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厄他培南

Ertapenem

Ertapenem sodium

碳青黴烯類抗生素IVIM

別名: Invanz · L-749345 · ML-0826 · ZD-4433 · ertapenemum

由 VetSheet 獸醫團隊審訂更新於 2026年4月5日本內容以實證獸醫文獻為本

15 mg/kg IV or IM every 12 hours (not to exceed a daily dosage of 1 gram)IV/IM· q12h
🐕

劑量為持牌獸醫專業人員的臨床參考。請務必對照最新藥品說明書及個別病患確認。

各物種劑量

🌎 NA — North America🌍 EU — Europe

適應症劑量途徑頻次療程地區
Susceptible infections (Investigational)15 mg/kg IV or IM every 12 hours (not to exceed a daily dosage of 1 gram)IV/IMq12h🌎 NA
  • Susceptible infections (Investigational): Monitor literature for additional data.

適應症劑量途徑頻次療程地區
Susceptible infections (Investigational)15 mg/kg IV or IM every 12 hours (not to exceed a daily dosage of 1 gram)IV/IMq12h🌎 NA
  • Susceptible infections (Investigational): Monitor literature for additional data.

劑量為持牌獸醫專業人員的臨床參考。請務必對照最新藥品說明書及個別病患確認。

正在為病患診症?VetSheet 的 AI 會把藥物、劑量與療程直接寫入結構化診症筆記。了解 VetSheet 如何運作

概覽

厄他培南是一種廣效的​碳青黴烯類抗生素​,結構上類似於亞胺培南 (imipenem) 和美羅培南 (meropenem),但抗菌譜較窄。

  • ​主要差異:​ 與其他碳青黴烯類不同,它對​綠膿桿菌 (Pseudomonas aeruginosa)​​不動桿菌 (Acinetobacter)​ 無效。
  • ​臨床應用:​ 特別適用於治療具抗藥性的革蘭氏陰性菌感染,尤其是當氨基醣苷類藥物有禁忌(如腎衰竭)或無效,且無法取得美羅培南時。
  • ​獸醫應用:​ 目前在犬貓使用的相關資訊非常有限;在獸醫學中被視為​試驗性用藥​

作用機制

Ertapenem is a beta-lactam antibiotic that exerts its bactericidal effect by inhibiting bacterial cell wall synthesis.

  • ​Mechanism:​ It binds to ​penicillin-binding proteins (PBPs)​ → inhibits peptidoglycan cross-linking → weakens the bacterial cell wall → causes cell lysis and death.
  • ​Enzyme Stability:​ It is highly resistant to degradation by most beta-lactamases, including penicillinases and cephalosporinases.
  • ​Renal Stability:​ Unlike imipenem, ertapenem is stable against renal dehydropeptidase I, meaning it does not require co-administration with cilastatin.

安全性與警告

禁忌症

  • Hypersensitivity to ertapenem or other carbapenems
  • History of anaphylaxis to any beta-lactam antibiotic
  • Hypersensitivity to lidocaine or amide-type local anesthetics (if using 1% lidocaine as an IM diluent)

不良反應

  • Injection site reactions (most common in humans)
  • Gastrointestinal effects (nausea, vomiting, diarrhea)
  • Headache
  • Tachycardia
  • Hypersensitivity reactions (rare)
  • CNS effects (hallucinations, agitation, seizures - rare)

注意事項

​Investigational Use:​ Consider its use in dogs and cats as investigational due to limited published data.

  • ​Diluent Warning:​ Do not use diluents containing dextrose.
  • ​IM Administration:​ If given IM, it must be diluted with 1% lidocaine HCl (without epinephrine) to minimize pain, and must be used within one hour. Do not give this lidocaine mixture IV.

藥物相互作用

Probenecid

Can increase ertapenem AUC by 25% and elimination half-life by about 20%. Not recommended to be used concurrently to extend half-life.

監測

  • Clinical efficacy (WBC count, resolution of fever, etc.)
  • Adverse effects (GI signs, neurotoxicity, hypersensitivity)
  • Hepatic, hematopoietic, and renal function (suggested for periodic assessment during prolonged use)

藥物動力學

吸收

Not appreciably absorbed after oral administration. Intramuscular bioavailability is about 90% with peak plasma levels occurring in approximately 2.3 hours (in humans).

分佈

Exhibits concentration-dependent binding to plasma proteins (85% to 95% bound depending on concentration).

代謝

Biotransformation is not dependent on hepatic mechanisms; the major inactive metabolite is formed by hydrolysis of the beta-lactam ring.

排除

Approximately 80% of an IV dose is excreted in the urine (evenly split between inactive metabolites and unchanged drug). Approximately 10% is excreted in feces.

過量

Inadvertent overdoses are unlikely. In humans, a 3-gram IV dose caused an increased incidence of nausea and diarrhea. If overdose occurs and adverse effects are noted, treat supportively.

可用產品

劑型

  • Lyophilized powder for injection

人用標示

  • Ertapenem Sodium Lyophilized Powder for Injection: 1 g (as 1.045 g ertapenem) in single-dose vials; Invanz®

各地核准狀態

暫無法規資料: 🇺🇸 US · 🇪🇺 EU · 🇬🇧 UK · 🇭🇰 HK · 🇹🇼 TW · 🇯🇵 JP · 🇰🇷 KR · 🇦🇺 AU

儲存與穩定性

Store unmixed vials at or below 25°C (77°F). Reconstitute with water for injection or 0.9% NaCl, then immediately transfer to a 50 mL bag of 0.9% NaCl. Once diluted in normal saline for IV use, it is stable at room temperature for 6 hours, or refrigerated for 24 hours (use within 4 hours of removal). Do not freeze. If diluted with lidocaine for IM use, use within 1 hour.

飼主須知

​重要提示:​ 此藥物在獸醫學中被視為試驗性用藥,通常僅保留用於高度抗藥性的感染。

  • ​給藥方式:​ 此藥物必須由獸醫專業人員透過注射給予。
  • ​監測:​ 密切觀察您的寵物是否有噁心、嘔吐、腹瀉或異常的神經行為(如焦躁或抽搐),若有發現請立即通知您的獸醫師。

VetSheet 藥物參考供持牌獸醫專業人員作臨床決策輔助之用,不能取代專業判斷或廠方最新藥品說明書。