G03XC01 raloxifene
GENITO URINARY SYSTEM AND SEX HORMONES ›SEX HORMONES AND MODULATORS OF THE GENITAL SYSTEM ›OTHER SEX HORMONES AND MODULATORS OF THE GENITAL SYSTEM ›Selective estrogen receptor modulators
健保收載品項 FDA 已核准 TFDA 在效許可證 4 健保給付條款 1
健保收載品名:"五洲"骨鬆膜衣錠60毫克、力骨實膜衣錠60毫克、希鈣膜衣錠60毫克、樂骨康膜衣錠60毫克、鈣穩膜衣錠60毫克、鈣穩膜衣錠60公絲
FDA 適應症
1 INDICATIONS AND USAGE Raloxifene hydrochloride is an estrogen agonist/antagonist indicated for: Treatment and prevention of osteoporosis in postmenopausal women. ( 1.1 ) Reduction in risk of invasive breast cancer in postmenopausal women with osteoporosis. ( 1.2 ) Reduction in risk of invasive breast cancer in postmenopausal women at high risk for invasive breast cancer. ( 1.3 ) Important Limitations: Raloxifene hydrochloride tablets are not indicated for the treatment of invasive breast cancer, reduction of the risk of recurrence of breast cancer, or reduction of risk of noninvasive breast cancer. ( 1.3 ) 1.1 Treatment and Prevention of Osteoporosis in Postmenopausal Women Raloxifene hydrochloride tablets are indicated for the treatment and prevention of osteoporosis in postmenopausal women [see Clinical Studies (14.1 , 14.2) ] . 1.2 Reduction in the Risk of Invasive Breast Cancer in Postmenopausal Women with Osteoporosis Raloxifene hydrochloride tablets are indicated for the reduction in risk of invasive breast cancer in postmenopausal women with osteoporosis [see Clinical Studies (14.3) ] . 1.3 Reduction in the Risk of Invasive Breast Cancer in Postmenopausal Women at High Risk of Invasive Breast Cancer Raloxifene hydrochloride tablets are indicated for the reduction in risk of invasive breast cancer in postmenopausal women at high risk of invasive breast cancer [see Clinical Studies (14.4) ] . The effect in the reduction in the incidence of breast cancer was shown in a study of postmenopausal women at high risk for breast cancer with a 5-year planned duration with a median follow-up of 4.3 years [see Clinical Studies (14.4) ] . Twenty-seven percent of the participants received drug for 5 years. The long-term effects and the recommended length of treatment are not known. High risk of breast cancer is defined as at least one breast biopsy showing lobular carcinoma in situ (LCIS) or atypical hyperplasia, one or more first-degree relatives with breast cancer, or a 5-year predicted risk of breast cancer ≥1.66% (based on the modified Gail model). Among the factors included in the modified Gail model are the following: current age, number of first-degree relatives with breast cancer, number of breast biopsies, age at menarche, nulliparity or age of first live birth. Healthcare professionals can obtain a Gail Model Risk Assessment Tool by dialing 1-800-545-5979. Currently, no single clinical finding or test result can quantify risk of breast cancer with certainty. After an assessment of the risk of developing breast cancer, the decision regarding therapy with raloxifene hydrochloride tablets should be based upon an individual assessment of the benefits and risks. Raloxifene hydrochloride tablets does not eliminate the risk of breast cancer. Patients should have breast exams and mammograms before starting raloxifene hydrochloride tablets and should continue regular breast exams and mammograms in keeping with good medical practice after beginning treatment with raloxifene hydrochloride tablets. Important Limitations of Use for Breast Cancer Risk Reduction There are no data available regarding the effect of raloxifene hydrochloride tablets on invasive breast cancer incidence in women with inherited mutations (BRCA1, BRCA2) to be able to make specific recommendations on the effectiveness of raloxifene hydrochloride tablets. Raloxifene hydrochloride tablets are not indicated for the treatment of invasive breast cancer or reduction of the risk of recurrence. Raloxifene hydrochloride tablets are not indicated for the reduction in the risk of noninvasive breast cancer.
資料來源:openFDA(美國 FDA Structured Product Labeling)。為英文原文,僅供對照。
TFDA 適應症
NHI 給付規定
直接適用條款
§ 5.6.1 抗骨質再吸收劑(anti- resorptive)(101/3/1、101/5/1、102/2/1、102/8/1、
激素及影響內分泌機轉藥物 › 骨質疏鬆症治療藥物(100/1/1)
抗骨質再吸收劑(anti-resorptive)(101/3/1、101/5/1、102/2/1、102/8/1、103/2/1、103/10/1、104/8/1、106/12/1、114/3/1)
1.藥品種類
(1)Bisphosphonates(雙磷酸鹽類):alendronate(如Fosamax)、zoledronate 5mg (如Aclasta 5mg/100mL solution for infusion)、risedronate(如Reosteo)、ibandronate 3mg/3mL (如Bonviva 3mg/3mL solution for injection)
(2)Selective estrogen receptor modulators (SERM,選擇性雌激素接受體調節劑):raloxifene(如Evista)、bazedoxifene(如Viviant)(102/2/1)
(3)Human monoclonal antibody for RANKL(RANKL單株抗體):denosumab(如Prolia)(101/3/1)
2.使用規定
(1)使用條件
Ⅰ.限用於停經後婦女(alendronate、zoledronate、denosumab及risedronate 35mg亦可使用於男性,risedronate 150mg不可使用於男性)因骨質疏鬆症(須經DXA 檢測BMD之T score≦ -2.5SD)引起脊椎或髖部骨折,或因骨質疏少症(osteopenia)(經DXA檢測BMD之-2.5SD <T score <-1.0SD)引起脊椎或髖部2處或2次(含)以上之骨折。使用Prolia及Alendronate Sandoz 70mg Tablets除上述條件外,亦可用於前述因骨質疏鬆症引起之遠端橈骨或近端肱骨骨折,或骨質疏少症引起之遠端橈骨、近端肱骨2處或2次(含)以上之骨折。 (101/5/1、102/8/1、103/10/1、104/8/1、106/12/1、114/3/1)
Ⅱ.用於骨質疏鬆症患者 (須經DXA檢測BMD之T-score≦-2.5),且合併下列至少一項骨質疏鬆性骨折高風險因子者,限使用Prolia及Alendronate Sandoz 70mg Tablets,且須於病歷上載明: (114/3/1)
ⅰ類風溼性關節炎。
ⅱ糖尿病且使用胰島素。
ⅲ使用糖皮質類固醇(>5毫克/天)超過3個月。
(2)治療時,一次限用一項藥物,不得併用其他骨質疏鬆症治療藥物。
(3)使用雙磷酸鹽類藥物,須先檢測病患之血清creatinine濃度,符合該項藥物仿單之建議規定。 歷史演變(11 次異動)
| 生效日 | 異動說明 |
|---|---|
| 101/3/1 | legacy_boan_parsed:ch05.txt |
| 101/5/1 | legacy_boan_parsed:ch05.txt |
| 101/7/1 | legacy_boan_parsed:ch05.txt |
| 102/2/1 | legacy_boan_parsed:ch05.txt |
| 102/8/1 | legacy_boan_parsed:ch05.txt |
| 103/2/1 | legacy_boan_parsed:ch05.txt |
| 103/10/1 | legacy_boan_parsed:ch05.txt |
| 104/8/1 | legacy_boan_parsed:ch05.txt |
| 106/12/1 | legacy_boan_parsed:ch05.txt |
| 110/5/1 | legacy_boan_parsed:ch05.txt |
| 114/3/1 | legacy_boan_parsed:ch05.txt |
實證補充
本藥品尚無實證補充整理(未來新增 Review/指引知識時補列)。
FDA 段:openFDA US SPL · TFDA 段:食藥署西藥許可證+ATC 分類開放資料 · NHI 段:健保署「全民健康保險藥品給付規定」(更新日 2026-05-31)· 實證補充段:人工彙整。 本頁為資訊整理,實際給付與適應症以主管機關公告為準。