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Search 255 medications, read preserved historical references, and inspect separately reviewed preparation statements.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

Desmopressin (DDAVP)

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.

Desmopressin (DDAVP ®) (opens in a new tab)Original source URL: https://globalrph.com/dilution/desmopressin-ddavp/ | 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/desmopressin-ddavp/ (opens in a new tab)
Source date
Not established in the retrieved source
Retrieved
2026-11-04T19:45:22.044825+00:00
Source location
div.post-content
Packaged content SHA-256
64f53ece15008cec8bb3cc77ee3c873323315566b440671aa1a4dc47ab1b73b1
Original response SHA-256
a89725f9083cf1ee3bcb5c67bf1703d5dd643e64e270944639afa39636caca9a
Source body SHA-256
4062a2138899d2512cf00594d5cd14e9fadc1c28ee3955eaf50ef79cde153f2c

DESMOPRESSIN (DDAVP ®)

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

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

[0 to 35 mcg] [50 ml] [15 - 30min]

Stability / Miscellaneous

Stability data:

Drug Stability
Refrigerated
Stability
Room Temp.
Reconstituted
Vial/Powder
Notes
Desmopressin Store refrigerated 2° to 8°C (36° to 46°F). Solution Preserve in tight containers, protected from light.


Supplied
: 4 mcg/ml-1 ml vial.

Indications: Hemophilia (increases factor VIII levels): 0.3 mcg/kg in 50ml normal saline over 15-30 minutes.
Diabetes insipidus: 2-4 mcg/day IV push or SC.
Decrease bleeding following cardiac bypass: 0.3 mcg/kg ivpb.
Provide short term protection for uremic hemorrhagic tendency: 0.3 mcg/kg ivpb q8h x 2 doses (diminishing response).

Greatly enhanced ADH activity. Less vasopressor activity. Longer DOA. (Synthetic analog of vasopressin-posterior pituitary hormone).

ADH activity : Pressor activity [DDAVP: 2000-4000: 1 Vasopressin: 1:1]

WARNINGS
When Desmopressin Acetate Injection is administered to patients who do not have need of antidiuretic hormone for its antidiuretic effect, in particular in pediatric and geriatric patients, fluid intake should be adjusted downward to decrease the potential occurrence of water intoxication and hyponatremia with accompanying signs and symptoms (headache, nausea/vomiting, decreased serum sodium and weight gain).

Particular attention should be paid to the possibility of the rare occurrence of an extreme decrease in plasma osmolality that may result in seizures which could lead to coma.

Desmopressin acetate should not be used to treat patients with Type IIB von Willebrand's disease since platelet aggregation may be induced.

DOSAGE AND ADMINISTRATION
Hemophilia A and von Willebrand's Disease (Type I): Desmopressin Acetate Injection 4 mcg/mL is administered as an intravenous infusion at a dose of 0.3 mcg desmopressin acetate/kg body weight diluted in sterile physiological saline and infused slowly over 15 to 30 minutes. In adults and children weighing more than 10 kg, 50 mL of diluent is recommended; in children weighing 10 kg or less, 10 mL of diluent is recommended. Blood pressure and pulse should be monitored during infusion. If Desmopressin Acetate Injection 4 mcg/mL is used preoperatively, it should be administered 30 minutes prior to the scheduled procedure.

The necessity for repeat administration of desmopressin acetate or use of any blood products for hemostasis should be determined by laboratory response as well as the clinical condition of the patient. The tendency toward tachyphylaxis (lessening of response) with repeated administration given more frequently than every 48 hours should be considered in treating each patient.

Diabetes Insipidus: This formulation is administered subcutaneously or by direct intravenous injection. Desmopressin Acetate Injection 4 mcg/mL dosage must be determined for each patient and adjusted according to the pattern of response. Response should be estimated by two parameters: adequate duration of sleep and adequate, not excessive, water turnover.

The usual dosage range in adults is 0.5 mL (2 mcg) to 1 mL (4 mcg) daily, administered intravenously or subcutaneously, usually in two divided doses. The morning and evening doses should be separately adjusted for an adequate diurnal rhythm of water turnover. For patients who have been controlled on intranasal desmopressin acetate and who must be switched to the injection form, either because of poor intranasal absorption or because of the need for surgery, the comparable antidiuretic dose of the injection is about one-tenth the intranasal dose.

Parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration whenever solution and container permit.

HOW SUPPLIED
Desmopressin Acetate Injection 4 mcg/mL is available as a clear colorless sterile solution as follows:
Ampul - 4 mcg/mL - 1 mL - 10 per Box

KEEP REFRIGERATED AT 2° to 8°C (36° to 46°F).

September, 2004
©Hospira 2004 EN-0511 Printed in USA
HOSPIRA, INC., LAKE FOREST, IL 60045 USA

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
      desmopressin-ddavp
      Source IDH51-6DD2B935361A2C3306423935
      Generic name
      Desmopressin (DDAVP)
      Source IDH51-0A1FCF9A91C14E367C4686BB
      Class
      Endocrine and metabolic
      Source IDH51-C3F6C39B340F011F506EC6B2
      Subclass
      Legacy GlobalRPh directory entry
      Source IDH51-A45CC93D3A685035F9DB7115
      Primary uses
      1. Acute endocrine, metabolic, obstetric, or hemostatic indications that match the named hormone or metabolic agent.
        Source IDH51-96498D99EBD6536BF0661AC3
      Mechanism
      Selectively stimulates V2 receptors, increases renal water reabsorption, and releases von Willebrand factor and factor VIII.
      Source IDH51-868DAEFFA53EEA6DC80529C0
      Mechanism level
      drug_specific
      Source IDH51-B602DAF001777899038B0287
      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 IDH51-3C72456DB0B86052CB79A74A
      Administration orientation
      Route, dilution, concentration, and administration details load automatically from the existing GlobalRPh quick reference below; current exact-product verification remains required.
      Source IDH51-5B6C7F8894EDA3EB6541A4A9
      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 IDH51-8EF291E1258621142BBA8C4D
      Key safety orientation
      1. Legacy content must be reconciled against current labeling and institutional policy before clinical use.
        Source IDH51-068B0F589F09DB9F281DABFE
      Coverage path
      automatic_legacy_quick_reference
      Source IDH51-263F1C25E0910C74225D6865
      Coverage path label
      Automatic legacy GlobalRPh quick reference
      Source IDH51-A9430142BE714877ECE41343
      Legacy title
      Desmopressin (DDAVP)
      Source IDH51-39509E3E42AB2469B7F40CE7
      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 IDH51-336C960190F92CCD185117B3
      Search text
      Desmopressin (DDAVP) Endocrine and metabolic Legacy GlobalRPh directory entry Acute endocrine, metabolic, obstetric, or hemostatic indications that match the named hormone or metabolic agent. Selectively stimulates V2 receptors, increases renal water reabsorption, and releases von Willebrand factor and factor VIII. 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 IDH51-88C9FE1981EF27597F50B969
      Official access mode
      none
      Source IDH51-E12117BA2E33FA1C4F4FBA9E
      Official access reason
      No source-backed DailyMed action has been verified for this umbrella or legacy record; identify the exact product before searching.
      Source IDH51-531E9E055B5B548D810762AB

      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 IDH51-5B3898D3882D27C182B0BDB4
      Summary
      Renal dosing status has not been locally normalized; use the current package insert before ordering or administration.
      Source IDH51-1289C49E08BAAD9B1354A60F
      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-B211EBD143C17AAE9BD83BBE

      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-D11FBC88BC2E91CBD78056A5

      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-F666789C8A6D5CEF4EA01E3D
      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
      desmopressin-ddavp
      Source IDH51-1D10ACCA3E65A053F6660AFE
      Legacy title
      Desmopressin (DDAVP)
      Source IDH51-AC63BDCACC6AA3B7EE897FD6
      Generic name
      Desmopressin (DDAVP)
      Source IDH51-68EAC81784DD165208679344
      Class
      Endocrine and metabolic
      Source IDH51-BD1B758F9602BE49D23316BA
      Subclass
      Legacy GlobalRPh directory entry
      Source IDH51-86049A89E02F888DD5AA84FD
      Summary
      Existing GlobalRPh IV dilution monograph retained for migration into the unified reference.
      Source IDH51-D9570A2D7F25A70B34279B48
      Populations
      1. Population not yet normalized
        Source IDH51-A5EA4FF0AE57D14F90DA82A9
      Evidence tier
      Legacy catalog - migration review required
      Source IDH51-FD503659A0906D64D1C959F8
      High alert
      false
      Source IDH51-077BFB648A725119DD7202C5
      Hazardous
      false
      Source IDH51-9354ED6E806C1894AE8D04B5
      Status
      Legacy migration
      Source IDH51-1528B401B3549D0A814808D2
      Version added
      Legacy
      Source IDH51-CF4946D74881CB01474BD7E7
      Sources
      LabelUrlKind
      Source IDH51-D566DFE2718A705AB7503027
      GlobalRPh legacy IV dilution monograph
      Source IDH51-AA8AB69F72E5B898C764DD4E
      legacy:auto
      Source IDH51-5051FE37F35F967920F567E0
      Legacy
      Source IDH51-6701DD71AC0055F19677150C
      Clinical release verification
      Audit version
      3.4
      Source IDH51-6DA8E8421D9ABE44E5280420
      Audited on
      2026-08-30
      Source IDH51-13731DCE9561DEFA2D24AC03
      Level
      red
      Source IDH51-0D701286085DB78BC1AD7D90
      Release gate
      unverified_or_unclassified_sources_do_not_release_as_current
      Source IDH51-89478E4D769FE1EBA0F27D1D
      Exact current label candidate
      false
      Source IDH51-C2503D11FD250F294DB63073
      Reference url count
      0
      Source IDH51-9516136462FA43C6BFE0CB86
      Broken reference count
      0
      Source IDH51-9E302298C723553AAFE2F089
      Point of use confirmation required
      true
      Source IDH51-C484515A179EECD012F74CAE
      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-A71DBA63FEB5348AF6027ED0

      Dosing source fields

      Id
      desmopressin-ddavp
      Source IDH51-DD41B3FB27969415C4AD1ACF
      Generic name
      Desmopressin (DDAVP)
      Source IDH51-40B13A1872BFD88B25F0A149
      Coverage status
      direct_official_label_access_plus_legacy_reference
      Source IDH51-64E80386D6A97706436FECA2
      Package insert
      Query name
      Desmopressin
      Source IDH51-346C0D447FDE79F9E88007E3
      Product and route must match
      true
      Source IDH51-995545A3DCA2E75F848E8970
      Live current label enabled
      false
      Source IDH51-1800178EFEA146691CA02312
      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-B9A0AD41D013F18086965496
      Direct official label access enabled
      true
      Source IDH51-8D6EAA3660030ED4965A4EFD
      Outbound server request required
      false
      Source IDH51-736829AB36BDD47A95E08943
      Local summary status
      not_bundled
      Source IDH51-595F2A0402623A351217128B
      Clinical review
      Locally normalized
      false
      Source IDH51-BCA9A9645C5884F5233E7475
      Reviewed
      2026-08-29
      Source IDH51-7A92EB5A45EFFBA3AEA3C49B
      Status
      Direct official package-insert access enabled; indication-specific local normalization pending.
      Source IDH51-94606168CEB2E574F8D13939
      Clinical release verification
      Audit version
      3.4
      Source IDH51-87877C736D51E21E43094E95
      Audited on
      2026-08-30
      Source IDH51-6C9A1F943C23F72F318A3B1F
      Level
      red
      Source IDH51-D828F17D6EF8B83D7270632C
      Release gate
      unverified_or_unclassified_sources_do_not_release_as_current
      Source IDH51-28A14CE75EAD1A2B3F926D76
      Exact current label candidate
      false
      Source IDH51-CD88ACF8E4364CA1ABAE42D9
      Reference url count
      0
      Source IDH51-380FF30359327781A1625AC0
      Broken reference count
      0
      Source IDH51-54F65B556151AFED7F906A8A
      Point of use confirmation required
      true
      Source IDH51-8D0325FF548494FCEFE5CDB9
      Note
      Do not treat this record as a fully current product-specific monograph until the exact IV formulation and current sources are confirmed.
      Source IDH51-61C96B6C66A8D67D562D5DC6
      Historical preparation assessment

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

      Id
      desmopressin-ddavp
      Source IDH51-B064B9BC1D8566B4B30C2794
      Name
      Desmopressin (DDAVP)
      Source IDH51-ACF276B62437075E90A0EB2D
      Therapeutic class
      Endocrine and metabolic
      Source IDH51-33A92E8E73DB5FFA149CD208
      Review version
      3.1
      Source IDH51-86277D4CDB25FE8BCF886DB0
      Review date
      2026-08-30
      Source IDH51-ED8CD9F934DD0E9159379D94
      Release status
      no_released_dilution_current_label_review_required
      Source IDH51-6FB4B65A20FCDA18523A4D54
      Market status
      Status
      no_current_us_iv_spl_confirmed
      Source IDH51-0FF8A7A4486A88ABE639CA0B
      Basis
      No high-confidence current IV SPL was automatically selected; legacy information is segregated
      Source IDH51-1A161982FD00C478B05DF567
      Ten point assessment
      Exact formulation
      Not established in the currently normalized record. Use the current-label panel before clinical use.
      Source IDH51-B9EB2B34ECDB68AE109D4A58
      Reconstitution concentration
      Not established in the currently normalized record. Use the current-label panel before clinical use.
      Source IDH51-31EC91CE6E37D9169EEE6323
      Maximum or recommended final concentration
      Not established in the currently normalized record. Use the current-label panel before clinical use.
      Source IDH51-6D2585622FB480B038C44762
      Appropriate standardized containers
      Not established in the currently normalized record. Use the current-label panel before clinical use.
      Source IDH51-566B51F1D5242124D9697554
      Adult dosing range
      Not established in the currently normalized record. Use the current-label panel before clinical use.
      Source IDH51-92A6C08D52E3A941CB5AF981
      Pediatric dosing range
      Not established in the currently normalized record. Use the current-label panel before clinical use.
      Source IDH51-FCBC6EF16C632533FF5E26D4
      Neonatal dosing range
      Not established in the currently normalized record. Use the current-label panel before clinical use.
      Source IDH51-4CEF03891FDA0867FF7944F3
      Infusion time
      Not established in the currently normalized record. Use the current-label panel before clinical use.
      Source IDH51-88B0FAED756E975D8C3B63E5
      Fluid restriction alternatives
      Not established in the currently normalized record. Use the current-label panel before clinical use.
      Source IDH51-924273216715A5D536E085EA
      Current manufacturer labeling
      Match confidence
      unresolved
      Source IDH51-C2B4956E8BF87A1C102C2007
      Field provenance
      Exact formulation
      Primary
      not_found
      Source IDH51-96C89A234B3065CA9153CFC5
      Reconstitution concentration
      Primary
      not_found
      Source IDH51-4454B84272FAC2AD8561E3F9
      Maximum or recommended final concentration
      Primary
      not_found
      Source IDH51-08FA184D4D1422164359506C
      Appropriate standardized containers
      Primary
      not_found
      Source IDH51-72D9FF5D5AA660E7F014AA5E
      Adult dosing range
      Primary
      not_found
      Source IDH51-8E200DDF815F84B94448686A
      Pediatric dosing range
      Primary
      not_found
      Source IDH51-0CE7B8FFF7518C46FC6B5658
      Neonatal dosing range
      Primary
      not_found
      Source IDH51-62D266A0515A3599D9DD0A5E
      Infusion time
      Primary
      not_found
      Source IDH51-60A20C700ABBA6CFE1D40549
      Fluid restriction alternatives
      Primary
      not_found
      Source IDH51-21014784F54995A0141B6358
      Current manufacturer labeling
      Primary
      DailyMed search gateway
      Source IDH51-A8FCF71D4C701F6EE88A50C6
      Population applicability
      Adult
      Applicability
      not_established
      Source IDH51-3263B5753761B7BECB12D875
      Guide generation allowed
      false
      Source IDH51-D52C6F83B576A74F1FDADFE8
      Pediatric
      Applicability
      not_established
      Source IDH51-3FCC50E89CEFEBA0A0089F03
      Guide generation allowed
      false
      Source IDH51-FEE7A38ECBF7654ADE2A967D
      Neonatal
      Applicability
      not_established
      Source IDH51-E7CB6C3DCC17368EC42582F6
      Guide generation allowed
      false
      Source IDH51-DC73AF70DD854609BF9AEE84
      Route presence
      Structured dilution
      false
      Source IDH51-7038768C355977128C776545
      Iv push
      false
      Source IDH51-3B01EBAE4FB273F022C5C38D
      Continuous infusion
      false
      Source IDH51-6B4A0F70D6765113B2CB1A0C
      Pediatric source
      false
      Source IDH51-64DCA2ABE4BD4D44298138AE
      Neonatal source
      false
      Source IDH51-76423482EB71716A8FBD7926
      Legacy reference
      Status
      not_available
      Source IDH51-338329989DF2E2AB9ECAD132
      Label resolution
      Status
      build_environment_network_unavailable
      Source IDH51-1970F69FDF66B16EAF9E7369
      Source files
      1. catalog.json
        Source IDH51-584190CC67F08C9F79E1D30C
      2. dosing.json
        Source IDH51-E3552DCBB9DBD0D1267EA6AC
      3. legacy-map.json
        Source IDH51-B835C621CE7795038CC30076
      4. review-queue.json
        Source IDH51-66C676C754BC1B7F74547F09
      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 IDH51-1F1A9FB3B4E7EF1EC502727C
      Historical statement IDs and source locations

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

      Historical IDOriginal source locationStatus
      H51-1D10ACCA3E65A053F6660AFEcatalog.json
      /records/75/id
      Historical; current review incomplete
      H51-AC63BDCACC6AA3B7EE897FD6catalog.json
      /records/75/legacy_title
      Historical; current review incomplete
      H51-68EAC81784DD165208679344catalog.json
      /records/75/generic_name
      Historical; current review incomplete
      H51-BD1B758F9602BE49D23316BAcatalog.json
      /records/75/class
      Historical; current review incomplete
      H51-86049A89E02F888DD5AA84FDcatalog.json
      /records/75/subclass
      Historical; current review incomplete
      H51-D9570A2D7F25A70B34279B48catalog.json
      /records/75/summary
      Historical; current review incomplete
      H51-D11FBC88BC2E91CBD78056A5catalog.json
      /records/75/warnings/0
      Historical; current review incomplete
      H51-F666789C8A6D5CEF4EA01E3Dcatalog.json
      /records/75/stability_notes/0
      Historical; current review incomplete
      H51-A5EA4FF0AE57D14F90DA82A9catalog.json
      /records/75/populations/0
      Historical; current review incomplete
      H51-FD503659A0906D64D1C959F8catalog.json
      /records/75/evidence_tier
      Historical; current review incomplete
      H51-077BFB648A725119DD7202C5catalog.json
      /records/75/high_alert
      Historical; current review incomplete
      H51-9354ED6E806C1894AE8D04B5catalog.json
      /records/75/hazardous
      Historical; current review incomplete
      H51-1528B401B3549D0A814808D2catalog.json
      /records/75/status
      Historical; current review incomplete
      H51-68700F18FD528716B404B009catalog.json
      /records/75/reviewed
      Historical; current review incomplete
      H51-CF4946D74881CB01474BD7E7catalog.json
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