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Fluad Quadrivalent

Generic Name: influenza vaccine, adjuvanted
Dosage Form: injection, suspension

Medically reviewed by Drugs.com. Last updated on June 1, 2020.

Indications and Usage for Fluad Quadrivalent

Fluad Quadrivalent is an inactivated influenza vaccine indicated for active immunization against influenza disease caused by influenza virus subtypes A and types B contained in the vaccine. Fluad Quadrivalent is approved for use in persons 65 years of age and older. This indication is approved under accelerated approval based on the immune response elicited by Fluad Quadrivalent [see Clinical Studies (14.1)]. Continued approval for this indication may be contingent upon verification and description of clinical benefit in a confirmatory trial.

Fluad Quadrivalent Dosage and Administration

For intramuscular injection only

. Dosage and Schedule

Administer Fluad Quadrivalent as a single 0.5 mL intramuscular injection in adults 65 years of age and older.

. Administration

  • Gently shake each syringe. Fluad Quadrivalent has a milky-white appearance. Parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration whenever solution and container permit [see Description (11)]. If either condition exists, Fluad Quadrivalent should not be administered.
  • To use a pre-filled syringe fitted with a Luer Lok system, remove the tip cap by unscrewing it in a counter-clockwise direction. Once the tip cap is removed, attach a needle to the syringe by screwing it on in a clockwise direction until it locks. Once the needle is locked in place, remove the needle protector and administer the vaccine.
  • The vaccine should be administered by intramuscular injection, preferably in the region of the deltoid muscle of the upper arm. Do not inject the vaccine in the gluteal region or areas where there may be a major nerve trunk.

Dosage Forms and Strengths

Fluad Quadrivalent is a sterile injectable emulsion supplied in 0.5 mL single-dose pre-filled syringes.

Contraindications

Do not administer Fluad Quadrivalent to anyone with a history of severe allergic reaction (e.g. anaphylaxis) to any component of the vaccine, including egg protein [see Description (11)], or to a previous influenza vaccine.

Warnings and Precautions

. Guillain-Barré Syndrome

If Guillain-Barré syndrome (GBS) has occurred within 6 weeks of receipt of prior influenza vaccine, the decision to give Fluad Quadrivalent should be based on careful consideration of the potential benefits and risks. The 1976 swine influenza vaccine was associated with an elevated risk of GBS. [see References (1)] Evidence for a causal relationship of GBS with other influenza vaccines is inconclusive; if an excess risk exists, it is probably slightly more than 1 additional case per 1 million persons vaccinated.

. Preventing and Managing Allergic Reactions

Appropriate medical treatment and supervision must be available to manage possible anaphylactic reactions following administration of the vaccine.

Altered Immunocompetence

The immune response to Fluad Quadrivalent in immunocompromised persons, including individuals receiving immunosuppressive therapy, may be lower than in immunocompetent individuals. [see Concurrent Use With Immunosuppressive Therapies (7.2)]

Syncope

Syncope (fainting) may occur in association with administration of injectable vaccines including Fluad Quadrivalent. Ensure procedures are in place to avoid injury from falling associated with syncope.

Limitations of Vaccine Effectiveness

Vaccination with Fluad Quadrivalent may not protect all vaccine recipients against influenza disease.

Adverse Reactions

The most common (≥10%) local and systemic reactions in elderly subjects 65 years of age and older were injection site pain (16.3%), headache (10.8%) and fatigue (10.5%).

. Clinical Trials Experience

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.

The safety of Fluad Quadrivalent was evaluated in two clinical studies in 4269 elderly subjects 65 years of age and older. Study 1 (NCT02587221) was a multi-center, randomized, observer-blind, non-influenza comparator-controlled efficacy and safety study conducted in 12 countries during the 2016-2017 Northern Hemisphere and 2017 Southern Hemisphere seasons. In this study, 3381 subjects received Fluad Quadrivalent and 3380 subjects received a US-licensed non-influenza comparator vaccine (Tetanus Toxoid, Reduced Diphtheria Toxoid and Acellular Pertussis Vaccine, Boostrix® [GlaxoSmithKline Biologicals]).

The mean age of subjects at enrollment was 72 years, 62% were female, 48% White, 34% Asian, 16% Other, 2% American Indian/Alaska Native, and 18% of Hispanic/Latino ethnicity.

Solicited local and systemic adverse reactions were collected for 7 days after vaccination in a subset of 665 subjects who received Fluad Quadrivalent and 667 subjects who received the comparator vaccine. The percentages of subjects reporting solicited local adverse reactions are presented in Table 1a and systemic adverse reactions are presented in Table 1b. Onset usually occurred within the first 2 days after vaccination. The majority of solicited reactions resolved within 3 days.

Table 1a. Percentages of Subjects Reporting Solicited Local Adverse Reactionsa in the Solicited Safety Populationb within 7 Days of Vaccination (Study 1)

Study 1: NCT02587221

Abbreviation: N=number of subjects with solicited safety data

Non-Influenza Comparator Vaccine = combined Tetanus Toxoid, Reduced Diphtheria Toxoid and Acellular Pertussis Vaccine, Boostrix® (GlaxoSmithKline Biologicals)

a All solicited local adverse events reported within 7 days of vaccination are included

b Solicited Safety Population: all subjects in the exposed population who received a study vaccine and provided post-vaccination solicited safety data

c Severe reactions of each type were reported in 1.1% or fewer subjects receiving Fluad Quadrivalent; severe reactions of each type were also reported in the comparator group at similar percentages. Severe definitions: Erythema, Induration and Ecchymosis = >100 mm diameter; Injection site pain, = prevents daily activity.

Local (Injection site) Reactionsc Fluad Quadrivalent
N=595-659
Non-Influenza Comparator Vaccine
N=607-664
Injection site pain 16.3 11.2
Erythema ≥25mm 3.8 1.8
Induration ≥25mm 4.0 2.6
Ecchymosis ≥25mm 0.5 0.7
Table 1b. Percentages of Subjects Reporting Solicited Systemic Adverse Reactionsa in the Solicited Safety Populationb within 7 Days of Vaccination (Study 1)

Study 1: NCT02587221

Abbreviation: N=number of subjects with solicited safety data

Non-Influenza Comparator Vaccine = combined Tetanus Toxoid, Reduced Diphtheria Toxoid and Acellular Pertussis Vaccine, Boostrix® (GlaxoSmithKline Biologicals)

a All solicited systemic adverse events reported within 7 days of vaccination are included

b Solicited Safety Population: all subjects in the exposed population who received a study vaccine and provided post-vaccination solicited safety data

c Severe reactions of each type were reported in 1.1% or fewer subjects receiving Fluad Quadrivalent; severe reactions of each type were also reported in the comparator group at similar percentages. Severe definitions: Nausea, Fatigue, Myalgia, Arthralgia, Headache, and Chills = prevents daily activity; Loss of appetite = not eating at all; Vomiting = 6 or more times in 24 hours or requires intravenous hydration; Diarrhea = 6 or more loose stools in 24 hours or requires intravenous hydration; Fever = ≥102.2°F (39°C).

Systemic Reactionsc Fluad Quadrivalent
N=595-659
Non-Influenza Comparator Vaccine
N=607-664
Headache 10.8 8.3
Fatigue 10.5 8.8
Myalgia 7.7 6.1
Arthralgia 7.3 6.6
Chills 5.0 3.9
Diarrhea 4.1 3.0
Nausea 3.8 2.3
Loss of appetite 3.6 3.6
Fever ≥100.4°F (38°C) 1.7 1.2
Vomiting 0.8 1.1

Unsolicited adverse events (AEs) were collected for all subjects for 21 days after vaccination. Related unsolicited AEs were reported by 303 (9.0%) and by 261 (7.7%) of the subjects for Fluad Quadrivalent and Boostrix, respectively. For Fluad Quadrivalent, injection site pain and influenza-like illness were the only unsolicited adverse reactions reported in ≥ 1% of subjects (1.7% and 1.5%, respectively).

Serious adverse events (SAEs) and potentially immune-mediated adverse events of special interest (AESIs) were collected up to 366 days after vaccination. SAEs were reported by 238 (7.0%) Fluad Quadrivalent recipients and 234 (6.9%) comparator recipients. There were no SAEs, AESIs or deaths in this study that were related to Fluad Quadrivalent.

Study 2 (NCT03314662) was a multicenter, randomized, double-blind, comparator-controlled study conducted during the 2017-18 Northern Hemisphere influenza season. In this study, 888 subjects received Fluad Quadrivalent, 444 subjects received the licensed adjuvanted trivalent vaccine (aTIV-1 - FLUAD® (trivalent formulation)) and 444 subjects received an adjuvanted trivalent influenza vaccine with an alternate B strain (aTIV-2).

The mean age of subjects at enrollment who received Fluad Quadrivalent was 72.5 years. Female subjects represented 56.6% of the study population and the racial distribution of subjects was 91.6% Caucasian, 7.0% Black or African American, and ≤ 1% each for Asian, Native Hawaiian or Pacific Islander, American Indian or Alaska Native or Other.

Solicited local and systemic adverse reactions reported within 7 days after vaccination were similar to those reported for Study 1. Unsolicited AEs were collected for 21 days after vaccination. Related unsolicited AEs were reported by 39 (4.4%) and by 17-19 (3.8%-4.3%) of subjects administered Fluad Quadrivalent or aTIV, respectively. For Fluad Quadrivalent, injection site bruising (1.0%) was the only unsolicited adverse reaction reported in ≥ 1% of subjects.

Serious AEs and AESIs were collected up to 181 days after vaccination. Within 6 months after vaccination, 37 (4.2%) Fluad Quadrivalent recipients and 18-28 (4.1%-6.3%) aTIV recipients experienced an SAE. There were no SAEs, AESIs or deaths in this study that were related to the study vaccine. There were no AEs leading to withdrawal from the study.

. Postmarketing Experience

There are no postmarketing data available for Fluad Quadrivalent. However, the post-marketing experience with FLUAD (trivalent formulation) is relevant to Fluad Quadrivalent because both vaccines are manufactured using the same process and have overlapping compositions.

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 causal relationship to the vaccine.

Blood and lymphatic system disorders:

Thrombocytopenia (some cases were severe with platelet counts less than 5,000 per mm3), lymphadenopathy

General disorders and administration site conditions:

Extensive swelling of injected limb lasting more than one week, injection site cellulitis-like reactions (some cases of swelling, pain, and redness extending more than 10 cm and lasting more than 1 week)

Immune system disorders:

Allergic reactions including anaphylactic shock, anaphylaxis, and angioedema

Musculoskeletal and connective tissue disorders:

Muscular weakness

Nervous system disorders:

Encephalomyelitis, Guillain-Barré Syndrome, convulsions, neuritis, neuralgia, parasthesia, syncope, presyncope

Skin and subcutaneous tissue disorders:

Generalized skin reactions including erythema multiforme, urticaria, pruritis or non-specific rash

Vascular disorders:

Vasculitis, renal vasculitis

Drug Interactions

. Concomitant Use With Other Vaccines

No clinical data on concomitant administration of Fluad Quadrivalent with other vaccines is available.

If Fluad Quadrivalent is given at the same time as other injectable vaccine(s), the vaccine(s) should be administered at different injection sites.

Do not mix Fluad Quadrivalent with any other vaccine in the same syringe.

. Concurrent Use With Immunosuppressive Therapies

Immunosuppressive or corticosteroid therapies may reduce the immune response to Fluad Quadrivalent.

USE IN SPECIFIC POPULATIONS

. Pregnancy

Risk Summary

Fluad Quadrivalent is not approved for use in persons < 65 years of age. There are insufficient human data to establish whether there is a vaccine-associated risk with use of Fluad Quadrivalent in pregnancy.

There were no developmental toxicity studies of Fluad Quadrivalent performed in animals. A developmental toxicity study has been performed in female rabbits administered FLUAD (trivalent formulation) prior to mating and during gestation. A 0.5 mL dose was injected on each occasion (a single human dose is 0.5 mL). (see 8.1 Animal Data).

Animal Data

In a developmental toxicity study, the effect of FLUAD (trivalent formulation) was evaluated in pregnant rabbits. Animals were administered FLUAD (trivalent formulation) 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 (45 mcg)/rabbit/occasion. No vaccine-related fetal malformations or variations and no adverse effects on pre-weaning development were observed in the study.

. Lactation

Fluad Quadrivalent is not approved for use in persons < 65 years of age. No human or animal data are available to assess the effects of Fluad Quadrivalent on the breastfed infant or on milk production/excretion.

. Pediatric Use

The safety and effectiveness of Fluad Quadrivalent in the pediatric population have not been established.

. Geriatric Use

Safety and immunogenicity of Fluad Quadrivalent have been evaluated in adults 65 years of age and older. [See Adverse Reactions (6.1) and Clinical Studies (14)]

Fluad Quadrivalent Description

Fluad Quadrivalent (Influenza Vaccine, Adjuvanted), a sterile injectable emulsion for intramuscular use, is a quadrivalent, inactivated influenza vaccine prepared from virus propagated in the allantoic cavity of embryonated hens' eggs inoculated with a specific type of influenza virus.

Fluad Quadrivalent is standardized according to United States Public Health Service requirements and each 0.5 mL dose is formulated to contain 15 mcg of hemagglutinin (HA) from each of the following four influenza strains recommended for the 2020-2021 influenza season: A/Victoria/2454/2019 IVR-207 (an A/Guangdong-Maonan/SWL1536/2019 (H1N1)pdm09-like virus), A/Hong Kong/2671/2019 IVR-208 (an A/Hong Kong/2671/2019 (H3N2)-like virus), B/Victoria/705/2018 BVR-11 (a B/Washington/02/2019-like virus), B/Phuket/3073/2013 BVR-1B (a B/Phuket/3073/2013-like virus).

Fluad Quadrivalent also contains MF59C.1 adjuvant (MF59®), a squalene based oil-in-water emulsion.

Each of the strains is harvested and clarified separately by centrifugation and filtration prior to inactivation with formaldehyde. 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 cetyltrimethylammonium bromide (CTAB). The antigen preparation is further purified.

Fluad Quadrivalent is prepared by combining the four virus antigens with the MF59C.1 adjuvant. After combining, Fluad Quadrivalent is a sterile, milky-white injectable emulsion supplied in single-dose pre-filled syringes containing 0.5 mL dose. Each 0.5 mL dose contains 15 mcg of hemagglutinin (HA) from each of the four recommended influenza strains and MF59C.1 adjuvant (9.75 mg squalene, 1.175 mg of polysorbate 80, 1.175 mg of sorbitan trioleate, 0.66 mg of sodium citrate dihydrate and 0.04 mg of citric acid monohydrate) at pH 6.9-7.7.

Fluad Quadrivalent may contain trace amounts of neomycin (≤ 0.02 mcg by calculation), kanamycin (≤ 0.03 mcg by calculation) and hydrocortisone (≤ 0.005 ng by calculation) which are used during the initial stages of manufacture, as well as residual egg protein (ovalbumin) (≤ 1.0 mcg), formaldehyde (≤ 10 mcg) or CTAB (≤ 18 mcg).

Fluad Quadrivalent does not contain a preservative. The syringe, syringe plunger stopper and tip caps are not made with natural rubber latex.

Fluad Quadrivalent - 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 induced by vaccination with inactivated influenza virus vaccine have not been correlated with protection from influenza illness. In some human studies, HI antibody titers of 1:40 or greater have been associated with protection from influenza illness in up to 50% of subjects. [see References (2,3)]

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 quadrivalent influenza vaccines are standardized to contain the hemagglutinin of influenza virus strains (two subtypes A and two types B), representing the influenza viruses likely to be circulating in the United States in the upcoming influenza season.

Annual influenza vaccination is recommended because immunity declines during the year after vaccination, and because circulating strains of influenza virus change from year to year.

Nonclinical Toxicology

. Carcinogenesis, Mutagenesis, Impairment of Fertility

Fluad Quadrivalent has not been evaluated for carcinogenic or mutagenic potential, or for impairment of male fertility in animals. FLUAD (trivalent formulation) did not affect female fertility in a rabbit developmental toxicity study [see Pregnancy (8.1)].

Clinical Studies

Immunogenicity of Fluad Quadrivalent

Immunogenicity of Fluad Quadrivalent was evaluated in Study 1 (NCT02587221), a randomized, observer-blind, non-influenza comparator-controlled multicenter efficacy study conducted in 12 countries during the 2016-2017 Northern Hemisphere and 2017 Southern Hemisphere seasons. In this study, elderly subjects 65 years of age and older received one dose of either Fluad Quadrivalent (N=3379) or a US-licensed non-influenza comparator vaccine (Boostrix; N=3382). Immunogenicity was evaluated 21 days after vaccination in a subgroup of subjects in a 4:1 ratio: Fluad Quadrivalent (N=1324) and non-influenza control vaccines (N=332). In the immunogenicity set, the mean age across both vaccination groups was 72 years and females represented 59% of subjects. The racial distribution of subjects consisted of 89% Caucasian, 11% Asian and <1% American Indian or Alaska Native.

Immunogenicity endpoints measured 3 weeks after vaccination included percentage of subjects with HI titer ≥1:40 and percentage of subjects who achieved seroconversion. Success criteria required the lower bound of the 2-sided 95% CI for the proportion of subjects with an HI titer ≥1:40 to be ≥60% and for the lower bound of the 2-sided 95% CI for the proportion of subjects with seroconversion to be ≥30%. Antibody responses for all 4 strains are presented in Table 2.

Table 2: Immune Responses 21 Days After Vaccination with Fluad Quadrivalent or a Non-Influenza Comparator Vaccine in Elderly Subjects 65 years of Age and Older (Study 1)

Abbreviations: CI=Confidence Interval, N=number of subjects in full analysis immunogenicity set.

Non-Influenza Comparator Vaccine = combined Tetanus Toxoid, Reduced Diphtheria Toxoid and Acellular Pertussis Vaccine, Boostrix® (GlaxoSmithKline Biologicals)

b Seroconversion is defined as a pre-vaccination HI titer <1:10 and post-vaccination HI titer ≥ 1:40 or at least a 4-fold increase in HI from pre-vaccination HI titer ≥ 1:10. Success criteria: the LB of the 95% CI for the SCR must be ≥30%.

Strain Proportion of subjects with HI titer ≥1:40a
(95% CI)
Fluad Quadrivalent
N=1324
Proportion of subjects with HI titer ≥1:40a
(95% CI)
Non-Influenza Comparator Vaccine
N=332
Seroconversionb
(95% CI)
Fluad Quadrivalent

N=1324
Seroconversionb
(95% CI)
Non-Influenza Comparator Vaccine

N=332
A/H1N1 96.2%
(95.1%, 97.2%)
46.7%
(41.2%, 52.2%)
78.0%
(75.7%, 80.2%)
2.1%
(0.9%, 4.3%)
A/H3N2 95.6%
(94.4%, 96.7%)
41.7%
(36.3%, 47.2%)
84.6%
(82.5%, 86.5%)
3.9%
(2.1%, 6.6%)
B/Yamagata 79.2%
(77.0%, 81.4%)
21.5%
(17.2%, 26.4%)
60.8%
(58.1%, 63.4%)
3.6%
(1.9%, 6.3%)
B/Victoria 81.6%
(79.4%, 83.7%)
18.4%
(14.4%, 23.0%)
65.5%
(62.9%, 68.1%)
2.1%
(0.9%, 4.3%)

REFERENCES

  1. Lasky T, Terracciano GJ, Magder L, et al. The Guillain-Barre syndrome and the 1992-1993 and 1993-1994 influenza vaccines. N Engl J Med 1998; 339(25): 1797-1802.

  2. Hannoun C, Megas F, Piercy J. Immunogenicity and protective efficacy of influenza vaccination. Virus Res 2004; 103:133-138.

  3. 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.

How Supplied/Storage and Handling

Fluad Quadrivalent is supplied in the product presentation listed below:

Presentation Carton
NDC Number
Components
Pre-Filled Syringe 70461-120-03 0.5 mL dose in a pre-filled syringe (needle not supplied), package of 10 syringes per carton [NDC 70461-120-04]

Store Fluad Quadrivalent refrigerated at 2°C to 8°C (36°F to 46°F). Protect from light. Do not freeze. Discard if the vaccine has been frozen. Do not use after expiration date.

The syringe, syringe plunger stopper and tip cap are not made with natural rubber latex.

Patient Counseling Information

  • Inform vaccine recipients of the potential benefits and risks of immunization with Fluad Quadrivalent.
  • Educate vaccine recipients regarding the potential side effects. Clinicians should emphasize that (1) Fluad Quadrivalent contains non-infectious particles and cannot cause influenza and (2) Fluad Quadrivalent is intended to help provide protection against illness due to influenza viruses only.
  • Instruct vaccine recipients to report adverse reactions to their healthcare provider and/or to Vaccine Adverse Event Reporting System (VAERS) at 1-800-822-7967 and www.vaers.hhs.gov. Provide vaccine recipients with the Vaccine Information Statements which are required by the National Childhood Vaccine Injury Act of 1986. These materials are available free of charge at the Centers for Disease Control and Prevention (CDC) website (www.cdc.gov/vaccines).
  • Inform vaccine recipients that annual vaccination is recommended.

Fluad Quadrivalent is a registered trademark of Seqirus UK Limited or its affiliates.

MF59® is a trademark of Novartis AG.

Manufactured by: Seqirus Inc., 475 Green Oaks Parkway, Holly Springs, NC 27540, USA

Distributed by: Seqirus USA Inc., 25 Deforest Avenue, Summit, NJ 07901, USA

Tel: 1-855-358-8966

US License No. 2049

Principal Display Panel – Carton Label

NDC 70461-120-03

2020-2021 Formula

Influenza
Vaccine,
Adjuvanted

FLUAD®
QUADRIVALENT

FOR ADULTS

65 YEARS
AND OLDER

For Intramuscular Injection only

Ten 0.5 mL, single-dose, pre-filled syringes

Rx Only

Seqirus™

Principal Display Panel – Syringe Label

Influenza Vaccine,
Adjuvanted

FLUAD® QUADRIVALENT

2020 – 2021 Formula

NDC 70461-120-04

Fluad Quadrivalent
influenza vaccine, adjuvanted injection, suspension
Product Information
Product Type VACCINE Item Code (Source) NDC:70461-120
Route of Administration INTRAMUSCULAR DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
INFLUENZA A VIRUS A/VICTORIA/2454/2019 IVR-207 (H1N1) ANTIGEN (FORMALDEHYDE INACTIVATED) (INFLUENZA A VIRUS A/VICTORIA/2454/2019 IVR-207 (H1N1) HEMAGGLUTININ ANTIGEN (FORMALDEHYDE INACTIVATED)) INFLUENZA A VIRUS A/VICTORIA/2454/2019 IVR-207 (H1N1) ANTIGEN (FORMALDEHYDE INACTIVATED) 15 ug in 0.5 mL
INFLUENZA A VIRUS A/HONG KONG/2671/2019 IVR-208 (H3N2) ANTIGEN (FORMALDEHYDE INACTIVATED) (INFLUENZA A VIRUS A/HONG KONG/2671/2019 IVR-208 (H3N2) HEMAGGLUTININ ANTIGEN (FORMALDEHYDE INACTIVATED)) INFLUENZA A VIRUS A/HONG KONG/2671/2019 IVR-208 (H3N2) ANTIGEN (FORMALDEHYDE INACTIVATED) 15 ug in 0.5 mL
INFLUENZA B VIRUS B/VICTORIA/705/2018 BVR-11 ANTIGEN (FORMALDEHYDE INACTIVATED) (INFLUENZA B VIRUS B/VICTORIA/705/2018 BVR-11 HEMAGGLUTININ ANTIGEN (FORMALDEHYDE INACTIVATED)) INFLUENZA B VIRUS B/VICTORIA/705/2018 BVR-11 ANTIGEN (FORMALDEHYDE INACTIVATED) 15 ug in 0.5 mL
INFLUENZA B VIRUS B/PHUKET/3073/2013 BVR-1B ANTIGEN (FORMALDEHYDE INACTIVATED) (INFLUENZA B VIRUS B/PHUKET/3073/2013 BVR-1B HEMAGGLUTININ ANTIGEN (FORMALDEHYDE INACTIVATED)) INFLUENZA B VIRUS B/PHUKET/3073/2013 BVR-1B ANTIGEN (FORMALDEHYDE INACTIVATED) 15 ug in 0.5 mL
Inactive Ingredients
Ingredient Name Strength
sodium chloride
potassium chloride
potassium phosphate, monobasic
sodium phosphate, dibasic, dihydrate
magnesium chloride
calcium chloride
citric acid monohydrate
sorbitan trioleate
trisodium Citrate dihydrate
water
squalene
polysorbate 80
Packaging
# Item Code Package Description
1 NDC:70461-120-03 10 SYRINGE, GLASS in 1 CARTON
1 NDC:70461-120-04 0.5 mL in 1 SYRINGE, GLASS
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA125510 02/21/2020 07/31/2021
Labeler - Seqirus, Inc. (080102141)
Seqirus, Inc.

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