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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.
Source-content exception: the live original page is empty apart from its heading. This does not establish a no-adjustment recommendation.
The separate CRIXIVAN label summary supplies actual historical dosing. It is not presented as missing text recovered from the original GlobalRPh page.
Check source scope before reading a dose
CRIXIVAN (indinavir sulfate) capsules
Product / population
Historical adult oral HIV product. Not an assertion of current U.S. marketing.
Renal method
Not specified
Source revision
05/2018
Retrieved
2026-09-05
Local review status
Historical exact U.S. label imported to fill the empty original source page; current availability is not established.
NIH/NLM DailyMed - U.S. prescribing information · Historical adult oral HIV product. Not an assertion of current U.S. marketing.
Renal method: Not specified in this summary. Source date: 05/2018 Retrieved: 2026-09-05
Historical exact U.S. label imported to fill the empty original source page; current availability is not established.
Historical labeled adult dose
The labeled adult regimen is 800 mg orally every 8 hours. Take with water, at least 1 hour before or 2 hours after a meal; a light meal is an alternative. Combination therapy and interacting medicines require separate review.
indinavir:dm-e19405d9-d9a1-4072-5b9e-40cd3ae4bf1f-1 · Source locator: DOSAGE AND ADMINISTRATION; PDF page 25
Renal evidence and limitations
The label reports no renal-impairment pharmacokinetic study and supplies no numeric renal-adjustment table. Removal by hemodialysis or peritoneal dialysis is unknown. Nephrolithiasis or urolithiasis may require temporary interruption for 1-3 days or discontinuation, with clinical management of hydration.
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.