36 hours ago NAMZARIC® (memantine hydrochloride extended-release and donepezil hydrochloride) capsules, for oral use. Therapeutic Area: Central Nervous System. OZURDEX® (dexamethasone intravitreal implant) 0.7 mg. Therapeutic Area: Eye Care. PRED FORTE® (prednisolone acetate ophthalmic suspension, USP) 1%. Therapeutic Area: >> Go To The Portal
NAMZARIC® (memantine hydrochloride extended-release and donepezil hydrochloride) capsules, for oral use. Therapeutic Area: Central Nervous System. OZURDEX® (dexamethasone intravitreal implant) 0.7 mg. Therapeutic Area: Eye Care. PRED FORTE® (prednisolone acetate ophthalmic suspension, USP) 1%. Therapeutic Area:
The Allergan Patient Assistance Program (“Program”) provides medication to qualifying applicants at no charge. The products available through the Program include certain products formerly supported under the Actavis, Aptalis, Forest, Merck, and Watson Patient Assistance Programs. Please see the accompanying list
Background: Growing evidence that patient engagement improves health outcomes and reduces health care costs has fueled health providers' focus on patient portals as the primary access point for personal health information and patient-provider communication. Whereas much attention has been given to identifying characteristics of older adults who do and do not adopt patient …
Patient Portals Welcome to Ascension Borgess Allegan Hospital’s secure, online patient portals. Once you are successfully registered and accepted, our online portal allows patients to have easy, instant access to their information 24/7. We utilize a variety of electronic medical record (EMR) systems in our hospital and affiliated clinics.
JUVÉDERM ® VOLUMA ™ XC 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.
Breast augmentation for women at least 18 years old for saline-filled implants. Breast augmentation includes primary breast augmentation to increase breast size, as well as revision surgery to correct or improve the result of a primary breast augmentation surgery. Breast reconstruction.
These may include asthenia, generalized muscle weakness , diplopia, ptosis, dysphagia, dysphonia, dysarthria, urinary incontinence, and breathing difficulties. These symptoms have been reported hours to weeks after injection. Swallowing and breathing difficulties can be life threatening and there have been reports of death. The risk of symptoms is probably greatest in children treated for spasticity, but symptoms can also occur in adults treated for spasticity and other conditions, particularly in those patients who have an underlying condition that would predispose them to these symptoms. In unapproved uses and approved indications, cases of spread of effect have been reported at doses comparable to those used to treat cervical dystonia and spasticity and at lower doses.
The CoolTone ® device is indicated for improvement of abdominal tone, strengthening of the abdominal muscles, and development for firmer abdomen. CoolTone ® is also indicated for strengthening, toning, and firming of buttocks and thighs.
Treatment with BOTOX ® and other botulinum toxin products can result in swallowing or breathing difficulties. Patients with pre-existing swallowing or breathing difficulties may be more susceptible to these complications. 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 (see Boxed Warning ).
The REVOLVE ™ Advanced Adipose System (REVOLVE™ System) is used for aspiration,harvesting, filtering, and transferring of autologous adipose tissue for aesthetic body contouring. This system should be used with a legally marketed vacuum or aspirator apparatus as a source of suction. If harvested fat is to be re-implanted, the harvested fat is only to be used without any additional manipulation. 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.
There have been reports of dry eye associated with BOTOX ® Cosmetic injection in or near the orbicularis oculi muscle. If symptoms of dry eye (eg, eye irritation, photophobia, or visual changes) persist, consider referring patients to an ophthalmologist.
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