Healthcare Professionals

The flu is serious. Now your patients aged 4 years and older have another option to help prevent the flu: FLUCELVAX QUADRIVALENT.

It's time to reshape the way you think about flu shots

Introducing a flu shot that could transform flu protection

For decades, there have been few improvements in flu shot manufacturing.1 Now, there's a vaccine made using modern techniques that may reshape the way you think about the flu shot. FLUCELVAX QUADRIVALENT is made using cell culture technology, which does not rely on eggs for manufacturing and has the potential to rapidly increase production of flu shots in times of need.1,2 It's also antibiotic, preservative, and latex free, and it helps protect against 4 strains of the flu in people aged 4 years and older.2 This flu season, consider a flu shot that’s on the cutting edge of flu protection. Choose FLUCELVAX QUADRIVALENT.

Purchase Information

You can purchase FLUCELVAX QUADRIVALENT in one of three ways:

Order FLUCELVAX QUADRIVALENT online at www.flu.seqirus.com

Call 855-358-8966 or email cs.flu@seqirus.com

Contact your Seqirus account manager

FLUCELVAX QUADRIVALENT Important Safety Information

Indication and Usage for FLUCELVAX QUADRIVALENT® (Influenza Vaccine)

FLUCELVAX QUADRIVALENT® is an inactivated vaccine indicated for active immunization for the prevention of influenza disease caused by influenza A subtype viruses and type B viruses contained in the vaccine. FLUCELVAX QUADRIVALENT is approved for use in persons 4 years of age and older.

Important Safety Information
Contraindication
  • Do not administer FLUCELVAX QUADRIVALENT to anyone with a history of severe allergic reaction (e.g. anaphylaxis) to any component of the vaccine.
Warnings & Precautions
  • Guillain-Barré Syndrome (GBS): If GBS has occurred within 6 weeks of receipt of a prior influenza vaccine, the decision to give FLUCELVAX QUADRIVALENT should be based on careful consideration of the potential benefits and risks.
  • Preventing and Managing Allergic Reactions: Appropriate medical treatment and supervision must be available to manage possible anaphylactic reactions following administration of the vaccine.
  • Syncope: Syncope (fainting) can occur in association with administration of injectable vaccines, including FLUCELVAX QUADRIVALENT. 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.
  • Altered Immunocompetence: After vaccination with FLUCELVAX QUADRIVALENT, immunocompromised individuals, including those receiving immunosuppressive therapy, may have a reduced immune response.
  • Limitations of Vaccine Effectiveness: Vaccination with FLUCELVAX QUADRIVALENT may not protect all vaccine recipients against influenza disease.
Most Common Adverse Reactions
  • The most common (≥10%) local and systemic reactions in adults 18-64 years of age were injection site pain (45.4%) headache (18.7%), fatigue (17.8%) and myalgia (15.4%), injection site erythema (13.4%), and induration (11.6%).
  • The most common (≥10%) local and systemic reactions in adults ≥65 years of age were injection site pain (21.6%) and injection site erythema (11.9%).
  • The most common (≥10%) local and systemic reactions in children 4 to < 6 years of age were tenderness at the injection site (46%), injection site erythema (18%), sleepiness (19%), irritability (16%), injection site induration (13%), and change in eating habits (10%).
  • The most common (≥10%) local and systemic reactions in children 6 through 8 years of age were pain at the injection site (54%), injection site erythema (22%), injection site induration (16%), headache (14%), fatigue (13%), and myalgia (12%).
  • The most common (≥10%) local and systemic reactions in children and adolescents 9 through 17 years of age were pain at the injection site (58%), headache (22%), injection site erythema (19%), fatigue (18%) myalgia (16%), and injection site induration (15%).

Please see accompanying US Full Prescribing Information for FLUCELVAX QUADRIVALENT.

Seqirus Vaccines maintains the FLUCELVAX QUADRIVALENT Pregnancy Registry for pregnant women immunized with FLUCELVAX QUADRIVALENT (Influenza Vaccine) during pregnancy. The Registry is strictly observational and is designed to collect prospective data on pregnancy outcomes. To enroll in the Registry, determine eligibility or for more information, please call 1-877-413-4759 or click here.

References

1. Perdue ML, Arnold F, Li S, et al. The future of cell culture-based influenza vaccine production. Expert Rev Vaccines. 2011;10(8):1183-1194. doi: 10.1586/erv.11.82.

2. FLUCELVAX QUADRIVALENT [package insert]. Holly Springs, NC. Seqirus, Inc: 2016.