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CLINICAL PHARMACOLOGY Mechanism Of Action Influenza illness and its complications follow infection with influenza viruses. Global surveillance of influenza identifies yearly antigenic variants. For example, since 1977, antigenic variants of influenza A (H1N1 and H3N2) viruses and influenza B viruses have been in global circulation. Specific levels of hemagglutination inhibition (HI) antibody titers post-vaccination with inactivated influenza virus vaccine have not been correlated with protection from influenza illness. In some human studies, antibody titer of ≥1:40 have been associated with protection from influenza illness in up to 50% of subjects [see REFERENCES]. Antibody against one influenza virus type or subtype confers limited or no protection against another. Furthermore, antibody to one antigenic variant of influenza virus might not protect against a new antigenic variant of the same type or subtype. Frequent development of antigenic variants through antigenic drift is the virologic basis for seasonal epidemics and the reason for the usual change of one or more new strains in each year's influenza vaccine. Therefore, inactivated influenza vaccines are standardized to contain the hemagglutinin of strains (i.e., typically two type A and one type B), representing the influenza viruses likely to be circulating in the United States in the upcoming winter. Annual revaccination with the current vaccine is recommended because immunity declines during the year after vaccination, and because circulating strains of influenza virus change from year to year [see REFERENCES]. Clinical Studies Between 1982 and 1991, twelve clinical studies were conducted in healthy adult and geriatric subjects and one in children between 4 and 12 years of age who were considered to be 'at risk'. Since 1991 an annual clinical study has been conducted in the UK in healthy adults aged 18 years or older. FLUVIRIN® was also used as a control in a US clinical trial in adults (18-49 years of age). In all the trials, blood samples were taken prior to vaccination and approximately three weeks after vaccination to assess the immunogenic response to vaccination by measurement of anti-HA antibodies. Three clinical studies were carried out between 1995 and 2004 in a total of 520 pediatric subjects (age range 6-47 months). Of these, 285 healthy subjects plus 41 'at risk' pediatric subjects received FLUVIRIN®. FLUVIRIN® should only be used for the immunization of persons aged 4 years and over. TABLE 5 : Summary of the Seroconversion and Proportion of Subjects Achieving an HI titer ≥1:40 for Adult Subjects Year/Strain No. of subjects Seroconversion∞ HI titer ≥1:40¥ N % 95% CIφ n % 95% CIφ 1998-1999 A/H1N1 66 48 73 (62, 83) 50 76 (65, 86) A/H3N2 43 65 (54, 77) 47 71 (60, 82) B 42 64 (52, 75) 62 94 (88, 100) 1999-2000 A/H1N1 76 45 59 (48, 70) 50 66 (55, 76) A/H3N2 51 67 (57, 78) 66 87 (79, 94) B 53 70 (59, 80) 75 99 (96, 100) 2000-2001 A/H1N1 74 41 55 (44, 67) 41 55 (44, 67) A/H3N2 45 61 (50, 72) 52 84 (75, 92) B 50 68 (57, 78) 73 99 (96, 100) 2001-2002 A/H1N1 75 44 59 (48, 70) 48 64 (53, 75) A/H3N2 46 61 (50, 72) 68 91 (84, 97) B 42 56 (45, 67) 66 88 (81, 95) 2002-2003 A/H1N1 106 62 58 (49, 68) 73 69 (60, 78) A/H3N2 72 68 (59, 77) 93 88 (81, 94) B 78 74 (65, 82) 101 95 (91, 99) 2004-2005 A/H1N1 74 52 70 (59, 80) 66 89 (80, 95) A/H3N2 60 81 (70, 89) 73 99 (93, 100) B 57 77 (66, 86) 69 93 (85, 98) 2005-2006 A/H1N1 303 191 63 (57, 68) 296 98 (95, 99) A/H3N2 273 90 (86, 93) 294 97 (94, 99) B 213 70 (65, 75) 263 87 (82, 90) ∞Seroconversion: proportion of subjects with either a post-vaccination HI titer ≥1:4 0 from a pre-vaccination titer <1:10 or at least a four-fold increase from pre-vaccination HI titer ≥1:10 in antibody titer. ¥HI titer ≥1:4 0: proportion of subjects with a post-vaccination titer ≥ 1:4 0. φ95% CI: 95% confidence interval Immunogenicity In Adults (18 To 64 Years Of Age) Tables 5 and 6 show the immunogenicity data for the adult age group. The seven clinical studies presented enrolled a total of 774 adult subjects. In the adult group, for all antigens (A/H1N1, A/H3N2 and B) at least one of the following point estimate criteria was met: the proportion of subjects with seroconversion (post-vaccination titer ≥1:40 from a pre-vaccination titer <1:10) or significant increase (at least a four-fold increase from pre-vaccination titer ≥1:10) in antibody titer was greater than 40%; the geometric mean titer (GMT) increase was >2.5; the proportion of subjects with a post-vaccination hemagglutination inhibition (HI) antibody titer ≥1:40 was greater than 70%. Immunogenicity In Geriatric Subjects (65 Years Of Age And Older) Tables 7 and 8 show the immunogenicity of FLUVIRIN® in the geriatric age group. The six clinical studies presented enrolled a total of 296 geriatric subjects. For each of the influenza antigens, the percentage of subjects who achieved seroconversion and the percentage of subjects who achieved HI titers of ≥1:40 are shown, as well as the fold increase in GMT. TABLE 6 : Summary of the Geometric Mean Hemagglutination Inhibition Antibody Titers, Preand Post-Immunization, for Adult Subjects Year/Strain No. of subjects Geometric Mean Titer (GMT) Pre- vaccination Post- vaccination Fold Increase (95% CI)* 1998-1999 A/H1N1 66 7.26 160.87 22.16 (14.25, 34.46) A/H3N2 8.23 87.02 10.57 (6.91, 16.16) B 20.97 231.07 110.2 (6.90, 17.59) 1999-2000 A/H1N1 76 7.43 58.95 7.93 (5.73, 10.97) A/H3N2 15.29 122.83 8.03 (5.80, 11.13) B 25.70 254.76 9.91 (6.97, 14.10) 2000-2001 A/H1N1 74 5.42 33.80 6.24 (4.49, 8.69) A/H3N2 15.98 126.01 7.89 (5.61, 11.09) B 26.24 308.25 11.75 (7.73, 17.85) 2001-2002 A/H1N1 75 7.76 54.78 7.06 (5.24, 9.52) A/H3N2 23.67 153.81 6.50 (4.78, 8.84) B 19.91 107.53 5.40 (3.95, 7.38) 2002-2003 A/H1N1 106 7.78 60.39 7.77 (5.81, 10.39) A/H3N2 23.32 292.03 12.52 (8.77, 17.87) B 30.20 314.11 10.40 (7.54, 14.34) 2004-2005 A/H1N1 74 13 159 12 (8.39, 17) A/H3N2 37 658 18 (12, 26) B 15 156 11 (7.87, 14) 2005-2006 A/H1N1 303 29 232 8 (6.68, 9.59) A/H3N2 14 221 15 (14, 17) B 13 83 6.5 (5.73, 7.37) * 95% CI: 95% confidence interval TABLE 7 : Summary of the Seroconversion and Proportion of Subjects Achieving an HI titer ≥1:40 for Geriatric Subjects Year/Strain No. of subjects Seroconversion∞ HI titer ≥1:40¥ N % 95% CIφ N % 95% CIφ 1998-1999 A/H1N1 42 33 79 (66, 91) 38 90 (82, 99) A/H3N2 33 79 (66, 91) 36 86 (75, 96) B 13 31 (17, 45) 42 100 (100, 100) 1999-2000 A/H1N1 34 10 29 (14, 45) 23 68 (52, 83) A/H3N2 18 53 (36, 70) 31 91 (82, 100) B 9 26 (12, 41) 32 94 (86, 100) 2000-2001 A/H1N1 35 5 14 (3, 26) 10 29 (14, 44) A/H3N2 22 63 (47, 79) 31 89 (78, 99) B 13 37 (21, 53) 33 94 (87, 100) 2001-2002 A/H1N1 35 5 14 (3, 26) 14 40 (24, 56) A/H3N2 15 43 (26, 59) 33 94 (87, 100) B 6 17 (5, 30) 32 91 (82, 100) 2002-2003 A/H1N1 89 24 27 (18, 36) 52 58 (48, 69) A/H3N2 42 47 (37, 58) 85 96 (91, 100) B 41 46 (36, 56) 86 97 (93, 100) 2004-2005 A/H1N1 61 17 28 (17, 41) 46 75 (63, 86) A/H3N2 29 48 (35, 61) 60 98 (91, 100) B 38 62 (49, 74) 51 84 (72, 92) ∞Seroconversion: proportion of subjects with either a post-vaccination HI titer ≥1:4 0 from a pre-vaccination titer <1:10 or at least a four-fold increase from pre-vaccination HI titer ≥1:10 in antibody titer ¥HI titer ≥1:4 0: proportion of subjects with a post-vaccination titer ≥1:4 0 φ95% CI: 95% confidence interval For all antigens (A/H1N1, A/H3N2 and B) at least one of the following point estimate criteria was met: the proportion of subjects with seroconversion (post- vaccination titer ≥1:40 from a pre-vaccination titer <1:10) or significant increase (at least a four-fold increase from pre-vaccination titer ≥1:10) in antibody titer was greater than 30%; the geometric mean titer (GMT) increase was >2.0; the proportion of subjects with a post-vaccination hemagglutination inhibition (HI) antibody titer ≥1:40 was greater than 60%. The pre-specified efficacy criteria were met in each study, although a relatively lower immunogenicity of A/H1N1 strain was seen in the last four studies (the same strain was in each of the formulations). Immunogenicity In Pediatric Subjects A small-scale study, was conducted in 1987 to evaluate safety and immunogenicity of FLUVIRIN® in 38 'at risk' children, with diabetes and/or asthma, or lymphoid leukemia. Thirty-eight participants aged between 4 and 12 years of age were assessed. Ten subjects had diabetes, 21 had asthma, two had both diabetes and asthma, and one had lymphoid leukemia. There were four healthy control subjects. All participants received a single 0.5-mL dose of FLUVIRIN®. Immunogenicity results were obtained for 19 of the 38 subjects enrolled in the study. The point estimate of the percentage of subjects achieving a titer of ≥ 1:40 was 84% for the A/H1N1 strain 79% for the B strain, and 53% for the A/H3N2 strain. The GMT fold increases were 5.8 for the A/H1N1 strain, 40 for the B strain and 17.7 for the A/H3N2 strain. Three clinical studies were carried out between 1995 and 2004 in a total of 520 TABLE 8 : Summary of the Geometric Mean Hemagglutination Inhibition Antibody Titers, Preand Post-Immunization, for Geriatric Subjects Year/Strain No. of subjects Geometric Mean Titer (GMT) Pre- vaccination Post- vaccination Fold Increase (95% CI)* 1998-1999 A/H1N1 42 13.92 176.65 12.69 (8.24, 19.56) A/H3N2 10.69 124.92 11.69 (7.02, 19.46) B 114.1 273.56 2.40 (1.82, 3.17) 1999-2000 A/H1N1 34 15.82 50.58 3.20 (2.13, 4.80) A/H3N2 28.00 133.19 4.76 (2.92, 7.76) B 57.16 127.86 2.24 (1.56, 3.20) 2000-2001 A/H1N1 35 6.66 18.85 2.83 (1.91, 4.18) A/H3N2 25.87 140.68 5.44 (3.72, 7.96) B 61.24 191.23 3.12 (2.13, 4.59) 2001-2002 A/H1N1 35 12.69 26.65 2.10 (1.55, 2.84) A/H3N2 47.33 114.26 2.41 (1.73, 3.38) B 45.49 91.89 2.02 (1.47, 2.78) 2002-2003 A/H1N1 89 13.29 31.92 2.40 (1.90, 3.03) A/H3N2 65.86 272.79 4.14 (3.09, 5.55) B 74.87 288.57 3.85 (2.89, 5.13) 2004-2005 A/H1N1 61 21 64 3.13 (2.33, 4.2) A/H3N2 72 320 4.43 (3.13, 6.27) B 20 114 5.69 (4.39, 7.38) * 95% CI: 95% confidence interval pediatric subjects (age range 6-47 months). Of these, 285 healthy subjects plus 41 'at risk' pediatric subjects, received FLUVIRIN®. In a 1995/1996 clinical study, 41 subjects (aged 6-36 months) at increased risk for influenza-related complications received two 0.25-mL doses of FLUVIRIN®. At least 49% of subjects showed a ≥4- fold increase in HI antibody titer to all three strains. HI antibody titers of 1:40 or greater were seen in at least 71% of the subjects for all three influenza strains, with increases in geometric mean titer of 6.0- fold or greater to all three strains. Two clinical studies (1999-2000 and 2004) indicated a lower immunogenicity profile for FLUVIRIN® compared with two commercial split vaccines; in a study in the age group 6-47 months the comparator was a US licensed vaccine, Fluzone®, and in another study in the age group 6-36 months the comparator was a non-US licensed inactivated influenza vaccine. Despite the small sample size (a total of 285 healthy subjects received FLUVIRIN® in these two clinical studies) the lower immunogenicity profile of FLUVIRIN® was greatest versus the comparator vaccines in children <36months but was also evident in those 36-47 months of age, though the differences were less. FLUVIRIN® should only be used for the immunization of persons aged 4 years and over. REFERENCES 1. Hannoun C, Megas F, Piercy J. Immunogenicity and protective efficacy of influenza vaccination. Virus Res 2004; 103:133-138. 2. Hobson D, Curry RL, Beare A, et. al. The role of serum hemagglutinin- inhibiting antibody in protection against challenge infection with influenza A2 and B viruses. J Hyg Camb 1972; 767-777. 3. Centers for Disease Control and Prevention. Prevention and Control of Influenza with Vaccines. Recommendations of the Advisory Committee on Immunization Practices (ACIP). MMWR 2011; 60(33):1128-1132.

FLUVIRIN® (influenza virus vaccine) Suspension for Intramuscular Injection DESCRIPTION FLUVIRIN® is a trivalent, sub-unit (purified surface antigen) influenza virus vaccine prepared from virus propagated in the allantoic cavity of embryonated hens' eggs inoculated with a specific type of influenza virus suspension containing neomycin and polymyxin. Each of the influenza virus strains is harvested and clarified separately by centrifugation and filtration prior to inactivation with betapropiolactone. The inactivated virus is concentrated and purified by zonal centrifugation. The surface antigens, hemagglutinin and neuraminidase, are obtained from the influenza virus particle by further centrifugation in the presence of nonylphenol ethoxylate, a process which removes most of the internal proteins. The nonylphenol ethoxylate is removed from the surface antigen preparation. FLUVIRIN® is a homogenized, sterile, slightly opalescent suspension in a phosphate buffered saline. FLUVIRIN® has been standardized according to USPHS requirements for the 2017/2018 influenza season and is formulated to contain 45 mcg hemagglutinin (HA) per 0.5-mL dose in the recommended ratio of 15 mcg HA of each of the following 3 viruses: A/Singapore/GP1908/2015,IVR-180 (an A/Michigan/45/2015 (H1N1)pdm09- like virus; A/Hong Kong/4801/2014, NYMC X-263B (H3N2) (an A/Hong Kong/4801/2014- like virus); and B/Brisbane/60/2008, wild type (a B/Brisbane/60/2008-like virus). The 0.5-mL prefilled syringe presentation is formulated without preservative. However, thimerosal, a mercury derivative used during manufacturing, is removed by subsequent purification steps to a trace amount (≤ 1 mcg mercury per 0.5-mL dose). The 5-mL multidose vial formulation contains thimerosal, a mercury derivative, added as a preservative. Each 0.5-mL dose from the multidose vial contains 25 mcg mercury. Each dose from the multidose vial or from the prefilled syringe may also contain residual amounts of egg proteins (≤ 1 mcg ovalbumin), polymyxin (≤ 3.75 mcg), neomycin (≤ 2.5 mcg), betapropiolactone (not more than 0.5 mcg) and nonylphenol ethoxylate (not more than 0.015% w/v). The tip caps of the FLUVIRIN® prefilled syringes may contain natural rubber latex. The multidose vial stopper and the syringe stopper/plunger do not contain latex.

INDICATIONS FLUVIRIN® is an inactivated influenza virus vaccine indicated for immunization of persons 4 years of age and older against influenza virus disease caused by influenza virus subtypes A and type B contained in the vaccine [see Dosage Forms And Strengths]. FLUVIRIN® is not indicated for children less than 4 years of age because there is evidence of diminished immune response in this age group. DOSAGE AND ADMINISTRATION Preparation For Administration Shake the syringe vigorously before administering the vaccine and shake the multidose vial preparation each time before withdrawing a dose of vaccine. Inspect FLUVIRIN® syringes and multidose vials visually for particulate matter and/or discoloration prior to administration [see DESCRIPTION]. If either of these conditions exists, the vaccine should not be administered. Between uses, return the multidose vial to the recommended storage conditions between 2° and 8°C (36° and 46°F). Do not freeze. Discard if the vaccine has been frozen. A separate sterile syringe and needle must be used for each injection to prevent transmission of infectious agents from one person to another. Needles should be disposed of properly and not recapped. It is recommended that small syringes (0.5 mL or 1 mL) should be used to minimize any product loss. For intramuscular us e only. Recommended Dose And Schedule The dose and schedule for Fluvirin is presented in Table 1. TABLE 1 : Fluvirin Dose and Schedule Age Dose Schedule 4 years through 8 years One or two dosesa, 0.5 mL each If 2 doses, administer at least 1 month apart 9 years and older One dose, 0.5 mL - a 1 or 2 doses depends on vaccination history as per Advisory Committee on Immunization Practices annual recommendations on prevention and control of influenza with vaccines. “-” indicates information is not applicable In children, the needle size may range from 7/8 to 1¼ inches, depending on the size of the child's deltoid muscle, and should be of sufficient length to penetrate the muscle tissue. The anterolateral thigh can be used, but the needle should be longer, usually 1 inch. In adults, a needle of ≥1 inch is preferred because needles <1 inch might be of insufficient length to penetrate muscle tissue in certain adults. The preferred site for intramuscular injection is the deltoid muscle of the upper arm. The vaccine should not be injected in the gluteal region or areas where there may be a major nerve trunk. HOW SUPPLIED Dosage Forms And Strengths FLUVIRIN®, a sterile suspension for intramuscular injection, is supplied in two presentations: 0.5 mL single-dose prefilled syringe 5.0 mL multi-dose vial containing 10 doses (each dose is 0.5 mL) FLUVIRIN® product presentations are listed in Table 9 below: TABLE 9 : Fluvirin Product Presentations Presentation Carton NDC Number Components Pre-filled syringe 70461-120-02 0.5 mL single dose pre-filled syringe, package of 10 syringes per carton (may contain latex) [NDC 70461-120-12] Multi-dose vial 70461-120-10 5.0 mL multi-dose vial, individually packaged in a carton (contains no latex) [NDC 70461-120-11] Storage And Handling Store FLUVIRIN® refrigerated between 2° and 8°C (36° and 46°F). Do not freeze. Discard if the vaccine has been frozen. Store in the original package to protect from light. Do not use after the expiration date. Between uses, return the multidose vial to the recommended storage conditions. Manufactured by: Seqirus Vaccines Limited, Speke, Liverpool, UK. Distributed by: Seqirus USA Inc. 25 Deforest Avenue, Summit, NJ 07901, USA, 1-855-358-8966. Revised: Mar 2017

PATIENT INFORMATION Vaccine recipients and guardians should be informed by their health care provider of the potential benefits and risks of immunization with FLUVIRIN®. When educating vaccine recipients and guardians regarding the potential side effects, clinicians should emphasize that (1) FLUVIRIN® contains noninfectious particles and cannot cause influenza and (2) FLUVIRIN® is intended to provide protection against illness due to influenza viruses only, and cannot provide protection against all respiratory illness. Vaccine recipients and guardians should be instructed to report any severe or unusual adverse reactions to their healthcare provider. Vaccine recipients and guardians should be instructed that annual vaccination is recommended.

OVERDOSE No information provided. CONTRAINDICATIONS Hypersensitivity Do not administer FLUVIRIN® to anyone with known history of severe allergic reactions (e.g., anaphylaxis) to egg proteins (eggs or egg products), or to any component of FLUVIRIN®, or who has had a life-threatening reaction to previous influenza vaccinations.

SIDE EFFECTS Overall Adverse Reaction Profile Serious allergic reactions, including anaphylactic shock, have been observed in individuals receiving FLUVIRIN® during postmarketing surveillance. Clinical Trial Experience Adverse event information from clinical trials provides a basis for identifying adverse events that appear to be related to vaccine use and for approximating the rates of these events. However, because clinical trials are conducted under widely varying conditions, the adverse reaction rates observed in the clinical trials of a vaccine cannot be directly compared to rates in the clinical trials of another vaccine, and may not reflect rates observed in clinical practice. Adult And Geriatric Subjects Safety data were collected in a total of 2768 adult and geriatric subjects (18 years of age and older) who have received FLUVIRIN® in 29 clinical studies since 1982. In 9 clinical studies since 1997, among 1261 recipients of FLUVIRIN®, 745 (59%) were women; 1211 (96%) were White, 23 (2%) Asian, 15 (1%) Black and 12 (1%) other; 370 (29%) of subjects were elderly (≥65 years of age). All studies have been conducted in the UK, apart from a study run in the US in 2005-2006 where FLUVIRIN® was used as a comparator for an unlicensed vaccine. After vaccination, the subjects were observed for 30 minutes for hypersensitivity or other immediate reactions. Subjects were instructed to complete a diary card for three days following immunization (i.e. Day 1 to 4) to collect local and systemic reactions (see Tables 2 and 3). All local and systemic adverse events were considered to be at least possibly related to the vaccine. Local and systemic reactions mostly began between day 1 and day 2. The overall adverse events reported in clinical trials since 1998 in at least 5% of the subjects are summarized in Table 4. Adults (18 To 64 Years Of Age) In adult subjects, solicited local adverse events occurred with similar frequency in all trials. The most common solicited adverse events occurring in the first 96 hours after administration (Tables 2 and 3) were associated with the injection site (such as pain, erythema, mass, induration and swelling) but were generally mild/moderate and transient. The most common solicited systemic adverse events were headache and myalgia. The most common overall events in adult subjects (18-64 years of age) were headache, fatigue, injection site reactions (pain, mass, erythema, and induration) and malaise (Table 4). Geriatric Subjects (65 Years Of Age And Older) In geriatric subjects, solicited local and systemic adverse events occurred less frequently than in adult subjects. The most common solicited local and systemic adverse events were injection site pain, and headache (Tables 2 and 3). All were considered mild/moderate and were transient. The most common overall events in elderly subjects (≥65 years of age) were headache and fatigue. Only 11 serious adverse events in adult and geriatric subjects (18 years and older) have been reported to date from all the trials performed. These serious adverse events were a minor stroke experienced by a 67 year old subject 14 days after vaccination (1990), death of an 82 year old subject 35 days after TABLE 2 : Solicited Adverse Events in the First 72-96 Hours After Administration of FLUVIRIN® in Adult (18-64 years of age) and Geriatric (≥65 years of age) Subjects 1998-1999*§ 1999-2000*§ 2000-2001*§ 18-64 yrs N = 66 ≥ 65 yrs N = 44 18-64 yrs N = 76 ≥ 65 yrs N = 34 18-64 yrs N = 75 ≥ 65 yrs N = 35 Local Adverse Events Pain 16 (24%) 4 (9%) 16 (21%) - 9 (12%) - Mass 7 (11%) 1 (2%) 4 (5%) - 8 (11%) 1 (3%) Inflammation 5 (8%) 2 (5%) 6 (8%) - 7 (9%) 1 (3%) Ecchymosis 4 (6%) 1 (2%) 3 (4%) 1 (3%) 4 (5%) - Edema 2 (3%) 1 (2%) 1 (1%) 2 (6%) 3 (4%) 1 (3%) Reaction 2 (3%) - 2 (3%) - 4 (5%) 1 (3%) Hemorrhage - - 1 (1%) - - - Systemic Adverse Events Headache 7 (11%) 1 (2%) 17 (22%) 3 (9%) 4 (5%) - Fatigue 3 (5%) 2 (5%) 4 (5%) 1 (3%) 3 (4%) - Malaise 2 (3%) 1 (2%) 2 (3%) 1 (3%) 1 (1%) - Myalgia 1 (2%) - 2 (3%) - - - Fever 1 (2%) - 1 (1%) - - - Arthralgia - 1 (2%) - 1 (3%) - - Sweating - - 3 (4%) - 1 (1%) 1 (3%) 2001-2002*^ 2002-2003*^ 2004-2005*^ 18-64 yrs N = 75 ≥ 65 yrs N = 35 18-64 yrs N = 107 ≥ 65 yrs N = 88 18-64 yrs N = 74 ≥ 65 yrs N = 61 Local Adverse Events Pain 12 (16%) 1 (3%) 14 (13%) 7 (8%) 15 (20%) 9 (15%) Mass 4 (5%) 1 (3%) - - - - Ecchymosis 2 (3%) - 3 (3%) 3 (3%) 2 (3%) 1 (2%) Edema 2 (3%) 1 (3%) 6 (6%) 2 (2%) - - Erythema 5 (7%) - 11 (10%) 5 (6%) 16 (22%) 5 (8%) Swelling - - - - 11 (15%) 4 (7%) Reaction - - 2 (2%) - - - Induration - - 14 (13%) 3 (3%) 11 (15%) 1 (2%) Pruritus - - 1 (1%) - - - Systemic Adverse Events Headache 8 (11%) 1 (3%) 12 (11%) 9 (10%) 14 (19%) 3 (5%) Fatigue 1 (1%) 1 (3%) - - 5 (7%) 2 (3%) Malaise 3 (4%) - 3 (3%) 4 (5%) 1 (1%) 1 (2%) Myalgia 3 (4%) - 5 (5%) 3 (3%) 8 (11%) 1 (2%) Fever - - - 1 (1%) - - Arthralgia - - 2 (2%) - 1 (1%) - Sweating 3 (4%) 1 (3%) - 2 (2%) - - Shivering - - - 1 (1%) - - Results reported to the nearest whole percent; Fever defined as >38°C – not reported * Solicited adverse events in the first 72 hours after administration of FLUVIRIN §Solicited adverse events reported by COSTART preferred term ^ Solicited adverse events reported by MEDDRA preferred term TABLE 3 : Solicited Adverse Events in the First 72 Hours After Administration of FLUVIRIN® in Adult Subjects (18-49 years of age). 2005-2006 US Trial FLUVIRIN® N = 304 Local Adverse Events Pain 168 (55%) Erythema 48 (16%) Ecchymosis 22 (7%) Induration 19 (6%) Swelling 16 (5%) Systemic Adverse Events Headache 91 (30%) Myalgia 64 (21%) Malaise 58 (19%) Fatigue 56 (18%) Sore throat 23 (8%) Chills 22 (7%) Nausea 21 (7%) Arthralgia 20 (7%) Sweating 17 (6%) Cough 18 (6%) Wheezing 4 (1%) Chest tightness 4 (1%) Other difficulties breathing 3 (1%) Facial edema - Results reported to the nearest whole percent – not reported TABLE 4 : Adverse Events Reported by at least 5% of Subjects in Clinical Trials since 1998 1998-1999§ 1999-2000§ 2000-2001§ 18-64 yrs N=66 ≥ 65 yrs N = 44 18-64 yrs N=67 ≥ 65 yrs N = 34 18-64 yrs N=75 ≥ 65 yrs N=35 Adverse Events Fatigue 8 (12%) 2 (5%) 8 (11%) 2 (6%) 5 (7%) - Back pain 4 (6%) 3 (7%) - - - - Cough increased 2 (3%) 2 (5%) - - - - Ecchymosis 4 (6%) 1 (2%) 4 (5%) 1 (3%) 5 (7%) - Fever 3 (5%) - - - - - Headache 12 (18%) 5 (11%) 22 (29%) 5 (15%) 14 (19%) 2 (6%) Infection 3 (5%) 2 (5%) - - - - Malaise 4 (6%) 4 (9%) 4 (5%) 1 (3%) - - Migraine 4 (6%) 1 (2%) - - - - Myalgia 4 (6%) 1 (2%) - - - - Sweating 5 (8%) 1 (2%) - - - - Rhinitis 3 (5%) 1 (2%) - - 5 (7%) 2 (6%) Pharingitis 6 (9%) 1 (2%) 10 (13%) - 6 (8%) - Arthralgia - - - 2 (6%) - - Injection site pain 16 (24%) 4 (9%) 16 (21%) - 9 (12%) - Injection site ecchymosis 4 (6%) 1 (2%) - - 4 (5%) - Injection site mass 7 (11%) 1 (2%) 4 (5%) - 8 (11%) 1 (3%) Injection site edema - - 1 (1%) 2 (6%) - - Injection site inflammation 5 (8%) 2 (5%) 6 (8%) - 7 (9%) 1 (3%) Injection site reaction - - - - 4 (5%) 1 (3%) 2001-2002^ 2002-2003^ 2004-2005^ 18-64 yrs N = 75 ≥ 65 yrs N = 35 18-64 yrs N = 107 ≥ 65 yrs N = 88 18-64 yrs N = 74 ≥ 65 yrs N = 61 Adverse Events Fatigue 5 (7%) 4 (11%) 11 (10%) 8 (9%) 4 (5%) 2 (3%) Hypertension - - 1 (1%) 4 (5%) - - Rinorrhea - - 2 (2%) 5 (6%) - - Headache 20 (27%) 2 (6%) 35 (33%) 18 (20%) 12 (16%) 1 (2%) Malaise 6 (8%) 1 (3%) 13 (12%) 8 (9%) - - Myalgia 4 (5%) 1 (3%) 10 (9%) 4 (5%) - - Sweating 3 (4%) 3 (9%) 2 (2%) 5 (6%) - - Rhinitis 4 (5%) - - - - - Pharingitis - - - - 6 (8%) - Arthralgia - - 5 (5%) 4 (5%) - - Sore throat 4 (5%) 1 (3%) 5 (5%) 4 (5%) - - Injection site pain 13 (17%) 3 (9%) 14 (13%) 7 (8%) 6 (8%) 2 (3%) Injection site ecchymosis 4 (5%) 1 (3%) 4 (4%) 4 (5%) - - Injection site erythema 5 (7%) 2 (6%) 11 (10%) 5 (6%) 4 (5%) - Injection site mass 4 (5%) 1 (3%) - - - - Injection site edema - - 6 (6%) 2 (2%) 4 (5%) 1 (2%) Injection site induration - - 14 (13%) 3 (3%) 7 (9%) - Results reported to the nearest whole percent; Fever defined as >38°C – not reaching the cut-off of 5% §Solicited adverse events reported by COSTART preferred term ^ Solicited adverse events reported by MEDDRA preferred term vaccination (1990) in very early studies; death of a 72 year old subject 19 days after vaccination (1998- 1999), a hospitalization for hemorrhoidectomy of a 38 year old male subject (1999-2000), a severe respiratory tract infection experienced by a 74 year old subject 12 days after vaccination (2002-2003), a planned transurethral resection of the prostate in a subject with prior history of prostatism (2004-2005), two cases of influenza (2005-2006), a drug overdose (2005-2006), cholelithiasis (2005-2006) and a nasal septal operation (2005- 2006). None of these events were considered causally related to vaccination. Clinical Trial Experience In Pediatric Subjects In 1987 a clinical study was carried out in 38 'at risk' children aged between 4 and 12 years (17 females and 21 males). To record the safety of FLUVIRIN®, participants recorded their symptoms on a diary card during the three days after vaccination and noted any further symptoms they thought were attributable to the vaccine. The only reactions recorded were tenderness at the site of vaccination in 21% of the participants on day 1, which was still present in 16% on day 2 and 5% on day 3. In one child, the tenderness was also accompanied by redness at the site of injection for two days. The reactions were not age-dependent and there was no bias towards the younger children. Three clinical studies were carried out between 1995 and 2004 in a total of 520 pediatric subjects (age range 6 - 47 months). Of these, 285 healthy subjects plus 41'at risk'subjects received FLUVIRIN®. No serious adverse events were reported. FLUVIRIN® should only be used for the immunization of persons aged 4 years and over. Postmarketing Experience The following additional adverse reactions have been reported during post- approval use of FLUVIRIN®. 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 vaccine exposure. Adverse events described here are included because: a) they represent reactions which are known to occur following immunizations generally or influenza immunizations specifically; b) they are potentially serious; or c) the frequency of reporting. Body as a whole: Local injection site reactions (including pain, pain limiting limb movement, redness, swelling, warmth, ecchymosis, induration), hot flashes/flushes; chills; fever; malaise; shivering; fatigue; asthenia; facial edema. Immune system disorders: Hypersensitivity reactions (including throat and/ or mouth edema). In rare cases, hypersensitivity reactions have lead to anaphylactic shock and death. Cardiovascular disorders: Vasculitis (in rare cases with transient renal involvement), presyncope, syncope shortly after vaccination. Digestive disorders: Diarrhea; nausea; vomiting; abdominal pain. Blood and lymphatic disorders: Local lymphadenopathy; thrombocytopenia (some very rare cases were severe with platelet counts less than 5,000 per mm³). Metabolic and nutritional disorders: Loss of appetite. Musculoskeletal: Arthralgia; myalgia; myasthenia. Nervous system disorders: Headache; dizziness; neuralgia; paraesthesia; confusion; febrile  convulsions; Guillain-Barré Syndrome; myelitis (including encephalomyelitis and transverse myelitis); neuropathy (including neuritis); paralysis (including Bell's Palsy). Respiratory disorders: Dyspnea; chest pain; cough; pharyngitis; rhinitis. Skin and appendages: Stevens-Johnson syndrome; sweating; pruritus; urticaria; rash (including nonspecific, maculopapular, and vesiculobulbous). General disorders and administration site conditions: Injection site cellulitis- like reaction (very rare cases of swelling, pain, and redness were large and extended to the entire arm) Other Adverse Reactions Associated With Influenza Vaccination Anaphylaxis has been reported after administration of FLUVIRIN®. Although FLUVIRIN® contains only a limited quantity of egg protein, this protein can induce immediate hypersensitivity reactions among persons who have severe egg allergy. Allergic reactions include hives, angioedema, allergic asthma, and systemic anaphylaxis [see CONTRAINDICATIONS]. The 1976 swine influenza vaccine was associated with an increased frequency of Guillain-Barré syndrome (GBS). Evidence for a causal relation of GBS with subsequent vaccines prepared from other influenza viruses is unclear. If influenza vaccine does pose a risk, it is probably slightly more than 1 additional case/1 million persons vaccinated. Neurological disorders temporally associated with influenza vaccination such as encephalopathy, optic neuritis/neuropathy, partial facial paralysis, and brachial plexus neuropathy have been reported. Microscopic polyangiitis (vasculitis) has been reported temporally associated with influenza vaccination. DRUG INTERACTIONS Concomitant Administration With Other Vaccines There are no data to assess the concomitant administration of FLUVIRIN® with other vaccines. If FLUVIRIN® is to be given at the same time as another injectable vaccine(s), the vaccines should always be administered at different injection sites. FLUVIRIN® should not be mixed with any other vaccine in the same syringe or vial. Concurrent Use With Immunosuppressive Therapies Immunosuppressive therapies, including irradiation, antimetabolites, alkylating agents, cytotoxic drugs, and corticosteroids (used in greater than physiologic doses), may reduce the immune response to FLUVIRIN®.

WARNINGS Included as part of the PRECAUTIONS section. PRECAUTIONS Guillain-Barré Syndrome If Guillain-Barré syndrome has occurred within 6 weeks of receipt of prior influenza vaccine, the decision to give FLUVIRIN® should be based on careful consideration of the potential benefits and risks. Altered Immunocompetence If FLUVIRIN® is administered to immunocompromised persons, including individuals receiving immunosuppressive therapy, the expected immune response may not be obtained. Preventing And Managing Allergic Reactions Prior to administration of any dose of FLUVIRIN®, the healthcare provider should review the patient's prior immunization history for possible adverse events, to determine the existence of any contraindication to immunization with FLUVIRIN® and to allow an assessment of benefits and risks. Appropriate medical treatment and supervision must be available to manage possible anaphylactic reactions following administration of the vaccine. The tip caps of the FLUVIRIN® prefilled syringes may contain natural rubber latex which may cause allergic reactions in latex sensitive individuals. Limitations Of Vaccine Effectiveness Vaccination with FLUVIRIN® may not protect all individuals. Syncope Syncope (fainting) can occur in association with administration of injectable vaccines, including Fluvirin. Syncope can be accompanied by transient neurological signs such as visual disturbance, paresthesia, and tonic-clonic limb movements. Procedures should be in place to avoid falling injury and to restore cerebral perfusion following syncope by maintaining a supine or Trendelenburg position. Nonclinical Toxicology Carcinogenesis, Mutagenesis, Impairment Of Fertility FLUVIRIN® has not been evaluated for carcinogenic or mutagenic potential, or for impairment of fertility. Use In Specific Populations Pregnancy Pregnancy Category B A reproductive and developmental toxicity study has been performed in rabbits at a dose level that was approximately 15 times the human dose based on body weight. The study revealed no evidence of impaired fertility or harm to the fetus due to FLUVIRIN®. There are, however, no adequate and well-controlled studies in pregnant women. Because animal reproduction studies are not always predictive of human response, this vaccine should be used during pregnancy only if clearly needed. In a reproductive and developmental toxicity study, the effect of FLUVIRIN® on embryo-fetal and postnatal development was evaluated in pregnant rabbits. Animals were administered FLUVIRIN® by intramuscular injection twice prior to gestation, during the period of organogenesis (gestation day 7) and later in pregnancy (gestation day 20), 0.5 mL/rabbit/occasion (approximately 15-fold excess relative to the projected human dose on a body weight basis). No adverse effects on mating, female fertility, pregnancy, embryo-fetal development, or post-natal development were observed. There were no vaccine related fetal malformations or other evidence of teratogenicity. Nursing Mothers It is not known whether FLUVIRIN® is excreted in human milk. Because many drugs are excreted in human milk, caution should be exercised when FLUVIRIN® is administered to a nursing woman. Pediatric Use The safety and immunogenicity of FLUVIRIN® have not been established in children under 4 years of age. The safety and immunogenicity of FLUVIRIN® have been established in the age group 4 years to 16 years. The use of FLUVIRIN® in these age groups is supported by evidence from adequate and well controlled studies of FLUVIRIN® in adults that demonstrate the immunogenicity of FLUVIRIN® [see ADVERSE REACTIONS and Clinical Studies]. Geriatric Use Since 1997, of the total number of geriatric subjects (n = 397) in clinical studies of FLUVIRIN®, 29% were 65 years and over, while 2.1% were 75 years and over. Antibody responses were lower in the geriatric population than in younger subjects. Adverse events occurred less frequently in geriatric subjects (≥65 years) than in younger adults. Other reported clinical experience has not identified differences in responses between the elderly and younger patients. [See ADVERSE REACTION and Clinical Studies].