Cases of injection site ulceration and necrosis have been reported with administration of KYBELLA. What are possible side effects of treatment? Tell your doctor if you have any medical conditions including recent surgery, pre-existing hernia, and any known sensitivities or allergies. Allergan deals in Medicine Research. Do you wish to leave this site? Some common adverse effects associated with fat transfer are unevenness, over- and/or under-correction, tissue lumps, bleeding, and scarring. 3. 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soft-tissue fillers; for example, after insertion of the needle and just before injection, the plunger rod can be withdrawn slightly to aspirate and verify the needle is not intravascular, inject the product slowly, and apply the least amount of pressure necessary. We are collecting this personal information in order to respond to the inquiry you are sending via this Contact Us form. Report a Side Effect or Adverse Event. For more information, please talk to your doctor. 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. Contact Allergan to report a suspected adverse event at 1-800-377-7790. To place an order or for general customer service, please call: 1 800-377-7790. Your doctor may choose to treat side effects persisting over 30 days with antibiotics, steroids, or hyaluronidase (an enzyme that breaks down hyaluronic acid). These products have not been approved by the FDA, and the statements on these pages have not been evaluated by the FDA. Email: MR-Pharmacovigilance@allergan.com CoolTone should not be applied over swollen, infected, inflamed areas or skin eruptions. Allergan, Inc. is a global provider of eye care and specialty pharmaceutical products. What warnings should I be aware of? For patients/caregivers, please consult with your physician or contact our. Serious and/or immediate allergic reactions have been reported. No cases of transmission of viral diseases, CJD or vCJD have ever been identified for licensed albumin or albumin contained in other licensed products. Company Allergan. CONSUMER INDICATIONS AND IMPORTANT SAFETY INFORMATION. One fatal case of anaphylaxis has been reported in which lidocaine was used as the diluent and, consequently, the causal agent cannot be reliably determined. Contact Us Allergan in New Zealand. 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. The current location address for Allergan Sales Puerto Rico Inc is Carr 1 Km 21.1, Sector La Muda, Guaynabo, Puerto Rico and the contact number is 787-766-4565 and fax number is --. 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. Natrelle Breast Implants are approved for the following: Breast implant surgery should NOT be performed in: Tell your doctor if you have any of the following conditions, as the risks of breast implant surgery may be higher: What are key complications with breast implants? For information, eligibility, and enrollment contact your Allergan Sales Representative or call All Support at 1-888-912-1572. BOTOX (onabotulinumtoxinA) Important Information. REVOLVE System must be used within the same surgical procedure. 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. 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. * This number, only available 3 minutes, is not your correspondant's number but the number of a service putting you through to that person. SL7 1YL, UK. Customer Relations & Medical Affairs. Excessive weakness may also be exaggerated by administration of a muscle relaxant before or afteradministration of BOTOXCosmetic. Rare side effects may happen in 1 to 10 out of 10,000 CoolSculpting treatments (between 0.01% to 0.1%). The link below will take you out of the AbbVie family of websites. 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. 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. 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. Madison, NJ 07940 Cases of injection site alopecia have been reported with administration of KYBELLA. Contact Number : 1(800) 272-5525: Founder : Abhijeet Patil: No of employees : 20431: Founded : 1948: Revenue :-Allergan top contacts. CoolTone should not be used in the heart or head areas, areas of new bone growth, over the carotid sinus nerves, or over the neck or mouth. Call the company . Please visit JuvedermDFU.com for more information. These side effects are consistent with other facial injection procedures and most will resolve with time. . This information is not intended to replace a discussion with your surgeon. If you believe this case requires a track other than that provided above . Eyelash changes are usually reversible upon discontinuation of treatment. 2022 AbbVie. 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. All trademarks are the property of their respective owners. interview or hiring process can contact us by sending an email to the appropriate contact listed on the Reasonable Accommodations . To report a side effect, please call Allergan . 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. Administrative Headquarters To report an adverse reaction, please call Allergan at 1.800.367.5737. 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. If you are experiencing a medical emergency, please consult your healthcare provider. Claims for Ocumend are based on traditional homeopathic practice, not accepted medical evidence. 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. Lack of Interchangeability Between Botulinum Toxin Products. They include: itching, rash, red itchy welts, wheezing, asthma symptoms, or dizziness or feeling faint. Tell your provider if you are pregnant or lactating, or if you have any medical conditions, including allergies, and if you are using topical medications on the area to be treated. The most frequently reported adverse reaction following injection of BOTOXCosmetic for lateral canthal lines was eyelid edema (1%). 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. Do you wish to continue to this product-specific site? The safety of injecting greater amounts has not been established, 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, Follow recommended fill volumes for saline implants to decrease possibility of shell wrinkling and crease-fold failure, Autoimmune diseases (eg, lupus and scleroderma), A compromised immune system (eg, currently receiving immunosuppressive therapy), Planned chemotherapy or radiation 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. If you later choose to have your implants removed and not replaced, you may experience dimpling, puckering, wrinkling, or other cosmetic changes, which may be permanent, Breast implantation is likely not a one-time surgery. Allergan shipped expired products. Reason: Incorrect or no expiration date. we cannot provide this information. Consult the CoolTone User Manual for a complete list of Contraindications, Warnings, Precautions, and potential side effects. Phone: ? Marginal Mandibular Nerve Injury Lumps, persistent pain, swelling, hardening, or changes in implant shape should be reported to your surgeon and possibly evaluated with imaging. Caution should be used for patients with suspected or diagnosed heart problems. Please refer to Boxed Warning for Distant Spread of Toxin Effect. BOTOX Cosmetic may cause loss of strength or general muscle weakness, vision problems, or dizziness within hours to weeks of taking BOTOX Cosmetic. 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). Medical Information Department. Patients with neuromuscular disorders may be at increased risk of clinically significant effects including generalized muscle weakness, diplopia, ptosis, dysphonia, dysarthria, severe dysphagia, and respiratory compromise from onabotulinumtoxinA (seeWarnings and Precautions). Introduction of these products into the vasculature may lead to embolization, occlusion of the vessels, ischemia, or infarction. By clicking "Accept" you understand that you are directing Allergan to disclose your personal information, including internet tracking data (like cookies and the IP address you used to access this website), to these third parties for the purposes stated above. 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. Allergan Training Center Central 12331-A Riata Trace Parkway, Building 3, Floor 1 Austin, TX 78727 USA CSUCentral@allergan.com Phone: (512) 214-6800. Typical side effects include a scratchy, stinging sensation during the treatment and temporary tightness, redness or slight swelling after the treatment. AbbVie is a global company so a response to your inquiry may require assistance from AbbVie organizations in other countries. Allergan plc FETZIMA (levomilnacipran) extended-release capsules, for oral use. What are the possible side effects of KYBELLA? Do not administer KYBELLA into affected area until complete resolution. Natrelle CUI Series Tissue Expanders. Address: 5 Giralda Farms Madison, NJ, 07940-1027 United States See other locations. 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. For more information, please see theInstructions for Use (IFU)andUser Manualfor REVOLVE Systemavailable atwww.allergan.com/REVOLVEIFUor call 1.800.678.1605. 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. What is KYBELLA? Contact Email: thomas_terry@allergan.com. Email: MR-Pharmacovigilance@allergan.com These SkinMedica products are not intended to be drug products that diagnose, treat, cure, or prevent any disease or condition. Contact Address: 2525 Dupont DriveMail Code: MN-1AIrvine, CA 92623-9534United States. For technical support, contact Allergan Web Services at 844-246-2461. Hair may grow outside the treatment area. CUSTOMER RELATIONS 1-800-678-1605; U.S. DRUG SAFETY 1-800-678-1605, OPTION 1; U.S. MEDICAL . Patients or caregivers should be advised to seek immediate medical care if swallowing, speech, or respiratory disorders occur. Box 1873, Auckland 1, New Zealand Telephone: +64 (0) 800-659-912 Fax: +64 (0) 800-659-913 For legacy Allergan Healthcare providers, Patients and Caregivers. Please see full Important Safety Information for additional information at coolsculpting.com/cooltone. Contact Information (phone number, email address, fax number) Direct email address for your HCP and business owners (for AbbVie QuickSign powered by Adobe Sign) EIN number(s) for your business (if applicable) . Your one-stop online destination to access Allergan Aesthetics programs and manage your account. Allergan $16.09 b in annual revenue in FY 2019. Please contact the Marketing Authorization Holder for the product. 5) Media Inquiries: (518) 795-1174. Breast implants are not considered lifetime devices. . Aegon UK Aegon UK support . Tell your doctor about all your muscle or nerve conditions, such as ALS or Lou Gehrigs disease, myasthenia gravis, or Lambert-Eaton syndrome, as you may be at increased risk of serious side effects including difficulty swallowing and difficulty breathing from typical doses of BOTOX Cosmetic. Need help figuring out if you qualify? Check Eligibility by visiting the myAbbVie Assist page. CONTACT ABBVIE'S CUSTOMER SERVICE TEAM AT: Phone: +1-800-255-5162 opt. BOTOX Cosmetic may cause serious side effects that can be life threatening. 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. BOTOX Cosmetic is a prescription medicine that is injected into muscles and used to temporarily improve the look of moderate to severe forehead lines, crow's feet lines, and frown lines between the eyebrows in adults. Facial injection procedures and most will resolve with time the AbbVie family websites..., over- and/or under-correction, tissue lumps, bleeding, and any known sensitivities or allergies lead to embolization occlusion. Effects include a scratchy, stinging sensation during the treatment and temporary tightness, redness slight! 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Also be exaggerated by administration of a muscle relaxant before or afteradministration of BOTOXCosmetic not be applied over,. Diagnosed heart problems you wish to continue to this product-specific site applied over swollen, infected, areas... Vessels, ischemia, or dizziness or feeling faint discussion with your or... Precautions, and the statements on these pages have not been evaluated by the FDA, and potential effects...