Consumer medicine information

Teriparatide Lupin

Teriparatide

BRAND INFORMATION

Brand name

Teriparatide Lupin

Active ingredient

Teriparatide

Schedule

S4

 

Consumer medicine information (CMI) leaflet

Please read this leaflet carefully before you start using Teriparatide Lupin.

SUMMARY CMI

TERIPARATIDE LUPIN

Consumer Medicine Information (CMI) summary

The full CMI on the next page has more details. If you are worried about using this medicine, speak to your doctor or pharmacist.

▼ This medicine is new or being used differently. Please report side effects. See the full CMI for further details.

1. Why am I using Teriparatide Lupin?

This product contains the active ingredient teriparatide, which is used to treat osteoporosis in women after menopause and in men.

For more information, see Section 1. Why am I using Teriparatide Lupin? in the full CMI.

2. What should I know before I use Teriparatide Lupin?

Do not use if you have ever had an allergic reaction to teriparatide or any of the ingredients listed at the end of the CMI.

Talk to your doctor if you have any other medical conditions, take any other medicines, or are pregnant or plan to become pregnant or are breastfeeding.

You will be required to sign your consent that you understand the 24-month lifetime limit. Keep this consent form as you may need to show this to your doctor in the future. Your pharmacist may also ask to see your consent form.

For more information, see Section 2. What should I know before I use Teriparatide Lupin? in the full CMI.

3. What if I am taking other medicines?

Some medicines may interfere with Teriparatide Lupin and affect how it works.

A list of these medicines is in Section 3. What if I am taking other medicines? in the full CMI.

4. How do I use Teriparatide Lupin?

The usual dose is 20 micrograms once a day, given by injection under the skin (subcutaneous) into the thigh or abdomen.

Your healthcare professional should teach you how to use the Teriparatide Lupin pen (multidose pre-filled delivery device). A Leaflet and a Pen User Manual containing information on how to use the Teriparatide Lupin pen are inserted in the carton.

Carefully follow all directions given to you by your doctor or healthcare professional. If you do not understand the user manual, ask your doctor or healthcare professional for help. Refer to the user manual each time you inject this medicine.

More instructions can be found in Section 4. How do I use Teriparatide Lupin? in the full CMI.

5. What should I know while using Teriparatide Lupin?

Things you should do
  • Remind any doctor, surgeon, anaesthetist, dentist, or pharmacist you visit that you are using Teriparatide Lupin or about to be started on any new medicine or about to have any blood tests.
  • Tell your doctor immediately if you become pregnant while using this medicine.
  • Keep all your doctor's appointments so that your progress can be checked.
Things you should not do
  • Do not stop using this medicine or use it to treat any other complaints unless your doctor tells you to.
  • Do not give or share your medicine with anyone else, even if they have the same condition as you and you have changed the needle.
Driving or using machines
  • This medicine is not expected to affect your ability to drive a car or use machinery.
  • Do not drive or operate machinery, if you experience dizziness.
Looking after your medicine
  • Keep Teriparatide Lupin in the refrigerator where the temperature stays between 2°C to 8°C. Do not allow Teriparatide Lupin to freeze. Do not store your pen with the needle attached.
  • Each Teriparatide Lupin pen can be used for up to 28 days after the first injection.

For more information, see Section 5. What should I know while using Teriparatide Lupin? in the full CMI.

6. Are there any side effects?

Feeling sick (nausea), leg cramps, muscle spasms, dizziness (light-headedness) after injection, a high level of uric acid or calcium in the blood, and discomfort around the area of injection, such as redness of the skin, pain, swelling, itching, bruising or minor bleeding are commonly seen side effects. The serious side effects include allergic reactions such as shortness of breath, wheezing or difficulty breathing, swelling of the face, lips or tongue, rash, itching or hives on the skin.

For more information, including what to do if you have any side effects, see Section 6. Are there any side effects? in the full CMI.

▼ This medicine is subject to additional monitoring. This will allow quick identification of new safety information. You can help by reporting any side effects you may get. You can report side effects to your doctor, or directly at www.tga.gov.au/reporting-problems.



FULL CMI

TERIPARATIDE LUPIN

Active ingredient(s): teriparatide

Consumer Medicine Information (CMI)

This leaflet provides important information about using Teriparatide Lupin. You should also speak to your doctor or pharmacist if you would like further information or if you have any concerns or questions about using Teriparatide Lupin.

Where to find information in this leaflet:

1. Why am I using Teriparatide Lupin?
2. What should I know before I use Teriparatide Lupin?
3. What if I am taking other medicines?
4. How do I use Teriparatide Lupin?
5. What should I know while using Teriparatide Lupin?
6. Are there any side effects?
7. Product details

1. Why am I using Teriparatide Lupin?

Teriparatide Lupin contains the active ingredient teriparatide.

Teriparatide is used to treat osteoporosis in women after menopause and in men.

Osteoporosis is a disease which causes bones to become less dense, gradually making them weaker, more brittle, and likely to break. This disease is especially common in women after the menopause. Osteoporosis is also common in patients receiving corticosteroids such as prednisone or cortisone.

Although it may have no symptoms at first, osteoporosis makes you more likely to break bones, especially in your spine, hips and wrists and may cause back pain, loss of height and a curved back.

Teriparatide Lupin works by activating cells in the bone to form new bone. Using this medicine each day will protect your bones by making them stronger and your risk of fracture will be reduced.

2. What should I know before I use Teriparatide Lupin?

Warnings

In rats that were treated with teriparatide for more than a quarter of their lifetime, teriparatide caused some rats to develop osteosarcoma, a bone cancer. The potential to cause osteosarcoma in rats was increased with higher doses and longer periods of treatment.

Osteosarcoma in humans is a serious but very rare cancer. Osteosarcoma occurs in about 4 out of every million people each year.

There is one report of osteosarcoma in a patient administered teriparatide for 14 months. Due to the complex medical history, cause and effect between teriparatide and osteosarcoma could not be established. At present, it is not known whether humans treated with teriparatide would have an increased chance of getting osteosarcoma.

You should discuss any safety concerns you have about the use of teriparatide with your doctor.

Do not use Teriparatide Lupin if:

  • you are allergic to teriparatide, or any of the ingredients listed at the end of this leaflet. Some of the symptoms of an allergic reaction may include shortness of breath, wheezing or difficulty breathing; swelling of the face, lips, tongue, or other parts of the body; rash, itching or hives on the skin.
    Always check the ingredients to make sure you can use this medicine.
  • you have previously received teriparatide therapy for a total of 24 months. This total of 24 months therapy may have been made up of several shorter courses of teriparatide. If you are not sure if you have previously received teriparatide, speak to your doctor or pharmacist.
  • you are pregnant or breastfeeding.
  • you have high calcium levels in the blood (hypercalcaemia).
  • you have severe kidney disease.
  • you have ever had metabolic bone disease (including Paget's disease of the bone or hyperparathyroidism) other than primary osteoporosis or glucocorticoid-induced osteoporosis.
  • you have ever had bone cancer or other cancers that have spread (metastasised) to your bones.
  • you have unexplained high levels of a liver enzyme called alkaline phosphatase (ALP) in the blood.
  • you have ever had external beam or implant irradiation therapy to the skeleton.
  • you have an open epiphysis (rounded portion of the bone).
  • the expiry date printed on the pack has passed or if the packaging is torn or shows signs of tampering.

Check with your doctor if you:

  • have any other medical conditions like:
    - allergies to any other medicines, foods, preservatives, or dyes.
    - high calcium levels in the blood (pre-existing hypercalcaemia). Signs and symptoms of high calcium in the blood may include continuing nausea, vomiting, constipation, low energy, or muscle weakness. Teriparatide Lupin may cause an increase in the amount of calcium in your blood or urine.
    - bone disorders other than osteoporosis (including hyperparathyroidism).
    - high levels of alkaline phosphatase.
    - have had radiation therapy.
    - calculi or stones (mineral deposits) in the urinary tract.
    - low blood pressure.
    - kidney disease.
  • take any medicines for any other condition.

You will be required to sign your consent that you understand the 24-month lifetime limit. Keep this consent form as you may need to show this to your doctor in the future. Your pharmacist may also ask to see your consent form.

Your healthcare professional should teach you how to use the Teriparatide Lupin pen. You should also read the user manual for information on how to use the pen before beginning therapy. Read the user manual and package leaflet each time you get a new pen, in case something has changed.

This medicine should not be used in children or in young adults if their bones have not finished growing (open epiphyses).

During treatment, you may be at risk of developing certain side effects. It is important you understand these risks and how to monitor for them. See additional information under Section 6. Are there any side effects?

Pregnancy and breastfeeding

Check with your doctor if you are pregnant or intend to become pregnant.

Talk to your doctor if you are breastfeeding or intend to breastfeed.

Teriparatide should not be used if you are pregnant or breastfeeding.

This medicine may affect your developing baby. It is not known whether this medicine passes into breast milk. Your doctor can discuss with you the risks and benefits involved.

3. What if I am taking other medicines?

Tell your doctor or pharmacist if you are taking any other medicines, including any that you get without a prescription from your pharmacy, supermarket, or health food shop.

Some medicines may interfere with Teriparatide Lupin and affect how it works.

Medicines that may increase the effect of Teriparatide Lupin include:

  • diuretics (medicines used to help the kidneys get rid of salt and water by increasing the amount of urine produced, such as hydrochlorothiazide and frusemide).

The effect of medicines that may be greatly increased by Teriparatide Lupin include:

  • anti-coagulants (medicines used to prevent blood clotting);
  • digoxin (medicine used to treat heart failure).

These medicines may be affected by Teriparatide Lupin or may affect how well it works. You may need different amounts of your medicines or you may need to use different medicines.

You can take calcium or vitamin D supplements (or both) while you are using Teriparatide Lupin. You should discuss with your doctor how much calcium and vitamin D to take each day.

Your doctor and pharmacist have more information on medicines to be careful with or avoid while using Teriparatide Lupin.

Check with your doctor or pharmacist if you are not sure about what medicines, vitamins or supplements you are taking and if these affect Teriparatide Lupin.

4. How do I use Teriparatide Lupin?

Carefully follow all directions given to you by your doctor or healthcare professional.

They may differ from the information contained in this leaflet. Read the user manual, inserted in the pack, for instructions on how to use the pen.

The cartridge must be used for multiple injections by one person only.

If you do not understand the user manual, ask your doctor or healthcare professional for help.

How much to use

The usual dose is 20 micrograms given once a day.

Follow the instructions provided and use Teriparatide Lupin until your doctor tells you to stop.

When to use Teriparatide Lupin

Teriparatide Lupin should be used at any time of day.

Using it at the same time each day will have the best effect.

How to inject Teriparatide Lupin

Teriparatide Lupin is given by injection under the skin (subcutaneous) into the thigh or abdomen.

Your healthcare professional (doctor or nurse) should teach you how to use the Teriparatide Lupin pen (multidose pre-filled delivery device).

It is a good idea to refer to the user manual each time you inject this medicine.

How long to use Teriparatide Lupin

The safety and efficacy of teriparatide have not been evaluated beyond 2 years (median treatment is 19 months in postmenopausal women).

Use of the drug for more than 24 months lifetime duration is not recommended.

You will be required to sign your consent that you understand the 24-month lifetime limit.

If you forget to use Teriparatide Lupin

Teriparatide Lupin should be used regularly at the same time each day. If you miss your dose at the usual time, have it as soon as possible on that day.

Do not have more than one injection on the same day. Then go back to using your medicine as you would normally.

If it is almost time for your next injection, skip the injection you missed and take your next injection when you are meant to.

Do not have double injections to make up for the injection that you missed.

This may increase the chance of you having an unwanted side effect.

If you are not sure what to do, ask your doctor or healthcare professional.

If you have trouble remembering to use your medicine, ask your healthcare professional for some hints.

If you use too much Teriparatide Lupin

If you think that you have used too much Teriparatide Lupin, you may need urgent medical attention.

Symptoms of an overdose may include high blood serum calcium levels, dizziness, or light-headedness on standing up. Nausea, vomiting, dizziness, and headache may also occur.

You should immediately:

  • phone the Poisons Information Centre
    (by calling 13 11 26); or
  • contact your doctor; or
  • go to the Emergency Department at your nearest hospital.

You should do this even if there are no signs of discomfort or poisoning.

5. What should I know while using Teriparatide Lupin?

Things you must do

If you are about to be started on any new medicine, remind your doctor and pharmacist that you are using Teriparatide Lupin.

If you are going to have surgery, tell the surgeon or anaesthetist that you are using this medicine. It may affect other medicines used during surgery.

If you are about to have any blood tests, tell your doctor that you are using this medicine. This medicine can cause small, temporary increases in blood calcium levels. If blood samples are taken, this needs to be done at least 16 hours after the last injection.

Keep all your doctor's appointments so that your progress can be checked. Your doctor may do some tests (like bone mineral density tests and blood tests) from time to time to make sure the medicine is working and to prevent unwanted side effects.

Call your doctor straight away if you:

  • become pregnant while using this medicine.

Remind any doctor, dentist pharmacist, or anaesthetist you visit that you are using Teriparatide Lupin.

Things you should not do

  • Do not stop using this medicine without checking with your doctor.
  • Do not use Teriparatide Lupin to treat any other complaints unless your doctor tells you to.
  • Do not give or share your medicine with anyone else, even if they have the same condition as you and you have changed the needle.
  • Do not use this medicine after the expiry date.

Driving or using machines

Be careful before you drive or use any machines or tools until you know how Teriparatide Lupin affects you.

This medicine is not expected to affect your ability to drive a car or use machinery.

Some patients may feel dizzy after injecting Teriparatide Lupin.

If you feel dizzy you should not drive or use machines until you feel better.

Looking after your medicine

  • Keep the Teriparatide Lupin pen in the refrigerator where the temperature stays between 2°C to 8°C. Do not allow Teriparatide Lupin to freeze.
  • Do not store your pen with the needle attached.
  • You should have your Teriparatide Lupin injection shortly after you take the pen out of the refrigerator as described in the user manual. Put the pen back into the refrigerator immediately after you have used it.
  • You should use a new needle for each injection. Do not store your pen with the needle attached. If you do this, it may allow solution to leak from the pen and air bubbles to form in the cartridge.
  • Teriparatide Lupin is a clear and colourless liquid. Do not use if solid particles appear or if the solution is cloudy or coloured.

Follow the instructions in the user manual on how to take care of your medicine properly.

Keep it where young children cannot reach it.

When and how to discard your medicine

Each Teriparatide Lupin pen can be used for up to 28 days after the first injection. After the 28-day use period, discard the pen even if it contains some unused solution.

Empty Teriparatide Lupin pens and any needles should be disposed of in a ‘sharps’ container or similar puncture proof container composed of hard plastic or glass.

Ask your doctor or nurse where you can dispose of the container once it is full.

Getting rid of any unwanted medicine

If you no longer need to use this medicine or it is out of date, take it to any pharmacy for safe disposal.

Do not use this medicine after the expiry date.

6. Are there any side effects?

All medicines can have side effects. If you do experience any side effects, most of them are minor and temporary. However, some side effects may need medical attention.

See the information below and, if you need to, ask your doctor or pharmacist if you have any further questions about side effects.

Less serious side effects

Less serious side effectsWhat to do
More common side effects
  • Discomfort around the area of injection, such as:
    - redness of the skin;
    - pain;
    - swelling;
    - itching; or
    - bruising or minor bleeding.
  • Feeling sick (nausea).
  • Leg cramps.
  • Muscle spasms.
  • Dizziness (light-headedness) after injection.
Less common side effects
The below side effects may occur in some people and can only be found when your doctor does tests from time to time to check your progress. These are:
  • a high level of uric acid or calcium levels, or al ow level of red blood cells in blood (anaemia).
Speak to your doctor if you have any of these less serious side effects and they worry you.
If you become dizzy (light-headed) after your injection, you should sit or lie down until you feel better. If you do not feel better, you should call a doctor before you continue treatment.

Serious side effects

Serious side effectsWhat to do

Allergic reactions may occur in some people. These can be seen as:

  • shortness of breath;
  • wheezing or difficulty breathing;
  • swelling of the face, lips, or tongue;
  • rash, itching or hives on the skin.
Call your doctor straight away or go straight to the Emergency Department at your nearest hospital if you notice any of these serious side effects.

Tell your doctor or pharmacist if you notice anything else that may be making you feel unwell.

Other side effects not listed here may occur in some people.

Reporting side effects

After you have received medical advice for any side effects you experience, you can report side effects to the Therapeutic Goods Administration online at www.tga.gov.au/reporting-problems. By reporting side effects, you can help provide more information on the safety of this medicine.

Always make sure you speak to your doctor or pharmacist before you decide to stop taking any of your medicines.

7. Product details

This medicine is only available with a doctor's prescription.

What Teriparatide Lupin contains

Active ingredient
(main ingredient)		Teriparatide
Other ingredients
(inactive ingredients)		Glacial acetic acid
Sodium acetate
Mannitol
Metacresol
Water for injections
Hydrochloric acid (for pH adjustment)
Sodium hydroxide (for pH adjustment)
Potential allergensNot applicable

Do not take this medicine if you are allergic to any of these ingredients.

What Teriparatide Lupin looks like

Teriparatide Lupin is pre-filled injection pen containing a 2.4 mL solution cartridge (siliconised Type I glass) with a plunger, rubber disc and aluminium cap assembled into a disposable pen. (AUST R 373604).

Teriparatide Lupin is available in the following pack sizes:

  • 1 pen;
  • 3 pens.

Each pen contains 28 doses of 20 micrograms (per 80 microlitres).

Not all pack sizes may be marketed.

Who distributes Teriparatide Lupin

Generic Health Pty Ltd
Suite 2, Level 2
19-23 Prospect Street
Box Hill, VIC, 3128

ii1390701  [email protected]

ii1390702  +61 3 9809 7900

ii1390703  www.generichealth.com.au

This leaflet was prepared in December 2022.

Pen User Manual - Instructions for Use
Overview of Pen Parts

Teriparatide Lupin is a solution for injection supplied in a pen. The pen contains medicine for a once daily injection on 28 consecutive days.

Use a new needle for each injection.

Needles are not included with the pen. It is recommended to use a CE Certified 31 gauge needle, 5 mm in length. Pen needles that meet the following specifications can also be used:

  • 29-31 gauge;
  • 5 mm to 12.7 mm in length;
  • CE Certified.

Ask your doctor or pharmacist which needle is most suitable for you.

  1. Pen cap
  2. Cartridge with medicine
  3. Label
  4. Dose window
  5. Dose knob
  6. Dose activator
  7. Large outer cap
  8. Small inner cap
  9. Needle
  10. Seal foil

For Your Safety

Important information

  • Read the instructions for use completely. Follow all directions carefully.
  • Read the package leaflet provided with your pen.
  • In case of questions, contact your doctor, pharmacist or caregiver.

Prevention of infectious diseases

  • Do not share your pen as this may risk transmission of infectious diseases.
  • Use a new sterile needle for each injection. Used needles pose a risk of transmission of infectious diseases.

Use of pen

  • Check the pen label when taking the pen out of the refrigerator. Ensure that you use the right medicine.
  • Check the expiry date, do not use the pen in case the expiry date is exceeded.
  • Check the solution: it must be clear, colourless and free of particles.
  • Do not transfer the medicine to a syringe. Teriparatide Lupin has to be administered using this pen only.
  • Do not use the pen for more than 28 injections. Note the first day of injection in the Injection Diary at the end of these Instructions for Use. Calculate the date for 28th injection by using a calendar and also note this date in the Injection Diary.
  • The pen is not recommended for use by the blind or visually impaired without help from a supporting person.

Storage

  • Keep pen in the refrigerator, preferably in a door compartment.
  • Keep pen and needles out of the reach of children.

Troubleshooting

  • If you encounter an issue during the injection where some medicine was injected, do not give a second injection the same day.
  • Read the section “What to do if...” in these Instructions for Use.
  • Do not use the pen if it is damaged.
  • Only use the pen if the solution is clear, colourless and free of particles.
  • If you cannot solve the issue by yourself or if you are uncertain, contact your doctor, pharmacist or caregiver.

Preparing the Pen Before the First Injection

Before FIRST injection, you have to prepare your pen as described here.

You have to perform this step only once. You do NOT need to repeat this procedure for the second and any following injection.

Attaching the needle

  1. Remove pen cap.
  2. Take a new needle and remove the seal foil from the needle cap.

  1. Attach needle with large outer cap to the pen. Screw large outer cap clockwise until hard stop.

  1. Remove large outer cap from the needle and keep it for later use (refer Step 9).

Dialling the Dose

  1. Turn the dose knob to the hard stop. Make sure the figure “80” is fully visible and centred in the dose window with the white mark aligned in the window notch.

  1. Remove small inner cap from the needle and dispose it.

  1. Hold pen with needle up. Push the dose activator to the hard stop and hold for 5 seconds. Collect the expelled liquid with a tissue.

  1. Confirm dose. Make sure the figure "0" is fully visible and centred in the dose window, the white mark is aligned in the window notch and the debossed marks of dose knob and pen body are aligned.

Removing the needle

Remove needle after preparation of pen, as it poses a risk of being contaminated.

  1. Carefully push needle into the large outer cap kept aside before in Step 4. To prevent injury, do not touch the needle directly.

  1. Unscrew needle by turning the large outer cap counter clockwise and pull needle from pen.

  1. Dispose of the needle in a puncture safe container which can be obtained from your pharmacy or caregiver.
  2. Re-attach pen cap to pen.

Now your pen is prepared for the first and all further injections as described in the following chapter.

Injecting Teriparatide Lupin

Prepare yourself for injection

  • Wash your hands before every injection.
  • Prepare the injection site (on thigh or abdomen) as directed by your doctor, pharmacist or caregiver.

Use a new needle for every injection because a new needle is sharp and allows an almost pain-free injection. A used needle poses a risk of being clogged or contaminated.

Attaching the needle

  1. Remove pen cap.
  2. Take a new needle and remove the seal foil from the needle cap.

  1. Attach needle with large outer cap to the pen. Screw large outer cap clockwise until hard stop.

  1. Remove large outer cap from the needle and keep it for later use (refer Step 9).

Dialling the Dose

  1. Turn the dose knob to the hard stop. Make sure the figure “80” is fully visible and centred in the dose window with the white mark aligned in the window notch.

  1. Remove small inner cap from the needle and dispose it.

  1. Gently hold a fold of skin from thigh or abdomen.
  2. Insert the needle preferably at a 90 degree angle at the prepared injection site. Push the dose activator to the hard stop and hold for 5 seconds. Count up slowly to 5.

  1. Pull out the needle from the skin.

  1. Confirm dose. Make sure the figure "0" is fully visible and centred in the dose window, the white mark is aligned in the window notch and the debossed marks of dose knob and pen body are aligned.

Removing needle

Always remove needle immediately after use of pen.

  1. Carefully push needle into the large outer cap kept aside before in Step 4. To prevent injury, do not touch the needle directly.

  1. Unscrew needle by turning the large outer cap counter clockwise and pull needle from pen.

  1. Dispose of the needle in a puncture safe container which can be obtained at your pharmacy or from your caregiver.
  2. Re-attach pen cap to pen.

Keeping the Injection Diary

  1. Note the current date of injection next to the relevant day, and calculate the date of the 28th injection, if not already done so, in the Injection Diary at the end of these Instructions for Use.

Storing the Pen

Do not store pen with a needle attached. Doing this may cause air bubbles to form in the medicine cartridge. Always close pen with pen cap.

Only take pen out of the refrigerator for use. Store pen in the refrigerator, preferably in a door compartment. Don't store pen next to the back wall of refrigerator or in the freezer. The solution becomes unusable if frozen.

If your pen has been left out of the refrigerator for a period of time, don't throw it away. Put pen back in the refrigerator and contact your doctor, pharmacist or caregiver.

Disposing Pen

The pen must be disposed of at the day of the last injection (see Injection Diary). Dispose of the pen even if there is solution remaining in the cartridge.

Dispose of the pen as directed by your doctor or pharmacist.

Attach the pen cap before disposal. Don't dispose of the pen with the needle attached.

What to do if…

Air bubble in cartridge: You can use your pen without any concern.

While preparing the pen for first use, no solution is expelled: Perform steps as described in ‘Dialling the dose’ again (Steps 5 through 8 under “Preparing the Pen Before the First Injection” above).

The dose activator is blocked or you have the impression you have not injected the full dose: Do not give a second injection the same day. Proceed with your regular injection the next day. Make sure you turn the dose knob to the hard stop and the figure “80” is fully visible and centred in the dose window with the white mark aligned in the window notch.

Injection Diary

Date of first injection:Day 1 
 Day 2 
Day 3 
Day 4 
Day 5 
Day 6 
Day 7 
Day 8 
Day 9 
Day 10 
Day 11 
Day 12 
Day 13 
Day 14 
Day 15 
Day 16 
Day 17 
Day 18 
Day 19 
Day 20 
Day 21 
Day 22 
Day 23 
Day 24 
Day 25 
Day 26 
Day 27 
Date of last injection:Day 28 

This user manual was last updated in March 2023.

Published by MIMS September 2024

BRAND INFORMATION

Brand name

Teriparatide Lupin

Active ingredient

Teriparatide

Schedule

S4

 

1 Name of Medicine

Teriparatide.

2 Qualitative and Quantitative Composition

One pre-filled pen of Teriparatide Lupin of 2.4 mL contains 600 microgram of teriparatide (corresponding to 250 microgram per mL).
For the full list of excipients, see Section 6.1 List of Excipients.

3 Pharmaceutical Form

Solution for injection.
Teriparatide Lupin is a sterile, colourless, clear, isotonic solution in pre-filled pens.

4 Clinical Particulars

4.1 Therapeutic Indications

Teriparatide Lupin is indicated for the treatment of osteoporosis in postmenopausal women and the treatment of primary osteoporosis in men when other agents are considered unsuitable and when there is a high risk of fractures.
Teriparatide Lupin is indicated for the treatment of osteoporosis associated with sustained systemic glucocorticoid therapy in women and men at high risk for fracture.

4.2 Dose and Method of Administration

Each dose of 80 microlitre contains 20 microgram of teriparatide.
The recommended dose of Teriparatide Lupin is 20 microgram administered once daily by subcutaneous injection in the thigh or abdomen.
Based on clinical experience, treatment with Teriparatide Lupin is recommended for a lifetime duration of 24 months treatment (for post-treatment efficacy, see Section 5.1 Pharmacodynamic Properties, Clinical trials). Teriparatide Lupin should be prescribed to patients with a full explanation and their informed consent on the lifetime duration of 24 months treatment.
Calcium and vitamin D supplements are advised in patients with a low dietary intake of these nutrients.

Use in males.

Primary or secondary hypogonadism should first be excluded and, if relevant, be treated (see Section 5.1 Pharmacodynamic Properties, Clinical trials).

Instructions for use/handling.

To prevent the possible transmission of disease, each pen must be used by one patient only, even if the needle is changed.
Following cessation of Teriparatide Lupin therapy, patients may be continued on other osteoporosis therapies.
The pen delivers 20 microgram per dose and contains dosing for 28 treatment days. Patients must be educated to use the proper injection techniques. Please refer to the User Manual for instructions for the pen.
Teriparatide Lupin is a clear and colourless liquid. Do not use if solid particles appear or if the solution is cloudy or coloured. The Teriparatide Lupin pen should not be used after the stated expiration date.
Data are not available on the safety or efficacy of intravenous or intramuscular injection of Teriparatide Lupin.

4.3 Contraindications

Teriparatide Lupin should not be given to patients with hypersensitivity to teriparatide or to any of its excipients.
Pregnancy and breastfeeding (see Section 4.6 Fertility, Pregnancy and Lactation).
Pre-existing hypercalcaemia.
Severe renal impairment.
Metabolic bone diseases (including hyperparathyroidism and Paget's disease of the bone) other than primary osteoporosis or glucocorticoid-induced osteoporosis.
Unexplained elevations of alkaline phosphatase.
Prior external beam or implant radiation therapy to the skeleton.
Patients with skeletal malignancies or bone metastases should be excluded from treatment with teriparatide.

4.4 Special Warnings and Precautions for Use

Duration of treatment.

The maximum lifetime exposure to teriparatide for an individual patient is 24 months (see Section 4.2 Dose and Method of Administration). For post-treatment efficacy, see Section 5.1 Pharmacodynamic Properties, Clinical trials.

Risk of osteosarcoma.

In male and female rats, teriparatide caused an increase in the incidence of osteosarcoma (a malignant bone tumour) that was dependent on dose and treatment duration. The effect was observed at systemic exposures to teriparatide ranging from 3 to 60 times the exposure in humans given a 20 microgram dose.
However no increased risk was identified in a study in which 30 monkeys were treated with teriparatide for 18 months and then observed for a further 3 years. Post-marketing data in humans has not identified an increased risk.
To minimise the potential risk of osteosarcoma (seen in the life-time rat studies):
1. The maximum lifetime exposure to Teriparatide Lupin for an individual patient is 24 months (see Section 4.2 Dose and Method of Administration; Section 5.1 Pharmacodynamic Properties).
2. Teriparatide should not be prescribed to patients where there is an increased background risk of osteosarcoma (such as Paget's disease of bone, prior radiation therapy involving the skeleton, open epiphysis, unexplained elevations of alkaline phosphatase). (See Section 4.3 Contraindications; Section 5.3 Preclinical Safety Data, Carcinogenicity).
Teriparatide Lupin should be prescribed to patients with a full explanation and their informed consent on the lifetime duration of 24 months treatment.

Information for patients.

For safe and effective use of Teriparatide Lupin, the physician should inform the patient on the following:

General.

Patients will need to read the Consumer Medicine Information leaflet and pen User Manual before starting therapy with Teriparatide Lupin and re-read them each time the prescription is renewed.

Osteosarcoma in rats.

Patients should be made aware that Teriparatide Lupin caused osteosarcoma in rats and that the clinical relevance of these findings is unknown.

Consent form.

Use of Teriparatide Lupin is restricted to 24 months lifetime duration. To access or download a copy of the consent form, visit: https://www.generichealth.com.au/.

Hypercalcaemia.

Teriparatide has not been studied in patients with pre-existing hypercalcaemia. Patients with pre-existing hypercalcaemia should be excluded from treatment with teriparatide because of the possibility of exacerbating hypercalcaemia (see Section 4.3 Contraindications).
In normocalcaemic patients, slight and transient elevations of serum calcium concentrations have been observed following teriparatide injection. Serum calcium concentrations reach a maximum between 4 and 6 hours and return to baseline by 16 to 24 hours after each dose of teriparatide. Routine calcium monitoring during therapy is not required.

Bone disorders other than osteoporosis.

Patients with metabolic bone diseases other than primary osteoporosis (including hyperparathyroidism and Paget's disease of the bone) (see Section 4.3 Contraindications) and those with otherwise unexplained elevations of alkaline phosphatase, should generally be excluded from treatment with teriparatide. Patients with skeletal malignancies or bone metastases should also be excluded from treatment with teriparatide.

Urolithiasis.

Teriparatide has not been studied in patients with active urolithiasis. Teriparatide should be used with caution in patients with active or recent urolithiasis because of the potential to exacerbate this condition.

Hypotension.

In short-term clinical studies with teriparatide, isolated episodes of transient orthostatic hypotension were observed. Typically, an event began within 4 hours of dosing and spontaneously resolved within a few minutes to a few hours. When transient orthostatic hypotension occurred, it happened within the first several doses, was relieved by placing subjects in a reclining position and did not preclude continued treatment.

Use in the elderly.

No differences in teriparatide pharmacokinetics were detected with regard to age (range 31 to 85 years). Dosage adjustment based on age is not required.

Paediatric use.

Teriparatide has not been studied in paediatric populations. Teriparatide should not be used in paediatric patients or young adults with open epiphyses.

Effects on laboratory tests.

Serum calcium.

Teriparatide transiently increases serum calcium, with the maximal effect observed at approximately 4 to 6 hours post-dose. By 16 hours post-dose, serum calcium generally has returned to, or near, baseline. These effects should be kept in mind because serum calcium concentrations observed within 16 hours after a dose may reflect the pharmacologic effect of teriparatide. Persistent hypercalcaemia was not observed in clinical trials with teriparatide. If persistent hypercalcaemia is detected, treatment with teriparatide should be discontinued pending further evaluation of the cause of hypercalcaemia. Patients known to have an underlying hypercalcaemic disorder, such as primary hyperparathyroidism, should not be treated with teriparatide (see Section 4.4 Special Warnings and Precautions for Use, Hypercalcaemia).
Teriparatide has not been studied in non-ambulant patients, thus monitoring of serum calcium may be appropriate when a previously ambulant patient is confined to bed.

Urinary calcium.

Teriparatide may cause small increases in urinary calcium excretion. However, in the clinical trials, the incidence of hypercalciuria in teriparatide patients did not differ from that in the placebo-treated patients.

Use in renal impairment.

No significant adverse renal effects were observed in long-term clinical studies. Assessments included creatinine clearance, measurements of blood urea nitrogen (BUN), creatinine, and electrolytes in serum, urine specific gravity and pH and examination of urine sediment. Long-term evaluation of patients with severe renal insufficiency, patients undergoing acute or chronic dialysis, or patients who have a functioning renal transplant has not been performed.
Caution should be exercised in patients with moderate renal impairment.
Contraindicated for use in severe renal impairment.

Younger adult population.

Experience in the younger adult population, including premenopausal women, is limited (see Section 5.1 Pharmacodynamic Properties). Treatment should only be initiated if the benefit clearly outweighs risks in this population.

Contraception and women of childbearing potential.

Women of childbearing potential should use effective methods of contraception during treatment with teriparatide. If pregnancy occurs, teriparatide should be discontinued (see Section 4.6 Fertility, Pregnancy and Lactation).

Serum uric acid.

Teriparatide may cause small increases in serum uric acid concentrations. In clinical trials, 2.8% of teriparatide patients had an elevated serum uric acid concentration compared to 0.7% of placebo patients. However, the hyperuricaemia did not result in an increase in gout, urolithiasis or arthralgia.

Anti-PTH antibody formation.

Anti-PTH antibodies, while apparently clinically irrelevant and only occurring in a small number of treated individuals, have the potential to interfere with serum PTH estimations.

PTH receptors.

As is generally known, PTH/PTH-related peptide receptors are on multiple tissues. There was no increase in non-osseous tumours in the two 24-month (lifetime) rat studies and in the two 18-month primate studies. There was no increase in incidence of any specific cancer or cancer overall in 2,074 patients in long-term clinical studies or in follow-up studies conducted in a number of these patients for a median of 18 months after teriparatide treatment. Osteosarcoma is a very rare cancer that occurs in 4 out of every million people each year. None of the patients in the clinical trials or post-treatment follow-up developed osteosarcomas.

Other.

New or worsened spinal stenosis was observed in 2 (0.3%) patients who received placebo, 3 (0.4%) patients who received teriparatide 20 microgram, and 3 (0.4%) patients who received teriparatide 40 microgram. One patient who received teriparatide 20 microgram had worsening conductive hearing loss. One patient who received teriparatide 40 microgram required removal of a bone spur and another patient receiving teriparatide 40 microgram required surgical removal of a hyperostosis.

4.5 Interactions with Other Medicines and Other Forms of Interactions

No clinically relevant drug interactions have been identified in studies administering teriparatide 40 microgram (twice the recommended dose of teriparatide).

Hydrochlorothiazide.

In a study of healthy subjects, the co-administration of 25 mg hydrochlorothiazide with teriparatide did not affect the serum calcium response to teriparatide 40 microgram. The 24-hour urine excretion of calcium was reduced by a clinically insignificant amount (15%).

Frusemide.

In a study of healthy subjects and patients with mild, moderate and severe renal insufficiency (creatinine clearance 13 to 72 mL/min), co-administration of intravenous frusemide (20 to 100 mg) with teriparatide 40 microgram resulted in small, clinically insignificant increases in serum calcium (2%) and in 24-hour urine calcium (37%).

Calcium channel antagonists.

In a study of women with hypertension treated with an extended release preparation of either diltiazem, nifedipine or felodipine, the blood pressure observed after injection of teriparatide 40 microgram was similar when administered alone or in combination with the long-acting calcium channel antagonists.

Atenolol.

In a study of women with hypertension treated with atenolol, the blood pressure observed after injection of teriparatide 40 microgram was similar when administered alone or in combination with atenolol.

Digoxin.

In a study of 15 healthy people administered digoxin daily to steady state, a single teriparatide dose did not alter the effect of digoxin on the systolic time interval (from electrocardiographic Q-wave onset to aortic valve closure, a measure of digoxin's calcium-mediated cardiac effect). However, sporadic case reports have suggested that hypercalcaemia may predispose patients to digitalis toxicity. Because teriparatide transiently increases serum calcium, teriparatide should be used with caution in patients taking digoxin.

Raloxifene.

In a study of healthy postmenopausal women, the co-administration of raloxifene with teriparatide 40 microgram did not alter the effects of teriparatide on serum or urine calcium or on clinical adverse events.

Anticoagulants.

While this has not been studied, co-administration of anti-coagulants would not be expected to alter the effects of teriparatide. Patients co-administering anticoagulants and teriparatide need to be advised to take appropriate precautions against the formation of haematomas at the injection sites.

4.6 Fertility, Pregnancy and Lactation

Effects on fertility.

Teriparatide had no adverse effects on fertility of male or female rats at doses up to 300 microgram/kg/day SC (about 120 times the human dose based on body surface area). In juvenile rats, treatment with teriparatide was associated with degeneration of the testes at doses ≥ 10 microgram/kg/day SC (about 4 times the human dose based on body surface area). Teriparatide should not be used in paediatric patients or young adults (also see Section 4.4 Special Warnings and Precautions for Use).
(Category B3)
In pregnant rats given subcutaneous teriparatide doses up to 1000 microgram/kg/day, there were no findings. In pregnant mice given subcutaneous doses of ≥ 30 microgram/kg/day (6 times the human dose based on body surface area) from gestation Day 6 through 15, the fetuses showed an increased incidence of skeletal deviations or variations (interrupted rib, extra vertebra or rib).
Developmental effects in a perinatal/postnatal study in pregnant rats given subcutaneous doses of teriparatide from gestation Day 6 through postpartum Day 20 included mild growth retardation in female offspring at doses of 225 microgram/kg/day (approximately 95 times the human dose based on BSA) and in male offspring at 1000 microgram/kg/day (420 times the human dose based on BSA). There was also reduced motor activity in both male and female offspring at 1000 microgram/kg/day. There were no developmental or reproductive effects in rats at a dose of 30 microgram/kg (12 times the human dose based on BSA).
The effects of teriparatide on the human fetus have not been studied. Teriparatide should not be used in pregnant women (see Section 4.3 Contraindications).

Contraception and women of childbearing potential.

Women of childbearing potential should use effective methods of contraception during use of teriparatide. If pregnancy occurs, teriparatide should be discontinued (see Section 4.3 Contraindications).
 It is not known whether teriparatide is excreted in human milk. Teriparatide should not be administered to women who are breastfeeding their children (see Section 4.3 Contraindications).

4.7 Effects on Ability to Drive and Use Machines

Teriparatide has no or negligible influence on the ability to drive and use machines. Transient, orthostatic hypotension or dizziness was observed in some patients. These patients should refrain from driving or the use of machines until symptoms have subsided.

4.8 Adverse Effects (Undesirable Effects)

Clinical trials were conducted with the reference medicine Forteo. The safety of teriparatide has been evaluated in 21 clinical trials in over 2,800 women and men. Four long-term, Phase 3 clinical trials included one large placebo-controlled, double-blind multinational trial with 1,637 postmenopausal women, one placebo-controlled, double-blind multinational trial with 437 men and two active-controlled trials including 393 postmenopausal women. Teriparatide doses ranged from 5 to 100 microgram/day in short-term trials and 20 to 40 microgram/day in the long-term trials. A total of 1,970 of the patients studied received teriparatide, including 738 patients at 20 microgram/day and 1,107 patients at 40 microgram/day. In the long-term clinical trials, 1,137 patients were exposed to teriparatide for greater than 1 year (500 at 20 microgram/day and 637 at 40 microgram/day). The maximum exposure duration to teriparatide was 2 years. Adverse events associated with teriparatide were usually mild and generally did not require discontinuation of therapy.
In the two Phase 3, placebo-controlled clinical trials in men and postmenopausal women, early discontinuation due to an adverse event occurred in 5.6% of patients on placebo and 7.1% of patients on teriparatide. Adverse events considered to be related to teriparatide therapy were nausea and leg cramps.
Table 1 lists adverse events occurring in the Phase 3, placebo-controlled clinical trials in postmenopausal women and in men at a frequency ≥ 2.0% in the teriparatide groups and in more teriparatide-treated patients than in placebo-treated patients. Adverse events are shown without attributing causality.

Immunogenicity.

In a large clinical trial, antibodies that cross-reacted with teriparatide were detected in 2.8% of female patients receiving teriparatide. Generally, antibodies were first detected following 12 months of treatment and diminished after withdrawal of therapy. There were no hypersensitivity reactions, allergic reactions, effects on serum calcium or effects on BMD response, which indicates that the antibodies did not cause any clinically significant adverse effects.

Spontaneous data.

Table 2 of adverse reactions is based on post-marketing spontaneous reports since market introduction. The following convention has been used for the classification of the adverse reactions: very common (> 1/10), common (> 1/100, < 1/10), uncommon (> 1/1000, < 1/100), rare (> 1/10,000, < 1/1000), very rare (< 1/10,000).
There has been a report of metastatic osteosarcoma with subsequent fatal outcome in a 72 year old woman with osteoporosis and low back pain who had received teriparatide for 14 months prior to presentation. Causality cannot be established on the basis of this single case and a surveillance program continues. Osteosarcoma occurs at a rate of approximately 4 in one million per year (1 in 250,000 per year) in the general population over 60 years old and at the same rate in women over the age of 70 years. At present it is not known if humans treated with teriparatide have an increased risk of osteosarcoma. However, post-marketing data in humans has not identified an increased risk.

Reporting suspected adverse effects.

Reporting suspected adverse reactions after registration of the medicinal product is important. It allows continued monitoring of the benefit-risk balance of the medicinal product. Healthcare professionals are asked to report any suspected adverse reactions at www.tga.gov.au/reporting-problems.

4.9 Overdose

No cases of overdose were reported during clinical trials. Teriparatide has been safely administered in single doses of up to 100 microgram. In a clinical study, doses of 60 microgram/day for 6 weeks were safely tolerated. The effects of overdose that might be expected include delayed hypercalcaemia and risk of orthostatic hypotension. Nausea, vomiting, dizziness and headache might also occur.
In post-marketing spontaneous reports, there have been cases of medication error in which the entire contents (up to 800 microgram) of the teriparatide pen have been administered as a single dose. Transient events reported have included nausea, weakness/ lethargy and hypotension. In some cases, no adverse events occurred as a result of the overdose. No fatalities associated with overdose have been reported.
In single-dose rodent studies using subcutaneous injection of teriparatide, no mortality was seen in rats given doses of 1000 microgram/kg (526 times the human dose based on body surface area) or in mice given 10,000 microgram/kg (2,635 times the human dose).

Overdose management.

There is no specific antidote for teriparatide. Treatment of suspected overdose should include discontinuation of teriparatide, monitoring of serum calcium, and implementation of appropriate supportive measures, such as hydration.
For information on the management of overdose, contact the Poisons Information Centre on 13 11 26 (Australia).

5 Pharmacological Properties

5.1 Pharmacodynamic Properties

Osteoporosis is characterised by low bone mass and microarchitectural deterioration of bone tissue, leading to bone fragility and an increase in the risk of vertebral and non-vertebral fractures. The diagnosis of osteoporosis may be confirmed by the finding of low bone mass or the presence or history of osteoporotic fracture. While non-vertebral fractures are usually clinically apparent, vertebral fractures also may be manifested by back pain, height loss or kyphosis.

Mechanism of action.

Endogenous 84-amino-acid parathyroid hormone (PTH) is the primary regulator of calcium and phosphate metabolism in bone and kidney. Physiological actions of PTH include regulation of bone metabolism, renal tubular reabsorption of calcium and phosphate, and intestinal calcium absorption. The biological actions of PTH and teriparatide are mediated through binding to specific PTH cell surface receptors. Teriparatide is the synthetic active fragment (1-34) of endogenous human PTH. The proposed teriparatide product is not manufactured using recombinant DNA technology. Teriparatide binds to these receptors with similar affinity as PTH, and has the same actions in bone and kidney as PTH. Like endogenous PTH, teriparatide is not expected to accumulate in bone or other tissues.

Pharmacodynamic effects.

The skeletal effects of teriparatide depend upon the pattern of systemic exposure. Once-daily administration of teriparatide increases apposition of new bone on trabecular and cortical (endosteal and periosteal) bone surfaces by preferential stimulation of osteoblastic activity over osteoclastic activity. In contrast, continuous excess of endogenous PTH, as occurs in hyperparathyroidism, may be detrimental to the skeleton because bone resorption may be stimulated more than bone formation. In monkey studies, teriparatide improved trabecular microarchitecture and increased bone mass and strength by stimulating new bone formation in both cancellous and cortical bone.
In humans, teriparatide affects calcium and phosphorus metabolism in a pattern consistent with the known actions of endogenous PTH.

Clinical trials.

Clinical trials were conducted with the reference medicine Forteo. The clinical program included treatment studies in women and men with osteoporosis. Postmenopausal women were treated for up to 24 months to evaluate effects on vertebral fractures. Men were treated for up to 14 months to evaluate the effect on BMD. Of the women and men who participated in the teriparatide treatment studies, 1,930 have been systematically observed for 18 months in a post-treatment follow-up study.
Treatment of postmenopausal women with osteoporosis. The pivotal study included 1,637 postmenopausal women (mean age 69.5 years). At baseline, ninety percent of the patients had one or more vertebral fractures. All patients received 1000 mg of calcium per day and at least 400 IU of vitamin D per day. Results from a treatment period of up to 24 months (median 19 months), with teriparatide, demonstrate significant anti-fracture efficacy.

Effect on vertebral fractures.

Teriparatide, relative to placebo, given for a median of 19 months, significantly reduced the risk and severity of new vertebral fractures in postmenopausal women with osteoporosis. The relative risk for the incidence of 1 or more new vertebral fractures was reduced by 65% and multiple fractures by 77% with teriparatide treatment (Table 3 includes data on absolute risk reduction). Eleven women would need to be treated with teriparatide for a median of 19 months to prevent one or more new vertebral fractures.

Effect on non-vertebral fractures.

Teriparatide significantly reduced (by 53%) the overall incidence of non-vertebral fragility fractures including wrist, ribs, ankle, humerus, hip, foot, pelvis and others (see Figure 1).

Effect on BMD.

Teriparatide rapidly increased lumbar spine BMD. Significant increases were seen as early as 3 months and continued throughout the treatment period, as shown in Figure 2. After a median treatment period of 19 months, BMD had increased 9% and 4% in the lumbar spine and total hip, respectively, compared with placebo (p < 0.001). Teriparatide was effective regardless of age, baseline rate of bone turnover and baseline BMD.

Effect on back pain.

Teriparatide significantly reduced the incidence and severity of back pain. In women with postmenopausal osteoporosis, there was a significant (p=0.017) 26% reduction in the spontaneous reports of new or worsened back pain compared to placebo.

Effects on height loss.

For the 86 postmenopausal women who experienced vertebral fractures, those treated with teriparatide had significantly less height loss when compared to placebo (p=0.001).

Bone histology.

The effects of teriparatide on bone histology were evaluated in iliac crest biopsies of 61 postmenopausal women treated for up to 24 months with placebo or teriparatide 20 microgram or 40 microgram per day. The increases in BMD and resistance to fracture achieved with teriparatide occurred without evidence of cellular toxicity or adverse effects on bone architecture or mineralisation. The findings in human bone samples paralleled those seen in preclinical primate studies.

Post-treatment fracture efficacy.

Following treatment with teriparatide, 1,262 postmenopausal women from the pivotal trial enrolled in a post-treatment follow-up study. After 18 months, approximately 50% of the women in each former treatment group had begun an approved osteoporosis therapy (not including teriparatide) at the discretion of their physician. All women were offered 1000 mg of calcium per day and at least 400 IU of vitamin D per day.
During a median of 18 months following discontinuation of teriparatide treatment, there was a significant 40% reduction in relative risk for new vertebral fractures in women previously treated with teriparatide, compared to placebo. (The relative risk reduction was similar for women with and without osteoporosis treatment, 41% and 37%, respectively.) During the same observation period, there was a 42% risk reduction for non-vertebral fragility fractures in women previously treated with teriparatide, compared with placebo.
Data from this study demonstrate that regardless of the follow-up treatment options, fracture risk was reduced for women previously treated with teriparatide.
A 24-month, randomised, double-blind, comparator-controlled Phase 4 study included 1,360 postmenopausal women with established osteoporosis. 680 subjects were randomised to teriparatide and 680 subjects were randomised to oral risedronate 35 mg/week. At baseline, the women had a mean age of 72.1 years and a median of 2 prevalent vertebral fractures; 57.9% of patients had received previous bisphosphonate therapy and 18.8% took concomitant glucocorticoids during the study. 1,013 (74.5%) Patients completed the 24-month follow-up. The mean (median) cumulative dose of glucocorticoid was 474.3 (66.2) mg in the teriparatide arm and 898.0 (100.0) mg in the risedronate arm. The mean (median) vitamin D intake for the teriparatide arm was 1408.4 IU/day (1380.4 IU/day) and for the risedronate arm was 1206.4 IU/day (900 IU/day). For those subjects who had baseline and follow-up spine radiographs, the incidence of new vertebral fractures was 28/516 (5.4%) in teriparatide and 64/533 (12.0%) in risedronate-treated patients, relative risk (95% CI) = 0.44 (0.29-0.68), p < 0.0001. The cumulative incidence of pooled clinical fractures (clinical vertebral and non-vertebral fractures) was 4.8% in teriparatide and 9.8% in risedronate-treated patients, hazard ratio (95% CI) = 0.48 (0.32-0.74), p=0.0009.
In an open-label study, 503 postmenopausal women with severe osteoporosis and a fragility fracture within the previous 3 years (83% had received previous osteoporosis therapy) were treated with teriparatide for up to 24 months. At 24 months, the mean increase from baseline in lumbar spine, total hip and femoral neck BMD was 10.5%, 2.6% and 3.9% respectively. The mean increase in BMD from 18 to 24 months was 1.4%, 1.2% and 1.6% at the lumbar spine, total hip and femoral neck, respectively.
Male osteoporosis. The efficacy of teriparatide was demonstrated in a double-blind, placebo-controlled clinical study in 437 men with either hypogonadal or idiopathic osteoporosis. All patients received 1000 mg of calcium per day and at least 400 IU of vitamin D per day and were treated for up to 14 months.
In this study, teriparatide rapidly increased lumbar spine BMD in men, with significant increases as early as 3 months. This increase continued throughout the treatment period, as shown in Figure 3. After a median treatment period of 11 months, BMD in the spine had (on average) increased by 5% and in the hip by 1%, compared to placebo. Increases in BMD were similar in men with hypogonadal or idiopathic osteoporosis. Teriparatide was effective regardless of age, baseline rate of bone turnover and baseline BMD.
All male patients presenting with osteoporosis should be checked for primary or secondary hypogonadism, investigated and treated appropriately as a prerequisite.
Glucocorticoid-induced osteoporosis. The efficacy of teriparatide in men and women (N=428) receiving sustained systemic glucocorticoid therapy (equivalent to 5 mg or greater of prednisone for at least 3 months) was demonstrated in a 36 month (18-month primary phase plus 18-month continuation phase), randomised, double-blind, comparator-controlled study (alendronate 10 mg/day). Twenty-eight percent of patients had one or more radiographic vertebral fractures at baseline. All patients were offered 1000 mg calcium per day and 800 IU vitamin D per day.
This study included postmenopausal women (N=277), premenopausal women (N=67), and men (N=83). At baseline, the postmenopausal women had a mean age of 61 years, mean lumbar spine BMD T score (number of standard deviations above or below the mean in healthy young women) of -2.7, median prednisone equivalent dose of 7.5 mg/day, and 34% had one or more radiographic vertebral fractures; premenopausal women had a mean age of 37 years, mean lumbar spine BMD T score of -2.5, median prednisone equivalent dose of 10 mg/day, and 9% had one or more radiographic vertebral fractures; and men had a mean age of 57 years, mean lumbar spine BMD T score of -2.2, median prednisone equivalent dose of 10 mg/day, and 24% had one or more radiographic vertebral fractures.

Effects on vertebral and non-vertebral BMD.

The primary objective was the change in lumbar spine BMD from baseline to the 18-month endpoint (last observation carried forward) in men and women combined. Sixty-nine percent of patients completed the 18-month primary phase. At the 18-month endpoint (men and women combined), teriparatide increased lumbar spine BMD (7.2%) significantly more than alendronate (3.4%) (p < 0.001).
Figure 4 shows the time course of mean percent change from baseline in lumbar spine BMD through 36 months for men and women combined. There was a significant difference between groups at all measured timepoints and endpoint. At 36 months (Figure 4) the mean percent change from baseline in lumbar spine BMD was 11.0% in the teriparatide group versus 5.3% in the alendronate group, a difference of 5.7% (p < 0.001).
Table 4 presents the mean percent change in lumbar spine BMD in the women only subgroup.
In men and women combined, changes from baseline in femoral neck BMD were significantly greater in the teriparatide compared with the alendronate group at all timepoints and at endpoint (Figure 5). The mean percent change in femoral neck BMD from baseline to endpoint was 5.1% in the teriparatide group compared with 2.6% in the alendronate group, (p < 0.001).
In men and women combined, changes from baseline in total hip BMD were significantly greater in the teriparatide group compared with the alendronate group at all timepoints and at endpoint (Figure 6). The mean increase in total hip BMD from baseline to endpoint was 4.4% in the teriparatide group versus 2.2% in the alendronate group (p < 0.001).
In premenopausal women, the increase in BMD from baseline to endpoint at 36 months was significantly greater in the teriparatide group compared with the alendronate group at the lumbar spine (4.6% versus -0.9%; p=0.017) and total hip (4.8% versus 1.5%; p=0.026). However, no significant effect on fracture rates was demonstrated in premenopausal women.
Analysis of vertebral and non-vertebral fractures: At 18 months, analysis of spinal X-rays from 165 alendronate patients and 171 teriparatide patients showed that 10 patients in the alendronate group (6.1%) had experienced a new vertebral fracture compared with 1 patient in the teriparatide group (0.6%). In addition, 9 patients in the alendronate group (4.2%) had experienced a non-vertebral fracture compared with 12 patients in the teriparatide group (5.6%).
Table 5 summarises the incident fractures at 36 months in men and women combined.

Effects on markers of bone turnover.

In patients with glucocorticoid-induced osteoporosis, daily administration of teriparatide stimulated new bone formation as shown by increases from baseline in the serum concentration of biochemical markers of bone formation including bone-specific alkaline phosphatase (BSAP), procollagen I carboxyterminal propeptide (PICP), and amino-terminal propeptide of type I collagen (PINP) (see Table 6). Teriparatide also stimulated bone resorption as shown by increases from baseline in serum concentrations of C-terminal telopeptide of type I collagen (CTX). Alendronate 10 mg/day induced decreases from baseline in the serum concentration of BSAP, PICP, PINP and CTX (see Table 6). The effects of teriparatide on bone turnover markers in patients with glucocorticoid-induced osteoporosis were qualitatively similar to the effects in postmenopausal women with osteoporosis not taking glucocorticoids.

5.2 Pharmacokinetic Properties

Absorption.

After subcutaneous (SC) injection, teriparatide has an absolute bioavailability of 95% (95% CI 0.824-1.07). Absorption and elimination are rapid. The half-life of teriparatide in serum is 5 minutes when administered by intravenous injection and approximately 1 hour when administered by subcutaneous injection. The longer half-life following subcutaneous administration reflects the time required for absorption from the injection site.
Following a subcutaneous injection of a 20 microgram dose, peak molar concentrations of teriparatide briefly exceed the upper limit of normal for endogenous PTH [65 picogram/mL (7.0 picomolar)] by 4 to 5-fold for about 30 minutes and then decline to non-quantifiable concentrations within 3 hours. The mean systemic exposure (endogenous PTH and teriparatide) over 24 hours does not exceed the upper limit of normal and is below the levels found in patients with mild hyperparathyroidism.

Distribution.

Volume of distribution is approximately 1.7 L/kg. Between-subject variability in systemic clearance and volume of distribution is 25% to 50%.

Metabolism.

No metabolism studies have been performed with teriparatide. However, the mechanisms of metabolism of PTH (1-34) and intact PTH have been extensively described. Metabolism of parathyroid hormone is believed to occur predominantly in liver and kidney.

Excretion.

Teriparatide is eliminated through hepatic and extra-hepatic clearance (approximately 62 L/hr in women and 94 L/hr in men). No excretion studies have been performed with teriparatide. However, the mechanism of elimination of PTH (1-34) and intact PTH have been extensively described.

Patient characteristics.

Geriatrics.

No differences in teriparatide pharmacokinetics were detected with regard to age (range 31 to 85 years). Dosage adjustment based on age is not required.

Gender.

Systemic exposure to teriparatide is approximately 20% to 30% lower in men than in women. There were, however, no gender differences with respect to safety, tolerability or pharmacodynamic responses. Dosage adjustment based on gender is not required.

Renal impairment.

No clinically relevant pharmacokinetic or safety differences were identified in patients with mild, moderate or severe chronic renal impairment administered a single dose of teriparatide. Dosage adjustment, based on renal function, is not required.
However, patients with renal impairment had reduced calcaemic and calciuric responses to teriparatide. Long-term safety and efficacy have not been evaluated in patients with serum creatinine concentrations > 177 micromol/L.

Heart failure.

No clinically relevant pharmacokinetic, blood pressure, pulse rate or other safety differences were identified in patients with stable heart failure (New York Heart Association Class I to III and additional evidence of cardiac dysfunction) administered two 20 microgram doses of teriparatide. Dosage adjustment based on the presence of mild or moderate heart failure is not required. There are no data from patients with severe heart failure.

Hepatic impairment.

Safety and efficacy have not been evaluated in patients with hepatic impairment. Preclinical data indicate that hepatic Kupffer cells are the primary site of metabolism for teriparatide. It is unlikely that disease states in which hepatocyte function is impaired will have a clinically significant effect on systemic exposure to teriparatide).

5.3 Preclinical Safety Data

Genotoxicity.

Teriparatide was not genotoxic in assays for gene mutations (Ames test and mouse lymphoma assay in vitro) and chromosomal damage (Chinese hamster ovary cells in vitro and the mouse micronucleus test in vivo).

Carcinogenicity.

Two carcinogenicity bioassays were conducted in rats. In the first study, male and female rats were given daily subcutaneous teriparatide injections of 5, 30, or 75 microgram/kg/day for 24 months from 2 months of age. These doses resulted in systemic exposures that were, respectively, 3, 20, and 60 times higher than the systemic exposure observed in humans following a subcutaneous dose of 20 microgram (based on AUC comparison). Teriparatide treatment resulted in a marked dose-related increase in the incidence of osteosarcoma, a rare malignant bone tumour, in both male and female rats. Osteosarcomas were observed at all doses, occurred after 17 to 20 months of treatment, and reached an incidence of 38% to 52% in the high-dose groups. Teriparatide also caused increased incidences of osteoblastoma and osteoma in both sexes. No osteosarcomas, osteoblastomas or osteomas were observed in untreated control rats. The bone tumours in rats occurred in association with a large increase in bone mass and focal osteoblast hyperplasia.
The second 2-year study was carried out in order to determine the effect of treatment duration and animal age on the development of bone tumours. Female rats were treated for different periods between 2 and 26 months of age with subcutaneous doses of 5 and 30 microgram/kg (equivalent to 3 and 20 times the human exposure at the 20 microgram dose, based on AUC). The study showed that the occurrence of osteosarcoma, osteoblastoma and osteoma was dependent upon dose and duration of exposure. Bone tumours were observed when immature 2-month old rats were treated with 30 microgram/kg/day for 6 or 24 months. Bone tumours were also observed when mature 6-month old rats were treated with 30 microgram/kg/day for 6 or 20 months. Tumours were not detected when mature 6-month old rats were treated with 5 microgram/kg/day for 6 or 20 months. The results did not demonstrate a difference in susceptibility to bone tumour formation, associated with teriparatide treatment, between mature and immature rats. The relevance of these rat findings to humans is uncertain.
No bone neoplasms or preneoplastic lesions were found in monkeys treated with teriparatide SC for 18 months, and then observed for a further 3 years, at a dose yielding 5-fold clinical exposure levels (based on AUC data).

6 Pharmaceutical Particulars

6.1 List of Excipients

Glacial acetic acid; sodium acetate; mannitol; metacresol; water for injections; hydrochloric acid (for pH adjustment); sodium hydroxide (for pH adjustment).

6.2 Incompatibilities

Incompatibilities were either not assessed or not identified as part of the registration of this medicine.
In the absence of compatibility studies, this medicinal product must not be mixed with other medicinal products.

6.3 Shelf Life

In Australia, information on the shelf life can be found on the public summary of the Australian Register of Therapeutic Goods (ARTG). The expiry date can be found on the packaging.
Each Teriparatide Lupin pen can be used for up to 28 days after the first injection.

6.4 Special Precautions for Storage

Store at 2°C to 8°C. Refrigerate. Do not freeze.
Chemical, physical and microbiological in-use stability has been demonstrated for 28 days at 2-8°C. Once opened, the product may be stored for a maximum of 28 days at 2°C to 8°C.
The dose may be delivered immediately following removal from the refrigerator. Do not allow Teriparatide Lupin to freeze. Do not use Teriparatide Lupin if it has been frozen. During the use period, minimise the time the pen remains out of the refrigerator.
Close the pen with the pen cap after use (due to light sensitivity of the solution for injection). The pen should be returned to the refrigerator immediately after use. Do not store the injection device with the needle attached.

6.5 Nature and Contents of Container

Teriparatide Lupin pre-filled injection pen contains 2.4 mL solution in a cartridge (siliconised Type I glass) with a plunger, rubber disc and aluminium cap assembled into a disposable pen.
Teriparatide Lupin is available in the following pack sizes: 1 pen; 3 pens.
Each pen contains 28 doses of 20 microgram (per 80 microlitre).
Not all pack sizes may be marketed.

6.6 Special Precautions for Disposal

In Australia, any unused medicine or waste material should be disposed of by taking to your local pharmacy.

6.7 Physicochemical Properties

Chemical structure.

Teriparatide, synthetically derived, is identical to the 34 N-terminal amino acid sequence of endogenous human parathyroid hormone.
Teriparatide is a polypeptide which molecular weight, molecular formula and molecular structure are as follows.
Molecular weight: 4117.72 g/mol (average mass of the isotopes).
Molecular formula: C181H291N55O51S2 (as free base).
Molecular structure:

CAS number.

The CAS number for teriparatide is 52232-67-4.

7 Medicine Schedule (Poisons Standard)

Schedule 4 - Prescription Only Medicine.

Summary Table of Changes