NATPARA® (NPS Pharmaceuticals, Inc., Bedminster NJ) for subcutaneous injection was approved by the US Food and Drug Administration on January 23, 2015. Natpara is a parathyroid hormone indicated as an adjunct to calcium and vitamin D to control hypocalcemia in patients with hypoparathyroidism.1 It is injected daily to help regulate the body’s calcium levels.
Hypoparathyroidism is a rare endocrine disease that affects approximately 60,000 people in the United States. Symptoms can be caused by low blood calcium levels (hypocalcemia). Patients with hypoparathyroidism may experience symptoms, including:
The most common cause of hypoparathyroidism is the loss of active parathyroid tissue following thyroid or parathyroid surgery. More rare is a defect present at birth (congenital), where a person is born without parathyroid glands. Occasionally, the specific cause of hypoparathyroidism cannot be determined.
How Natpara is Supplied
Natpara is supplied as a medication cartridge, which is available in four dosage strengths (25, 50, 75, and 100 mcg/dose). The medication cartridge is disposable and designed for use with a “reusable mixing device for product reconstitution and reusable Q-Cliq™ pen injector for drug delivery.”1
1. NATPARA® Full Prescribing Information. 22Jan2015. http://www.npsp.com/file_depot/0-10000000/0-10000/262/folder/2023/NatparaPI.pdf. Accessed January 27, 2015.
January 27, 2015