Selecting here opens the current stored cards. The pinned link below records their fingerprints. Do not enter patient information in links or searches.
Share or print this source review
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.
Copy is optional; the link can be selected and copied manually. No patient data or dose decision is collected.
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.
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
<30
Avoid use
30-89
Exposure 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
<30
Avoid use
30-89
Exposure 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.
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.