Natpara

Natpara is a prescription medication used to control hypocalcemia (low blood calcium levels) in patients with hypoparathyroidism.

Natpara belongs to a group of drugs called hormones. It helps to regulate the body’s calcium levels. Natpara should be used with calcium and vitamin D supplementation.

This medication is available in an injectable form to be given under the skin (subcutaneous) once daily.

Common side effects of Natpara include sensations of tingling, tickling, pricking, or burning of the skin (paraesthesia), low blood calcium, headache, high blood calcium, and nausea.

Natpara is a prescription parathyroid hormone (PTH) used with calcium and vitamin D supplementation to control low blood calcium (hypocalcemia) in people with low PTH blood levels (hypoparathyroidism).

This medication may be prescribed for other uses. Ask your doctor or pharmacist for more information.

Take this medication exactly as prescribed by your doctor. Follow the directions on your prescription label carefully.

The dose your doctor recommends may be based on the following:

• the condition being treated
• other medical conditions you have
• other medications you are taking
• how to respond to this medication

The dose of Natpara should be individualized based on calcium levels in the blood and urine.

WARNING: POTENTIAL RISK OF OSTEOSARCOMA

• In male and female rats, parathyroid hormone caused an increase in the incidence of osteosarcoma (a malignant bone tumor). The occurrence of osteosarcoma was dependent on parathyroid hormone dose and treatment duration. This effect was observed at parathyroid hormone exposure levels ranging from 3 to 71 times the exposure levels in humans receiving a 100 mcg dose of Natpara. These data could not exclude a risk to humans.
• Because of a potential risk of osteosarcoma, use NATPARA only in patients who cannot be well-controlled on calcium and active forms of vitamin D alone and for whom the potential benefits are considered to outweigh this potential risk.
• Avoid use of Natpara in patients who are at increased baseline risk for osteosarcoma such as patients with Paget's disease of bone or unexplained elevations of alkaline phosphatase, pediatric and young adult patients with open epiphyses, patients with hereditary disorders predisposing to osteosarcoma or patients with a prior history of external beam or implant radiation therapy involving the skeleton.
• Because of the risk of osteosarcoma, Natpara is available only through a restricted program under a Risk Evaluation and Mitigation Strategy (REMS) called the Natpara REMS Program.

Serious side effects have been reported with Natpara including the following:

• Osteosarcoma (a type of bone cancer). Natpara should not be used in patients with an increased risk of osteosarcoma.
• Severe hypercalcemia (high levels of calcium in the blood). Calcium levels should be monitored while patients are receiving Natpara.
• Severe hypocalcemia (low levels of calcium in the blood). Hypocalcemia can occur when Natpara therapy is interrupted or discontinued. Calcium levels should be monitored while patients are receiving Natpara.

Do not take Natpara if you:

• are allergic to Natpara or to any of its ingredients.

Serious side effects have been reported with Natpara. See the “Natpara Precautions” section.

Common side effects of Natpara include the following:

• sensations of tingling, tickling, pricking, or burning of the skin (paraesthesia)
• low blood calcium
• headache
• high blood calcium
• nausea
• diarrhea
• vomiting
• joint pain
• calcium in the urine
• pain in the extremities

This is not a complete list of Natpara side effects. Ask your doctor or pharmacist for more information.

Tell your doctor if you have any side effect that bothers you or that does not go away.

Call your doctor for medical advice about side effects. You may report side effects to the FDA at 1-800-FDA-1088.

Tell your doctor about all the medicines you take, including prescription and non-prescription medicines, vitamins, and herbal supplements. Especially tell your doctor if you take:

• digoxin (Lanoxin)

This is not a complete list of Natpara drug interactions. Ask your doctor or pharmacist for more information.

Tell your doctor if you are pregnant or plan to become pregnant.

The FDA categorizes medications based on safety for use during pregnancy. Five categories - A, B, C, D, and X - are used to classify the possible risks to an unborn baby when a medication is taken during pregnancy.

Natpara falls into category C. In animal studies, pregnant animals were given this medication and had some babies born with problems. No well-controlled studies have been done in humans. Therefore, this medication may be used if the potential benefits to the mother outweigh the potential risks to the unborn child.

Tell your doctor if you are breastfeeding or plan to breastfeed.

It is not known if Natpara crosses into human milk. Because many medications can cross into human milk and because of the possibility for serious adverse reactions in nursing infants with use of this medication, a choice should be made whether to stop nursing or stop the use of this medication. Your doctor and you will decide if the benefits outweigh the risk of using Natpara.