FDA label e2080615-8066-4141-836c-3c40e7c81f29

5 WARNINGS AND PRECAUTIONS • Hepatic adverse reactions were reported with the use of the combination regimen of Pretomanid Tablets, bedaquiline, and linezolid. Monitor symptoms and signs and liver-related laboratory tests. Interrupt treatment with the entire regimen if evidence of liver injury occurs. ( 5.2 ) • Myelosuppression was reported with the use of the combination regimen of Pretomanid Tablets, bedaquiline, and linezolid. Monitor complete blood counts. Decrease or interrupt linezolid dosing if significant myelosuppression develops or worsens. ( 5.3 ) • Peripheral and optic neuropathy were reported with the use of the combination regimen of Pretomanid Tablets, bedaquiline, and linezolid. Monitor visual function. Obtain an ophthalmologic evaluation if there are symptoms of visual impairment. Decrease or interrupt linezolid dosing if neuropathy develops or worsens. ( 5.4 ) • QT prolongation was reported with the use of the combination regimen of Pretomanid Tablets, bedaquiline, and linezolid. Use with drugs that prolong the QT interval may cause additive QT prolongation. Monitor ECGs. Discontinue the combination regimen of Pretomanid Tablets, bedaquiline, and linezolid if significant ventricular arrhythmia or if QTcF interval prolongation of greater than 500 ms develops. ( 5.5 ) • Reproductive effects: Pretomanid caused testicular atrophy and impaired fertility in male rats. Advise patients of reproductive toxicities seen in animal studies and that the potential effects on human male fertility have not been adequately evaluated. ( 5.7 , 13.1 ) • Lactic acidosis was reported with the use of the combination regimen of Pretomanid Tablets, bedaquiline, and linezolid. Consider interrupting linezolid or the entire combination regimen of Pretomanid Tablets, bedaquiline, and linezolid dosing if significant lactic acidosis develops. ( 5.8 ) 5.1 Risks Associated with the Combination Treatment Regimen Pretomanid Tablet is indicated for use as part of a regimen in combination with bedaquiline and linezolid. Refer to the prescribing information for bedaquiline and linezolid for additional risk information. Warnings and Precautions related to bedaquiline and linezolid also apply to their use in the combination regimen with Pretomanid Tablets. 5.2 Hepatotoxicity Hepatic adverse reactions were reported with the combination regimen of Pretomanid Tablets, bedaquiline, and linezolid [ see Warnings and Precautions (5.1) , and Adverse Reactions (6.1) ] . Avoid alcohol and hepatotoxic agents, including herbal supplements and drugs other than bedaquiline and linezolid [see Indications and Usage (1) ] while on Pretomanid Tablets, especially in patients with impaired hepatic function. Monitor symptoms and signs (such as fatigue, anorexia, nausea, jaundice, dark urine, liver tenderness, and hepatomegaly) and laboratory tests (ALT, AST, alkaline phosphatase, and bilirubin) at a minimum at baseline, at two weeks, and then monthly while on treatment and as needed. If evidence of new or worsening liver dysfunction occurs, test for viral hepatitides and discontinue other hepatotoxic medications. Interrupt treatment with the entire regimen if: • Aminotransferase elevations are accompanied by total bilirubin elevation greater than 2 times the upper limit of normal. • Aminotransferase elevations are greater than 8 times the upper limit of normal. • Aminotransferase elevations are greater than 5 times the upper limit of normal and persist beyond 2 weeks. 5.3 Myelosuppression Myelosuppression (including anemia, leukopenia, thrombocytopenia, and pancytopenia) was reported with the combination regimen of Pretomanid Tablets, bedaquiline, and linezolid. Myelosuppression is a known adverse reaction of linezolid. Anemia can be life threatening [see Warnings and Precautions (5.1) , and Adverse Reactions (6.1) ] . When linezolid dosing, as part of the combination regimen of Pretomanid Tablets, bedaquiline, and linezolid, was reduced, interrupted, or discontinued, the observed hematologic abnormalities were reversible. Complete blood counts should be monitored at a minimum at baseline, at two weeks, and then monthly in patients receiving linezolid as part of the combination regimen of Pretomanid Tablets, bedaquiline, and linezolid, and decreasing or interrupting linezolid dosing should be considered in patients who develop or have worsening myelosuppression [see Dosage and Administration (2.2) ] . 5.4 Peripheral and Optic Neuropathy Peripheral neuropathy and optic neuropathy were reported with the combination regimen of Pretomanid Tablets, bedaquiline, and linezolid [see Warnings and Precautions (5.1) , and Adverse Reactions (6.1) ] . Neuropathy is a known adverse reaction of long-term linezolid use. Neuropathy associated with linezolid is generally reversible or improved with appropriate monitoring and interruption, dose reduction, or discontinuation of linezolid dosing. Monitor visual function in all patients receiving the combination regimen of Pretomanid Tablets, bedaquiline, and linezolid; if a patient experiences symptoms of visual impairment, interrupt linezolid dosing and obtain prompt ophthalmologic evaluation. 5.5 QT Prolongation QT prolongation was reported with the combination regimen of Pretomanid Tablets, bedaquiline, and linezolid [see Warnings and Precautions (5.1) , Adverse Reactions (6.1) , and Clinical Pharmacology (12.2) ] . QT prolongation is a known adverse reaction of bedaquiline. Obtain an ECG before initiation of treatment, and at least 2, 12, and 24 weeks after starting treatment with the combination regimen of Pretomanid Tablets, bedaquiline, and linezolid. Obtain serum potassium, calcium, and magnesium at baseline and correct if abnormal. Monitor these electrolytes if QT prolongation is detected [see Adverse Reactions (6.1) ] . The following may increase the risk for QT prolongation when patients are receiving bedaquiline as part of the combination regimen of Pretomanid Tablets, bedaquiline, and linezolid: a history of Torsade de Pointes, congenital long QT syndrome, ongoing hypothyroidism, ongoing bradyarrhythmia, uncompensated heart failure, or serum calcium, magnesium, or potassium levels below the lower limits of normal. If necessary, bedaquiline treatment initiation could be considered in these patients after a favorable benefit-risk assessment and with frequent ECG monitoring. Discontinue the combination regimen of Pretomanid Tablets, bedaquiline, and linezolid if the patient develops clinically significant ventricular arrhythmia or a QTcF interval of greater than 500 ms (confirmed by repeat ECG). If syncope occurs, obtain an ECG to detect QT prolongation. 5.6 Drug Interactions CYP3A4 Inducers Pretomanid may be in part metabolized by CYP3A4 [see Drug Interactions (7.1) and Clinical Pharmacology 12.3) ]. Avoid co-administration of strong or moderate CYP3A4 inducers, such as rifampin or efavirenz, during treatment with pretomanid. 5.7 Reproductive Effects Pretomanid caused testicular atrophy and impaired fertility in male rats. Advise patients of reproductive toxicities seen in animal studies and that the potential effects on human male fertility have not been adequately evaluated [see Use in Specific Populations (8.3) and Nonclinical Toxicology (13.1) ] . 5.8 Lactic Acidosis Lactic acidosis was reported with the combination regimen of Pretomanid Tablets, bedaquiline, and linezolid [see Warnings and Precautions (5.1) and Adverse Reactions (6.1) ] . Lactic acidosis is a known adverse reaction of linezolid. Patients who develop recurrent nausea or vomiting should receive immediate medical evaluation, including evaluation of bicarbonate and lactic acid levels, and interruption of linezolid or the entire combination regimen of Pretomanid Tablets, bedaquiline, and linezolid should be considered.

6 ADVERSE REACTIONS The following serious adverse reactions are discussed here and elsewhere in the labeling: • Hepatotoxicity [see Warnings and Precautions (5.2) ] • Myelosuppression [see Warnings and Precautions (5.3) ] • Peripheral and Optic Neuropathy [see Warnings and Precautions (5.4) ] • QT Prolongation [see Warnings and Precautions (5.5) ] • Reproductive Effects [see Warnings and Precautions (5.7) ] • Lactic Acidosis [see Warnings and Precautions (5.8) ] Most common adverse reactions (≥10%) are peripheral neuropathy, acne, anemia, nausea, vomiting, headache, increased transaminases, dyspepsia, decreased appetite, rash, pruritus, abdominal pain, pleuritic pain, increased gamma-glutamyltransferase, lower respiratory tract infection, hyperamylasemia, hemoptysis, back pain, cough, visual impairment, hypoglycemia, abnormal loss of weight, and diarrhea. ( 6 ) To report SUSPECTED ADVERSE REACTIONS, contact Mylan at 1-877-446-3679 (1-877-4-INFO-RX) or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch. 6.1 Clinical Trials Experience Because clinical studies are conducted under widely varying conditions, adverse reaction rates observed in the clinical studies of a drug cannot be directly compared to the rates in the clinical studies of another drug and may not reflect the rates observed in clinical practice. When Pretomanid Tablets are administered in combination with bedaquiline and linezolid, refer to the prescribing information for the respective drugs for a description of the adverse reactions associated with their use. A total of 1168 subjects, 879 patients with tuberculosis and 289 healthy volunteers, have been exposed to Pretomanid Tablets, either alone or as part of a combination therapy in 19 trials. Study 1 (NCT02333799) was a single-arm, open-label study conducted in three sites in South Africa in which patients with XDR, treatment-intolerant MDR, or non-responsive MDR pulmonary TB received the combination regimen of Pretomanid Tablets, bedaquiline, and linezolid for 6 months (extendable to 9 months) with 24 months of follow-up. One hundred and nine subjects were treated; 76% were black, and 23% were of mixed race. Their ages ranged from 17 years to 60 years (mean 36 years), and all patients were from South Africa. Fifty-six (51%) patients were HIV-positive. There were 8 deaths. Six patients died while receiving treatment; all surviving patients, excluding one patient who withdrew consent, completed treatment. Two patients died during follow-up at Day 369 and Day 486, respectively. Common Adverse Reactions Reported in Study 1 Table 1 summarizes the incidence of select adverse reactions occurring in ≥5% of patients in Study 1. Table 1: Select Adverse Reactions (All Grades) Reported in ≥5% of Subjects Receiving the Combination Regimen of Pretomanid Tablets, Bedaquiline, and Linezolid in Study 1 Pretomanid Tablets, Bedaquiline and Linezolid Combination Regimen (N = 109) Adverse Reactions All Grades n (%) Peripheral neuropathy Select terms are collapsed, as follows: peripheral neuropathy (burning sensation, hypoesthesia, hyporeflexia, neuropathy peripheral, paresthesia, peripheral motor neuropathy, peripheral sensorimotor neuropathy, peripheral sensory neuropathy); acne (acne, dermatitis acneiform); anemia (anemia); musculoskeletal pain (arthralgia, back pain, costochondritis, myalgia, pain in extremity); transaminases increased (alanine aminotransferase [ALT]) increased, aspartate aminotransferase [AST] increased, drug-induced liver injury, hepatic enzyme increased, hepatic function abnormal, liver function test increased, transaminases increased); rash (rash, rash erythematous, rash maculo-papular, rash papular, rash vesicular); pruritus (pruritus, pruritus generalized, rash pruritic); abdominal pain (abdominal pain, abdominal pain lower, abdominal pain upper, abdominal tenderness); lower respiratory tract infection (bronchitis, influenza, lower respiratory tract infection, pneumonia); hyperamylasemia (amylase increased, hyperamylasemia); cough (cough, productive cough); visual impairment (vision blurred, visual acuity reduced, visual impairment); neutropenia (neutropenia); hypertension (blood pressure increased, hypertension); hyperlipasemia (hyperlipasemia, lipase increased); thrombocytopenia (thrombocytopenia). 88 (81) Acne 42 (39) Anemia 40 (37) Nausea 40 (37) Vomiting 37 (34) Musculoskeletal Pain 32 (29) Headache 30 (28) Transaminases increased 30 (28) Dyspepsia 26 (24) Decreased appetite 24 (22) Rash 23 (21) Pruritus 22 (20) Abdominal pain 21 (19) Pleuritic pain 21 (19) Gamma-glutamyltransferase increased 19 (17) Lower respiratory tract infection 16 (15) Hyperamylasemia 15 (14) Hemoptysis 14 (13) Cough 13 (12) Visual impairment 13 (12) Hypoglycemia 12 (11) Abnormal loss of weight 11 (10) Diarrhea 11 (10) Constipation 9 (8) Gastritis 9 (8) Neutropenia 9 (8) Dry skin 8 (7) Hypertension 8 (7) Electrocardiogram QT prolonged 6 (6) Hyperlipasemia 6 (6) Insomnia 6 (6) Thrombocytopenia 6 (6) The following select adverse reactions were reported in patients receiving the combination regimen of Pretomanid Tablets, bedaquiline and linezolid at a rate of less than 5% in Study 1: Gastrointestinal Disorders: pancreatitis, dysgeusia Laboratory Investigations : blood creatine phosphokinase increase, blood creatinine increase, blood alkaline phosphatase increase Blood and Lymphatic System Disorders: leukopenia Metabolism and Nutrition Disorders: hypomagnesemia, hyperglycemia, hypokalemia, hyperkalemia, hyponatremia Nervous System Disorders : dizziness, seizure Laboratory Abnormalities Reported in Study 1 Table 2 summarizes select laboratory abnormalities. Table 2: Select Laboratory Abnormalities in Study 1 Parameter Multiples of Upper Limit of Normal (× ULN) Combination Regimen of Pretomanid Tablets, Bedaquiline, and Linezolid (N = 109) n (%) ULN = upper limit of normal Transaminases and Bilirubin Alanine Aminotransferase (ALT) >3 and ≤ 5 × ULN 6 (6) >5 and ≤ 8 × ULN 5 (5) >8 × ULN 1 (1) Aspartate Aminotransferase (AST) >3 and ≤ 5 × ULN 7 (6) >5 and ≤ 8 × ULN 2 (2) >8 × ULN 1 (1) Total Bilirubin >1 × ULN and ≤ 2 × ULN 6 (6) >2 × ULN 2 (2) Hematology Hemoglobin ≤7.9 mg/dL 6 (6) Neutrophils Absolute Count ≤749/mm 3 5 (5) Platelets ≤49,999/mm 3 2 (2) Serum Chemistry Lipase > 2 × ULN 5 (5) In Study 1, 28% of patients experienced increased transaminases. Except for one patient who died due to pneumonia and sepsis, all patients who experienced increased transaminases were able to continue therapy and complete the full course of treatment. Myelosuppression is a known adverse reaction of linezolid. The most common hematopoietic cytopenia was anemia (37%). The majority of cytopenias began after 2 weeks of treatment. Three patients experienced cytopenias that were considered serious: neutropenia in 1 patient and anemia in 2 patients. All 3 serious adverse reactions resulted in interruption of linezolid or all components of the combination regimen of Pretomanid Tablets, bedaquiline, and linezolid, and all resolved. Peripheral and Optic Neuropathy Peripheral neuropathy is a known adverse reaction of linezolid. In Study 1, peripheral neuropathy was reported in 81% of patients. Most of these adverse reactions (64%) occurred after 8 weeks of treatment and resulted in dosing interruption, dose reduction, or discontinuation of linezolid. Severe, moderate, and mild peripheral neuropathy occurred in 22%, 32%, and 26% of patients, respectively. No adverse reaction related to peripheral neuropathy led to a discontinuation of the entire study regimen. Optic neuropathy is a known adverse reaction of linezolid. Two patients (2%) in Study 1 developed optic neuropathy after 16 weeks of treatment. Both were serious, confirmed on retinal examination as optic neuropathy/neuritis, and resulted in discontinuation of linezolid; both adverse reactions resolved. Overall, patients administered a linezolid dose of 600 mg twice daily had a similar safety profile to those administered a dose of 1,200 mg once daily.

<table ID="_RefID0EMJAE" width="75%"> <caption>Table 1: Select Adverse Reactions (All Grades) Reported in &#x2265;5% of Subjects Receiving the Combination Regimen of Pretomanid Tablets, Bedaquiline, and Linezolid in Study 1</caption> <col width="40%"/> <col width="47%"/> <thead> <tr> <th align="left" styleCode="Rrule Botrule Lrule Toprule " valign="top"/> <th align="left" styleCode="Rrule Botrule Toprule " valign="top"> <content styleCode="bold">Pretomanid Tablets, Bedaquiline and Linezolid Combination Regimen</content> <content styleCode="bold">(N = 109)</content> </th> </tr> <tr> <th align="left" styleCode="Rrule Lrule Botrule " valign="top"> <content styleCode="bold">Adverse Reactions</content> </th> <th align="left" styleCode="Rrule Botrule " valign="top"> <content styleCode="bold">All Grades</content> <content styleCode="bold">n (%)</content> </th> </tr> </thead> <tbody> <tr> <td styleCode="Rrule Lrule Toprule Botrule " valign="top"> <paragraph> Peripheral neuropathy<footnote ID="_Reffoot11">Select terms are collapsed, as follows: <content styleCode="bold">peripheral neuropathy</content> (burning sensation, hypoesthesia, hyporeflexia, neuropathy peripheral, paresthesia, peripheral motor neuropathy, peripheral sensorimotor neuropathy, peripheral sensory neuropathy); <content styleCode="bold">acne</content> (acne, dermatitis acneiform);<content styleCode="bold"> anemia</content> (anemia); <content styleCode="bold">musculoskeletal pain</content> (arthralgia, back pain, costochondritis, myalgia, pain in extremity); <content styleCode="bold">transaminases increased</content> (alanine aminotransferase [ALT]) increased, aspartate aminotransferase [AST] increased, drug-induced liver injury, hepatic enzyme increased, hepatic function abnormal, liver function test increased, transaminases increased); <content styleCode="bold">rash</content> (rash, rash erythematous, rash maculo-papular, rash papular, rash vesicular); <content styleCode="bold">pruritus</content> (pruritus, pruritus generalized, rash pruritic); <content styleCode="bold">abdominal pain</content> (abdominal pain, abdominal pain lower, abdominal pain upper, abdominal tenderness); <content styleCode="bold">lower respiratory tract infection</content> (bronchitis, influenza, lower respiratory tract infection, pneumonia); <content styleCode="bold">hyperamylasemia </content>(amylase increased, hyperamylasemia);<content styleCode="bold">cough</content> (cough, productive cough); <content styleCode="bold">visual impairment</content> (vision blurred, visual acuity reduced, visual impairment); <content styleCode="bold">neutropenia</content> (neutropenia); <content styleCode="bold">hypertension</content> (blood pressure increased, hypertension); <content styleCode="bold">hyperlipasemia</content> (hyperlipasemia, lipase increased); <content styleCode="bold">thrombocytopenia </content>(thrombocytopenia).</footnote> </paragraph> </td> <td styleCode="Rrule Toprule Botrule " valign="top"> <paragraph>88 (81)</paragraph> </td> </tr> <tr> <td styleCode="Rrule Lrule Botrule " valign="top"> <paragraph> Acne<footnoteRef IDREF="_Reffoot11"/> </paragraph> </td> <td styleCode="Rrule Botrule " valign="top"> <paragraph>42 (39)</paragraph> </td> </tr> <tr> <td styleCode="Rrule Lrule Botrule " valign="top"> <paragraph> Anemia<footnoteRef IDREF="_Reffoot11"/> </paragraph> </td> <td styleCode="Rrule Botrule " valign="top"> <paragraph>40 (37)</paragraph> </td> </tr> <tr> <td styleCode="Rrule Lrule Botrule " valign="top"> <paragraph> Nausea</paragraph> </td> <td styleCode="Rrule Botrule " valign="top"> <paragraph>40 (37)</paragraph> </td> </tr> <tr> <td styleCode="Rrule Lrule Botrule " valign="top"> <paragraph> Vomiting</paragraph> </td> <td styleCode="Rrule Botrule " valign="top"> <paragraph>37 (34)</paragraph> </td> </tr> <tr> <td styleCode="Rrule Lrule Botrule " valign="top"> <paragraph> Musculoskeletal Pain<footnoteRef IDREF="_Reffoot11"/> </paragraph> </td> <td styleCode="Rrule Botrule " valign="top"> <paragraph>32 (29)</paragraph> </td> </tr> <tr> <td styleCode="Rrule Lrule Botrule " valign="top"> <paragraph> Headache</paragraph> </td> <td styleCode="Rrule Botrule " valign="top"> <paragraph>30 (28)</paragraph> </td> </tr> <tr> <td styleCode="Rrule Lrule Botrule " valign="top"> <paragraph> Transaminases increased<footnoteRef IDREF="_Reffoot11"/> </paragraph> </td> <td styleCode="Rrule Botrule " valign="top"> <paragraph>30 (28)</paragraph> </td> </tr> <tr> <td styleCode="Rrule Lrule Botrule " valign="top"> <paragraph> Dyspepsia</paragraph> </td> <td styleCode="Rrule Botrule " valign="top"> <paragraph>26 (24)</paragraph> </td> </tr> <tr> <td styleCode="Rrule Lrule Botrule " valign="top"> <paragraph> Decreased appetite</paragraph> </td> <td styleCode="Rrule Botrule " valign="top"> <paragraph>24 (22)</paragraph> </td> </tr> <tr> <td styleCode="Rrule Lrule Botrule " valign="top"> <paragraph> Rash<footnoteRef IDREF="_Reffoot11"/> </paragraph> </td> <td styleCode="Rrule Botrule " valign="top"> <paragraph>23 (21)</paragraph> </td> </tr> <tr> <td styleCode="Rrule Lrule Botrule " valign="top"> <paragraph> Pruritus<footnoteRef IDREF="_Reffoot11"/> </paragraph> </td> <td styleCode="Rrule Botrule " valign="top"> <paragraph>22 (20)</paragraph> </td> </tr> <tr> <td styleCode="Rrule Lrule Botrule " valign="top"> <paragraph> Abdominal pain<footnoteRef IDREF="_Reffoot11"/> </paragraph> </td> <td styleCode="Rrule Botrule " valign="top"> <paragraph>21 (19)</paragraph> </td> </tr> <tr> <td styleCode="Rrule Lrule Botrule " valign="top"> <paragraph> Pleuritic pain</paragraph> </td> <td styleCode="Rrule Botrule " valign="top"> <paragraph>21 (19)</paragraph> </td> </tr> <tr> <td styleCode="Rrule Lrule Botrule " valign="top"> <paragraph> Gamma-glutamyltransferase increased</paragraph> </td> <td styleCode="Rrule Botrule " valign="top"> <paragraph>19 (17)</paragraph> </td> </tr> <tr> <td styleCode="Rrule Lrule Botrule " valign="top"> <paragraph> Lower respiratory tract infection<footnoteRef IDREF="_Reffoot11"/> </paragraph> </td> <td styleCode="Rrule Botrule " valign="top"> <paragraph>16 (15)</paragraph> </td> </tr> <tr> <td styleCode="Rrule Lrule Botrule " valign="top"> <paragraph> Hyperamylasemia<footnoteRef IDREF="_Reffoot11"/> </paragraph> </td> <td styleCode="Rrule Botrule " valign="top"> <paragraph>15 (14)</paragraph> </td> </tr> <tr> <td styleCode="Rrule Lrule Botrule " valign="top"> <paragraph> Hemoptysis</paragraph> </td> <td styleCode="Rrule Botrule " valign="top"> <paragraph>14 (13)</paragraph> </td> </tr> <tr> <td styleCode="Rrule Lrule Botrule " valign="top"> <paragraph> Cough<footnoteRef IDREF="_Reffoot11"/> </paragraph> </td> <td styleCode="Rrule Botrule " valign="top"> <paragraph>13 (12)</paragraph> </td> </tr> <tr> <td styleCode="Rrule Lrule Botrule " valign="top"> <paragraph> Visual impairment<footnoteRef IDREF="_Reffoot11"/> </paragraph> </td> <td styleCode="Rrule Botrule " valign="top"> <paragraph>13 (12)</paragraph> </td> </tr> <tr> <td styleCode="Rrule Lrule Botrule " valign="top"> <paragraph> Hypoglycemia</paragraph> </td> <td styleCode="Rrule Botrule " valign="top"> <paragraph>12 (11)</paragraph> </td> </tr> <tr> <td styleCode="Rrule Lrule Botrule " valign="top"> <paragraph> Abnormal loss of weight</paragraph> </td> <td styleCode="Rrule Botrule " valign="top"> <paragraph>11 (10)</paragraph> </td> </tr> <tr> <td styleCode="Rrule Lrule Botrule " valign="top"> <paragraph> Diarrhea</paragraph> </td> <td styleCode="Rrule Botrule " valign="top"> <paragraph>11 (10)</paragraph> </td> </tr> <tr> <td styleCode="Rrule Lrule Botrule " valign="top"> <paragraph> Constipation</paragraph> </td> <td styleCode="Rrule Botrule " valign="top"> <paragraph>9 (8)</paragraph> </td> </tr> <tr> <td styleCode="Rrule Lrule Botrule " valign="top"> <paragraph> Gastritis</paragraph> </td> <td styleCode="Rrule Botrule " valign="top"> <paragraph>9 (8)</paragraph> </td> </tr> <tr> <td styleCode="Rrule Lrule Botrule " valign="top"> <paragraph> Neutropenia<footnoteRef IDREF="_Reffoot11"/> </paragraph> </td> <td styleCode="Rrule Botrule " valign="top"> <paragraph>9 (8)</paragraph> </td> </tr> <tr> <td styleCode="Rrule Lrule Botrule " valign="top"> <paragraph> Dry skin</paragraph> </td> <td styleCode="Rrule Botrule " valign="top"> <paragraph>8 (7)</paragraph> </td> </tr> <tr> <td styleCode="Rrule Lrule Botrule " valign="top"> <paragraph> Hypertension<footnoteRef IDREF="_Reffoot11"/> </paragraph> </td> <td styleCode="Rrule Botrule " valign="top"> <paragraph>8 (7)</paragraph> </td> </tr> <tr> <td styleCode="Rrule Lrule Botrule " valign="top"> <paragraph> Electrocardiogram QT prolonged</paragraph> </td> <td styleCode="Rrule Botrule " valign="top"> <paragraph>6 (6)</paragraph> </td> </tr> <tr> <td styleCode="Rrule Lrule Botrule " valign="top"> <paragraph> Hyperlipasemia<footnoteRef IDREF="_Reffoot11"/> </paragraph> </td> <td styleCode="Rrule Botrule " valign="top"> <paragraph>6 (6)</paragraph> </td> </tr> <tr> <td styleCode="Rrule Lrule Botrule " valign="top"> <paragraph> Insomnia</paragraph> </td> <td styleCode="Rrule Botrule " valign="top"> <paragraph>6 (6)</paragraph> </td> </tr> <tr> <td styleCode="Rrule Botrule Lrule " valign="top"> <paragraph> Thrombocytopenia<footnoteRef IDREF="_Reffoot11"/> </paragraph> </td> <td styleCode="Rrule Botrule " valign="top"> <paragraph>6 (6)</paragraph> </td> </tr> </tbody> </table>

<table ID="_RefID0EQUAE" width="60%"> <caption>Table 2: Select Laboratory Abnormalities in Study 1</caption> <col width="30%"/> <col width="39%"/> <thead> <tr> <th align="center" styleCode="Rrule Botrule Lrule Toprule " valign="top"> <content styleCode="bold">Parameter</content> <content styleCode="bold">Multiples of Upper Limit of Normal (&#xD7; ULN)</content> </th> <th align="left" styleCode="Rrule Botrule Toprule " valign="top"> <content styleCode="bold">Combination Regimen of Pretomanid Tablets, Bedaquiline, and Linezolid</content> <content styleCode="bold">(N = 109)</content> <content styleCode="bold">n (%)</content> </th> </tr> </thead> <tfoot> <tr> <td align="left" colspan="2" styleCode="Botrule" valign="top">ULN = upper limit of normal</td> </tr> </tfoot> <tbody> <tr> <td styleCode="Rrule Lrule Toprule Botrule " valign="top"> <paragraph> <content styleCode="bold">Transaminases and Bilirubin</content> </paragraph> </td> <td styleCode="Rrule Toprule Botrule " valign="top"/> </tr> <tr> <td styleCode="Rrule Lrule Botrule " valign="top"> <paragraph>Alanine Aminotransferase (ALT)</paragraph> </td> <td styleCode="Rrule Botrule " valign="top"/> </tr> <tr> <td styleCode="Rrule Lrule Botrule " valign="top"> <paragraph> &gt;3 and &#x2264; 5 &#xD7; ULN</paragraph> </td> <td styleCode="Rrule Botrule " valign="top"> <paragraph>6 (6)</paragraph> </td> </tr> <tr> <td styleCode="Rrule Lrule Botrule " valign="top"> <paragraph> &gt;5 and &#x2264; 8 &#xD7; ULN</paragraph> </td> <td styleCode="Rrule Botrule " valign="top"> <paragraph>5 (5)</paragraph> </td> </tr> <tr> <td styleCode="Rrule Lrule Botrule " valign="top"> <paragraph> &gt;8 &#xD7; ULN</paragraph> </td> <td styleCode="Rrule Botrule " valign="top"> <paragraph>1 (1)</paragraph> </td> </tr> <tr> <td styleCode="Rrule Lrule Botrule " valign="top"> <paragraph>Aspartate Aminotransferase (AST)</paragraph> </td> <td styleCode="Rrule Botrule " valign="top"/> </tr> <tr> <td styleCode="Rrule Lrule Botrule " valign="top"> <paragraph> &gt;3 and &#x2264; 5 &#xD7; ULN</paragraph> </td> <td styleCode="Rrule Botrule " valign="top"> <paragraph>7 (6)</paragraph> </td> </tr> <tr> <td styleCode="Rrule Lrule Botrule " valign="top"> <paragraph> &gt;5 and &#x2264; 8 &#xD7; ULN</paragraph> </td> <td styleCode="Rrule Botrule " valign="top"> <paragraph>2 (2)</paragraph> </td> </tr> <tr> <td styleCode="Rrule Lrule Botrule " valign="top"> <paragraph> &gt;8 &#xD7; ULN</paragraph> </td> <td styleCode="Rrule Botrule " valign="top"> <paragraph>1 (1)</paragraph> </td> </tr> <tr> <td styleCode="Rrule Lrule Botrule " valign="top"> <paragraph>Total Bilirubin</paragraph> </td> <td styleCode="Rrule Botrule " valign="top"/> </tr> <tr> <td styleCode="Rrule Lrule Botrule " valign="top"> <paragraph> &gt;1 &#xD7; ULN and &#x2264; 2 &#xD7; ULN</paragraph> </td> <td styleCode="Rrule Botrule " valign="top"> <paragraph>6 (6)</paragraph> </td> </tr> <tr> <td styleCode="Rrule Lrule Botrule " valign="top"> <paragraph> &gt;2 &#xD7; ULN</paragraph> </td> <td styleCode="Rrule Botrule " valign="top"> <paragraph>2 (2)</paragraph> </td> </tr> <tr> <td styleCode="Rrule Lrule Botrule " valign="top"> <paragraph> <content styleCode="bold">Hematology </content> </paragraph> </td> <td styleCode="Rrule Botrule " valign="top"/> </tr> <tr> <td styleCode="Rrule Lrule Botrule " valign="top"> <paragraph>Hemoglobin</paragraph> </td> <td styleCode="Rrule Botrule " valign="top"/> </tr> <tr> <td styleCode="Rrule Lrule Botrule " valign="top"> <paragraph> &#x2264;7.9 mg/dL</paragraph> </td> <td styleCode="Rrule Botrule " valign="top"> <paragraph>6 (6)</paragraph> </td> </tr> <tr> <td styleCode="Rrule Lrule Botrule " valign="top"> <paragraph>Neutrophils Absolute Count</paragraph> </td> <td styleCode="Rrule Botrule " valign="top"/> </tr> <tr> <td styleCode="Rrule Lrule Botrule " valign="top"> <paragraph> &#x2264;749/mm³ </paragraph> </td> <td styleCode="Rrule Botrule " valign="top"> <paragraph>5 (5)</paragraph> </td> </tr> <tr> <td styleCode="Rrule Lrule Botrule " valign="top"> <paragraph>Platelets</paragraph> </td> <td styleCode="Rrule Botrule " valign="top"/> </tr> <tr> <td styleCode="Rrule Lrule Botrule " valign="top"> <paragraph> &#x2264;49,999/mm³ </paragraph> </td> <td styleCode="Rrule Botrule " valign="top"> <paragraph>2 (2)</paragraph> </td> </tr> <tr> <td styleCode="Rrule Lrule Botrule " valign="top"> <paragraph> <content styleCode="bold">Serum Chemistry</content> </paragraph> </td> <td styleCode="Rrule Botrule " valign="top"/> </tr> <tr> <td styleCode="Rrule Lrule Botrule " valign="top"> <paragraph>Lipase</paragraph> </td> <td styleCode="Rrule Botrule " valign="top"/> </tr> <tr> <td styleCode="Rrule Botrule Lrule " valign="top"> <paragraph>&gt; 2 &#xD7; ULN</paragraph> </td> <td styleCode="Rrule Botrule " valign="top"> <paragraph>5 (5)</paragraph> </td> </tr> </tbody> </table>