GlobalRPh Renal Dosing Masterv6.6
Evidence addition

Ceftobiprole medocaril sodium (Zevtera, adult IV)

Zevtera / ceftobiprole medocaril

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Official source

Ceftobiprole medocaril sodium (Zevtera, adult IV) - selected U.S. label sections

Product / population
U.S. ZEVTERA IV prodrug doses: 667 mg ceftobiprole medocaril sodium is equivalent to 500 mg ceftobiprole; 333 mg is equivalent to 250 mg. Not an international 500 mg vial instruction.
Renal measure
Creatinine clearance in mL/min; adult U.S. product table

Selected renal sections only, not a complete monograph. Exact product, indication, patient population, renal method and all other contraindications/interactions remain controlling.

Second independent renal reference and clinician adjudication remain pending; no all-indication, dialysis or pediatric dose may be inferred from an omitted field.

Adult renal table - U.S. prodrug dose units

CrClS. aureus bacteremiaABSSSI or community-acquired bacterial pneumonia
30 to below 50667 mg every 8 hours on days 1-8, then every 12 hours667 mg every 12 hours
15 to below 30333 mg every 8 hours on days 1-8, then every 12 hours333 mg every 12 hours
Below 15, including hemodialysis333 mg every 24 hours333 mg every 24 hours

Administer each dose by a 2-hour IV infusion. On hemodialysis days, administer after dialysis.

Augmented renal clearance

For adult CrCl above 150 mL/min, the label specifies 667 mg every 6 hours. This is not a pediatric schedule.

Source revision: Revision not captured; 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=2bd685df-7dc6-78a6-e063-6294a90a580b

Scope: Local label summary; independent clinical review pending. Not a two-source validated protocol. GlobalRPh v6.6.

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Evidence sources and renal implications

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Official product label

Ceftobiprole medocaril sodium (Zevtera, adult IV) - selected U.S. label sections

U.S. ZEVTERA IV prodrug doses: 667 mg ceftobiprole medocaril sodium is equivalent to 500 mg ceftobiprole; 333 mg is equivalent to 250 mg. Not an international 500 mg vial instruction.

Renal method: Creatinine clearance in mL/min; adult U.S. product table
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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Renal dosing and precautions

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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.

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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=2bd685df-7dc6-78a6-e063-6294a90a580b

Product and population scope

U.S. ZEVTERA IV prodrug doses: 667 mg ceftobiprole medocaril sodium is equivalent to 500 mg ceftobiprole; 333 mg is equivalent to 250 mg. Not an international 500 mg vial instruction.

RDM32-ceftobiprole-zevtera-scope · Source section: Editorial scope for the selected U.S. labelRenal section finder
Separate U.S. product-label layer

FDA / DailyMed dosing and renal information

Official

Ceftobiprole medocaril sodium (Zevtera, adult IV) - selected U.S. label sections

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U.S. product labeling / DailyMed · U.S. ZEVTERA IV prodrug doses: 667 mg ceftobiprole medocaril sodium is equivalent to 500 mg ceftobiprole; 333 mg is equivalent to 250 mg. Not an international 500 mg vial instruction.

Renal method: Creatinine clearance in mL/min; adult U.S. product table
Source date: Revision not captured; retrieval date is not the revision date.
Retrieved: 2026-09-05

Local label summary; independent clinical review pending. Not a two-source validated protocol.

Adult renal table - U.S. prodrug dose units

CrClS. aureus bacteremiaABSSSI or community-acquired bacterial pneumonia
30 to below 50667 mg every 8 hours on days 1-8, then every 12 hours667 mg every 12 hours
15 to below 30333 mg every 8 hours on days 1-8, then every 12 hours333 mg every 12 hours
Below 15, including hemodialysis333 mg every 24 hours333 mg every 24 hours

Administer each dose by a 2-hour IV infusion. On hemodialysis days, administer after dialysis.

RDM32-ceftobiprole-zevtera-1 · Source locator: 2.3, Table 3; 8.6

Augmented renal clearance

For adult CrCl above 150 mL/min, the label specifies 667 mg every 6 hours. This is not a pediatric schedule.

RDM32-ceftobiprole-zevtera-2 · Source locator: 2.3

Source-specific limits

Selected renal sections only, not a complete monograph. Exact product, indication, patient population, renal method and all other contraindications/interactions remain controlling.

Second independent renal reference and clinician adjudication remain pending; no all-indication, dialysis or pediatric dose may be inferred from an omitted field.

Source identity and provenance
Source
https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=2bd685df-7dc6-78a6-e063-6294a90a580b
Retrieved
2026-09-05
DailyMed Set ID
2bd685df-7dc6-78a6-e063-6294a90a580b
Renal-function method
Creatinine clearance in mL/min; adult U.S. product table
Source date/version
Revision not captured; retrieval date is not the revision date.
Hash meaning
SHA-256 identifies this local summary, not original SPL XML or a label PDF.
Local summary SHA-256
7dcf7afff9a5e2f1f2d6275f70deaa03a33b2b9754f138b2dc943b4f3380b883

Provenance and preservation

Additional summaries stored on this page: 1 official-label, 0 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://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=2bd685df-7dc6-78a6-e063-6294a90a580b
Source retrieval
2026-09-05. This is not the source publication or label revision date.
Original source type
multisource addition
Local text SHA-256
02efa0421a9276bb270723646cd9ab148f9031b6e628c1ab3bee8410435d95fb
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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