Component

Human modafinil-associated serious rash and hypersensitivity reports

1 recorded relationships. Experimental role, claim status and evidence remain attached to each record.

How nutrients influence it

Every nutrient with a recorded effect on this component, credited to the nutrient that acted rather than the chapter that recorded it. Open a nutrient to see the findings and the conditions they were measured under.

How nutrients reach it in more than one step

Chains of two or more recorded steps that end here, grouped by the nutrient they start from. Each step is a separate finding, so a chain is a route a mechanism could take, not proof that it does.

Tracing routes…

What it does

Every recorded relationship this component is part of, grouped by its role. Plain wording comes first; the technical statement follows.

Recorded relationships

What acts on it

  1. Official labeling reports serious rash including SJS/TEN and systemic hypersensitivity; pediatric rash discontinuations are not equivalent to SJS incidence.

    Experimental context and source evidence
    evidence_access
    Official label description, pharmacology, pharmacokinetics, indications, interactions and relevant warnings checked.
    experimental_model
    Official U.S. label; safety reports and pediatric trial discontinuations, not supported adult incidence denominator.
    interpretation_status
    Source-derived extraction of a fact-checked reference; access is explicit, not independent raw-data verification.
    limitations
    Interpret only within the recorded preparation, exposure and comparator. The complete source passage retains qualifications; unspecified doses/timing have not been extracted here. No clinical efficacy, nutrient deficiency or unique molecular mediation is inferred.
    plain_language
    Official labeling reports serious rash including SJS/TEN and systemic hypersensitivity; pediatric rash discontinuations are not equivalent to SJS incidence.
    primary_references
    PROVIGIL U.S. prescribing information | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=3b8d1c32-dac9-50e6-e063-6394a90aa5a5
    source_locator
    Reviewed reference lines 166-166; exact primary location described in quoted passage where extracted.

    Modafinil: detailed mechanisms of action (reviewed 3 October 2026) · lines 166–166

    Original AI-assisted review of primary studies and, where relevant, official regulatory records. Access level is retained per claim. Corrections, null results and unresolved questions remain explicit. Not publisher full text or independent replication. · supports · Official U.S. label; safety reports and pediatric trial discontinuations, not supported adult incidence denominator. · Recorded from source · Recorded from source

    The U.S. product is Schedule IV, approved for adult excessive sleepiness associated with narcolepsy, OSA or shift-work disorder. Serious rash is a warning, **not a boxed warning**; 13/1,585 pediatric rash-related discontinuations are not 13 SJS cases. It is not approved for children. Reported reactions include SJS/TEN and systemic hypersensitivity. The cited label provides no supported adult “1 in 3,000–10,000” incidence. It instructs discontinuation at the first rash unless clearly unrelated. [U.S. label](https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=3b8d1c32-dac9-50e6-e063-6394a90aa5a5)
    Complete structured claim and evidence

In the sources

Preserved passages that mention this component, quoted exactly. Open one to read it in context.

    This is a research prototype built from draft material. It is not medical advice, and its statements still await verification against the original studies.