What precautions should I be aware of? 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. Bimatoprost has been reported to cause pigment changes (darkening) to periorbital pigmented tissues and eyelashes. Allergan $16.09 b in annual revenue in FY 2019. It does not describe all the potential risks associated with fat grafting procedures. . 5 Giralda Farms Become A Provider. This product contains albumin, a derivative of human blood. Learn more about AbbVie. Dates: June 18, 2015 to Dec. 16, 2015. 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). Investor Relations: (518) 795-1408. As with any medical procedure, a consultation should be done by a licensed healthcare professional to determine if the patient is a candidate for treatment. 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. . Talk to your doctor about other complications. If you are experiencing a medical emergency, please consult your healthcare provider. Allergan phone numbers. In clinical trials, 72% of subjects treated with KYBELLA experienced hematoma/bruising. 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. Tell your healthcare provider about all the medicines you take, including prescription and over-the-counter medicines, vitamins, and herbal supplements. In addition to its wide-ranging line of contact lens care products, Allergan also develops and markets products used in the treatment of glaucoma, cataracts, dry eye, psoriasis, acne, and various cancers. Injection-Site Hematoma/Bruising 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. CoolTone is also contraindicated in placing the active applicator over menstruating uterus, over areas of the skin that lack normal sensation, and in patients with fever, malignant tumor, hemorrhagic conditions, epilepsy, recent surgical procedure, pulmonary insufficiency, or pregnancy. Check out how easy it is to complete and eSign documents online using fillable templates and a powerful editor. AbbVie is a global company so a response to your inquiry may require assistance from AbbVie organizations in other countries. Rare side effects may also occur. If you would like to access our global sites please click Yes. BOTOX Cosmetic may cause loss of strength or general muscle weakness, vision problems, or dizziness within hours to weeks of taking BOTOX Cosmetic. Do not start any new medicines until you have told your doctor that you have received BOTOX Cosmetic in the past. 5 Giralda Farms Do not use LATISSE if you are allergic to one of its ingredients. CONTACT Allergan Access for medical aesthetics customer support Fill in the form below or call us at (800) 832 - 1925 . 1 844-639-2246, Allergan Partner Privileges What warnings should I be aware of? Results of the procedure may or may not be permanent. Please visitJuvedermDFU.comfor more information. If you are a resident of a country other than those to which the site is directed, please return to AbbVie.com or contact your local AbbVie affiliate to obtain the appropriate product information for your country of residence. To report a side effect with any JUVDERM product, please call Allergan at 1-800-433-8871. . The Internet site that you have requested may not be optimized to your screen size. 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. For patients/caregivers, please consult with your physician or contact our. IMPORTANT SAFETY INFORMATION and PRESCRIBING INFORMATION FOR General. Some patients have died from BIA-ALCL. These SkinMedica products are not intended to be drug products that diagnose, treat, cure, or prevent any disease or condition. . May cause brown darkening of the colored part of the eye which is likely permanent. Customer Relations and Medical Affairs Some of these patients had risk factors including pre-existing cardiovascular disease. The sale and distribution of this device is restricted to users and/or user facilities that provide information to patients about the risks and benefits of this device in the form and manner specified in the approved labeling provided by Allergan. The most commonly reported side effects with JUVDERM injectable gels were redness, swelling, pain, tenderness, firmness, lumps/bumps, bruising, discoloration, and itching. Results of this procedure will vary depending upon patient age, surgical site, and experience of the physician. Contact Us Allergan in India. Customer Service. We are collecting this personal information in order to respond to the inquiry you are sending via this Contact Us form. 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. Allergan India. Singapore. The longer people have them, the greater the chances are that they will develop complications, some of which will require more surgery. 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. The head office for Allergan Australia is based in North Sydney less than a 10 minute walk from North Sydney station. These products have not been approved by the FDA and the statements have not been evaluated by the FDA. As with all skin injection procedures, there is a risk of infection. Not FDA evaluated. Free and open company data on California (US) company ALLERGAN, INC. (company number 0815360), 2525 DUPONT DRIVE IRVINE CA 92612 For more information, see the patient brochures at www.allergan.com/products. Use of anticholinergic drugs after administration of BOTOXCosmetic may potentiate systemic anticholinergic effects. Allergan Aesthetics U.S. J23-3 North Chicago, IL 60064 USA. Cases of marginal mandibular nerve injury, manifested as an asymmetric smile or facial muscle weakness, were reported in 4% of subjects in the clinical trials; all cases resolved spontaneously (range 1-298 days, median 44 days). 1 (800) 377-7790. LATISSE may cause eyelid skin darkening which may be reversible. In several of the cases, patients had pre-existing dysphagia or other significant disabilities. These sensations lessen as the area becomes numb. To report an adverse reaction, please call Allergan at 1.800.367.5737. Please contact Allergan at 1-844-NEW-2AGN to setup your account. CoolSculpting is not a treatment for weight loss. If the product of interest is not present, please contact our, The information you provide will be treated in accordance with our. criminal minds fanfiction reid changes CONTACT YOUR ALLERGAN REPRESENTATIVE TODAY OR CALL ALLERGAN CUSTOMER SERVICE AT 1.800.367.5737 REIMBURSEMENT HOTLINE: . Injection Site Ulceration and Necrosis CONTRAINDICATIONS How can I change my email address and login information? Adverse Reactions:The most frequently reported adverse reactions were eye pruritus, conjunctival hyperemia, skin hyperpigmentation, ocular irritation, dry eye symptoms, and periorbital erythema. 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. Caution should be used for patients with suspected or diagnosed heart problems. Contact Allergan to report a suspected adverse event at 1-800-377-7790. 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. Contact via email: customer.care@aegonlife.com. What is KYBELLA? Patients receiving breast implants have reported a variety of systemic symptoms, such as joint pain, muscle aches, confusion, chronic fatigue, autoimmune diseases, and others. If such reactions occur, further injection of BOTOXCosmetic should be discontinued and appropriate medical therapy immediately instituted. 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. 3. JUVDERM VOLLURE XC injectable gel is for adults over 21. The potency units of BOTOXCosmetic are specific to the preparation and assay method utilized. AbbVie is providing these links to you only as a convenience and the inclusion of any link does not imply endorsement of the linked site by AbbVie. Please refer to Boxed Warning for Distant Spread of Toxin Effect. The safety of JUVDERM VOLLURE XC and JUVDERM VOLBELLA XC has not been studied in patients under 22 years, and the safety of JUVDERM Ultra Plus XC and JUVDERM Ultra XC has not been studied in patients under 18 years, The safety and effectiveness of treatment with JUVDERM products in anatomical regions outside of their approved uses have not been established in clinical studies, If you have a history of excessive scarring (thick, hard scars) or pigmentation disorders, treatment in these patients has not been studied and may result in additional scars or changes in pigmentation, If you are planning other procedures including laser treatments or a chemical peel, there is a possible risk of inflammation at the treatment site if these procedures are performed closely before or after JUVDERM injectable gel treatment, Tell your doctor if you are on therapy used to reduce your bodys natural defense system (such as steroids, chemotherapy, and medicines to treat autoimmune diseases, HIV, and AIDs), as these may increase your risk of infection; and medications that can prolong bleeding (such as aspirin, ibuprofen, or other blood thinners), as these may result in increased bruising or bleeding at the injection site, Minimize strenuous exercise, exposure to extensive sun or heat, and alcoholic beverages within the first 24 hours following treatment, as these may cause temporary redness, swelling, and/or itching at the injection site, JUVDERM VOLUMA XC was not studied in patients with significant loose skin of the chin, neck, or jaw, The effect of JUVDERM VOLUMA XC injection into the chin on facial hair growth has not been studied, Patients who experience skin injury near the site of JUVDERM VOLUMA XC injection may be at a higher risk for adverse events, Injection site problems including: a collection of blood under the skin (hematoma) or bruising, damage to an artery or vein if KYBELLA is inadvertently injected into it, hair loss, open sores (ulcers), damage and tissue cell-death (necrosis) around the injection site. REVOLVE System is available by prescription only. Please see LATISSE full Prescribing Information. Allergan - email id & phone of 1 top management contacts like Founder, CEO, CFO, CMO, CTO, Marketing or HR or Finance head & all company details. Do not receive KYBELLA if you have an infection in the treatment area. These are not all of the possible side effects of KYBELLA. Patients with a diagnosis of depression, or other mental health disorders, should wait until resolution or stabilization of these conditions prior to undergoing breast implantation surgery. . Typical side effects include a scratchy, stinging sensation during the treatment and temporary tightness, redness or slight swelling after the treatment. The mailing address for Allergan Sales Puerto Rico Inc is Po Box 195409, , San Juan, Puerto Rico - 00919-5409 (mailing address contact number - --). Madison, NJ 07940. Allergan is a pharmaceutical Company and healthcare Company in which the headquarter is situated in Irvine, California. The most commonly reported adverse reactions in the pivotal clinical trials were: injection site edema/swelling, hematoma/bruising, pain, numbness, erythema, and induration. All rights reserved. JUVDERM VOLUMA XC injectable gel is indicated for deep (subcutaneous and/or supraperiosteal) injection for cheek augmentation to correct age-related volume deficit in the mid-face and for augmentation of the chin region to improve the chin profile in adults over the age of 21. For more information refer to the Medication Guide or talk with your doctor. Lumps, persistent pain, swelling, hardening, or changes in implant shape should be reported to your surgeon and possibly evaluated with imaging. Do not use these products if you have a history of multiple severe allergies or severe allergic reactions (anaphylaxis), if you are allergic to lidocaine or the Gram-positive bacterial proteins used in these products, or if you have had previous allergic reactions to hyaluronic acid fillers. Media Enquiries: 1-905-940-7327 MR-Canada_Communications@Allergan.com Use of this device is limited to those physicians who have the appropriate level of medical education and surgical experience in the appropriate surgical procedures. 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. Natrelle Breast Implants are indicated for women for the following: CONTRAINDICATIONS Any personal data you provide us will be processed according to our. Products in the JUVDERM Collection are available only by a licensed physician or properly licensed practitioner. DO NOT APPLY to lower lid. There have been reports of dry eye associated with BOTOXCosmetic injection in or near the orbicularis oculi muscle. Patients or caregivers should be advised to seek immediate medical care if swallowing, speech, or respiratory disorders occur. 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 report a problem with Natrelle Breast Implants, please call Allergan at 1-800-624-4261 . +1 862 261 7000. Serious adverse reactions, including excessive weakness, dysphagia, and aspiration pneumonia, with some adverse reactions associated with fatal outcomes, have been reported in patients who received BOTOXinjections for unapproved uses. This device should be used by your physician with extreme caution if you have a chronic medical condition such as diabetes, heart, lung, or circulatory system disease, or obesity. Please contact the Marketing Authorization Holder for the product. Do you wish to leave this site? Please also visit Juvederm.com or talk to your doctor for more information. 1 (862) 261-7000. REVOLVE System must be used within the same surgical procedure. 5) Media Inquiries: (518) 795-1174. 2022 AbbVie. To place an order or for general customer service, please call: 1 800-377-7790.