Boostrix® Pregnancy Registry

for Boostrix® Tetanus Toxoid, Reduced Diphtheria Toxoid and Acellular Pertussis Vaccine, Adsorbed

This is a pregnancy registry for Boostrix vaccine (GSK) approved and marketed in the United States. To participate in this registry: Registration should take place as early in the pregnancy as possible and prior to any knowledge of the pregnancy outcome. Healthcare providers(HCPs) are encouraged to notify the registry staff of ongoing pregnancies where exposure to the vaccine has already occurred. HCPs can enroll the patients by completing the enrollment form available below. We include a “patient inform consent form” with information regarding this registry, and we encourage HCPs to review this form with their patient and have it signed at the time of enrollment. All forms can be sent by fax or email to the Pregnancy Registry.

Patients can be registered by calling GlaxoSmithKline directly at 1-888-452-9622 (toll-free).

GlaxoSmithKline's Boostrix® Pregnancy Registry is managed at:

Boostrix® Pregnancy Registry
Global Clinical Safety and Pharmacovigilance
PO Box 13398
Research Triangle Park, NC 27709-3398
Phone: 888-825-5249
Fax: 1-919-483-5404

Information collected at the time of registration includes date(s) of vaccine exposure, estimated date of delivery, and sufficient contact information to allow for follow-up of the subsequent pregnancy outcome. Measures are in place to protect patient confidentiality. If Registration is initiated from a consumer, permission is requested to obtain confirmation and follow-up from their health care provider. Around the patient’s estimated date of delivery, a short follow-up form is sent to the registering healthcare provider to report on the pregnancy course and outcome.

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