Denosumab [Stoboclo®]
Yes
No
No
Active ingredient: Denosumab
General information
Subsidy Information and Financing Scheme
Not Applicable
Drug Guidance for Subsidy
01/04/2023 Review of cancer supportive care medicines>
[R] The Ministry of Health’s Drug Advisory Committee has reviewed the available clinical evidence for cancer supportive care medicines routinely used in public healthcare institutions to update the MOH List of Subsidised Drugs in line with local clinical practice. The following medicines have been recommended for inclusion on the MOH Standard Drug List (SDL) or Medication Assistance Fund (MAF) in line with their registered indications or specific clinical criteria for cancer supportive care, in view of clinical need and acceptable clinical and cost-effectiveness:
Aprepitant 125 mg and 80 mg tri-pack capsules;
Cetirizine 10 mg tablet;
Denosumab 60 mg/mL prefilled syringe;
Denosumab 120 mg/1.7 mL solution for injection;
Epoetin alfa 10,000 international units/mL and 40,000 international units/mL prefilled syringes;
Epoetin beta 10,000 international units/0.6 mL and 30,000 international units/0.6 mL prefilled syringes;
Folic acid 400 mcg tablet;
Granisetron 1 mg tablet;
Granisetron 1 mg/mL and 3 mg/3 mL solution for injection;
Ketamine 500 mg/10 mL solution for injection;
Montelukast 10 mg tablet;
Oxycodone 5 mg and 10 mg capsules;
Posaconazole 100 mg delayed-release tablet;
Pegfilgrastim (Neulastim) 6 mg/0.6 mL prefilled syringe;
Pegfilgrastim biosimilar (Fulphila) 6 mg/0.6 mL prefilled syringe;
Pregabalin 25 mg, 50 mg, 75 mg, 100 mg, 150 mg and 300 mg capsules;
Ranitidine 150 mg tablet; and
Voriconazole 50 mg and 200 mg tablets.
[NR] Medicines that have not been recommended for subsidy due to unacceptable cost-effectiveness are listed in the Annex.
The clinical indications, subsidy class and subsidy implementation dates (if applicable) for all medicines included in the review are provided in the Annex.
01/07/2022 Denosumab for treating osteoporosis and glucocorticoid-associated bone loss
The Ministry of Health’s Drug Advisory Committee has recommended:
Denosumab 60 mg/mL prefilled syringe for treating patients with osteoporosis (T-score ≤ -2.5) at high risk of fracture.
Patients must also receive adequate calcium and vitamin D supplementation whilst undergoing treatment.
Subsidy status
[R] Denosumab 60 mg/mL prefilled syringe is recommended for inclusion on the Medication Assistance Fund (MAF) for the abovementioned indication with effect from 1 July 2022.
[NR] MAF assistance does not apply to denosumab 60 mg/mL prefilled syringe when used for treating glucocorticoid-associated bone loss.
Registered Product(s) Information
Clinical and product info
Clinical info | Product Info |
|---|---|
Information under the Indication, Dosage and Contraindication sections are extracted from the relevant Package Insert/Patient Information Leaflet of the product available on HSA Infosearch. For more information, please refer to the product's Package Insert/ Patient Information Leaflet available on HSA Infosearch. The information provided is for informational purposes only, and is not exhaustive. The information provided is not a substitute for professional medical advice. Please consult a qualified healthcare provider for any medical advice. | Information available here are product details as registered with the HSA. As this website is updated monthly, please refer to HSA Infosearch for the most updated product information. |
Subcutaneous
* Clinical information is available for this product.
