Boostrix Vaccine

Boostrix contains inactivated components of the bacteria responsible for diphtheria, tetanus, and pertussis. When administered, it stimulates the body's immune system to produce antibodies against these pathogens without causing the diseases themselves. This immune response equips the body to recognize and combat these infections effectively in the future.

• Administration: The Boostrix Vaccine is administered as a single 0.5 ml intramuscular injection, preferably into the deltoid muscle of the upper arm.
• Schedule: Boostrix can be given regardless of previous vaccination history. For pregnant women, it is recommended during the third trimester to help protect newborns from pertussis.
• Healthcare Supervision: Always ensure that a qualified healthcare professional administers the vaccine.

• Inform if you have a history of severe allergic reactions to any vaccine components.
• Inform if you experienced encephalopathy of unknown origin within seven days of a previous pertussis-containing vaccine.
• Inform if you suffer from progressive neurological disorders.
• Inform if you have a bleeding disorder or are on anticoagulant therapy.
• Inform if you are immunocompromised or undergoing immunosuppressive therapy.

• Protection Against Diphtheria: Boostrix Vaccine prevents a serious infection that affects the mucous membranes of the throat and nose.
• Protection Against Tetanus: Prevents a bacterial infection that causes painful muscle stiffness and spasms, often referred to as "lockjaw."
• Protection Against Pertussis: Prevents whooping cough, a highly contagious respiratory disease known for severe coughing fits.

• Common side effects may include: Pain, redness, or swelling at the injection site, Headache., Fatigue, Gastrointestinal symptoms such as nausea, vomiting, diarrhea, or abdominal pain.
• These side effects are usually mild and resolve on their own. If they persist or become bothersome, consult your healthcare provider.