Login www.allerganadvantage.com All For information, eligibility, and enrollment contact your Allergan Sales Representative or call All Support at 1-888-912-1572 Medical Information Contact Allergan to report a suspected adverse event at 1-800-377-7790. To set up an Allergan Aesthetics account, please call 844-NEW-2AGN (844-639-2246). Results of this procedure will vary depending upon patient age, surgical site, and experience of the physician. The most commonly reported side effects for JUVDERM injectable gels were redness, swelling, pain, tenderness, firmness, lumps/bumps, bruising, discoloration, and itching. The REVOLVE Advanced Adipose System (REVOLVE System) is used for aspiration, harvesting, filtering, and transferring of autologous adipose tissue for aesthetic body contouring. In clinical trials, 72% of subjects treated with KYBELLA experienced hematoma/bruising. These reactions occurred in less than 4% of patients. Hashtags. At Allergan Aesthetics, we believe in the remarkable impact confidence can have on the lives, businesses, and careers of those we serve through our history of a company built on patient-care, education and support of our customers, and our commitment to putting the patients we serve first. For legacy Allergan Healthcare providers, Patients and Caregivers, submit inquiry here. For healthcare providers please tell us what information you are requesting, being as specific as possible. Accounts payable and accrued liabilities $ 12,788 . Possible adverse events with breast implant surgery include implant rupture with silicone implants, implant deflation with saline-filled implants, capsular contracture, reoperation, implant removal, pain, changes in nipple and breast sensation, infection, scarring, asymmetry, wrinkling, implant displacement/migration, implant palpability/visibility, breastfeeding complications, hematoma/seroma, implant extrusion, necrosis, delayed wound healing, infection, breast tissue atrophy/chest wall deformity, calcium deposits, and lymphadenopathy. Our company is built on patient-care and education and support of our customers. Injections that are too superficial into the dermis may result in skin ulceration and necrosis. Our goal is to consistently provide our customers with innovation, education, exceptional. All is the next-generation patient loyalty program by Allergan Aesthetics. At Allergan Aesthetics, an AbbVie company, we develop, manufacture, and market a portfolio of leading aesthetics brands and products. In most cases, this is a consequence of weakening of muscles in the area of injection that are involved in breathing or oropharyngeal muscles that control swallowing or breathing (seeBoxed Warning). Our goal is to consistently provide our customers with innovation, education, exceptional service, and a . Some common adverse effects associated with autologous fat transfer are asymmetry, over- and/or under-correction of the treatment site, tissue lumps, bleeding, and scarring. Lack of Interchangeability Between Botulinum Toxin Products. For JUVDERM VOLBELLA XC, dryness was also reported. Cases of injection site alopecia have been reported with administration of KYBELLA. Take extra care when injecting soft-tissue fillers; for example, after insertion of the needle and just before injection, the plunger rod can be withdrawn slightly to aspirate and verify the needle is not intravascular, inject the product slowly, and apply the least amount of pressure necessary. The safety and effectiveness of BOTOXfor unapproved uses have not been established. Women who are close to menstruation may find that it comes sooner, or cramping is increased or intensified with CoolTone treatments, therefore, it is recommended to not undergo treatment during this time of the month. In several of the cases, patients had pre-existing dysphagia or other significant disabilities. Pfizer COVID-19 vaccine FDA EUA This product contains albumin, a derivative of human blood. Pfizer COVID-19 vaccine UK EUA See our locations. BOTOX is approved in 98 countries worldwide1* and in several therapeutics and aesthetics indications.2, For aesthetics indications BOTOX is indicated for the temporary improvement in the appearance of moderate to severe vertical lines between the eyebrows (glabellar lines) seen at maximum frown and/or moderate to severe lateral canthal lines (crows feet lines) seen at maximum smile and/or moderate to severe forehead lines seen at maximum eyebrow elevation when the severity of the facial lines has an important psychological impact in adult patients.2, For full list of approved indications, please refer to theSummary of Product Characteristics, Product Status: Prescription Medicine The system should be used with a legally marketed vacuum or aspirator . ABOUT KYBELLA The first-of-its-kind FDA-approved injectable, KYBELLA is a nonsurgical option to improve the appearance of submental fullness in adults. Breast implant surgery should not be performed in: PRECAUTIONS BOTOX Botulinum toxin type-A is a prescription only medicine that should only be given by physicians with appropriate qualifications, and expertise in the treatment and the use of the required equipment. Injection Site Alopecia Consult the CoolSculpting System User Manual for a complete list of Contraindications, Warnings, Precautions, and potential side effects. Your Practice. About Allergan Aesthetics At Allergan Aesthetics, an AbbVie company, we develop, manufacture, and market a portfolio of leading aesthetics brands and products. Human Albumin and Transmission of Viral Diseases. JUVDERM Ultra Plus XC and JUVDERM Ultra XC injectable gels are indicated for injection into the mid-to-deep dermis for correction of moderate to severe facial wrinkles and folds (such as nasolabial folds). Co-administration of BOTOXCosmetic and aminoglycosides or other agents interfering with neuromuscular transmission (eg, curare-like compounds) should only be performed with caution as the effect of the toxin may be potentiated. If you have additional questions on other products, please submit another request form. Your browser currently is not set to accept Cookies. Safety and effectiveness have not been established in patients with the following: ADVERSE EVENTS is an exciting partnership designed to support new physicians, like you, transitioning to new medical practices. Serious Adverse Reactions With Unapproved Use. These sensations subside as the area becomes numb. The input we received from practitioners and consumers provides a unique view of what tomorrow may hold for aesthetics. Filling the device with adipose tissue over the maximum fill volume line can lead to occlusion of the mesh resulting in mesh tear. Please visit JuvedermDFU.com for more information. There have been reports following administration of BOTOXof adverse events involving the cardiovascular system, including arrhythmia and myocardial infarction, some with fatal outcomes. They are not interchangeable with other preparations of botulinum toxin products and, therefore, units of biological activity of BOTOXCosmetic cannot be compared to nor converted into units of any other botulinum toxin products assessed with any other specific assay method. Treatment results may vary. WARNINGS Patients should receive prompt medical attention and, possibly, evaluation by an appropriate healthcare professional specialist should an intravascular injection occur, Product use at specific sites in which an active inflammatory process (skin eruptions such as cysts, pimples, rashes, or hives) or infection is present should be deferred until the underlying process has been controlled, To minimize the risks of potential complications, this product should only be used by healthcare professionals with appropriate experience and training on facial anatomy and product use in indicated area(s), vasculature, safe injection techniques, and identification and management of potential adverse events, including intravascular complications, The potential risks of soft-tissue injections should be discussed with patients prior to treatment to ensure they are aware of signs and symptoms of complications, The safety and effectiveness for the treatment of anatomic regions other than indicated areas for each product have not been established in controlled clinical studies, The safety for use of these products during pregnancy, in breastfeeding females, and in patients with known susceptibility to keloid formation, hypertrophic scarring, and pigmentation disorders has not been studied, The safety for use of JUVDERM VOLUMA XC has been established in patients between 35 and 65 years of age for cheek augmentation and in patients between 22 and 80 years of age for chin augmentation, The safety for use of JUVDERM Ultra Plus XC and JUVDERM Ultra XC in patients under 18 years, and JUVDERM VOLLURE XC and JUVDERM VOLBELLA XC in patients under 22 years, has not been established, As with all transcutaneous procedures, dermal filler implantation carries a risk of infection, Dermal fillers should be used with caution in patients on immunosuppressive therapy, Patients taking medications that can prolong bleeding (such as aspirin, nonsteroidal anti-inflammatory drugs, and warfarin) may experience increased bruising or bleeding at treatment sites, Patients who experience skin injury near the site of implantation may be at a higher risk for adverse events, If laser treatment, chemical peel, or any other procedure based on active dermal response is considered after treatment, or before skin has healed from a procedure prior to treatment, there is a possible risk of eliciting an inflammatory reaction at the injection site, The safety for use of JUVDERM VOLUMA XC injectable gel in patients with very thin skin in the mid-face has not been established, The safety of JUVDERM VOLUMA XC with cannula for cheek augmentation has not been established in patients with Fitzpatrick Skin Types V and VI, JUVDERM VOLUMA XC was not evaluated in subjects with significant skin laxity of the chin, neck, or jaw in the chin augmentation study, The effect of JUVDERM VOLUMA XC injection into the chin on facial hair growth has not been studied, Patients may experience late-onset adverse events with use of these dermal fillers, and late-onset nodules with use of JUVDERM VOLUMA XC, Based on preclinical studies, patients should be limited to 20 mL of any JUVDERM injectable gel per 60 kg (130 lbs) body mass per year. Please login to your account to access resources, take e-learning courses, update your account, and read industry insights. CoolTone treatment is contraindicated in placing the active applicator over metal, electrical, or electronic implants/devices in the treatment area like cardiac pacemakers, cochlear implants, intrathecal pumps, implanted defibrillators, implanted neurostimulators, drug pumps, or hearing aids. Cases of injection site alopecia have been reported with administration of KYBELLA. Dysphagia All Rights Reserved. These sensations subside as the area becomes numb. Filling the device with adipose tissue over the maximum fill volume line can lead to occlusion of the mesh resulting in mesh tear. Reuse of this device in the same patient in a subsequent surgical procedure, or for more than one patient, may result in infection and/or transmission of communicable diseases. Your one-stop online destination to access Allergan Aesthetics programs and manage your account. Our aesthetics portfolio includes facial injectables,. Reuse of this device in the same patient in a subsequent surgical procedure, or for more than one patient, may result in infection and/or transmission of communicable diseases. Funding support is never intended to induce, incentivize or reward past, current or future prescribing, purchasing, formulary inclusion . Learn about your reporting options for select products. update your account, and read industry insights. All unsolicited grants are independently managed by the Grants and Donations Committee. 2022 AbbVie. There have been reports of dry eye associated with BOTOXCosmetic injection in or near the orbicularis oculi muscle. This device will not, in and of itself, produce significant weight reduction. Use of this device is limited to those physicians who, by means of formal professional training or sanctioned continuing medical education (including supervised operative experience), have attained proficiency in suction lipoplasty and tissue transfer. WARNINGS AND PRECAUTIONS CoolSculpting is contraindicated in patients with cryoglobulinemia, cold agglutinin disease, or paroxysmal cold hemoglobinuria. Care should be taken to avoid inadvertent injection directly into an artery or a vein as it can result in vascular injury. Search for Careers Working at Allergan A dynamic organization that offers exciting and unique opportunities at all levels. Based on effective donor screening and product manufacturing processes, it carries an extremely remote risk for transmission of viral diseases and variant Creutzfeldt-Jakob disease (vCJD). Box 19534 Irvine, CA 92623, USA. Please login to your account to access resources, take e-learning courses, If harvested fat is to be re-implanted, the harvested fat is only to be used without any additional manipulation. If symptoms of dry eye (eg, eye irritation, photophobia, or visual changes) persist, consider referring patients to an ophthalmologist. The potency units of BOTOXCosmetic are specific to the preparation and assay method utilized. KYBELLA is contraindicated in the presence of infection at the injection sites. We use cookies on this site to enhance your user experience. SkinMedica Total Defense + Repair Broad Spectrum Sunscreens (SPF 34, SPF 34 Tinted, and SPF 50+) and Essential Defense Broad Spectrum Sunscreens (Everyday Clear SPF 47, Mineral Shield Tinted SPF 32, and Mineral Shield SPF 35) are over-the-counter drug products which are formulated and marketed pursuant to FDAs governing regulations set forth at 21 C.F.R. JUVDERM VOLBELLA XC injectable gel is indicated for injection into the lips for lip augmentation and correction of perioral rhytids, and for the improvement of infraorbital hollowing in adults over the age of 21. AU-ABBV-210497 V1 DoP: November 2021. All rights reserved. At Allergan Aesthetics, an AbbVie company, we develop, manufacture, and market a portfolio of leading aesthetics brands and products. . This rating has decreased by -3% over the last 12 months. At Allergan Aesthetics, we are inspired by possibilities. Based on effective donor screening and product manufacturing processes, it carries an extremely remote risk for transmission of viral diseases and variant Creutzfeldt-Jakob disease (vCJD). For JUVDERM VOLUMA XC, most resolved within 2 to 4 weeks. Cases of injection site ulceration and necrosis have been reported with administration of KYBELLA. Rare side effects may also occur. For more information, please see theInstructions for Use (IFU)andUser Manualfor REVOLVE Systemavailable atwww.allergan.com/REVOLVEIFUor call 1.800.678.1605. Some of these patients had risk factors including pre-existing cardiovascular disease. Allergan Aesthetics, an AbbVie company, and a global leader in medical aesthetics treatments, today launched 'The Future of Aesthetics' global trends report via a high-profile virtual event for . 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, blindness, cerebral ischemia or cerebral hemorrhage leading to stroke, skin necrosis, and damage to underlying facial structures. Allergan Access for Medical Aesthetics is a Web-based suite of practice management tools and resources. Allergan, Inc. has retained the services of BSM Consulting ("BSM") to develop and manage Allergan Access and BSM is solely responsible for the content on this website. Adverse product reactions. Allergan Aesthetics | An AbbVie Company . We may also use cookies to . CoolTone is also indicated for strengthening, toning, and firming of buttocks and thighs. Allergan Physician Log In will sometimes glitch and take you a long time to try different solutions. These SkinMedica products are not intended to be drug products that diagnose, treat, cure, or prevent any disease or condition. We create the products and technologies that drive the advancement of aesthetic medicine. All trademarks are the property of their respective owners. The CoolSculpting procedure is FDA-cleared for the treatment of visible fat bulges in the thigh, abdomen and flank, along with bra fat, back fat, underneath the buttocks (also known as banana roll), and upper arm in patients with a Body Mass Index (BMI) of 30 and in submental and submandibular areas in patients with a BMI of 46.2. when working with non-allergan customers who are considering aesthetics, duties include: assessment of customer needs, gathering of basic customer info, education on the value of working with allergan (sales support, program support, business development support, etc.) Do not administer KYBELLA into affected area until complete resolution. CONTRAINDICATIONS Terms of Use and Online Service Agreement. Patients should be advised about the potential for increased brown iris pigmentation, which is likely to be permanent. KYBELLA should be used with caution in patients with bleeding abnormalities or who are currently being treated with antiplatelet or anticoagulant therapy as excessive bleeding or bruising in the treatment area may occur. Regular price gift cards are also always available. Pre-existing Conditions at the Injection Site. Built on robust market research from a world-class forecasting think tank, crafted through social listening data, industry research, academic studies and Allergan Aesthetics proprietary global market research into consumer attitudes, and validated by interviews with leading aesthetics practitioners. SkinMedica Purifying Foaming Wash is an over-the-counter drug product that are formulated and marketed pursuant to the FDAs governing regulations set forth at 21 CFR Part 333 Subpart D. LATISSE(bimatoprost ophthalmic solution) 0.03% is indicated to treat hypotrichosis of the eyelashes by increasing their growth, including length, thickness, and darkness. To report an adverse reaction, please call Allergan at 1.800.367.5737. IRVINE, Calif., Nov. 3, 2022 /PRNewswire/ -- Allergan Aesthetics, an AbbVie company (NYSE: ABBV), is continuing its commitment to provide education and support for breast health, restoration, and . We are dedicated to promoting excellence in clinical practice and improving patient outcomes. Do you wish to leave this site? Possible adverse events with breast implant surgery include implant rupture with silicone implants, implant deflation with saline-filled implants, capsular contracture, reoperation, implant removal, pain, changes in nipple and breast sensation, infection, scarring, asymmetry, wrinkling, implant displacement/migration, implant palpability/visibility, breastfeeding complications, hematoma/seroma, implant extrusion, necrosis, delayed wound healing, infection, breast tissue atrophy/chest wall deformity, calcium deposits, and lymphadenopathy. Treatment applications that deviate from the guidelines are not recommended. Increased iris pigmentation has occurred when bimatoprost solution was administered. Natrelle Breast Implants are indicated for women for the following: CONTRAINDICATIONS Increased Risk of Clinically Significant Effects With Pre-existing Neuromuscular Disorders. Postmarketing Experience:The following adverse reactions have been identified during postapproval use ofLATISSE: dry skin of the eyelid and/or periocular area, eye swelling, eyelid edema, hordeolum, hypersensitivity (local allergic reactions), lacrimation increased, madarosis and trichorrhexis (temporary loss of a few eyelashes to loss of sections of eyelashes, and temporary eyelash breakage, respectively), periorbital and lid changes associated with a deepening of the eyelid sulcus, rash (including macular and erythematous), skin discoloration (periorbital), trichiasis, and vision blurred. Active Ingredient: Botulinum toxin type-A. Explore the vast array of educational resources available to you as part of the AMI. Association Guidance: The REVOLVE Advanced Adipose System (REVOLVE System) is used for aspiration, harvesting, filtering, and transferring of autologous adipose tissue for aesthetic body contouring. Human Albumin and Transmission of Viral Diseases. All is the next-generation patient loyalty program by Allergan Aesthetics. Ensure that persons with pacemakers are not present in vicinity of the device during treatment. Allergan Aesthetics Allergan Aesthetics, an AbbVie Company #AllerganAesthetics . Join All 01 Point Events From Double Points to Bonus Points, Members can earn points even faster with our seasonal point events. For aesthetics indications BOTOX is indicated for the temporary improvement in the appearance of moderate to severe vertical lines between the eyebrows (glabellar lines) seen at maximum frown and/or moderate to severe lateral canthal lines (crow's feet lines) seen at maximum smile and/or moderate to severe forehead lines seen at maximum eyebrow elevation when the severity of the . Furthermore, you can find the "Troubleshooting Login Issues" section which can answer your unresolved problems and equip you . For more information on LATISSE, please see the full Prescribing Information. Our aesthetics portfolio includes facial injectables and body contouring. Breast implant surgery should not be performed in: PRECAUTIONS Earn & Redeem Allergan Brilliant Distinctions coupons for more . Injection Site Ulceration and Necrosis For physicians in need of a sales rep and/or samples, please call: 1 800-678-1605. A cookie can be used to enable a site to remember information that you previously input. ADVERSE REACTIONS Patients with pre-existing swallowing or breathing difficulties may be more susceptible to these complications. Specializing in our breast implant and tissue related products, our Reimbursement Support Team is available to provide tailored support for your Allergan Aesthetics products. Use of anticholinergic drugs after administration of BOTOXCosmetic may potentiate systemic anticholinergic effects. Customer Experience Team New accounts, payment inquiries, and more 1-800-377-7790 . Don't have an account yet? At Allergan Aesthetics, an AbbVie company, we develop, manufacture, and market a portfolio of leading aesthetics brands and products. Please see KYBELLA fullPrescribing Information. We create the products and technologies that drive the advancement of aesthetic medicine. This is a statement regarding the global business. The goal of this role is the development of sales of Allergan products at the assigned group of customer accounts through building and maintaining effective long-term relationship . 2022 AbbVie. Consider withholding subsequent treatments until resolution. Argentina Australia Austria Brazil Canada Chile China France Germany India Italy Japan Mexico Netherlands Portugal Spain Switzerland Taiwan Thailand Turkey UK US * This special opportunity provides substantial savings on select Allergan Aesthetics products and programs. Individuals with peripheral motor neuropathic diseases, amyotrophic lateral sclerosis, or neuromuscular junction disorders (eg, myasthenia gravis or Lambert-Eaton syndrome) should be monitored when given botulinum toxin. The majority were mild or moderate in severity. REVOLVE System is intended for use in the following surgical specialties when the aspiration of soft tissue is desired: plastic and reconstructive surgery, gastrointestinal and affiliated organ surgery, urological surgery, general surgery, orthopedic surgery, gynecological surgery, thoracic surgery, and laparoscopic surgery. CoolTone should be used with caution in patients with Graves disease, active bleeding disorders, or seizure disorders. Commissioned by Allergan Aesthetics and independently developed by specialist trend forecasting agency Wunderman Thompson Intelligence, the report aims to help the industry understand the developments driving today's aesthetics market, and to highlight the key trends that may shape it in the years ahead. The CoolTone device is indicated for improvement of abdominal tone, strengthening of the abdominal muscles, and development for firmer abdomen. 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