The REVOLVE System is intended for use in the following surgeries when drawing fat is desired: plastic and reconstructive surgery, gastrointestinal and affiliated organ surgery, urological surgery, general surgery, bone or muscle surgery, gynecological surgery, thoracic surgery, and minimally invasive surgery. Customer Relations & Medical Affairs Allergan Contact Number, Email, Support, Information - Complaints Board To report a side effect, please call Allergan . Medical Information Department. Allergan Aesthetics U.S. 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. Tell your doctor about all your medical conditions, including: plans to have surgery; had surgery on your face; have trouble raising your eyebrows; drooping eyelids; any other abnormal facial change; are pregnant or plan to become pregnant (it is not known if BOTOX Cosmetic can harm your unborn baby); are breast-feeding or plan to (it is not known if BOTOX Cosmetic passes into breast milk). Please see LATISSE full Prescribing Information. Only apply at base of upper lashes. Gastroenterology. Refresh Eye Drops for Contact Lens Wearers | Refresh Brand - Allergan The chances of this happening are very small, but if it does happen, the complications can be serious and may be permanent. Is There a Way to Check the Authenticity of Botox Via the Serial Number FRN 0028728244; Registration Date: 01/14/2002 05:38:10 PM: Last Updated: 09/13/2004 05:03:29 PM: Business Name: ALLERGAN: Business Type: Private Sector , Corporation: Contact Organization: Allergan: Contact Position: Manager Facilities: Contact Name: Mr Terry W Thomas: Contact Address: 2525 Dupont DriveMail . The mailing address for Allergan Sales Puerto Rico Inc is Po Box 195409, , San Juan, Puerto Rico - 00919-5409 (mailing address contact number - --). Caution should be used when BOTOXCosmetic treatment is used in the presence of inflammation at the proposed injection site(s) or when excessive weakness or atrophy is present in the target muscle(s). CoolTone should not be applied over swollen, infected, inflamed areas or skin eruptions. Do not inject into blood vessels. At Holdings Channel, we have reviewed 4,124 13F filings for the 06/30/2016 reporting period, and noticed that Allergan PLC (NYSE: AGN) was held by 11 of the particular managers we have flagged as . The longer implants are in place, the greater the potential risk for complications. KYBELLA (deoxycholic acid) injection is indicated for improvement in the appearance of moderate to severe convexity or fullness associated with submental fat in adults. What precautions should I be aware of? Most of the SkinMedica products described on this website are intended to meet the FDAs definition of a cosmetic product, an article applied to the human body to cleanse, beautify, promote attractiveness, and alter appearances. DO NOT APPLY to lower lid. All rights reserved. Mar 25, 2021. 634 Allergan Biocell Textured Breast Implants 635 Tasigna 636 Strattice Hernia Mesh 637 Singulair 638 Elmiron . Answer: Botox. Investor Relations: (518) 795-1408. These are not all of the possible side effects of KYBELLA. Phone: 1-800-668-6424 or 905-940-6393. 1 (800) 678-1605. In several of the cases, patients had pre-existing dysphagia or other significant disabilities. Allergan is a company that will inspire you to aim high with your ambition. The amount of fat removed should be limited to that necessary to achieve a desired cosmetic effect. 1-844-241-5011 www.abbviemedinfo.com . 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. To place an order or for general customer service, please call: 1 800-377-7790. Please note that our response to your inquirywill be sent through Internet emailwhich is not secure and may include the personal information you provided usin your inquiry. For technical support, contact Allergan Web Services at 844-246-2461. DURYSTA (bimatoprost implant) 10 mcg. By checking "I accept," I authorize Allergan, or any contracted third parties acting on its behalf, to install cookies on my browser to remember the information that I input, track how I use sections of websites, enable Allergan to remember my user custom preferences, and to tailor my access to the website . If you need a response during the same business day, please call the appropriate number below: Customer Service: (800) 772-6446 (opt. * REFRESH Family of Products, Ipsos Healthcare, 2021 REFRESH ECP Recommendation Survey During the procedure you may experience sensations of pulling, tugging, mild pinching, intense cold, tingling, stinging, aching, and cramping at the treatment site. Allergan Training Center East 12110 Sunset Hills Road, Suite 110 Reston, VA 20190 USA CSUEast@allergan.com Phone: (703) 574-5702. BOTOX Cosmetic (onabotulinumtoxinA) , JUVDERM Injectable Gel Fillers, KYBELLA (deoxycholic acid) injection 10 mg/mL , CoolSculpting Treatment, CoolTone Treatment, Natrelle Breast Implants including Boxed Warning, REVOLVE ADVANCED ADIPOSE SYSTEM, SkinMedica, LATISSE (bimatoprost ophthalmic solution) 0.03%. All Rights Reserved. Serious and/or immediate hypersensitivity reactions have been reported. Common adverse effects may include, but may not be limited to muscular pain, temporary muscle spasm, temporary joint or tendon pain, and local erythema or skin redness. 1 North Waukegan Road Dept. If you have any additional questions, please call us at 1-800-222-6885. Results of the procedure will vary depending upon your age, surgical site, and experience of the physician. Use caution when administering to patients with pre-existing cardiovascular disease. The longer people have them, the greater the chances are that they will develop complications, some of which will require more surgery. Allergan Contact Information - Contact | AbbVie For JUVDERM VOLLURE XC, JUVDERM Ultra Plus XC, or JUVDERM Ultra XC, most resolved within 14 days; and for JUVDERM VOLBELLA XC, most resolved within 30 days. . If you believe this case requires a track other than that provided above . Breast implant surgery should not be performed in: PRECAUTIONS Use of anticholinergic drugs after administration of BOTOXCosmetic may potentiate systemic anticholinergic effects. Vice President, Allergan Aesthetics Operations - LinkedIn Contact Number (714) ***-**** Engage via Phone. The DiamondGlow treatment is not for everyone. LATISSEshould be used with caution in aphakic patients, in pseudophakic patients with a torn posterior lens capsule, or in patients with known risk factors for macular edema. Allergan FCC ID Applications (UH7) If you're . 1 (800) 377-7790, If you are experiencing a medical emergency, please consult your healthcare provider. Lack of Interchangeability Between Botulinum Toxin Products. Risk of Injecting Into or in Proximity to Vulnerable Anatomic Structures Breast implants are not considered lifetime devices. For information, eligibility, and enrollment contact your Allergan Sales Representative or call All Support at 1-888-912-1572. See Approved Uses, Important Safety Information, and Prescribing Information, APPROVED USES, IMPORTANT SAFETY INFORMATION AND PRESCRIBING INFORMATION. More phone numbers. JUVDERM VOLLURE XC injectable gel is for adults over 21. ESTRACE (estradiol vaginal cream, USP, 0.01%) Other. (Canada) 1 0. HQ Phone +353 1 435 7700. For legacy Allergan Healthcare providers, Patients and Caregivers. AbbVie and AbbVie partners understand the importance of protecting your information and will use your information for the sole purpose of responding to your inquiry. Allergan headquarters and office locations - Craft.co REVOLVE System will not, in and of itself, produce significant weight loss. J23-3 North Chicago, IL 60064 USA. CONSUMER INDICATIONS AND IMPORTANT SAFETY INFORMATION. What is KYBELLA? 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. Do not administer KYBELLA into affected area until complete resolution. BOTOX Cosmetic may cause serious side effects that can be life threatening. For more information on LATISSE, please see the full Prescribing Information. For more information, please see the full Directions for Use atwww.allergan.com/products. BOTOX Savings Program: Save on Treatment Costs DL-InsideSales-CS-Pleasanton@Allergan.com If you are experiencing a medical emergency, please consult your healthcare provider. REVOLVE System is available by prescription only. CoolSculpting is FDA-cleared for the treatment of visible fat bulges in the submental (under the chin) and submandibular (under the jawline) areas, thigh, abdomen, and flank, along with bra fat, back fat, underneath the buttocks (also known as banana roll), and upper arm. Any personal data you provide us will be processed according to our Privacy Notices. BOTOXCosmetic (onabotulinumtoxinA) is indicated in adult patients for the temporary improvement in the appearance of: - Moderate to severe glabellar lines associated with corrugator and/or procerus muscle activity, - Moderate to severe lateral canthal lines associated with orbicularis oculi activity, - Moderate to severe forehead lines associated with frontalis activity, IMPORTANT SAFETY INFORMATION, INCLUDING BOXED WARNING. Allergan Training Center Central 12331-A Riata Trace Parkway, Building 3, Floor 1 Austin, TX 78727 USA CSUCentral@allergan.com Phone: (512) 214-6800. Reason: Incorrect or no expiration date. Email: MR-Pharmacovigilance@allergan.com Any personal data you provide us will be processed according to our. Please note we do not provide medical treatment recommendations. Do not start any new medicines until you have told your doctor that you have received BOTOX Cosmetic in the past. Immediately stop the injection if a patient exhibits any of the following symptoms: changes in vision, signs of a stroke, blanching of the skin, unusual pain during or shortly after the procedure. Check out how easy it is to complete and eSign documents online using fillable templates and a powerful editor. 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. The CoolTone device is FDA-cleared for improvement of abdominal tone, strengthening of the abdominal muscles, and development for firmer abdomen. 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. , contact Allergan Web Services at 844-246-2461 eSign documents online using fillable templates and a powerful editor effects can... 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