Interaction Guide · Research summary

Can I take Vitamin E with Fluoxetine?

Review Vitamin E with Fluoxetine: possible adverse effects, 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

Review supplemental vitamin E with the prescriber, particularly before procedures or when other bleeding-risk medicines are used. A fluoxetine co-use case exists, but several stronger competing explanations prevent isolating vitamin E.

What this answer covers

Supplemental vitamin E with fluoxetine; the reported case used a multivitamin containing 50 IU, not a high-dose isolated vitamin E regimen.

Supplement or preparation
Vitamin E
Medication ingredient
fluoxetine

Both dose and other medicines matter

Fluoxetine carries a bleeding warning. ODS notes that large vitamin E supplement doses can affect clotting, but the dose producing clinically significant effects is uncertain.

The case was a complex procedural event

A patient taking fluoxetine, fish oil and a multivitamin developed a spinal hematoma after an epidural procedure and ketorolac administration. The authors proposed multiple contributors.

Do not mislabel the vitamin exposure

The multivitamin contained 50 IU of vitamin E. This was not proof that isolated high-dose vitamin E caused the event, nor that a particular lower dose guarantees safety.

Make a procedure plan with the team

Disclose the vitamin amount, fish oil and all pain medicines before a procedure. Report unusual bleeding promptly; do not copy an automatic stopping interval or stop fluoxetine independently.

Evidence and practical considerations

Side effects & toxicity

Conditional bleeding review with strongly confounded exact coexposure evidence; no automatic restriction of dietary vitamin E.

Exact scope
Supplemental vitamin E with fluoxetine; the reported case used a multivitamin containing 50 IU, not a high-dose isolated vitamin E regimen. with Exact oral fluoxetine hydrochloride capsules. RxNorm IN 4493/PIN 227224 hydrochloride capsules. Active norfluoxetine and prolonged elimination matter. Not the combined olanzapine product.
Medication form and route
oral
Timing or duration
Source-specific single-dose, repeated-dose and observational exposures distinguished.

What remains uncertain

  • One procedural case with ketorolac, fish oil, renal disease and spinal disease; no causal allocation or safe-dose threshold.

Factors that may matter: preparation and plant part; clinical indication; dose; other medicines; baseline alertness.

Research conclusion: supported with conditions · Evidence assessment: low

Read the supporting source summaries

Source 1: current product label

dailymed.nlm.nih.gov · Source check Sep 10, 2026

Population: People prescribed oral fluoxetine.

Exact label names tryptophan and St John’s wort in serotonin warnings, warns about bleeding and mania, and describes long elimination of fluoxetine and norfluoxetine.

How this applies: RxNorm IN 4493/PIN 227224 hydrochloride capsules. Active norfluoxetine and prolonged elimination matter. Not the combined olanzapine product.

No universal supplement interval, event rate or preparation equivalence established. Original label distinguishes warnings from measured pair-specific results.

Source 2: official nutrient guidance

ods.od.nih.gov · Source check Sep 10, 2026

Population: People using vitamin E.

Large supplemental amounts may affect platelets/clotting and increase bleeding with anticoagulant or antiplatelet treatment.

How this applies: General nutrient bleeding context with actual dose and formulation required.

Clinically significant dose threshold unknown; proposed amounts above 400 IU/day are not a guaranteed safety boundary. No exact fluoxetine event rate.

Source 3: original case report

pubmed.ncbi.nlm.nih.gov · Source check Sep 10, 2026

Population: One 66-year-old with renal impairment and spinal disease undergoing cervical epidural injection.

Spinal epidural hematoma occurred; authors proposed multiple contributors to impaired hemostasis.

How this applies: Only the named drug, preparation, route and measured endpoints apply.

Procedure, ketorolac, fish oil and comorbidities strongly confound causality. Vitamin E was a multivitamin dose, not isolated high-dose supplementation; no pair-specific incidence or universal stopping rule.

Research assessment: · Open full citations ↗

Review and change history

Publication status
Published research summary
Clinical review
Not yet recorded
DateUpdate
Article prepared
Current exact available claims adjudicated using original captures and explicit identity and comparator limits.
Research summary published

Article revision: 81a1818bd1f7e3da

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.

Taking other supplements or medications?

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