Interaction Guide · Research summary

Can I take St. John's Wort with Dextroamphetamine Saccharate?

Review St. John's Wort with Dextroamphetamine Saccharate: possible adverse effects and timing and monitoring, preparation details, evidence limits, and sources.

Prepared by Dr. Edward M.Kim, PharmD · Clinical Director, SupplementSafety editorial team

Research summary published · Prepared · Editorial update

The short answer

St. John's wort can increase the risk of serotonin syndrome when used with dextroamphetamine saccharate. If co-use is necessary, the prescriber may need a lower stimulant starting dose and monitoring, especially when starting or increasing treatment. Do not adjust an existing dose yourself.

What this answer covers

Applies to dextroamphetamine saccharate with St. John's wort products; the risk concerns overlapping effects on serotonin. Evidence includes a mixed-salt product containing this ingredient, with the finding limited to its documented active-ingredient mechanism.

Supplement or preparation
St. John's wort
Medication ingredient
dextroamphetamine saccharate

Evidence and practical considerations

Side effects & toxicity

Current dextroamphetamine labeling explicitly names St. John's wort as a serotonergic agent and provides management, supporting a clinically major conditional serotonin-toxicity interaction. Exact dextroamphetamine-saccharate labeling or an explicit noncausal-saccharate active-moiety bridge supports the PIN applicability stated here.

Exact scope
St. John's wort with dextroamphetamine saccharate
Medication form and route
systemic dextroamphetamine
Timing or duration
Risk is most relevant during overlapping systemic serotonergic exposure and dose initiation or escalation.

What remains uncertain

  • Pair-specific incidence and dose-response are unknown.
  • A distinct cardiovascular or neuropsychiatric interaction beyond serotonin toxicity was not independently established.
  • St. John's wort enzyme induction is not assumed to change dextroamphetamine exposure without exact evidence.
  • Active-moiety evidence was bridged to RxCUI 221088 only where sulfate is noncausal; mixed salts, other salts, combinations, prodrugs, brands, and formulation-specific effects were not transferred.
  • No standalone dextroamphetamine-saccharate finished-product effect was assumed.
  • The component-containing product bridge is allowed only because the adjudicated mechanism concerns dextroamphetamine or amphetamine and the saccharate counterion is noncausal; other components and formulation effects are excluded.

Factors that may matter: higher stimulant dose; other serotonergic drugs or supplements; CYP2D6 inhibitors; history of serotonin toxicity; product variability.

Research conclusion: supported with conditions · Evidence assessment: moderate

Read the supporting source summaries

Source 1: FDA prescribing information (dextroamphetamine-saccharate-containing product)

dailymed.nlm.nih.gov · Source check Jul 24, 2026

Population: Patients prescribed an oral extended-release mixed-amphetamine product containing dextroamphetamine saccharate.

St. John's wort is explicitly listed as a serotonergic drug; lower initial doses and monitoring are instructed when co-use is warranted.

The finished product also contains dextroamphetamine sulfate and two amphetamine salts. Applicability to RxCUI 221088 is limited to the label's dextroamphetamine- or amphetamine-moiety mechanism; formulation-specific magnitude and other-component effects are not transferred.

Source 2: United States government supplement safety resource

nccih.nih.gov · Source check Jul 24, 2026

Population: Users of St. John's wort and medicines affecting serotonin.

NCCIH warns that combining St. John's wort with serotonin-affecting medicines can cause serious serotonin-related effects.

Not an exact-dextroamphetamine pair study.

Research assessment: · Open full citations ↗

Timing & monitoring

Exact government and regulatory sources support disclosure, avoidance when feasible, and monitoring if concomitant use is clinically warranted. Exact dextroamphetamine-saccharate labeling or an explicit noncausal-saccharate active-moiety bridge supports the PIN applicability stated here.

Exact scope
St. John's wort with dextroamphetamine saccharate
Medication form and route
systemic dextroamphetamine
Timing or duration
During overlapping systemic exposure; timing separation is not an adequate risk-control strategy.

What remains uncertain

  • This is a pharmacodynamic risk; time separation is not a reliable workaround.
  • Use is not automatically prohibited in every circumstance, but requires clinician judgment.
  • Enzyme-induction hypotheses are not used for management here.
  • Active-moiety evidence was bridged to RxCUI 221088 only where sulfate is noncausal; mixed salts, other salts, combinations, prodrugs, brands, and formulation-specific effects were not transferred.
  • No standalone dextroamphetamine-saccharate finished-product effect was assumed.
  • The component-containing product bridge is allowed only because the adjudicated mechanism concerns dextroamphetamine or amphetamine and the saccharate counterion is noncausal; other components and formulation effects are excluded.

Factors that may matter: other serotonergic agents; higher dextroamphetamine dose; CYP2D6 inhibitors; product variability.

Research conclusion: supported with conditions · Evidence assessment: moderate

Read the supporting source summaries

Source 1: United States government drug information

medlineplus.gov · Source check Jul 24, 2026

Population: Patients taking exact dextroamphetamine.

St. John's wort is named and should not be started without discussion.

No dose or interval.

Source 2: FDA prescribing information (dextroamphetamine-saccharate-containing product)

dailymed.nlm.nih.gov · Source check Jul 24, 2026

Population: Patients prescribed an oral extended-release mixed-amphetamine product containing dextroamphetamine saccharate.

St. John's wort is a named serotonergic drug; lower starting dose and monitoring are advised if co-use is warranted.

The finished product also contains dextroamphetamine sulfate and two amphetamine salts. Applicability to RxCUI 221088 is limited to the label's dextroamphetamine- or amphetamine-moiety mechanism; formulation-specific magnitude and other-component effects are not transferred.

Research assessment: · Open full citations ↗

Review and change history

Publication status
Published research summary
Clinical review
Not yet recorded
DateUpdate
Article prepared
Research summary published

Article revision: 2877ef28fb72ff32

This guide brings together the evidence records used by our interaction checker. Each finding retains its own preparation limits, research date, and source summaries.

Full citations require verification. Reading this answer and the source summaries does not.

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Information, not medical advice. Do not change prescribed treatment based on this guide.