GlobalRPh Renal Dosing Masterv6.6
Evidence addition

Viloxazine extended-release capsules (Qelbree, adult renal comments)

Qelbree

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Official source

Viloxazine extended-release capsules (Qelbree, adult renal comments) - selected U.S. label sections

Product / population
Adult QELBREE extended-release oral capsules; not an immediate-release preparation.
Renal measure
eGFR in mL/min/1.73 m2

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.

Severe renal impairment

At eGFR below 30, initiate 100 mg once daily. Titrate in weekly increments of 50-100 mg, to a maximum of 200 mg once daily. This reduced maximum must not be replaced with the usual adult maximum.

Scope

This entry contains the severe-impairment modification, not the full ADHD titration, interaction or safety algorithm. No dialysis supplement is derived.

Source revision: Revision not captured; retrieval date is not the revision date. | Retrieved: 2026-09-05. Retrieval date is not the revision date.

Source: https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=aedf408d-0f84-418d-9416-7c39ddb0d29a

Scope: Local label summary; independent clinical review pending. Not a two-source validated protocol. GlobalRPh v6.6.

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Official product label

Viloxazine extended-release capsules (Qelbree, adult renal comments) - selected U.S. label sections

Adult QELBREE extended-release oral capsules; not an immediate-release preparation.

Renal method: eGFR in mL/min/1.73 m2
Retrieved: 2026-09-05

Source presence is not independent validation. A label mirror is not a second independent source; review the original reference and exact formulation.

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New source summary - independent clinical review pending. Summaries of the identified label sections are included locally. Source import and numeric transcription checks are not independent two-reference validation. Do not treat this card as an approved institutional dosing protocol.
Official source

Viloxazine extended-release capsules (Qelbree, adult renal comments) - selected U.S. label sections

Adult QELBREE extended-release oral capsules; not an immediate-release preparation.

Method: eGFR in mL/min/1.73 m2

No dialysis or renal heading shown? Read the complete source summary. Absence of a heading is not evidence that dose adjustment is unnecessary.

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Exact product and population matter. This added page contains locally stored, source-specific clinical summaries. Historical handbook information, when present, is identified separately and may conflict with U.S. labeling. Confirm indication, population, kidney-function method, monitoring and the full prescribing information before applying a regimen.
Locally stored source content

Exact product and population

Product identity selected for the separately displayed source protocols below. Reference: https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=aedf408d-0f84-418d-9416-7c39ddb0d29a

Product and population scope

Adult QELBREE extended-release oral capsules; not an immediate-release preparation.

RDM32-viloxazine-qelbree-er-scope · Source section: Editorial scope for the selected U.S. labelRenal section finder
Separate U.S. product-label layer

FDA / DailyMed dosing and renal information

Official

Viloxazine extended-release capsules (Qelbree, adult renal comments) - selected U.S. label sections

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U.S. product labeling / DailyMed · Adult QELBREE extended-release oral capsules; not an immediate-release preparation.

Renal method: eGFR in mL/min/1.73 m2
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

At eGFR below 30, initiate 100 mg once daily. Titrate in weekly increments of 50-100 mg, to a maximum of 200 mg once daily. This reduced maximum must not be replaced with the usual adult maximum.

RDM32-viloxazine-qelbree-er-1 · Source locator: 2.4; 8.6

Scope

This entry contains the severe-impairment modification, not the full ADHD titration, interaction or safety algorithm. No dialysis supplement is derived.

RDM32-viloxazine-qelbree-er-2 · Source locator: 2; 8.6

Source-specific limits

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.

Source identity and provenance
Source
https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=aedf408d-0f84-418d-9416-7c39ddb0d29a
Retrieved
2026-09-05
DailyMed Set ID
aedf408d-0f84-418d-9416-7c39ddb0d29a
Renal-function method
eGFR in mL/min/1.73 m2
Source date/version
Revision not captured; retrieval date is not the revision date.
Hash meaning
SHA-256 identifies this local summary, not original SPL XML or a label PDF.
Local summary SHA-256
dcf677fedb744d9be61971d9c538978688c58610261e6a47e5926b2b58a0fdde

Provenance and preservation

Additional summaries stored on this page: 1 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://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=aedf408d-0f84-418d-9416-7c39ddb0d29a
Source retrieval
2026-09-05. This is not the source publication or label revision date.
Original source type
multisource addition
Local text SHA-256
15486c0e9e17c27401b95bc07e85960b1bb3bae05ae7bb641c71ab24284df190
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.

This page is an additional exact-product entry, not a recovered GlobalRPh monograph. Its primary scope text and separately attributed clinical summaries are locally included.

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