Is Faricimab (anti-vascular endothelial growth factor) injections contraindicated in a female of childbearing age with a history of eye conditions, taking Diane 35 (cyproterone acetate and ethinyl estradiol)?

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Last updated: January 27, 2026View editorial policy

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Faricimab is NOT contraindicated with Diane-35

There is no known drug interaction or contraindication between faricimab (intravitreal anti-VEGF injection) and Diane-35 (cyproterone acetate/ethinyl estradiol oral contraceptive). These medications work through completely different mechanisms in separate anatomical compartments—faricimab acts locally in the eye while Diane-35 works systemically—and no evidence suggests any pharmacological interaction between them.

Key Clinical Considerations

Pregnancy Prevention is Critical

  • The primary concern with faricimab in women of childbearing age is pregnancy prevention, not drug interactions. Anti-VEGF medications including faricimab are FDA pregnancy category C, with animal studies showing embryo-fetal toxicity and theoretical risks to the developing fetal vasculature 1.
  • Diane-35 actually serves a protective role here by providing effective contraception while the patient receives faricimab treatment 1.

No Systemic Absorption Issues

  • Intravitreal faricimab has minimal systemic absorption due to local administration directly into the vitreous cavity 1.
  • The small molecular amounts that might reach systemic circulation would not interact with oral contraceptive metabolism or efficacy 2, 3.

Documented Safety of Combined Use

  • One clinical trial specifically evaluated exenatide + metformin + Diane-35 in women with PCOS, demonstrating that Diane-35 can be safely combined with other therapeutic agents without contraindication 1.
  • While this study involved different medications, it establishes precedent that Diane-35 does not have broad contraindications with injectable therapies.

Practical Management Algorithm

For women of childbearing age requiring faricimab:

  1. Verify effective contraception is in place - Diane-35 fulfills this requirement 1.

  2. Counsel about pregnancy risks - Document that patient understands anti-VEGF therapy must be discontinued immediately if pregnancy occurs 1.

  3. Proceed with faricimab treatment - No dose adjustment or special monitoring needed for the Diane-35 interaction 2, 3.

  4. Monitor for faricimab-specific adverse events - Watch for ocular complications (endophthalmitis, retinal vasculitis, intraocular inflammation) which occur independently of contraceptive use 4, 5.

Important Caveats

Thrombotic Risk Considerations

  • Diane-35 (containing cyproterone acetate) carries a 50-80% higher VTE risk compared to levonorgestrel-containing contraceptives, with rates of approximately 10 per 10,000 woman-years 1.
  • However, this is a contraceptive-related risk, not a faricimab interaction. The decision to use Diane-35 should be based on standard contraceptive risk assessment, not concerns about faricimab 1.

If Pregnancy Occurs

  • Discontinue faricimab immediately and switch to alternative treatments such as macular laser photocoagulation or intravitreal corticosteroids, which are reasonable first-line approaches during pregnancy 1.
  • Anti-VEGF use in pregnancy may only be justified if potential benefit clearly outweighs fetal risk 1.

Gender-Specific Faricimab Adverse Events

  • Recent pharmacovigilance data suggests some ocular adverse events with faricimab may differ between genders, though this does not relate to contraceptive use 4.
  • Most adverse events occur within 91-180 days of treatment initiation 4.

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Faricimab Administration and Usage Guidelines

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2026

Guideline

Intravitreal Anti-VEGF Injections for Age-Related Macular Degeneration

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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