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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.
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Voclosporin capsules (Lupkynis) - selected U.S. label sections
Product / population
Adult LUPKYNIS oral capsules for active lupus nephritis with the labeled background therapy.
Renal method
eGFR in mL/min/1.73 m2, including percentage change from baseline
Source revision
10/2025
Retrieved
2026-09-05
Local review status
Local label summary; independent clinical review pending. Not a two-source validated protocol.
Official
Voclosporin capsules (Lupkynis) - selected U.S. label sections
U.S. product labeling / DailyMed · Adult LUPKYNIS oral capsules for active lupus nephritis with the labeled background therapy.
Renal method: eGFR in mL/min/1.73 m2, including percentage change from baseline Source date: 10/2025 Retrieved: 2026-09-05
Local label summary; independent clinical review pending. Not a two-source validated protocol.
Baseline renal eligibility
Baseline eGFR at or below 45: generally not recommended unless benefit exceeds risk; this population was not studied. If treatment is chosen despite severe impairment, the reduced starting dose is 15.8 mg twice daily.
Monitor eGFR every 2 weeks in month 1, every 4 weeks through year 1, then quarterly.
If eGFR is below 60 and falls more than 20% but less than 30% from baseline, reduce each twice-daily dose by 7.9 mg. Recheck within 2 weeks; if the fall remains above 20%, reduce again by 7.9 mg twice daily.
If eGFR is below 60 and the fall is at least 30%, discontinue. Recheck within 2 weeks; consider restarting 7.9 mg twice daily only after recovery to at least 80% of baseline. After a renal-driven reduction, consider increasing by 7.9 mg twice daily for each measurement at least 80% of baseline, without exceeding the starting dose.
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.