FDA label 86b61495-b29e-46c4-9b40-491f35b4b8bf

5 WARNINGS AND PRECAUTIONS Enablex should be administered with caution to patients with clinically significant bladder outflow obstruction because of the risk of urinary retention ( 5.1 ) Enablex should be administered with caution to patients with gastrointestinal obstructive disorders because of the risk of gastric retention ( 5.2 ) Enablex should be used with caution in patients being treated for narrow-angle glaucoma and only where the potential benefits outweigh the risks ( 5.3 ) Central Nervous System Effects: Somnolence has been reported with Enablex. Advise patients not to drive or operate heavy machinery until they know how Enablex affects them ( 5.5 ) 5.1 Risk of Urinary Retention Enablex should be administered with caution to patients with clinically significant bladder outflow obstruction because of the risk of urinary retention. 5.2 Decreased Gastrointestinal Motility Enablex should be administered with caution to patients with gastrointestinal obstructive disorders because of the risk of gastric retention. Enablex, like other anticholinergic drugs, may decrease gastrointestinal motility and should be used with caution in patients with conditions such as severe constipation, ulcerative colitis, and myasthenia gravis. 5.3 Controlled Narrow-Angle Glaucoma Enablex should be used with caution in patients being treated for narrow-angle glaucoma and only where the potential benefits outweigh the risks. 5.4 Angioedema Angioedema of the face, lips, tongue, and/or larynx have been reported with darifenacin. In some cases angioedema occurred after the first dose. Angioedema associated with upper airway swelling may be life threatening. If involvement of the tongue, hypopharynx, or larynx occurs, darifenacin should be promptly discontinued and appropriate therapy and/or measures necessary to ensure a patent airway should be promptly provided. 5.5 Central Nervous System Effects Enablex is associated with anticholinergic central nervous system (CNS) effects [see Adverse Reactions ( 6.2 )] . A variety of CNS anticholinergic effects have been reported, including headache, confusion, hallucinations and somnolence. Patients should be monitored for signs of anticholinergic CNS effects, particularly after beginning treatment or increasing the dose. Advise patients not to drive or operate heavy machinery until they know how Enablex affects them. If a patient experiences anticholinergic CNS effects, dose reduction or drug discontinuation should be considered. 5.6 Patients with Hepatic Impairment The daily dose of Enablex should not exceed 7.5 mg for patients with moderate hepatic impairment (Child-Pugh B). Enablex has not been studied in patients with severe hepatic impairment (Child-Pugh C) and therefore is not recommended for use in this patient population [see Dosage and Administration ( 2 ) Use in Specific Populations ( 8.6 ) and Clinical Pharmacology ( 12.3 )] .

6 ADVERSE REACTIONS The most frequently reported adverse reactions (greater than 3%) for Enablex are: constipation, dry mouth, headache, dyspepsia, nausea, urinary tract infection, accidental injury, and flu symptoms ( 6 ) To report SUSPECTED ADVERSE REACTIONS, contact Allergan at 1-800-678-1605 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch 6.1 Clinical Trials Experience Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in practice. The safety of Enablex was evaluated in controlled clinical trials in a total of 8,830 patients, 6,001 of whom were treated with Enablex. Of this total, 1,069 patients participated in three, 12-week, randomized, placebo-controlled, fixed-dose efficacy and safety studies (Studies 1, 2 and 3). Of this total, 337 and 334 patients received Enablex 7.5 mg daily and 15 mg daily, respectively. In all long-term trials combined, 1,216 and 672 patients received treatment with Enablex for at least 24 and 52 weeks, respectively. In Studies 1, 2 and 3 combined, the serious adverse reactions to Enablex were urinary retention and constipation. In Studies 1, 2 and 3 combined, dry mouth leading to study discontinuation occurred in 0%, 0.9%, and 0% of patients treated with Enablex 7.5 mg daily, Enablex 15 mg daily and placebo, respectively. Constipation leading to study discontinuation occurred in 0.6%, 1.2%, and 0.3% of patients treated with Enablex 7.5 mg daily, Enablex 15 mg daily and placebo, respectively. Table 1 lists the rates of identified adverse reactions, derived from all reported adverse events in 2% or more of patients treated with 7.5 mg or 15 mg Enablex, and greater than placebo in Studies 1, 2 and 3. In these studies, the most frequently reported adverse reactions were dry mouth and constipation. The majority of the adverse reactions were mild or moderate in severity and most occurred during the first two weeks of treatment. Table 1: Incidence of Identified Adverse Reactions, Derived from All Adverse Events Reported in greater than or equal to 2% of Patients Treated with Enablex Extended-Release Tablets and More Frequent with Enablex than with Placebo in Studies 1, 2, and 3 Body System Adverse Reaction % of Subjects Enablex 7.5 mg N = 337 Enablex 15 mg N = 334 Placebo N = 388 Digestive Dry Mouth 20.2 35.3 8.2 Constipation 14.8 21.3 6.2 Dyspepsia 2.7 8.4 2.6 Abdominal Pain 2.4 3.9 0.5 Nausea 2.7 1.5 1.5 Diarrhea 2.1 0.9 1.8 Urogenital Urinary Tract Infection 4.7 4.5 2.6 Nervous Dizziness 0.9 2.1 1.3 Body as a Whole Asthenia 1.5 2.7 1.3 Eye Dry Eyes 1.5 2.1 0.5 Other adverse reactions reported by 1% to 2% of Enablex-treated patients include: abnormal vision, accidental injury, back pain, dry skin, flu syndrome, hypertension, vomiting, peripheral edema, weight gain, arthralgia, bronchitis, pharyngitis, rhinitis, sinusitis, rash, pruritus, urinary tract disorder and vaginitis. Study 4 was a randomized, 12-week, placebo-controlled, dose-titration regimen study in which Enablex was administered in accordance with dosing recommendations [see Dosage and Administration ( 2 )] . All patients initially received placebo or Enablex 7.5 mg daily, and after two weeks, patients and physicians were allowed to adjust upward to Enablex 15 mg if needed. In this study, the most commonly reported adverse reactions were also constipation and dry mouth. Table 2 lists the identified adverse reactions, derived from all adverse events reported in greater than 3% of patients treated with Enablex and greater than placebo. Table 2: Number (%) of Adverse Reactions, Derived from All Adverse Events Reported in greater than 3% of Patients Treated with Enablex Extended-Release Tablets, and More Frequent with Enablex than Placebo, in Study 4 Adverse Reaction Enablex 7.5 mg/15 mg N = 268 Placebo N = 127 Constipation 56 (20.9%) 10 (7.9%) Dry Mouth 50 (18.7%) 11 (8.7%) Headache 18 (6.7%) 7 (5.5%) Dyspepsia 12 (4.5%) 2 (1.6%) Nausea 11 (4.1%) 2 (1.6%) Urinary Tract Infection 10 (3.7%) 4 (3.1%) Accidental Injury 8 (3.0%) 3 (2.4%) Flu Syndrome 8 (3.0%) 3 (2.4%) 6.2 Post Marketing Experience The following adverse reactions have been reported during post-approval use of Enablex extended-release tablets (darifenacin). Because these reactions are reported voluntarily from a population of uncertain size, it is not always possible to reliably estimate frequency or establish a causal relationship to drug exposure. Dermatologic: erythema multiforme, interstitial granuloma annulare General: hypersensitivity reactions, including angioedema with airway obstruction and anaphylactic reaction Central Nervous: confusion, hallucinations and somnolence Cardiovascular: palpitations and syncope

<table><caption>Table 1: Incidence of Identified Adverse Reactions, Derived from All Adverse Events Reported in greater than or equal to 2% of Patients Treated with Enablex Extended-Release Tablets and More Frequent with Enablex than with Placebo in Studies 1, 2, and 3</caption><col width="222"/><col width="204"/><col width="113"/><col width="91"/><col width="42"/><tbody><tr><td styleCode="Toprule "> <content styleCode="bold">Body System</content></td><td styleCode="Toprule "> <content styleCode="bold">Adverse Reaction</content></td><td styleCode="Toprule " colspan="3" align="center"> <content styleCode="bold">% of Subjects</content></td></tr><tr><td styleCode="Toprule "> </td><td styleCode="Toprule "> </td><td styleCode="Toprule "> <content styleCode="bold">Enablex</content> <content styleCode="bold">7.5 mg</content> <content styleCode="bold">N = 337</content></td><td styleCode="Toprule "> <content styleCode="bold">Enablex</content> <content styleCode="bold">15 mg</content> <content styleCode="bold">N = 334</content></td><td styleCode="Toprule "> <content styleCode="bold">Placebo</content> <content styleCode="bold">N = 388</content></td></tr><tr><td styleCode="Toprule "> <content styleCode="bold">Digestive</content></td><td styleCode="Toprule "> Dry Mouth</td><td styleCode="Toprule "> 20.2</td><td styleCode="Toprule "> 35.3</td><td styleCode="Toprule "> 8.2</td></tr><tr><td> </td><td> Constipation</td><td> 14.8</td><td> 21.3</td><td> 6.2</td></tr><tr><td> </td><td> Dyspepsia</td><td> 2.7</td><td> 8.4</td><td> 2.6</td></tr><tr><td> </td><td> Abdominal Pain</td><td> 2.4</td><td> 3.9</td><td> 0.5</td></tr><tr><td> </td><td> Nausea</td><td> 2.7</td><td> 1.5</td><td> 1.5</td></tr><tr><td> </td><td> Diarrhea</td><td> 2.1</td><td> 0.9</td><td> 1.8</td></tr><tr><td> <content styleCode="bold">Urogenital</content></td><td> Urinary Tract Infection</td><td> 4.7</td><td> 4.5</td><td> 2.6</td></tr><tr><td> <content styleCode="bold">Nervous</content></td><td> Dizziness</td><td> 0.9</td><td> 2.1</td><td> 1.3</td></tr><tr><td> <content styleCode="bold">Body as a Whole</content></td><td> Asthenia</td><td> 1.5</td><td> 2.7</td><td> 1.3</td></tr><tr><td> <content styleCode="bold">Eye</content></td><td> Dry Eyes</td><td> 1.5</td><td> 2.1</td><td> 0.5</td></tr></tbody></table>

<table><caption>Table 2: Number (%) of Adverse Reactions, Derived from All Adverse Events Reported in greater than 3% of Patients Treated with Enablex Extended-Release Tablets, and More Frequent with Enablex than Placebo, in Study 4</caption><col width="228"/><col width="239"/><col width="255"/><tbody><tr><td styleCode="Toprule "> <content styleCode="bold">Adverse Reaction</content></td><td styleCode="Toprule " align="center"> <content styleCode="bold">Enablex 7.5 mg/15 mg</content> <content styleCode="bold">N = 268</content></td><td styleCode="Toprule " align="center"> <content styleCode="bold">Placebo</content> <content styleCode="bold">N = 127</content></td></tr><tr><td styleCode="Toprule "> Constipation</td><td styleCode="Toprule " align="center"> 56 (20.9%)</td><td styleCode="Toprule " align="center"> 10 (7.9%)</td></tr><tr><td> Dry Mouth</td><td align="center"> 50 (18.7%)</td><td align="center"> 11 (8.7%)</td></tr><tr><td> Headache</td><td align="center"> 18 (6.7%)</td><td align="center"> 7 (5.5%)</td></tr><tr><td> Dyspepsia</td><td align="center"> 12 (4.5%)</td><td align="center"> 2 (1.6%)</td></tr><tr><td> Nausea</td><td align="center"> 11 (4.1%)</td><td align="center"> 2 (1.6%)</td></tr><tr><td> Urinary Tract Infection</td><td align="center"> 10 (3.7%)</td><td align="center"> 4 (3.1%)</td></tr><tr><td> Accidental Injury</td><td align="center"> 8 (3.0%)</td><td align="center"> 3 (2.4%)</td></tr><tr><td> Flu Syndrome</td><td align="center"> 8 (3.0%)</td><td align="center"> 3 (2.4%)</td></tr></tbody></table>