Benzathine benzylpenicillin 1.2million unit powder for suspension for injection vials
Requires a prescription from a doctor or prescriber
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MHRA alerts for Benzathine benzylpenicillin
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Yellow Card reports
The MHRA Yellow Card scheme collects reports of suspected side effects from healthcare professionals and patients. View the Drug Analysis Profile (iDAP) for real-world adverse reaction data.
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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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Suspected adverse reactions reported for Benzathine benzylpenicillin
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Benzathine benzylpenicillin 1.2million unit powder for suspension for injection vials
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: 4 · Randomised trials: 6 · 2000–2026
Showing the 50 most relevant studies, sorted by most relevant.
O. Mitjà, R. Hays, Anthony Ipai, et al.
Lancet, 2012
A. Bowen, Steven Y. C. Tong, R. Andrews, et al.
Lancet, 2014
Zhang, Fu-Ren, Qu, Hui-Qing, Wang, Xiu-Min, et al.
Pharmacotherapy Group, Faculty of Pharmacy, University of Benin, Benin City, Nigeria, 2018
Suzanne J. Serruya (380985), Ricardo Fescina (380988), Tais F Galvao, et al.
Public Library of Science (PLoS), 2013
OBJECTIVE: To estimate the risk of serious adverse reactions to benzathine penicillin in pregnant women for preventing congenital syphilis. METHODS: We searched for clinical trials or cohorts that assessed the incidence of serious adverse reactions to benzathine penicillin in pregnant women and the general population (indirect evidence). MEDLINE, EMBASE, Scopus and other databases were searched up to December 2012. The GRADE approach was used to assess quality of evidence. Absolute risks of each study were calculated along with their 95% confidence intervals (95% CI). We employed the DerSimonian and Laird random effects model in the meta-analyses. RESULTS: From 2,765 retrieved studies we included 13, representing 3,466,780 patients. The studies that included pregnant women were conducted to demonstrate the effectiveness of benzathine penicillin: no serious adverse reactions were reported among the 1,244 pregnant women included. In the general population, among 2,028,982 patients treated, 4 died from an adverse reaction. The pooled risk of death was virtually zero. Fifty-four cases of anaphylaxis were reported (pooled absolute risk = 0.002%; 95% CI: 0%-0.003% I(2) = 12%). From that estimate, penicillin treatment would be expected to result in an incidence of 0 to 3 cases of anaphylaxis per 100,000 treated. Any adverse reactions were reported in 6,377 patients among 3,465,322 treated with penicillin (pooled absolute risk = 0.169%; 95% CI: 0.073%-0.265% I(2) = 97%). The quality of evidence was very low. CONCLUSION: Studies that assessed the risk of serious adverse events due to benzathine penicillin treatment in pregnant women were scarce, but no reports of adverse reactions were found. The incidence of severe adverse outcomes was very low in the general population. The risk of treating pregnant women with benzathine penicillin to prevent congenital syphilis appears very low and does not outweigh its benefits. Further research is needed to improve the quality of evidence
Abstract licence: CC BY
Trevor Duke, Harry Poka, Frank Dale, et al.
The Lancet, 2002
Halük Demiroglu, Osman I Özcebe, Ibrahim Barista, et al.
The Lancet, 2000
A. V. Ganesh Kumar, V. M. Kothari, A. Krishnan, et al.
Annals of Tropical Medicine & Parasitology, 2004
L. Gutiérrez, H. Sumano, L. Ocampo, et al.
Veterinaria México OA, 2023
Andrews, Ross M., Carapetis, Jonathan R., Tong, Steven Y.C., et al.
Wiley-Blackwell, 2010
Deborah Watson‐Jones, Balthazar Gumodoka, Helen Weiss, et al.
The Journal of Infectious Diseases, 2002
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.