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Takeda, in alignment with the U.S. Food and Drug Administration (FDA), will close the U.S. Special Use Program (SUP) for NATPARA® (parathyroid hormone) for Injection at the end of 2025. TAKEDA WILL CEASE SHIPMENTS OF NATPARA BY DECEMBER 31, 2025 AND NATPARA WILL NO LONGER BE AVAILABLE TO SUP PATIENTS. Learn How This May Affect You
NATPARA logo.
NATPARA logo.

Injection Training

We help prepare your patients to self-administer NATPARA

Nurse showing the NATPARA kit.

How we can help your patients get started

All patients prescribed NATPARA are provided injection training by a Registered Nurse through the NATPARA Nurse Educator team. A Patient Support Manager works with the Nurse Educator team to assign each patient a specially trained NATPARA Nurse Educator. The Nurse Educator will contact the patient within 2 business days of receiving his/her NATPARA shipment to schedule up to 4 sessions of complimentary training in the patient's home, including:

Nurse showing the NATPARA kit.
  • Delivering the injection device and demonstrating how to assemble it
  • Walking through the reconstitution and administration process for the first 3 cartridges (Days 1, 15, and 29 of treatment)
  • Calling the patient after each training to check in and answer any questions
  • Providing materials to help patients take an active role in their treatment

When patients are mixing the cartridge alone for the first time, there will be a Nurse Educator on the phone

Questions or concerns?

Please call 1-866-888-0660, Monday through Friday,
8:30 AM to 8:00 PM ET

Reference: 1. NATPARA [package insert]. Shire Pharmaceuticals, Inc.

NATPARA® and the NATPARA Logo® are registered trademarks of Takeda Pharmaceuticals, U.S.A,. Inc.