Patient support and resources

3 Ways to help your patients get started with FORTEO

forteo savings copay card

Forteo Savings Card*

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forteo connect patient support

FORTEO Connect

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forteo patient starter kit

Forteo starter kit

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*Governmental beneficiaries excluded, subject to terms and conditions.

Forteo Savings Card

  • Commercially insured patients pay as little as $4 per month with the FORTEO Savings Card
  • Up to 12 months

Download their FORTEO Savings Card below

Subject to Lilly USA, LLC’s (Lilly’s) right to terminate, rescind, revoke or amend the Forteo Savings Card Program ( “Card”) eligibility criteria and/or Card terms and conditions which may occur at Lilly’s sole discretion, without notice, and for any reason, the Card expires and savings end on 12/31/2024. Card savings are not available to patients without commercial drug insurance or who are enrolled in any state, federal, or government funded healthcare program, including, without limitation, Medicaid, Medicare, Medicare Part D, Medicare Advantage, Medigap, DoD, VA, TRICARE®/CHAMPUS, or any state prescription drug assistance program.

For patients with commercial drug insurance coverage for Forteo: You must have commercial drug insurance that covers Forteo and a prescription consistent with FDA-approved product labeling to pay as little as $4 for a 1-month prescription fill of Forteo. Month is defined as 28-days. Card savings are subject to a maximum monthly savings of wholesale acquisition cost plus usual and customary pharmacy charges and separate maximum annual savings of up to $9,450 per calendar year. Card may be used for a maximum of up to 13 prescription fills per calendar year. Subject to Lilly USA, LLC’s (“Lilly”) right to terminate, rescind, revoke, or amend Card eligibility criteria and/or Card terms and conditions which may occur at Lilly’s sole discretion, without notice, and for any reason, Card expires and savings end on 12/31/2024.

Help eligible patients lower out-of-pocket costs to as little as $4 per month for FORTEO for up to 12 months. Help your patients by downloading their card below or contact FORTEO Connect.

Patient Savings Card

Eligible commercially insured patients pay as little as $4 for a month's supply of FORTEO*.

If you are a healthcare professional in Vermont, ask for a savings card from your representative.

Each card has a unique ID number. Please do not make copies.

*See terms and conditions above

Enroll them in FORTEO Connect

Information and injection training

  • Patients learn how to get off to a good start on FORTEO with personalized support

Insurance investigation

You can enroll your patients online or by calling 1-866-4-FORTEO (1-866-436-7836), 8 am-10 pm ET (M-F).

Give them a FORTEO starter kit

Call The Lilly Answers Center (TLAC) at 1-800-LillyRx (1-800-545-5979) to receive kits

  • FORTEO Travel Bag with room for their FORTEO delivery device and needles
  • FORTEO User Manual
  • FORTEO Patient Guide
  • FORTEO Prescribing Information and Medication Guide

Note: There is a limit of 1 kit per person.

For more information about FORTEO

Please see full Prescribing Information



FORTEO is contraindicated in patients with hypersensitivity to teriparatide or to any of its excipients. Reactions have included angioedema and anaphylaxis.


Osteosarcoma: Osteosarcoma has been reported in patients treated with FORTEO in the post marketing setting; however, an increased risk of osteosarcoma has not been observed in observational studies in humans. Avoid use in patients with increased baseline risk of osteosarcoma including patients with open epiphyses (pediatric and young adult patients), metabolic bone diseases including Paget’s disease of the bone, bone metastases or history of skeletal malignancies, prior external beam or implant radiation therapy involving the skeleton, and hereditary disorders predisposing to osteosarcoma. There is limited data assessing the risk of osteosarcoma beyond 2 years.

Hypercalcemia and Cutaneous Calcification: FORTEO may cause hypercalcemia and may exacerbate hypercalcemia in patients with pre-existing hypercalcemia. Avoid FORTEO in patients known to have an underlying hypercalcemic disorder, such as primary hyperparathyroidism.

Serious reports of calciphylaxis and worsening of previously stable cutaneous calcification have been reported in the post-marketing setting in patients taking FORTEO. Risk factors for development of calciphylaxis include underlying autoimmune disease, kidney failure, and concomitant warfarin or systemic corticosteroid use. Discontinue in patients developing calciphylaxis or worsening of previously stable cutaneous calcification.

Risk of Urolithiasis: Consider the risks and benefits in patients with active or recent urolithiasis because of risk of exacerbation. If FORTEO-treated patients have pre-existing hypercalciuria or suspected/known active urolithiasis, consider measuring urinary calcium excretion.

Orthostatic Hypotension: Transient orthostatic hypotension may occur with initial doses of FORTEO. FORTEO should be administered initially under circumstances in which the patient can sit or lie down if symptoms of orthostatic hypotension occur. In short-term clinical pharmacology studies of FORTEO in healthy volunteers, transient episodes of symptomatic orthostatic hypotension were observed in 5% of volunteers.

Risk of Digoxin Toxicity: Hypercalcemia may predispose patients to digitalis toxicity because FORTEO transiently increases serum calcium. Consider the potential onset of signs and symptoms of digitalis toxicity when FORTEO is used in patients receiving digoxin.


The most common adverse reactions in clinical trials included: arthralgia (10.1% FORTEO vs. 8.4% placebo), pain (21.3% FORTEO vs. 20.5% placebo), and nausea (8.5% FORTEO vs. 6.7% placebo). Other adverse reactions included: dizziness, leg cramps, joint aches, and injection site reactions.

FORTEO may increase serum calcium, urinary calcium, and serum uric acid.


Pregnancy & Lactation
There are no available data on FORTEO use in pregnant women to evaluate for drug-associated risk of major birth defects, miscarriage, or adverse maternal or fetal outcomes. Consider discontinuing FORTEO when pregnancy is recognized. It is not known whether teriparatide is excreted in human milk, affects human milk production, or has effects on the breastfed infant. Avoid FORTEO use in women who are breastfeeding.

Pediatric Use
The safety and effectiveness of FORTEO have not been established in pediatric patients. Pediatric patients are at higher baseline risk of osteosarcoma because of open epiphyses. Avoid use due to increased baseline risk of osteosarcoma.

For more safety information, please click to see Medication Guide and Full Prescribing Information . Click to see Full User Manual that accompanies the delivery device.

FORTEO® is a registered trademark owned or licensed by Eli Lilly and Company, its subsidiaries, or affiliates.



FORTEO is indicated:

  • for the treatment of postmenopausal women with osteoporosis at high risk for fracture (defined herein as having a history of osteoporotic fracture or multiple risk factors for fracture) or who have failed or are intolerant to other available osteoporosis therapy. In postmenopausal women with osteoporosis, FORTEO reduces the risk of vertebral and nonvertebral fractures.
  • to increase bone mass in men with primary or hypogonadal osteoporosis at high risk for fracture or who have failed or are intolerant to other available osteoporosis therapy.
  • for the treatment of men and women with osteoporosis associated with sustained systemic glucocorticoid therapy (daily dosage equivalent to 5 mg or greater of prednisone) at high risk for fracture or who have failed or are intolerant to other available osteoporosis therapy.