Botox Consent Form Template
Streamline Your Botox Procedure with a Clear Consent
Navigating patient consent can be challenging, especially when it comes to cosmetic procedures like Botox. This Botox consent form template is designed specifically for practitioners and clinics, ensuring your patients are fully informed and protected. By using this template, you can clearly outline treatment risks, document patient understanding, and maintain organized records, all while ensuring compliance with WCAG-aligned standards. It's the straightforward way to enhance patient communication and streamline your administrative processes. Try the live template to see how easy it can be.
When to use this form
Use this template any time you need informed consent before cosmetic or therapeutic Botox injections. It fits med spas, dermatology and plastic surgery clinics, and neurology practices treating chronic migraine or spasticity. Send it before the visit to screen for contraindications, allergies, and medications; at the chair, it documents risks, benefits, alternatives, and aftercare, then captures a signature. For remote intakes or paperless workflows, pair it with the Electronic informed consent form. If the treatment is part of a study, add the Research consent form to cover study-specific disclosures. For eligible therapeutic patients who need help with medication costs, point them to the Botox patient assistance program application form.
Must Ask Botox Consent Questions
- Do you have any medical conditions, neuromuscular disorders, or recent facial procedures?
This surfaces contraindications (for example, myasthenia gravis, infection, or recent surgery) and helps you time treatment safely. Clear history lowers complication risk and guides dosing.
- Are you pregnant, trying to conceive, or breastfeeding?
Botulinum toxin is not recommended in these situations, so this determines whether to proceed or defer. Documenting this status protects patient safety and your compliance.
- Have you had Botox or similar botulinum toxin treatments before, and did you have any reactions?
Past response, duration of effect, or adverse events (such as eyelid ptosis or headache) inform product choice and units. It prevents over- or under-treatment and flags possible resistance.
- Which areas do you want treated, and what results are you expecting?
This aligns goals, maps injection sites, and sets realistic timelines. It reduces dissatisfaction by clarifying limits, asymmetries, and the need for touch-ups.
- Do you understand the risks, benefits, alternatives, costs, and aftercare, and do you consent to treatment today?
This confirms informed consent and creates a clear record for clinical and legal standards. It also ensures the patient knows aftercare to reduce bruising, swelling, or toxin spread.
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