Botox: 

IMPORTANT INFORMATION:

Botox® is a prescription medicine for the treatment of frown lines , horizontal forehead lines and crow’s feet round the eyes. Botox® has risks and benefits. Ask your doctor if Botox is right for you. If you have side effects, see your doctor. You will need to pay for Botox® and clinic fees will apply. For details on precautions & side effects consult your healthcare professional or the Consumer Medicine Information (CMI) at www.medsafe.govt.nz . Botox® treatment lasts about 4 months and further courses of treatment may be necessary. Should only be administered by trained medical professionals. (contains botulinum toxin A 50,100 & 200 units) Allergan (NZ) Limited, Auckland.

 Treat forehead 8 units, treat frown 20 units, treat crows-feet 20 units these are the manufacturer’s recommended minimum dosages per area.

While the recommended dosage serves as a guideline based on clinical trials and expert consensus, healthcare professionals have the discretion to adjust the dosage based on individual patient factors and clinical judgment.

Each patient is unique, and their characteristics, such as age, weight, overall health, and response to treatment, can influence the appropriate dosage. A medical professional may adjust the dosage based on these factors to ensure optimal efficacy and safety for the individual patient.

Healthcare professionals may prescribe a medication for an indication or in a dosage that is not specifically approved by regulatory authorities. This is known as off-label use. Off-label use may be appropriate in certain cases where the healthcare professional determines that the potential benefits outweigh the risks.

If a patient has previously received a medication and did not respond adequately or experienced side effects at the recommended dosage, a medical professional may consider adjusting the dosage to achieve a better response or minimise adverse effects.

Clinical judgment and expertise: Healthcare professionals rely on their clinical judgment, expertise, and knowledge of the latest research and medical guidelines to make informed decisions about dosage adjustments. They may take into account factors such as the severity of the condition, the patient’s overall treatment plan, and their experience with similar cases.

Always consult with a healthcare professional for personalized advice regarding medication dosages.

Dysport: 

IMPORTANT INFORMATION: Dysport® (Clostridium botulinum type A toxin-haemagglutinin complex, 300 or 500 IPSEN units) is a Prescription Medicine for the treatment of vertical frown lines between the eyebrows. DYSPORT® has risks and benefits. For more information, talk to your medical professional or read the Consumer Medicine Information available at www.medsafe.govt.nz. Ask your Doctor if DYSPORT® is right for you. Do not use in patients with allergIndividy to active ingredients, in patients diagnosed with myasthenic gravis. Do not use if there is sign of infection at injection site. If you experience side effects and they concern you, see your medical professional. You will need to pay for DYSPORT® and for the administration and consultation charges. Galderma c/o Healthcare Logistics, Auckland 0800 174 104.

treat frown 50 units, treat crows-feet 60 units which are the manufacturer’s recommended minimum dosages per area.

While the recommended dosage serves as a guideline based on clinical trials and expert consensus, healthcare professionals have the discretion to adjust the dosage based on individual patient factors and clinical judgment.

Each patient is unique, and their characteristics, such as age, weight, overall health, and response to treatment, can influence the appropriate dosage. A medical professional may adjust the dosage based on these factors to ensure optimal efficacy and safety for the individual patient.

Healthcare professionals may prescribe a medication for an indication or in a dosage that is not specifically approved by regulatory authorities. This is known as off-label use. Off-label use may be appropriate in certain cases where the healthcare professional determines that the potential benefits outweigh the risks.

If a patient has previously received a medication and did not respond adequately or experienced side effects at the recommended dosage, a medical professional may consider adjusting the dosage to achieve a better response or minimise adverse effects.

Healthcare professionals rely on their clinical judgment, expertise, and knowledge of the latest research and medical guidelines to make informed decisions about dosage adjustments. They may take into account factors such as the severity of the condition, the patient’s overall treatment plan, and their experience with similar cases.

Always consult with a healthcare professional for personalized advice regarding medication dosages.

Dermal Filler

JUVEDERM ULTRA® & JUVEDERM ULTRA PLUS® injectable gels are Prescription Medicines containing 24 mg/mL cross linked hyaluronic acid. They are used for the filling of medium size and deep facial wrinkles by injection into the skin and for creating definition and volume in the lips. They should be administered only by trained medical professionals. Talk to your specialist about the benefits/risks of this procedure in appearance medicine. Cautions: Use in an area that has been treated with another dermal filler. People with autoimmune disease; or who are pregnant, breastfeeding, age under 18; or have an increased susceptibility to keloid formation and hypertrophic scarring. Possible Side Effects: Injection site inflammatory reactions (redness/swelling /itching/pain on pressure); induration or nodules; discolouration; weak filling effect. If you have any side effects or concerns speak to your doctor. Note: Juvederm® treatment lasts from about 12-24 months. Allergan New Zealand Ltd. PO Box 1873 Auckland 1140, New Zealand.

 BELOTERO® is hyaluronic acid dermal filler. It is used to improve the look of facial fold and wrinkles and restore volume, including contouring, shaping and volumising of the lips. Always read the label and consult your Healthcare Professional for more information. This medical device must be administered by a Healthcare Professional.You should tell your practitioner and avoid treatment with BELOTERO® if you: have had an allergic reaction to any of the ingredients; if you tend to develop keloids or heavy scars; have any bleeding disorders, poor wound healing, inflamed or infected skin, or general infection; are under the age of 18; are pregnant or breastfeeding. Please inform your practitioner of any diseases you have or have had. These include in particular cardiovascular diseases, autoimmune diseases, diabetes, epilepsy, liver or kidney problems, skin infections or severe allergies. If you take medication or vitamins, have had previous cosmetic procedures, or have been treated with other implants, please inform your practitioner. Pharmacy Retailing NZ Limited t/a Healthcare Logistics (HCL). 58 Richard Pearse Drive, Mangere, Auckland 2022. Botulinum toxin injections are prescription medicine for the treatment of frown lines , horizontal forehead lines and crow’s feet round the eyes. Botulinum toxin injections have risks and benefits. Ask your doctor if botulinum toxin injection is right for you. If you have side effects, see your doctor. You will need to pay for your botulinum toxin injection and clinic fees will apply. For details on precautions & side effects consult your doctor or go to www.medsafe.govt.nz . Botulinum toxin injections lasts about 4 months and further courses of treatment may be necessary. Should only be administered by trained medical professionals.

JUVÉDERM ULTRA® & JUVÉDERM ULTRA PLUS® injectable gels are Prescription Medicines containing 24 mg/mL cross linked hyaluronic acid. They are used for the filling of medium size and deep facial wrinkles by injection into the skin and for creating definition and volume in the lips. They should be administered only by trained medical professionals. Talk to your specialist about the benefits/risks of this procedure in appearance medicine. Cautions: Use in an area that has been treated with another dermal filler. People with autoimmune disease; or who are pregnant, breastfeeding, age under 18; or have an increased susceptibility to keloid formation and hypertrophic scarring.Possible Side Effects: Injection site inflammatory reactions (redness/swelling/itching/pain on pressure); induration or nodules; discolouration; weak filling effect. If you have any side effects or concerns speak to your doctor. You will need to pay for this medicine. Normal Doctors visit fees apply. Speak to your specialist about your own situation.JUVÉDERM® VOLUMA® injectable gel is a Prescription Medicine containing 20mg/mL cross linked hyaluronic acid. It is used to restore volume of the face. It should be administered only by trained medical professionals. Talk to your specialist about the benefits/risks of this procedure in appearance medicine. Cautions: Use in an area that has been treated with another dermal filler. People who have autoimmune disease; severe multiple allergies; a history of anaphylactic shock; acute rheumatic fever with heart complications; streptococcal disease; undergoing anti-coagulant treatment; in combination with drugs that reduce or inhibit hepatic metabolism.Possible Side Effects: Injection site inflammatory reactions (redness, swelling) which may be associated with itching and/or pain on pressure, bruising, indurations or nodules, discolouration, weak filling effects, abscess formation, granuloma, hypersensitivity. If you have any side effects or concerns speak to your doctor. You will need to pay for this medicine. Normal Doctors visit fees apply. Speak to your specialist about your own situation. JUVÉDERM®, VOLUMA®, JUVÉDERM ULTRA® and JUVÉDERM ULTRA PLUS® are registered trademarks. Allergan New Zealand Ltd. PO Box 1873 Auckland 1000, New Zealand.

TEOSYAL RHA ® 1, TEOSYAL RHA ® 2, TEOSYAL RHA ® 3, TEOSYAL RHA ® 4, TEOSYAL ® PURESENSE REDENSITY 1, TEOSYAL ® PURESENSE REDENSITY 2, TEOSYAL PURESENSE KISS ® , TEOSYAL® PURESENSE GLOBAL ACTION, TEOSYAL ® PURESENSE DEEP LINES, TEOSYAL ® PURESENSE ULTIMATE and TEOSYAL ® PURESENSE ULTRA DEEP TEOSYAL KISS ® , RHA KISS ® , TEOSYAL ® MESO, TEOSYAL ® GLOBAL ACTION, TEOSYAL ® DEEP LINES, , TEOSYAL ® ULTIMATE and TEOSYAL ® ULTRA DEEP are trademark of the firm TEOXANE SA. These products are gel that contains hyaluronic acid, and 0.3% by weight of lidocaine hydrochloride They are class III medical devices. Caution for people on blood thinning medicines. Local side effects: inflammatory reactions (redness, oedema, pain at the point of injection), haematomas, itching, temporary loss of sensitivity around the injected area, disorders of pigmentation in skin and hair, abscesses, indurations, nodules (possibly ranulomas). General manifestations: immediate hypersensitivity up to anaphylactic shock, migration of the implant. Rare but serious adverse events associated with the intravascular injection of soft tissue fillers in the face have been reported and include temporary or permanent vision impairment or blindness, skin necrosis and stroke. Lasts 9 -12 months. Please consult your doctor pharmacist for more information. Please refer to instructions for use, local distributor. Healthcare Logistics, Auckland.