Testosterone enantate 250mg/1ml solution for injection ampoules
Requires a prescription from a doctor or prescriber
Minimal controls; includes benzodiazepines and anabolic steroids
Legal requirements and restrictions
Anabolic steroids and related substances. Possession for personal use is not an offence, but supply is controlled.
Legal requirements
- Prescriptions valid for 28 days
- No controlled drugs register required
- No safe custody requirements
- Import/export restrictions apply
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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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6 branded products available
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Testosterone enantate 250mg/1ml solution for injection ampoules
Testosterone enantate 250mg/1ml solution for injection ampoules
Testosterone enantate 250mg/1ml solution for injection ampoules
Testosterone enantate 250mg/1ml solution for injection ampoules
Testosterone enantate 250mg/1ml solution for injection ampoules
Testosterone enantate 250mg/1ml solution for injection ampoules
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.
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: 2 · 1980–2026
Showing the 50 most relevant studies, sorted by most relevant.
Melissa E. Paulen, Kathryn M. Curtis
Contraception, 2009
- Fertility
- Norethindrone
- Injections, Intramuscular
Curtis KM, Nguyen AT, Tepper NK, et al.
2024
- Contraception
- Contraceptive Agents
- United States
The 2024 U.S. Selected Practice Recommendations for Contraceptive Use (U.S. SPR) addresses a selected group of common, yet sometimes complex, issues regarding initiation and use of specific contraceptive methods. These recommendations for health care providers were updated by CDC after review of the scientific evidence and a meeting with national experts in Atlanta, Georgia, during January 25-27, 2023. The information in this report replaces the 2016 U.S. SPR (CDC. U.S. Selected Practice Recommendations for Contraceptive Use, 2016. MMWR 2016;65[No. RR-4]:1-66). Notable updates include 1) updated recommendations for provision of medications for intrauterine device placement, 2) updated recommendations for bleeding irregularities during implant use, 3) new recommendations for testosterone use and risk for pregnancy, and 4) new recommendations for self-administration of injectable contraception. The recommendations in this report are intended to serve as a source of evidence-based clinical practice guidance for health care providers. The goals of these recommendations are to remove unnecessary medical barriers to accessing and using contraception and to support the provision of person-centered contraceptive counseling and services in a noncoercive manner. Health care providers should always consider the individual clinical circumstances of each person seeking contraceptive services. This report is not intended to be a substitute for professional medical advice for individual patients; when needed, patients should seek advice from their health care providers about contraceptive use.
Abstract licence: Public domain
M Krotkiewski, John G. Kral, J. Karlsson
Acta Physiologica Scandinavica, 1980
- Adipose Tissue
- Body Composition
- Body Weight
Geoffrey Hackett, Amar Mann, Ahmad Haider, et al.
The World Journal of Men s Health, 2024
Anina Neidhart, Viktor von Wyl, Benno Käslin, et al.
Frontiers in Endocrinology, 2025
- Hypogonadism
- Polycythemia
- Androgens
Aksam Yassin
Testosterone, 2023
Ilpo Huhtaniemi
Good and Bad Testosterone, 2024
Thomas A, Thelen J, Sakellariou P, et al.
2025
- Esters
- Steroids
- Tandem Mass Spectrometry
Steroidal esters (e.g., testosterone, nandrolone and boldenone esters) belong to the substance class prohibited in professional sport that is particularly frequently abused due to its considerable performance-enhancing effects. Thus, a high number of adverse analytical findings in doping controls is reported every year. Unfortunately, the analysis of steroids that are not exclusively of exogenous nature and, in particular, their differentiation from endogenously produced steroids is very time-consuming and resource-intensive (necessitating isotope-ratio mass spectrometric analysis). The direct detection of the applied (unequivocally exogenous) steroidal esters in blood or dried blood spots (DBS) can offer a much simpler approach. In the present project, the analysis of 17 underivatized steroidal esters (composed of testosterone, nandrolone and boldenone species) is reported, employing liquid chromatography-(low-resolution)-MSn. The results show that all included esters can be selectively and sensitively detected in MS3 mode at sub-ng/mL levels in DBS. The detection limits for most analytes extracted from a single spot were below 0.1 ng/mL, and recovery rates were determined at 40%-80%. The overall procedure was controlled using four different stable isotope-labelled internal standards. Notably, the obtained results are largely independent from the sampling device, and the method works for cellulose-based DMPK cards as well as polymer-based TASSO devices. Proof-of-concept and applicability of the method to authentic samples were demonstrated by analysing post-administration samples collected after an oral administration of 80 mg of testosterone undecanoate.
Abstract licence: CC BY
Alyssa Hill, Cristina Rabaza
Evidence-Based Practice, 2024
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.