Neurotoxin Treatment — Sample Consent Template
A sample informed-consent structure for neurotoxin treatment — a starting point for your attorney and medical director to complete and approve.
A sample structure only, for neurotoxin (e.g., botulinum toxin) treatment. Complete every [bracketed] field, and have your medical director verify the risks are complete and accurate and your attorney adapt and approve it for your state before any use.
Patient & practice information
The treatment
I consent to treatment with a neurotoxin (product: [____]) to the following area(s): [____], to soften the appearance of dynamic lines from muscle movement. My provider has explained the treatment, the expected onset and duration, and that effects develop over a period of time rather than instantly.
Risks and possible complications I understand and accept
- Temporary effects such as redness, swelling, bruising, or tenderness at injection sites
- Headache or temporary discomfort
- Asymmetry, drooping (e.g., of the brow or eyelid), or an unintended effect on nearby muscles
- Less-than-expected or short-lived effect, or diminished response over time
- Allergic or hypersensitivity reaction, and other risks specific to neurotoxin treatment that my provider has discussed: [clinicians must list the complete, accurate, current risks here]
Important acknowledgments
- I understand effects are temporary and that repeat treatment is needed to maintain results.
- I have disclosed any pregnancy, breastfeeding, neuromuscular conditions, medications, and relevant history.
- I will follow the aftercare instructions I am given.
Results are not guaranteed
I understand results vary, that no specific outcome is guaranteed, and that touch-ups or additional units may be discussed.
Acknowledgments
- I have read (or had read to me) and understand this document.
- My questions have been answered to my satisfaction.
- My disclosed medical history, medications, and allergies are accurate.
- I am consenting voluntarily.