Safety monitoring of oral iron supplements in pregnant women with anemia: a multi-center observational clinical study.

IF 3.4 3区 医学 Q2 PHARMACOLOGY & PHARMACY Therapeutic Advances in Drug Safety Pub Date : 2023-01-01 DOI:10.1177/20420986231181335
Chang Liu, Qianqian Zhang, Peiye Hui, Yan Wang, Guohui Li, Guangchao Cao, Zicheng Xue, Jing Zhang, Heng Zhang, Xin Huang, Jiyong Wu, Fusehng Sun, Meixing Yan
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Abstract

Aims: To investigate the safety of oral iron therapy in pregnant women with iron-deficiency anemia (IDA) in the real world.

Methods: A retrospective analysis was performed on 1792 pregnant patients with IDA who received oral iron supplements from 12 hospitals in Shandong Province from 1 April to 31 June 2021; follow-up and adverse reactions were recorded. They were divided into six groups according to the treatment drugs.

Results: The overall adverse reaction rate was 15.4%, and the main adverse reaction site was the digestive system. The incidence of all kinds of oral iron adverse reactions from high to low in order: compound ferrous sulfate and folic acid tablets (21.88%); iron proteinsuccinylate oral solution (20.90%); ferrous succinate tablets (19.76%); ferrous succinate sustained-release tablets (18.00%); iron polysaccharide complex capsule (12.06%); and iron dextran oral solution (6.94%). It was found that there was a significant difference in the incidence of adverse reactions among the six drugs (p < 0.05). Pairwise comparison showed that the incidence of adverse reactions was higher in the iron proteinsuccinylate oral solution than that in the iron polysaccharide complex capsule (p < 0.05). There was no significant difference in the incidence of adverse reactions in different ages (p > 0.05), but there was a significant difference in the incidence of adverse reactions in different gestational ages (p < 0.05). In Adverse Drug Reaction (ADR) patients, the adverse reaction result of most patients is recovery or improvement, and there was no serious adverse reaction outcome such as sequela and death.

Conclusion: All the adverse reactions of oral iron were mainly gastrointestinal adverse reactions, and no heavy adverse reactions were found. Iron proteinsuccinylate oral solution has a higher incidence of adverse reactions than iron polysaccharide complex capsule. The results showed that oral iron was safer for anemia patients during pregnancy.

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贫血孕妇口服铁补充剂的安全性监测:一项多中心观察性临床研究
目的:探讨现实世界中孕妇缺铁性贫血(IDA)口服铁治疗的安全性。方法:回顾性分析2021年4月1日至6月31日山东省12家医院1792例口服补铁的妊娠IDA患者;记录随访及不良反应。根据治疗药物分为6组。结果:总不良反应率为15.4%,主要不良反应部位为消化系统。各类口服铁类药物不良反应发生率由高到低依次为:复方硫酸亚铁叶酸片(21.88%);琥珀酸铁蛋白口服溶液(20.90%);琥珀酸亚铁片(19.76%);琥珀酸亚铁缓释片(18.00%);铁多糖复合胶囊(12.06%);右旋糖酐铁口服液(6.94%)。结果发现,6种药物的不良反应发生率差异有统计学意义(p p > 0.05),但不同胎龄的不良反应发生率差异有统计学意义(p结论:口服铁的不良反应均以胃肠道不良反应为主,未发现重度不良反应。琥珀酸铁蛋白口服液的不良反应发生率高于铁多糖复合胶囊。结果表明,妊娠期贫血患者口服铁更安全。
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来源期刊
Therapeutic Advances in Drug Safety
Therapeutic Advances in Drug Safety Medicine-Pharmacology (medical)
CiteScore
6.70
自引率
4.50%
发文量
31
审稿时长
9 weeks
期刊介绍: Therapeutic Advances in Drug Safety delivers the highest quality peer-reviewed articles, reviews, and scholarly comment on pioneering efforts and innovative studies pertaining to the safe use of drugs in patients. The journal has a strong clinical and pharmacological focus and is aimed at clinicians and researchers in drug safety, providing a forum in print and online for publishing the highest quality articles in this area. The editors welcome articles of current interest on research across all areas of drug safety, including therapeutic drug monitoring, pharmacoepidemiology, adverse drug reactions, drug interactions, pharmacokinetics, pharmacovigilance, medication/prescribing errors, risk management, ethics and regulation.
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