Prolia® is licensed for treating:1
- Osteoporosis in women after the menopause (postmenopausal) and men who have an increased risk of fracture (broken bones), reducing the risk of spinal, non-spinal and hip fractures.
- Bone loss that results from a reduction in hormone (testosterone) level caused by surgery or treatment with medicines in patients with prostate cancer.
- Bone loss that results from long-term treatment with glucocorticoids in patients who have an increased risk of fracture.
What do I need to remember?
- While being treated, you should maintain good oral hygiene and receive routine dental check-ups. If you wear dentures you should make sure these fit properly. If you are under dental treatment or will undergo dental surgery (e.g. tooth extractions), inform your doctor about your dental treatment and tell your dentist that you are being treated with Prolia®.1 Please refer to the Patient reminder card .
- If your doctor has prescribed calcium and/or vitamin D it is important that you take this as instructed during your Prolia® treatment (until advised otherwise by your doctor).1
If you get any side effects, talk to your doctor, pharmacist or nurse. This includes any possible side effects not listed in the package leaflet. Side effects can be reported directly to the Health Products Regulatory Authority (HPRA) using the available methods via www.hpra.ie. Side effects should also be reported to Amgen Limited on +44 (0) 1223 436441 or Freephone 1800 535 160.
Don't forget to take Prolia® as prescribed or please consult your doctor on the date for a potential next injection. The benefits of Prolia® start from the first injection but because the treatment effect does wear off, if you miss an injection you might increase your risk of fracture.
Both calcium and vitamin D play a vital role in maintaining strong bones. Calcium supplements ensure your body has the right level of calcium for different functions in your body and vitamin D helps ensure that the calcium you take (through supplements or through your diet) is transferred into the bloodstream.
Prolia® may lower the calcium levels in your blood. If you have low blood calcium, it may get worse during treatment, so your low blood calcium must be treated before you receive Prolia®.1
You can get calcium from dairy products such as milk and cheese and you can boost your vitamin D levels through exposure to sunlight. Your doctor may prescribe supplements to increase your calcium and vitamin D.
The amount of calcium and vitamin D you need will depend on your levels to start with, so will be specific to you. Your doctor can measure these levels through single blood tests and will then decide on the correct dose of supplements, and may advise you on maintaining or increasing your levels through lifestyle changes such as diet and exposure to sunlight.
Administer your injection (if you were trained to do it) or book in for an injection as soon as it is convenient for you and your healthcare provider.1 The treatment effect of Prolia® does wear off if treatment is stopped, so it is important you continue to get your injection every six months. If you miss an injection you might increase your risk of a fracture.2,3
Mark the injection date on your calendar, phone, and/or Prolia®
Passport card to keep a record of the next injection date. You can download the Prolia®
Passport card on the More Resources
For more information on what support services are available, please visit the Irish Osteoporosis Society website - www.irishosteoporosis.ie
- or ring
the National Helpline on 01 637 5050.