Forteo (for-TAY-o) : Appendix 1. Medication Guide
Forteo (for-TAY-o) : Appendix 1. Medication Guide
Forteo (for-TAY-o) : Appendix 1. Medication Guide
FORTEO® (for-TAY-o)
teriparatide (rDNA origin)
injection
Read this Medication Guide before you start taking FORTEO® and each time you get a refill.
There may be new information. Also, read the User Manual that comes with the FORTEO
delivery device (pen) for information on how to use the device to inject your medicine the right
way. This Medication Guide does not take the place of talking with your healthcare provider
about your medical condition or your treatment.
What is the most important information I should know about FORTEO?
1. Possible bone cancer. During drug testing, the medicine in FORTEO caused some rats to
develop a bone cancer called osteosarcoma. In people, osteosarcoma is a serious but rare
cancer. Osteosarcoma has rarely been reported in people who took FORTEO. It is not
known if people who take FORTEO have a higher chance of getting osteosarcoma.
2. You should not take FORTEO for more than 2 years over your lifetime.
3. There is a voluntary Patient Registry for people who take FORTEO. The purpose of the
registry is to collect information about the possible risk of osteosarcoma in people who take
FORTEO. For information about how to sign up for this patient registry, call 1-866-382
6813 or go to www.forteoregistry.rti.org.
What is FORTEO?
• FORTEO is a prescription medicine that is like a hormone made by the body called
parathyroid hormone or PTH. FORTEO may help to form new bone, increase bone
mineral density and bone strength.
• FORTEO can lessen the number of fractures of the spine and other bones in
FORTEO should not be used in children and young adults whose bones are still growing.
Tell your healthcare provider about all the medicines you take including prescription and
non-prescription medicines, vitamins, and herbal supplements. Your healthcare provider needs
this information to help keep you from taking FORTEO with other medicines that may harm
you.
• Especially tell your doctor if you take medicines that contain digoxin (Digoxin*,
Lanoxicaps*, Lanoxin*).
• FORTEO should look clear and colorless. Do not use FORTEO if it has particles in it, or
if it is cloudy or colored.
• Inject FORTEO right away after you take the delivery device out of the refrigerator.
• After each use, safely remove the needle, recap the delivery device, and put it back in the
refrigerator right away.
• You can take FORTEO at any time of the day. To help you remember to take FORTEO,
take it at about the same time each day.
• If you forget or cannot take FORTEO at your usual time, take it as soon as you can on
that day. Do not take more than one injection in the same day.
• If you take more FORTEO than prescribed, call your healthcare provider. If you take too
much FORTEO, you may have nausea, vomiting, weakness, or dizziness.
Follow your healthcare provider’s instructions about other ways you can help your osteoporosis,
such as exercise, diet, and reducing or stopping your use of tobacco and alcohol. If your
healthcare provider recommends calcium and vitamin D supplements, you can take them at the
same time you take FORTEO.
• See “What is the most important information I should know about FORTEO?”
• Decrease in blood pressure when you change positions. Some people feel dizzy, get a
fast heartbeat, or feel faint right after the first few doses. This usually happens within 4
hours of taking FORTEO and goes away within a few hours. For the first few doses, take
your injections of FORTEO in a place where you can sit or lie down right away if you get
these symptoms. If your symptoms get worse or do not go away, stop taking FORTEO
and call your healthcare provider.
• Increased calcium in your blood. Tell your healthcare provider if you have nausea,
vomiting, constipation, low energy, or muscle weakness. These may be signs there is too
much calcium in your blood.
Common side effects of FORTEO include:
• nausea
• joint aches
• pain
Your healthcare provider may take samples of blood and urine during treatment to check your
response to FORTEO. Also, your healthcare provider may ask you to have follow-up tests of
bone mineral density.
Tell your healthcare provider if you have any side effect that bothers you or that does not go
away.
These are not all the possible side effects of FORTEO. For more information, ask your doctor or
pharmacist.
Call your doctor for medical advice about side effects. You may report side effects to FDA at 1
800-FDA-1088.
This Medication Guide summarizes the most important information about FORTEO. If you
would like more information, talk with your healthcare provider. You can ask your pharmacist or
healthcare provider for information about FORTEO that is written for healthcare professionals.
For more information, go to www.FORTEO.com or call Lilly at 1-866-436-7836.
Inactive ingredients: glacial acetic acid, sodium acetate (anhydrous), mannitol, metacresol, and
water for injection. In addition, hydrochloric acid solution 10% and/or sodium hydroxide
solution 10% may have been added to adjust the product to pH 4.
What is Osteoporosis?
Osteoporosis is a disease in which the bones become thin and weak, increasing the chance of
having a broken bone. Osteoporosis usually causes no symptoms until a fracture happens. The
most common fractures are in the spine (backbone). They can shorten height, even without
causing pain. Over time, the spine can become curved or deformed and the body bent over.
Fractures from osteoporosis can also happen in almost any bone in the body, for example, the
wrist, rib, or hip. Once you have had a fracture, the chance for more fractures greatly increases.
The following risk factors increase your chance of getting fractures from osteoporosis:
• past broken bones from osteoporosis
• very low bone mineral density (BMD)
• frequent falls
• limited movement, such as using a wheelchair
• medical conditions likely to cause bone loss, such as some kinds of arthritis
• taking steroid medicines called glucocorticoids, such as prednisone
• other medicines that may cause bone loss, for example: seizure medicines (such as
phenytoin), blood thinners (such as heparin), and high doses of vitamin A
This Medication Guide has been approved by the U.S. Food and Drug Administration.
*The brands listed are trademarks of their respective owners and are not trademarks of Eli Lilly
and Company.
Copyright © 2002, 2013, Eli Lilly and Company. All rights reserved.
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