通用中文 | 奥马达环素粉针剂 | 通用外文 | Omadacycline |
品牌中文 | 品牌外文 | Nuzyra | |
其他名称 | |||
公司 | Paratek(Paratek) | 产地 | 美国(USA) |
含量 | 10mg | 包装 | 10支/盒 |
剂型给药 | 粉针剂 | 储存 | 室温 |
适用范围 | 四环素类 用于治疗获得性细菌性肺炎和急性细菌性皮肤和皮下结构感染 |
通用中文 | 奥马达环素粉针剂 |
通用外文 | Omadacycline |
品牌中文 | |
品牌外文 | Nuzyra |
其他名称 | |
公司 | Paratek(Paratek) |
产地 | 美国(USA) |
含量 | 10mg |
包装 | 10支/盒 |
剂型给药 | 粉针剂 |
储存 | 室温 |
适用范围 | 四环素类 用于治疗获得性细菌性肺炎和急性细菌性皮肤和皮下结构感染 |
Nuzyra (omadacycline)使用说明书
公司: Paratek Pharmaceuticals
批准状态: 2018年10月批准
特殊治疗: 社区-获得性细菌性肺炎和急性细菌性皮肤和皮下结构感染
治疗领域:皮肤学 肺/呼吸疾病感染 细菌性感染肺炎皮肤感染/疾病
一般资料
Nuzyra (omadacycline)是一种现代化四环素,特异性地被设计克服四环素抗性。
Nuzyra是特异性地适用为以下:
成年患者有社区-获得性细菌性肺炎(CABP) 被以下易感性微生物所致: 链球菌肺炎,金黄色葡萄球菌(甲氧西林敏感菌株),流感嗜血杆菌,流感嗜血杆菌,克雷白氏杆菌,嗜肺性军团病杆菌,支原体 肺炎,和嗜衣原体肺炎.
成年患者有急性细菌性皮肤和皮结构感染(ABSSSI)被以下易感性微生物所致: 金黄色葡萄球菌(甲氧西林-易感和-抗性分离株),葡萄球菌卢古德南锡斯,链球菌生脓的,链球菌咽峡炎grp. (包括S. 咽峡炎,S. 中间炳,和S. constellatus),粪肠球菌,阴沟肠杆菌,和克雷白氏杆菌.
临床结果
FDA批准
Nuzyra的FDA批准是根据以下研究:
社区获得性细菌性肺炎
总共774成年有CABP被随机化至一项多国家,双盲,双-模拟试验比较Nuzyra与莫西沙星。Nuzyra 被给予100-mg静脉地每12小时共两剂量在天1,接着被100-mg 静脉地每天,或300mg口服,每天。莫西沙星 400-mg被给予静脉地或口服地,每天。总治疗时间为7-14天。Omadacycline符合 FDA-说明的原发性终点的统计学非-劣效性在医学治疗人群与莫西沙星比较在早期临床反应(ECR) 72-120小时治疗的开始后。对omadacycline和莫西沙星治疗臂的ECR率分别为81.1 %和82.7%。
急性细菌性皮肤和皮肤结构感染
总共1,390成年有ABSSSI被随机化至两项多中心,多国家,双盲,双模拟试验(试验2和试验3)。两项试验比较Nuzyra的7至14天至利奈唑胺[inezolid]。患者有蜂窝组织炎,重大脓肿,或伤口感染被纳入在试验中。在试验2中,患者被随机化至Nuzyra(100-mg静脉地每12小时共2剂接着被 100-mg静脉地每24小时,有选择至转至300-mg口服每24小时)或患者被随机化至利奈唑胺(600-mg静脉地每12小时,与选择至转至600-mg口服每12小时)。在试验3中,患者被随机化至Nuzyra (450-mg口服一天一次在天1和2,接着被300-mg口服一天1次)或患者被随机化至利奈唑胺(600-mg口服每12小时)。在两项试验中,疗效被确定通过成功的早期临床反应在48至72小时after the在mITT人群首次剂量后和被定义为在病变大小一个20%或更大减低。在试验 2 临床反应是达到of Nuzyra臂的84.8%和利奈唑胺臂的85.5%。在试验3 临床反应是达到 Nuzyra臂的87.3%和利奈唑胺臂的82.2% 。
副作用
不良反应伴随Nuzyra的使用可能包括,但是不限于,以下:
恶心
呕吐
输注部位反应
丙氨酸氨基转氨酶增加
天门冬氨酸氨基转氨酶增加
Г-谷氨酰转移酶增加
高血压
头痛
腹泻
失眠
便秘
作用机制
Nuzyra (omadacycline)是一种现代化的四环素,被特殊地设计克服四环素抗性和表现活性跨越一个谱的细菌包括革兰氏-阳性,革兰氏-阴性,不典型,和其他药物-抗性株。
FDA Approved: Yes (First approved October 2, 2018)
Brand name: Nuzyra
Generic name: omadacycline
Dosage form: for Injection and Tablets
Company: Paratek Pharmaceuticals, Inc.
Treatment for: Skin and Structure Infection, Pneumonia
Nuzyra (omadacycline) is an aminomethylcycline tetracycline antibiotic for the treatment of community-acquired bacterial pneumonia (CABP) and acute bacterial skin and skin structure infections (ABSSSI).
Antibacterial Resistance
Patients should be advised that antibacterial drugs including Nuzyra should only be used to treat bacterial infections. They do not treat viral infections (e.g., the common cold). When Nuzyra is prescribed to treat a bacterial infection, patients should be told that although it is common to feel better early in the course of therapy, the medication should be taken exactly as directed. Skipping doses or not completing the full course of therapy may decrease the effectiveness of the immediate treatment and increase the likelihood that bacteria will develop resistance and will not be treatable by Nuzyra or other antibacterial drugs in the future.
Administration with Food
Patients are advised to fast 4 hours before and 2 hours after taking Nuzyra tablets and not to consume dairy products, antacids, or multivitamins for 4 hours after taking Nuzyra tablets.
Allergic Reactions
Patients are advised that allergic reactions, including serious allergic reactions, could occur and that serious allergic reactions require immediate treatment. Patients should be asked about any previous hypersensitivity reactions to Nuzyra, or other tetracycline class antibacterials.
Tooth Discoloration and Inhibition of Bone Growth
Patients are advised that Nuzyra, like other tetracycline-class drugs, may cause permanent tooth discoloration of deciduous teeth and reversible inhibition of bone growth when administered during the second and third trimesters of pregnancy. Tell your healthcare provider right away if you become pregnant during treatment.
Diarrhea
Patients are advised that diarrhea is a common problem caused by antibacterial drugs, including Nuzyra, which usually ends when the antibacterial drugs is discontinued. Sometimes after starting treatment with antibacterial drugs, patients can develop watery or bloody stools (with or without stomach cramps and fever). If this occurs, patients should contact their physician as soon as possible.
Nausea and Vomiting
Patients are advised that nausea and vomiting can be an adverse reaction to Nuzyra. A greater proportion of patients who received the oral loading dose of Nuzyra for treatment of ABSSSI experienced nausea and vomiting.
Lactation
Women are advised not to breastfeed during treatment with Nuzyra and for 4 days after the last dose.
Adverse Reactions
The most common adverse reactions (incidence ≥2%) are nausea, vomiting, infusion site reactions, alanine aminotransferase increased, aspartate aminotransferase increased, gamma-glutamyl transferase increased, hypertension, headache, diarrhea, insomnia, and constipation.