Insulin isophane porcine 100units/ml suspension for injection 10ml vials
Requires a prescription from a doctor or prescriber
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MHRA alerts for Insulin isophane porcine
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Yellow Card reports
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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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4 branded products available
Part of the Hypurin brand family (generic: Insulin isophane porcine)
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View all licensed products for Insulin isophane porcine on the MHRA register
Hypurin Porcine Isophane 100units/ml suspension for injection 10ml vials
Hypurin Porcine Isophane 100units/ml suspension for injection 10ml vials
This is the NHS Drug Tariff indicative price used for reimbursement purposes. It may not reflect the price paid by patients or pharmacies.
View full Drug TariffSource: NHS Drug Tariff via NHSBSA. Derived from dm+d VMPP (Virtual Medicinal Product Pack) pricing data. Contains public sector information licensed under the Open Government Licence v3.0.
WHO defined daily dose (DDD)
40 unit
Not a recommended dose. The DDD is the assumed average maintenance dose per day for a drug used for its main indication in adults. It is a statistical measure used for research and comparison purposes only.
Source: WHO Collaborating Centre for Drug Statistics Methodology, distributed via the NHS dm+d supplementary mapping files (NHSBSA). Contains public sector information licensed under the Open Government Licence v3.0.
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: 10 · Randomised trials: 1 · 1973–2025
Showing the 50 most relevant studies, sorted by most relevant.
Vos RC, van Avendonk MJ, Jansen H, et al.
2016
Hemmingsen B, Metzendorf MI, Richter B
2021
- Myocardial Infarction
- Diabetes Mellitus, Type 1
- Hypoglycemia
B. M. Frier, D. Russell‐Jones, T. Heise
Diabetes, Obesity and Metabolism, 2013
Cristiane Patricia Pissinato Pere, Sophia Economidou, G. Lall, et al.
International Journal of Pharmaceutics, 2018
Eden E. L. Tanner, K. Ibsen, S. Mitragotri
Journal of Controlled Release, 2018
Tricco AC, Ashoor HM, Soobiah C, et al.
2013
- Research Design
- Meta-Analysis as Topic
- Systematic Reviews as Topic
Z. J. Zhang, L. Davidson, G. Eisenbarth, et al.
Proceedings of the National Academy of Sciences of the United States of America, 1991
Dahl-Jørgensen K, Brinchmann-Hansen O, Hanssen KF, et al.
1985
- Diabetic Retinopathy
- Diabetes Mellitus, Type 1
- Insulin
Hirsch IB, Juneja R, Beals JM, et al.
2020
- Diabetes Mellitus
- Hypoglycemic Agents
- Insulins
Insulin has been available for the treatment of diabetes for almost a century, and the variety of insulin choices today represents many years of discovery and innovation. Insulin has gone from poorly defined extracts of animal pancreata to pure and precisely controlled formulations that can be prescribed and administered with high accuracy and predictability of action. Modifications of the insulin formulation and of the insulin molecule itself have made it possible to approximate the natural endogenous insulin response. Insulin and insulin formulations had to be designed to produce either a constant low basal level of insulin or the spikes of insulin released in response to meals. We discuss how the biochemical properties of endogenous insulin were exploited to either shorten or extend the time-action profiles of injectable insulins by varying the pharmacokinetics (time for appearance of insulin in the blood after injection) and pharmacodynamics (time-dependent changes in blood sugar after injection). This has resulted in rapid-acting, short-acting, intermediate-acting, and long-acting insulins, as well as mixtures and concentrated formulations. An understanding of how various insulins and formulations were designed to solve the challenges of insulin replacement will assist clinicians in meeting the needs of their individual patients.
Abstract licence: CC BY
J. Baranao, James M. Hammond
Biochemical and biophysical research communications, 1984
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.