. 1 (862) 261-7000. Allergan FCC Registration Number. Free and open company data on California (US) company ALLERGAN, INC. (company number 0815360), 2525 DUPONT DRIVE IRVINE CA 92612 Thus, you should also consider the complication rates for later (revision) surgery since you may experience these risks in the future, Cancer treatments and surgery will affect the outcome and timing of breast reconstruction, Breast implants may affect your ability to breastfeed, either by reducing or eliminating milk production, Rupture of a silicone-filled breast implant is most often silent. Breast implant surgery should not be performed in: PRECAUTIONS Allergan - email id & phone of 1 top management contacts like Founder, CEO, CFO, CMO, CTO, Marketing or HR or Finance head & all company details. CoolTone should be used with caution in patients with Graves disease, active bleeding disorders, or seizure disorders. Login to your CoolNet Customer Account. The Internet site that you have requested may not be optimized to your screen size. HQ Phone +353 1 435 7700. Call your healthcare provider if you: begin to develop weakness in the muscles of your face, or your smile becomes uneven; have difficulty swallowing, or if any of the symptoms that you already have get worse; develop open sores or drainage from the treatment area, Women with active infection anywhere in their body, Women with existing cancer or precancer of their breast who have not received adequate treatment for those conditions, Women who are currently pregnant or nursing, Autoimmune diseases (eg, lupus and scleroderma), A weakened immune system (eg, taking medications to decrease the bodys immune response), Planned chemotherapy or radiation therapy following breast implant placement, Conditions or medications that interfere with wound healing and blood clotting, Clinical diagnosis of depression or other mental health disorders, including body dysmorphic disorder and eating disorders, Those with a diagnosis of depression or other mental health disorders should wait for resolution or stabilization of these conditions prior to undergoing breast implantation surgery, There is a Boxed Warning for breast implants. You should also be aware that the linked site is not subject to the same terms and conditions and may be governed by its own set of regulations. To avoid the potential of tissue damage, KYBELLA should not be injected into or in close proximity (1 cm-1.5 cm) to salivary glands, lymph nodes, and muscles. 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. Please talk to your provider for additional information. How can I contact Customer Support for Allergan One? 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 is an FDA-approved treatment to grow eyelashes for people with inadequate or not enough lashes. . If you have eye problems/surgery, consult your doctor. Contact Lens Use LUMIGAN 0.01% contains benzalkonium chloride, which may be absorbed by and cause discoloration of soft contact lenses. Please see KYBELLA full Prescribing Information,or ask your healthcare provider, or visit MyKybella.com. Do not inject into blood vessels. Allergan shipped expired products. Do not receive KYBELLA if you have an infection in the treatment area. JUVDERM Ultra XC injectable gel is also indicated for injection into the lips and perioral area for lip augmentation in adults over the age of 21. North Chicago1401 Sheridan RoadNorth Chicago, Illinois 60085AbbVie Customer Service: 800-255-5162. If you have symptoms of or uncertain ultrasound results for breast implant rupture, an MRI is recommended. ADVERSE REACTIONS For healthcare providers please tell us what information you are requesting, being as specific as possible. There has not been a confirmed serious case of spread of toxin effect when BOTOX, Tell your doctor if you have received any other botulinum toxin product in the last 4 months; have received injections of botulinum toxin such as, One of the risks with using dermal fillers is the unintentional injection into a blood vessel. Allergan Aesthetics, an AbbVie company, is providing these links to you only as a convenience. Safety and effectiveness have not been established in patients with the following: ADVERSE EVENTS This Website is not intended for receiving reports of adverse effects of drugs and medical devices. Common side effects may include, but may not be limited to, muscular pain, temporary muscle spasm, temporary joint or tendon pain, and redness at or near the treatment site. To report a problem withNatrelle Breast Implants, please call Allergan at 1-800-624-4261. The longer implants are in place, the greater the potential risk for complications. 2. 2022 AbbVie. How can I change my email address and login information? These products should not be used in patients who have severe allergies, marked by a history of anaphylaxis or history or presence of multiple severe allergies, and should not be used in patients with a history of allergies to Gram-positive bacterial proteins or lidocaine contained in these products. What are the possible side effects of KYBELLA? Caution should be used for patients with suspected or diagnosed heart problems. Allergan is a pharmaceutical company that acquires, develops, manufactures and markets brand name drugs and medical devices in the areas of medical aesthetics, eye care, central nervous system, and . Allergan Direct. For more information, please talk to your doctor. This product contains albumin, a derivative of human blood. Company Allergan. Thank you! These are not all the possible side effects of LATISSE. Lumps, persistent pain, swelling, hardening, or changes in implant shape should be reported to your surgeon and possibly evaluated with imaging. Potential adverse effects associated with REVOLVE System include fat necrosis, cyst formation, infection, chronic foreign body response, allergic reaction, and inflammation. 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). Contact Number (714) ***-**** Engage via Phone. 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. Introduction of these products into the vasculature may lead to embolization, occlusion of the vessels, ischemia, or infarction. 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. CoolTone should be used with caution in patients with Graves disease (an autoimmune disorder that causes overactive thyroid), active bleeding disorders, or seizure disorders. Mobile Number (***) ***-**** Engage via Mobile. These sensations lessen as the area becomes numb. Customer Relations & Medical Affairs United States: Austin: 12331a Riata Trace Pkwy: United States: Irvine: 2525 Dupont Dr: United States: Madison: 5 Giralda Farms: United States: Washington: 500 North Capitol St NW #330washington As a result, the site may contain information on pharmaceuticals that are not approved in other countries or region. Email: MR-Pharmacovigilance@allergan.com BOTOX Cosmetic may cause serious side effects that can be life threatening. Ask your patient about any medical conditions including recent surgery, pre-existing hernia, and any known sensitivities or allergies. RESTASIS and RESTASIS MultiDose Ophthalmic Emulsion help increase your eyes' natural ability to produce tears, which may be reduced by inflammation due to Chronic Dry Eye. Results of this procedure may or may not be permanent. Dysphagia 2022 AbbVie. The link below will take you out of the AbbVie family of websites. Contact details for Marketing Authorization Holder are listed in the leaflet or labeling accompanying a product. . 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. Are there any reasons why I should not receive any JUVDERM formulation? Cultivating a Diverse & Inclusive Workplace, Protecting Human Rights & Workplace Safety, Providing Resources & Support for Employee Well-Being. You are now leaving the Allergan Aesthetics Reimbursement page. 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. Lack of Interchangeability Between Botulinum Toxin Products. CoolSculpting is not a treatment for weight loss. Following the procedure, typical side effects include temporary redness, swelling, blanching, bruising, firmness, tingling, stinging, tenderness, cramping, aching, itching, or skin sensitivity, and sensation of fullness in the back of the throat after submental or submandibular area treatment. Allergan Aesthetics, an AbbVie company, is providing these links to you only as a convenience. Other complications include breast pain, swelling, asymmetry, wrinkling/rippling, implant malposition nipple complications, hypertrophic scarring, and implant palpability/visibility. Breast implants are not considered lifetime devices. Box 1873, Auckland 1, New Zealand Telephone: +64 (0) 800-659-912 Fax: +64 (0) 800-659-913 Our Customer Support number is 1-844-246-2461. Phone: ? If you have additional questions on other products, please submit another request form. Offer good only with a valid prescription for BOTOX (onabotulinumtoxinA). This procedure is not for everyone. See Approved Uses, Important Safety Information, and Prescribing Information, APPROVED USES, IMPORTANT SAFETY INFORMATION AND PRESCRIBING INFORMATION. Any personal data you provide us will be processed according to our. Aegon Asset Management Aegon Asset Management website. The most frequently reported adverse reactions following injection of BOTOXCosmetic for forehead lines with glabellar lines were headache (9%), brow ptosis (2%), and eyelid ptosis (2%). For more information, please see theInstructions for Use (IFU)andUser Manualfor REVOLVE Systemavailable atwww.allergan.com/REVOLVEIFUor call 1.800.678.1605. Excessive neuromuscular weakness may be exacerbated byadministration of another botulinum toxin prior to the resolution of the effects of a previously administered botulinum toxin. Please see BOTOX Cosmetic fullPrescribing Informationincluding Boxed Warning andMedication Guide. It is also FDA-cleared to affect the appearance of lax tissue with submental area treatments. If you are a healthcare provider, pleasesubmit a Medical Information Request. If you have any specific questions, please contact your health care professional. These changes include increased length, thickness, and number of lashes. Your doctor may choose to treat side effects persisting over 30 days with antibiotics, steroids, or hyaluronidase (an enzyme that breaks down hyaluronic acid). Other side effects of BOTOX and BOTOX Cosmetic include dry mouth, discomfort or pain at the injection site; tiredness; headache; neck pain; eye problems such as double vision, blurred vision, decreased eyesight, drooping eyelids, swelling of your eyelids, dry eyes; drooping eyebrows; and upper respiratory tract infection. Part 352. You can find their contact details below. The most common side effects of KYBELLA include swelling, pain, numbness, redness, and areas of hardness in the treatment area. General. All trademarks are the property of their respective owners. To report a side effect with any JUVDERM product, please call Allergan at 1-800-433-8871. . In clinical trials, 72% of subjects treated with KYBELLA experienced hematoma/bruising. Please see LATISSE full Prescribing Information. Other side effects of BOTOX Cosmetic include: dry mouth; discomfort or pain at the injection site; tiredness; headache; neck pain; and eye problems: double vision, blurred vision, decreased eyesight, drooping eyelids and eyebrows, swelling of your eyelids and dry eyes. What warnings should my doctor advise me about? 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. This system should be used with a legally marketed vacuum or aspirator apparatus as a source of suction. Injection Site Alopecia CoolTone should not be applied over swollen, infected, inflamed areas or skin eruptions. Injection-Site Hematoma/Bruising RESTASIS and RESTASIS MultiDose did not increase tear production in patients using anti-inflammatory eye drops or tear duct plugs. Do not receive BOTOX Cosmetic if you: are allergic to any of the ingredients in BOTOX Cosmetic (see Medication Guide for ingredients); had an allergic reaction to any other botulinum toxin product such as Myobloc (rimabotulinumtoxinB), Dysport (abobotulinumtoxinA), or Xeomin (incobotulinumtoxinA); have a skin infection at the planned injection site. BOTOX (onabotulinumtoxinA) Important Information. JUVDERM VOLLURE XC, JUVDERM Ultra Plus XC, and JUVDERM Ultra XC injectable gels are for injection into the facial tissue for the correction of moderate to severe facial wrinkles and folds, such as nasolabial folds. The Parkway. All rights reserved. Human Albumin and Transmission of Viral Diseases. ADVERSE EFFECTS Key complications include reoperation, implant removal with or without replacement, implant rupture with silicone-filled implants, implant deflation with saline-filled implants, and capsular contracture (severe scar tissue around the implant). CoolTone is also indicated for strengthening, toning, and firming of buttocks and thighs. * REFRESH Family of Products, Ipsos Healthcare, 2021 REFRESH ECP Recommendation Survey Even if you have no symptoms, you should have your first ultrasound or MRI at 5 to 6 years after your initial implant surgery and then every 2 to 3 years thereafter regardless of whether your implants are for augmentation or reconstruction. Need help figuring out if you qualify? Allergan Aesthetics U.S. Paradoxical hyperplasia (visibly enlarged tissue volume in the treated area) may develop 2-5 months after treatment, will not resolve on its own, and may require surgical intervention for correction. If harvested fat is to be re-implanted, the harvested fat is only to be used without any additional manipulation. Some common adverse effects associated with fat transfer are unevenness, over- and/or under-correction, tissue lumps, bleeding, and scarring. KYBELLA (deoxycholic acid) injection is indicated for improvement in the appearance of moderate to severe convexity or fullness associated with submental fat in adults. The sale and distribution of Natrelle Breast Implants is restricted to licensed physicians who provide information to patients about the risks and benefits of breast implant surgery. These products have not been approved by the FDA, and the statements on these pages have not been evaluated by the FDA. Allergan Aesthetics U.S. All trademarks are the property of their respective owners. Neither Allergan, Inc. nor any of its employees, officers, directors, subsidiaries or affiliates (collectively, the "Allergan Parties") warrant or guarantee the accuracy, adequacy or current relevance of such content and none of the Allergan Parties are responsible or liable for such content. Increased Risk of Clinically Significant Effects With Pre-existing Neuromuscular Disorders. Contact Us Allergan in India. Report a Side Effect or Adverse Event. Bimatoprost has been reported to cause pigment changes (darkening) to periorbital pigmented tissues and eyelashes. For inquiries regarding products in countries outside the US, please refer to the Allergan Global Medical Information Contacts list. Use caution when administering to patients with pre-existing cardiovascular disease. The DiamondGlow device is a general dermabrasion device that gently removes the top layer of skin and delivers topical cosmetic serums onto the skin. No use of any AbbVie trademark, trade name, or trade dress in this site may be made without the prior written authorization of AbbVie Inc., except to identify the product or services of the company. Overactive Bladder In clinical trials, 6.5% of patients (36/552) initiated CIC for urinary retention following treatment with BOTOX 100 Units, as compared to 0.4% of patients (2/542) treated with placebo. For more information on LATISSE, please see the accompanying full Prescribing Information. SL7 1YL, UK. Tell your doctor if you have received any other botulinum toxin product in the last 4 months; have received injections of botulinum toxin such as Myobloc, Dysport, or Xeomin in the past (tell your doctor exactly which product you received); have recently received an antibiotic by injection; take muscle relaxants; take an allergy or cold medicine; take a sleep medicine; take aspirin-like products or blood thinners. All gives you points on over 50 products and treatments at participating dermatologists, plastic surgeons, and med spas. The CoolTone device is FDA-cleared for improvement of abdominal tone, strengthening of the abdominal muscles, and development for firmer abdomen. 1 (862) 261-7000. Medical Information Department. 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.

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