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Search 255 medications, read preserved historical references, and inspect separately reviewed preparation statements.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

Isoproterenol

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.

Isoproterenol (opens in a new tab)Original source URL: https://globalrph.com/dilution/isoproterenol/ | 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/isoproterenol/ (opens in a new tab)
Source date
Not established in the retrieved source
Retrieved
2026-11-04T19:49:36.570202+00:00
Source location
div.post-content
Packaged content SHA-256
a06f8d3a5f3683c4a807fb495914f7b873e5e95c02e1fdfc072cde57f5fdce26
Original response SHA-256
bdfc9398ac0bb2075113830f5c922b7143fb9071d01be7dc61c3b93b067c9a4f
Source body SHA-256
d71b3d1ea9602d46a4a8171ebceb28b74d9e80a5848a54356c35d017da187521

Isoproterenol (Isuprel ®)

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

D5W, NS

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

[1 mg] [250 ml] [Titrate]

[1 - 2 mg] [250-500 ml] [Titrate]

Stability / Miscellaneous

EXP: 1 DAY (RT).

(B1/B2) agonist. IV infusion: 2 to 20 mcg/ min.
Usual initial rate: 5 mcg/min.
Titrate to HR/BP.
May give IV-push (must use 1:50,000 dilution).

Calculation of drip rate:
1 mg/250 ml (ml/hr) = 15 x mcg/min. eg: 5 mcg/min = 75 ml/hr

DOSAGE AND ADMINISTRATION
ISUPREL injection 1:5000 should generally be started at the lowest recommended dose and the rate of administration gradually increased if necessary while carefully monitoring the patient. The usual route of administration is by intravenous infusion or bolus intravenous injection. In dire emergencies, the drug may be administered by intracardiac injection. If time is not of the utmost importance, initial therapy by intramuscular or subcutaneous injection is preferred.

Recommended dosage for adults with heart block, Adams-Stokes attacks, and cardiac arrest:
Route of Administration Preparation of Dilution Initial Dose Subsequent Dose Range*
Bolus intravenous injection Dilute 1 mL (0.2 mg) to 10 mL with Sodium Chloride Injection, USP, or 5% Dextrose Injection, USP 0.02 mg to 0.06 mg (1 mL to 3 mL of diluted solution) 0.01 mg to 0.2 mg (0.5 mL to 10 mL of diluted solution)
Intravenous infusion Dilute 10 mL (2 mg) in 500 mL of 5% Dextrose Injection, USP 5 mcg/min. (1.25 mL of diluted solution per minute)
Intramuscular Use Solution 1:5000 undiluted 0.2 mg (1 mL) 0.02 mg to 1 mg (0.1 mL to 5 mL)
Subcutaneous Use Solution 1:5000 undiluted 0.2 mg (1 mL) 0.15 mg to 0.2 mg (0.75 mL to 1 mL)
Intracardiac Use Solution 1:5000 undiluted 0.02 mg (0.1 mL)

*Subsequent dosage and method of administration depend on the ventricular rate and the rapidity with which the cardiac pacemaker can take over when the drug is gradually withdrawn.

There are no well-controlled studies in children to establish appropriate dosing; however, the American Heart Association recommends an initial infusion rate of 0.1 mcg/kg/min, with the usual range being 0.1 mcg/kg/min to 1 mcg/kg/min.

Recommended dosage for adults with shock and hypoperfusion states:

Route of Administration

Preparation of Dilution†

Infusion Rate††

Intravenous infusion

Dilute 5 mL (1 mg) in 500 mL of 5% Dextrose Injection, USP

0.5 mcg to 5 mcg per minute (0.25 mL to 2.5 mL of diluted solution)

†Concentrations up to 10 times greater have been used when limitation of volume is essential.

††Rates over 30 mcg per minute have been used in advanced stages of shock. The rate of infusion should be adjusted on the basis of heart rate, central venous pressure, systemic blood pressure, and urine flow. If the heart rate exceeds 110 beats per minute, it may be advisable to decrease or temporarily discontinue the infusion.

Recommended dosage for adults with bronchospasm occurring during anesthesia:

Route of Administration

Preparation of Dilution

Initial Dose

Subsequent Dose

Bolus

intravenous

injection

Dilute 1 mL (0.2 mg) to 10 mL with Sodium Chloride Injection, USP, or 5% Dextrose Injection, USP

0.01 mg to 0.02 mg (0.5 mL to 1 mL of diluted solution)

The initial dose may be

repeated when necessary

Parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration, whenever solution and container permit. Such solution should not be used.

HOW SUPPLIED
Ampul
0.2 mg (0.2 mg/mL)
1 mL
UNI-AMP® pak of 25

Ampul
1 mg (0.2 mg/mL)
5 mL
10 ampuls per carton

Protect from light. Keep in opaque container until used.
Store at controlled room temperature 20° to 25°C (68° to 77°F). [See USP.]
Do not use if the injection is pinkish or darker than slightly yellow or contains a precipitate.

©Hospira 2004
EN-0427

HOSPIRA, INC., LAKE FOREST, IL 60045 USA
Source: [package insert]

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
      isoproterenol
      Source IDH51-F181905C81E9792346B2D8B4
      Generic name
      Isoproterenol
      Source IDH51-78ADF6B12AC1D4E64858EF47
      Class
      Cardiovascular and vasoactive
      Source IDH51-EE6646D0A31B676919CC1F6F
      Subclass
      Legacy GlobalRPh directory entry
      Source IDH51-DC19CCFED37A1BAB27DE34BB
      Primary uses
      1. Acute rhythm, hemodynamic, blood-pressure, perfusion, or volume-management indications, depending on the named agent.
        Source IDH51-3430703694712314CDFE7206
      Mechanism
      Nonselectively stimulates beta-1 and beta-2 receptors, increasing cardiac activity and peripheral vasodilation.
      Source IDH51-F68EAFA41502B3FDE2002941
      Mechanism level
      drug_specific
      Source IDH51-F5510E5DA855BFE72C8A603F
      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-E9F007F3C4A4887D6691BD35
      Administration orientation
      Route, dilution, concentration, and administration details load automatically from the existing GlobalRPh quick reference below; current exact-product verification remains required.
      Source IDH51-57E9D43C80C0B783637099EC
      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-E04DFCF5FC506E28DED73495
      Key safety orientation
      1. Legacy content must be reconciled against current labeling and institutional policy before clinical use.
        Source IDH51-A3FFA607A0118203583EB453
      Coverage path
      automatic_legacy_quick_reference
      Source IDH51-0BDE0D0D050352E14A5DA1B4
      Coverage path label
      Automatic legacy GlobalRPh quick reference
      Source IDH51-59E21DFEBD67DEDA39B5B388
      Legacy title
      Isoproterenol
      Source IDH51-FD98AE39D3FFE98D1D5EE111
      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 IDH51-59B6D48D5C511A03F53A8C5C
      Search text
      Isoproterenol Cardiovascular and vasoactive Legacy GlobalRPh directory entry Acute rhythm, hemodynamic, blood-pressure, perfusion, or volume-management indications, depending on the named agent. Nonselectively stimulates beta-1 and beta-2 receptors, increasing cardiac activity and peripheral vasodilation. 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-C03929FABF2D4107F218AAC7
      Official access mode
      none
      Source IDH51-F13249CA818D6E29171FB543
      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-F5232B33D79877FD71B8CFAB

      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-FEA0AD8256FEA9208E2A9181
      Summary
      Renal dosing status has not been locally normalized; use the current package insert before ordering or administration.
      Source IDH51-6CBA58EA43EF6953D9B606EC
      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-C73522571BD6369EC2DEE068

      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-C4CA0CCFC1BFF70554779047

      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 IDH51-83DB7BF43FDF0709CC67D3CC
      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
      isoproterenol
      Source IDH51-3CF6171DD3F466BC3F2ACB3E
      Legacy title
      Isoproterenol
      Source IDH51-2F2F6B6AE0BE919263748812
      Generic name
      Isoproterenol
      Source IDH51-01FDFDCE23B32A62782F1D0E
      Class
      Cardiovascular and vasoactive
      Source IDH51-731F96E25E43765CEA5C78BF
      Subclass
      Legacy GlobalRPh directory entry
      Source IDH51-FE571E33C51021BB3C73526A
      Summary
      Existing GlobalRPh IV dilution monograph retained for migration into the unified reference.
      Source IDH51-4EAF0E40D2235520EED55934
      Populations
      1. Population not yet normalized
        Source IDH51-E62BB287977562C8DDD68FD8
      Evidence tier
      Legacy catalog - migration review required
      Source IDH51-47ACD5444EDD9C9AEE0D5106
      High alert
      false
      Source IDH51-6DF848638C61CC683FCF93F8
      Hazardous
      false
      Source IDH51-3B1435A5F0B7E96E1D93B56C
      Status
      Legacy migration
      Source IDH51-F8661D101427199C8EBCFDB8
      Version added
      Legacy
      Source IDH51-036E67317DC0CE6A3B269337
      Sources
      LabelUrlKind
      Source IDH51-87C5341EE75385DB52098244
      GlobalRPh legacy IV dilution monograph
      Source IDH51-1D6B796CE59992765CDF0836
      legacy:auto
      Source IDH51-FD391E4E2FD1C9B4413646F5
      Legacy
      Source IDH51-5E0C67ED7457205F256B3911
      Clinical release verification
      Audit version
      3.4
      Source IDH51-C1C5C6603865474B692E3519
      Audited on
      2026-08-30
      Source IDH51-FDA937D65125F6CF6E2C95FC
      Level
      red
      Source IDH51-32DADF9FB654B8E5FA5E69DC
      Release gate
      unverified_or_unclassified_sources_do_not_release_as_current
      Source IDH51-468A9BD5D4F67C1B49268133
      Exact current label candidate
      false
      Source IDH51-B1D72D500E3B6862806F42F1
      Reference url count
      0
      Source IDH51-FEE32161C29B9C175036397D
      Broken reference count
      0
      Source IDH51-F062A9722914955BEC37DAD5
      Point of use confirmation required
      true
      Source IDH51-36035D0A82A7E82BE9485413
      Note
      Do not treat this record as a fully current product-specific monograph until the exact IV formulation and current sources are confirmed.
      Source IDH51-311D63F4FE8E258660C689CA

      Dosing source fields

      Id
      isoproterenol
      Source IDH51-8D9210FABA671938EF39A07E
      Generic name
      Isoproterenol
      Source IDH51-8037BEACA623481E33F5B0A9
      Coverage status
      direct_official_label_access_plus_legacy_reference
      Source IDH51-FBF5E9205ECC8373146A0E0A
      Package insert
      Query name
      Isoproterenol
      Source IDH51-F56D7BDA140AD0EC1D4F7FD6
      Product and route must match
      true
      Source IDH51-E8D0CCB981F5C1D5E0C98645
      Live current label enabled
      false
      Source IDH51-55CF62F28EE0D70964B79152
      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 IDH51-4D870C1DB5ADF1B2E0E750E8
      Direct official label access enabled
      true
      Source IDH51-33AD4905F0E84BDA02C3E0E8
      Outbound server request required
      false
      Source IDH51-BE0B3B0C87F64E0C52AF9080
      Local summary status
      not_bundled
      Source IDH51-4A6C07F124A8F20C607D4990
      Clinical review
      Locally normalized
      false
      Source IDH51-0BEE9FE962B0E7005997FFF8
      Reviewed
      2026-08-29
      Source IDH51-0D980081F93DF7E1E2A7ADB9
      Status
      Direct official package-insert access enabled; indication-specific local normalization pending.
      Source IDH51-416F18F1E6289E0277C39159
      Clinical release verification
      Audit version
      3.4
      Source IDH51-769AD89BC3B2722CD3B4F1E2
      Audited on
      2026-08-30
      Source IDH51-54E7BF3A54FD0C11A9364EAD
      Level
      red
      Source IDH51-D92A606972397BF535A99F48
      Release gate
      unverified_or_unclassified_sources_do_not_release_as_current
      Source IDH51-E2C0285D2D99575A6B22C100
      Exact current label candidate
      false
      Source IDH51-DBEA6D90AE420B476E6AD04C
      Reference url count
      0
      Source IDH51-BB9E32703CBDF6EC71607120
      Broken reference count
      0
      Source IDH51-51DFB4054FD8DCBFB299B5FB
      Point of use confirmation required
      true
      Source IDH51-D2746A3DBE7264FA235DDDAD
      Note
      Do not treat this record as a fully current product-specific monograph until the exact IV formulation and current sources are confirmed.
      Source IDH51-06263ACC8280205E9C0037CE
      Historical preparation assessment

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

      Id
      isoproterenol
      Source IDH51-C2311A0E35E3E74E22DC869C
      Name
      Isoproterenol
      Source IDH51-BA7B9A2912C9D33F80EAEC65
      Therapeutic class
      Cardiovascular and vasoactive
      Source IDH51-F58E76DBC2B6C6FDB634830E
      Review version
      3.1
      Source IDH51-6552C6EDA5DEE483D99D5B42
      Review date
      2026-08-30
      Source IDH51-84F3888DCB198AAB86D6E85F
      Release status
      no_released_dilution_current_label_review_required
      Source IDH51-B689B6CBC2529C181BFF8766
      Market status
      Status
      no_current_us_iv_spl_confirmed
      Source IDH51-7DF7AABFE2C825A68ABE74FD
      Basis
      No high-confidence current IV SPL was automatically selected; legacy information is segregated
      Source IDH51-44CE594CC046C1256974FBEE
      Ten point assessment
      Exact formulation
      Not established in the currently normalized record. Use the current-label panel before clinical use.
      Source IDH51-8E722EDEA979D4C697CD38B1
      Reconstitution concentration
      Not established in the currently normalized record. Use the current-label panel before clinical use.
      Source IDH51-265D9AB37C13A2E89A318434
      Maximum or recommended final concentration
      Not established in the currently normalized record. Use the current-label panel before clinical use.
      Source IDH51-9950DB1A99D2A0FDD9F0F448
      Appropriate standardized containers
      Not established in the currently normalized record. Use the current-label panel before clinical use.
      Source IDH51-9152F17486597B24A81324F6
      Adult dosing range
      Not established in the currently normalized record. Use the current-label panel before clinical use.
      Source IDH51-B0BEAFF5DFB4C37D39B68297
      Pediatric dosing range
      Not established in the currently normalized record. Use the current-label panel before clinical use.
      Source IDH51-2BB390FE4B69C612D99A214D
      Neonatal dosing range
      Not established in the currently normalized record. Use the current-label panel before clinical use.
      Source IDH51-3BFED49EEC9D968D8E5EF99E
      Infusion time
      Not established in the currently normalized record. Use the current-label panel before clinical use.
      Source IDH51-0CABD8EE77B84044B24675B2
      Fluid restriction alternatives
      Not established in the currently normalized record. Use the current-label panel before clinical use.
      Source IDH51-9B77D93DD55BCFC49287DCE5
      Current manufacturer labeling
      Match confidence
      unresolved
      Source IDH51-77BCED3F16E676525EC6638A
      Field provenance
      Exact formulation
      Primary
      not_found
      Source IDH51-FDFEC58F8C5B3987C5651AEC
      Reconstitution concentration
      Primary
      not_found
      Source IDH51-C984C5C0C0513DD1A0B6109C
      Maximum or recommended final concentration
      Primary
      not_found
      Source IDH51-FE10D53EDF8321D6FFE83661
      Appropriate standardized containers
      Primary
      not_found
      Source IDH51-A9A10F32C48E136379A9692B
      Adult dosing range
      Primary
      not_found
      Source IDH51-B5E3F65559008D58A236E728
      Pediatric dosing range
      Primary
      not_found
      Source IDH51-F8106312B2396E26672A8D32
      Neonatal dosing range
      Primary
      not_found
      Source IDH51-EBE2507932F66935684274B9
      Infusion time
      Primary
      not_found
      Source IDH51-F43C6DD9987C74C3A68B9126
      Fluid restriction alternatives
      Primary
      not_found
      Source IDH51-03D7EB7A3AE9584A7956B9A3
      Current manufacturer labeling
      Primary
      DailyMed search gateway
      Source IDH51-53B72D0C532E4718982949EB
      Population applicability
      Adult
      Applicability
      not_established
      Source IDH51-4DE6DA29D503A4FE85AC54D5
      Guide generation allowed
      false
      Source IDH51-C3587CFCD32A64CF2B5E6B69
      Pediatric
      Applicability
      not_established
      Source IDH51-1E717357FBECFC96602B2BB5
      Guide generation allowed
      false
      Source IDH51-30763195E47CCEBB34435896
      Neonatal
      Applicability
      not_established
      Source IDH51-5A88B9CED420AEAADA947769
      Guide generation allowed
      false
      Source IDH51-A0C214A9D0ECFD92104F5BF0
      Route presence
      Structured dilution
      false
      Source IDH51-9542EB5BF8E54F5BC185BFD7
      Iv push
      false
      Source IDH51-1E8798AF37A133A3A7FADF34
      Continuous infusion
      false
      Source IDH51-CC0C740F733EF524F7243741
      Pediatric source
      false
      Source IDH51-BD62BF9DD8FEC376D36D852E
      Neonatal source
      false
      Source IDH51-285DE7334D98A96EA927873D
      Legacy reference
      Status
      not_available
      Source IDH51-DFC1720D6901515098367378
      Label resolution
      Status
      build_environment_network_unavailable
      Source IDH51-84F9F91C5991DE59A00A68BC
      Source files
      1. catalog.json
        Source IDH51-60ABF87112F14E9CBD009F1B
      2. dosing.json
        Source IDH51-3C65EE7654FD9B2BB25AFD4A
      3. legacy-map.json
        Source IDH51-ACFD9D19E5C85A345F29362E
      4. review-queue.json
        Source IDH51-E9CE67B8E5AFCAF62B86B5E0
      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 IDH51-73E46298CF7627482ED83EC8
      Historical statement IDs and source locations

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

      Historical IDOriginal source locationStatus
      H51-3CF6171DD3F466BC3F2ACB3Ecatalog.json
      /records/139/id
      Historical; current review incomplete
      H51-2F2F6B6AE0BE919263748812catalog.json
      /records/139/legacy_title
      Historical; current review incomplete
      H51-01FDFDCE23B32A62782F1D0Ecatalog.json
      /records/139/generic_name
      Historical; current review incomplete
      H51-731F96E25E43765CEA5C78BFcatalog.json
      /records/139/class
      Historical; current review incomplete
      H51-FE571E33C51021BB3C73526Acatalog.json
      /records/139/subclass
      Historical; current review incomplete
      H51-4EAF0E40D2235520EED55934catalog.json
      /records/139/summary
      Historical; current review incomplete
      H51-C4CA0CCFC1BFF70554779047catalog.json
      /records/139/warnings/0
      Historical; current review incomplete
      H51-83DB7BF43FDF0709CC67D3CCcatalog.json
      /records/139/stability_notes/0
      Historical; current review incomplete
      H51-E62BB287977562C8DDD68FD8catalog.json
      /records/139/populations/0
      Historical; current review incomplete
      H51-47ACD5444EDD9C9AEE0D5106catalog.json
      /records/139/evidence_tier
      Historical; current review incomplete
      H51-6DF848638C61CC683FCF93F8catalog.json
      /records/139/high_alert
      Historical; current review incomplete
      H51-3B1435A5F0B7E96E1D93B56Ccatalog.json
      /records/139/hazardous
      Historical; current review incomplete
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