Fig 500microlitres/5ml / Senna fruit 400microlitres/5ml oral solution
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Data from the MHRA Yellow Card scheme. A reported reaction does not necessarily mean the medicine caused it. Contains public sector information licensed under the Open Government Licence v3.0.
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Therapeutically similar medicines
Similarity is based on WHO Anatomical Therapeutic Chemical (ATC) classification and on a factual NHS dm+d therapeutic-grouping code prefix. Source data: NHS dm+d via TRUD (OGL v3.0), WHO ATC/DDD Index.
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SNOMED CT and dm+d codes from NHS TRUD (Technology Reference data Update Distribution), licensed under the Open Government Licence v3.0. ATC codes from the WHO Collaborating Centre for Drug Statistics Methodology (whocc.no).
Active and completed clinical studies from ClinicalTrials.gov
Source: ClinicalTrials.gov, a database of the U.S. National Library of Medicine (NLM), National Institutes of Health (NIH). Data accessed via ClinicalTrials.gov API v2. Trial information is provided for research purposes and does not constitute medical advice.
Academic studies and reviews for this medicine's active substance
Showing the 50 most relevant studies.
Reviews & meta-analyses: 12 · Randomised trials: 5 · 1997–2025
Showing the 50 most relevant studies, sorted by most relevant.
Bo Jiang, Shaoyu Chen, Bencheng Liao, et al.
International Journal of Computer Vision, 2024
D. Morishita, T. Tomita, Sumire Mori, et al.
The American journal of gastroenterology, 2020
Natsumi Maeda, Akira Higashimori, Daijiro Kabata, et al.
The American Journal of Gastroenterology, 2025
INTRODUCTION: No bowel preparation (BP) for colonoscopy achieves optimal efficacy and tolerability. Combining polyethylene glycol plus ascorbic acid (PEG-Asc) with adjuvants has been explored to enhance cleansing efficacy and reduce the required volume. The aim of this study was to evaluate whether adding 0.5 mg linaclotide to 1 L PEG-Asc (1 L-PEG/AL) improves superior cleansing compared with adding 24 mg senna (1 L-PEG/AS), which we previously reported to be noninferior to the standard regimen of 2 L PEG-Asc. METHODS: A multicenter, endoscopist-blinded, randomized controlled trial was conducted at 5 centers in Japan with outpatients scheduled for colonoscopy. The primary outcome was adequate BP, evaluated using the Boston Bowel Preparation Scale. Analyses were stratified based on low-risk and high-risk groups for inadequate BP. RESULTS: Between April 2022 and April 2023, 1,464 patients were randomized to the 1L-PEG/AL (n = 731) or 1L-PEG/AS (n = 733). The 1L-PEG/AL demonstrated higher adequate BP rates (92% vs 86%, P = 0.001) compared with 1L-PEG/AS. Both groups experienced similar adverse events and expressed high willingness for repeat BP (83% vs 81%, P = 0.49). In high-risk patients (n = 892), 1L-PEG/AL had significantly higher adequate BP rates (94% vs 86%, P < 0.001), whereas rates were comparably high in low-risk patients (n = 539) (94% vs 94%, P = 0.66). DISCUSSION: The linaclotide regimen was superior to the senna regimen reagrding BP efficacy without reducing tolerability. It can be a promising new option for BP, especially in patients at a high risk of inadequate BP.
Abstract licence: CC BY-NC-ND
O. Oladeji, F. Adelowo, A. Oluyori, et al.
Evidence-based Complementary and Alternative Medicine : eCAM, 2020
Espoir K. Kambale, C. Nkanga, Blaise-Pascal I. Mutonkole, et al.
Heliyon, 2020
Chengchun Tang, Yoshio Bando, Tadao Sato, et al.
Chemical Communications, 2002
Mohammed M. Alshehri, Cristina Quispe, Jesús Herrera‐Bravo, et al.
Oxidative Medicine and Cellular Longevity, 2022
- Anti-Infective Agents
- Antioxidants
- Phytotherapy
A. Vilanova-Sanchez, A. Gasior, Nicole Toocheck, et al.
Journal of pediatric surgery, 2018
Natsumi Maeda, Akira Higashimori, M. Nakatani, et al.
Digestive Endoscopy, 2022
N. Nata, Supaporn Suebsiripong, B. Satirapoj, et al.
International Journal of Nephrology and Renovascular Disease, 2021
Sources: aggregated from Europe PMC (EMBL-EBI), OpenAlex, Crossref, PubMed and other open scholarly databases. Retracted articles are excluded. Study information is provided for research purposes and does not constitute medical advice.
Scientific data (pharmacology, interactions, ADME) is not yet available for this medicine. Clinical sections are sourced from the NHS dm+d database.