Submit a MedWatch Report
If you or someone you know experienced an adverse event after being induced with Cytotec, please fill out an FDA MedWatch Online Voluntary Reporting Form. It is important that these adverse events are reported, because NO ONE ELSE is collecting this information. The more cases that are reported to the FDA, the more it pushes the Agency to take action on Cytotec and prevent it from being used for labor induction. If you have any questions about how to submit a MedWatch report, see the materials below or email us at zorah@tatia.org.
Resources:
- Tatia Foundation’s How to Submit a MedWatch Report video
- FDA MedWatch Online Reporting Form
- FDA MedWatch PDF Reporting Form
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