GlobalRPh Renal Dosing Masterv6.6
GlobalRPh source record

Dapagliflozin (Farxiga)

READ THE SOURCE-SPECIFIC ANSWER

Renal guidance at a glance

Cautions / source differences (1)
Review first - source-specific qualification

Indication, initiation and continuation are separate

The older mirror and June 2026 label retain different thresholds for glycemic and other adult indications. The official surgery paragraph no longer limits its wording to major surgery.

Before applying: Use the newer source wording within its scope; a continuation statement below 25 is not a general initiation/dialysis rule.

Evidence for this qualification

Source-specific interpretation; independent clinician adjudication pending.

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

Choose a source to read (5)

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

FARXIGA - official indication-specific renal guidance

Product / population
FARXIGA adult indication-specific renal instructions.
Renal measure
eGFR (mL/min/1.73 m2)
Before using this finding

Use the indication-specific threshold and distinguish initiation from continuation.

Renal guidance and important limits

For glycemic control, use is not recommended below eGFR 45 mL/min/1.73 m2. For other adult indications, the recommended dose is 10 mg daily; do not initiate below 25. Patients already receiving it whose eGFR declines below 25 may continue 10 mg daily for the specified cardiorenal risk reduction. Renal function and volume status require assessment; correct depletion before starting. Withhold at least 3 days, if possible, before surgery or prolonged-fasting procedures; restart when clinically stable and eating. Trials did not enroll patients initially below eGFR 25 or on dialysis; trial continuation after decline or dialysis initiation is not universal permission to start in dialysis. Glycemic and cardiorenal indications must remain separate.

Source revision: 6/2026 | Retrieved: 2026-09-10. Retrieval date is not the revision date.

Source: https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=72ad22ae-efe6-4cd6-a302-98aaee423d69

Scope: Selected source sections stored locally. Not a complete monograph or independent clinical approval. GlobalRPh v6.6.

Full source card / provenance

All sources, comparison tools and evidence navigation
Source-specific interpretation

What the dialysis evidence actually supports

Removal information alone does not define a maintenance dose, supplemental dose or dialysis schedule. A reported regimen still requires its product, indication, renal measure and dialysis assumptions to match the patient.

FARXIGA - official indication-specific renal guidance

Authored v6.1; retrieved 2026-09-10 - retained source, not freshly reviewed in this release

No dialysis regimen established in selected content

Read the source and its limits

GlobalRPh RX List - FARXIGA

Authored v6.1; retrieved 2026-09-10 - retained source, not freshly reviewed in this release

No dialysis regimen established in selected content

Read the source and its limits

These manual classifications apply only to the identified selected sections, not every retained source or the entire prescribing information. They are not dosing clearance.

Source-first renal review

Evidence sources and renal implications

Choose a source to jump directly to its locally stored result. Qualitative precautions and evidence gaps remain visible even when no numerical clearance schedule is supplied.

Read 1 source difference / applicability notes

Preserved GlobalRPh source

Preserved original GlobalRPh source

Preserved historical content; not revalidated as current prescribing guidance.

Renal method: Read the measure and population stated in the original source sections.
Retrieved: 2026-09-05

Official product label

FARXIGA - official indication-specific renal guidance

Dose or interval guidance. Use only the product, indication, renal metric and population described in this source.
Before using this finding

Use the indication-specific threshold and distinguish initiation from continuation.

Dialysis evidence: No dialysis regimen established in selected content

FARXIGA adult indication-specific renal instructions.

Renal method: eGFR (mL/min/1.73 m2)
Retrieved: 2026-09-10

GlobalRPh RX List

GlobalRPh RX List - FARXIGA

Dose or interval guidance. Use only the product, indication, renal metric and population described in this source.
Before using this finding

Confirm the indication before applying 45 or 25; a continuation statement is not permission to initiate below the threshold.

Dialysis evidence: No dialysis regimen established in selected content

FARXIGA: adult glycemic versus cardiorenal indications, not a common threshold for all SGLT2 inhibitors.

Renal method: eGFR (mL/min/1.73 m2)
Retrieved: 2026-09-10

Handbook

Renal Drug Handbook, fifth edition

Historical 2019 reference; renal bands retain the book's own method labels.

Renal method: See source.
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.

Find text within this drug
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Search the stored clinical text

Locate a word or phrase within this drug's source summaries. Choose all sources or one source to focus the search. The selection never hides warnings or source text, changes a dose, or proves that a renal finding is absent.

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

Check the setting. Compare whole sources.

No patient-specific dose is calculated. Context choices only display reminders; they do not validate, hide or change any regimen.

Share a reproducible source review

Choose sources below, then open a print-ready comparison with product scope, renal method, dates and cautions. Links can pin the exact local cards; they never contain patient values or choose a dose.

Open / share selected sources

Select two distinct source versions. The complete stored summaries will appear below.

Build a source-review outline for documentation

This creates a blank decision outline with the source identities you select, not a dose recommendation or completed clinical assessment. No patient fields are collected, saved or sent. Complete the clinical decisions in your approved documentation system.

Choose one or two sources above or use the source checkboxes below.

Renal-context checklist: population, kidney trend and dialysis

These prompts are a reading aid, not a prescription checklist or proof that all requirements have been met. No selections are stored or sent to a server.

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.

Read before choosing a regimen

Source differences and product cautions

Search differences across all drugs

These are specific issues found during source review, not an automated judgment that one source is universally correct. A label mirror and its original label are not independent evidence.

source scope and renal guidance

Indication, initiation and continuation are separate

The older mirror and June 2026 label retain different thresholds for glycemic and other adult indications. The official surgery paragraph no longer limits its wording to major surgery.

How to use this: Use the newer source wording within its scope; a continuation statement below 25 is not a general initiation/dialysis rule.

Source-specific interpretation; independent clinician adjudication pending.

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.

New source summary - independent clinical review pending. Summaries of the identified label sections are included locally. Source import and numeric transcription checks are not independent two-reference validation. Do not treat this card as an approved institutional dosing protocol.

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

All content below is stored locally. Read a whole source version; do not combine its dose with another source's interval, renal metric or dialysis assumptions.

Choose two source checkboxes below.
Historical source content is not a current prescription. Original GlobalRPh recommendations are preserved, not automatically certified as current. Product-label and professional additions below are separately attributed. Confirm indication, population, kidney-function method, monitoring and the full prescribing information before applying a regimen.

Important source distinctions

The original GlobalRPh and 2019 handbook eGFR 60 restriction is historical. Use the indication-specific FARXIGA label addition below; the glycemic threshold is not the HF/CKD initiation threshold.

Locally stored source content

Original GlobalRPh protocol

Clinical facts and comments transcribed into a structured reading format. This is not a byte-for-byte HTML archive. Original source: https://globalrph.com/renal/medications-with-general-renal-dosing-statements/

GlobalRPh general renal statement

The recommended starting dose of FARXIGA is 5 mg once daily, taken in the morning, with or without food. In patients tolerating FARXIGA 5 mg once daily who require additional glycemic control, the dose can be increased to 10 mg once daily.

Patients with Renal Impairment: Assessment of renal function is recommended prior to initiation of FARXIGA therapy and periodically thereafter. FARXIGA should not be initiated in patients with an eGFR less than 60 mL/min/1.73 m2. No dose adjustment is needed in patients with mild renal impairment (eGFR of 60 mL/min/1.73 m2 or greater). FARXIGA should be discontinued when eGFR is persistently less than 60 mL/min/1.73 m2.

GRPH-general-dapagliflozin-01 · Source section: GlobalRPh general renal statementRenal section finder
Separate U.S. product-label layer

FDA / DailyMed dosing and renal information

Official

FARXIGA (dapagliflozin) tablets

Open original reference

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NIH/NLM DailyMed - U.S. prescribing information · Adult oral single-agent product; glycemic and cardiorenal indications are different.

Renal method: Not specified in this summary.
Source date:
Retrieved: 2026-09-05

Source-read local summary; source-specific recommendations are not automatically interchangeable.

Usual adult dose and kidney-function limits

For glycemic control, start 5 mg once daily; increase to 10 mg if needed. Glycemic use is not recommended below eGFR 45 mL/min/1.73 m2. For the labeled HF/CKD and other adult cardiorenal indications, use 10 mg daily; initiation requires eGFR >=25. Existing treatment may continue at 10 mg if eGFR subsequently falls below 25.

general-dapagliflozin:dm-72ad22ae-efe6-4cd6-a302-98aaee423d69-1 · Source locator: 2.2-2.3

Precautions

Correct volume depletion before treatment. Withhold for at least 3 days before surgery or prolonged fasting when possible; resume after clinical stability and oral intake return. Do not interpret continuation below 25 as permission to initiate on dialysis.

general-dapagliflozin:dm-72ad22ae-efe6-4cd6-a302-98aaee423d69-2 · Source locator: 2.1, 2.4; 8.6

Source identity and provenance
Source
https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=72ad22ae-efe6-4cd6-a302-98aaee423d69
Retrieved
2026-09-05
Exact label title
FARXIGA (dapagliflozin) tablets
DailyMed Set ID
72ad22ae-efe6-4cd6-a302-98aaee423d69
Labeler
AstraZeneca Pharmaceuticals LP
DailyMed page updated
2026-06-03
FDA application
New Drug Application
U.S. product identity basis
Exact named product and route appear in the selected U.S. prescription label; current retail availability was not independently assessed.
Hash meaning
Locally authored source summary, not original SPL/XML/PDF bytes
Local summary SHA-256
64a9ce09c5a6eeea7643cd1906a2bbbb4ddb94be88952380ceb0908c40ebb4ab
Official

FARXIGA - official indication-specific renal guidance

Open original reference

Open / share this exact local source

National Library of Medicine / manufacturer labeling · FARXIGA adult indication-specific renal instructions.

Renal method: eGFR (mL/min/1.73 m2)
Source date: 6/2026
Retrieved: 2026-09-10

Dose or interval guidance. Use only the product, indication, renal metric and population described in this source.
Before using this finding

Use the indication-specific threshold and distinguish initiation from continuation.

Dialysis evidence: No dialysis regimen established in selected content

Selected source sections stored locally. Not a complete monograph or independent clinical approval.

Renal guidance and important limits

For glycemic control, use is not recommended below eGFR 45 mL/min/1.73 m2. For other adult indications, the recommended dose is 10 mg daily; do not initiate below 25. Patients already receiving it whose eGFR declines below 25 may continue 10 mg daily for the specified cardiorenal risk reduction. Renal function and volume status require assessment; correct depletion before starting. Withhold at least 3 days, if possible, before surgery or prolonged-fasting procedures; restart when clinically stable and eating. Trials did not enroll patients initially below eGFR 25 or on dialysis; trial continuation after decline or dialysis initiation is not universal permission to start in dialysis. Glycemic and cardiorenal indications must remain separate.

RDM61-official-general-dapagliflozin-44ff2ec02c-C1 · Source locator: 2.1-2.4 and 8.6

Source identity and provenance
Source family
product_label
Source
https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=72ad22ae-efe6-4cd6-a302-98aaee423d69
Retrieved
2026-09-10
Exact label title
FARXIGA - official indication-specific renal guidance
DailyMed Set ID
72ad22ae-efe6-4cd6-a302-98aaee423d69
DailyMed page updated
2026-06-03
Label revision
6/2026
Renal-function method
eGFR (mL/min/1.73 m2)
Source date/version
6/2026
Hash meaning
Local authored summary, not source HTML/XML/PDF bytes
Local summary SHA-256
4df28debfbe880c2725f03d0728e87d02ac590848e343fd43ab2df36366c9cfd
Locally imported selected renal sections

GlobalRPh RX List renal information

Rxlist

GlobalRPh RX List - FARXIGA

Open original reference

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GlobalRPh-hosted RX List · FARXIGA: adult glycemic versus cardiorenal indications, not a common threshold for all SGLT2 inhibitors.

Renal method: eGFR (mL/min/1.73 m2)
Source date: June 2024 (mirror)
Retrieved: 2026-09-10

Label mirror, not independent corroboration. This is selected locally stored RX List content. Full monograph import and current official-label review are not implied.
Dose or interval guidance. Use only the product, indication, renal metric and population described in this source.
Before using this finding

Confirm the indication before applying 45 or 25; a continuation statement is not permission to initiate below the threshold.

Dialysis evidence: No dialysis regimen established in selected content

Selected source sections stored locally. Not a complete monograph or independent clinical approval.

Renal guidance and important limits

The June 2024 mirror separates glycemic control from other adult indications. Glycemic use is not recommended below eGFR 45 mL/min/1.73 m2. For other adult indications, use 10 mg daily; initiation is not recommended below 25, but patients whose eGFR falls below 25 while taking it may continue 10 mg daily for the stated cardiorenal outcomes. Assess renal function and correct volume depletion before initiation. The mirror advises withholding at least 3 days, if possible, before major surgery or prolonged-fasting procedures. Current official wording is separately displayed; no universal dialysis-start recommendation is inferred.

RDM61-rxlist-general-dapagliflozin-61f2f20e52-C1 · Source locator: Dosage and Administration: renal impairment; named precautions

Source identity and provenance
Source family
product_label_mirror
Source
https://globalrph.com/rx-list/farxiga-drug/
Retrieved
2026-09-10
Renal-function method
eGFR (mL/min/1.73 m2)
Source date/version
June 2024 (mirror)
Hash meaning
Local authored summary, not source HTML/XML/PDF bytes
Local summary SHA-256
9930370f6229dc32830b18b3d878bf3b91c6838f60869c3fd73264af238ea2ad
Separate handbook layer

Renal Drug Handbook cross-check

Handbook

Renal Drug Handbook, fifth edition

Open / share this exact local source

UK Renal Pharmacy Group / Ashley and Dunleavy / CRC Press · Historical 2019 reference; renal bands retain the book's own method labels.

Renal method: Not specified in this summary.
Source date: Not established
Retrieved: 2026-09-05

Historical handbook facts locally summarized; not a current U.S. label or a modern CRRT protocol.

Historical renal and replacement-therapy statements

The handbook advises avoidance in its 20-60, 10-20 and <10 mL/min bands and across APD/CAPD, HD, high-flux and continuous replacement therapies. Its accompanying manufacturer note uses GFR <60. These historical glycemic-era limits differ from the subsequently expanded U.S. cardiorenal labeling.

general-dapagliflozin:rdh5-281-1 · Source locator: Renal impairment; renal replacement therapies; Other information

Source-specific limits

Do not use this older avoidance table as the current HF/CKD eligibility rule.

Source identity and provenance
Retrieved
2026-09-05
Handbook page
Printed page 281; PDF page 300
Hash meaning
Locally authored source summary, not original SPL/XML/PDF bytes
Local summary SHA-256
c00b97b838dec95f6f02e8743a40950d6cedb2935bcb9a95a9d1ddfe4519f36a

Provenance and preservation

Additional summaries stored on this page: 2 official-label, 1 RX List, 0 professional, 1 handbook. Empty additional-source groups are not shown. A missing layer is not a no-adjustment recommendation.

Original source
https://globalrph.com/renal/medications-with-general-renal-dosing-statements/
Source retrieval
2026-09-05. This is not the source publication or label revision date.
Original source type
globalrph general · Numbered general entry 6
Local text SHA-256
87f63ceb476ab9419d059ab1c205e99f5ac1446248e231ae0392ed54c337d9b6
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.

The original individual GlobalRPh pages commonly cite NIH/NLM DailyMed and instruct readers to review the applicable package insert for updates. That historical reference is preserved as context; it is not counted as an independently retrieved current label.

Read the full coverage report