Indications

Prolia® is a prescription medicine used to treat osteoporosis in women after menopause who are at high risk for fracture or cannot use another osteoporosis medicine or other osteoporosis medicines did not work well. Read More

Prolia® is a prescription medicine used to increase bone mass in men with osteoporosis who are at high risk for fracture.

Prolia® is a prescription medicine used to treat osteoporosis in men and women who will be taking corticosteroid medicines (such as prednisone) for at least six months and are at high risk for fracture.

Prolia® is a prescription medicine used to treat bone loss in men who are at high risk for fracture receiving certain treatments for prostate cancer that has not spread to other parts of the body.

Prolia® is a prescription medicine used to treat bone loss in women who are at high risk for fracture receiving certain treatments for breast cancer that has not spread to other parts of the body. Read Less

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For women with osteoporosis after menopause at high risk for fracture

See whether Prolia® is right for you by selecting an option below

Learn more if you're starting with Prolia® (denosumab)

Starting with Prolia®

I’ve been diagnosed with postmenopausal osteoporosis at high risk for fracture and am exploring treatment options.

Starting with Prolia®

If you have postmenopausal osteoporosis at high risk for fracture but are not currently taking medication, find out why Prolia® might be the right first treatment for you:

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I thought my bones were fine. I exercise, I eat right, I’m very healthy. But I found out my bones weren’t as great as I thought.

—Rebecca,

taking Prolia® since 2015

Individual results
may vary.

Rebecca, taking Prolia® (denosumab) since 2015
  1. 1

    Osteoporosis is progressive and bone loss will worsen if not treated.

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    Though exercise, calcium, and vitamin D are a good start, those elements alone may not be enough to protect you from breaking a bone.

    Talk to your doctor to see if you can start slowing down bone loss and help reduce your risk of fracture with Prolia®.

  2. 2

    Over 18 million women have been treated with Prolia® worldwide.*

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    Gain perspective from real women who have experience with Prolia® here.

    *Estimates of patients treated reflect global data since launch (June 2010-Sept 2022; US=approximately 26% of data). Patient counts are based on syringes sold and IQVIA prescription data.

  3. 3

    Prolia® is proven to help strengthen bones and reduce spine fracture risk by 68% with 1 shot every 6 months.

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    In a 3-year study, women not treated with Prolia® had more new spine fractures (7.2%) compared to women treated with Prolia® (2.3%). Study consisted of 7393 patients who received either Prolia® or a placebo (a treatment containing no medicine).

    You should take calcium and vitamin D as your doctor tells you to while you receive Prolia®.

    After your treatment with Prolia® is stopped, or if you skip or delay taking a dose, your risk for breaking bones, including bones in your spine, is increased. Do not stop, skip or delay taking Prolia® without first talking with your doctor.

Talk to your doctor about Prolia®

Download the personalized Doctor Discussion Guide to be proactive before your next doctor's visit.

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Learn more if you're considering switching to Prolia® (denosumab)

Switching to Prolia®

I have postmenopausal osteoporosis at high risk for fracture and I am on an oral medication, but I’m not happy with my current treatment.

Switching to Prolia®

If you are not satisfied with your current treatment or are finishing a treatment, it’s important to talk to your doctor about the next step in your treatment journey.

I had tried other treatments before, but I wasn't seeing the great results I wanted. So, I talked to my doctor about Prolia®. My scan showed improvement within that first year.

—Anita,

taking Prolia® since 2011

Individual results
may vary.

  1. 1

    Only Prolia® is proven to help strengthen and protect bones from fracture with 1 shot every 6 months.

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    That could mean fewer doses than most other osteoporosis treatments. You should take calcium and vitamin D as your doctor tells you to while you receive Prolia®.

    After your treatment with Prolia® is stopped, or if you skip or delay taking a dose, your risk for breaking bones, including bones in your spine, is increased. Do not stop, skip or delay taking Prolia® without first talking with your doctor.

  2. 2

    Prolia® has been studied in two head-to-head bone mineral density (BMD) studies against other common treatments.

    dot line See the data
  3. 3

    Over 18 million women have been treated with Prolia® worldwide.*

    dot line

    Gain perspective from real women who have experience with Prolia® here.

    *Estimates of patients treated reflect global data since launch (June 2010-Sept 2022; US=approximately 26% of data). Patient counts are based on syringes sold and IQVIA prescription data.

Talk to your doctor about Prolia®

Download the personalized Doctor Discussion Guide to be proactive before your next doctor's visit.

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Nearly 500,000 women were included in the largest
Real-World study for postmenopausal osteoporosis.

Compare fracture results between Prolia® and alendronate (Fosamax).

Learn about another treatment option for people who’ve already had a fracture or who are at very high risk for fracture due to osteoporosis.

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Important Safety Information

What is the most important information I should know about Prolia®?
If you receive Prolia, you should not receive XGEVA® (denosumab). Prolia contains the same medicine as XGEVA®.
Prolia® can cause serious side effects (including):
Increased risk of severe low calcium levels in your blood (hypocalcemia). Prolia may lower the calcium levels in your blood. If you have low blood calcium before you start receiving Prolia, it may get worse during treatment. Your low blood calcium must be treated before you receive Prolia. Talk to your doctor before starting Prolia. Your doctor may prescribe calcium and vitamin D to help prevent low calcium levels in your blood while you take Prolia. Take calcium and vitamin D as your doctor tells you to.
If you have advanced chronic kidney disease (may or may not be on kidney dialysis), Prolia may increase your risk for severe low calcium levels in your blood, which could result in hospitalization, life-threatening events and death. A mineral and bone disorder associated with kidney disease called chronic kidney disease mineral bone disorder (CKD-MBD) may increase your risk for severe low calcium levels in blood. Before you start PROLIA and during treatment, your doctor may need to do certain blood tests to check for CKD-MBD.
Most people with low blood calcium levels do not have symptoms, but some people may have symptoms. Call your doctor right away if you have symptoms of low blood calcium such as:
Serious allergic reactions have happened in people who take Prolia®. Call your doctor or go to your nearest emergency room right away if you have any symptoms of a serious allergic reaction, including low blood pressure (hypotension); trouble breathing; throat tightness; swelling of your face, lips, or tongue; rash; itching; or hives.
Severe jaw bone problems (osteonecrosis) may occur. Your doctor should examine your mouth before you start Prolia® and may tell you to see your dentist. It is important for you to practice good mouth care during treatment with Prolia®.
Unusual thigh bone fractures. Some people have developed unusual fractures in their thigh bone. Symptoms of a fracture include new or unusual pain in your hip, groin, or thigh.
Increased risk of broken bones, including broken bones in the spine, after stopping, skipping or delaying Prolia®Talk with your doctor before starting Prolia® treatment. After your treatment with Prolia® is stopped, or if you skip or delay taking a dose, your risk for breaking bones, including bones in your spine, is increased. Your risk for having more than 1 broken bone in your spine is increased if you have already had a broken bone in your spine. Do not stop, skip or delay taking Prolia® without first talking with your doctor. If your Prolia® treatment is stopped, talk to your doctor about other medicine that you can take.
Serious infections in your skin, lower stomach area (abdomen), bladder, or ear may happen. Inflammation of the inner lining of the heart (endocarditis) due to an infection may also happen more often in people who take Prolia®. You may need to go to the hospital for treatment.
Prolia® is a medicine that may affect the ability of your body to fight infections. People who have weakened immune systems or take medicines that affect the immune system may have an increased risk for developing serious infections.
Skin problems such as inflammation of your skin (dermatitis), rash, and eczema have been reported.
Bone, joint, or muscle pain. Some people who take Prolia® develop severe bone, joint, or muscle pain.
Do not take Prolia® if you: have low blood calcium; or are pregnant or plan to become pregnant, as Prolia® may harm your unborn baby; or are allergic to denosumab or any ingredients in Prolia®.
Before taking Prolia®, tell your doctor about all of your medical conditions, including if you:

What are the possible side effects of Prolia®?

It is not known if the use of Prolia® over a long period of time may cause slow healing of broken bones. The most common side effects of Prolia® in women being treated for osteoporosis after menopause are back pain, pain in your arms and legs, high cholesterol, muscle pain, and bladder infection.

The most common side effects of Prolia® in men with osteoporosis are back pain, joint pain, and common cold (runny nose or sore throat).

The most common side effects of Prolia® in patients with corticosteroid-induced osteoporosis are back pain, high blood pressure, lung infection (bronchitis), and headache.

The most common side effects of Prolia® in patients receiving certain treatments for prostate or breast cancer are joint pain, back pain, pain in your arms and legs, and muscle pain. Additionally, in Prolia®-treated men with nonmetastatic prostate cancer receiving ADT, a greater incidence of cataracts was observed.

These are not all the possible side effects of Prolia®. Call your doctor for medical advice about side effects.

You are encouraged to report negative side effects of prescription drugs to the FDA. Visit www.fda.gov/medwatch, or call 1-800-FDA-1088. 

Indications

Prolia® is a prescription medicine used to treat osteoporosis in women after menopause who are at high risk for fracture or cannot use another osteoporosis medicine or other osteoporosis medicines did not work well.

Prolia® is a prescription medicine used to increase bone mass in men with osteoporosis who are at high risk for fracture.

Prolia® is a prescription medicine used to treat osteoporosis in men and women who will be taking corticosteroid medicines (such as prednisone) for at least six months and are at high risk for fracture.

Prolia® is a prescription medicine used to treat bone loss in men who are at high risk for fracture receiving certain treatments for prostate cancer that has not spread to other parts of the body.

Prolia® is a prescription medicine used to treat bone loss in women who are at high risk for fracture receiving certain treatments for breast cancer that has not spread to other parts of the body.

Please see Prolia® full Prescribing Information and Medication Guide.

Important Safety Information

What is the most important information I should know about Prolia®?
If you receive Prolia, you should not receive XGEVA® (denosumab). Prolia contains the same medicine as XGEVA®.
Prolia® can cause serious side effects (including):
Increased risk of severe low calcium levels in your blood (hypocalcemia). Prolia may lower the calcium levels in  
Read More