Gonadorelin 100microgram powder for solution for injection vials
Requires a prescription from a doctor or prescriber
Gonadorelin is another name for gonadotropin-releasing hormone (GnRH).
Official documents, adverse reaction reporting, and safety monitoring
Report a side effect
Submit a Yellow Card report to the MHRA
Official medicine documents
Yellow Card
Report side effects (MHRA)
Drug safety updates
MHRA alerts for Gonadorelin
Safety monitoring data
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.
View Drug Analysis Profile
Suspected adverse reactions reported for Gonadorelin
Browse all iDAP reports
Interactive Drug Analysis Profiles for all medicines
Report a side effect
Submit a Yellow Card report to the MHRA
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.
EudraVigilance
The European Medicines Agency (EMA) collects suspected adverse reaction reports from across the EU/EEA through the EudraVigilance system. Search for safety data on this medicine.
View EudraVigilance report
Suspected adverse reactions reported for Gonadorelin
About EudraVigilance
Learn about EU pharmacovigilance and safety monitoring
EudraVigilance data is published by the European Medicines Agency (EMA). A suspected adverse reaction is not necessarily caused by the medicine.
2 branded products available
MHRA licensed products
View all licensed products for Gonadorelin on the MHRA register
Gonadorelin 100microgram powder for solution for injection vials
Therapeutically similar medicines
Injectables
(1)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.
NHS prescribing volume and spending trends
Check stock at pharmacies and supply information
Pharmacy stock checkers
Search for this medicine at major UK pharmacy chains. These links open the retailer's own website — results depend on their current online catalogue.
Supply & safety information
Official UK regulator monitoring and safety alerts
Pharmacy links redirect to the retailer's own search and do not represent real-time stock levels. Shortage and safety information sourced from MHRA drug safety updates (gov.uk, Crown Copyright under OGL v3.0).
Codes for healthcare professionals and prescribing systems
These codes are used by healthcare IT systems and prescribers to identify this medicine.
NHS UK identifiers
Browse tools
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 · Randomised trials: 1 · 1988–2026
Showing the 50 most relevant studies, sorted by most relevant.
V. Caldwell, R. Martineau
American Association of Bovine Practitioners Conference Proceedings, 2016
J. R. Chenault, D. Kratzer, R. A. Rzepkowski, et al.
Theriogenology, 1990
Francesca Torrini, Simona Scarano, Pasquale Palladino, et al.
Journal of Pharmaceutical and Biomedical Analysis, 2023
- Peptide Hormones
- Molecular Imprinting
- Polymers
T.J. Valdés-Arciniega, I.M.R. Leão, E. Anta-Galván, et al.
Journal of Dairy Science, 2023
- Progesterone
- Lactation
- Cattle
D. Melo, W. Coelho, T. C. Marques, et al.
Journal of dairy science, 2024
- Progesterone
- Insemination, Artificial
- Estrus Synchronization
Iago M.R. Leão, Marcelo S. El Azzi, Everaldo Anta-Galván, et al.
Journal of Dairy Science, 2024
- Estrus Synchronization
- Lactation
- Cattle
Gifford RM, O'Leary TJ, Knight RL, et al.
2025
- Pituitary-Adrenal System
- Hypothalamo-Hypophyseal System
- Saliva
Reproductive endocrine function adapts to psychological, environmental, and energy-associated stressors. Multistressor environments upregulate hypothalamic-pituitary-adrenal (HPA) axis, causing suppression of the hypothalamic-pituitary-gonadal (HPG) axis, but it is not known if this pattern or its magnitude is sex biased. We compared HPG and HPA axis activity in 9 men and 34 women undergoing Army training. One-hour low-dose gonadorelin and Synacthen tests were conducted at 1 and 29 wk, measuring gonadotrophins and cortisol. Cortisol was measured from hair every 3 mo. Morning and evening salivary cortisol and psychometric questionnaires were measured at six timepoints. Sexes were compared over time by two-way ANOVA. Gonadotrophin responses were significantly higher in women than men in week 1, but no sex difference was seen at week 29 (no significant sex × time interaction). Week 1 cortisol response was higher among men, but week 29 cortisol response was higher among women (sex × time F(1,44) = 18.0, P months 5-11 (F(3,15) = 3.25, P = 0.024). Morning salivary cortisol was higher among women in weeks 8 and 14, but higher among men in week 29 (F(4,76) = 4.0, P = 0.005). No differences were seen in evening salivary cortisol. Psychometrics did not change or differ between sexes. HPA axis responses to military training were greater among women than men. HPG axis responses suggest greater downregulation among women. These findings will enable equitable and individualized management of people undergoing periods of intensive physical stress.NEW & NOTEWORTHY We conducted a comprehensive comparison of adrenal and reproductive function in men and women undergoing 11-mo military training. We found progressively elevated cortisol levels and dynamic cortisol response to stress among women, but not men, and suppression of reproductive function among women. The physiological impact of stressful military training was greater among women than men; this could not be explained by energy balance, and sex-specific effects of sleep, socio-ethnographic, or other stressors may be responsible.
Abstract licence: CC BY
Thomas A, Walpurgis K, Thevis M
2024
- Body Fluids
- Doping in Sports
- Cattle
Peptides with a molecular mass between 2 and 10 kDa that are prohibited in elite sports usually require dedicated sample preparation and mass spectrometric detection that commonly cannot be combined with other (lower molecular mass) substances. In most instances, the physicochemical differences are too significant to allow for a generic analytical procedure. A simplification of established and comparably complex analytical approaches is therefore desirable and has been accomplished in the context of this study. With urine samples representing still the most frequently collected doping control specimens, efficient extraction of peptidic analytes from this matrix was a major goal of this method, as demonstrated for the included compounds such as insulins (human, lispro, aspart, glulisine, tresiba, glargine metabolite, bovine insulin, porcine insulin), growth hormone-releasing hormones (sermorelin, CJC-1295, tesamorelin) incl. their respective metabolites, insulin-like-growth factors (long-R3 -IGF-I, R3 -IGF-I, des1-3 -IGF-I), synacthen, gonadorelin and mechano growth factors (human MGF, MGF-Goldspink). Sample preparation and detection are controlled by five internal standards, covering all five included peptide drug categories. Nearly all requirements of the recent technical documents from the World Anti-Doping Agency (WADA) considering their minimum required performance levels (MRPL) are fulfilled, and the method was validated for its utilisation as initial testing procedure in doping controls. Finally, the approach was applied to authentic post-administration study urine samples (for insulins and gonadorelin) in order to provide proof of principle.
Abstract licence: CC BY-NC-ND
F.S. Lima, R.G.S. Bruno, R.M. Cleale, et al.
Journal of Dairy Science, 2026
- Luteinizing Hormone
- Estrus Synchronization
- Ovulation
Jeong Ho Seo, Myoung Jin Yoo, Kyeongmi Lee, et al.
Annals of Pediatric Endocrinology & Metabolism, 2025
following GnRHa stimulation in boys. This retrospective study analyzed boys evaluated for precocious puberty at the Division of Pediatric Endocrinology at Hanyang University Hospital in Seoul and Guri, between March 2019 and August 2024. The study included all patients who underwent a GnRH or GnRHa stimulation test and showed advanced bone age (BA), with testicular volumes confirmed to be ≥4 mL before the age of 9. For patients whose initial visit occurred at age 9 or older, inclusion criteria were based on clinical suspicions of a testicular volume ≥4 mL before age 9, based on findings of a volume of ≥6 mL before age 9.5 or ≥8 mL before age 10. A total of 55 boys met these criteria: 23 underwent a GnRH stimulation test, and 32 underwent a GnRHa stimulation test. From these, 17 boys from each group (totaling 34) were matched in a 1:1 ratio using propensity score matching based on BA. After matching, the standardized mean difference was 0.026, indicating negligible covariate imbalance between the 2 groups, and multiple regression analysis showed no significant differences in any clinical characteristics between the groups ( P >0.05). Differences between the 2 groups were evaluated using the Mann-Whitney U -test. The clinical characteristics, including age, height, weight, body mass index, testicular volume, and basal levels of LH, and testoste rone, showed no significant differences between the 2 groups, except for follicle-stimulating hormone, which has
Abstract licence: CC BY-NC 4.0
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.
Pharmacology and chemical data from DrugBank
Key facts
Drug status
Approved
Major interactions
None known
Half-life
2 to 10 minutes
Mechanism
Systemic - Like naturally occurring gonadotropin-releasing hormone (GnRH), gonad…
Food interactions
None known
Human targets
2 targets
Data: DrugBank · CC BY-NC 4.0
Pharmacokinetics at a glance
Absorption
Half-life
2 to 10 minutes
Metabolism
Pharmacokinetic data: DrugBank · CC BY-NC 4.0
Known interactions with other medicines. Always consult a healthcare professional.
Showing 3 of 3 interactions
How the body processes this drug — absorption, distribution, metabolism, and elimination
Proteins and enzymes this drug interacts with in the body
ATC V04CM01
ATC H01CA01
Chemical identifiers
CAS, UNII, InChI Key and database cross-references
Show
Chemical identifiers
CAS, UNII, InChI Key and database cross-references
Linked compound data from DrugBank Open Data (CC BY-NC 4.0)
Gonadorelin
Additional database identifiers
Drugs Product Database (DPD)
7330
Drugs Product Database (DPD)
11313
Drugs Product Database (DPD)
7361
Drugs Product Database (DPD)
7362
ChemSpider
33562
HUGO Gene Nomenclature Committee (HGNC)
HGNC:4421
GenAtlas
GNRHR
GeneCards
GNRHR
GenBank Gene Database
L03380
GenBank Protein Database
183422
Guide to Pharmacology
256
UniProt Accession
GNRHR_HUMAN
HUGO Gene Nomenclature Committee (HGNC)
HGNC:16341
GenAtlas
GNRHR2
GeneCards
GNRHR2
GenBank Gene Database
AF403014
GenBank Protein Database
16589056
UniProt Accession
GNRR2_HUMAN
DrugBank citations
If you use DrugBank data in your research, please cite:
- DrugBank 6.02024Recommended citationKnox C., Wilson M., Klinger C.M., et alDrugBank 6.0: the DrugBank Knowledgebase for 2024Nucleic Acids Res. 2024 Jan 552(D1):D1265-D1275
- DrugBank 5.02018Wishart D.S., Feunang Y.D., Guo A.C., et alDrugBank 5.0: a major update to the DrugBank database for 2018Nucleic Acids Res. 2017 Nov 846(D1):D1074-D1082
- DrugBank 4.02014Law V., Knox C., Djoumbou Y., et alDrugBank 4.0: shedding new light on drug metabolismNucleic Acids Res. 2014 Jan 142(1):D1091-7
- DrugBank 3.02011Knox C., Law V., Jewison T., et alDrugBank 3.0: a comprehensive resource for 'omics' research on drugsNucleic Acids Res. 2011 Jan39(Database issue):D1035-41
- DrugBank 2.02008Wishart D.S., Knox C., Guo A.C., et alDrugBank: a knowledgebase for drugs, drug actions and drug targets.Nucleic Acids Research2008 Jan36(Database issue):D901-6
- DrugBank 1.02006Wishart D.S., Knox C., Guo A.C., et alDrugBank: a comprehensive resource for in silico drug discovery and exploration.Nucleic Acids Research2006 Jan 134(Database issue):D668-72