Safety of Remdesivir in 20 Children with COVID-19-Case Series-

Shuji Manabe1, Shinsuke Mizuno1, Tsuyoshi Jinda2

  • 1Department of Infection, Kobe Children's Hospital.

Insights

Remdesivir (RDV) treatment for hospitalized children with COVID-19 showed positive outcomes. This study found RDV safe and effective in pediatric patients, with no serious adverse events reported.

Area of Science:

  • Pediatric Infectious Diseases
  • Virology
  • Clinical Pharmacology

Background:

  • Coronavirus disease 2019 (COVID-19), caused by SARS-COV-2, is a global health concern.
  • Remdesivir (RDV) is an established treatment for severe COVID-19 in adults.
  • Limited data exists on RDV's safety and efficacy in pediatric populations.

Purpose of the Study:

  • To evaluate the safety and efficacy of remdesivir (RDV) in hospitalized children diagnosed with COVID-19.
  • To assess adverse events and clinical outcomes in pediatric patients receiving RDV.

Main Methods:

  • Retrospective study of 20 hospitalized pediatric patients with COVID-19 treated with RDV.
  • Data collected from February to June 2022 at Kobe Children's Hospital, Japan.
  • Analysis of patient demographics, underlying conditions, adverse events, and recovery.

Main Results:

  • All 20 pediatric patients recovered without sequelae.
  • No serious adverse events were reported during RDV treatment.
  • Reported adverse events included elevated liver enzymes (20%), leukopenia (5%), neutropenia (5%), and hypokalemia (5%).

Conclusions:

  • Remdesivir (RDV) appears to be safe and effective for treating COVID-19 in hospitalized children.
  • The study suggests RDV can be a viable treatment option for pediatric COVID-19 cases.
  • Further research is warranted to confirm these findings in larger pediatric cohorts.

Related Concept Videos

Teratogenicity01:07

Teratogenicity

The ability of a drug to produce structural deformations and functional abnormalities in the developing embryo or the fetus is called teratogenicity, and the drug producing this effect is known as a teratogen. Teratogenic effects include stillbirth, miscarriage, intrauterine growth restriction, and neurocognitive delay. A teratogen may affect the embryo at different stages of development, which is important in determining the type and extent of the damage. During blastocyst formation, the early...
2.6K
Factors Affecting Drug Response: Overview01:21

Factors Affecting Drug Response: Overview

When it comes to infants and young children, they are typically administered smaller doses of medication in comparison to adults. This is primarily because their organ functions still need to fully develop, meaning their bodies are not as efficient at metabolizing or eliminating drugs. Additionally, their blood-brain barrier is more permeable than in adults. As a result, high concentrations of drugs can easily penetrate the central nervous system (CNS), potentially leading to neurological...
2.1K
Rous Sarcoma Virus (RSV) and Cancer01:03

Rous Sarcoma Virus (RSV) and Cancer

Rous Sarcoma virus or RSV was discovered by F. Peyton Rous in the year 1911 as a filterable transmissible agent that could cause tumors in chickens. He won a Nobel Prize for this discovery in 1966. His experiments clearly demonstrated that some cancers could be caused by infectious agents and led to the discovery of many more cancer-causing viruses in animals as well as humans.
RSV is a retrovirus that contains two copies of a plus-strand  RNA genome. Its genome consists of four main open...
5.3K
Relative Risk01:12

Relative Risk

Relative risk (RR) is a statistical measure commonly used in epidemiology to compare the likelihood of a particular event occurring between two groups. This metric is important for evaluating the relationship between exposure to a specific risk factor and the probability of a particular outcome. It plays a crucial role in medical research, public health studies, and risk assessment. Relative risk quantifies how much more (or less) likely an event is to occur in an exposed group compared to an...
295
Pharmacovigilance01:19

Pharmacovigilance

Post-marketing surveillance is a critical component of pharmaceutical regulation, often uncovering unanticipated adverse drug reactions (ADRs) once a drug is widely used over an extended period.
This process, termed pharmacovigilance, aims to detect, evaluate, and minimize harmful effects related to medication use. The data collection for pharmacovigilance depends on spontaneous reporting systems, where healthcare professionals or patients voluntarily report suspected ADRs.
In some cases, there...
963
Subviral Agents01:29

Subviral Agents

Subviral agents are infectious entities that resemble viruses but lack one or more viral components, such as a capsid or essential replication machinery. These agents include viroids, prions, and satellites, each possessing distinct structural and functional characteristics that influence their mode of infection and replication.Viroids are the simplest subviral agents, consisting of circular, single-stranded RNA molecules without a protein coat. They exclusively infect plants, relying entirely...
82