status
      no_released_dilution_current_label_review_required
      Source IDH51-07E8EED9B5429885AB12E950
      Market status
      Status
      no_current_us_iv_spl_confirmed
      Source IDH51-063EC30D51E0B49E442AC3EA
      Basis
      No high-confidence current IV SPL was automatically selected; legacy information is segregated
      Source IDH51-E2016015802A5AF2385FB0F9
      Ten point assessment
      Exact formulation
      Not established in the currently normalized record. Use the current-label panel before clinical use.
      Source IDH51-F727CC779FD1278F3F5A7CDE
      Reconstitution concentration
      Not established in the currently normalized record. Use the current-label panel before clinical use.
      Source IDH51-E3B6AAF4486B6A083A574443
      Maximum or recommended final concentration
      Not established in the currently normalized record. Use the current-label panel before clinical use.
      Source IDH51-9B6E033B169AF7551A421842
      Appropriate standardized containers
      Not established in the currently normalized record. Use the current-label panel before clinical use.
      Source IDH51-62215095846189DB6E6B8F8B
      Adult dosing range
      Adult commonly 0.2 to 0.3 mg/kg; pediatric weight based Adult commonly 0.2 to 0.3 mg/kg; pediatric weight based
      Source IDH51-EE31B1E7A9B4427E96949DD8
      Pediatric dosing range
      Separate renal reference: Open Renal Dosing Master (opens in a new tab)Do not interchange Cockcroft-Gault CrCl, indexed eGFR, and de-indexed eGFR without confirming the dosing source. | existing_route_snapshots: route: IV push | population: Adult / Pediatric | indication: Adult commonly 0.2 to 0.3 mg/kg; pediatric weight based | dose: Adult commonly 0.2 to 0.3 mg/kg; pediatric weight based | interval: Patient- and indication-specific | duration: See current package insert | administration: Over 30 to 60 seconds | source_level: Existing GlobalRPh IV push snapshot | notes: Use only when ordered and supported by current labeling or institutional policy Provides no analgesia. Myoclonus is common; transient adrenal suppression should be considered in context. | warnings: Apnea, hypotension, myoclonus, nausea/vomiting, and adrenal suppression. | monitoring: Continuous ECG, blood pressure, oxygenation, and ventilation | populations: Adult | Pediatric | evidence_tier: IV push safety normalization - verify stocked product | high_alert: true | hazardous: false | status: Active | reviewed: 2026-08-29 | version_added: 1.2 | sources: label: DailyMed label search | url: https://dailymed.nlm.nih.gov/dailymed/search.cfm?query=Etomidate | kind: Primary | label: GlobalRPh legacy IV dilution monograph | url: legacy:auto | kind: Legacy
      Source IDH51-FBDEB0E8CD8164B8003345BC
      Neonatal dosing range
      Not established in the currently normalized record. Use the current-label panel before clinical use.
      Source IDH51-9FB2B73935B662708C0D8417
      Infusion time
      Over 30 to 60 seconds
      Source IDH51-22F9D9CAACFF832189979E96
      Fluid restriction alternatives
      Not established in the currently normalized record. Use the current-label panel before clinical use.
      Source IDH51-9C3DD0791B51A1E25CB7AD17
      Current manufacturer labeling
      Match confidence
      unresolved
      Source IDH51-CE70BF54577501ED46CF4BBF
      Field provenance
      Exact formulation
      Primary
      not_found
      Source IDH51-4FF2F16DCD9AB93B4EE7EBAC
      Reconstitution concentration
      Primary
      not_found
      Source IDH51-8DE9494503282F809124EF65
      Maximum or recommended final concentration
      Primary
      not_found
      Source IDH51-EB3D98F4D71E36306AE52495
      Appropriate standardized containers
      Primary
      not_found
      Source IDH51-C0114D26AB429AFC64420022
      Adult dosing range
      Primary
      existing_structured_record
      Source IDH51-24741DC9AFC0E96E46871168
      Pediatric dosing range
      Primary
      existing_record_text
      Source IDH51-8ED43AC89356410FFA1C0B35
      Neonatal dosing range
      Primary
      not_found
      Source IDH51-0DDD8811944247DBF0B22C85
      Infusion time
      Primary
      existing_structured_record
      Source IDH51-282A72B53F4C36A05911EAFF
      Fluid restriction alternatives
      Primary
      not_found
      Source IDH51-68A053B807D66A184018FAB8
      Current manufacturer labeling
      Primary
      DailyMed search gateway
      Source IDH51-196179B535A9DF6D9511632C
      Population applicability
      Adult
      Applicability
      supported_or_source_present
      Source IDH51-313C395B27A7CBC776F94AF4
      Guide generation allowed
      true
      Source IDH51-950091A64C4B4CCD1BB4490A
      Pediatric
      Applicability
      supported_or_source_present
      Source IDH51-3B7D0E914CC42B897BA0C2B2
      Guide generation allowed
      false
      Source IDH51-AEB7D583453C65F625840FF3
      Neonatal
      Applicability
      not_established
      Source IDH51-C924F3093B0472EBAAC7F676
      Guide generation allowed
      false
      Source IDH51-0CD91BA8986808694A705EF9
      Route presence
      Structured dilution
      false
      Source IDH51-548179955BEA9054049393C4
      Iv push
      true
      Source IDH51-E9EC76E813926C824082F059
      Continuous infusion
      false
      Source IDH51-674EF6C15E7C8DAD72AD617E
      Pediatric source
      true
      Source IDH51-C306F7735AD68FADEEDED279
      Neonatal source
      false
      Source IDH51-9EDB1698422BED95E7E03DF8
      Legacy reference
      Status
      not_available
      Source IDH51-E71E663E867158C47532A019
      Label resolution
      Status
      build_environment_network_unavailable
      Source IDH51-6245A1ABEE7FBFCA2F80B2B0
      Source files
      1. catalog.json
        Source IDH51-C6F3038267F9822784A4D999
      2. dosing.json
        Source IDH51-4C83AB824BBEA857BD071566
      3. new-in-v1.2.json
        Source IDH51-C820FA5A4C4034A3F087230A
      Clinical release note
      Preparation instructions are released only at the evidence level shown. Legacy content remains visibly separate. Exact product, NDC, route, current labeling, and institutional policy must be confirmed.
      Source IDH51-A36EF40D6C2A2D064A787187
      Historical statement IDs and source locations

      These IDs identify recovered source units. They are not evidence-qualified clinical claims.

      Historical IDOriginal source locationStatus
      H51-8F85D16C73C3B9FE4C3EFB0Dcatalog.json
      /records/98/id      		Historical; current review incomplete
      H51-0E1860B71120A30B9CF295E3catalog.json
      /records/98/generic_name      		Historical; current review incomplete
      H51-3A6704B23A79FC0A54D297C3catalog.json
      /records/98/brand_names/0      		Historical; current review incomplete
      H51-EC897F81C83C864F28A7D897catalog.json
      /records/98/class      		Historical; current review incomplete
      H51-E5599A970F613A618806BA6Dcatalog.json
      /records/98/subclass      		Historical; current review incomplete
      H51-5726F0D7E1454E286958FE71catalog.json
      /records/98/summary      		Historical; current review incomplete
      H51-B38BC49A094930D1A0FBDD0Fcatalog.json
      /records/98/common_uses/0      		Historical; current review incomplete
      H51-A36726970C94375433201AFBcatalog.json
      /records/98/iv_push/0      		Historical; current review incomplete
      H51-5A74F8C64FD1DCC77CED80B5catalog.json
      /records/98/iv_push/0/population      		Historical; current review incomplete
      H51-57ACC2011552C199A20FAE63catalog.json
      /records/98/iv_push/0/dose_scope      		Historical; current review incomplete
      H51-DAE5495B85C86D3AA5EBCE71catalog.json
      /records/98/iv_push/0/concentration      		Historical; current review incomplete
      H51-B6AEED9F3C8957655E41678Dcatalog.json
      /records/98/iv_push/0/rate      		Historical; current review incomplete
      H51-FCE31AB28A142A1F2DDF085Ecatalog.json
      /records/98/iv_push/0/status      		Historical; current review incomplete
      H51-E4AC6D16A8958366D57D6701catalog.json
      /records/98/iv_push/0/notes      		Historical; current review incomplete
      H51-3DAFECFB3B42583DCDE887B0catalog.json
      /records/98/warnings/0      		Historical; current review incomplete
      H51-BD16DEF33686FA65B93C9BC7catalog.json
      /records/98/monitoring/0      		Historical; current review incomplete
      H51-4F19D6CF32E2E57A457A307Ecatalog.json
      /records/98/populations/0      		Historical; current review incomplete
      H51-C012D62605A953A8938D9396catalog.json
      /records/98/populations/1      		Historical; current review incomplete
      H51-5A8BCDFCE6D2A721D9AC64CFcatalog.json
      /records/98/evidence_tier      		Historical; current review incomplete
      H51-C5EBE631F04BD19A3C5C9870catalog.json
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      H51-3D7563AFCF87F88F452D4503catalog.json
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      H51-FE2B9D6402725FB5C878A471catalog.json
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      H51-18B8A4B328C0C1A003165A84catalog.json
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      H51-8DCAB6E1A3F3A8D4CFD5E42Acatalog.json
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      H51-278D3C1456764FCB1C4942D2catalog.json
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      H51-AAAAAC02FD6EBE71F5AD75E4catalog.json
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      H51-D72DCFCE06A4AD13C80195BFcatalog.json
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      H51-C60E3A773BC8BAD9FA0D513Bdosing.json
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      H51-5E602D1231C1F39ECC543AB6dosing.json
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      H51-16CD075E7D84393A1A81923Adosing.json
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      H51-78C3AC718B203D2034835E27dosing.json
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      H51-B94E9F932C979DBE6B234A2Cdosing.json
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      H51-CB0516ADD0830D505DD6FDA1dosing.json
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      H51-E1404832C09941172B5A9029dosing.json
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      H51-7B23A058C3F1DA5AD3BFB06Fdosing.json
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      H51-6A708BC6C6AA468F032D8610dosing.json
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      H51-D641A792CC3568CC410B60B2dosing.json
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      H51-BA791C6166BB02930BB0F6D4dosing.json
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      H51-CFCA4114313913021AF855FCdosing.json
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      H51-BCC56E3FDA7E95C337B5DDA8dosing.json
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      H51-F050A1E3A582DBCF0E66BEC3dosing.json
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      H51-4B3F4B09D25A9DAEAF38E286dosing.json
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      H51-5768772D5C3120D821A1CBEEdosing.json
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      H51-1C562C33D4E50861BEC73C1Edosing.json
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      H51-0FAC9FB990D2A1D09BCD833Edosing.json
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      H51-5893B305405F701739544432dosing.json
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      H51-89BBFC3D4C4314900DB7E7C1first-look-v5.1.json
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      H51-7BB87ED415651AF3FCF43D33preparation-assessments-v3.8.json
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