Vortioxetine

وورتیوکستین

⚠ Unverified

🧠 Nervous SystemMultimodal antidepressant

Market / country: 🇺🇸 USA

Trintellix (US)

🧮 Dose calculator

Major depressive disorder · Regimen source: FDA Trintellix · 2.1

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🛡️ Safety & information

Contraindications

  • ⛔ Hypersensitivity; MAOIs, within 14 days of stopping an MAOI or 21 days of stopping vortioxetine; linezolid or IV methylene blue. FDA Trintellix · 4

Warnings

Formulations

👥 Special populations

  • 🤰 PregnancyUse with caution

    Label states no clear risk or has limited data; use only if needed, under medical advice. FDA Trintellix · 8.1

    “Risk Summary Based on data from published observational studies, exposure to SSRIs or SNRIs, particularly in the month before delivery, has been associated with a less than 2-fold increase in the risk of postpartum hemorrhage [see Warnings and Precautions (5.3) and Clinical Considerations ] .”
  • 🤱 BreastfeedingUse with caution

    Label: use with caution while breastfeeding; see the label text. FDA Trintellix · 8.2

    “Risk Summary There is no information regarding the presence of vortioxetine in human milk, the effects on the breastfed infant, or the effects on milk production.”
  • 👶 ChildrenDangerous / avoid

    Boxed warning in the label about children. FDA Trintellix · Boxed Warning

    “Antidepressants increased the risk of suicidal thoughts and behavior in pediatric and young adult patients in short-term studies.”
  • 👴 Older adultsUse with caution

    Label: use with caution in older adults, usually starting at the low end of the dose range. FDA Trintellix · 8.5

    “Serotonergic antidepressants have been associated with cases of clinically significant hyponatremia in elderly patients, who may be at greater risk for this adverse event [see Warnings and Precautions (5.7) ] .”
  • ⚥ Females & males of reproductive potentialNo data

    The source for this drug has no section for this group.

📚 Reference status for this drug

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