Hospira Inc.
产品描述: LACTATED RINGER'S and 5% DEXTROSE Injection USP, 1000 mL, flexible containers, Rx Only, Hospira, Inc., Lake Forest, IL 600045, NDC 0409-7929-09
地位: 正在进行
城市: Lake Forest
状态: IL
国家: 我们
自愿/要求: 自愿:公司发起的公司
Initial Firm Notification: 新闻稿
分配模式: Nationwide
分类: Class I
产品数量: 142,644袋
Reason For Recall: 非智力:确认的客户对主要容器解决方案中颗粒物的抱怨,与模具一致。
记起Initiation Date: 20140710
报告日期: 20150225

Lactated Ringers And Dextrose

Lactated Ringers And Dextrose

Lactated Ringers And Dextrose Recall

Get an alertwhen a recall is issued.

Questions & Answers

Side Effects & Adverse Reactions

由于凝结的可能性,不应通过与血液相同的给药组同时给予含有钙离子的溶液。

Solutions which contain potassium should be used with great care, if at all, in patients with hyperkalemia, severe renal failure and in conditions in which potassium retention is present.

在充血性心力衰竭,严重的肾功能不全以及存在钠含钠的水肿的临床状态下,应格外小心地使用含有钠离子的溶液。

In patients with diminished renal function, administration of solutions containing sodium or potassium ions may result in sodium or potassium retention.

Solutions containing lactate ions should be used with great care in patients with metabolic or respiratory alkalosis. The administration of lactate ions should be done with great care where there is an increased level or an impaired utilization of lactate ions, as in severe hepatic insufficiency.

这些溶液的静脉内给药会导致液体和/或溶质过载,从而导致血清电解质浓度稀释,过度渗透,充血状态或肺水肿。稀释状态的风险与管理肠胃外溶液的电解质浓度成反比。

溶质超负荷的风险与外围和肺水肿引起拥挤状态与此类溶液的电解质浓度成正比。

Legal Issues

目前尚无该药物可用的法律信息。

FDA Safety Alerts

There are currently no FDA safety alerts available for this drug.

Manufacturer Warnings

目前尚无该药物可用的制造商警告信息。

FDA Labeling Changes

目前,该药物尚无FDA标签更改。

用途

这些解决方案指示用于肠外替代流体和电解质的细胞外损失,无论是否有或没有最少的碳水化合物卡路里,如患者的临床状况所要求。

历史

There is currently no drug history available for this drug.

其他信息

These products are sterile, nonpyrogenic solutions each containing isotonic concentrations of electrolytes (with or without dextrose) in water for injection. The solutions containing dextrose and electrolytes are hypertonic; those containing only electrolytes are isotonic. They are administered by intravenous infusion for parenteral replacement of extracellular losses of fluid and electrolytes, with or without minimal carbohydrate calories.

USP每100毫升乳铃的注射均含有氯化钠600 mg,乳酸钠,无水310 mg,氯化钾30 mg和氯化钙,二水合物20 mg。可能含有盐酸和/或氢氧化钠进行pH调节。一升提供9卡路里(来自乳酸),钠(Na)+), 130 mEq, potassium (K+)4 MEQ,钙(CA)++) 3 mEq, chloride (Cl-) 109 mEq and lactate [CH3CH(OH) COO-] 28 mEq. The electrolyte content is isotonic (273 mOsmol/liter, calc.) in relation to the extracellular fluid (approx. 280 mOsmol/liter). The pH of the solution is 6.6 (6.0 − 7.5).

USP每100毫升泌乳的铃声和5%的葡萄糖注射,含有葡萄糖,含水为5 g,以及与乳酸林格注入相同的成分和MEQ值,USP(仅包含盐酸进行盐酸进行pH调节)。一升可提供179卡路里(来自葡萄糖和乳酸),高渗渗透浓度为525 MOSMOL(CALC。)。pH为4.9(4.0 - 6.5)。

该溶液不包含杆菌,抗菌剂或添加的缓冲液(调整pH调节除外),并且每种都仅用于单剂量注射。当需要较小剂量时,应丢弃未使用的部分。

溶液是肠胃液,营养和/或电解质补充剂。

Dextrose, USP is chemically designated D-glucose, monohydrate (C6H12o6• H2o),己糖自由溶于水。它具有以下结构公式:

结构配方葡萄糖

Calcium Chloride, USP is chemically designated calcium chloride, dihydrate (CaCl2•2 h2o),白色碎片或颗粒自由溶于水。

Potassium Chloride, USP is chemically designated KCl, a white granular powder freely soluble in water.

Sodium Chloride, USP is chemically designated NaCl, a white crystalline powder freely soluble in water.


乳酸钠,USP是化学指定的乳酸单钠[CH3CH(OH)Coona],一种60%的水溶液在水中混乱。

它具有以下结构公式:

乳酸钠钠

注射水,USP被化学指定h2O.

柔性塑料容器由特殊配方的聚氯乙烯制成。水可以从容器内部渗透到覆盖物中,但不足以显着影响溶液。在达到到期期之前,塑料容器内的溶液还可以在很少的量中浸出某些化学成分。然而,根据USP生物学标准,塑料容器的测试证实了塑料的安全性。

Lactated Ringers And Dextrose Manufacturers


  • Hospira,Inc。
    Lactated Ringers And Dextrose (Sodium Chloride, Sodium Lactate, Potassium Chloride, Calcium Chloride, And Dextrose Monohydrate) Injection, Solution Lactated Ringers (Sodium Chloride, Sodium Lactate, Potassium Chloride, And Calcium Chloride) Injection, Solution [Hospira, Inc.]
  • 百特医疗保健公司
    Lactated Ringers And Dextrose (Sodium Chloride, Sodium Lactate, Potassium Chloride, Calcium Chloride And Dextrose Monohydrate) Injection, Solution [Baxter Healthcare Corporation]

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