M03BX01 baclofen

MUSCULO-SKELETAL SYSTEM MUSCLE RELAXANTS MUSCLE RELAXANTS, CENTRALLY ACTING AGENTS Other centrally acting agents

健保收載品項 TFDA 在效許可證 32 FDA 已核准

台灣藥品與外觀

台灣食藥署在效西藥許可證 32 張;以下列出 24 個品項(13 項有外觀照)。

健保收載品名:"優生"巴可舒錠10公絲(貝可芬)、"元宙"巴氯芬錠 25 毫克 (巴克樂芬)、"十全"背克痛錠10公絲(貝可芬)、"壽元"百克芬10公絲錠(貝可芬)、"安星" 貝可舒錠10公絲(貝可芬)、"強生" 貝可芬錠5毫克(巴克樂芬)、"強生"貝可芬錠10公絲(巴克樂芬)、"應元"痙可避錠10毫克、"正和"普樂芬錠10公絲(貝可芬)、"正和"普樂芬錠5公絲(貝可芬)、"永勝"肉舒錠10公絲(貝可芬)、"海默尼"脊舒錠10毫克(貝可芬)、"美時"倍鬆錠10毫克(貝可芬)、"美時"倍鬆錠5毫克(貝可芬)、"達德士"舒肌錠10毫克、"達德士"舒肌錠10毫克

無外觀照
巴克樂芬
無外觀照
巴克樂芬
無外觀照
巴克樂芬
"海默尼"脊舒錠10毫克(貝可芬) 外觀
"海默尼"脊舒錠10毫克(貝可芬)
橢圓形 · 黃 · 刻痕:直線 · 9.7 mm
無外觀照
"壽元"百克芬10公絲錠(貝可芬)
舒樂疼錠10公絲(貝可芬) 外觀
舒樂疼錠10公絲(貝可芬)
圓形 · 粉 · 刻痕:無 · 標記:GP / 242 · 6.7 mm
痛獲平10毫克錠(貝可芬) 外觀
痛獲平10毫克錠(貝可芬)
圓形 · 白 · 刻痕:十字 · 6 mm
無外觀照
"正和"普樂芬錠5公絲(貝可芬)
必克痛錠 外觀
必克痛錠
圓形 · 白 · 刻痕:直線 · 6 mm
無外觀照
"應元"痙可避錠10毫克
力健芬錠(貝可芬) 外觀
力健芬錠(貝可芬)
圓形 · 藍 · 刻痕:直線 · 7 mm
無外觀照
"安星" 貝可舒錠10公絲(貝可芬)
"美時"倍鬆錠10毫克(貝可芬) 外觀
"美時"倍鬆錠10毫克(貝可芬)
圓形 · 白 · 刻痕:直線 · 標記:M S · 7 mm
"美時"倍鬆錠5毫克(貝可芬) 外觀
"美時"倍鬆錠5毫克(貝可芬)
圓形 · 白 · 刻痕:無 · 標記:LO / B · 8 mm
速鎮錠10毫克(貝可芬) 外觀
速鎮錠10毫克(貝可芬)
橢圓形 · 粉 · 刻痕:直線 · 標記:HS HS / K 2 · 10 mm
"強生"貝可芬錠10公絲(巴克樂芬) 外觀
"強生"貝可芬錠10公絲(巴克樂芬)
圓形 · 白 · 刻痕:直線 · 6.4 mm
"強生" 貝可芬錠5毫克(巴克樂芬) 外觀
"強生" 貝可芬錠5毫克(巴克樂芬)
圓形 · 白 · 刻痕:無 · 6.4 mm
無外觀照
"永勝"肉舒錠10公絲(貝可芬)
"十全"背克痛錠10公絲(貝可芬) 外觀
"十全"背克痛錠10公絲(貝可芬)
圓形 · 橘 · 刻痕:直線 · 6.5 mm
無外觀照
巴芬錠10公絲(巴克樂芬)
肌利健錠5公絲 外觀
肌利健錠5公絲
圓形 · 白 · 刻痕:直線 · 標記:M3 · 7 mm
痛獲平錠5毫克 外觀
痛獲平錠5毫克
圓形 · 白 · 刻痕:無 · 標記:S / 5 · 6 mm
無外觀照
鋇克瓏錠10毫克
無外觀照
鋇克瓏錠5毫克

資料來源:食藥署「西藥許可證」+「藥品 ATC 碼」+「藥品外觀」+「藥品仿單或外盒」開放資料。外觀照與仿單連結指向食藥署原始檔。

適應症

台灣 TFDA 核准適應症

  1. 限用於脊髓和大腦之疾病或損傷所引起之肌肉痙攣。
  2. 限於脊髓和大腦疾病或損傷引起的肌肉痙攣。
  3. 限於脊髓和大腦疾病或損傷引的肌肉痙攣。
  4. 限於脊髓和腦疾病或損傷引起的肌肉痙攣。
  5. 脊髓和大腦疾病或損傷引起的肌肉痙攣。
  6. 骨骼肌弛緩劑。
  7. 骨骼肌鬆弛劑。

美國 FDA 適應症(英文原文對照)

美國 FDA 核准成分 baclofen (商品名 BACLOFEN / Baclofen / Baclofen (Intrathecal) / Gablofen) · 仿單更新 2026-04-01

INDICATIONS AND USAGE Baclofen injection (intrathecal) is indicated for use in the management of severe spasticity. Patients should first respond to a screening dose of intrathecal baclofen prior to consideration for long term infusion via an implantable pump. For spasticity of spinal cord origin, chronic infusion of baclofen injection (intrathecal) via an implantable pump should be reserved for patients unresponsive to oral baclofen therapy, or those who experience intolerable CNS side effects at effective doses. Patients with spasticity due to traumatic brain injury should wait at least one year after the injury before consideration of long term intrathecal baclofen therapy. Baclofen injection (intrathecal) is intended for use by the intrathecal route in single bolus test doses (via spinal catheter or lumbar puncture) and, for chronic use, only in implantable pumps approved by the FDA specifically for the administration of baclofen injection (intrathecal) into the intrathecal space. Spasticity of Spinal Cord Origin: Evidence supporting the efficacy of baclofen injection (intrathecal) was obtained in randomized, controlled investigations that compared the effects of either a single intrathecal dose or a three day intrathecal infusion of baclofen injection (intrathecal) to placebo in patients with severe spasticity and spasms due to either spinal cord trauma or multiple sclerosis. Baclofen injection (intrathecal) was superior to placebo on both principal outcome measures employed: change from baseline in the Ashworth rating of spasticity and the frequency of spasms. Spasticity of Cerebral Origin: The efficacy of baclofen injection (intrathecal) was investigated in three controlled clinical trials; two enrolled patients with cerebral palsy and one enrolled patients with spasticity due to previous brain injury. The first study, a randomized controlled cross-over trial of 51 patients with cerebral palsy, provided strong, statistically significant results; baclofen injection (intrathecal) was superior to placebo in reducing spasticity as measured by the Ashworth Scale. A second cross-over study was conducted in 11 patients with spasticity arising from brain injury. Despite the small sample size, the study yielded a nearly significant test statistic (p= 0.066) and provided directionally favorable results. The last study, however, did not provide data that could be reliably analyzed. Baclofen injection (intrathecal) therapy may be considered an alternative to destructive neurosurgical procedures. Prior to implantation of a device for chronic intrathecal infusion of baclofen injection (intrathecal), patients must show a response to baclofen injection (intrathecal) in a screening trial (see Dosage and Administration ).

資料來源:食藥署西藥許可證適應症(中文)、openFDA US SPL(英文,僅供對照)。

健保給付規定

查無健保特殊給付規定條款;本藥品依一般健保藥品支付規定給付。

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)。


台灣藥品與適應症:食藥署西藥許可證+ATC+外觀+仿單開放資料 · FDA:openFDA US SPL · 健保給付:健保署「全民健康保險藥品給付規定」(更新日 2026-06-09)· 實證補充: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。