GlobalRPh Renal Dosing Masterv6.6
Evidence addition

Amphotericin B liposomal (AmBisome)

AmBisome

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Renal guidance at a glance

Confirm the product, indication and renal measure. The selected summary is not a complete prescribing monograph.

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Display order is not a clinical ranking. Date of retrieval is not the label revision date. Sources are never merged into one regimen. Other sources and conflicts remain below.

Official source

Amphotericin B liposomal (AmBisome) - selected U.S. labeling

Product / population
Adults receiving intravenous liposomal amphotericin B, specifically AmBisome. Not interchangeable with deoxycholate, lipid-complex or other amphotericin formulations.
Renal measure
Qualitative renal/PK evidence; no label CrCl-based reduction table.
Labeled basic dosing

Labeled adult initial doses: empirical therapy 3 mg/kg IV daily; systemic fungal infection 3-5 mg/kg daily; HIV-associated cryptococcal meningitis 6 mg/kg daily. Infuse initially over about 120 minutes; approximately 60 minutes may be used when tolerated.

Renal information and dialysis

Renal-impairment pharmacokinetics have not been studied, although patients with pre-existing dysfunction received treatment. No numeric CrCl reduction is provided. Hemodialysis/peritoneal dialysis do not appear to materially increase elimination.

Selected warnings and limits

Monitor renal function and electrolytes. This product cannot be substituted milligram-for-milligram for another amphotericin formulation. Use only its own preparation instructions.

Source revision: Label revision date not separately recorded; retrieval date is not the revision date. | Retrieved: 2026-09-05. Retrieval date is not the revision date.

Source: https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=f7be6506-4d20-401e-a0ff-02ad7c33158a

Scope: Selected dosing/renal sections read; concise local summary, not full prescribing information. GlobalRPh v6.6.

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Source-first renal review

Evidence sources and renal implications

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Official product label

Amphotericin B liposomal (AmBisome) - selected U.S. labeling

Adults receiving intravenous liposomal amphotericin B, specifically AmBisome. Not interchangeable with deoxycholate, lipid-complex or other amphotericin formulations.

Renal method: Qualitative renal/PK evidence; no label CrCl-based reduction table.
Retrieved: 2026-09-05

Professional guidance

UCSF AmBisome - renal and dialysis protocols

Adults receiving intravenous liposomal amphotericin B, specifically AmBisome. Not interchangeable with deoxycholate, lipid-complex or other amphotericin formulations.

Renal method: No renal dose reduction; source-specific weight convention
Retrieved: 2026-09-05

Source presence is not independent validation. A label mirror is not a second independent source; review the original reference and exact formulation.

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All source summaries, original wording and provenance
Before applying a renal protocol

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Renal-context checklist: population, kidney trend and dialysis

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Read the exact source scope, renal metric and date before selecting a row. No applicability assessment has been performed.

See source-specific renal methods and the clinical interpretation guide for the supporting context.

Go directly to the relevant source section

Renal dosing and precautions

Choose a source, then jump to its renal or dialysis section. These links locate stored text; they do not merge regimens or certify that sources agree.

Official source

Amphotericin B liposomal (AmBisome) - selected U.S. labeling

Adults receiving intravenous liposomal amphotericin B, specifically AmBisome. Not interchangeable with deoxycholate, lipid-complex or other amphotericin formulations.

Method: Qualitative renal/PK evidence; no label CrCl-based reduction table.

Professional source

UCSF AmBisome - renal and dialysis protocols

Adults receiving intravenous liposomal amphotericin B, specifically AmBisome. Not interchangeable with deoxycholate, lipid-complex or other amphotericin formulations.

Method: No renal dose reduction; source-specific weight convention

No dialysis or renal heading shown? Read the complete source summary. Absence of a heading is not evidence that dose adjustment is unnecessary.

Compare or copy source versions

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Exact product and population matter. This added page contains locally stored, source-specific clinical summaries. Historical handbook information, when present, is identified separately and may conflict with U.S. labeling. Confirm indication, population, kidney-function method, monitoring and the full prescribing information before applying a regimen.
Locally stored source content

Exact product and population

Product identity selected for the separately displayed source protocols below. Reference: https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=f7be6506-4d20-401e-a0ff-02ad7c33158a

Product and population scope

Adults receiving intravenous liposomal amphotericin B, specifically AmBisome. Not interchangeable with deoxycholate, lipid-complex or other amphotericin formulations.

RDM31-amphotericin-b-liposomal-scope · Source section: Editorial scope tied to selected U.S. labelRenal section finder
Separate U.S. product-label layer

FDA / DailyMed dosing and renal information

Official

Amphotericin B liposomal (AmBisome) - selected U.S. labeling

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U.S. product labeling / DailyMed · Adults receiving intravenous liposomal amphotericin B, specifically AmBisome. Not interchangeable with deoxycholate, lipid-complex or other amphotericin formulations.

Renal method: Qualitative renal/PK evidence; no label CrCl-based reduction table.
Source date: Label revision date not separately recorded; retrieval date is not the revision date.
Retrieved: 2026-09-05

Selected dosing/renal sections read; concise local summary, not full prescribing information.

Labeled basic dosing

Labeled adult initial doses: empirical therapy 3 mg/kg IV daily; systemic fungal infection 3-5 mg/kg daily; HIV-associated cryptococcal meningitis 6 mg/kg daily. Infuse initially over about 120 minutes; approximately 60 minutes may be used when tolerated.

RDM31-amphotericin-b-liposomal-label-dose · Source locator: Dosage and Administration

Renal information and dialysis

Renal-impairment pharmacokinetics have not been studied, although patients with pre-existing dysfunction received treatment. No numeric CrCl reduction is provided. Hemodialysis/peritoneal dialysis do not appear to materially increase elimination.

RDM31-amphotericin-b-liposomal-label-renal · Source locator: Clinical Pharmacology: Special Populations; Overdosage

Selected warnings and limits

Monitor renal function and electrolytes. This product cannot be substituted milligram-for-milligram for another amphotericin formulation. Use only its own preparation instructions.

RDM31-amphotericin-b-liposomal-label-limits · Source locator: Precautions: Laboratory Tests; Dosage and Administration

Source identity and provenance
Source
https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=f7be6506-4d20-401e-a0ff-02ad7c33158a
Retrieved
2026-09-05
DailyMed Set ID
f7be6506-4d20-401e-a0ff-02ad7c33158a
Renal-function method
Qualitative renal/PK evidence; no label CrCl-based reduction table.
Source date/version
Label revision date not separately recorded; retrieval date is not the revision date.
Hash meaning
SHA-256 identifies this local summary, not original SPL XML or label PDF.
Local summary SHA-256
75ba65d98cd36b11e4933e15015ef7e21bf7a96f4d481b8c5410682b2c3d2066
Separate professional-source layer

University and professional protocols

Professional

UCSF AmBisome - renal and dialysis protocols

Open original reference

Open / share this exact local source

University of California San Francisco (UCSF) · Adults receiving intravenous liposomal amphotericin B, specifically AmBisome. Not interchangeable with deoxycholate, lipid-complex or other amphotericin formulations.

Renal method: No renal dose reduction; source-specific weight convention
Source date: Revision date not stated on the reviewed page.
Retrieved: 2026-09-05

Separate professional-source protocol; not automatically equivalent to product labeling.

Source-specific renal protocol

UCSF uses 4 mg/kg IV every 24 hours with flucytosine for cryptococcal meningitis, 5 mg/kg daily for invasive fungal infection, and 3 mg/kg daily for heme/BMT mold prophylaxis. These schedules are also listed for IHD and continuous dialysis. Monitor creatinine/electrolytes. Use total body weight unless it exceeds 120% of ideal weight, when adjusted weight is used.

RDM31-amphotericin-b-liposomal-prof-1 · Source locator: Dosing Weights; adult and dialysis tables; Dialysis Notes

Source-specific limits

The cryptococcal 4 mg/kg combination regimen differs from the label's 6 mg/kg regimen; preserve the entire selected treatment plan. The source's optional saline hydration requires assessment of fluid tolerance; it is not an instruction to mix saline into AmBisome.

Source identity and provenance
Source
https://idmp.ucsf.edu/content/ambisome-liposomal-amphotericin-b
Retrieved
2026-09-05
Renal-function method
No renal dose reduction; source-specific weight convention
Source date/version
Revision date not stated on the reviewed page.
Hash meaning
SHA-256 identifies the local paraphrase, not original source bytes.
Local summary SHA-256
2c61f9bcc77b3a4838965b0e224beef13a2a4695bd01d2c20c4023a5a2fa8bba

Provenance and preservation

Additional summaries stored on this page: 1 official-label, 0 RX List, 1 professional, 0 handbook. Empty additional-source groups are not shown. A missing layer is not a no-adjustment recommendation.

Original source
https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=f7be6506-4d20-401e-a0ff-02ad7c33158a
Source retrieval
2026-09-05. This is not the source publication or label revision date.
Original source type
multisource addition
Local text SHA-256
fc75cabca760a591e92fc68aabdcff3e52858e34dbd18f5fe3ce4b0349fb37e2
Import versus clinical validation
Source-section locators identify where retained content came from. A source-section identifier does not assert that every numeric statement has been independently corroborated. The local text hash is not a hash of original HTML, an FDA PDF or SPL XML.

This page is an additional exact-product entry, not a recovered GlobalRPh monograph. Its primary scope text and separately attributed clinical summaries are locally included.

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