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Status and Safety Signals of Cephalosporins in Children: A Spontaneous Reporting Database Study
Yuanxuan Cai1, Linhui Yang1, Xiaofang Shangguan1
1School of Pharmacy, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Insights
Adverse drug reactions (ADRs) are common in young children treated with cephalosporins, but usually not severe. Specific cephalosporins like ceftezole and ceftriaxone showed higher rates of serious ADRs, necessitating improved drug safety information.
Area of Science:
- Pediatric Pharmacology
- Drug Safety Surveillance
- Clinical Pharmacy
Background:
- Cephalosporins are frequently prescribed for children, yet robust safety data from clinical trials are limited.
- Adverse drug reactions (ADRs) in pediatric populations represent a significant public health concern.
Purpose of the Study:
- To analyze ADR reports for cephalosporins in children to assess their safety profile.
- To identify specific cephalosporins and patient demographics associated with higher ADR risks.
Main Methods:
- Descriptive analysis of ADR reports from 2014-2019.
- Application of three signal-mining methods: Reporting Odds Ratio (ROR), Proportional Reporting Ratio (PRR), and MHRA method.
Main Results:
- Children aged 0-4 years had the highest ADR reporting rates, with a low proportion of severe reactions (6.63%).
- Ceftezole, ceftazidime, cefoperazone/sulbactam, cefotaxime, and ceftriaxone were associated with more numerous and severe ADRs.
- Compound cephalosporin preparations showed a higher proportion of severe ADRs compared to single components; 99.18% of cases improved, with four deaths primarily due to anaphylaxis.
Conclusions:
- ADRs are frequent but generally mild in children under 4 years old.
- The incidence of serious ADRs increases with age in pediatric patients over 4 years.
- Safety concerns exist for certain cephalosporins and compound preparations in children, highlighting the need for improved labeling and allergy history recording.
Abstract:
Introduction: Cephalosporins are widely used in clinical treatment of children, but it is difficult to carry out clinical trials and there is no strong evidence of their safety. Therefore, adverse drug reactions (ADR) of cephalosporins can be a public health problem that deserves attention. Methods: ADR reports collected by the Hubei Adverse Drug Reaction Monitoring Center from 2014 to 2019 were analysed. The safety of Cephalosporins was described by descriptive analysis and three signal mining methods, including the reporting odd ratio (ROR), proportional reporting ratio (PRR), and comprehensive standard method (MHRA). Results: The findings indicated that the age groups of 0-1 and 2-3 years had the highest rates of reporting ADRs. Children aged 0-4 years reported more ADRs, while the proportion of severe ADRs was lower than the average (6.63%). Among the 37 cephalosporins, the severe ADRs of ceftezole, ceftazidime, cefoperazone/sulbactam, cefotaxime, ceftriaxone were reported more and the proportion of severe ADRs was higher. The proportion of severe ADRs of most cephalosporin compound preparations was higher than that of corresponding single components. A total of 99.18% of the cases improved after treatment. There were four deaths whose ADRs were mainly anaphylactic shock, dyspnoea, and anaphylactoid reaction. In signal mining, the three methods produced 206 signals that were the same, and 73 of them were off-label ADRs. Conclusion: ADRs were common but not serious in children aged 0-4 years. And the reported rate of serious ADRs in children aged over 4 years increased with age. ADR reports of ceftezole, ceftazidime, cefoperazone/sulbactam, cefotaxime, ceftriaxone were numerous and serious, and the safety of cephalosporin compound preparations in children was doubtful. Ceftezole may cause off-label ADRs including tremor, face oedema, cyanosis, pallor, rigors, and palpitation. The labeling of ADRs in children in cephalosporin instructions and the record of allergic history need to be improved.
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