Assessing the safety and adverse effects of paracetamol, ibuprofen, and their combination in paediatric pain and fever management: A prospective observational study.

IF 1 Q4 PRIMARY HEALTH CARE Journal of Family Medicine and Primary Care Pub Date : 2025-02-01 Epub Date: 2025-02-21 DOI:10.4103/jfmpc.jfmpc_348_24
Vivek Charde, Mukesh Sanklecha, Priyank Rajan, Babar Naeem, Mayur Wanjari, Gaurav Mittal, Tanjmi Djabo Eric Adrien
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Abstract

Purpose: Pain and fever are common paediatric complaints that demand meticulous symptom alleviation to ensure the child's holistic well-being. Paracetamol, ibuprofen, and their synergistic coadministration occupy a crucial position, rendering the management of these symptoms efficacious. This study aims to evaluate the safety and adverse effects of paracetamol, ibuprofen, and their combination comprehensively.

Methods: A prospective observational study was conducted at the Department of Paediatrics, Bombay Hospital Institute of Medical Sciences, Mumbai, India. 108 paediatric patients aged 6 months to 18 years experiencing fever, pain, or both. Patients were assigned to receive one of the three medications and were randomized into one of the three groups: paracetamol, ibuprofen, or a combination. Baseline and 48-hour assessments included vital signs, adverse effects, and biochemical markers including SGOT, SGPT, serum creatinine, platelet count, and occult blood in stool samples.

Results: Paracetamol, ibuprofen, and their combination were found to be equally effective in relieving symptoms associated with fever and pain. The most common adverse effect observed was vomiting, with minimal occurrences of rash, cough, and diarrhoea. Biochemical markers, including SGOT, SGPT, serum creatinine, platelet count, and occult blood in stool samples, remained within normal ranges after 48 h of drug administration.

Conclusion: This study affirms the safety of paracetamol, ibuprofen, and their combination for paediatric pain and fever management. Minimal adverse effects and the absence of significant biochemical derangements support their favourable risk-benefit profiles, emphasizing their importance in paediatric clinical practice.

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评估扑热息痛、布洛芬及其复方制剂在儿科疼痛和发烧治疗中的安全性和不良反应:前瞻性观察研究。
目的:疼痛和发烧是常见的儿科主诉,需要细致的症状缓解,以确保儿童的整体福祉。扑热息痛、布洛芬及其协同共给药在这些症状的治疗中起着至关重要的作用。本研究旨在综合评价扑热息痛、布洛芬及其联用的安全性和不良反应。方法:在印度孟买孟买医院医学研究所儿科进行了一项前瞻性观察研究,108例6个月至18岁的儿童患者出现发烧、疼痛或两者兼有。患者被分配接受三种药物中的一种,并随机分为三组:扑热息痛、布洛芬或联合用药。基线和48小时评估包括生命体征、不良反应和生化指标,包括SGOT、SGPT、血清肌酐、血小板计数和粪便样本中的隐血。结果:扑热息痛、布洛芬及其组合在缓解发烧和疼痛症状方面同样有效。观察到的最常见的不良反应是呕吐,很少出现皮疹、咳嗽和腹泻。给药48小时后,生化指标(SGOT、SGPT、血清肌酐、血小板计数、粪便隐血)均在正常范围内。结论:本研究肯定了扑热息痛、布洛芬及其联用治疗小儿疼痛和发热的安全性。最小的不良反应和缺乏显著的生化紊乱支持其有利的风险-效益特征,强调其在儿科临床实践中的重要性。
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