FDA label f864feae-7eb2-4e8b-8aee-3c35fd4cb5e3

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b2eb10c8-9d8c-41e6-a045-01e425c3f8a7
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f864feae-7eb2-4e8b-8aee-3c35fd4cb5e3
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3156
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2019-10-29
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Warnings cross-check#

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warnings

WARNINGS Suicidal Behavior and Ideation Antiepileptic drugs (AEDs), including levetiracetam tablets, increase the risk of suicidal thoughts or behavior in patients taking these drugs for any indication. Patients treated with any AED for any indication should be monitored for the emergence or worsening of depression, suicidal thoughts or behavior, and/or any unusual changes in mood or behavior. Pooled analyses of 199 placebo-controlled clinical trials (mono- and adjunctive therapy) of 11 different AEDs showed that patients randomized to one of the AEDs had approximately twice the risk (adjusted Relative Risk 1.8, 95% CI:1.2, 2.7) of suicidal thinking or behavior compared to patients randomized to placebo. In these trials, which had a median treatment duration of 12 weeks, the estimated incidence rate of suicidal behavior or ideation among 27,863 AED-treated patients was 0.43%, compared to 0.24% among 16,029 placebo-treated patients, representing an increase of approximately one case of suicidal thinking or behavior for every 530 patients treated. There were four suicides in drug-treated patients in the trials and none in placebo-treated patients, but the number is too small to allow any conclusion about drug effect on suicide. The increased risk of suicidal thoughts or behavior with AEDs was observed as early as one week after starting drug treatment with AEDs and persisted for the duration of treatment assessed. Because most trials included in the analysis did not extend beyond 24 weeks, the risk of suicidal thoughts or behavior beyond 24 weeks could not be assessed. The risk of suicidal thoughts or behavior was generally consistent among drugs in the data analyzed. The finding of increased risk with AEDs of varying mechanisms of action and across a range of indications suggests that the risk applies to all AEDs used for any indication. The risk did not vary substantially by age (5-100 years) in the clinical trials analyzed. Table 5 shows absolute and relative risk by indication for all evaluated AEDs. Table 5 Risk by indication for antiepileptic drugs in the pooled analysis Indication Placebo Patients Drug Patients Relative Risk: Risk Difference: with Events Per with Events Per Incidence of Events Additional Drug 1000 Patients 1000 Patients in Drug Patients with Patients/Incidence Events Per 1000 in Placebo Patients Patients Epilepsy 1.0 3.4 3.5 2.4 Psychiatric 5.7 8.5 1.5 2.9 Other 1.0 1.8 1.9 0.9 Total 2.4 4.3 1.8 1.9 The relative risk for suicidal thoughts or behavior was higher in clinical trials for epilepsy than in clinical trials for psychiatric or other conditions, but the absolute risk differences were similar for the epilepsy and psychiatric indications. Anyone considering prescribing levetiracetam tablets or any other AED must balance the risk of suicidal thoughts or behaviors with the risk of untreated illness. Epilepsy and many other illnesses for which AEDs are prescribed are themselves associated with morbidity and mortality and an increased risk of suicidal thoughts and behavior. Should suicidal thoughts and behavior emerge during treatment, the prescriber needs to consider whether the emergence of these symptoms in any given patient may be related to the illness being treated. Patients, their caregivers, and families should be informed that AEDs increase the risk of suicidal thoughts and behavior and should be advised of the need to be alert for the emergence or worsening of the signs and symptoms of depression, any unusual changes in mood or behavior, or the emergence of suicidal thoughts, behavior, or thoughts about self-harm. Behaviors of concern should be reported immediately to healthcare providers. Neuropsychiatric Adverse Events Partial Onset Seizures Adults In adults, experiencing partial onset seizures, levetiracetam use is associated with the occurrence of central nervous system adverse events that can be classified into the following categories: 1) somnolence and fatigue, 2) coordination difficulties, and 3) behavioral abnormalities. In controlled trials of adult patients with epilepsy experiencing partial onset seizures, 14.8% of levetiracetam treated patients reported somnolence, compared to 8.4% of placebo patients. There was no clear dose response up to 3000 mg/day. In a study where there was no titration, about 45% of patients receiving 4000 mg/day reported somnolence. The somnolence was considered serious in 0.3% of the treated patients, compared to 0% in the placebo group. About 3% of levetiracetam treated patients discontinued treatment due to somnolence, compared to 0.7% of placebo patients. In 1.4% of treated patients and in 0.9% of placebo patients the dose was reduced, while 0.3% of the treated patients were hospitalized due to somnolence. In controlled trials of adult patients with epilepsy experiencing partial onset seizures, 14.7% of treated patients reported asthenia, compared to 9.1% of placebo patients. Treatment was discontinued in 0.8% of treated patients as compared to 0.5% of placebo patients. In 0.5% of treated patients and in 0.2% of placebo patients the dose was reduced. A total of 3.4% of levetiracetam-treated patients experienced coordination difficulties, (reported as either ataxia, abnormal gait, or incoordination) compared to 1.6% of placebo patients. A total of 0.4% of patients in controlled trials discontinued levetiracetam treatment due to ataxia, compared to 0% of placebo patients. In 0.7% of treated patients and in 0.2% of placebo patients the dose was reduced due to coordination difficulties, while one of the treated patients was hospitalized due to worsening of pre-existing ataxia. Somnolence, asthenia and coordination difficulties occurred most frequently within the first 4 weeks of treatment. In controlled trials of patients with epilepsy experiencing partial onset seizures, 5 (0.7%) of levetiracetam treated patients experienced psychotic symptoms compared to 1 (0.2%) placebo patient. Two (0.3%) levetiracetam-treated patients were hospitalized and their treatment was discontinued. Both events, reported as psychosis, developed within the first week of treatment and resolved within 1 to 2 weeks following treatment discontinuation. Two other events, reported as hallucinations, occurred after 1-5 months and resolved within 2-7 days while the patients remained on treatment. In one patient experiencing psychotic depression occurring within a month, symptoms resolved within 45 days while the patient continued treatment. A total of 13.3% of levetiracetam patients experienced other behavioral symptoms (reported as aggression, agitation, anger, anxiety, apathy, depersonalization, depression, emotional lability, hostility, irritability etc.) compared to 6.2% of placebo patients. Approximately half of these patients reported these events within the first 4 weeks. A total of 1.7% of treated patients discontinued treatment due to these events, compared to 0.2% of placebo patients. The treatment dose was reduced in 0.8% of treated patients and in 0.5% of placebo patients. A total of 0.8% of treated patients had a serious behavioral event (compared to 0.2% of placebo patients) and were hospitalized. Pediatric Patients In pediatric patients experiencing partial onset seizures, levetiracetam is associated with somnolence, fatigue, and behavioral abnormalities. In the double-blind, controlled trial in children with epilepsy experiencing partial onset seizures, 22.8% of levetiracetam-treated patients experienced somnolence, compared to 11.3% of placebo patients. The design of the study prevented accurately assessing dose-response effects. No patient discontinued treatment for somnolence. In about 3.0% of Levetiracetam tablets -treated patients and in 3.1% of placebo patients the dose was reduced as a result of somnolence. Asthenia was reported in 8.9% of levetiracetam-treated patients, compared to 3.1% of placebo patients. No patient discontinued treatment for asthenia, but asthenia led to a dose reduction in 3.0% of levetiracetam-treated patients compared to 0% of placebo patients. A total of 37.6% of the levetiracetam-treated patients experienced behavioral symptoms (reported as agitation, anxiety, apathy, depersonalization, depression, emotional lability, hostility, hyperkinesia, nervousness, neurosis, and personality disorder), compared to 18.6% of placebo patients. Hostility was reported in 11.9% of levetiracetam-treated patients, compared to 6.2% of placebo patients. Nervousness was reported in 9.9% of levetiracetam-treated patients, compared to 2.1% of placebo patients. Depression was reported in 3.0% of levetiracetam-treated patients, compared to 1.0% of placebo patients. A total of 3.0% of levetiracetam-treated patients discontinued treatment due to psychotic and nonpsychotic adverse events, compared to 4.1% of placebo patients. Overall, 10.9% of levetiracetam- treated patients experienced behavioral symptoms associated with discontinuation or dose reduction, compared to 6.2% of placebo patients. Withdrawal Seizures Antiepileptic drugs, including levetiracetam, should be withdrawn gradually to minimize the potential of increased seizure frequency.

warnings table

<table width="698" ID="id_1f16b162-9bf7-4bab-9cc6-5653d74c42ac"> <caption ID="id_dd392c5e-4ffb-437a-8325-96a9e0492ad9">Table 5 Risk by indication for antiepileptic drugs in the pooled analysis</caption> <col width="16.5%"/> <col width="18.9%"/> <col width="18.1%"/> <col width="24.5%"/> <col width="22.1%"/> <tbody> <tr ID="id_e7cdd195-06fa-4997-aec9-fe7a1d464545"> <td align="left" valign="bottom" styleCode="Toprule">Indication</td> <td align="left" valign="bottom" styleCode="Toprule">Placebo Patients</td> <td align="left" valign="bottom" styleCode="Toprule">Drug Patients</td> <td align="left" valign="bottom" styleCode="Toprule">Relative Risk:</td> <td align="left" valign="bottom">Risk Difference:</td> </tr> <tr ID="id_3e9fa66f-259d-43ee-bff4-ce042945150f"> <td align="left" valign="bottom"/> <td align="left" valign="bottom">with Events Per</td> <td align="left" valign="bottom">with Events Per</td> <td align="left" valign="bottom">Incidence of Events</td> <td align="left" valign="bottom">Additional Drug</td> </tr> <tr ID="id_2c638ab5-b84f-4d8c-92e4-325f5d753d8c"> <td align="left" valign="bottom"/> <td align="left" valign="bottom">1000 Patients</td> <td align="left" valign="bottom">1000 Patients</td> <td align="left" valign="bottom">in Drug</td> <td align="left" valign="bottom">Patients with</td> </tr> <tr ID="id_cbe83505-65fb-4350-a7f6-f757fb089c47"> <td align="left" valign="bottom"/> <td align="left" valign="bottom"/> <td align="left" valign="bottom"/> <td align="left" valign="bottom">Patients/Incidence</td> <td align="left" valign="bottom">Events Per 1000</td> </tr> <tr ID="id_4f0a0e85-dd55-4ace-b889-997acfa94486"> <td align="left" valign="bottom" styleCode="Botrule"/> <td align="left" valign="bottom" styleCode="Botrule"/> <td align="left" valign="bottom" styleCode="Botrule"/> <td align="left" valign="bottom" styleCode="Botrule">in Placebo Patients</td> <td align="left" valign="bottom" styleCode="Botrule">Patients</td> </tr> <tr ID="id_8da8b965-b870-4198-92ef-b8a011fe6575"> <td align="left" valign="bottom">Epilepsy</td> <td align="left" valign="bottom">1.0</td> <td align="left" valign="bottom">3.4</td> <td align="left" valign="bottom">3.5</td> <td align="left" valign="bottom">2.4</td> </tr> <tr ID="id_32891238-9ce3-44dc-8b99-bb548ab4d62f"> <td align="left" valign="bottom">Psychiatric</td> <td align="left" valign="bottom">5.7</td> <td align="left" valign="bottom">8.5</td> <td align="left" valign="bottom">1.5</td> <td align="left" valign="bottom">2.9</td> </tr> <tr ID="id_9b3a182e-f542-4401-92df-6b22d287a156"> <td align="left" valign="bottom">Other</td> <td align="left" valign="bottom">1.0</td> <td align="left" valign="bottom">1.8</td> <td align="left" valign="bottom">1.9</td> <td align="left" valign="bottom">0.9</td> </tr> <tr ID="id_705c6b1c-e4ea-465e-8ec0-369db8743b88"> <td align="left" valign="bottom" styleCode="Botrule">Total</td> <td align="left" valign="bottom" styleCode="Botrule">2.4</td> <td align="left" valign="bottom" styleCode="Botrule">4.3</td> <td align="left" valign="bottom" styleCode="Botrule">1.8</td> <td align="left" valign="bottom" styleCode="Botrule">1.9</td> </tr> </tbody> </table>

Adverse reactions cross-check#

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adverse reactions

ADVERSE REACTIONS The prescriber should be aware that adverse event incidence figures in the following tables, obtained when levetiracetam was added to concurrent AED therapy, cannot be used to predict the frequency of adverse experiences in the course of usual medical practice where patient characteristics and other factors may differ from those prevailing during clinical studies. Similarly, the cited frequencies cannot be directly compared with figures obtained from other clinical investigations involving different treatments, uses, or investigators. An inspection of these frequencies, however, does provide the prescriber with one basis to estimate the relative contribution of drug and non-drug factors to the adverse event incidences in the population studied. Partial Onset Seizures In well-controlled clinical studies in adults with partial onset seizures, the most frequently reported adverse events associated with the use of levetiracetam in combination with other AEDs, not seen at an equivalent frequency among placebo-treated patients, were somnolence, asthenia, infection and dizziness. In the well-controlled pediatric clinical study in children 4 to 16 years of age with partial onset seizures, the adverse events most frequently reported with the use of levetiracetam in combination with other AEDs, not seen at an equivalent frequency among placebo-treated patients, were somnolence, accidental injury, hostility, nervousness, and asthenia. Table 6 lists treatment-emergent adverse events that occurred in at least 1% of adult epilepsy patients treated with levetiracetam participating in placebo-controlled studies and were numerically more common than in patients treated with placebo. Table 7 lists treatment-emergent adverse events that occurred in at least 2% of pediatric epilepsy patients (ages 4-16 years) treated with levetiracetam participating in the placebo-controlled study and were numerically more common than in pediatric patients treated with placebo. In these studies, either levetiracetam or placebo was added to concurrent AED therapy. Adverse events were usually mild to moderate in intensity. Table 6: Incidence (%) of Treatment-Emergent Adverse Events in Placebo-Controlled, Add-On Studies in Adults Experiencing Partial Onset Seizures by Body System (Adverse Events occurred in at least 1% of Levetiracetam-Treated Patients and occurred more frequently than Placebo-Treated Patients) Body System/ Adverse Event Levetiracetam (N=769) % Placebo (N=439) % Body as a Whole Asthenia 15 9 Headache 14 13 Infection 13 8 Pain 7 6 Digestive System Anorexia 3 2 Nervous System Somnolence 15 8 Dizziness 9 4 Depression 4 2 Nervousness 4 2 Ataxia 3 1 Vertigo 3 1 Amnesia 2 1 Anxiety 2 1 Hostility 2 1 Paresthesia 2 1 Emotional Lability 2 0 Respiratory System Pharyngitis 6 4 Rhinitis 4 3 Cough Increased 2 1 Sinusitis 2 1 Special Senses Diplopia 2 1 Other events reported by 1% of adult patients treated with levetiracetam but as or more frequent in the placebo group were the following: abdominal pain, accidental injury, amblyopia, arthralgia, back pain, bronchitis, chest pain, confusion, constipation, convulsion, diarrhea, drug level increased, dyspepsia, ecchymosis, fever, flu syndrome, fungal infection, gastroenteritis, gingivitis, grand mal convulsion, insomnia, nausea, otitis media, rash, thinking abnormal, tremor, urinary tract infection, vomiting and weight gain. Table 7: Incidence (%) of Treatment-Emergent Adverse Events in a Placebo-Controlled, Add-On Study in Pediatric Patients ages 4-16 years by Experiencing Partial Onset Seizures Body System (Adverse Events occurred in at least 2% of Levetiracetam-Treated Patients and occurred more frequently than Placebo-Treated Patients) Body System/ Adverse Event Levetiracetam (N=101) % Placebo (N=97) % Body as a Whole Accidental Injury 17 10 Asthenia 9 3 Pain 6 3 Flu Syndrome 3 2 Face Edema 2 1 Neck Pain 2 1 Viral Infection 2 1 Digestive System Vomiting 15 13 Anorexia 13 8 Diarrhea 8 7 Gastroenteritis 4 2 Constipation 3 1 Hemic and Lymphatic System Ecchymosis 4 1 Metabolic and Nutritional Dehydration 2 1 Nervous System Somnolence 23 11 Hostility 12 6 Nervousness 10 2 Personality Disorder 8 7 Dizziness 7 2 Emotional Lability 6 4 Agitation 6 1 Depression 3 1 Vertigo 3 1 Reflexes Increased 2 1 Confusion 2 0 Respiratory System Rhinitis 13 8 Cough Increased 11 7 Pharyngitis 10 8 Asthma 2 1 Skin and Appendages Pruritis 2 0 Skin Discoloration 2 0 Vesiculobullous Rash 2 0 Special Senses Conjunctivits 3 2 Amblyopia 2 0 Ear Pain 2 0 Urogenital System Albuminuria 4 0 Urine Abnormality 2 1 Other events occurring in 2% or more of pediatric patients treated with levetiracetam but as or more frequent in the placebo group were the following: abdominal pain, allergic reaction, ataxia, convulsion, epistaxis, fever, headache, hyperkinesia, infection, insomnia, nausea, otitis media, rash, sinusitis, status epilepticus (not otherwise specified), thinking abnormal, tremor, and urinary incontinence. Time Course of Onset of Adverse Events For Partial Onset Seizures Of the most frequently reported adverse events in adults experiencing partial onset seizures, asthenia, somnolence and dizziness appeared to occur predominantly during the first 4 weeks of treatment with levetiracetam. Discontinuation or Dose Reduction in Well-Controlled Clinical Studies Partial Onset Seizures In well-controlled adult clinical studies, 15.0% of patients receiving levetiracetam and 11.6% receiving placebo either discontinued or had a dose reduction as a result of an adverse event. Table 8 lists the most common (>1%) adverse events that resulted in discontinuation or dose reduction. Table 8: Adverse Events that most commonly resulted in Discontinuation or Dose Reduction in Placebo-Controlled Studies in Adult Patients with Epilepsy Experiencing Partial Onset Seizures Number (%) Levetiracetam (N=769) Placebo (N=439) Asthenia 10 (1.3%) 3 (0.7%) Convulsion 23 (3.0%) 15 (3.4%) Dizziness 11 (1.4%) 0 Rash 0 5 (1.1%) Somnolence 34 (4.4%) 7 (1.6%) In the well-controlled pediatric clinical study, 16.8% of patients receiving levetiracetam and 20.6% receiving placebo either discontinued or had a dose reduction as a result of an adverse event. The adverse events most commonly associated (≥3% in patients receiving levetiracetam) with discontinuation or dose reduction in the well-controlled study are presented in Table 9. Table 9: Adverse Events most commonly associated with Discontinuation or Dose Reduction in the Placebo-Controlled Study In Pediatric Patients ages 4-16 Years with Epilepsy Experiencing Partial Onset Seizures Number (%) Levetiracetam (N=101) Placebo (N=97) Asthenia 3 (3.0%) 0 (0.0%) Hostility 7 (6.9%) 2 (2.1%) Somnolence 3 (3.0%) 3 (3.1%) Comparison of Gender, Age and Race The overall adverse experience profile of levetiracetam was similar between females and males. There are insufficient data to support a statement regarding the distribution of adverse experience reports by age and race. Postmarketing Experience The following adverse events have been identified during postapproval use of levetiracetam tablets. Because these events are reported voluntarily from a population of uncertain size, it is not always possible to reliably estimate their frequency or establish a casual relationship to drug exposure. In addition to the adverse experiences listed above, the following have been reported in patients receiving marketed levetiracetam worldwide. The listing is alphabetized: abnormal liver function test, hepatic failure, hepatitis, leukopenia, neutropenia, pancreatitis, pancytopenia (with bone marrow suppression identified in some of the cases), thrombocytopenia and weight loss. Alopecia has been reported with levetiracetam use; recovery was observed in majority of cases where levetiracetam was discontinued. These adverse experiences have not been listed above, and data are insufficient to support an estimate of their incidence or to establish causation.

adverse reactions table

<table border="single" width="572" ID="id_bef4838a-2f27-455f-bbf7-6aa286962d73"> <caption ID="id_64302e6a-2554-4316-b953-ded09d68f559">Table 6: Incidence (%) of Treatment-Emergent Adverse Events in Placebo-Controlled, Add-On Studies in Adults Experiencing Partial Onset Seizures by Body System (Adverse Events occurred in at least 1% of Levetiracetam-Treated Patients and occurred more frequently than Placebo-Treated Patients)</caption> <col width="42.3%"/> <col width="28.8%"/> <col width="28.8%"/> <tbody> <tr ID="id_98a7f728-58d6-47f3-9425-5d73924484dc"> <td align="center" valign="top" styleCode="Botrule Toprule Rrule Lrule"> <paragraph> <content styleCode="bold">Body System/</content> </paragraph> <paragraph> <content styleCode="bold">Adverse Event</content> </paragraph> </td> <td align="center" valign="top" styleCode="Botrule Rrule"> <paragraph> <content styleCode="bold">Levetiracetam</content> </paragraph> <paragraph> <content styleCode="bold">(N=769)</content> </paragraph> <content styleCode="bold">%</content> </td> <td align="center" valign="top" styleCode="Botrule Rrule"> <paragraph> <content styleCode="bold">Placebo</content> </paragraph> <paragraph> <content styleCode="bold">(N=439)</content> </paragraph> <content styleCode="bold">%</content> </td> </tr> <tr ID="id_ec46347e-8cf2-49ec-acbf-167aba9aac66"> <td align="justify" valign="top" styleCode="Lrule Botrule Rrule"> <content styleCode="bold">Body as a Whole</content> </td> <td align="center" valign="top" styleCode="Botrule Rrule"/> <td align="center" valign="top" styleCode="Botrule Rrule"/> </tr> <tr ID="id_6bdc1193-05ad-4242-bcaf-d874175967de"> <td align="justify" valign="top" styleCode="Lrule Botrule Rrule"> Asthenia</td> <td align="center" valign="top" styleCode="Botrule Rrule">15</td> <td align="center" valign="top" styleCode="Botrule Rrule">9</td> </tr> <tr ID="id_57928509-1182-46e2-8f9a-9a9771ec388a"> <td align="justify" valign="top" styleCode="Lrule Botrule Rrule"> Headache</td> <td align="center" valign="top" styleCode="Botrule Rrule">14</td> <td align="center" valign="top" styleCode="Botrule Rrule">13</td> </tr> <tr ID="id_128cd7ef-d803-4e36-93dd-61d88a72b924"> <td align="justify" valign="top" styleCode="Lrule Botrule Rrule"> Infection</td> <td align="center" valign="top" styleCode="Botrule Rrule">13</td> <td align="center" valign="top" styleCode="Botrule Rrule">8</td> </tr> <tr ID="id_198b7978-8456-4de4-b46e-9bb0c97048f0"> <td align="justify" valign="top" styleCode="Lrule Botrule Rrule"> Pain</td> <td align="center" valign="top" styleCode="Botrule Rrule">7</td> <td align="center" valign="top" styleCode="Botrule Rrule">6</td> </tr> <tr ID="id_41dc0c84-cc6e-4e1a-951c-960e9ca7d981"> <td align="justify" valign="top" styleCode="Lrule Botrule Rrule"> <content styleCode="bold">Digestive System</content> </td> <td align="center" valign="top" styleCode="Botrule Rrule"/> <td align="center" valign="top" styleCode="Botrule Rrule"/> </tr> <tr ID="id_cb91c30a-7978-492c-bef1-e74d42c88330"> <td align="justify" valign="top" styleCode="Lrule Botrule Rrule"> Anorexia</td> <td align="center" valign="top" styleCode="Botrule Rrule">3</td> <td align="center" valign="top" styleCode="Botrule Rrule">2</td> </tr> <tr ID="id_c839ad60-7c5d-4daf-92db-827d21e73702"> <td align="justify" valign="top" styleCode="Lrule Botrule Rrule"> <content styleCode="bold">Nervous System</content> </td> <td align="center" valign="top" styleCode="Botrule Rrule"/> <td align="center" valign="top" styleCode="Botrule Rrule"/> </tr> <tr ID="id_a8fb4fe6-bbcb-4022-a41e-2b56c70fc6ec"> <td align="justify" valign="top" styleCode="Lrule Botrule Rrule"> Somnolence</td> <td align="center" valign="top" styleCode="Botrule Rrule">15</td> <td align="center" valign="top" styleCode="Botrule Rrule">8</td> </tr> <tr ID="id_d0913b1f-9a87-4dcf-98b1-5fd3292a7860"> <td align="justify" valign="top" styleCode="Lrule Botrule Rrule"> Dizziness</td> <td align="center" valign="top" styleCode="Botrule Rrule">9</td> <td align="center" valign="top" styleCode="Botrule Rrule">4</td> </tr> <tr ID="id_f99a01c5-672f-4c60-91d7-becbcbcc7ee4"> <td align="justify" valign="top" styleCode="Lrule Botrule Rrule"> Depression</td> <td align="center" valign="top" styleCode="Botrule Rrule">4</td> <td align="center" valign="top" styleCode="Botrule Rrule">2</td> </tr> <tr ID="id_2508ac44-6046-47f8-a412-a1c424987b03"> <td align="justify" valign="top" styleCode="Lrule Botrule Rrule"> Nervousness</td> <td align="center" valign="top" styleCode="Botrule Rrule">4</td> <td align="center" valign="top" styleCode="Botrule Rrule">2</td> </tr> <tr ID="id_8800aac2-18e7-4cfa-a9c5-410eafe122e8"> <td align="justify" valign="top" styleCode="Lrule Botrule Rrule"> Ataxia</td> <td align="center" valign="top" styleCode="Botrule Rrule">3</td> <td align="center" valign="top" styleCode="Botrule Rrule">1</td> </tr> <tr ID="id_466d491d-c5cc-463a-952b-0c1a44353691"> <td align="justify" valign="top" styleCode="Lrule Botrule Rrule"> Vertigo</td> <td align="center" valign="top" styleCode="Botrule Rrule">3</td> <td align="center" valign="top" styleCode="Botrule Rrule">1</td> </tr> <tr ID="id_8a386829-ede7-4dac-9cee-d6fa45d48c94"> <td align="justify" valign="top" styleCode="Lrule Botrule Rrule"> Amnesia</td> <td align="center" valign="top" styleCode="Botrule Rrule">2</td> <td align="center" valign="top" styleCode="Botrule Rrule">1</td> </tr> <tr ID="id_d5176596-e91d-421d-b90a-3c15e10cad1c"> <td align="justify" valign="top" styleCode="Lrule Botrule Rrule"> Anxiety</td> <td align="center" valign="top" styleCode="Botrule Rrule">2</td> <td align="center" valign="top" styleCode="Botrule Rrule">1</td> </tr> <tr ID="id_29ccb4d4-aba6-49b7-82b7-753548502b38"> <td align="justify" valign="top" styleCode="Lrule Botrule Rrule"> Hostility</td> <td align="center" valign="top" styleCode="Botrule Rrule">2</td> <td align="center" valign="top" styleCode="Botrule Rrule">1</td> </tr> <tr ID="id_869fb308-a443-42f3-8efc-3e8a692601c6"> <td align="justify" valign="top" styleCode="Lrule Botrule Rrule"> Paresthesia</td> <td align="center" valign="top" styleCode="Botrule Rrule">2</td> <td align="center" valign="top" styleCode="Botrule Rrule">1</td> </tr> <tr ID="id_b32b5b59-83fa-486b-8f12-61b70a789031"> <td align="justify" valign="top" styleCode="Lrule Botrule Rrule"> Emotional Lability</td> <td align="center" valign="top" styleCode="Botrule Rrule">2</td> <td align="center" valign="top" styleCode="Botrule Rrule">0</td> </tr> <tr ID="id_c5c13b31-afdc-4221-87e2-f4a9423666c3"> <td align="justify" valign="top" styleCode="Lrule Botrule Rrule"> <content styleCode="bold">Respiratory System</content> </td> <td align="center" valign="top" styleCode="Botrule Rrule"/> <td align="center" valign="top" styleCode="Botrule Rrule"/> </tr> <tr ID="id_c2a58614-7ab8-4bbd-ae6d-92c15ae54ff3"> <td align="justify" valign="top" styleCode="Lrule Botrule Rrule"> Pharyngitis</td> <td align="center" valign="top" styleCode="Botrule Rrule">6</td> <td align="center" valign="top" styleCode="Botrule Rrule">4</td> </tr> <tr ID="id_ccf7bab1-68d4-4972-beda-bd5d975d61f3"> <td align="justify" valign="top" styleCode="Lrule Botrule Rrule"> Rhinitis</td> <td align="center" valign="top" styleCode="Botrule Rrule">4</td> <td align="center" valign="top" styleCode="Botrule Rrule">3</td> </tr> <tr ID="id_80b89ba0-49f1-42bb-a333-c25b646d0f6a"> <td align="justify" valign="top" styleCode="Lrule Botrule Rrule"> Cough Increased</td> <td align="center" valign="top" styleCode="Botrule Rrule">2</td> <td align="center" valign="top" styleCode="Botrule Rrule">1</td> </tr> <tr ID="id_8378383c-bfb0-4b3b-8708-625f97431525"> <td align="justify" valign="top" styleCode="Lrule Botrule Rrule"> Sinusitis</td> <td align="center" valign="top" styleCode="Botrule Rrule">2</td> <td align="center" valign="top" styleCode="Botrule Rrule">1</td> </tr> <tr ID="id_50f7f1cc-d5e9-4cd8-858a-d33cad3c570f"> <td align="justify" valign="top" styleCode="Lrule Botrule Rrule"> <content styleCode="bold">Special Senses</content> </td> <td align="center" valign="top" styleCode="Botrule Rrule"/> <td align="center" valign="top" styleCode="Botrule Rrule"/> </tr> <tr ID="id_cac9e850-e821-4429-9877-0b479b735f32"> <td align="justify" valign="top" styleCode="Lrule Botrule Rrule"> Diplopia</td> <td align="center" valign="top" styleCode="Rrule">2</td> <td align="center" valign="top" styleCode="Botrule Rrule">1</td> </tr> </tbody> </table>

adverse reactions table

<table border="single" width="522" ID="id_68e453bf-e425-4e3c-92c9-669749bb1f68"> <caption ID="id_f79ac087-36db-4fd6-9452-a40c0aa7b066">Table 7: Incidence (%) of Treatment-Emergent Adverse Events in a Placebo-Controlled, Add-On Study in Pediatric Patients ages 4-16 years by Experiencing Partial Onset Seizures Body System (Adverse Events occurred in at least 2% of Levetiracetam-Treated Patients and occurred more frequently than Placebo-Treated Patients)</caption> <col width="49.4%"/> <col width="23.2%"/> <col width="27.4%"/> <tbody> <tr ID="id_58a8b14b-7593-45d3-a949-097db0c70009"> <td align="center" valign="top" styleCode="Botrule Toprule Rrule Lrule"> <paragraph> <content styleCode="bold">Body System/</content> </paragraph> <paragraph> <content styleCode="bold">Adverse Event</content> </paragraph> </td> <td align="center" valign="top" styleCode="Botrule Rrule"> <paragraph> <content styleCode="bold">Levetiracetam</content> </paragraph> <paragraph> <content styleCode="bold">(N=101)</content> </paragraph> <content styleCode="bold">%</content> </td> <td align="center" valign="top" styleCode="Botrule Rrule"> <paragraph> <content styleCode="bold">Placebo</content> </paragraph> <paragraph> <content styleCode="bold">(N=97)</content> </paragraph> <content styleCode="bold">%</content> </td> </tr> <tr ID="id_aeb74c64-4f19-4628-aa68-70dea60c183a"> <td align="justify" valign="top" styleCode="Lrule Botrule Rrule"> <content styleCode="bold">Body as a Whole</content> </td> <td align="center" valign="top" styleCode="Botrule Rrule"/> <td align="center" valign="top" styleCode="Botrule Rrule"/> </tr> <tr ID="id_8970cef5-5518-49ca-9e61-5e9a0e535d6a"> <td align="justify" valign="top" styleCode="Lrule Botrule Rrule"> Accidental Injury</td> <td align="center" valign="top" styleCode="Botrule Rrule">17</td> <td align="center" valign="top" styleCode="Botrule Rrule">10</td> </tr> <tr ID="id_2bcbaca9-694f-4f47-8bce-7edbfac97c3d"> <td align="justify" valign="top" styleCode="Lrule Botrule Rrule"> Asthenia</td> <td align="center" valign="top" styleCode="Botrule Rrule">9</td> <td align="center" valign="top" styleCode="Botrule Rrule">3</td> </tr> <tr ID="id_b1c701cf-1ae2-4b2f-81fb-61870b377821"> <td align="justify" valign="top" styleCode="Lrule Botrule Rrule"> Pain</td> <td align="center" valign="top" styleCode="Botrule Rrule">6</td> <td align="center" valign="top" styleCode="Botrule Rrule">3</td> </tr> <tr ID="id_789b9938-24b0-4019-baa3-d3ec4f944e51"> <td align="justify" valign="top" styleCode="Lrule Botrule Rrule"> Flu Syndrome</td> <td align="center" valign="top" styleCode="Botrule Rrule">3</td> <td align="center" valign="top" styleCode="Botrule Rrule">2</td> </tr> <tr ID="id_2f2be2b8-c8cf-48f9-9cb4-74052a2f6220"> <td align="justify" valign="top" styleCode="Lrule Botrule Rrule"> Face Edema</td> <td align="center" valign="top" styleCode="Botrule Rrule">2</td> <td align="center" valign="top" styleCode="Botrule Rrule">1</td> </tr> <tr ID="id_6b8dc22f-1cb2-4dea-9cac-8ae12b05f9e6"> <td align="justify" valign="top" styleCode="Lrule Botrule Rrule"> Neck Pain</td> <td align="center" valign="top" styleCode="Botrule Rrule">2</td> <td align="center" valign="top" styleCode="Botrule Rrule">1</td> </tr> <tr ID="id_291b02fd-4c2f-45c1-88f0-27d92971b70a"> <td align="justify" valign="top" styleCode="Lrule Botrule Rrule"> Viral Infection</td> <td align="center" valign="top" styleCode="Botrule Rrule">2</td> <td align="center" valign="top" styleCode="Botrule Rrule">1</td> </tr> <tr ID="id_63c3f6c7-a7e7-4642-9357-7f6ba1b53a11"> <td align="justify" valign="top" styleCode="Lrule Botrule Rrule"> <content styleCode="bold">Digestive System</content> </td> <td align="center" valign="top" styleCode="Botrule Rrule"/> <td align="center" valign="top" styleCode="Botrule Rrule"/> </tr> <tr ID="id_fc66742c-9212-4f54-bb04-f31ea9082a84"> <td align="justify" valign="top" styleCode="Lrule Botrule Rrule"> Vomiting</td> <td align="center" valign="top" styleCode="Botrule Rrule">15</td> <td align="center" valign="top" styleCode="Botrule Rrule">13</td> </tr> <tr ID="id_ba90df72-b673-4bad-8f4b-23acd2fa5d00"> <td align="justify" valign="top" styleCode="Lrule Botrule Rrule"> Anorexia</td> <td align="center" valign="top" styleCode="Botrule Rrule">13</td> <td align="center" valign="top" styleCode="Botrule Rrule">8</td> </tr> <tr ID="id_38d14a33-62e6-4e26-95dc-86d15f739aff"> <td align="justify" valign="top" styleCode="Lrule Botrule Rrule"> Diarrhea</td> <td align="center" valign="top" styleCode="Botrule Rrule">8</td> <td align="center" valign="top" styleCode="Botrule Rrule">7</td> </tr> <tr ID="id_9200b9ef-cf88-4586-b0e7-657a760cde57"> <td align="justify" valign="top" styleCode="Lrule Botrule Rrule"> Gastroenteritis</td> <td align="center" valign="top" styleCode="Botrule Rrule">4</td> <td align="center" valign="top" styleCode="Botrule Rrule">2</td> </tr> <tr ID="id_5f232ddf-e30f-4722-bef9-8cffb8666491"> <td align="justify" valign="top" styleCode="Lrule Botrule Rrule"> Constipation</td> <td align="center" valign="top" styleCode="Botrule Rrule">3</td> <td align="center" valign="top" styleCode="Botrule Rrule">1</td> </tr> <tr ID="id_c23cf8db-0ac7-4eb0-a022-b78d0c454aec"> <td align="left" valign="top" styleCode="Lrule Botrule Rrule"> <content styleCode="bold">Hemic and Lymphatic System</content> </td> <td align="center" valign="top" styleCode="Botrule Rrule"/> <td align="center" valign="top" styleCode="Botrule Rrule"/> </tr> <tr ID="id_9f084bf1-5f15-42ea-8d18-681ef9bcae7a"> <td align="justify" valign="top" styleCode="Lrule Botrule Rrule"> Ecchymosis</td> <td align="center" valign="top" styleCode="Botrule Rrule">4</td> <td align="center" valign="top" styleCode="Botrule Rrule">1</td> </tr> <tr ID="id_b596bc3e-b986-4bf3-9f98-979be3da72c0"> <td align="justify" valign="top" styleCode="Lrule Botrule Rrule"> <content styleCode="bold">Metabolic and Nutritional</content> </td> <td align="center" valign="top" styleCode="Botrule Rrule"/> <td align="center" valign="top" styleCode="Botrule Rrule"/> </tr> <tr ID="id_6dd567c1-1a50-42dd-adc7-c54db7e29a78"> <td align="justify" valign="top" styleCode="Lrule Botrule Rrule"> Dehydration</td> <td align="center" valign="top" styleCode="Botrule Rrule">2</td> <td align="center" valign="top" styleCode="Botrule Rrule">1</td> </tr> <tr ID="id_e1f087d1-786b-4f07-863e-932af18f3769"> <td align="justify" valign="top" styleCode="Lrule Botrule Rrule"> <content styleCode="bold">Nervous System</content> </td> <td align="center" valign="top" styleCode="Botrule Rrule"/> <td align="center" valign="top" styleCode="Botrule Rrule"/> </tr> <tr ID="id_aad64315-e139-4ed9-bbf3-e1cb7f04b50c"> <td align="justify" valign="top" styleCode="Lrule Botrule Rrule"> Somnolence</td> <td align="center" valign="top" styleCode="Botrule Rrule">23</td> <td align="center" valign="top" styleCode="Botrule Rrule">11</td> </tr> <tr ID="id_8161254c-1c36-4785-bca7-b41ae497ffcc"> <td align="justify" valign="top" styleCode="Lrule Botrule Rrule"> Hostility</td> <td align="center" valign="top" styleCode="Botrule Rrule">12</td> <td align="center" valign="top" styleCode="Botrule Rrule">6</td> </tr> <tr ID="id_8a780759-3cdf-41d8-bb20-b22dc6151c60"> <td align="justify" valign="top" styleCode="Lrule Botrule Rrule"> Nervousness</td> <td align="center" valign="top" styleCode="Botrule Rrule">10</td> <td align="center" valign="top" styleCode="Botrule Rrule">2</td> </tr> <tr ID="id_6d0455be-5bc3-40e2-a51f-c6fc834cdfb0"> <td align="justify" valign="top" styleCode="Lrule Botrule Rrule"> Personality Disorder</td> <td align="center" valign="top" styleCode="Botrule Rrule">8</td> <td align="center" valign="top" styleCode="Botrule Rrule">7</td> </tr> <tr ID="id_0c3e43ab-22d8-4034-8b67-2967eff1eb5e"> <td align="justify" valign="top" styleCode="Lrule Botrule Rrule"> Dizziness</td> <td align="center" valign="top" styleCode="Botrule Rrule">7</td> <td align="center" valign="top" styleCode="Botrule Rrule">2</td> </tr> <tr ID="id_e48600d5-bfcd-46a7-84f6-1af120cd4aad"> <td align="justify" valign="top" styleCode="Lrule Botrule Rrule"> Emotional Lability</td> <td align="center" valign="top" styleCode="Botrule Rrule">6</td> <td align="center" valign="top" styleCode="Botrule Rrule">4</td> </tr> <tr ID="id_fff2501e-7329-4e64-b81a-ff6882f1035e"> <td align="justify" valign="top" styleCode="Lrule Botrule Rrule"> Agitation</td> <td align="center" valign="top" styleCode="Botrule Rrule">6</td> <td align="center" valign="top" styleCode="Botrule Rrule">1</td> </tr> <tr ID="id_a2104b87-fcdf-43ae-ab30-03efa4b0ce5e"> <td align="justify" valign="top" styleCode="Lrule Botrule Rrule"> Depression</td> <td align="center" valign="top" styleCode="Botrule Rrule">3</td> <td align="center" valign="top" styleCode="Botrule Rrule">1</td> </tr> <tr ID="id_5c1cbf43-6362-4496-b66c-dc54651e4707"> <td align="justify" valign="top" styleCode="Lrule Botrule Rrule"> Vertigo</td> <td align="center" valign="top" styleCode="Botrule Rrule">3</td> <td align="center" valign="top" styleCode="Botrule Rrule">1</td> </tr> <tr ID="id_b481702a-bd16-4edf-81e8-041d6bf9acf9"> <td align="justify" valign="top" styleCode="Lrule Botrule Rrule"> Reflexes Increased </td> <td align="center" valign="top" styleCode="Botrule Rrule">2</td> <td align="center" valign="top" styleCode="Botrule Rrule">1</td> </tr> <tr ID="id_81213e3a-8cc9-4862-8664-c3b560f9a0bd"> <td align="justify" valign="top" styleCode="Lrule Botrule Rrule"> Confusion</td> <td align="center" valign="top" styleCode="Botrule Rrule">2</td> <td align="center" valign="top" styleCode="Botrule Rrule">0</td> </tr> <tr ID="id_d3b3a7ae-df50-4a49-a4ab-a37c83d64489"> <td align="justify" valign="top" styleCode="Lrule Botrule Rrule"> <content styleCode="bold">Respiratory System</content> </td> <td align="center" valign="top" styleCode="Botrule Rrule"/> <td align="center" valign="top" styleCode="Botrule Rrule"/> </tr> <tr ID="id_8774b1e6-8de5-427f-a770-a875a45709cf"> <td align="justify" valign="top" styleCode="Lrule Botrule Rrule"> Rhinitis</td> <td align="center" valign="top" styleCode="Botrule Rrule">13</td> <td align="center" valign="top" styleCode="Botrule Rrule">8</td> </tr> <tr ID="id_97956264-5d2e-4bd5-9b0c-5b732ad14939"> <td align="justify" valign="top" styleCode="Lrule Botrule Rrule"> Cough Increased</td> <td align="center" valign="top" styleCode="Botrule Rrule">11</td> <td align="center" valign="top" styleCode="Botrule Rrule">7</td> </tr> <tr ID="id_9e2bffd5-973e-4582-a6f1-c32c48120bcb"> <td align="justify" valign="top" styleCode="Lrule Botrule Rrule"> Pharyngitis</td> <td align="center" valign="top" styleCode="Botrule Rrule">10</td> <td align="center" valign="top" styleCode="Botrule Rrule">8</td> </tr> <tr ID="id_42d5239a-2260-4b7b-a246-06c77c659cf8"> <td align="justify" valign="top" styleCode="Lrule Botrule Rrule"> Asthma</td> <td align="center" valign="top" styleCode="Botrule Rrule">2</td> <td align="center" valign="top" styleCode="Botrule Rrule">1</td> </tr> <tr ID="id_afd7542b-82d4-4ca9-a630-9793480e0362"> <td align="left" valign="top" styleCode="Lrule Botrule Rrule"> <content styleCode="bold">Skin and Appendages</content> </td> <td align="center" valign="top" styleCode="Botrule Rrule"/> <td align="center" valign="top" styleCode="Botrule Rrule"/> </tr> <tr ID="id_70d51b98-d3a3-41d7-83f5-2297ca1608af"> <td align="justify" valign="top" styleCode="Lrule Botrule Rrule"> Pruritis</td> <td align="center" valign="top" styleCode="Botrule Rrule">2</td> <td align="center" valign="top" styleCode="Botrule Rrule">0</td> </tr> <tr ID="id_a667bfcd-a97b-4ea1-a31f-17d6342bb663"> <td align="justify" valign="top" styleCode="Lrule Botrule Rrule"> Skin Discoloration</td> <td align="center" valign="top" styleCode="Botrule Rrule">2</td> <td align="center" valign="top" styleCode="Botrule Rrule">0</td> </tr> <tr ID="id_eb50529e-e7bd-4b1c-9d88-22419b22dde9"> <td align="justify" valign="top" styleCode="Lrule Botrule Rrule"> Vesiculobullous Rash</td> <td align="center" valign="top" styleCode="Botrule Rrule">2</td> <td align="center" valign="top" styleCode="Botrule Rrule">0</td> </tr> <tr ID="id_8c75b98d-dc1c-4af6-9bf4-7ae9c5787292"> <td align="justify" valign="top" styleCode="Lrule Botrule Rrule"> <content styleCode="bold">Special Senses</content> </td> <td align="center" valign="top" styleCode="Botrule Rrule"/> <td align="center" valign="top" styleCode="Botrule Rrule"/> </tr> <tr ID="id_5ae93bd5-ef11-4263-923e-7970375a68b6"> <td align="justify" valign="top" styleCode="Lrule Botrule Rrule"> Conjunctivits</td> <td align="center" valign="top" styleCode="Botrule Rrule">3</td> <td align="center" valign="top" styleCode="Botrule Rrule">2</td> </tr> <tr ID="id_a8cfa81a-0240-47b4-aa12-a7421ad06512"> <td align="justify" valign="top" styleCode="Lrule Botrule Rrule"> Amblyopia</td> <td align="center" valign="top" styleCode="Botrule Rrule">2</td> <td align="center" valign="top" styleCode="Botrule Rrule">0</td> </tr> <tr ID="id_6452f9f5-4577-4d3c-809a-d610b3f0a827"> <td align="justify" valign="top" styleCode="Lrule Botrule Rrule"> Ear Pain</td> <td align="center" valign="top" styleCode="Botrule Rrule">2</td> <td align="center" valign="top" styleCode="Botrule Rrule">0</td> </tr> <tr ID="id_e98c9770-a073-4f63-833d-0c03e777377a"> <td align="left" valign="top" styleCode="Lrule Botrule Rrule"> <content styleCode="bold">Urogenital System</content> </td> <td align="center" valign="top" styleCode="Botrule Rrule"/> <td align="center" valign="top" styleCode="Botrule Rrule"/> </tr> <tr ID="id_38ae17f7-d3e1-49f8-b01e-00e49a204cf7"> <td align="justify" valign="top" styleCode="Lrule Botrule Rrule"> Albuminuria</td> <td align="center" valign="top" styleCode="Botrule Rrule">4</td> <td align="center" valign="top" styleCode="Botrule Rrule">0</td> </tr> <tr ID="id_997efc1e-a9f0-4223-8aa4-ccddada8cb37"> <td align="justify" valign="top" styleCode="Lrule Botrule Rrule"> Urine Abnormality</td> <td align="center" valign="top" styleCode="Rrule">2</td> <td align="center" valign="top" styleCode="Botrule Rrule">1</td> </tr> </tbody> </table>

adverse reactions table

<table border="single" width="521" ID="id_4132536d-5e33-4f4a-a96f-38ea9573d794"> <caption ID="id_1850299d-78cf-456e-8fb1-9cb0a09a8d2b">Table 8: Adverse Events that most commonly resulted in Discontinuation or Dose Reduction in Placebo-Controlled Studies in Adult Patients with Epilepsy Experiencing Partial Onset Seizures</caption> <col width="39.0%"/> <col width="34.7%"/> <col width="26.3%"/> <tbody> <tr ID="id_ecac3a74-8c53-438e-8eab-b024408b8590"> <td align="justify" valign="top" rowspan="2" styleCode="Botrule Toprule Rrule Lrule"/> <td align="center" valign="top" colspan="2" styleCode="Botrule Rrule"> <content styleCode="bold">Number (%)</content> </td> </tr> <tr ID="id_3ecc3f53-7f2b-4596-8ba6-891bb2edca55"> <td align="center" valign="top" styleCode="Lrule Botrule Rrule"> <paragraph> <content styleCode="bold">Levetiracetam </content> </paragraph> <content styleCode="bold">(N=769)</content> </td> <td align="center" valign="top" styleCode="Botrule Rrule"> <paragraph> <content styleCode="bold">Placebo</content> </paragraph> <content styleCode="bold">(N=439)</content> </td> </tr> <tr ID="id_e0c8015d-a9d0-44c5-ba2f-81b6987357cc"> <td align="justify" valign="top" styleCode="Lrule Botrule Rrule">Asthenia</td> <td align="center" valign="top" styleCode="Botrule Rrule">10 (1.3%)</td> <td align="center" valign="top" styleCode="Botrule Rrule">3 (0.7%)</td> </tr> <tr ID="id_a441c402-a77e-4585-a443-71cc00dff46f"> <td align="justify" valign="top" styleCode="Lrule Botrule Rrule">Convulsion</td> <td align="center" valign="top" styleCode="Botrule Rrule">23 (3.0%)</td> <td align="center" valign="top" styleCode="Botrule Rrule">15 (3.4%)</td> </tr> <tr ID="id_a15dbd1f-c6ad-44ff-9425-970bd1b961ea"> <td align="justify" valign="top" styleCode="Lrule Botrule Rrule">Dizziness</td> <td align="center" valign="top" styleCode="Botrule Rrule">11 (1.4%)</td> <td align="center" valign="top" styleCode="Botrule Rrule">0 </td> </tr> <tr ID="id_c520e5c6-19b0-483e-ba9b-3cfd922902cc"> <td align="justify" valign="top" styleCode="Lrule Botrule Rrule">Rash</td> <td align="center" valign="top" styleCode="Botrule Rrule">0</td> <td align="center" valign="top" styleCode="Botrule Rrule">5 (1.1%)</td> </tr> <tr ID="id_2acd1e00-8032-4531-9e73-f0ca717c799b"> <td align="justify" valign="top" styleCode="Lrule Botrule Rrule">Somnolence</td> <td align="center" valign="top" styleCode="Rrule">34 (4.4%)</td> <td align="center" valign="top" styleCode="Botrule Rrule">7 (1.6%)</td> </tr> </tbody> </table>