GlobalRPh Renal Dosing Masterv6.6
GlobalRPh source record

Cefixime

GlobalRPh source pageBase record retrieved 2026-09-05See the evidence for this drug1 sources available - open source summaries, references and comparisons
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Renal measure
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Source summary and narrative differ at exactly 20 and 60 mL/min. Both are retained; do not silently resolve the boundary.

Usual Dosing (Adults)

400 mg orally every 24 hours or 200 mg every 12 hours.

Renal Dosing

Source summary: CrCl >60 mL/min: 400 mg/day; 21 to 60: 300 mg/day; <=20: 200 mg/day.

Suprax may be administered in the presence of impaired renal function. Normal dose and schedule may be employed in patients with creatinine clearances of 60 mL/min or greater. Patients whose clearance is between 21 and 60 mL/min or who are on renal hemodialysis may be given 75% of the standard dosage at the standard dosing interval (300 mg daily). Patients whose clearance is <20 mL/min, or who are on continuous ambulatory peritoneal dialysis, may be given half the standard dosage (200 mg daily). Neither hemodialysis nor peritoneal dialysis removes significant amounts of the drug from the body.

Hemodialysis

See the renal dosing text above.

Source revision: Historical source; revision not established here | Retrieved: 2026-09-05. Retrieval date is not the revision date.

Source: https://globalrph.com/renal/cefixime/

Scope: Preserved historical source; no fresh clinical approval GlobalRPh v6.6.

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Preserved GlobalRPh source

Preserved original GlobalRPh source

Preserved historical content; not revalidated as current prescribing guidance.

Renal method: Read the measure and population stated in the original source sections.
Retrieved: 2026-09-05

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Renal dosing and precautions

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Original content / product scope
Historical source content is not a current prescription. Original GlobalRPh recommendations are preserved, not automatically certified as current. Product-label and professional additions below are separately attributed. Confirm indication, population, kidney-function method, monitoring and the full prescribing information before applying a regimen.

Important source distinctions

Source summary and narrative differ at exactly 20 and 60 mL/min. Both are retained; do not silently resolve the boundary.

Locally stored source content

Original GlobalRPh protocol

Clinical facts and comments transcribed into a structured reading format. This is not a byte-for-byte HTML archive. Original source: https://globalrph.com/renal/cefixime/

Usual Dosing (Adults)

400 mg orally every 24 hours or 200 mg every 12 hours.

GRPH-cefixime-01 · Source section: Usual Dosing (Adults)Renal section finder

Renal Dosing

Source summary: CrCl >60 mL/min: 400 mg/day; 21 to 60: 300 mg/day; <=20: 200 mg/day.

Suprax may be administered in the presence of impaired renal function. Normal dose and schedule may be employed in patients with creatinine clearances of 60 mL/min or greater. Patients whose clearance is between 21 and 60 mL/min or who are on renal hemodialysis may be given 75% of the standard dosage at the standard dosing interval (300 mg daily). Patients whose clearance is <20 mL/min, or who are on continuous ambulatory peritoneal dialysis, may be given half the standard dosage (200 mg daily). Neither hemodialysis nor peritoneal dialysis removes significant amounts of the drug from the body.

GRPH-cefixime-02 · Source section: Renal DosingRenal section finder

Hemodialysis

See the renal dosing text above.

GRPH-cefixime-03 · Source section: HemodialysisRenal section finder

Provenance and preservation

Additional summaries stored on this page: 0 official-label, 0 RX List, 0 professional, 0 handbook. Empty additional-source groups are not shown. A missing layer is not a no-adjustment recommendation.

Original source
https://globalrph.com/renal/cefixime/
Source retrieval
2026-09-05. This is not the source publication or label revision date.
Original source type
globalrph individual
Local text SHA-256
50d886b4260041097c8b490d18f9b4786de9b014a2ec839ed589678ce9c61ef1
Import versus clinical validation
Source-section locators identify where retained content came from. A source-section identifier does not assert that every numeric statement has been independently corroborated. The local text hash is not a hash of original HTML, an FDA PDF or SPL XML.

The original individual GlobalRPh pages commonly cite NIH/NLM DailyMed and instruct readers to review the applicable package insert for updates. That historical reference is preserved as context; it is not counted as an independently retrieved current label.

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