GlobalRPh Renal Dosing Masterv6.6
Evidence addition

Delafloxacin - BAXDELA intravenous infusion

Local official-label summaryBase record retrieved 2026-09-10See the evidence for this drug2 sources available - open source summaries, references and comparisons

BAXDELA IV / delafloxacin IV / delafloxacin

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Renal guidance at a glance

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

Vehicle accumulation remains part of the IV decision

A reduced IV amount does not remove the SBECD precaution.

Before applying: Keep renal monitoring, oral-switch consideration and the below-15 restriction attached.

Evidence for this qualification

Source-specific qualification; independent clinician review pending.

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

Choose a source to read (2)

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

DailyMed / BAXDELA IV exact product label

Product / population
Adult intravenous BAXDELA for labeled ABSSSI or CABP. Every dose is infused over 60 minutes.
Renal measure
MDRD eGFR, mL/min/1.73 m2

Exact DailyMed HTML label identity and selected named sections checked. A page update is not proof that renal instructions changed.

No raw SPL XML, original XML hash or separate Drugs@FDA revision-history review was performed.

Renal dosing, restrictions and evidence limits

Use 300 mg IV every 12 hours at MDRD eGFR 30-89 and 200 mg every 12 hours at 15-29 mL/min/1.73 m2, over 60 minutes. Not recommended below 15, including hemodialysis. Monitor severe-renal patients for SBECD accumulation; consider oral therapy with rising creatinine and discontinue below 15. The table's older MDRD equation is source context, not a newly implemented calculation.

Source revision: 6/2021 | Retrieved: 2026-09-10. Retrieval date is not the revision date.

Source: https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=fb77637a-88d9-4aea-958f-e270030ce30d

Scope: Selected source text imported locally; independent clinical review pending. Not a complete prescribing monograph. GlobalRPh v6.6.

Full source card / provenance

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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

Official product label

DailyMed / BAXDELA IV exact product label

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

Adult intravenous BAXDELA for labeled ABSSSI or CABP. Every dose is infused over 60 minutes.

Renal method: MDRD eGFR, mL/min/1.73 m2
Retrieved: 2026-09-10

Read local renal resultOpen original reference
GlobalRPh RX List

GlobalRPh RX List - BAXDELA IV

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

Adult intravenous BAXDELA for labeled ABSSSI or CABP. Every dose is infused over 60 minutes.

Renal method: MDRD eGFR, mL/min/1.73 m2
Retrieved: 2026-09-10

Read local renal resultOpen original reference

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

Product / population check

Confirm the exact formulation before using a renal source

These links compare product identities, not interchangeable doses. A selected summary is not a complete prescribing monograph.

Source-specific review points

Vehicle accumulation remains part of the IV decision

Read the attributed comparison notes and source cards below. No conflict has been silently adjudicated.

Source-quality holds
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All source summaries, original wording and provenance
Before applying a renal protocol

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

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Jump to renal guidanceRead 1 difference / caution notesClinician guide

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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.

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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

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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.

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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.

Original content / product scopeDailyMed / BAXDELA IV exact product labelGlobalRPh RX List - BAXDELA IV
Choose two source checkboxes below.
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://globalrph.com/rx-list/baxdela-drug/

Exact product and population

Adult intravenous BAXDELA for labeled ABSSSI or CABP. Every dose is infused over 60 minutes.

RDM56-SCOPE-delafloxacin-baxdela-iv · Source section: Selected source product scopeRenal section finder
Separate U.S. product-label layer

FDA / DailyMed dosing and renal information

Official

DailyMed / BAXDELA IV exact product label

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DailyMed / Melinta Therapeutics, LLC · Adult intravenous BAXDELA for labeled ABSSSI or CABP. Every dose is infused over 60 minutes.

Renal method: MDRD eGFR, mL/min/1.73 m2
Source date: 6/2021
Retrieved: 2026-09-10

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

Selected source text imported locally; independent clinical review pending. Not a complete prescribing monograph.

Renal dosing, restrictions and evidence limits

Use 300 mg IV every 12 hours at MDRD eGFR 30-89 and 200 mg every 12 hours at 15-29 mL/min/1.73 m2, over 60 minutes. Not recommended below 15, including hemodialysis. Monitor severe-renal patients for SBECD accumulation; consider oral therapy with rising creatinine and discontinue below 15. The table's older MDRD equation is source context, not a newly implemented calculation.

RDM56-official-delafloxacin-baxdela-iv-af1549ad09-C1 · Source locator: Sections 2.2-2.3 Table 2 and 8.7

Source-specific limits

Exact DailyMed HTML label identity and selected named sections checked. A page update is not proof that renal instructions changed.

No raw SPL XML, original XML hash or separate Drugs@FDA revision-history review was performed.

Source identity and provenance
Source family
product_label
Source
https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=fb77637a-88d9-4aea-958f-e270030ce30d
Retrieved
2026-09-10
Exact label title
BAXDELA - delafloxacin meglumine tablets and injection
DailyMed Set ID
fb77637a-88d9-4aea-958f-e270030ce30d
Labeler
Melinta Therapeutics, LLC
Label revision
6/2021
Renal-function method
MDRD eGFR, mL/min/1.73 m2
Source date/version
6/2021
Hash meaning
SHA-256 of local authored summary only; not original HTML, PDF or SPL bytes.
Local summary SHA-256
ae565ea3d78209e10a2e238f6d4ff3697db7903b9b7c19e4942d35ed482f76f9
Locally imported selected renal sections

GlobalRPh RX List renal information

Rxlist

GlobalRPh RX List - BAXDELA IV

Open original reference

Open / share this exact local source

GlobalRPh-hosted RX List · Adult intravenous BAXDELA for labeled ABSSSI or CABP. Every dose is infused over 60 minutes.

Renal method: MDRD eGFR, mL/min/1.73 m2
Source date: Source revision date not established in selected retrieval.
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.

Selected source text imported locally; independent clinical review pending. Not a complete prescribing monograph.

Renal dosing, restrictions and evidence limits

At indexed eGFR 30-89, retain 300 mg IV every 12 hours; at 15-29 mL/min/1.73 m2, use 200 mg IV every 12 hours. Infuse over 60 minutes. Below 15, including hemodialysis, use is not recommended. The SBECD vehicle accumulates in renal impairment. Monitor creatinine/eGFR closely in severe impairment; consider oral therapy if creatinine rises and discontinue below eGFR 15.

RDM56-rxlist-delafloxacin-baxdela-iv-25a9af963e-C1 · Source locator: Dosage Table 2; Renal Impairment; infusion instructions

Source-specific limits

Selected sections only. A hosted mirror is not independent confirmation of the underlying label.

Source identity and provenance
Source family
product_label_mirror
Source
https://globalrph.com/rx-list/baxdela-drug/
Retrieved
2026-09-10
Renal-function method
MDRD eGFR, mL/min/1.73 m2
Source date/version
Source revision date not established in selected retrieval.
Hash meaning
SHA-256 of local authored summary only; not original HTML, PDF or SPL bytes.
Local summary SHA-256
3a3ec3867e616a12af002737882059a1e3f86dd47d04a00dbcc46fb8c1212912

Provenance and preservation

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

Original source
https://globalrph.com/rx-list/baxdela-drug/
Source retrieval
2026-09-10. This is not the source publication or label revision date.
Original source type
rxlist summary
Local text SHA-256
d947976ec924f8b5484f38df3e05d82ce59ca77ea6540d972449542438c858a6
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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