
Building on a nearly 70-year heritage in ophthalmology with expertise in discovering and developing new therapeutic agents to preserve and protect vision, these presentations further establish
The scheduled times of the 19
Retina Poster Presentations (
- Pegylation of Abicipar Increases Vitreal Half-Life, Supporting a Potential for up to 3-Month Duration of Action in the Clinic
- In Vitro and In Vivo Characterization of Abicipar Pegol, an anti-VEGF DARPin® Therapeutic
- Simulation of Ocular Drug Distribution Following Zero Order Release of Intravitreally Dosed Bevacizumab Using 3D Computational Fluid Dynamic Model
Glaucoma Poster Presentations
- A Rabbit Model for Glaucoma Filtration Surgery
- Patient-reported Outcomes of Bimatoprost Ocular Ring in an Open-label Extension Study in Patients with Open-angle Glaucoma or Ocular Hypertension
- Intravitreal Brimonidine Drug Delivery System (Brimo DDS Generation 1) Enhances Spatial Sweep Visual Evoked Potential (sVEP) in a Nonhuman Primate Model of Chronic Glaucoma
- In Vivo Angiographic Study of Rabbit Aqueous Outflow following Ab Interno Gelatin Stent Implantation
- Visualization of Conjunctival Lymphatic Vessels in Normotensive Rabbits
- A Novel Iridocorneal Angle Measurement Technique: Assessment of Inter-and Intra-Scorer Variability
- Complete Responders Following Ab Interno Gelatin Stent at 12M in Refractory Glaucoma Patients
- Treatment Experience of Open Angle Glaucoma Patients Undergoing Trabeculectomy in the US
- Using a Novel Anterior Segment Optical Coherence Tomography (AS-OCT) Method to Assess Iridocorneal Angle
- fMRI shows Functional Recovery by Intravitreal Brimonidine Drug Delivery System (Brimo DDS Generation 1) in a Rabbit Model of Retinal Ganglion Cell (RGC) Degeneration
Ocular Surface Treatment Poster Presentations
- Effect of TrueTearTM on Dry Eye Symptoms During Exposure to a Controlled Adverse Environment
- The Repeatability of Tear Film Measurements in Subjects with Dry Eye
- Evaluation of the Durability of Dry Symptom Relief Following Daily Use of TrueTearTM
- Changes in Tear Lipid Layer Thickness with Omega-3 Eye Drop
- Organic Osmolytes as Osmotic Agents vs. Salts in Artificial Tears
- Sodium Concentration Affects the
INDICATION
TrueTear™ provides a temporary increase in tear production during neurostimulation in adult patients.
IMPORTANT SAFETY INFORMATION
CONTRAINDICATIONS
Do not use TrueTear™ if you have a cardiac pacemaker, implanted or wearable defibrillator, or other implanted metallic or electronic device (eg, cochlear implant) in the head or neck, chronic or recurrent nosebleeds, a bleeding disorder (eg, hemophilia), a condition that can lead to increased bleeding, or a known hypersensitivity (allergy) to the hydrogel material.
WARNINGS
Do not use TrueTear™ around electronic monitoring equipment (eg, heart monitors or electrocardiogram alarms), in the bath/shower, while driving, operating machinery, or during activity in which sneezing/watery eyes may cause risk, areas other than the nose, within 3 feet of shortwave or microwave therapy equipment, around flammable anesthetic mixture (air, oxygen or nitrous oxide). Do not continue using TrueTear™ if your nose is irritated. Safety/effectiveness not established for longer than 6 months or for treating aqueous-deficient dry eye disease. Safety not established in pregnancy, patients under 22 years of age, patients with nasal or sinus surgery (including nasal cautery) or significant trauma, severe nasal airway obstruction or vascularized polyp; active, severe systemic or chronic seasonal allergies; rhinitis or sinusitis requiring treatment; untreated nasal infection; and disabling arthritis, neuropathy, severe dexterity impairment or limited motor coordination.
PRECAUTIONS
Consult your doctor on TrueTear™ instructions before use and on discontinuing use if pain, discomfort or numbness in the nose persists after reducing for higher levels/longer sessions. Remove studs, nose rings, or other nose jewelry before use. Do not use prescription eye medications or nasal sprays 30 minutes before or after using TrueTear™. Consult your doctor before use if you have suspected or diagnosed heart disease. Keep away from children.
ADVERSE EVENTS
Nasal pain, discomfort or burning; short-term electrical discomfort; nosebleed; nasal congestion; headaches; trace blood in nostril; facial pain; sore eye; sinus pain; pain around the eye; runny nose; nasal ulcers; and light-headedness. Caution: Federal law restricts this device to sale by or on the order of a licensed physician. For the full Directions for Use, please visit www.allergan.com/truetear/usa.htm or call 1-800-678-1605. Please call 1-800-433-8871 to report an adverse event.
About Allergan Eye Care
As a leader in eye care,
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Forward-Looking Statement
Statements contained in this press release that refer to future events or other non-historical facts are forward-looking statements that reflect
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