PRECEDEX

5 WARNINGS AND PRECAUTIONS 5.1 Drug Administration PRECEDEX should be administered only by persons skilled in the management of patients in the intensive care or operating room setting. Due to the known pharmacological effects of PRECEDEX, patients should be continuously monitored while receiving PRECEDEX. 5.2 Hypotension, Bradycardia, and Sinus Arrest Clinically significant episodes of bradycardia and sinus arrest have been reported with PRECEDEX administration in young, healthy adult volunteers with high vagal tone or with different routes of administration including rapid intravenous or bolus administration. Reports of hypotension and bradycardia have been associated with PRECEDEX infusion. Some of these cases have resulted in fatalities. If medical intervention is required, treatment may include decreasing or stopping the infusion of PRECEDEX, increasing the rate of intravenous fluid administration, elevation of the lower extremities, and use of pressor agents. Because PRECEDEX has the potential to augment bradycardia induced by vagal stimuli, clinicians should be prepared to intervene. The intravenous administration of anticholinergic agents (e.g., glycopyrrolate, atropine) should be considered to modify vagal tone. In clinical trials, glycopyrrolate or atropine were effective in the treatment of most episodes of PRECEDEX-induced bradycardia. However, in some patients with significant cardiovascular dysfunction, more advanced resuscitative measures were required. Caution should be exercised when administering PRECEDEX to patients with advanced heart block and/or severe ventricular dysfunction. Because PRECEDEX decreases sympathetic nervous system activity, hypotension and/or bradycardia may be expected to be more pronounced in patients with hypovolemia, diabetes mellitus, or chronic hypertension and in elderly patients. In clinical trials where other vasodilators or negative chronotropic agents were co-administered with PRECEDEX an additive pharmacodynamic effect was not observed. Nonetheless, caution should be used when such agents are administered concomitantly with PRECEDEX. 5.3 Transient Hypertension Transient hypertension has been observed primarily during the loading dose in association with the initial peripheral vasoconstrictive effects of PRECEDEX. Treatment of the transient hypertension has generally not been necessary, although reduction of the loading infusion rate may be desirable. 5.4 Arousability Some patients receiving PRECEDEX have been observed to be arousable and alert when stimulated. This alone should not be considered as evidence of lack of efficacy in the absence of other clinical signs and symptoms. 5.5 Withdrawal Intensive Care Unit Sedation With administration up to 7 days, regardless of dose, 12 (5%) PRECEDEX adult subjects experienced at least 1 event related to withdrawal within the first 24 hours after discontinuing study drug and 7 (3%) PRECEDEX adult subjects experienced at least 1 event 24 to 48 hours after end of study drug. The most common events were nausea, vomiting, and agitation [see Adverse Reactions (6.1)]. In adult subjects, tachycardia and hypertension requiring intervention in the 48 hours following study drug discontinuation occurred at frequencies of <5%. Procedural Sedation In adult subjects, withdrawal symptoms were not seen after discontinuation of short‑term infusions of PRECEDEX (<6 hours). In pediatric patients, mild transient withdrawal symptoms of emergence delirium or agitation were seen after discontinuation of short‑term infusions of PRECEDEX (<2 hours) [see Adverse Reactions (6.1)]. 5.6 Tolerance and Tachyphylaxis Use of dexmedetomidine beyond 24 hours has been associated with tolerance and tachyphylaxis and a dose‑related increase in adverse reactions [see Adverse Reactions (6.1)]. 5.7 Hyperthermia or Pyrexia PRECEDEX may induce hyperthermia or pyrexia, which may be resistant to traditional cooling methods, such as administration of cooled intravenous fluids and antipyretic medications. Discontinue PRECEDEX if drug‑related hyperthermia or pyrexia is suspected and monitor patients until body temperature normalizes. 5.8 Hepatic Impairment Since PRECEDEX clearance decreases with severity of hepatic impairment, dose reduction should be considered in patients with impaired hepatic function [see Dosage and Administration (2.2, 2.3)]. •Monitoring: Continuously monitor patients while receiving PRECEDEX. (5.1) • Bradycardia and Sinus Arrest: Have occurred in young healthy volunteers with high vagal tone or with different routes of administration, e.g., rapid intravenous or bolus administration. (5.2) • Hypotension and Bradycardia: May necessitate medical intervention. May be more pronounced in patients with hypovolemia, diabetes mellitus, or chronic hypertension, and in the elderly. Use with caution in patients with advanced heart block or severe ventricular dysfunction. (5.2) • Co-administration with Other Vasodilators or Negative Chronotropic Agents: Use with caution due to additive pharmacodynamic effects. (5.2) • Transient Hypertension: Observed primarily during the loading dose. Consider reduction in loading infusion rate. (5.3) • Arousability: Patients can become aroused/alert with stimulation; this alone should not be considered as lack of efficacy. (5.4) • Tolerance and Tachyphylaxis: Prolonged exposure to dexmedetomidine beyond 24 hours may be associated with tolerance and tachyphylaxis and a dose-related increase in adverse events. (5.7)

6 ADVERSE REACTIONS The following clinically significant adverse reactions are described elsewhere in the labeling: Hypotension, bradycardia and sinus arrest [see WARNINGS AND PRECAUTIONS (5.2)] Transient hypertension [see WARNINGS AND PRECAUTIONS (5.3)] 6.1 Clinical Studies Experience Because clinical trials are conducted under widely varying conditions, adverse reactions rates observed in the clinical trials of a drug cannot be directly compared to rates in clinical trials of another drug and may not reflect the rates observed in practice. Most common treatment-emergent adverse reactions, occurring in greater than 2% of patients in both Intensive Care Unit and procedural sedation studies include hypotension, bradycardia and dry mouth. Intensive Care Unit Sedation Adverse reaction information is derived from the continuous infusion trials of PRECEDEX for sedation in the Intensive Care Unit setting in which 1,007 adult patients received PRECEDEX. The mean total dose was 7.4 mcg/kg (range: 0.8 to 84.1), mean dose per hour was 0.5 mcg/kg/hr (range: 0.1 to 6.0) and the mean duration of infusion of 15.9 hours (range: 0.2 to 157.2). The population was between 17 to 88 years of age, 43% 65 years of age, 77% male and 93% Caucasian. Treatment-emergent adverse reactions occurring at an incidence of >2% are provided in Table 3. The most frequent adverse reactions were hypotension, bradycardia and dry mouth [see Warnings and Precautions (5.2)]. Table 3: Adverse Reactions with an Incidence >2%-Adult Intensive Care Unit Sedation Population <24 hours* Adverse Event All Precedex (N = 1007) (%) Randomized Precedex (N = 798) (%) Placebo (N = 400) (%) Propofol (N = 188) (%) *26 subjects in the all PRECEDEX group and 10 subjects in the randomized PRECEDEX group had exposure for greater than 24 hours. Hypotension 25% 24% 12% 13% Hypertension 12% 13% 19% 4% Nausea 9% 9% 9% 11% Bradycardia 5% 5% 3% 0 Atrial Fibrillation 4% 5% 3% 7% Pyrexia 4% 4% 4% 4% Dry Mouth 4% 3% 1% 1% Vomiting 3% 3% 5% 3% Hypovolemia 3% 3% 2% 5% Atelectasis 3% 3% 3% 6% Pleural Effusion 2% 2% 1% 6% Agitation 2% 2% 3% 1% Tachycardia 2% 2% 4% 1% Anemia 2% 2% 2% 2% Hyperthermia 2% 2% 3% 0 Chills 2% 2% 3% 2% Hyperglycemia 2% 2% 2% 3% Hypoxia 2% 2% 2% 3% Post-procedural Hemorrhage 2% 2% 3% 4% Pulmonary Edema 1% 1% 1% 3% Hypocalcemia 1% 1% 0 2% Acidosis 1% 1% 1% 2% Urine Output Decreased 1% 1% 0 2% Sinus Tachycardia 1% 1% 1% 2% Ventricular Tachycardia <1% 1% 1% 5% Wheezing <1% 1% 0 2% Edema Peripheral <1% 0 1% 2% Adverse reaction information was also derived from the placebo-controlled, continuous infusion trials of PRECEDEX for sedation in the surgical intensive care unit setting in which 387 adult patients received PRECEDEX for less than 24 hours. The most frequently observed treatment-emergent adverse events included hypotension, hypertension, nausea, bradycardia, fever, vomiting, hypoxia, tachycardia and anemia (see Table 4). Table 4: Treatment-Emergent Adverse Events Occurring in >1% Of All Dexmedetomidine-Treated Adult Patients in the Randomized Placebo-Controlled Continuous Infusion <24 Hours ICU Sedation Studies Adverse Event Randomized Dexmedetomidine (N = 387) Placebo (N = 379) Hypotension 28% 13% Hypertension 16% 18% Nausea 11% 9% Bradycardia 7% 3% Fever 5% 4% Vomiting 4% 6% Atrial Fibrillation 4% 3% Hypoxia 4% 4% Tachycardia 3% 5% Hemorrhage 3% 4% Anemia 3% 2% Dry Mouth 3% 1% Rigors 2% 3% Agitation 2% 3% Hyperpyrexia 2% 3% Pain 2% 2% Hyperglycemia 2% 2% Acidosis 2% 2% Pleural Effusion 2% 1% Oliguria 2% <1% Thirst 2% <1% In a controlled clinical trial, PRECEDEX was compared to midazolam for ICU sedation exceeding 24 hours duration in adult patients. Key treatment emergent adverse events occurring in dexmedetomidine or midazolam treated patients in the randomized active comparator continuous infusion long-term intensive care unit sedation study are provided in Table 5. The number (%) of subjects who had a dose-related increase in treatment-emergent adverse events by maintenance adjusted dose rate range in the Precedex group is provided in Table 6. Table 5: Key Treatment-Emergent Adverse Events Occurring in Dexmedetomidine- or Midazolam-Treated Adult Patients in the Randomized Active Comparator Continuous Infusion Long-Term Intensive Care Unit Sedation Study Includes any type of hypertension. 1 Hypotension was defined in absolute terms as Systolic blood pressure of <80 mmHg or Diastolic blood pressure of <50 mmHg or in relative terms as 30% lower than pre-study drug infusion value. 2 Bradycardia was defined in absolute terms as <40 bpm or in relative terms as 30% lower than pre-study drug infusion value. 3 Hypertension was defined in absolute terms as Systolic blood pressure >180 mmHg or Diastolic blood pressure of >100 mmHg or in relative terms as 30% higher than pre-study drug infusion value. 4 Tachycardia was defined in absolute terms as >120 bpm or in relative terms as 30% greater than pre-study drug infusion value. Adverse Event Dexmedetomidine (N = 244) Midazolam (N = 122) Hypotension 1 56% 56% Hypotension Requiring Intervention 28% 27% Bradycardia 2 42% 19% Bradycardia Requiring Intervention 5% 1% Systolic Hypertension 3 28% 42% Tachycardia 4 25% 44% Tachycardia Requiring Intervention 10% 10% Diastolic Hypertension 3 12% 15% Hypertension 3 11% 15% Hypertension Requiring Intervention 19% 30% Hypokalemia 9% 13% Pyrexia 7% 2% Agitation 7% 6% Hyperglycemia 7% 2% Constipation 6% 6% Hypoglycemia 5% 6% Respiratory Failure 5% 3% Renal Failure Acute 2% 1% Acute Respiratory Distress Syndrome 2% 1% Generalized Edema 2% 6% Hypomagnesemia 1% 7% The following adverse events occurred between 2 and 5% for PRECEDEX and Midazolam, respectively: renal failure acute (2.5%, 0.8%), acute respiratory distress syndrome (2.5%, 0.8%), and respiratory failure (4.5%, 3.3%). Table 6. Number (%) of Adult Subjects Who Had a Dose-Related Increase in Treatment Emergent Adverse Events by Maintenance Adjusted Dose Rate Range in the Precedex Group *Average maintenance dose over the entire study drug administration Precedex mcg/kg/hr Adverse Event 0.7* (N = 95) >0.7 to 1.1* (N = 78) >1.1* (N = 71) Constipation 6% 5% 14% Agitation 5% 8% 14% Anxiety 5% 5% 9% Edema Peripheral 3% 5% 7% Atrial Fibrillation 2% 4% 9% Respiratory Failure 2% 6% 10% Acute Respiratory Distress Syndrome 1% 3% 9% Adult Procedural Sedation Adverse reaction information is derived from the two trials for adult procedural sedation [see Clinical Studies (14.2)] in which 318 adult patients received PRECEDEX. The mean total dose was 1.6 mcg/kg (range: 0.5 to 6.7), mean dose per hour was 1.3 mcg/kg/hr (range: 0.3 to 6.1) and the mean duration of infusion of 1.5 hours (range: 0.1 to 6.2). The population was between 18 to 93 years of age, ASA IIV, 30% 65 years of age, 52% male and 61% Caucasian. Treatment-emergent adverse reactions occurring in adults at an incidence of >2% are provided in Table 7. The most frequent adverse reactions were hypotension, bradycardia, and dry mouth [see Warnings and Precautions (5.2)]. Pre-specified criteria for the vital signs to be reported as adverse reactions are footnoted below the table. The decrease in respiratory rate and hypoxia was similar between PRECEDEX and comparator groups in both studies. Table 7: Adverse Reactions With an Incidence > 2%Procedural Sedation Population Adverse Event Precedex (N = 318) (%) Placebo (N = 113) (%) 1 Hypotension was defined in absolute and relative terms as Systolic blood pressure of <80 mmHg or 30% lower than pre-study drug infusion value, or Diastolic blood pressure of <50 mmHg. 2 Respiratory depression was defined in absolute and relative terms as respiratory rate (RR) <8 beats per minute or > 25% decrease from baseline. 3 Bradycardia was defined in absolute and relative terms as <40 beats per minute or 30% lower than pre-study drug infusion value. 4 Hypertension was defined in absolute and relative terms as Systolic blood pressure >180 mmHg or 30% higher than pre-study drug infusion value or Diastolic blood pressure of >100 mmHg. 5 Tachycardia was defined in absolute and relative terms as >120 beats per minute or 30% greater than pre-study drug infusion value. 6 Hypoxia was defined in absolute and relative terms as SpO2 <90% or 10% decrease from baseline. Hypotension 1 54% 30% Respiratory Depression 2 37% 32% Bradycardia 3 14% 4% Hypertension 4 13% 24% Tachycardia 5 5% 17% Nausea 3% 2% Dry Mouth 3% 1% Hypoxia 6 2% 3% Bradypnea 2% 4% Pediatric Sedation for Magnetic Resonance Imaging Adverse reaction information is derived from a trial for sedation of pediatric procedural during a non‑invasive procedure [see Clinical Studies (14.2)] in which 122 pediatric patients aged 1 month to less than 17 years undergoing magnetic resonance imaging (MRI) scans received PRECEDEX. In pediatric patients 1 month to less than 2 years old, the median total dose for the PRECEDEX low, middle, and high dose treatment groups was 8.30, 18.90, and 22.75 mcg, respectively. The median duration of treatment ranged from 52.5 to 69 minutes across treatment groups. In pediatric patients 2 to less than 17 years old, the median total dose for the PRECEDEX low, middle, and high dose treatment groups was 21.30, 43.90, and 80.25 mcg, respectively. The median duration of treatment ranged from 56.5 to 66 minutes across treatment groups. All-causality treatment-emergent adverse reactions occurring in the combined age group of pediatric patients during the procedure at an incidence of >5% are provided in Table 8. The most frequent treatment-emergent adverse events were bradypnea, bradycardia, hypertension, and hypotension [see Warnings and Precautions (5.2, 5.3)]. In the combined age group and in each age group, increased incidence in bradycardia and hypertension was observed with increasing PRECEDEX dose. Mild transient withdrawal symptoms of emergence delirium or agitation occurred in 3 of 122 patients after discontinuation of PRECEDEX infusion [see Warnings and Precautions (5.5)]. All reported treatment‑emergent adverse reactions were mild to moderate in severity and the majority resolved without medical intervention. No subject in the study required airway intervention, including a jaw thrust or insertion of a nasal or oral airway. A similar profile was observed in the pediatric patients 1 month to less than 2 years old and in pediatric patients 2 to less than 17 years old. Pre‑specified criteria for the vital signs to be reported as adverse events are footnoted below the table. Table 8: Treatment-Emergent Adverse Events with Incidence >5%—Pediatric Patients During Non-invasive Procedure PRECEDEX Low Dose (N = 42) PRECEDEX Middle Dose (N = 42) PRECEDEX High Dose (N = 38) Total (N = 122) Number (%) of Pediatric Patients n (%) n (%) n (%) n (%) Adverse Event Bradypnea 1 33 (79) 27 (64) 22 (58) 82 (67) Bradycardia 2 24 (57) 24 (57) 27 (71) 75 (62) Hypertension 3 11 (26) 17 (41) 18 (47) 46 (38) Hypotension 4 13 (31) 11 (26) 6 (16) 30 (25) Hypoxia 5 6 (14) 3 (7) 1 (3) 10 (8) Diastolic Hypertension 3 3 (7) 3 (7) 4 (11) 10 (8) Systolic Hypertension 3 1 (2) 5 (12) 3 (8) 9 (7) Tachycardia 3 (7) 1 (2) 1 (3) 5 (4) N = Number of pediatric patients evaluable for adverse events. 1 Bradypnea was defined as respiratory rate <1st centile of the age adjusted normal range. 2 Bradycardia was defined as a decrease in HR of 30% from baseline or absolute HR ≤1st centile of the age adjusted normal range. 3 For pediatric patients 1 month to less than 1 year old, hypertension was defined as supine systolic blood pressure ≥104 mm/Hg and/or diastolic blood pressure ≥56 mmHg measurements. For pediatric patients 1 to less than 17 years old: hypertension was defined as supine systolic blood pressure and/or diastolic blood pressure measurements ≥95th percentile for gender, age, and height. 4 Hypotension was defined as a decrease in systolic blood pressure ≥30% from baseline. 5 Hypoxia was defined as oxygen saturation <90% for any duration. 6.2 Postmarketing Experience The following adverse reactions have been identified during post‑approval use of PRECEDEX. Because these reactions are reported voluntarily from a population of uncertain size, it is not always possible to reliably estimate their frequency or establish a causal relationship to drug exposure. Hypotension and bradycardia were the most common adverse reactions associated with the use of PRECEDEX during post‑approval use of the drug. Table 9: Adverse Reactions Experienced During Post-approval Use of Precedex System Organ Class Preferred Term Blood and Lymphatic System Disorders Anemia Cardiac Disorders Arrhythmia, atrial fibrillation, atrioventricular block, bradycardia, cardiac arrest, cardiac disorder, extrasystoles, myocardial infarction, supraventricular tachycardia, tachycardia, ventricular arrhythmia, ventricular tachycardia Eye Disorders Photopsia, visual impairment Gastrointestinal Disorders Abdominal pain, diarrhea, nausea, vomiting General Disorders and Administration Site Conditions Chills, hyperpyrexia, pain, pyrexia, thirst Hepatobiliary Disorders Hepatic function abnormal, hyperbilirubinemia Investigations Alanine aminotransferase increased, aspartate aminotransferase increased, blood alkaline phosphatase increased, blood urea increased, electrocardiogram T wave inversion, gammaglutamyltransferase increased, electrocardiogram QT prolonged Metabolism and Nutrition Disorders Acidosis, hyperkalemia, hypoglycemia, hypovolemia, hypernatremia Nervous System Disorders Convulsion, dizziness, headache, neuralgia, neuritis, speech disorder Psychiatric Disorders Agitation, confusional state, delirium, hallucination, illusion Renal and Urinary Disorders Oliguria, polyuria Respiratory, Thoracic and Mediastinal Disorders Apnea, bronchospasm, dyspnea, hypercapnia, hypoventilation, hypoxia, pulmonary congestion, respiratory acidosis Skin and Subcutaneous Tissue Disorders Hyperhidrosis, pruritus, rash, urticaria Surgical and Medical Procedures Light anesthesia Vascular Disorders Blood pressure fluctuation, hemorrhage, hypertension, hypotension The most common adverse reactions (incidence >2%) in adults are hypotension, bradycardia, and dry mouth. (6.1) The most common adverse reactions (incidence >5%) in pediatric patients aged 1 month to less than 17 years are bradypnea, bradycardia, hypertension, and hypotension. (6.1) Adverse reactions in adults, associated with infusions >24 hours in duration include ARDS, respiratory failure, and agitation. (6.1) To report SUSPECTED ADVERSE REACTIONS, contact Hospira, Inc. at 1-800-441-4100, or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch.

<table width="97.72%"><caption>Table 3: Adverse Reactions with an Incidence &gt;2%-Adult Intensive Care Unit Sedation Population &lt;24 hours*</caption><colgroup><col width="43%"/><col width="16%"/><col width="15%"/><col width="14%"/><col width="12%"/></colgroup><thead><tr styleCode="First Last"><th styleCode="Botrule Rrule Toprule" align="left" valign="bottom">Adverse Event</th><th styleCode="Botrule Lrule Rrule Toprule" align="center" valign="bottom">All Precedex (N = 1007) (%)</th><th styleCode="Botrule Lrule Rrule Toprule" align="center" valign="bottom">Randomized Precedex (N = 798) (%)</th><th styleCode="Botrule Lrule Rrule Toprule" align="center" valign="bottom">Placebo (N = 400) (%)</th><th styleCode="Botrule Lrule Toprule" align="center" valign="bottom">Propofol (N = 188) (%)</th></tr></thead><tfoot><tr styleCode="First Last"><td styleCode="Footnote" colspan="5" align="left">*26 subjects in the all PRECEDEX group and 10 subjects in the randomized PRECEDEX group had exposure for greater than 24 hours.</td></tr></tfoot><tbody><tr><td styleCode="Botrule Rrule Toprule" valign="top"><paragraph>Hypotension</paragraph></td><td styleCode="Botrule Lrule Rrule Toprule" align="center" valign="bottom"><paragraph>25%</paragraph></td><td styleCode="Botrule Lrule Rrule Toprule" align="center" valign="bottom"><paragraph>24%</paragraph></td><td styleCode="Botrule Lrule Rrule Toprule" align="center" valign="bottom"><paragraph>12%</paragraph></td><td styleCode="Botrule Lrule Toprule" align="center" valign="bottom"><paragraph>13%</paragraph></td></tr><tr><td styleCode="Botrule Rrule" valign="top"><paragraph>Hypertension</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>12%</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>13%</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>19%</paragraph></td><td styleCode="Botrule Lrule" align="center" valign="bottom"><paragraph>4%</paragraph></td></tr><tr><td styleCode="Botrule Rrule" valign="top"><paragraph>Nausea</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>9%</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>9%</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>9%</paragraph></td><td styleCode="Botrule Lrule" align="center" valign="bottom"><paragraph>11%</paragraph></td></tr><tr><td styleCode="Botrule Rrule" valign="top"><paragraph>Bradycardia</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>5%</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>5%</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>3%</paragraph></td><td styleCode="Botrule Lrule" align="center" valign="bottom"><paragraph>0</paragraph></td></tr><tr><td styleCode="Botrule Rrule" valign="top"><paragraph>Atrial Fibrillation</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>4%</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>5%</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>3%</paragraph></td><td styleCode="Botrule Lrule" align="center" valign="bottom"><paragraph>7%</paragraph></td></tr><tr><td styleCode="Botrule Rrule" valign="top"><paragraph>Pyrexia</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>4%</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>4%</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>4%</paragraph></td><td styleCode="Botrule Lrule" align="center" valign="bottom"><paragraph>4%</paragraph></td></tr><tr><td styleCode="Botrule Rrule" valign="top"><paragraph>Dry Mouth</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>4%</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>3%</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>1%</paragraph></td><td styleCode="Botrule Lrule" align="center" valign="bottom"><paragraph>1%</paragraph></td></tr><tr><td styleCode="Botrule Rrule" valign="top"><paragraph>Vomiting</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>3%</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>3%</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>5%</paragraph></td><td styleCode="Botrule Lrule" align="center" valign="bottom"><paragraph>3%</paragraph></td></tr><tr><td styleCode="Botrule Rrule" valign="top"><paragraph>Hypovolemia</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>3%</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>3%</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>2%</paragraph></td><td styleCode="Botrule Lrule" align="center" valign="bottom"><paragraph>5%</paragraph></td></tr><tr><td styleCode="Botrule Rrule" valign="top"><paragraph>Atelectasis</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>3%</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>3%</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>3%</paragraph></td><td styleCode="Botrule Lrule" align="center" valign="bottom"><paragraph>6%</paragraph></td></tr><tr><td styleCode="Botrule Rrule" valign="top"><paragraph>Pleural Effusion</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>2%</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>2%</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>1%</paragraph></td><td styleCode="Botrule Lrule" align="center" valign="bottom"><paragraph>6%</paragraph></td></tr><tr><td styleCode="Botrule Rrule" valign="top"><paragraph>Agitation</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>2%</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>2%</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>3%</paragraph></td><td styleCode="Botrule Lrule" align="center" valign="bottom"><paragraph>1%</paragraph></td></tr><tr><td styleCode="Botrule Rrule" valign="top"><paragraph>Tachycardia</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>2%</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>2%</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>4%</paragraph></td><td styleCode="Botrule Lrule" align="center" valign="bottom"><paragraph>1%</paragraph></td></tr><tr><td styleCode="Botrule Rrule" valign="top"><paragraph>Anemia</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>2%</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>2%</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>2%</paragraph></td><td styleCode="Botrule Lrule" align="center" valign="bottom"><paragraph>2%</paragraph></td></tr><tr><td styleCode="Botrule Rrule" valign="top"><paragraph>Hyperthermia</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>2%</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>2%</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>3%</paragraph></td><td styleCode="Botrule Lrule" align="center" valign="bottom"><paragraph>0</paragraph></td></tr><tr><td styleCode="Botrule Rrule" valign="top"><paragraph>Chills</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>2%</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>2%</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>3%</paragraph></td><td styleCode="Botrule Lrule" align="center" valign="bottom"><paragraph>2%</paragraph></td></tr><tr><td styleCode="Botrule Rrule" valign="top"><paragraph>Hyperglycemia</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>2%</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>2%</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>2%</paragraph></td><td styleCode="Botrule Lrule" align="center" valign="bottom"><paragraph>3%</paragraph></td></tr><tr><td styleCode="Botrule Rrule" valign="top"><paragraph>Hypoxia</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>2%</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>2%</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>2%</paragraph></td><td styleCode="Botrule Lrule" align="center" valign="bottom"><paragraph>3%</paragraph></td></tr><tr><td styleCode="Botrule Rrule" valign="top"><paragraph>Post-procedural Hemorrhage</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>2%</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>2%</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>3%</paragraph></td><td styleCode="Botrule Lrule" align="center" valign="bottom"><paragraph>4%</paragraph></td></tr><tr><td styleCode="Botrule Rrule" valign="top"><paragraph>Pulmonary Edema</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>1%</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>1%</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>1%</paragraph></td><td styleCode="Botrule Lrule" align="center" valign="bottom"><paragraph>3%</paragraph></td></tr><tr><td styleCode="Botrule Rrule" valign="top"><paragraph>Hypocalcemia</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>1%</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>1%</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>0</paragraph></td><td styleCode="Botrule Lrule" align="center" valign="bottom"><paragraph>2%</paragraph></td></tr><tr><td styleCode="Botrule Rrule" valign="top"><paragraph>Acidosis</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>1%</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>1%</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>1%</paragraph></td><td styleCode="Botrule Lrule" align="center" valign="bottom"><paragraph>2%</paragraph></td></tr><tr><td styleCode="Botrule Rrule" valign="top"><paragraph>Urine Output Decreased</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>1%</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>1%</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>0</paragraph></td><td styleCode="Botrule Lrule" align="center" valign="bottom"><paragraph>2%</paragraph></td></tr><tr><td styleCode="Botrule Rrule" valign="top"><paragraph>Sinus Tachycardia</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>1%</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>1%</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>1%</paragraph></td><td styleCode="Botrule Lrule" align="center" valign="bottom"><paragraph>2%</paragraph></td></tr><tr><td styleCode="Botrule Rrule" valign="top"><paragraph>Ventricular Tachycardia</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>&lt;1%</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>1%</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>1%</paragraph></td><td styleCode="Botrule Lrule" align="center" valign="bottom"><paragraph>5%</paragraph></td></tr><tr><td styleCode="Botrule Rrule" valign="top"><paragraph>Wheezing</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>&lt;1%</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>1%</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>0</paragraph></td><td styleCode="Botrule Lrule" align="center" valign="bottom"><paragraph>2%</paragraph></td></tr><tr><td styleCode="Botrule Rrule" valign="top"><paragraph>Edema Peripheral</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>&lt;1%</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>0</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>1%</paragraph></td><td styleCode="Botrule Lrule" align="center" valign="bottom"><paragraph>2%</paragraph></td></tr></tbody></table>

<table width="97.7%"><caption>Table 4: Treatment-Emergent Adverse Events Occurring in &gt;1% Of All Dexmedetomidine-Treated Adult Patients in the Randomized Placebo-Controlled Continuous Infusion &lt;24 Hours ICU Sedation Studies</caption><colgroup><col width="30%"/><col width="36%"/><col width="33%"/></colgroup><tbody><tr><td styleCode="Botrule Rrule Toprule" valign="bottom"><paragraph><content styleCode="bold">Adverse Event</content></paragraph></td><td styleCode="Botrule Lrule Rrule Toprule" align="center" valign="bottom"><paragraph><content styleCode="bold">Randomized Dexmedetomidine </content> <content styleCode="bold">(N = 387)</content></paragraph></td><td styleCode="Botrule Lrule Toprule" align="center" valign="bottom"><paragraph><content styleCode="bold">Placebo </content> <content styleCode="bold">(N = 379)</content></paragraph></td></tr><tr><td styleCode="Botrule Rrule" valign="top"><paragraph>Hypotension</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>28%</paragraph></td><td styleCode="Botrule Lrule" align="center" valign="bottom"><paragraph>13%</paragraph></td></tr><tr><td styleCode="Botrule Rrule" valign="top"><paragraph>Hypertension</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>16%</paragraph></td><td styleCode="Botrule Lrule" align="center" valign="bottom"><paragraph>18%</paragraph></td></tr><tr><td styleCode="Botrule Rrule" valign="top"><paragraph>Nausea</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>11%</paragraph></td><td styleCode="Botrule Lrule" align="center" valign="bottom"><paragraph>9%</paragraph></td></tr><tr><td styleCode="Botrule Rrule" valign="top"><paragraph>Bradycardia</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>7%</paragraph></td><td styleCode="Botrule Lrule" align="center" valign="bottom"><paragraph>3%</paragraph></td></tr><tr><td styleCode="Botrule Rrule" valign="top"><paragraph>Fever</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>5%</paragraph></td><td styleCode="Botrule Lrule" align="center" valign="bottom"><paragraph>4%</paragraph></td></tr><tr><td styleCode="Botrule Rrule" valign="top"><paragraph>Vomiting</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>4%</paragraph></td><td styleCode="Botrule Lrule" align="center" valign="bottom"><paragraph>6%</paragraph></td></tr><tr><td styleCode="Botrule Rrule" valign="top"><paragraph>Atrial Fibrillation</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>4%</paragraph></td><td styleCode="Botrule Lrule" align="center" valign="bottom"><paragraph>3%</paragraph></td></tr><tr><td styleCode="Botrule Rrule" valign="top"><paragraph>Hypoxia</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>4%</paragraph></td><td styleCode="Botrule Lrule" align="center" valign="bottom"><paragraph>4%</paragraph></td></tr><tr><td styleCode="Botrule Rrule" valign="top"><paragraph>Tachycardia</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>3%</paragraph></td><td styleCode="Botrule Lrule" align="center" valign="bottom"><paragraph>5%</paragraph></td></tr><tr><td styleCode="Botrule Rrule" valign="top"><paragraph>Hemorrhage</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>3%</paragraph></td><td styleCode="Botrule Lrule" align="center" valign="bottom"><paragraph>4%</paragraph></td></tr><tr><td styleCode="Botrule Rrule" valign="top"><paragraph>Anemia</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>3%</paragraph></td><td styleCode="Botrule Lrule" align="center" valign="bottom"><paragraph>2%</paragraph></td></tr><tr><td styleCode="Botrule Rrule" valign="top"><paragraph>Dry Mouth</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>3%</paragraph></td><td styleCode="Botrule Lrule" align="center" valign="bottom"><paragraph>1%</paragraph></td></tr><tr><td styleCode="Botrule Rrule" valign="top"><paragraph>Rigors</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>2%</paragraph></td><td styleCode="Botrule Lrule" align="center" valign="bottom"><paragraph>3%</paragraph></td></tr><tr><td styleCode="Botrule Rrule" valign="top"><paragraph>Agitation</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>2%</paragraph></td><td styleCode="Botrule Lrule" align="center" valign="bottom"><paragraph>3%</paragraph></td></tr><tr><td styleCode="Botrule Rrule" valign="top"><paragraph>Hyperpyrexia</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>2%</paragraph></td><td styleCode="Botrule Lrule" align="center" valign="bottom"><paragraph>3%</paragraph></td></tr><tr><td styleCode="Botrule Rrule" valign="top"><paragraph>Pain</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>2%</paragraph></td><td styleCode="Botrule Lrule" align="center" valign="bottom"><paragraph>2%</paragraph></td></tr><tr><td styleCode="Botrule Rrule" valign="top"><paragraph>Hyperglycemia</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>2%</paragraph></td><td styleCode="Botrule Lrule" align="center" valign="bottom"><paragraph>2%</paragraph></td></tr><tr><td styleCode="Botrule Rrule" valign="top"><paragraph>Acidosis</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>2%</paragraph></td><td styleCode="Botrule Lrule" align="center" valign="bottom"><paragraph>2%</paragraph></td></tr><tr><td styleCode="Botrule Rrule" valign="top"><paragraph>Pleural Effusion</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>2%</paragraph></td><td styleCode="Botrule Lrule" align="center" valign="bottom"><paragraph>1%</paragraph></td></tr><tr><td styleCode="Botrule Rrule" valign="top"><paragraph>Oliguria</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>2%</paragraph></td><td styleCode="Botrule Lrule" align="center" valign="bottom"><paragraph>&lt;1%</paragraph></td></tr><tr><td styleCode="Botrule Rrule" valign="top"><paragraph>Thirst</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>2%</paragraph></td><td styleCode="Botrule Lrule" align="center" valign="bottom"><paragraph>&lt;1%</paragraph></td></tr></tbody></table>

<table width="97.7%"><caption>Table 5: Key Treatment-Emergent Adverse Events Occurring in Dexmedetomidine- or Midazolam-Treated Adult Patients in the Randomized Active Comparator Continuous Infusion Long-Term Intensive Care Unit Sedation Study</caption><colgroup><col width="42%"/><col width="25%"/><col width="33%"/></colgroup><tfoot><tr styleCode="First Last"><td styleCode="Botrule" colspan="11" align="left" valign="top"><sup/> Includes any type of hypertension. ¹ Hypotension was defined in absolute terms as Systolic blood pressure of &lt;80 mmHg or Diastolic blood pressure of &lt;50 mmHg or in relative terms as 30% lower than pre-study drug infusion value. ² Bradycardia was defined in absolute terms as &lt;40 bpm or in relative terms as 30% lower than pre-study drug infusion value. ³ Hypertension was defined in absolute terms as Systolic blood pressure &gt;180 mmHg or Diastolic blood pressure of &gt;100 mmHg or in relative terms as 30% higher than pre-study drug infusion value. ⁴ Tachycardia was defined in absolute terms as &gt;120 bpm or in relative terms as 30% greater than pre-study drug infusion value.</td></tr></tfoot><tbody><tr><td styleCode="Botrule Rrule Toprule" valign="bottom"><paragraph><content styleCode="bold">Adverse Event</content></paragraph></td><td styleCode="Botrule Lrule Rrule Toprule" align="center" valign="bottom"><paragraph><content styleCode="bold">Dexmedetomidine </content> <content styleCode="bold">(N = 244)</content></paragraph></td><td styleCode="Botrule Lrule Toprule" align="center" valign="bottom"><paragraph><content styleCode="bold">Midazolam </content> <content styleCode="bold">(N = 122)</content></paragraph></td></tr><tr><td styleCode="Botrule Rrule" valign="top"><paragraph>Hypotension¹</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>56%</paragraph></td><td styleCode="Botrule Lrule" align="center" valign="bottom"><paragraph>56%</paragraph></td></tr><tr><td styleCode="Botrule Rrule" valign="top"><paragraph>Hypotension Requiring Intervention</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>28%</paragraph></td><td styleCode="Botrule Lrule" align="center" valign="bottom"><paragraph>27%</paragraph></td></tr><tr><td styleCode="Botrule Rrule" valign="top"><paragraph>Bradycardia²</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>42%</paragraph></td><td styleCode="Botrule Lrule" align="center" valign="bottom"><paragraph>19%</paragraph></td></tr><tr><td styleCode="Botrule Rrule" valign="top"><paragraph>Bradycardia Requiring Intervention</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>5%</paragraph></td><td styleCode="Botrule Lrule" align="center" valign="bottom"><paragraph>1%</paragraph></td></tr><tr><td styleCode="Botrule Rrule" valign="top"><paragraph>Systolic Hypertension³</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>28%</paragraph></td><td styleCode="Botrule Lrule" align="center" valign="bottom"><paragraph>42%</paragraph></td></tr><tr><td styleCode="Botrule Rrule" valign="top"><paragraph>Tachycardia⁴</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>25%</paragraph></td><td styleCode="Botrule Lrule" align="center" valign="bottom"><paragraph>44%</paragraph></td></tr><tr><td styleCode="Botrule Rrule" valign="top"><paragraph>Tachycardia Requiring Intervention</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>10%</paragraph></td><td styleCode="Botrule Lrule" align="center" valign="bottom"><paragraph>10%</paragraph></td></tr><tr><td styleCode="Botrule Rrule" valign="top"><paragraph>Diastolic Hypertension³</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>12%</paragraph></td><td styleCode="Botrule Lrule" align="center" valign="bottom"><paragraph>15%</paragraph></td></tr><tr><td styleCode="Botrule Rrule" valign="top"><paragraph>Hypertension³</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>11%</paragraph></td><td styleCode="Botrule Lrule" align="center" valign="bottom"><paragraph>15%</paragraph></td></tr><tr><td styleCode="Botrule Rrule" valign="top"><paragraph>Hypertension Requiring Intervention</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>19%</paragraph></td><td styleCode="Botrule Lrule" align="center" valign="bottom"><paragraph>30%</paragraph></td></tr><tr><td styleCode="Botrule Rrule" valign="top"><paragraph>Hypokalemia</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>9%</paragraph></td><td styleCode="Botrule Lrule" align="center" valign="bottom"><paragraph>13%</paragraph></td></tr><tr><td styleCode="Botrule Rrule" valign="top"><paragraph>Pyrexia</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>7%</paragraph></td><td styleCode="Botrule Lrule" align="center" valign="bottom"><paragraph>2%</paragraph></td></tr><tr><td styleCode="Botrule Rrule" valign="top"><paragraph>Agitation</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>7%</paragraph></td><td styleCode="Botrule Lrule" align="center" valign="bottom"><paragraph>6%</paragraph></td></tr><tr><td styleCode="Botrule Rrule" valign="top"><paragraph>Hyperglycemia</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>7%</paragraph></td><td styleCode="Botrule Lrule" align="center" valign="bottom"><paragraph>2%</paragraph></td></tr><tr><td styleCode="Botrule Rrule" valign="top"><paragraph>Constipation</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>6%</paragraph></td><td styleCode="Botrule Lrule" align="center" valign="bottom"><paragraph>6%</paragraph></td></tr><tr><td styleCode="Botrule Rrule" valign="top"><paragraph>Hypoglycemia</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>5%</paragraph></td><td styleCode="Botrule Lrule" align="center" valign="bottom"><paragraph>6%</paragraph></td></tr><tr><td styleCode="Botrule Rrule" valign="top"><paragraph>Respiratory Failure</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>5%</paragraph></td><td styleCode="Botrule Lrule" align="center" valign="bottom"><paragraph>3%</paragraph></td></tr><tr><td styleCode="Botrule Rrule" valign="top"><paragraph>Renal Failure Acute</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>2%</paragraph></td><td styleCode="Botrule Lrule" align="center" valign="bottom"><paragraph>1%</paragraph></td></tr><tr><td styleCode="Botrule Rrule" valign="top"><paragraph>Acute Respiratory Distress Syndrome</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>2%</paragraph></td><td styleCode="Botrule Lrule" align="center" valign="bottom"><paragraph>1%</paragraph></td></tr><tr><td styleCode="Botrule Rrule" valign="top"><paragraph>Generalized Edema</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>2%</paragraph></td><td styleCode="Botrule Lrule" align="center" valign="bottom"><paragraph>6%</paragraph></td></tr><tr><td styleCode="Botrule Rrule" valign="top"><paragraph>Hypomagnesemia</paragraph></td><td styleCode="Botrule Lrule Rrule" align="center" valign="bottom"><paragraph>1%</paragraph></td><td styleCode="Botrule Lrule" align="center" valign="bottom"><paragraph>7%</paragraph></td></tr></tbody></table>