GlobalRPh Renal Dosing Masterv6.6
Source review / handoff

Pacritinib (VONJO)

One or two intact local summaries. No averaged regimen, patient-specific dose or automatic source preference.

Selecting here opens the current stored cards. The pinned link below records their fingerprints. Do not enter patient information in links or searches.

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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.

Check source scope before reading a dose

Pacritinib - VONJO manufacturer prescribing information

Product / population
Adults with specified myelofibrosis and platelets below 50 x 10^9/L; accelerated-approval indication.
Renal method
MDRD-associated eGFR; source prints mL/min without indexed suffix.
Source revision
07/2026
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.

Before use: Pacritinib (VONJO)

A manufacturer document retrieved from a URL containing 2024-09 is actually revised July 2026. Its renal avoid-use restriction remains separate from newer hepatic dosing instructions.

What to reconcile: Read the document revision, not the URL folder date. Do not apply the hepatic dose reduction as a renal workaround.

Source-specific interpretation; independent clinician adjudication pending.

Open this note and its source references
Official

Pacritinib - VONJO manufacturer prescribing information

Open original reference

Sobi / VONJO manufacturer prescribing information · Adults with specified myelofibrosis and platelets below 50 x 10^9/L; accelerated-approval indication.

Renal method: MDRD-associated eGFR; source prints mL/min without indexed suffix.
Source date: 07/2026
Retrieved: 2026-09-10

Restriction or avoidance guidance. Read the specific threshold, age, formulation and dialysis exclusions; do not generalize across products.
Before using this finding

Read the document revision, not the URL folder date. Do not apply the hepatic dose reduction as a renal workaround.

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

Renal guidance and important limits

Limits that apply to these rows

The usual regimen is 200 mg twice daily. A lower severe-hepatic dose does not create a severe-renal regimen.

Review hemorrhage, QT/electrolytes, diarrhea, infection and interactions. Strong CYP3A4 inhibitors or inducers are contraindicated. No dialysis replacement dose is inferred.

VONJO - renal restriction
Printed eGFR (mL/min)Source-specific instruction
<30Avoid use
30-89Exposure similar to >=90 in the selected renal PK study; this is not an all-patient dosing authorization
Read the retained text before reformatting

VONJO - renal restriction

Printed eGFR (mL/min)Source-specific instruction
<30Avoid use
30-89Exposure similar to >=90 in the selected renal PK study; this is not an all-patient dosing authorization

The usual regimen is 200 mg twice daily. A lower severe-hepatic dose does not create a severe-renal regimen.

Review hemorrhage, QT/electrolytes, diarrhea, infection and interactions. Strong CYP3A4 inhibitors or inducers are contraindicated. No dialysis replacement dose is inferred.

RDM64-official-pacritinib-vonjo-bb997138e1-C1 · Source locator: Sections 1, 2.1-2.2, 4, 8.7 and 12.3; PDF renal PK page inspected.

Source-specific limits

The usual regimen is 200 mg twice daily. A lower severe-hepatic dose does not create a severe-renal regimen.

Review hemorrhage, QT/electrolytes, diarrhea, infection and interactions. Strong CYP3A4 inhibitors or inducers are contraindicated. No dialysis replacement dose is inferred.

Source identity and provenance
Source family
product_label
Source
https://www.vonjohcp.com/sites/default/files/2024-09/prescribing-information.pdf
Retrieved
2026-09-10
Exact label title
Pacritinib - VONJO manufacturer prescribing information
Label revision
07/2026
Renal-function method
MDRD-associated eGFR; source prints mL/min without indexed suffix.
Source date/version
07/2026
Hash meaning
Local authored summary, not source HTML/XML/PDF bytes
Local summary SHA-256
b15bdccde987402b9a710c420c759137ea1f6577a69ac99a5c0ab4f44015f838

Document the clinical decision separately

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.

Pinned reference: https://globalrph.com/blogCalcs/renal-dosing-master/compare.php?id=pacritinib-vonjo&s1=RDM64-official-pacritinib-vonjo-bb997138e1&h1=3e63ba3e34e2c90a151b32395116683273a06491eff52ed5ab7d773dcd7e9197