Forteo - Dosage Teriparatide

FORTEO (teriparatide injection, solution) comes in different strengths and amounts, which is referred to as the dosing of Forteo. The appearance of Forteo can differ based on the dosing. Your doctor may change the dosage and prescription of Forteo to get you the best results possible.

Dosage & Administration

  • Recommended dosage is 20 mcg subcutaneously once a day (2.1)
  • Consider supplemental calcium and Vitamin D based on individual patient needs (2.1)
  • Administer as a subcutaneous injection into the thigh or abdominal region (2.2)
  • Administer initially under circumstances in which the patient can sit or lie down if symptoms of orthostatic hypotension occur (2.2)
  • Use of FORTEO for more than 2 years during a patient's lifetime should only be considered if a patient remains at or has returned to having a high risk for fracture (2.3)

recommended dosage

The recommended dosage is 20 mcg given subcutaneously once a day. Instruct patients to take supplemental calcium and vitamin D if daily dietary intake is inadequate.

administration instructions

  • Administer FORTEO as a subcutaneous injection into the thigh or abdominal region. FORTEO is not approved for intravenous or intramuscular use.
  • FORTEO should be administered initially under circumstances in which the patient can sit or lie down if symptoms of orthostatic hypotension occur [see Warnings and Precautions (5.4)].
  • Parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration (FORTEO is a clear and colorless liquid). Do not use if solid particles appear or if the solution is cloudy or colored.
  • Patients and/or caregivers who administer FORTEO should receive appropriate training and instruction on the proper use of the FORTEO prefilled delivery device (pen) from a qualified health professional.

recommended treatment duration

Use of FORTEO for more than 2 years during a patient's lifetime should only be considered if a patient remains at or has returned to having a high risk for fracture [see Warnings and Precautions (5.1)].

Dosage Form & Strengths

Injection: 600 mcg/2.4 mL (250 mcg/mL) clear, colorless solution in a single-patient-use prefilled delivery device (pen) containing 28 daily doses of 20 mcg.

Injection: 600 mcg/2.4 mL (250 mcg/mL) in a single-patient-use prefilled delivery device (pen) containing 28 daily doses of 20 mcg (3)

Overdosage

In postmarketing spontaneous reports, there have been cases of medication errors in which the entire contents (up to 800 mcg) (40 times the recommended dose) of the FORTEO prefilled delivery device (pen) have been administered as a single dose. Transient events reported have included nausea, weakness/lethargy and hypotension. No fatalities associated with overdose have been reported. Additional signs, symptoms, and complications of FORTEO overdosage may include a delayed hypercalcemic effect, vomiting, dizziness, and headache.

Overdose Management — There is no specific antidote for a FORTEO overdosage. Treatment of suspected overdosage should include discontinuation of FORTEO, monitoring of serum calcium and phosphorus, and implementation of appropriate supportive measures, such as hydration.

Storage & Handling

how supplied

FORTEO (teriparatide injection) is a clear and colorless solution, available as single-patient-use prefilled delivery device (pen) in the following package size:

  • 600 mcg/2.4 mL (250 mcg/mL) [containing 28 daily doses of 20 mcg] NDC 0002-8400-01 (MS8400).

storage & handling

  • Store FORTEO under refrigeration at 2° to 8°C (36° to 46°F) at all times except when administering the product.
  • Recap the delivery device (pen) when not in use to protect the cartridge from physical damage and light.
  • When using FORTEO, minimize the time out of the refrigerator; deliver the dose immediately following removal from the refrigerator.
  • Do not freeze. Do not use FORTEO if it has been frozen.
This drug label information is as submitted to the Food and Drug Administration (FDA) and is intended for informational purposes only. If you think you may have a medical emergency, immediately call your doctor or dial 911. You are encouraged to report negative side effects of prescription drugs to the FDA. Visit the FDA MedWatch website or call 1-800-FDA-1088.
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