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Gardasil (HPV Type 6, 11,16 & 18) Vaccine

Gardasil is a recombinant quadrivalent vaccine designed to protect against Human Papillomavirus (HPV) types 6, 11, 16, and 18. It’s indicated for individuals aged 9 through 26 years to prevent cervical, vulvar, vaginal, and anal cancers, as well as genital warts and precancerous lesions associated with these HPV types. Administered via intramuscular injection, Gardasil plays a crucial role in reducing the risk of HPV-related diseases.

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Gardasil is a prophylactic vaccine that targets four HPV types: 6, 11, 16, and 18. HPV types 16 and 18 are responsible for approximately 70% of cervical cancer cases globally, while types 6 and 11 cause about 90% of genital warts. By eliciting an immune response against these HPV types, Gardasil effectively reduces the incidence of related cancers and genital warts.

The vaccine is formulated as a suspension for intramuscular injection, typically administered in a three-dose schedule over six months. Gardasil is suitable for both females and males aged 9 through 26 years, aiming to provide broad protection against HPV-related diseases.

Indications

Gardasil is indicated for use in females and males aged 9 through 26 years for the prevention of the following diseases caused by HPV types included in the vaccine:

  • Cancers:
    • Cervical, vulvar, vaginal, and anal cancers caused by HPV types 16 and 18.
  • Genital Warts:
    • Genital warts (condyloma acuminata) caused by HPV types 6 and 11.
  • Precancerous or Dysplastic Lesions:
    • Cervical intraepithelial neoplasia (CIN) grades 1, 2, and 3.
    • Cervical adenocarcinoma in situ (AIS).
    • Vulvar intraepithelial neoplasia (VIN) grades 2 and 3.
    • Vaginal intraepithelial neoplasia (VaIN) grades 2 and 3.
    • Anal intraepithelial neoplasia (AIN) grades 1, 2, and 3.

Composition

Each 0.5 mL dose of Gardasil contains:

  • Active Ingredients:
    • HPV Type 6 L1 protein: 20 µg.
    • HPV Type 11 L1 protein: 40 µg.
    • HPV Type 16 L1 protein: 40 µg.
    • HPV Type 18 L1 protein: 20 µg.
  • Adjuvant:
    • Amorphous aluminum hydroxyphosphate sulfate: 0.225 mg Al.
  • Excipients:
    • Sodium chloride.
    • L-histidine.
    • Polysorbate 80.
    • Sodium borate.
    • Water for injection.

Dosage and Administration

Gardasil is administered as a 0.5 mL intramuscular injection, preferably in the deltoid muscle of the upper arm or the higher anterolateral area of the thigh.

  • Standard Schedule:
    • Three-Dose Series: Administered at 0, 2, and 6 months.
  • Alternative Schedule:
    • Two-Dose Series: For individuals aged 9 through 14 years, administered at 0 and 6 months.

Note: The vaccination schedule may vary based on age and local health authority recommendations. It’s essential to complete the full vaccination series for optimal protection.

Precautions

  • Hypersensitivity: Contraindicated in individuals with hypersensitivity to any vaccine component, including yeast.
  • Acute Illness: Defer vaccination in individuals with moderate or severe acute illnesses until recovery.
  • Syncope: Syncope (fainting) can occur following vaccination; observe individuals for 15 minutes post-injection.
  • Pregnancy: Not recommended for use during pregnancy. If pregnancy is detected after initiation of the vaccination series, delay the remaining doses until after pregnancy.
  • Immunocompromised Individuals: The immune response may be diminished in immunocompromised individuals, including those receiving immunosuppressive therapy.

Limitations of Vaccine Effectiveness: Gardasil does not protect against all HPV types or existing HPV infections. Routine cervical cancer screening remains essential.

Storage

  • Store refrigerated at 2°C to 8°C (36°F to 46°F).
  • Do not freeze. Discard if the vaccine has been frozen.
  • Protect from light by storing in the original package until administration.
  • Shake well before use to obtain a uniform suspension.

Note

  • Cervical Cancer Screening: Vaccination does not eliminate the need for routine cervical cancer screening. Continue regular Pap tests as recommended.
  • Completion of Vaccine Series: Ensure the full vaccination series is completed for maximum efficacy.
  • Reporting of Adverse Events: Report any adverse events following vaccination to healthcare providers or local health authorities.

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