Bocouture 1 x 100 units

Aesthetic Enhancement Through Muscle Relaxation 
 
The primary function of BOCOUTURE lies in its ability to relax muscles when injected. This relaxation serves as the foundation for its use in addressing certain facial lines and wrinkles. By targeting specific muscle groups, BOCOUTURE plays a key role in temporarily improving upper facial lines in adults under the age of 65.
These lines, which can have a significant psychological impact, include:

• Vertical lines between the eyebrows, visible during frowning.
• Lateral periorbital lines, observed when smiling.
• Horizontal forehead lines, noticeable during maximum contraction.

Essential Considerations Before Using BOCOUTURE

Prior to Treatment: What You Need to Know 
Before administering BOCOUTURE treatment, it's important to be aware of certain conditions that might affect its suitability for your client. This medicine is not suitable for those who:

• Are allergic to Botulinum neurotoxin type A or its ingredients.
• Suffer from muscle activity disorders like myasthenia gravis or Lambert-Eaton syndrome.
• Have an infection or inflammation at the planned injection site. 

Ensuring Safety and Efficacy 
While BOCOUTURE offers transformative benefits, it's essential to exercise caution and adhere to the following precautions:

• Misplaced injections may lead to temporary muscle paralysis, causing unintended side effects.
• Rare reports of distant toxin spread causing muscle weakness or swallowing difficulties highlight the importance of proper injection techniques.
• Individuals who receive recommended doses may still experience excessive muscle weakness.
• Risk of breathing, swallowing, or speaking difficulties. 

 
Procedure for use of BOCOUTURE 
Navigating the Treatment Process with Precision 
 
BOCOUTURE is a potent medical tool that should only be administered by professionals with specialised knowledge of Botulinum neurotoxin type A treatments. Here's how the treatment process unfolds for different types of facial lines:

Vertical Lines Between Eyebrows (Glabellar Frown Lines)

• Standard dose: 20 units (adjustable up to 30 units based on patient needs).
• Results: Visible reduction in 2 to 3 days, with peak effect on day 30. Lasts up to 4 months.

Lateral Periorbital Lines (Crow’s Feet Lines)

• Standard dose: 24 units (12 units per eye).
• Results: Reduction in 6 days, peak effect on day 30. Lasts up to 4 months.

Horizontal Forehead Lines 

• Dose: 10 to 20 units (distributed across injection sites).
• Results: Visible reduction in 7 days, with peak effect on day 30. Lasts up to 4 months. 

 
Navigating Possible Side Effects and Management 
 
Understanding the Potential Outcomes 
Like any medical treatment, BOCOUTURE carries the potential for side effects, although they are typically temporary. Localized reactions near the injection site may include pain, inflammation, tenderness, itching, and swelling. Additionally, certain side effects are specific to each treated area. 
 
Storage and Disposal Considerations 
 
Safeguarding BOCOUTURE and Its Components 
To ensure the integrity of BOCOUTURE, store unopened vials below 25°C. After reconstitution, the solution remains stable for up to 24 hours at 2°C to 8°C. Remember that the solution should be discarded if it appears cloudy or contains particles. 
 
Proper Disposal for Safety 
Unused vials, remaining solutions, and used syringes must be disposed of safely. Autoclaving, inactivation with appropriate solutions, or other suitable methods are recommended to ensure the safe disposal of these materials. 
 
Professional Insights for Practitioners 
 
Guidelines for Administration and Handling 
BOCOUTURE should be reconstituted using sodium chloride 9 mg/ml (0.9 %) solution for injection. The proper preparation and administration of the solution demand meticulous care to prevent spillage and ensure patient safety. 
 
Addressing Incidents and Ensuring Safety 
In case of incidents during handling, quick and appropriate actions are crucial. Whether there's a spillage, contact with skin, or an adverse reaction, following recommended procedures can mitigate risks and safeguard both practitioners and patients. 

Contents | 1 x 100 units
Cold Chain | No
Storage Conditions | 2-25 °C
Legal Category | POM
Form | Vial
Prescription Only | Yes