Brand Name: Prolia, Xgeva
Generic Name: Denosumab
Drug Class: Monoclonal Antibodies, Endocrine; Antineoplastics, Monoclonal Antibody
What Is Denosumab and How Does It Work?
Dosages of Denosumab:
Dosage Forms and Strengths
- Prolia: 60mg/mL (1mL prefilled syringe or 1mL vial) (adult only)
- Xgeva: 70mg/mL (120mg/1.7mL vial) (adult and pediatric)
Dosage Considerations – Should be Given as Follows:
- Treatment of men and postmenopausal women with osteoporosis who are at high risk for fracture; treatment to increase bone mass in men at high risk for fracture who are receiving androgen deprivation therapy for non-metastatic prostate cancer; treatment to increase bone mass in women at high risk for fracture who are receiving adjuvant aromatase inhibitor therapy for breast cancer
- Prolia: 60 mg subcutaneously (SC) every 6 months
- Supplement with calcium 1000 mg/day and vitamin D 400 IU/day
Aromatase Inhibitor Induced Bone Loss
- Women with breast cancer: 60 mg (Prolia) subcutaneously (SC) every 6 months
Androgen Deprivation Induced Bone Loss
- Men with prostate cancer: 60 mg (Prolia) subcutaneously (SC) every 6 months
- Prevention of skeletal-related events (SREs; e.g., bone fractures and pain) in patients with bone metastases from solid tumors
- Xgeva: 120 mg (1.7 mL) subcutaneously (SC) every 4 weeks
- Adult: Treatment of adults and skeletally mature adolescents with giant cell tumor of bone in whom surgical resection is impossible or is likely to result in severe morbidity
- Xgeva: 120 mg subcutaneously (SC) every 4 weeks with additional 120 mg on days 8 and 15 during first month of therapy
- Pediatric: Treatment of skeletally mature adolescents with giant cell tumor of bone in whom surgical resection is impossible or is likely to result in severe morbidity
- Xgeva: 120 mg SC every 4 weeks, with additional 120 mg on days 8 and 15 during first month of therapy
- Indicated for treatment of hypercalcemia of malignancy refractory to bisphosphonate therapy
- Xgeva: 120 mg subcutaneously (SC) every 4 weeks
- Give 2 additional 120 mg doses during the first month of therapy on Days 8 and 15
- Must be administered by healthcare professional
- Administer SC in upper arm, upper thigh, or abdomen; do NOT administer intradermally, intramuscularly (IM), or intravenously (IV)
- Administer calcium and vitamin D as needed to treat or prevent hypocalcemia
- Avoid vigorous shaking of vial/syringe
- Store refrigerated at 2-8°C (36-46°F)
- Once removed from refrigerator, preparation must be used within 14 days
What Are Side Effects Associated with Using Denosumab?
Common side effects of denosumab include:
- Back pain
- Extremity pain
- Musculoskeletal pain
- Upper respiratory tract infection
- New malignancies
- Nonfatal serious infection
- Bone pain
- Upper abdominal pain
- Gas (flatulence)
- Osteonecrosis of jaw
- Low blood calcium (hypocalcemia)
- Joint pain
Serious side effects of denosumab include:
- Serious infection of abdomen resulting in hospitalization
- Serious infection of urinary tract resulting in hospitalization
- Serious infection resulting in death
- Serious infection of ear resulting in hospitalization
- Jaw pain
- New or unusual thigh/hip/groin pain
- Bone/joint/muscle pain
- Shortness of breath
Postmarketing side effects of denosumab reported include:
- Marked elevation in PTH in patients with severe renal impairment or receiving dialysis
- Multiple vertebral fractures following discontinuation of Prolia
This document does not contain all possible side effects and others may occur. Check with your physician for additional information about side effects.
What Other Drugs Interact with Denosumab?
If your doctor has directed you to use this medication, your doctor or pharmacist may already be aware of any possible drug interactions and may be monitoring you for them. Do not start, stop, or change the dosage of any medicine before checking with your doctor, health care provider or pharmacist first.
Denosumab has no known severe interactions with other drugs.
Serious interactions of denosumab include:
- influenza virus vaccine trivalent, adjuvanted
Denosumab has moderate interactions with at least 105 different drugs.
Denosumab has no known mild interactions with other drugs.
This information does not contain all possible interactions or adverse effects. Therefore, before using this product, tell your doctor or pharmacist of all the products you use. Keep a list of all your medications with you, and share this information with your doctor and pharmacist. Check with your health care professional or doctor for additional medical advice, or if you have health questions, concerns or for more information about this medicine.
What Are Warnings and Precautions for Denosumab?
This medication contains denosumab. Do not take Prolia or Xgeva if you are allergic to denosumab or any ingredients contained in this drug.
Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center immediately.
Effects of Drug Abuse
- No information available
- See "What Are Side Effects Associated with Using Denosumab?"
- See "What Are Side Effects Associated with Using Denosumab?"
- Denosumab is available as 2 distinct brands (Prolia and Xgeva) that have different dosage strengths for their respective indications; do not use concurrently.
- Low blood calcium (hypocalcemia) may occur; monitor calcium levels during therapy, especially in the first weeks of initiating therapy, and adequately supplement all patients with calcium and vitamin D.
- Severe symptomatic hypocalcemia has been reported; hypocalcemia may worsen, especially in patients who have CrCl less than 30 mL/minute or are on hemodialysis.
- Serious infections (including cellulitis) and dermatologic reactions (e.g., dermatitis, rashes, eczema) have been reported; advise patients to seek prompt medical attention if they develop signs or symptoms of infection, including cellulitis; consider discontinuing therapy if severe symptoms develop.
- Hypersensitivity (including anaphylaxis) has been reported.
- Bone turnover suppression may increase risk for osteonecrosis of jaw; perform an oral examination prior to initiating therapy; osteonecrosis of the jaw, can occur spontaneously and is generally associated with tooth extraction and/or local infection with delayed healing; known risk factors include invasive dental procedures (e.g., tooth extraction, dental implants, boney surgery), diagnosis of cancer, concomitant therapies (e.g., chemotherapy, corticosteroids, angiogenesis inhibitors), poor oral hygiene, and co-morbid disorders; risk of osteonecrosis of the jaw may increase with duration of therapy.
- Significant suppression demonstrated; monitor for consequences of bone over-suppression.
- Severe and occasionally incapacitating bone, joint, and/or muscle pain has been reported; discontinue use if severe symptoms develop.
- Monitor patients for signs and symptoms of high blood calcium (hypercalcemia) and treat appropriately.
- Atypical femoral fracture has been reported; evaluate patients with thigh or groin pain to rule out a femoral fracture.
- Following discontinuation of Prolia treatment, fracture risk increases, including risk of multiple vertebral fractures.
- Pancreatitis reported in clinical trials.
- Pediatric use is not recommended; drug may impair bone growth in children with open growth plates and may inhibit eruption of dentition.
- Latex allergy: If sensitive to latex, do not handle gray needle cap on single-use prefilled syringe, which contains dry natural rubber (a derivative of latex).
- Pregnancy; females of reproductive potential should be advised to use highly effective contraception during therapy and for at least 5 months after last dose (Prolia).
- Not indicated for the prevention of skeletal-related events in patients with multiple myeloma.
- Use caution in patients with renal impairment less than 30 mL/minute) or patients on dialysis; risk of hypocalcemia increased; dose adjustment not necessary when administered at 60 mg every 6 months; once monthly dosing not evaluated in patients with renal impairment.
- Not for intravenous, intradermal, or intramuscular administration.
Pregnancy and Lactation
- Do not use denosumab in pregnancy. The risks involved outweigh potential benefits. Safer alternatives exist.
- On the basis of animal studies, denosumab may cause fetal harm when administered pregnant women. In utero, there were results in increased fetal loss, stillbirths, and postnatal mortality, including absent lymph nodes, abnormal bone growth, and decreased neonatal growth.
- Women with reproductive potential must use highly effective contraception during therapy and for 5 months or more after the last dose of denosumab.
- On the basis of animal studies in pregnant mice lacking the RANK/RANK ligand (RANKL) signaling pathway that have shown altered maturation of the maternal mammary gland, leading to impaired lactation post partum, maternal exposure during pregnancy may impair mammary gland development and lactation.
- It is unknown whether denosumab is distributed in breast milk; caution is advised if breastfeeding.
RxList. Xgeva Side Effects Center.