Post-marketing safety re-evaluation of placental peptide injection in China: a large-scale multicenter real-world study
- PMID: 40103593
- PMCID: PMC11913665
- DOI: 10.3389/fphar.2025.1541005
Post-marketing safety re-evaluation of placental peptide injection in China: a large-scale multicenter real-world study
Abstract
Purpose: This study conducted a post-marketing safety re-evaluation of placental polypeptide injections in China to support updates to drug guidelines, pharmacovigilance efforts, and rational clinical use, facilitating its inclusion in essential drug lists and medical insurance coverage.
Methods: A hospital-based centralized monitoring system tracked 3,000 patients receiving placental polypeptide injections across three medical institutions. Adverse drug reactions (ADRs) and adverse drug events (AEs) were systematically collected and analyzed.
Results: The mean patient age was 49.65 years, with 96.47% being over 18 years of age. A single dose exceeding 4 mL was administered in 98.34% of the cases, with a median treatment duration of 7 days. Concomitant medication use was high (injectable, 98.43%; non-injectable, 75.43%). One case of vertigo was reported as an ADR in a patient aged >60 years who had melanoma.
Conclusion: The ADR rate was 0.03%, confirming the favorable safety profile of placental polypeptide injection. These findings support its safe clinical use and can inform future regulatory and policy decisions.
Keywords: adverse drug reactions; centralized hospital monitoring method; placental peptide injection; post-marketing safety re-evaluation; real-world study.
Copyright © 2025 Duan, An, Tian, Yan, Chen, Zhang, Liu, Wang, Zhang, Tong and Zhou.
Conflict of interest statement
Author XL was employed by Beijing Dehuijia Pharmaceutical Technology Co., Ltd. The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
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