Evidence map›Paper›PMID 36334809›Full record

ArticleJournal of pharmaceutical sciences2023

Basis to Aid Crisis: Favipiravir Oral Solution for Hospital Compounding During COVID-19 Drug Shortage.

Bodin Tuesuwan, Wunlapa Mueannoom, Promporn Jamnongtanachot, Ariya Khunvichai, Chiravi Pavitrapok, Kawinthida Wongpakdee, Supasil Sra-Ium, Nithi Mahanonda, Vorasit Vongsutilers

Abstract read
In one paragraph

Article in Journal of pharmaceutical sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Managing drug shortages in pediatric care.Frontiers in pharmacology · 2024
    Review
  6. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Bodin TuesuwanDepartment of Food and Pharmaceutical Chemistry, Faculty of Pharmaceutical Sciences, Chulalongkorn University, Bangkok, 10330, Thailand.
Wunlapa MueannoomMedica Innova Co., Ltd., Bangkok, 10310, Thailand.
Promporn JamnongtanachotMedica Innova Co., Ltd., Bangkok, 10310, Thailand.
Ariya KhunvichaiMedica Innova Co., Ltd., Bangkok, 10310, Thailand.
Chiravi PavitrapokMedica Innova Co., Ltd., Bangkok, 10310, Thailand.
Kawinthida WongpakdeeChulabhorn Hospital, Chulabhorn Royal Academy, Bangkok, 10210, Thailand.
Supasil Sra-IumChulabhorn Hospital, Chulabhorn Royal Academy, Bangkok, 10210, Thailand.
Nithi MahanondaChulabhorn Hospital, Chulabhorn Royal Academy, Bangkok, 10210, Thailand.
Vorasit VongsutilersDepartment of Food and Pharmaceutical Chemistry, Faculty of Pharmaceutical Sciences, Chulalongkorn University, Bangkok, 10330, Thailand. Electronic address: Vorasit.v@chula.ac.th.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The COVID-19 pandemic outbreak has been overwhelming the healthcare system worldwide. A rapidly growing number of younger pediatric patients in Thailand necessitated the formulation of favipiravir, the most locally accessible antiviral agent against COVID-19, into a child-friendly dosage form as a safer alternative to a dispersion of crushed tablets in simple syrup. While striving to quickly develop a liquid formulation that is feasible for any local hospital production units, an oral solution was chosen due to its simplicity. Despite the large dose and poor aqueous solubility of favipiravir, a combination of pH control and use of poloxamer as a solubilizing agent has enabled us to streamline the manufacturing process of a 200 mg/15 mL oral solution for hospital compounding. To ensure its efficacy and safety, a specification for quality control was also established in accordance with the ICH quality guidelines and USP. The finished product stability was subsequently demonstrated under the conditions of 5°C ± 3°C, 25°C ± 2°C/75% RH ± 5% RH, 30°C ± 2°C/75% RH ± 5% RH, and 40°C ± 2°C/75% RH ± 5% RH. The results indicated that our formulation can be stored at 30°C ± 2°C/75% RH for 30 days, which will very well serve the need to allow drug distribution and patient use during the crisis, while the shelf-life can be extended to 60 days when stored at 5°C ± 3°C. Thus, accessibility to an essential medical treatment has been successfully enhanced for pediatric patients in Thailand and neighboring countries during the COVID-19 outbreak.

Indexed as

COVID-19AmidesChildDrug CompoundingDrug StabilityHospitalsHumansPandemicsPyrazinesAmidesfavipiravirPyrazinesCOVID-19FavipiravirFormulation developmentHospital compoundingOral solutionSpecificationStability

Identifiers

PMID36334809
PMCPMC9628134

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.