GlobalRPh Renal Dosing Masterv6.6
GlobalRPh source record

Valganciclovir - adult tablets

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Renal guidance at a glance

Cautions / source differences (2)

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2 additional source qualifications - review before use
Adult tablet label versus UCSF intermittent-HD practice

The VALCYTE label provides no adult tablet dose for hemodialysis and says those tablets should not be used. UCSF lists institutional oral treatment and prophylaxis schedules in intermittent HD. This is a real label-versus-institution difference, not two independently agreeing labels.

Before applying: Confirm CMV indication, transplant context, formulation, dialysis schedule, cytopenias and infectious-disease input. The institutional regimen is not labeled approval; IV ganciclovir is preferred by UCSF for initiation in unstable renal function or dialysis.

Continuous-HD prophylaxis: institutional interval versus small PK study

UCSF lists prophylaxis every 48 hours during continuous HD. The Jarrell primary abstract studied daily enteral dosing in ten ICU transplant recipients on CVVHD and found that most reached a proposed trough target. These sources differ, but the study is not a comparative clinical-outcomes trial.

Before applying: Reconcile the actual dialysis modality and clearance, absorption, CMV risk, counts and monitoring. Full-text flow-rate details were not reviewed; no universal CRRT dose is derived or automatically preferred.

Also check: Adult tablet label versus UCSF intermittent-HD practice; Continuous-HD prophylaxis: institutional interval versus small PK study

Official source

VALCYTE: adult renal tablet table and hemodialysis restriction

Product / population
Adult VALCYTE 450 mg tablets; induction versus maintenance/prevention. Pediatric equations are not substituted.
Renal measure
Cockcroft-Gault CrCl in mL/min.

Renal dosing, restrictions and evidence limits

For CrCl >=60, induction is 900 mg twice daily and maintenance/prevention 900 mg daily. At 40-59, use 450 mg twice daily or 450 mg daily, respectively. At 25-39, use 450 mg daily or every two days. At 10-24, use 450 mg every two days or twice weekly. Below 10 on hemodialysis, the label provides no tablet dose and says the tablets should not be used; it directs clinicians to appropriately adjusted ganciclovir. Monitor kidney function and blood counts. Take with food and do not crush or split tablets. Institutional dialysis regimens are displayed separately, not called label-approved.

Source revision: December 2025 | Retrieved: 2026-09-07. Retrieval date is not the revision date.

Source: https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=4c517a39-2ded-4c5a-8d56-276853414b31

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

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Evidence sources and renal implications

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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

VALCYTE: adult renal tablet table and hemodialysis restriction

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

Adult VALCYTE 450 mg tablets; induction versus maintenance/prevention. Pediatric equations are not substituted.

Renal method: Cockcroft-Gault CrCl in mL/min.
Retrieved: 2026-09-07

Professional guidance

UCSF - valganciclovir: treatment, prevention and dialysis

Adults; source-specific institutional guidance. Match route, indication and renal replacement modality.

Renal method: CrCl in mL/min where specified; no equation inferred.
Retrieved: 2026-09-05

Professional guidance

UCSF: valganciclovir in intermittent and continuous hemodialysis

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

UCSF adult institutional CMV treatment/prophylaxis; dialysis regimens differ from the product label.

Renal method: Intermittent versus continuous hemodialysis; not automatically every CRRT modality.
Retrieved: 2026-09-07

Professional guidance

Jarrell et al.: valganciclovir prophylaxis during CVVHD (primary abstract)

Pharmacokinetic observation only. A drug-exposure observation is not itself a dose recommendation.

Single-center prospective pharmacokinetic study of ten adult solid-organ transplant recipients in ICU on CVVHD; abstract only.

Renal method: Continuous veno-venous hemodialysis; not intermittent dialysis.
Retrieved: 2026-09-07

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Source differences and product cautions

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label vs institution

Adult tablet label versus UCSF intermittent-HD practice

The VALCYTE label provides no adult tablet dose for hemodialysis and says those tablets should not be used. UCSF lists institutional oral treatment and prophylaxis schedules in intermittent HD. This is a real label-versus-institution difference, not two independently agreeing labels.

How to use this: Confirm CMV indication, transplant context, formulation, dialysis schedule, cytopenias and infectious-disease input. The institutional regimen is not labeled approval; IV ganciclovir is preferred by UCSF for initiation in unstable renal function or dialysis.

Source-specific interpretation; independent clinician adjudication pending.

institution vs primary study

Continuous-HD prophylaxis: institutional interval versus small PK study

UCSF lists prophylaxis every 48 hours during continuous HD. The Jarrell primary abstract studied daily enteral dosing in ten ICU transplant recipients on CVVHD and found that most reached a proposed trough target. These sources differ, but the study is not a comparative clinical-outcomes trial.

How to use this: Reconcile the actual dialysis modality and clearance, absorption, CMV risk, counts and monitoring. Full-text flow-rate details were not reviewed; no universal CRRT dose is derived or automatically preferred.

Source-specific interpretation; independent clinician adjudication pending.

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Renal dosing and precautions

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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

Adult 450 mg tablet source. No pediatric solution or institutional HD regimen is inferred.

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/valganciclovir/

Usual Dosing (Adults)

CMV-retinitis induction: 900 mg (two 450 mg tablets) twice daily for 21 days; maintenance after induction or for inactive disease: 900 mg daily. CMV prevention after heart or kidney-pancreas transplant: 900 mg daily starting within 10 days through post-transplant day 100. After kidney transplant: the same dose through day 200.

GRPH-valganciclovir-01 · Source section: Usual Dosing (Adults)Renal section finder

Renal Dosing

CrCl above 60 mL/min: usual doses. 40-59: induction 450 mg twice daily, maintenance 450 mg daily. 25-39: induction 450 mg daily, maintenance 450 mg every 2 days. 10-24: induction 450 mg every 2 days, maintenance 450 mg twice weekly. Exactly 60 is not explicitly assigned in the source summary.

GRPH-valganciclovir-02 · Source section: Renal DosingRenal section finder

Hemodialysis

The manufacturer statement on the source page says VALCYTE should not be prescribed to patients receiving hemodialysis.

GRPH-valganciclovir-03 · Source section: HemodialysisRenal section finder
Separate U.S. product-label layer

FDA / DailyMed dosing and renal information

Official

VALCYTE: adult renal tablet table and hemodialysis restriction

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DailyMed / Genentech · Adult VALCYTE 450 mg tablets; induction versus maintenance/prevention. Pediatric equations are not substituted.

Renal method: Cockcroft-Gault CrCl in mL/min.
Source date: December 2025
Retrieved: 2026-09-07

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

For CrCl >=60, induction is 900 mg twice daily and maintenance/prevention 900 mg daily. At 40-59, use 450 mg twice daily or 450 mg daily, respectively. At 25-39, use 450 mg daily or every two days. At 10-24, use 450 mg every two days or twice weekly. Below 10 on hemodialysis, the label provides no tablet dose and says the tablets should not be used; it directs clinicians to appropriately adjusted ganciclovir. Monitor kidney function and blood counts. Take with food and do not crush or split tablets. Institutional dialysis regimens are displayed separately, not called label-approved.

RDM40-official-valganciclovir-5fe607ba2e-C1 · Source locator: Sections 2.1, 2.5 (Table 2), 2.6, 5.1 and 8.6

Source identity and provenance
Source family
product_label
Source
https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=4c517a39-2ded-4c5a-8d56-276853414b31
Retrieved
2026-09-07
Exact label title
VALCYTE: adult renal tablet table and hemodialysis restriction
DailyMed Set ID
4c517a39-2ded-4c5a-8d56-276853414b31
Labeler
Genentech
Label revision
December 2025
Renal-function method
Cockcroft-Gault CrCl in mL/min.
Source date/version
December 2025
Hash meaning
SHA-256 of local authored summary only; not original HTML, PDF or SPL bytes.
Local summary SHA-256
da7a91960f5c759803bc71d50867a1747f8e5ee364a064affb9c209d8387b768
Separate professional-source layer

University and professional protocols

Professional

UCSF - valganciclovir: treatment, prevention and dialysis

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UCSF Infectious Diseases Management Program · Adults; source-specific institutional guidance. Match route, indication and renal replacement modality.

Renal method: CrCl in mL/min where specified; no equation inferred.
Source date: Revision date not stated in the reviewed page.
Retrieved: 2026-09-05

Locally included source-specific summary. Regimen differences are not automatically resolved.

Dosing / renal protocol and limits

Limits that apply to these rows

Exactly 60 is unassigned. Institutional HD regimens differ from U.S. tablet-label limitations. IV ganciclovir is preferred at initiation with unstable renal function or dialysis. Give oral doses with food.

CMV treatment - oral
CrCl, mL/minSource-specific dose / instruction
>60900 mg every 12 hours
40-59450 mg every 12 hours
25-39450 mg daily
10-24450 mg every other day
CMV prevention - oral
CrCl, mL/minSource-specific dose / instruction
>60900 mg daily
40-59450 mg daily
25-39450 mg every other day
10-24450 mg twice weekly
Dialysis guidance - separate source-specific schedules
Valganciclovir dialysis
Dialysis setting / indicationSource-specific schedule
IHD treatment450 mg initially, then after HD
IHD prevention450 mg twice weekly
Continuous HD treatment450 mg daily
Continuous HD prevention450 mg every other day
Read the retained text before reformatting

Adult CrCl bands: >60 / 40-59 / 25-39 / 10-24 mL/min; exactly 60 is not assigned by the displayed webpage. CMV treatment: 900 mg orally every 12 hours / 450 mg every 12 hours / 450 mg daily / 450 mg every other day. Prevention: 900 mg daily / 450 mg daily / 450 mg every other day / 450 mg twice weekly.

Intermittent HD treatment: 450 mg initially, then after HD. HD prevention: 450 mg twice weekly. Continuous-HD treatment: 450 mg daily; prevention: 450 mg every other day. These institutional HD regimens are distinct from U.S. tablet-label limitations. IV ganciclovir is preferred when starting therapy in unstable renal function or dialysis. Give oral doses with food.

RDM30-026-valganciclovir-1 · Source locator: UCSF - valganciclovir: treatment, prevention and dialysis; renal/dosing sections and stated qualifiers

Source identity and provenance
Source
https://idmp.ucsf.edu/content/valganciclovir-valcyte
Retrieved
2026-09-05
Renal-function method
CrCl in mL/min where specified; no equation inferred.
Source date/version
Revision date not stated in the reviewed page.
Hash meaning
Locally authored summary text; not original SPL, HTML or PDF bytes
Local summary SHA-256
e9d496f833efd6f7ae9de2a8643ec34e661a784711c7894611f5acd6d5e5d563
Professional

UCSF: valganciclovir in intermittent and continuous hemodialysis

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Open / share this exact local source

UCSF Infectious Diseases Management Program · UCSF adult institutional CMV treatment/prophylaxis; dialysis regimens differ from the product label.

Renal method: Intermittent versus continuous hemodialysis; not automatically every CRRT modality.
Source date: Source revision date not established in selected retrieval.
Retrieved: 2026-09-07

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

For intermittent HD, UCSF lists CMV treatment as 450 mg orally once now and after HD; prophylaxis is 450 mg twice weekly. For continuous HD it lists treatment 450 mg daily and prophylaxis 450 mg every 48 hours. IV ganciclovir is preferred when initiating treatment during unstable renal function or dialysis. Give with food. These are institution-specific regimens outside the label's adult tablet-HD recommendation. Confirm actual dialysis settings and specialist monitoring rather than treating continuous HD and intermittent HD as interchangeable.

RDM40-professional-valganciclovir-81c34aacfb-C1 · Source locator: Adult dialysis table and dialysis notes

Source identity and provenance
Source family
professional_guidance
Source
https://idmp.ucsf.edu/content/valganciclovir-valcyte
Retrieved
2026-09-07
Renal-function method
Intermittent versus continuous hemodialysis; not automatically every CRRT modality.
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
b38568266d3b557666b0504963bae7a5b4eb7ec3cf1d7810f5762d8b91e6faff
Professional

Jarrell et al.: valganciclovir prophylaxis during CVVHD (primary abstract)

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Jarrell et al. / primary study indexed by PubMed · Single-center prospective pharmacokinetic study of ten adult solid-organ transplant recipients in ICU on CVVHD; abstract only.

Renal method: Continuous veno-venous hemodialysis; not intermittent dialysis.
Source date: Clinical Infectious Diseases, 2021; published online 2020. PMID 32379860.
Retrieved: 2026-09-07

Pharmacokinetic observation only. A drug-exposure observation is not itself a dose recommendation.

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

Renal dosing, restrictions and evidence limits

Participants received 450 mg enterally every 24 hours for prophylaxis. Eight of ten achieved the proposed ganciclovir trough target of at least 0.60 microgram/mL; no neutropenia was documented, while significant thrombocytopenia occurred in six. The authors suggest daily dosing may be needed to achieve the desired exposure. This small pharmacokinetic study did not establish comparative clinical efficacy, universal safety or a prescription for every CRRT setting. Its daily schedule differs from UCSF's displayed continuous-HD prophylaxis interval; reconcile modality, clearance and monitoring with specialists.

RDM40-professional-valganciclovir-22f9e63629-C1 · Source locator: Primary-publication abstract: Methods, Results and Conclusions

Source-specific limits

Full text not re-reviewed; no exact dialysate or effluent-rate assumptions are invented.

Source identity and provenance
Source family
primary_research_abstract
Source
https://pubmed.ncbi.nlm.nih.gov/32379860/
Retrieved
2026-09-07
Renal-function method
Continuous veno-venous hemodialysis; not intermittent dialysis.
Source date/version
Clinical Infectious Diseases, 2021; published online 2020. PMID 32379860.
Hash meaning
SHA-256 of local authored summary only; not original HTML, PDF or SPL bytes.
Local summary SHA-256
e109b567ec9781f081d4c64ab3868a03e1bc842f1ec587ccd573ded8ffe0033e

Provenance and preservation

Additional summaries stored on this page: 1 official-label, 0 RX List, 3 professional, 0 handbook. Empty additional-source groups are not shown. A missing layer is not a no-adjustment recommendation.

Original source
https://globalrph.com/renal/valganciclovir/
Source retrieval
2026-09-05. This is not the source publication or label revision date.
Original source type
globalrph individual
Local text SHA-256
db1eb0b47aa6e44e50883e49b8acc304dbf1be50fe516f540b8cd134f4198f54
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.

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