Pharmacy Department, St. Mary Medical Center, 1201 Langhorne-Newtown Road, Langhorne, PA, 19047, USA.
American Regent, Norristown, PA, USA.
Drug Saf. 2021 Jan;44(1):107-119. doi: 10.1007/s40264-020-01022-2. Epub 2020 Nov 25.
Intravenous iron preparations rapidly correct iron deficiency anemia, with the notable drug class effect of rare, yet potentially life-threatening, administration-related hypersensitivity or anaphylactic reactions. The objective of this comparative study was to assess adverse events associated with four intravenous iron preparations and estimated medical costs, in the US Food and Drug Administration Adverse Event Reporting System (FAERS) database.
Cases of hypersensitivity reactions and anaphylaxis/anaphylactic shock associated with iron dextran, iron sucrose, ferumoxytol, and ferric carboxymaltose, spontaneously reported to FAERS (1 January, 2014 to 31 December, 2019), were extracted. The reporting odds ratio lower bound 90% confidence interval (ROR05) > 1 and cases ≥ 5 defined a likely signal for a drug-adverse event association. Adverse event-associated medical costs were estimated using Agency for Healthcare Research and Quality/Healthcare Cost and Utilization Project 2016 data.
For hypersensitivity reactions, ferumoxytol and iron dextran had the highest ROR05 values (5.00 and 4.35, respectively) and greatest proportions of associated deaths (7.1% and 5.3%), followed by iron sucrose (ROR05 3.94, deaths 2.4%), and ferric carboxymaltose (ROR05 3.03, deaths 0.2%). For anaphylaxis/anaphylactic shock, ROR05 for cases/deaths were: 39.32/13.4%, ferumoxytol; 37.80/4.5%, iron dextran; 17.60/4.7%, iron sucrose; and 8.77/no deaths, ferric carboxymaltose. Downstream medical costs per adverse event were highest with iron dextran (US$8615) and ferumoxytol (US$8164), followed by iron sucrose (US$4212), and ferric carboxymaltose (US$1832).
Reporting rates of hypersensitivity and anaphylaxis with intravenous iron preparations were highest with ferumoxytol and lowest with ferric carboxymaltose in the US FAERS database. Adverse event-related medical costs were highest for iron dextran and ferumoxytol, and lowest for ferric carboxymaltose.
静脉铁制剂可迅速纠正缺铁性贫血,具有显著的药物类别效应,即罕见但可能危及生命的与给药相关的过敏反应或过敏性休克。本研究旨在评估美国食品药品监督管理局不良事件报告系统(FAERS)数据库中四种静脉铁制剂相关的不良事件及估计的医疗费用。
提取 2014 年 1 月 1 日至 2019 年 12 月 31 日 FAERS 中自发报告的与铁右旋糖酐、蔗糖铁、ferumoxytol 和羧基麦芽糖铁相关的过敏反应和过敏性休克的病例。报告比值比下限 90%置信区间(ROR05)>1 且病例数≥5 定义为药物-不良事件关联的可能信号。使用医疗保健研究与质量/医疗保健成本和利用项目 2016 年的数据来估计与不良事件相关的医疗费用。
对于过敏反应,ferumoxytol 和铁右旋糖酐的 ROR05 值最高(分别为 5.00 和 4.35),且相关死亡比例最高(分别为 7.1%和 5.3%),其次是蔗糖铁(ROR05 为 3.94,死亡比例为 2.4%)和羧基麦芽糖铁(ROR05 为 3.03,死亡比例为 0.2%)。对于过敏性休克,病例/死亡的 ROR05 为:39.32/13.4%,ferumoxytol;37.80/4.5%,铁右旋糖酐;17.60/4.7%,蔗糖铁;8.77/无死亡,羧基麦芽糖铁。每个不良事件的下游医疗费用以铁右旋糖酐(8615 美元)和 ferumoxytol(8164 美元)最高,其次是蔗糖铁(4212 美元)和羧基麦芽糖铁(1832 美元)。
在 FAERS 数据库中,美国静脉铁制剂过敏反应和过敏性休克的报告率以 ferumoxytol 最高,以羧基麦芽糖铁最低。与不良事件相关的医疗费用以铁右旋糖酐和 ferumoxytol 最高,以羧基麦芽糖铁最低。