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Medication Reference

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Albumin

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Albumin (opens in a new tab)Original source URL: https://globalrph.com/dilution/albumin/ | Retrieved 2026-11-04

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

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https://globalrph.com/dilution/albumin/ (opens in a new tab)
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Not established in the retrieved source
Retrieved
2026-11-04T19:45:43.168897+00:00
Source location
div.post-content
Packaged content SHA-256
15332f0c2ea943448ff70b972ab9b16e85080c9d4bc8ad36acb6a4265455e17a
Original response SHA-256
d6adb1062163c8c550dd21549e64411228181b254e3737090379fac13de65580
Source body SHA-256
941036e6108e2d03fa343d3848f2e130505c2e559b728325b96bc6220a3ca56f

ALBUMIN

The authors make no claims of the accuracy of the information contained herein; and these suggested doses are not a substitute for clinical judgment. Neither GlobalRPh Inc. nor any other party involved in the preparation of this program 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. Read the disclaimer

Usual Diluents

NS, D5W

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

Pre-mixed vials:
[12.5 gm] [50 ml vial] [30 min]
[ 25 gm] [100ml ] [45 - 60 min]

Admixture:
[12.5 gm] [250ml (5%)] [30-60 min]
[25 gm] [500 ml (5%)] [1 - 3 hours]

Stability / Miscellaneous

Stability data:

Stability Refrigerated: May be stored for 36 months at +2°C to + 25°C (36°F to 77°F) from the date of manufacture.
Stability Room Temp: May be stored for 36 months at +2°C to + 25°C (36°F to 77°F) from the date of manufacture.
Reconstituted Vial/Powder: Solution


Notes: Intravenous use only. Store protected from light. Do not freeze. Do not use after expiration date. Do not use if turbid.


Infusion rate
:
25% vials: 2-3 ml/minute maximum.
5% solution: 5-10 ml/minute maximum.

Discard unused solution after 4 hours.
Dilute if necessary with D5W or NS.

Hypoproteinemia (Usual dose): 0.5- 1 gram/kg/dose q1-2 days as calculated to replace ongoing losses.
Maximum dose/day: 250 grams/48 hours.


Clinical Pharmacology
Albumin is a highly soluble, globular protein (MW 66,500), accounting for 70-80% of the colloid osmotic pressure of plasma.

Therefore, it is important in regulating the osmotic pressure of plasma. Human Albumin Grifols® 25% supplies the oncotic equivalent of approximately 5 times its volume of human plasma. It will increase the circulating plasma volume by an amount approximately 3.5 times the volume infused within 15 minutes, if the recipient is adequately hydrated3. This extra fluid reduces hemoconcentration and decreases blood viscosity. The degree and duration of volume expansion depend upon the initial blood volume.

When treating patients with diminished blood volume, the effect of infused albumin may persist for many hours. The hemodilution lasts for a shorter time when albumin is administered to individuals with normal blood volume.

Albumin is also a transport protein and binds naturally occurring, therapeutic, and toxic materials in the circulation.

Albumin is distributed throughout the extracellular water and more than 60% of the body albumin pool is located in the extravascular fluid compartment. The total body albumin in a 70 kg man is approximately 320 g; it has a circulating life span of 15-20 days, with a turnover of approximately 15 g per day.

3. INDICATIONS AND USAGE

3.1 General Principles

3.1.1 Volume Deficit
Since the oncotic pressure of AlbuRx® 25, Albumin (Human) 25% solution is about four times higher than that of normal human serum, it will expand the plasma volume if interstitial water is available for an inflow through the capillary walls. However, many patients suffering from an acute volume deficit also have some degree of interstitial dehydration. In the absence of hyperhydration, the treatment of an acute volume deficit with AlbuRx® 25 should therefore include isotonic electrolyte solutions with an albumin:electrolyte ratio of 1:3 or 1:4. By contrast, chronic volume deficits have usually been at least partially compensated for by the renal retention of sodium and water with some degree of tissue edema, and in these circumstances a trial with AlbuRx® 25 only is indicated. In any case, an anemia of clinically relevant magnitude requires specific treatment, and the metabolic needs of the patient with respect to fluid and electrolytes must be cared for.

3.1.2 Oncotic Deficit
The common causes of hypoproteinemia are protein-calorie malnutrition, defective absorption in gastro-intestinal disorders, faulty albumin synthesis in chronic hepatic failure, increased protein catabolism postoperatively or with sepsis, and abnormal renal losses of albumin with chronic kidney disease. In all these settings, the circulating albumin mass is initially maintained by a gradual transfer of extravascular albumin to the circulation, and hypoproteinemia ensues only when this compensatory potential has been exhausted. This implies that manifest hypoproteinemia is usually accompanied by a hidden extravascular albumin deficit of equal magnitude as the measurable intravascular deficit, which must be allowed for if AlbuRx® 25, Albumin (Human) 25% solution is infused because of the capillary permeability of that protein.

The primary sequel of the oncotic deficit resulting from hypoproteinemia is a loss of plasma and a gain of interstitial volume with increased lymphatic flow. As a secondary response, the kidney retains sodium and water which distribute themselves on both sides of the capillary walls and the plasma volume may be returned almost to normal when the interstitial hydrostatic pressure increases sufficiently to compensate for the decrease of the serum oncotic pressure. This chain of events is accelerated by the infusion of crystalloid fluids. The plasma volume is maintained at the price of interstitial edema.2

There is some evidence that a serum oncotic pressure near 20 mmHg - equaling a total serum protein (TSP) concentration of 5.2 g/100 mL - represents a threshold, below which the risk of complications increases.17 The target organs of hypoproteinemia include the skin, the lungs, and the intestine.10 Cutaneous edema lowers the oxygen tension of wounds and may thus impair the healing process.5 An oncotic deficit favors the development of interstitial pulmonary edema4 and the intestinal accumulation of fluids, which may progress to a paralytic ileus.9

Relief of the basic pathology is the definitive mode of therapy for the restoration of the plasma protein content, but this process takes time to become effective, and the rapid correction of a critical oncotic deficit by the administration of AlbuRx® 25, Albumin (Human) 25% solution - possibly in conjunction with a diuretic - may therefore be indicated, particularly in high-risk patients who have undergone abdominal, cardio-vascular, thoracic, or urologic surgery or who have acute bacteremia. In notably catabolic patients, attempts to raise the TSP level above 6 g/100 mL usually prove futile, even with massive doses of Albumin (Human).

It is emphasized that whereas AlbuRx® 25, Albumin (Human) 25% solution may be necessary to prevent or treat the aforementioned acute complications of hypoproteinemia, it is not indicated for treatment of the chronic condition itself.

3.2 Specific Indications

3.2.1 Acute circumstances in which AlbuRx® 25, Albumin (Human) 25% solution use is usually appropriate

Shock
Though electrolyte solutions such as Ringer's lactate and colloid-containing plasma substitutes may be used as an emergency treatment of shock, AlbuRx® 25, Albumin (Human) 25% solution used according to the aforementioned principles has a much longer intravascular half-life and may therefore be preferable. In addition, anemia of clinically relevant magnitude requires specific therapy with red cells.

Burns
Immediate therapy during the first 24 hours is directed at the administration of large volumes of crystalloid solutions and lesser amounts of AlbuRx® 25, Albumin (Human) 25% solution to maintain an adequate plasma volume and protein (colloid) content. For continuation of therapy beyond 24 hours, larger amounts of AlbuRx® 25 and lesser amounts of crystalloid are generally used .17 An optimum regimen for the use of Albumin (Human), electrolytes, and fluid in the early treatment of burns has, however, not yet been established.

With restoration of normal capillary function, a close relationship exists once again between infused Albumin (Human) and resultant increase in plasma oncotic pressure. A goal should be sought of maintaining a plasma albumin concentration of about 2.5 ±0.5 g/100 mL or a plasma oncotic pressure of 20 mmHg (equivalent to a TSP concentration of 5.2 g/100 mL).17 In the presence of extensive granulating wounds, a daily loss of up to 30 g of albumin may continue into the late post-burn period.1 Protein-rich oral feedings, or adequate parenteral nutrition should be included in the overall regimen to the fullest possible extent, though such treatment does not permit the rapid correction of an oncotic deficit.

3.2.2 Acute circumstances in which AlbuRx® 25, Albumin (Human) 25% solution use may be appropriate

Adult Respiratory Distress Syndrome
Several factors are usually involved in the development of the state now commonly called the adult respiratory distress syndrome, one of these being a hypoproteinemic fluid overload. If present, this may be corrected by the use of AlbuRx® 25, Albumin (Human) 25% solution and a diuretic.14,17

Cardiopulmonary Bypass
An adequate blood volume during cardiopulmonary bypass can be maintained with crystalloids as the only pump priming fluid, but only at the price of interstitial edema. A commonly employed program is an AlbuRx® 25, Albumin (Human) 25% solution and crystalloid pump prime adjusted so as to achieve a hematocrit of 20% and a plasma albumin level of 2.5 g/100 mL in the patient, but the level to which either may be lowered safely has not yet been defined.17

Pre- and postoperative Hypoproteinemia
Patients undergoing major surgery may lose more than half of their circulating albumin mass6,9,15, and complications attributable to an oncotic deficit may occur in such cases, as well as in septic and intensive care patients. Oncotic therapy with AlbuRx® 25, Albumin (Human) 25% solution may therefore be indicated in such patients, according to the principles outlined in 3.1.2. Temporary redistribution of protein is usually not an indication for Albumin (Human).

Third Space Problems of Infectious Origin
The sequestration of protein-rich fluid during acute peritonitis, pancreatitis, mediastinitis or extensive cellulitis may be of sufficient magnitude to require the treatment of a volume or an oncotic deficit with AlbuRx® 25, Albumin (Human) 25% solution3, although this occurrence is relatively rare.

Acute Liver Failure
In acute liver failure, AlbuRx® 25, Albumin (Human) 25% solution may serve the triple purpose of stabilizing the circulation, correcting an oncotic deficit and binding excessive serum bilirubin. The therapeutic approach is guided by the individual circumstances.17

Acute Nephrosis
Patients with acute nephrosis may prove refractory to cyclophosphamide or steroid therapy and their edema may even be aggravated initially by steroids. In such cases, a response may be elicited by combining 100 mL of 20-25% Albumin (Human) solution with an appropriate diuretic. This combination should be repeated daily for about one week, after which the patient may react satisfactorily to drug therapy.17

Ascites
The use of AlbuRx® 25, Albumin (Human) 25% solution for blood volume support may be indicated if circulatory instability follows the withdrawal of ascitic fluid.

Red Cell Resuspension Media
As a rule, the use of Albumin (Human) for resuspending red cells can be dispensed with. However, in exceptional circumstances such as certain types of exchange transfusions and the use of very large volumes of erythrocyte concentrates and frozen or washed red cells, the addition of AlbuRx® 25, Albumin (Human) 25% solution to the resuspension medium may be indicated in order to provide sufficient volume and/or avoid excessive hypoproteinemia during the subsequent transfusion. If necessary, 20-25 g or more of Albumin (Human) per liter of red cell suspension should be added as a concentrated solution to the isotonic, electrolyte suspension of erythrocytes immediately before transfusion, the individual dosage depending on the TSP level of the recipient.

Renal Dialysis
Patients undergoing long-term hemodialysis may need AlbuRx® 25, Albumin (Human) 25% solution for the treatment of a volume or an oncotic deficit. As a rule, the initial dose should not exceed 100 mL of a 20-25% solution, and the patients should be carefully observed for signs of a circulatory overload, to which they are particularly sensitive.

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

Hemolytic Disease of the Newborn
AlbuRx® 25, Albumin (Human) 25% solution may be indicated in order to bind and thus detoxify free serum bilirubin in severely hemolytic infants pending an exchange transfusion.

3.2.3 Circumstances in which AlbuRx® 25, Albumin (Human) 25% solution use is not justified
For the reasons set forth in sections 2. and 3.1, there is no valid reason for the use of AlbuRx® 25, Albumin (Human) 25% solution as an intravenous nutrient or for treating the stabilized hypoproteinemia accompanying chronic cirrhosis, chronic nephrosis, protein-losing enteropathy, malabsorption and pancreatic insufficiency.

If, however, a patient in this category has to cope with a superimposed acute stress, e.g. anesthesia, surgery or major infections, the patient's hemodynamic state, oncotic deficit and fluid balance should be carefully assessed and the appropriate steps taken as indicated by the individual circumstances.

4. CONTRAINDICATIONS
The only specific contraindication to the use of AlbuRx® 25, Albumin (Human) 25% solution is a history of an incompatibility reaction to Albumin (Human) in the individual recipient (see ADVERSE REACTIONS).

5. WARNINGS
AlbuRx® 25, Albumin (Human) 25% solution is made from human plasma. Products made from human plasma may contain infectious agents, such as viruses, that can cause disease. The risk that such products will transmit an infectious agent has been extremely reduced by screening plasma donors for prior exposure to certain viruses, by testing for the presence of certain current virus infections, and by inactivating and/or removing certain viruses through alcohol fractionation and through heat treatment of the product in the final container for 10 hours at 60°C. Despite these measures, such products can still potentially transmit disease. A theoretical risk for transmission of Creutzfeldt-Jakob Disease (CJD) is considered extremely remote. No cases of transmission of viral diseases or CJD have ever been identified for Albumin (Human). There is also the possibility that unknown infectious agents may be present in such products. All infections thought by a physician possibly to have been transmitted by this product should be reported by the physician or other healthcare provider to CSL Behring at 1-800-504-5434. The physician should discuss the risks and benefits of this product with the patient.

Turbid solutions must not be used. Do not begin administration more than 4 hours after introduction of the administration set. Partially used bottles must be discarded. There exists a risk of potentially fatal hemolysis and acute renal failure from the inappropriate use of sterile water for injection as a diluent for AlbuRx® 25, Albumin (Human) 25% solution. Acceptable diluents include 0.9% sodium chloride or 5% dextrose in water.

6. PRECAUTIONS
Adequate precautions should be taken against circulatory overload and may include pulmonary auscultation or X-ray as well as monitoring the central venous or pulmonary artery wedge pressure. Special caution is indicated in patients with stabilized chronic anemia, congestive heart failure and renal insufficiency.

Pregnancy Category C
Animal reproduction studies have not been conducted with AlbuRx® 25, Albumin (Human) 25% solution. It is also not known whether AlbuRx® 25 can cause fetal harm when administered to a pregnant woman or can affect reproduction capacity. AlbuRx® 25 should be given to a pregnant woman only if clearly needed. There is, however, no evidence for any contraindication to the use of AlbuRx® 25 specifically associated with reproduction, pregnancy or the fetus.

Use an intravenous infusion set suitable for the infusion of blood and blood products.

7. ADVERSE REACTIONS
Since AlbuRx® 25, Albumin (Human) 25% solution is sterile when coming from the manufacturer, bacterial contamination with the risk of post-infusion septicemia can only occur if the container has been damaged or following puncture of the rubber cap (see WARNINGS).

Though very rare, non-septic incompatibility reactions including nausea, chills, fever, urticaria, headache and hypotension following the administration of albumin-containing preparations have been recorded.8,11,12,17 A favorable response was observed to the intravenous administration of 50 to 100 mg of prednisolone.12

8. DOSAGE AND ADMINISTRATION
AlbuRx® 25, Albumin (Human) 25% solution must be administered intravenously. The venipuncture site should not be infected or traumatized, and should be prepared with standard aseptic technique. The solution is compatible with whole blood or packed red cells as well as the usual electrolyte and carbohydrate solutions intended for intravenous use. By contrast, it should not be mixed with protein hydrolysates, amino acid mixtures, or solutions containing alcohol. It is ready for use as contained in the bottle and may be given without regard to the blood group of the recipient.

The dosage of AlbuRx® 25, Albumin (Human) 25% solution is based on the principles outlined in the section on indications but should always be adapted to the individual situation. The quantities required may be underestimated because of hidden extravascular deficits, and the effect of AlbuRx® 25 infusion on the serum protein level should therefore be checked by laboratory analysis.

8.1 Volume Deficit
The appropriate AlbuRx® 25, Albumin (Human) 25% solution dose for the treatment of a volume deficit should be estimated from the recipient's hemodynamic response7, supplemented with the established safeguards against a circulatory overload. In the absence of active hemorrhage, the total dose should at any rate not exceed the normal circulating albumin mass, i.e. 2 g per kg body weight.

8.2 Oncotic Deficit
The appropriate AlbuRx® 25, Albumin (Human) 25% solution dose in grams of protein for the correction of an oncotic deficit can, as an average, be estimated from the difference between the desired and the actual TSP level x plasma volume (~40 mL/kg) × 2, the latter factor allowing for the hidden extravascular deficit. The individual effect is, however, variable and should be checked by measuring the post-infusion TSP level.10,17

8.3 Hemolytic Disease of the Newborn
The appropriate AlbuRx® 25, Albumin (Human) 25% solution dose for the binding of free serum bilirubin in severely hemolytic infants is 1 g/kg body weight, to be given about one hour prior to the exchange transfusion, and caution is recommended in hypervolemic infants.

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

9. HOW SUPPLIED
AlbuRx® 25, Albumin (Human) 25% solution is supplied in 50 mL (NDC 44206-251-05) and 100 mL (NDC 44206-251-10) vials, with complete directions for use.

10. STORAGE
AlbuRx® 25, Albumin (Human) 25% solution should be stored at a temperature not exceeding 30°C (86°F). It should not be used after the expiration date printed on the label.

REFERENCES

  1. Birke G, Liljedahl SO, Plantin LO, Reizenstein P. Acta Chir. Scand. 1968;134:27.
  2. Cervera AL, Moss G. J. Trauma. 1974;14:506.
  3. Clowes GH Jr, Vucinic M, Weidner MG. Ann. Surg. 1966;163:866.
  4. Gaar KA Jr, Taylor AE, Owens LJ, Guyton AC. Amer. J. Physiol. 1967;213:79.
  5. Heughan C, Niinikoski J, Hunt TK. Surg. Gynec. Obstet. 1972;135:257.
  6. Hoye RC, Paulson DF, Ketcham AS. Surg. Gynec. Obstet. 1970;131:943.
  7. Kinney JM, Egdahl RH, Zuidema GD. Manual of Preoperative and Postoperative Care, American College of Surgeons. Philadelphia: W. B. Saunders Co; 1971.
  8. Lowenstein E. In: Sgouris JT, René A, ed. Proceedings of the Workshop on Albumin, February 12-13. Bethesda, Maryland 20014: DHEW Publication NIH 76-925, NHLI; , p. 302, 1975.
  9. Moss G. Surg. Forum. 1967;18:333.
  10. Pappova E, Bachmeier W, Crevoisier JL, Kollar J, Kollar M, Tobler P, Zahler HW, Zaugg D, Lundsgaard-Hansen P. Vox Sang. 1977;33:307.
  11. Ring J, Messmer K. Lancet. 1977;1:466.
  12. Ring J, Seifert J, Lob G, Coulin K, Brendel W. Klin. Wschr. 1974;52:595.
  13. Sgouris JT, René A, ed. Proceedings of the Workshop on Albumin, February 12-13. Bethesda, Maryland 20014: DHEW Publication NIH 76-925, NHLI; 1975.
  14. Skillman JJ, Parikh BM, Tanenbaum BJ. Amer. J. Surg. 1970;119:440.
  15. Skillman JJ, Tanenbaum BJ. Current Topics in Surgical Research. New York: Academic Press; 1970;2:523.
  16. Starling EH. J. Physiol. 1896;19:312-326.
  17. Tullis JL. JAMA. 1977;237:355,460

Manufactured by:
CSL Behring AG
Bern, Switzerland
US License No. 1766

Distributed by:
CSL Behring LLC
Kankakee, IL 60901 USA

Revised: June 2007
Part number: 02771/907

Source: Package insert.

Albumin - Sample dosing for a 70 kg patient:

Generally, albumin 5% solution is used in hypovolemic or intravascularly depleted patients and albumin 25% solution is used in fluid and sodium restricted patients.2 Usual dose is 25 grams and may be repeated in 15-30 minutes if the desired response is not achieved (no more than 250 grams should be administered in a 48 hour period). 2
Depending on the indication, always review the appropriateness of alternative options such as crystalloid therapy or non-protein colloids/volume expanders.

-----------------------------------------------------------------------
Hypovolemia:
-----------------------------------------------------------------------

Give 5% albumin 0.5 - 1 gram/kg/dose = 35 grams to 70 grams based on the weight entered earlier (70.0 kg). This translates into a total volume (range) of 5% albumin of
700 to 1400 mL. Infusion rate - 5% albumin: commonly started at a rate of 1 to 2 mL/min and not exceeding 4 mL/minute in patients with normal plasma volume. 1,2 (possibly up to maximum of 5 to 10 mL/min in patients with concomitant hypoproteinemia2 ). May repeat infusion as needed.

If 5% albumin bags are not available, may dilute 25% albumin vials with NS or D5W:
Albumin 5% - 250ml:
Withdraw 50ml from 250ml NS IV bag and add 50mL 25% albumin (12.5g) albumin.

Albumin 5% - 500ml:
Withdraw 100ml from 500ml NS and add 100mL 25% albumin (25g) albumin.

Albumin vials: Do not use if the solution is turbid. Since this product contains no antimicrobial preservative, do not begin administration more than 4 hours after the container has been entered.

-----------------------------------------------------------------------
Large volume paracentesis - over 5 Liters:
-----------------------------------------------------------------------

Preventing post-paracentesis circulatory dysfunction (PPCD):
Albumin 25% - 5 to 8 grams for each liter removed or 50 grams total for paracentesis over 5 liters2.
Package insert4 - Adults: 8 grams for every 1,000 mL of ascitic fluid removed.

Infusion volumes (albumin 25%):
5 grams: 20 mL.
8 grams: 32 mL
50 grams: 200 mL

Infusion rate: Do not exceed 1 mL/min in patients with normal plasma volume.1,2,4 (or maximum rate of 2-3 mL/min in patients with hypoproteinemia.2 )

Some institutions provide guidelines for albumin (if use is justified) and less than 5 liters are removed.
Consider a rounding protocol if possible e.g.:
< 1.5 liters removed --------- albumin dose: 0 grams
1.6 to 2 liters removed ------- albumin dose: 12.5 grams (50 mL)
2.1 to 4 liters removed ------- albumin dose: 25 grams (100 mL)
4.5 liters removed -------------- albumin dose: 37.5 grams (150 mL)

-----------------------------------------------------------------------
Spontaneous bacterial peritonitis (SBP) in patients with cirrhosis:
-----------------------------------------------------------------------

Albumin 25% 1.5 grams/kg (105 grams based on weight entered above) on Day 1. Then give 1 gram/kg ( 70 grams based on weight entered above) on Day 3.2

Infusion rate: Do not exceed 1 mL/min in patients with normal plasma volume.1,2,4 (or maximum rate of 2-3 mL/min in patients with hypoproteinemia.2 )

-----------------------------------------------------------------------
Acute nephrosis:
-----------------------------------------------------------------------

Adults: Albumin: 25 grams together with diuretic once a day for 7-10 days4

References

[1] Hillyer, CD. Blood Banking and Transfusion Medicine: Basic Principles & Practice. Churchill Livingstone/ Elsevier Health Sciences, 2007. pp 281, 282.
Infusion rates: "Because high rates of albumin infusion can cause circulatory overload and pulmonary edema, 5% albumin solutions are commonly started at a rate of 1 to 2/mL/min and are not usually infused at a faster rate than 4 mL/min, and 25% albumin solutions are not infused at rates faster than 1 mL/min."

[2] Lexi-Comp, Inc. (Lexi-Drugs). Lexi-Comp, Inc.; Accessed: February 17, 2014.

[3] Package insert data: accessed Feb 17,2014. Albumin (Human) 25 % - 12.5 g in 50 mL. CSL Behring LLC. Kankakee, IL 60901 USA. US License No. 1767. Revised August, 2012.

[4] Package insert data: accessed Feb 17,2014. Albumin (Human) 25 % - 12.5 g in 50 mL. Octapharma USA Inc. 121 River Street, 12 th floor. Hoboken, NJ 07030. Revised: 8/2008.

[5] Package insert data: accessed Feb 17,2014. Albuminar?-5 - Albumin (Human) USP 5% 250 mL. CSL Behring LLC. Kankakee, IL 60901 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.

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Renal
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Original classification
current_label_review_required
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    Dialysis
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    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.
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        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
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      Historical first look: uses, mechanism, dosing context, and administration

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

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      Source IDH51-296DD4B4EA72989B8D785C48
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      Albumin
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      Source IDH51-86ED598878B7D0EE390BEDF0
      Search text
      Albumin Electrolytes and fluids Legacy GlobalRPh directory entry Correction of the named fluid, electrolyte, acid-base, or oncotic abnormality under monitored conditions. Raises plasma colloid oncotic pressure and expands intravascular volume while transporting multiple ligands. 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-C791F8506CA86F3542AA50BF
      Official access mode
      none
      Source IDH51-1729A5317D81159C75CA039A
      Official access reason
      No source-backed DailyMed action has been verified for this umbrella or legacy record; identify the exact product before searching.
      Source IDH51-3017B4C940DF5EA11DF66852

      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 IDH51-1CD478CBB6ACCE60B14C0B89
      Summary
      Renal dosing status has not been locally normalized; use the current package insert before ordering or administration.
      Source IDH51-60254733ECD9D795EBCD406B
      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 IDH51-18C5D8A56B35BB07F3BE0494

      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 IDH51-05995FA7595E3B7E6D45D138

      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 IDH51-80446E213D435D58965FFEFB
      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
      albumin
      Source IDH51-FE18C8ED122A532DEAA194D1
      Legacy title
      Albumin
      Source IDH51-F20BB4D7E6C92C6A07EC8FA0
      Generic name
      Albumin
      Source IDH51-073A3E1DD06A6B699F98FC4F
      Class
      Electrolytes and fluids
      Source IDH51-1DF90EBD64780838ABF08CAB
      Subclass
      Legacy GlobalRPh directory entry
      Source IDH51-71398121365E1A0EDD18F57C
      Summary
      Existing GlobalRPh IV dilution monograph retained for migration into the unified reference.
      Source IDH51-0380CF0426C53E5C7B076220
      Populations
      1. Population not yet normalized
        Source IDH51-5E837CCC8A863BA1D734B033
      Evidence tier
      Legacy catalog - migration review required
      Source IDH51-71D54C959631CB2DA8A66E82
      High alert
      false
      Source IDH51-DA2B58B6682A5860FBB62419
      Hazardous
      false
      Source IDH51-50387DEEAF1EB7B3C976597F
      Status
      Legacy migration
      Source IDH51-068D01F9D34E2101E9020D65
      Version added
      Legacy
      Source IDH51-099406AE21292C7701AEA9EC
      Sources
      LabelUrlKind
      Source IDH51-7E219547886FDD36F9D22F2B
      GlobalRPh legacy IV dilution monograph
      Source IDH51-DE3D72D9083C20CA910AF691
      legacy:auto
      Source IDH51-36B4F72454AE2AAB8304F962
      Legacy
      Source IDH51-45B0DD9925C6659BB21F802F
      Clinical release verification
      Audit version
      3.4
      Source IDH51-29CE38AE05D310642BF60129
      Audited on
      2026-08-30
      Source IDH51-0BB8072D8127BC91624A8D09
      Level
      red
      Source IDH51-C8AD96AEA9088DEC26874A00
      Release gate
      unverified_or_unclassified_sources_do_not_release_as_current
      Source IDH51-41892BC9A7C8F702722B61F9
      Exact current label candidate
      false
      Source IDH51-E40456346B783B1A4E961CB7
      Reference url count
      0
      Source IDH51-CEE3154D29149DAC349BB07C
      Broken reference count
      0
      Source IDH51-DC9E5B0AAD6D57AD0AC54404
      Point of use confirmation required
      true
      Source IDH51-708EDB6A759DB77F197CF766
      Note
      Do not treat this record as a fully current product-specific monograph until the exact IV formulation and current sources are confirmed.
      Source IDH51-5FD228EA6FAA4568E52E0E12
      Dailymed search url
      https://dailymed.nlm.nih.gov/dailymed/search.cfm?query=Albumin (opens in a new tab)
      Source IDH51-388AA7EBD45A8AA7BE4C10CC

      Dosing source fields

      Id
      albumin
      Source IDH51-0D7466EFC9B9EFF107C4C7D2
      Generic name
      Albumin
      Source IDH51-3CA6861F4258262A079F424D
      Coverage status
      direct_official_label_access_plus_legacy_reference
      Source IDH51-21B043CFFF9F9969A33B9F52
      Package insert
      Query name
      Albumin
      Source IDH51-08B0B8BFBE8E62D8CEE2340F
      Product and route must match
      true
      Source IDH51-429FCD0F6D47C156ED4A33FB
      Live current label enabled
      false
      Source IDH51-300715A25307B19003145FE0
      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 IDH51-649AE270F03092B7B288686D
      Direct official label access enabled
      true
      Source IDH51-5C55B9AF730643DF44F8066F
      Outbound server request required
      false
      Source IDH51-6913E9FB14A6EFD5E70357CF
      Local summary status
      not_bundled
      Source IDH51-E85B9179694DC1F0BBE49F0E
      Clinical review
      Locally normalized
      false
      Source IDH51-2D043EF22B515BEC0CA53A84
      Reviewed
      2026-08-29
      Source IDH51-C356637E52D88D478533DA2B
      Status
      Direct official package-insert access enabled; indication-specific local normalization pending.
      Source IDH51-FCF1A0C58C143F7A1F02EBB9
      Clinical release verification
      Audit version
      3.4
      Source IDH51-E755D94F52CDB3C67F4DECCE
      Audited on
      2026-08-30
      Source IDH51-E6E3902C9BFFBB9BFF0DBAEB
      Level
      red
      Source IDH51-12600EEA6C174033D6842FF5
      Release gate
      unverified_or_unclassified_sources_do_not_release_as_current
      Source IDH51-A95F6285B68925C94D2571AF
      Exact current label candidate
      false
      Source IDH51-7685E31EBE0E3DACD3DD2B62
      Reference url count
      0
      Source IDH51-9B40CAFFC84663269CF25937
      Broken reference count
      0
      Source IDH51-725611FDA9558A8D37739058
      Point of use confirmation required
      true
      Source IDH51-AF87866D4728DC0CDC238474
      Note
      Do not treat this record as a fully current product-specific monograph until the exact IV formulation and current sources are confirmed.
      Source IDH51-7302E4CB88AC1C848B5794AE
      Dailymed search url
      https://dailymed.nlm.nih.gov/dailymed/search.cfm?query=Albumin (opens in a new tab)
      Source IDH51-FBEE0D43DDC81217A52F0D02
      Historical preparation assessment

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

      Id
      albumin
      Source IDH51-4B567B0F490D40D19D653BDA
      Name
      Albumin
      Source IDH51-A555F93D83AFDBAB9842186D
      Therapeutic class
      Electrolytes and fluids
      Source IDH51-8CE7C6504A347FFB490B3918
      Review version
      3.1
      Source IDH51-D19B0781DC37C73B39AB15AE
      Review date
      2026-08-30
      Source IDH51-F517563155C7B518F5218E21
      Release status
      no_released_dilution_current_label_review_required
      Source IDH51-3CB0B9AB791D31D1797AE8A1
      Market status
      Status
      no_current_us_iv_spl_confirmed
      Source IDH51-251B43083733CD35410777E7
      Basis
      No high-confidence current IV SPL was automatically selected; legacy information is segregated
      Source IDH51-75471D601A694E8EEACB4448
      Ten point assessment
      Exact formulation
      Not established in the currently normalized record. Use the current-label panel before clinical use.
      Source IDH51-73B023662D021B06766F4F0B
      Reconstitution concentration
      Not established in the currently normalized record. Use the current-label panel before clinical use.
      Source IDH51-A9941E70E25781ECFBCD3500
      Maximum or recommended final concentration
      Not established in the currently normalized record. Use the current-label panel before clinical use.
      Source IDH51-8622A6D562F8C38CE8FDFDDB
      Appropriate standardized containers
      Not established in the currently normalized record. Use the current-label panel before clinical use.
      Source IDH51-E2220E5E89FE231E4177EA76
      Adult dosing range
      Not established in the currently normalized record. Use the current-label panel before clinical use.
      Source IDH51-79B64422351A8B4D59D1A138
      Pediatric dosing range
      Not established in the currently normalized record. Use the current-label panel before clinical use.
      Source IDH51-83F3DFC7B756B6C23721A9CF
      Neonatal dosing range
      Not established in the currently normalized record. Use the current-label panel before clinical use.
      Source IDH51-DB403934BB5F94617C5BCFD5
      Infusion time
      Not established in the currently normalized record. Use the current-label panel before clinical use.
      Source IDH51-7977E96E356B3E51AC720652
      Fluid restriction alternatives
      Not established in the currently normalized record. Use the current-label panel before clinical use.
      Source IDH51-C01F0C31D284FE32969E8E9B
      Current manufacturer labeling
      Match confidence
      unresolved
      Source IDH51-269AF25D336223401E449B44
      Field provenance
      Exact formulation
      Primary
      not_found
      Source IDH51-9B12B6654976495816007D75
      Reconstitution concentration
      Primary
      not_found
      Source IDH51-2C3D7D2C83A1A1D8FB489138
      Maximum or recommended final concentration
      Primary
      not_found
      Source IDH51-82C0624C0B39E403E2453E50
      Appropriate standardized containers
      Primary
      not_found
      Source IDH51-DF421D60555FBDA7DD5F2214
      Adult dosing range
      Primary
      not_found
      Source IDH51-AEA51CB259C9BCB11DD34114
      Pediatric dosing range
      Primary
      not_found
      Source IDH51-12CF865E61E5CC9C0CB08D68
      Neonatal dosing range
      Primary
      not_found
      Source IDH51-FE17695CFBF822B37D4F32A1
      Infusion time
      Primary
      not_found
      Source IDH51-0CD3863C944E11667B88059D
      Fluid restriction alternatives
      Primary
      not_found
      Source IDH51-A59461C7DA8603F238EF08A8
      Current manufacturer labeling
      Primary
      DailyMed search gateway
      Source IDH51-B5B315A192001E939A2BAB49
      Population applicability
      Adult
      Applicability
      not_established
      Source IDH51-B7DEF0ABFB15714D4538633E
      Guide generation allowed
      false
      Source IDH51-40A74FADD2D56C7F3D35A51C
      Pediatric
      Applicability
      not_established
      Source IDH51-6D3C420D105B3DB75EBDDB12
      Guide generation allowed
      false
      Source IDH51-A201709F7B001454C48284F7
      Neonatal
      Applicability
      not_established
      Source IDH51-9667729A71A0475E6922E0F4
      Guide generation allowed
      false
      Source IDH51-72E238A541CD8D3AFEF95386
      Route presence
      Structured dilution
      false
      Source IDH51-810105E3565DB99A7FFC7F2C
      Iv push
      false
      Source IDH51-64403CFFC9EB4A71384360F4
      Continuous infusion
      false
      Source IDH51-0BB7D355924AECED82318BD3
      Pediatric source
      false
      Source IDH51-C4E2845BD049A5592B07897B
      Neonatal source
      false
      Source IDH51-8CAF314EE1EDBA95D46BBFD3
      Legacy reference
      Status
      not_available
      Source IDH51-57B587FDF34313F1E40F4733
      Label resolution
      Status
      build_environment_network_unavailable
      Source IDH51-86B3C89C0423CC8B23144144
      Source files
      1. catalog.json
        Source IDH51-BC098C1F63E18FBB8160B42A
      2. dosing.json
        Source IDH51-43084032EFDFF3AF3CB1C6EF
      3. legacy-map.json
        Source IDH51-A93F4CFA77E366D1A5FF492E
      4. review-queue.json
        Source IDH51-8FE336849D3B27D8DAADC12D
      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 IDH51-87919D26C556BC7B986DDD8B
      Historical statement IDs and source locations

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

      Historical IDOriginal source locationStatus
      H51-FE18C8ED122A532DEAA194D1catalog.json
      /records/9/id
      Historical; current review incomplete
      H51-F20BB4D7E6C92C6A07EC8FA0catalog.json
      /records/9/legacy_title
      Historical; current review incomplete
      H51-073A3E1DD06A6B699F98FC4Fcatalog.json
      /records/9/generic_name
      Historical; current review incomplete
      H51-1DF90EBD64780838ABF08CABcatalog.json
      /records/9/class
      Historical; current review incomplete
      H51-71398121365E1A0EDD18F57Ccatalog.json
      /records/9/subclass
      Historical; current review incomplete
      H51-0380CF0426C53E5C7B076220catalog.json
      /records/9/summary
      Historical; current review incomplete
      H51-05995FA7595E3B7E6D45D138catalog.json
      /records/9/warnings/0
      Historical; current review incomplete
      H51-80446E213D435D58965FFEFBcatalog.json
      /records/9/stability_notes/0
      Historical; current review incomplete
      H51-5E837CCC8A863BA1D734B033catalog.json
      /records/9/populations/0
      Historical; current review incomplete
      H51-71D54C959631CB2DA8A66E82catalog.json
      /records/9/evidence_tier
      Historical; current review incomplete
      H51-DA2B58B6682A5860FBB62419catalog.json
      /records/9/high_alert
      Historical; current review incomplete
      H51-50387DEEAF1EB7B3C976597Fcatalog.json
      /records/9/hazardous
      Historical; current review incomplete
      H51-068D01F9D34E2101E9020D65catalog.json
      /records/9/status
      Historical; current review incomplete
      H51-1BCB765A5837111384DA22D7catalog.json
      /records/9/reviewed
      Historical; current review incomplete
      H51-099406AE21292C7701AEA9ECcatalog.json
      /records/9/version_added
      Historical; current review incomplete
      H51-7E219547886FDD36F9D22F2Bcatalog.json
      /records/9/sources/0
      Historical; current review incomplete
      H51-DE3D72D9083C20CA910AF691catalog.json
      /records/9/sources/0/label
      Historical; current review incomplete
      H51-36B4F72454AE2AAB8304F962catalog.json
      /records/9/sources/0/url
      Historical; current review incomplete
      H51-45B0DD9925C6659BB21F802Fcatalog.json
      /records/9/sources/0/kind
      Historical; current review incomplete
      H51-29CE38AE05D310642BF60129catalog.json
      /records/9/clinical_release_verification/audit_version
      Historical; current review incomplete
      H51-0BB8072D8127BC91624A8D09catalog.json
      /records/9/clinical_release_verification/audited_on
      Historical; current review incomplete
      H51-C8AD96AEA9088DEC26874A00catalog.json
      /records/9/clinical_release_verification/level
      Historical; current review incomplete
      H51-41892BC9A7C8F702722B61F9catalog.json
      /records/9/clinical_release_verification/release_gate
      Historical; current review incomplete
      H51-E40456346B783B1A4E961CB7catalog.json
      /records/9/clinical_release_verification/exact_current_label_candidate
      Historical; current review incomplete
      H51-CB556840529A082044EF97F9catalog.json
      /records/9/clinical_release_verification/selected_setid
      Historical; current review incomplete
      H51-EF42999BA147F6DA281005B1catalog.json
      /records/9/clinical_release_verification/selected_label_title
      Historical; current review incomplete
      H51-C8FA5F61F06289C3FD3F408Ecatalog.json
      /records/9/clinical_release_verification/numeric_support_ratio
      Historical; current review incomplete
      H51-CEE3154D29149DAC349BB07Ccatalog.json
      /records/9/clinical_release_verification/reference_url_count
      Historical; current review incomplete
      H51-DC9E5B0AAD6D57AD0AC54404catalog.json
      /records/9/clinical_release_verification/broken_reference_count
      Historical; current review incomplete
      H51-708EDB6A759DB77F197CF766catalog.json
      /records/9/clinical_release_verification/point_of_use_confirmation_required
      Historical; current review incomplete
      H51-5FD228EA6FAA4568E52E0E12catalog.json
      /records/9/clinical_release_verification/note
      Historical; current review incomplete
      H51-388AA7EBD45A8AA7BE4C10CCcatalog.json
      /records/9/clinical_release_verification/dailymed_search_url
      Historical; current review incomplete
      H51-0D7466EFC9B9EFF107C4C7D2dosing.json
      /records/9/id
      Historical; current review incomplete
      H51-3CA6861F4258262A079F424Ddosing.json
      /records/9/generic_name
      Historical; current review incomplete
      H51-21B043CFFF9F9969A33B9F52dosing.json
      /records/9/coverage_status
      Historical; current review incomplete
      H51-08B0B8BFBE8E62D8CEE2340Fdosing.json
      /records/9/package_insert/query_name
      Historical; current review incomplete
      H51-0750CAAA716C1DCC2012D3DDdosing.json
      /records/9/package_insert/preferred_setid
      Historical; current review incomplete
      H51-429FCD0F6D47C156ED4A33FBdosing.json
      /records/9/package_insert/product_and_route_must_match
      Historical; current review incomplete
      H51-300715A25307B19003145FE0dosing.json
      /records/9/package_insert/live_current_label_enabled
      Historical; current review incomplete
      H51-649AE270F03092B7B288686Ddosing.json
      /records/9/package_insert/source_priority
      Historical; current review incomplete
      H51-5C55B9AF730643DF44F8066Fdosing.json
      /records/9/package_insert/direct_official_label_access_enabled
      Historical; current review incomplete
      H51-6913E9FB14A6EFD5E70357CFdosing.json
      /records/9/package_insert/outbound_server_request_required
      Historical; current review incomplete
      H51-E85B9179694DC1F0BBE49F0Edosing.json
      /records/9/package_insert/local_summary_status
      Historical; current review incomplete
      H51-1CD478CBB6ACCE60B14C0B89dosing.json
      /records/9/renal/classification
      Historical; current review incomplete
      H51-60254733ECD9D795EBCD406Bdosing.json
      /records/9/renal/summary
      Historical; current review incomplete
      H51-18C5D8A56B35BB07F3BE0494dosing.json
      /records/9/renal/method_note
      Historical; current review incomplete
      H51-2D043EF22B515BEC0CA53A84dosing.json
      /records/9/clinical_review/locally_normalized
      Historical; current review incomplete
      H51-C356637E52D88D478533DA2Bdosing.json
      /records/9/clinical_review/reviewed
      Historical; current review incomplete
      H51-FCF1A0C58C143F7A1F02EBB9dosing.json
      /records/9/clinical_review/status
      Historical; current review incomplete
      H51-E755D94F52CDB3C67F4DECCEdosing.json
      /records/9/clinical_release_verification/audit_version
      Historical; current review incomplete
      H51-E6E3902C9BFFBB9BFF0DBAEBdosing.json
      /records/9/clinical_release_verification/audited_on
      Historical; current review incomplete
      H51-12600EEA6C174033D6842FF5dosing.json
      /records/9/clinical_release_verification/level
      Historical; current review incomplete
      H51-A95F6285B68925C94D2571AFdosing.json
      /records/9/clinical_release_verification/release_gate
      Historical; current review incomplete
      H51-7685E31EBE0E3DACD3DD2B62dosing.json
      /records/9/clinical_release_verification/exact_current_label_candidate
      Historical; current review incomplete
      H51-3E7953A3E734579576C9F48Edosing.json
      /records/9/clinical_release_verification/selected_setid
      Historical; current review incomplete
      H51-0CE92E618055C8D83D03528Cdosing.json
      /records/9/clinical_release_verification/selected_label_title
      Historical; current review incomplete
      H51-4011D20DE13420BB9669069Ddosing.json
      /records/9/clinical_release_verification/numeric_support_ratio
      Historical; current review incomplete
      H51-9B40CAFFC84663269CF25937dosing.json
      /records/9/clinical_release_verification/reference_url_count
      Historical; current review incomplete
      H51-725611FDA9558A8D37739058dosing.json
      /records/9/clinical_release_verification/broken_reference_count
      Historical; current review incomplete
      H51-AF87866D4728DC0CDC238474dosing.json
      /records/9/clinical_release_verification/point_of_use_confirmation_required
      Historical; current review incomplete
      H51-7302E4CB88AC1C848B5794AEdosing.json
      /records/9/clinical_release_verification/note
      Historical; current review incomplete
      H51-FBEE0D43DDC81217A52F0D02dosing.json
      /records/9/clinical_release_verification/dailymed_search_url
      Historical; current review incomplete
      H51-296DD4B4EA72989B8D785C48first-look-v5.1.json
      /records/9/id
      Historical; current review incomplete
      H51-51CF9E84B0357F400326EB7Afirst-look-v5.1.json
      /records/9/generic_name
      Historical; current review incomplete
      H51-9391ACAA242ACA9AA08176FBfirst-look-v5.1.json
      /records/9/class
      Historical; current review incomplete
      H51-89D07D810DBC337438239C05first-look-v5.1.json
      /records/9/subclass
      Historical; current review incomplete
      H51-38268034EA1A27A458FD0CEAfirst-look-v5.1.json
      /records/9/primary_uses/0
      Historical; current review incomplete
      H51-5E6851E885E282F60FC641C4first-look-v5.1.json
      /records/9/mechanism
      Historical; current review incomplete
      H51-FF48B5E20A252C97041C55F2first-look-v5.1.json
      /records/9/mechanism_level
      Historical; current review incomplete
      H51-A7CB53EF977B93C833140E08first-look-v5.1.json
      /records/9/basic_dosing_orientation
      Historical; current review incomplete
      H51-4DECEDBE4980AAF6EDF744A7first-look-v5.1.json
      /records/9/administration_orientation
      Historical; current review incomplete
      H51-24DE08EBC78A6201E227FB7Bfirst-look-v5.1.json
      /records/9/renal_and_population_orientation
      Historical; current review incomplete
      H51-A9D0D29D8D16AAFBA5981A36first-look-v5.1.json
      /records/9/key_safety_orientation/0
      Historical; current review incomplete
      H51-3031D0A0125E821B2D47475Bfirst-look-v5.1.json
      /records/9/coverage_path
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      H51-4B567B0F490D40D19D653BDApreparation-assessments-v3.8.json
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