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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
Pirtobrutinib tablets (Jaypirca) - selected U.S. label sections
Product / population
Adult JAYPIRCA oral tablets.
Renal method
eGFR; label reports mL/min
Source revision
Revision not captured; retrieval date is not the revision date.
Retrieved
2026-09-05
Local review status
Local label summary; independent clinical review pending. Not a two-source validated protocol.
Official
Pirtobrutinib tablets (Jaypirca) - selected U.S. label sections
U.S. product labeling / DailyMed · Adult JAYPIRCA oral tablets.
Renal method: eGFR; label reports mL/min 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.
Severe renal impairment - dose reduction
For eGFR 15-29 mL/min, reduce a current 200 mg once-daily dose to 100 mg once daily. For other current doses, reduce by 50 mg; discontinue if the current dose is already 50 mg once daily. At eGFR 30-89, no renal dose adjustment is recommended.
Concomitant CYP3A inhibitors and inducers have separate modification rules. This renal table does not authorize combining adjustments by simple arithmetic or extrapolating to dialysis.
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.
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.