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1 local source card selected. Local card fingerprints checked where supplied. This is not an original-document hash, source-currency guarantee or clinical approval. Record-level cautions below are the current library's cautions, not a frozen prior version.
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Clinical context remains essential
Independent clinical review is pending. Confirm indication, exact formulation/route, population, renal measure and units, kidney-function stability, dialysis prescription, interacting drugs, monitoring and source revision. An RX mirror and its original label are not independent corroboration. Missing disagreement notes do not certify agreement.
The source summary mentions an after-dialysis dose; the source package-insert paragraph says both during and at the end of dialysis. Both statements are retained and require product-specific reconciliation.
Check source scope before reading a dose
GlobalRPh RX List - AUGMENTIN
Product / population
Conventional AUGMENTIN adult renal paragraph; not extended-release or ES-600.
Renal method
GFR (mL/min), as printed
Source revision
Revision not established in selected retrieval
Retrieved
2026-09-10
Local review status
Selected source sections stored locally. Not a complete monograph or independent clinical approval.
Documented differences and cautions on this drug
All record notes are retained here, including notes about sources not selected in this review.
Conventional AUGMENTIN is not XR or ES-600
The conventional renal table cannot be transferred to XR, and clavulanate content differs among formulations.
What to reconcile: Match both component strengths and formulation before using any table.
GlobalRPh-hosted RX List · Conventional AUGMENTIN adult renal paragraph; not extended-release or ES-600.
Renal method: GFR (mL/min), as printed Source date: Revision 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.
Before using this finding
Match both component strengths and formulation; compare dialysis instructions as a whole protocol.
Dialysis evidence: A regimen is reported in selected content
Selected source sections stored locally. Not a complete monograph or independent clinical approval.
Renal guidance and important limits
The selected conventional-product renal paragraph excludes the 875 mg dose when GFR is below 30 mL/min.
GFR / treatment
Selected dose expressed by amoxicillin component
10-30 mL/min
250 or 500 mg every 12 hours, according to infection severity
Below 10 mL/min
250 or 500 mg every 24 hours, according to infection severity
Hemodialysis
250 or 500 mg every 24 hours; additional dose both during and at the end of dialysis
The adult 250 mg tablet and 250 mg chewable tablet have different clavulanate amounts. These instructions are not an AUGMENTIN XR or ES-600 conversion. Confirm the complete component strength, not amoxicillin milligrams alone.
RDM61-rxlist-amoxicillinclav-0a71e46ff2-C1 · Source locator: Dosage and Administration: renal impairment; named precautions
Source-specific limits
No new official-label card was obtained for this product in v6.1. Earlier source layers, if present, were retained but not rechecked.
This reference does not select a regimen. Complete the indication, measured/estimated renal function and trend, dialysis setting, source rationale, monitoring and reassessment plan in your institution's approved documentation system. Confirm the complete current source before adopting its regimen.
GlobalRPh v6.6 | RDM66-DIRECT-PHP-20260911 | Local library date 2026-09-11. Selected-card identity does not imply clinical verification.