Anaphylactic Reaction Following Injection Cefotaxime Sodium

IF 0.4 Q4 PHARMACOLOGY & PHARMACY Journal of Pharmacology & Pharmacotherapeutics Pub Date : 2021-07-01 DOI:10.4103/jpp.jpp_60_21
Bharat Satish Krishnan, Kavita M. Jaiswal, S. Dudhgaonkar, Latesh B. Raghute
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引用次数: 1

Abstract

This is a case study of anaphylactic reaction to cefotaxime sodium in a 23-year-old female who underwent a lower segment cesarean section under spinal anesthesia. Cefotaxime sodium, an antibiotic belonging to the class of cephalosporins, was administered intravenously postoperatively for prevention of infection. The patient complained of breathlessness, swelling around both eyes, and pruritus and urticarial rash over her abdomen, legs, and forehead. The case was successfully managed by withholding the medication and treatment of symptoms. According to the WHO-Uppsala Monitoring Centre causality assessment scale, a probable causal relationship between the suspected drug (cefotaxime sodium) and anaphylactic reaction was made. The severity was found to be moderate (Level 3). Although cefotaxime has well established place in surgical prophylaxis, this case study emphasizes on constant observation and meticulous follow-up of patients receiving it in clinical practice as there is possibility of an adverse drug reaction (ADR) which can be life-threatening. Such happenings can add to challenges faced by the treating physician in the present COVID-19 era. Recognizing ADR helps reduce morbidity and mortality. Reporting ADR helps in documentation and education of healthcare professionals.
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注射用头孢噻肟钠后的过敏反应
这是一例23岁女性在脊柱麻醉下接受下段剖宫产时对头孢噻肟钠过敏反应的病例研究。头孢噻肟钠是头孢菌素类抗生素,术后静脉注射预防感染。患者抱怨呼吸困难,双眼周围肿胀,腹部、腿部和前额瘙痒和荨麻疹。该病例通过扣留药物和症状治疗成功控制。根据世界卫生组织-尤普萨拉监测中心因果关系评估量表,对可疑药物(头孢噻肟钠)与过敏反应之间可能存在的因果关系进行了分析。严重程度为中度(3级)。尽管头孢噻肟在外科预防中有着良好的地位,但本病例研究强调在临床实践中对接受头孢噻肟治疗的患者进行持续观察和细致随访,因为可能会出现危及生命的药物不良反应(ADR)。这种情况可能会增加治疗医生在当前新冠肺炎时代面临的挑战。认识ADR有助于降低发病率和死亡率。报告ADR有助于记录和教育医疗保健专业人员。
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CiteScore
0.40
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37
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