Ganirelix 250micrograms/0.5ml solution for injection pre-filled syringes
Requires a prescription from a doctor or prescriber
Ganirelix is a synthetic decapeptide and a competitive gonadotropin-releasing hormone (GnRH) antagonist.
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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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Suspected adverse reactions reported for Ganirelix
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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
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Suspected adverse reactions reported for Ganirelix
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4 branded products available
MHRA licensed products
View all licensed products for Ganirelix on the MHRA register
Fyremadel 250micrograms/0.5ml solution for injection pre-filled syringes
Ovamex 250micrograms/0.5ml solution for injection pre-filled syringes
Ganirelix 250micrograms/0.5ml solution for injection pre-filled syringes
Orgalutran 250micrograms/0.5ml solution for injection pre-filled syringes
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.
NHS prescribing volume and spending trends
Check stock at pharmacies and supply information
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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
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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. BNF code shown is the factual mapping value distributed by NHS Business Services Authority (NHSBSA) in the dm+d supplementary file under OGL v3.0; it is not affiliated with, nor licensed from, the publishers of the British National Formulary. 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: 3 · Randomised trials: 13 · Trials: 7 · 1992–2025
Showing the 50 most relevant studies, sorted by most relevant.
The European Orgalutran® Study Group, George F. Borm, Bernadette Mannaerts
Human Reproduction, 2000
- Administration, Intranasal
- Buserelin
- Fertility Agents, Female
R. Begueria, Désirée García, Rita Vassena, et al.
Human Reproduction, 2019
- Birth Rate
- Embryo Transfer
- Endometrium
Bart C.J.M. Fauser, Diederick De Jong, F. Olivennes, et al.
The Journal of Clinical Endocrinology & Metabolism, 2002
- Fertilization in Vitro
- Endocrine Glands
- Fertility Agents, Female
Human Reproduction, 1998
- Embryo Transfer
- Estradiol
- Fertilization in Vitro
The European Middle East Orgalutran® Study Group
Human Reproduction, 2001
- Embryo Transfer
- Estradiol
- Follicle Stimulating Hormone
Margo R. Fluker, J. Grifo, Arthur Leader, et al.
Fertility and Sterility, 2001
- Embryo, Mammalian
- Fertilization in Vitro
- Follicle Stimulating Hormone
Joseph Itskovitz‐Eldor, Shahar Kol, Bernadette Mannaerts
Human Reproduction, 2000
- Ovulation Induction
- Embryo Transfer
- Estradiol
H. Out, A. Rutherford, R. Fleming, et al.
Human reproduction, 2004
- Estradiol
- Follicle Stimulating Hormone
- Hormone Antagonists
J. Wilcox, Daniel Potter, Marva Moore, et al.
Fertility and Sterility, 2005
- Analysis of Variance
- Infertility, Female
- Luteinizing Hormone
Andrea DiLuigi, Lawrence Engmann, David Schmidt, et al.
Fertility and Sterility, 2011
- Luteal Phase
- Administration, Cutaneous
- Connecticut
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
13 hours
Mechanism
Gonadotropin-releasing hormone (GnRH) is a hypothalamus-derived releasing hormon…
Food interactions
None known
Human targets
1 target
Data: DrugBank · CC BY-NC 4.0
Pharmacokinetics at a glance
Absorption
91%
[L43045]…
Half-life
13 hours
[L43040][L43045]
Protein binding
81.9%
[L43045]
Volume of distribution
Metabolism
[L43040]…
Elimination
50–70%
Clearance
2.4 L/h
[L43040]
Pharmacokinetic data: DrugBank · CC BY-NC 4.0
[L43040][L43045]
[L43065]
There have been no reports of overdosage with ganirelix in humans.
[L43045]
Clinical studies with subcutaneous administration of ganirelix at single doses up to 12 mg did not show systemic adverse reactions. In acute toxicity studies in rats and monkeys, non-specific toxic symptoms such as hypotension and bradycardia were only observed after intravenous administration of ganirelix over 1 and 3 mg/kg, respectively. As there is no known antidote for ganirelix, the drug should be discontinued in case of an overdose.
[L43040]
Controlled ovarian hyperstimulation (COH) is performed in conjunction with other interventions like in vitro fertilization (IVF) during assisted reproductive technology (ART).[A252205] COH is beneficial as it allows the scheduling of IVF treatments.[A252195] During this intervention, inhibiting premature surges of LH is important because premature elevated LH levels can hinder effective multiple follicular maturation [A252205] and can lead to an undesirable increase in progesterone levels.[A252190] Ganirelix aims to suppress premature LH surges by competitively blocking the GnRH receptors on the pituitary gonadotroph and subsequent transduction pathways. Ganirelix-induced suppression of gonadotropin secretion is rapid and reversible. The suppression of pituitary LH secretion by ganirelix is more pronounced than that of FSH. An initial release of endogenous gonadotropins has not been detected with ganirelix, which is consistent with an antagonist effect.[L43045]
In patients undergoing controlled ovarian stimulation, the median duration of ganirelix treatment was five days.[L43040] In one study, multiple-dose administration of 0.25 mg ganirelix decreased serum LH, FSH and estradiol (E2) concentrations from baseline by 74, 32, and 25% after the last dose, respectively.[A252190] Serum hormone levels returned to pre-treatment levels within two days after the last injection.[L43040][L43045]
How the body processes this drug — absorption, distribution, metabolism, and elimination
[L43045]
It has a Tmax ranging from one to two hours.
[L43040][L43045]
Ganirelix reaches steady-state serum concentrations after three days of administration.
[L43045]
[L43040][L43045]
[L43045]
[L43045]
[L43040]
The 1–4 peptide and 1–6 peptide of ganirelix are the primary metabolites observed in the feces.
[L43045]
Urinary excretion is virtually complete in 24 h, whereas fecal excretion starts to plateau 192 h after dosing.
[L43045]
[L43040]
Proteins and enzymes this drug interacts with in the body
ATC H01CC01
Chemical identifiers
CAS, UNII, InChI Key and database cross-references
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Chemical identifiers
CAS, UNII, InChI Key and database cross-references
Linked compound data from DrugBank Open Data (CC BY-NC 4.0)
Ganirelix
Additional database identifiers
Drugs Product Database (DPD)
12713
ChemSpider
17287671
BindingDB
50102454
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
DrugBank citations
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Structured knowledge from the free knowledge base
ATC classifications (Wikidata)
Linked open data from Wikidata (Q5521314), a free and open knowledge base operated by the Wikimedia Foundation. Data is available under the Creative Commons CC0 1.0 Public Domain Dedication.