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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Search 255 medications, read preserved historical references, and inspect separately reviewed preparation statements.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

Esomeprazole (Nexium)

Monograph awaiting updateThis monograph will be updated in the future.

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Historical source. Current clinical review is incomplete. This monograph will be updated in the future.

Esomeprazole - Nexium ® (opens in a new tab)Original source URL: https://globalrph.com/dilution/esomeprazole-nexium/ | Retrieved 2026-11-04

Source dates, location and integrity

This historical article is separate from the reviewed claim cards. Product formulations and source dates may differ.

Original source URL
https://globalrph.com/dilution/esomeprazole-nexium/ (opens in a new tab)
Source date
Not established in the retrieved source
Retrieved
2026-11-04T19:46:42.543155+00:00
Source location
div.post-content
Packaged content SHA-256
eace7afb527747efebae4feffab3978cd9f6ecbb2c89faf64ccd744e095d14f4
Original response SHA-256
ad3071aa731ef4297a13069e0c2a64317ef7326062e232f43c47dc190e8f1d42
Source body SHA-256
7a5a8c6d665969b52f5191749b6d1a95edd7e4cfdcde0f796b9603fd7fff8663

esomeprazole sodium - Nexium ®

The authors make no claims of the accuracy of the information contained herein; and these suggested doses and/or guidelines are not a substitute for clinical judgment. Neither GlobalRPh Inc. nor any other party involved in the preparation of this document shall be liable for any special, consequential, or exemplary damages resulting in whole or part from any user's use of or reliance upon this material. PLEASE READ THE DISCLAIMER CAREFULLY BEFORE ACCESSING OR USING THIS SITE. BY ACCESSING OR USING THIS SITE, YOU AGREE TO BE BOUND BY THE TERMS AND CONDITIONS SET FORTH IN THE DISCLAIMER.

Usual Diluents

NS , D5W

Standard Dilutions [Amount of drug] [Infusion volume] [Infusion rate]

[ 20 mg ] [ 50 ml ] [ 10 to 30 min]
[ 40 mg ] [ 50 ml ] [ 10 to 30 min ]
(Dilute each vial with 5 ml NS)

Label: Do not refrigerate.

Stability / Miscellaneous

Stability data:

Drug Stability
Refrigerated
Stability
Room Temp.
Reconstituted
Vial/Powder
Notes
Esomeprazole - Nexium Store at 20° to 25°C (68° to 77°F). The reconstituted solution of esomeprazole sodium for injection should be stored at room temperature up to 30°C (86°F) and administered within 12 hours after reconstitution. (Administer within 6 hours if 5% Dextrose Injection is used after reconstitution). No refrigeration is required Powder Protect from light. Store in carton until time of use.

Following reconstitution and administration, discard any unused portion of esomeprazole solution.


INDICATIONS
: NEXIUM I.V. for Injection is indicated for the short-term treatment (up to 10 days) of GERD patients with a history of erosive esophagitis as an alternative to oral therapy in patients when therapy with NEXIUM Delayed-Release Capsules is not possible or appropriate.

DOSAGE AND ADMINISTRATION:
GERD with a history of Erosive Esophagitis: The recommended adult dose is either 20 or 40 mg esomeprazole given once daily by intravenous injection (no less than 3 minutes) or intravenous infusion (10 to 30 minutes). NEXIUM I.V. for Injection should not be administered concomitantly with any other medications through the same intravenous site and or tubing. The intravenous line should always be flushed with either 0.9% Sodium Chloride Injection, Lactated Ringer's Injection, or 5% Dextrose Injection, both prior to and after administration. Safety and efficacy of NEXIUM I.V. for Injection as a treatment of GERD patients with a history of erosive esophagitis for more than 10 days have not been demonstrated.

Renal Insufficiency
The pharmacokinetics of esomeprazole in patients with renal impairment are not expected to be altered relative to healthy volunteers as less than 1% of esomeprazole is excreted unchanged in urine.

Separate renal reference: Open Renal Dosing Master (opens in a new tab)

Preparations for use:
No refrigeration is required. Parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration, whenever solution and container permit.

IV Injection: The freeze-dried powder should be reconstituted with 5 mL of 0.9% Sodium Chloride Injection, USP. Withdraw 5 mL of the reconstituted solution and administer as an intravenous injection over no less than 3 minutes. The reconstituted solution should be stored at room temperature up to 30°C (86°F) and administered within 12 hours after reconstitution.

Intravenous Infusion (20 or 40 mg) over 10 to 30 minutes: A solution for intravenous infusion is prepared by first reconstituting the contents of one vial with 5 mL of 0.9% Sodium Chloride Injection, Lactated Ringer's Injection, or 5% Dextrose Injection, and further diluting the resulting solution to a final volume of 50 mL. The solution (admixture) should be administered as an intravenous infusion over a period of 10 to 30 minutes. The admixture should be stored at room temperature up to 30°C (86°F) and should be administered within the designated time period as listed in the Table below.

Diluent

Administer within:

5% Dextrose Injection, USP

6 hours

Lactated Ringer’s Injection, USP

12 hours

0.9% Sodium Chloride Injection, USP

12 hours

Storage:
Store at 25°C (77°F); excursions permitted to 15°-30°C (59°-86°F). Protect from light. Store in carton until time of use.

HOW SUPPLIED:
NEXIUM I.V. for Injection is supplied as a freeze-dried powder containing 20 mg or 40 mg of esomeprazole per single-use vial.

Source: Nexium (package insert). Willmington, DE: AstraZeneca LP; April 2007. https://www.astrazeneca-us.com/pi/nexium_iv.pdf

Open this historical article on its own

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

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

      Id
      esomeprazole-nexium
      Source IDH51-007E06EA6289CDCAAA6C8675
      Generic name
      Esomeprazole (Nexium)
      Source IDH51-18F8D83FA50B70D93CF11544
      Class
      GI and antiemetic
      Source IDH51-762335BF325698C5D48301B8
      Subclass
      Legacy GlobalRPh directory entry
      Source IDH51-15D5F2485FF3801A8EEF5493
      Primary uses
      1. Acid suppression, nausea and vomiting control, or gastrointestinal motility therapy, depending on the named agent.
        Source IDH51-0CA6575CDA765D024F3D2DE5
      Mechanism
      Irreversibly inhibits the gastric hydrogen-potassium ATPase after acid-dependent activation.
      Source IDH51-41D0685AC3372B9D63EE8934
      Mechanism level
      drug_specific
      Source IDH51-B195734B70ACE03F3FD85D80
      Basic dosing orientation
      The existing GlobalRPh dose and preparation quick reference loads automatically below. Treat it as historical continuity, then confirm the exact current DailyMed label, population, indication, renal function, and institutional policy.
      Source IDH51-CC4A4E5C3C2D60E9C9D5343E
      Administration orientation
      Route, dilution, concentration, and administration details load automatically from the existing GlobalRPh quick reference below; current exact-product verification remains required.
      Source IDH51-6DE3FDDC7CBE15A85D0E6221
      Renal and population orientation
      Separate renal reference: Open Renal Dosing Master (opens in a new tab)Renal dosing status has not been locally normalized; use the current package insert before ordering or administration.
      Source IDH51-5E4D90872D891D8F92D4B360
      Key safety orientation
      1. Legacy content must be reconciled against current labeling and institutional policy before clinical use.
        Source IDH51-98C1B805C939901DF2FD688F
      Coverage path
      automatic_legacy_quick_reference
      Source IDH51-A7A1E7C10BBE5B0D09F514E2
      Coverage path label
      Automatic legacy GlobalRPh quick reference
      Source IDH51-BEE2A8C817AC506B016B5DBD
      Legacy title
      Esomeprazole (Nexium)
      Source IDH51-8735E54A5C733C87B07AD276
      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 IDH51-29D96B97CBA1508DB4F66A75
      Search text
      Esomeprazole (Nexium) GI and antiemetic Legacy GlobalRPh directory entry Acid suppression, nausea and vomiting control, or gastrointestinal motility therapy, depending on the named agent. Irreversibly inhibits the gastric hydrogen-potassium ATPase after acid-dependent activation. The existing GlobalRPh dose and preparation quick reference loads automatically below. Treat it as historical continuity, then confirm the exact current DailyMed label, population, indication, renal function, and institutional policy. Route, dilution, concentration, and administration details load automatically from the existing GlobalRPh quick reference below; current exact-product verification remains required. Renal dosing status has not been locally normalized; use the current package insert before ordering or administration. Legacy content must be reconciled against current labeling and institutional policy before clinical use. Automatic legacy GlobalRPh quick reference
      Source IDH51-B854A4776EF5F906CEF047D5
      Official access mode
      none
      Source IDH51-642C2D322BC5B07947654BD0
      Official access reason
      No source-backed DailyMed action has been verified for this umbrella or legacy record; identify the exact product before searching.
      Source IDH51-D79DF31FA03B648A63180E70

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

      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
      current_label_review_required
      Source IDH51-29918C802320737C5F11A1A4
      Summary
      Renal dosing status has not been locally normalized; use the current package insert before ordering or administration.
      Source IDH51-110CA018B55BA341D73D1438
      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 IDH51-99E2209869E822151B82F065

      Historical Warnings and safeguards

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

      1. Legacy content must be reconciled against current labeling and institutional policy before clinical use.
        Source IDH51-4803F546A5064D95BF3C3E05

      Historical Stability notes

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

      1. Legacy product stability information is not automatically equivalent to a USP <797> BUD.
        Source IDH51-C232DE8A4FE67FA2897CDE9E
      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
      esomeprazole-nexium
      Source IDH51-96E77D71AB366850295B53BB
      Legacy title
      Esomeprazole (Nexium)
      Source IDH51-39C82C00BDFCE32120F2A618
      Generic name
      Esomeprazole (Nexium)
      Source IDH51-F21171D74BD68DEDF4E7AD39
      Class
      GI and antiemetic
      Source IDH51-90A7234D5F0D8B16C0540C38
      Subclass
      Legacy GlobalRPh directory entry
      Source IDH51-5D1FA15924A6181FAEE83E17
      Summary
      Existing GlobalRPh IV dilution monograph retained for migration into the unified reference.
      Source IDH51-FF0CE77DA75E003693677A9D
      Populations
      1. Population not yet normalized
        Source IDH51-C48C1067648CD8CD5E424E72
      Evidence tier
      Legacy catalog - migration review required
      Source IDH51-B1A6C316770830F034F5EA8D
      High alert
      false
      Source IDH51-60F6201DB25501E28E8A569B
      Hazardous
      false
      Source IDH51-604774D718AE423B3692F699
      Status
      Legacy migration
      Source IDH51-E282735D82DB07F7E7205F6D
      Version added
      Legacy
      Source IDH51-67215216AECC37B9D82BEC5E
      Sources
      LabelUrlKind
      Source IDH51-65C7A4D802F0894875A8B946
      GlobalRPh legacy IV dilution monograph
      Source IDH51-9B9C7BB10F9B1F5267F9EE35
      legacy:auto
      Source IDH51-1A01B9A2C684B68C0DD5BE4F
      Legacy
      Source IDH51-562341BEAA17DE35F625746E
      Clinical release verification
      Audit version
      3.4
      Source IDH51-4FEEFBCC8A2355AE6E38A230
      Audited on
      2026-08-30
      Source IDH51-BA6D190058BAD152A0467E1C
      Level
      red
      Source IDH51-F918C135799217ED740F73EF
      Release gate
      unverified_or_unclassified_sources_do_not_release_as_current
      Source IDH51-458DD30636C5CDA419CEC5ED
      Exact current label candidate
      false
      Source IDH51-251F64729260665E82E84584
      Reference url count
      0
      Source IDH51-EC2DEE058F3EF49557A28FAA
      Broken reference count
      0
      Source IDH51-A43820D3487FCE9255F40D0A
      Point of use confirmation required
      true
      Source IDH51-C434B9D1D7DAC91E76536410
      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-AAF9566EB5FB77F2086A86E4

      Dosing source fields

      Id
      esomeprazole-nexium
      Source IDH51-C1CAA41DCD72C35D77064DF1
      Generic name
      Esomeprazole (Nexium)
      Source IDH51-943CCF81C2A457F1D3C41424
      Coverage status
      direct_official_label_access_plus_legacy_reference
      Source IDH51-60BA2A67CEF260922C291DAE
      Package insert
      Query name
      Esomeprazole
      Source IDH51-814E10B27D6672CE8C1717F1
      Product and route must match
      true
      Source IDH51-4DBB918320057C06C3C47792
      Live current label enabled
      false
      Source IDH51-55DB527D63036CD62CD8D1F4
      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 IDH51-893E01B58BA0FC5A235BF8F7
      Direct official label access enabled
      true
      Source IDH51-F419C3A6A2F6791C8606C180
      Outbound server request required
      false
      Source IDH51-A2B096A20B0929B8A1E4E99B
      Local summary status
      not_bundled
      Source IDH51-CA9BC3E1C951B868DC478314
      Clinical review
      Locally normalized
      false
      Source IDH51-F6FCBB3969E928D9F17CED16
      Reviewed
      2026-08-29
      Source IDH51-EB7E508E1C619D26B2AFCD62
      Status
      Direct official package-insert access enabled; indication-specific local normalization pending.
      Source IDH51-884F7FE0D74C65246403149F
      Clinical release verification
      Audit version
      3.4
      Source IDH51-91507570268CC31B19BB5C5C
      Audited on
      2026-08-30
      Source IDH51-A1D9F3C3F0B75B73902BB6E8
      Level
      red
      Source IDH51-79CED77C76F5A8DFE011066B
      Release gate
      unverified_or_unclassified_sources_do_not_release_as_current
      Source IDH51-52FA644CD7A7490A054173FC
      Exact current label candidate
      false
      Source IDH51-88CA789882D994BC4BFE2913
      Reference url count
      0
      Source IDH51-3B06C4CEBBFD2FF8014CA138
      Broken reference count
      0
      Source IDH51-70AC0EBD8D3C46237D5BE007
      Point of use confirmation required
      true
      Source IDH51-407B3879CF3AEE8F623D947D
      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-B2EBAD5909FE6807F6FF0153
      Historical preparation assessment

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

      Id
      esomeprazole-nexium
      Source IDH51-B03B676BF84B72D3E797697C
      Name
      Esomeprazole (Nexium)
      Source IDH51-430E90A0CE6F065D219B38A2
      Therapeutic class
      GI and antiemetic
      Source IDH51-4FF70EBF1441C6090AF27E9C
      Review version
      3.1
      Source IDH51-D784E37684B57D79C7CC1246
      Review date
      2026-08-30
      Source IDH51-0E5E568085ED52E0574784CE
      Release status
      no_released_dilution_current_label_review_required
      Source IDH51-2B06010CB06CF6F9B31CD1D1
      Market status
      Status
      no_current_us_iv_spl_confirmed
      Source IDH51-ABF28A2E1B15EED6DB320029
      Basis
      No high-confidence current IV SPL was automatically selected; legacy information is segregated
      Source IDH51-100A28D1FBE10AE817B48E35
      Ten point assessment
      Exact formulation
      Not established in the currently normalized record. Use the current-label panel before clinical use.
      Source IDH51-A1B0936862E94A6499E203B8
      Reconstitution concentration
      Not established in the currently normalized record. Use the current-label panel before clinical use.
      Source IDH51-8D8E3D6D7C934FCB70AD804C
      Maximum or recommended final concentration
      Not established in the currently normalized record. Use the current-label panel before clinical use.
      Source IDH51-63746C123F4F24BE79EDEC14
      Appropriate standardized containers
      Not established in the currently normalized record. Use the current-label panel before clinical use.
      Source IDH51-8D379A1DDEA8F0CBB94F9502
      Adult dosing range
      Not established in the currently normalized record. Use the current-label panel before clinical use.
      Source IDH51-160339B823811B7ABF6C3B5E
      Pediatric dosing range
      Not established in the currently normalized record. Use the current-label panel before clinical use.
      Source IDH51-7363F8CD79F898ADD85CB3CD
      Neonatal dosing range
      Not established in the currently normalized record. Use the current-label panel before clinical use.
      Source IDH51-367A88D9605F4F9B6FBD0FEF
      Infusion time
      Not established in the currently normalized record. Use the current-label panel before clinical use.
      Source IDH51-12E5FE65C772DE74B243D839
      Fluid restriction alternatives
      Not established in the currently normalized record. Use the current-label panel before clinical use.
      Source IDH51-1F227D4D6C03C5BFC2C49FBB
      Current manufacturer labeling
      Match confidence
      unresolved
      Source IDH51-1022F5D2529805AB00D4B255
      Field provenance
      Exact formulation
      Primary
      not_found
      Source IDH51-010ED3FCADD3AF5B3A1B927F
      Reconstitution concentration
      Primary
      not_found
      Source IDH51-590699A81C8473F9DC80C17E
      Maximum or recommended final concentration
      Primary
      not_found
      Source IDH51-2A41C2B2A9B94EE6FC8BB5E0
      Appropriate standardized containers
      Primary
      not_found
      Source IDH51-7E215932BEBE6245F90219E7
      Adult dosing range
      Primary
      not_found
      Source IDH51-68759093BDA745CC611A8D4B
      Pediatric dosing range
      Primary
      not_found
      Source IDH51-F33D377DBF048D9BFB04C9C7
      Neonatal dosing range
      Primary
      not_found
      Source IDH51-CC47E066BC3B4B013B216852
      Infusion time
      Primary
      not_found
      Source IDH51-8BD3FA28ACA7FC5D166A32DD
      Fluid restriction alternatives
      Primary
      not_found
      Source IDH51-87B46426FE132A69086CF055
      Current manufacturer labeling
      Primary
      DailyMed search gateway
      Source IDH51-CE8A93AED4DEF7ACD7676AF6
      Population applicability
      Adult
      Applicability
      not_established
      Source IDH51-A1F9D69DBF68F63E0BF5132A
      Guide generation allowed
      false
      Source IDH51-71EF2ACB3F45E70627620041
      Pediatric
      Applicability
      not_established
      Source IDH51-E4F0F2502A2D995B93A45583
      Guide generation allowed
      false
      Source IDH51-269988AD1E31A89F71C964A6
      Neonatal
      Applicability
      not_established
      Source IDH51-79D06F3D43E7568C9F49E9FE
      Guide generation allowed
      false
      Source IDH51-549186BFE66613FA61C11BAF
      Route presence
      Structured dilution
      false
      Source IDH51-B8B08C17F18D17CA5970CEE6
      Iv push
      false
      Source IDH51-C4971079DDA757F01B9F141B
      Continuous infusion
      false
      Source IDH51-14860C602F00B9CA237164E1
      Pediatric source
      false
      Source IDH51-38214D613D7C63E5AEBC9434
      Neonatal source
      false
      Source IDH51-578B9F742A08F099E2A0DA13
      Legacy reference
      Status
      not_available
      Source IDH51-4BDAF87E34404B088AED86DA
      Label resolution
      Status
      build_environment_network_unavailable
      Source IDH51-D8568251A93A1EE8CE9AEE84
      Source files
      1. catalog.json
        Source IDH51-AFBF7133BBB2CDE2CC4BDE0F
      2. dosing.json
        Source IDH51-B0D1A2ED66AACA6F37323004
      3. legacy-map.json
        Source IDH51-BF0FA0E84186C50B2891F6EC
      4. review-queue.json
        Source IDH51-571F5438026218ED358FA1FD
      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-A8C618432CFAE125B2EF1B5D
      Historical statement IDs and source locations

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

      Historical IDOriginal source locationStatus
      H51-96E77D71AB366850295B53BBcatalog.json
      /records/97/id
      Historical; current review incomplete
      H51-39C82C00BDFCE32120F2A618catalog.json
      /records/97/legacy_title
      Historical; current review incomplete
      H51-F21171D74BD68DEDF4E7AD39catalog.json
      /records/97/generic_name
      Historical; current review incomplete
      H51-90A7234D5F0D8B16C0540C38catalog.json
      /records/97/class
      Historical; current review incomplete
      H51-5D1FA15924A6181FAEE83E17catalog.json
      /records/97/subclass
      Historical; current review incomplete
      H51-FF0CE77DA75E003693677A9Dcatalog.json
      /records/97/summary
      Historical; current review incomplete
      H51-4803F546A5064D95BF3C3E05catalog.json
      /records/97/warnings/0
      Historical; current review incomplete
      H51-C232DE8A4FE67FA2897CDE9Ecatalog.json
      /records/97/stability_notes/0
      Historical; current review incomplete
      H51-C48C1067648CD8CD5E424E72catalog.json
      /records/97/populations/0
      Historical; current review incomplete
      H51-B1A6C316770830F034F5EA8Dcatalog.json
      /records/97/evidence_tier
      Historical; current review incomplete
      H51-60F6201DB25501E28E8A569Bcatalog.json
      /records/97/high_alert
      Historical; current review incomplete
      H51-604774D718AE423B3692F699catalog.json
      /records/97/hazardous
      Historical; current review incomplete
      H51-E282735D82DB07F7E7205F6Dcatalog.json
      /records/97/status
      Historical; current review incomplete
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