Medicine guide

XGEVA

As listed in the register: XGEVA

120 mg · solution

  • Prescription only
  • Muscles, joints and bones
Active substance
Denosumab
Made by
Amgen Canada Inc

Quoted from the official source. Not yet reviewed by Mediclarum — the leaflet in your pack is authoritative.

What it is for

Medicine groupMuscles, joints and bonesM05BX04

Mediclarum has not yet retrieved and stored the official label for this product, so none of its text is shown here. Open the official leaflet

How it works

From the US prescribing label for the same active substance (Bilprevda). It describes the substance, not this exact product.

Denosumab products bind to RANKL, a transmembrane or soluble protein essential for the formation, function, and survival of osteoclasts, the cells responsible for bone resorption, thereby modulating calcium release from bone.

Increased osteoclast activity, stimulated by RANKL, is a mediator of bone pathology in solid tumors with osseous metastases.Similarly, giant cell tumors of bone consist of stromal cells expressing RANKL and osteoclast-like giant cells expressing RANK receptor, and signaling through the RANK receptor contributes to osteolysis and tumor growth.

Half-life28 days
Mostly cleared after≈ 20 weeksfive half-lives — our arithmetic

Quoted from the prescribing label, sections “Mechanism of Action” and “Pharmacokinetics”. DailyMed · 2026-08-18

Safety of the active substance

From the US prescribing label for the same active substance (Bilprevda). It describes the substance, not this exact product.

Must not be used by
  • ( 4.1 ) Known clinically significant hypersensitivity to denosumab products.
  • ( 4.2 ) 4.1 Hypocalcemia Pre-existing hypocalcemia must be corrected prior to initiating therapy with Bilprevda [see Warnings and Precautions ( 5.3 )]. 4.2 Hypersensitivity Bilprevda is contraindicated in patients with known clinically significant hypersensitivity to denosumab products [see Warnings and Precautions ( 5.2 ) and Adverse Reactions ( 6.2 )].
Most common side effects

Most common adverse reactions (≥ 10%) were diarrhea, nausea, anemia, back pain, thrombocytopenia, peripheral edema, hypocalcemia, upper respiratory tract infection, rash, and headache.

Quoted from the US prescribing label for the same active substance. Your own pack’s leaflet is the authority for your product. DailyMed

Same active substance, strength and form in other countries

Matched on active substance, strength and kind of form only. This is not a statement that the products are equivalent or interchangeable: other ingredients, release and approved uses can differ — ask a pharmacist before swapping.

Medicine passport: one printable page to show a pharmacist abroad

United StatesNo exact match for this strength and form

European UnionNo exact match for this strength and form

SpainNo exact match for this strength and form

NetherlandsNo exact match for this strength and form

SwitzerlandNo exact match for this strength and form

Details

Made byAmgen Canada Inc
Active substanceDenosumab
Used inMuscles, joints and bones
Strength120 mg
Formsolution
ClassificationM05BX04 · Muscles, joints and bones
Routesubcutaneous
Dispensing (as stated by the register)SCHEDULE D · PRESCRIPTION
StatusMarketed
MarketedYes, according to the register
DIN02368153
DPD drug code85304

Source: Drug Product Database · 2026-09-30 · not reviewed by a clinician

Contains information licensed under the Open Government Licence – Canada. Reuse terms: Open Government Licence – Canada.

Same active substance

These contain the same substance. That does not mean one can replace another — ask a pharmacist.