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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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Naloxegol tablets (Movantik, adults) - selected U.S. label sections
Product / population
Adult MOVANTIK oral tablets for opioid-induced constipation.
Renal method
Creatinine clearance in 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.
Documented differences and cautions on this drug
All record notes are retained here, including notes about sources not selected in this review.
MOVANTIK: renal starting dose and conditional escalation
The higher dose is a conditional option after tolerance and inadequate response, not the default renal maintenance dose. CYP3A interactions can impose additional restrictions.
What to reconcile: Check the renal starting dose and interaction pathway before considering escalation.
U.S. product labeling / DailyMed · Adult MOVANTIK oral tablets for opioid-induced constipation.
Renal method: Creatinine clearance in 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.
Renal starting dose and cautious escalation
For CrCl below 60 mL/min, including severe or end-stage impairment, start 12.5 mg once daily. If well tolerated but constipation persists, the label permits increasing to 25 mg once daily after considering increased exposure and adverse-reaction risk. Mild impairment does not require adjustment.
The renal starting recommendation is not replaced with a larger dose solely because the patient receives hemodialysis. Review the contraindications, CYP3A interactions and gastrointestinal warnings separately.
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.