Menotrophin 1,200unit powder and solvent for solution for injection vials
Requires a prescription from a doctor or prescriber
Menotropins contains follicle stimulating hormone (FSH) and luteinizing hormone (LH) purified from the urine of postmenopausal women.
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Suspected adverse reactions reported for Menotrophin
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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 Menotrophin
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1 branded products available
Part of the Meriofert brand family (generic: Menotrophin)
MHRA licensed products
View all licensed products for Menotrophin on the MHRA register
Menopur 1,200unit powder and solvent for solution for injection vials
WHO defined daily dose (DDD)
75 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 BNF/ATC 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.
NHS prescribing volume and spending trends
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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: 4 · Trials: 26 · 1993–2025
Showing the 50 most relevant studies, sorted by most relevant.
Rina Agrawal, Jeremy Holmes, Howard S. Jacobs
Fertility and Sterility, 2000
- Fertilization in Vitro
- Clinical Protocols
- Follicle Stimulating Hormone
Philippe Lehert, Joan Schertz, D. Ezcurra
Reproductive Biology and Endocrinology, 2010
- Cell Count
- Fertility Agents, Female
- Infertility
Alviggi, Carlo, Casarini, Livio, Santi, Daniele, et al.
Frontiers in Endocrinology, 2017
Wex J, Abou-Setta AM
2013
Gonadotropin-releasing hormone-analog type, fertilization method, and number of embryos available for cryopreservation should be incorporated into economic evaluations of highly purified human menopausal gonadotropin (HP-hMG) and recombinant human follicle-stimulating hormone (r-hFSH), as they may affect treatment costs. We searched for randomized trials and meta-analyses comparing HP-hMG and r-hFSH. Meta-analysis showed no significant difference in live births (odds ratio 0.82, 95% confidence interval [CI] 0.66-1.01), but a greater number of oocytes with r-hFSH (mean difference [MD] 1.96, 95% CI 1.02-2.90). Using a cost-minimization model for Sweden, accounting for embryo availability, survival following thawing, and patient dropout, we simulated patients individually for up to three cycles. R-hFSH was found to be cost-saving, at 2,767 kr (95% CI 1,580-4,057) per patient (€315 or $411); baseline savings were 6.43% of the total HP-hMG cost. In fresh cycles only, the savings for r-hFSH were 1,752 kr (95% CI 48-3,658) per patient (€200 or $260). In univariate sensitivity analyses, savings were obtained until the price of r-hFSH increased by 30% or the dosage of HP-hMG decreased by 38%-62% of baseline value. In probabilistic sensitivity analysis, r-hFSH was cost-saving in 100% of the simulated cohort per patient and in 85% per live birth; the respective percentages for fresh cycles only were 97.3% and 73.1%. In conclusion, a greater number of oocytes with r-hFSH allows for more frozen embryo transfers, thereby reducing overall treatment cost.
Abstract licence: CC BY-NC
Marco Filicori
Human Reproduction, 2002
- Drug Combinations
- Fertility Agents, Female
- Follicle Stimulating Hormone
Peter Platteau, Anders Nyboe Andersen, Adam Balen, et al.
Human Reproduction, 2006
- Anovulation
- Ovarian Follicle
- Infertility, Female
Brader J, Ramphul R
2025
A woman in her 20s developed IgA vasculitis with nephritis (IgAVN), which started four days after oocyte donation (for in-vitro fertilisation (IVF) and transfer to another recipient). Prior to oocyte retrieval, the patient received a course of controlled ovarian stimulation (COS) with menotrophin, ganirelix acetate and choriogonadotropin alfa. Four days after COS, she developed a painful purpuric rash alongside knee pain and swelling. Prednisolone was started for presumed IgA vasculitis. Soon after, she developed de novo mononeuritis multiplex and renal dysfunction characterised by haematoproteinuria and nephrotic syndrome. A kidney biopsy confirmed the diagnosis of IgAVN. Symptoms improved over time; however, there remained questions about the possible trigger. The induced sex hormone changes associated with COS may have had an immunomodulatory effect, leading to disease development.
Abstract licence: CC BY
SUN N, Yin P, Yan H
2023
Abstract Object: This study was to investigate the effect of different human Menotrophin (hMG) initiation doses on in vitro fertilization (IVF) outcomes in aged poor ovarian response(POR) patients undergoing ovulation induction with Clomiphene Citrate (CC) combined with hMG; Method: The clinical data of 142 POR patients more than 40 years old were collected and were divided into 3 groups according to the initiation dose of hMG (Group A=75IU, Group B=150IU, Group C=225IU). The baseline characteristics and IVF outcomes were compared; Results: We found that with the increase of hMG initiation dose, the average number of oocytes retrieved increased, pair-to-pair comparison showed that the the average number of oocytes retrieved in Group Awas significantly lower than that in the Group B and Group C(PPP>0.05). Conclusions: For aged POR patients receiving CC combined with hMG, increasing hMG cannot improve patients' IVF outcomes and Pregnancy outcomes. 150IU of hMG initiation dose may be the better choice for aged POR patients.
Abstract licence: CC BY
Caixia Liu
Advances in Obstetrics and Gynecology Research, 2024
Richard Fleming, C. C. Chung, R. Yates, et al.
Human reproduction, 1996
- Follicular Phase
- Follicle Stimulating Hormone
- Hormones
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
Not available
Mechanism
Being a combination drug, Menotropins bind to the follicle stimulating hormone r…
Food interactions
None known
Human targets
2 targets
Data: DrugBank · CC BY-NC 4.0
Pharmacokinetics at a glance
Proteins and enzymes this drug interacts with in the body
PMID:11847099 PMID:24058690 PMID:24692546
Through cAMP production activates the downstream PI3K-AKT and ERK1/ERK2 signaling pathways PMID:24058690
PMID:11847099
The activity of this receptor is mediated by G proteins which activate adenylate cyclase PMID:11847099
ATC G03GA02
ATC G03GA03
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)
Menotropins
Matched from: Menotrophin
Additional database identifiers
Drugs Product Database (DPD)
7369
HUGO Gene Nomenclature Committee (HGNC)
HGNC:3969
GenAtlas
FSHR
GeneCards
FSHR
GenBank Gene Database
M65085
GenBank Protein Database
182771
Guide to Pharmacology
253
UniProt Accession
FSHR_HUMAN
HUGO Gene Nomenclature Committee (HGNC)
HGNC:6585
GenAtlas
LHCGR
GeneCards
LHCGR
GenBank Gene Database
M73746
GenBank Protein Database
903746
Guide to Pharmacology
254
UniProt Accession
LSHR_HUMAN
DrugBank citations
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Structured knowledge from the free knowledge base
ATC classifications (Wikidata)
Linked open data from Wikidata (Q416821), a free and open knowledge base operated by the Wikimedia Foundation. Data is available under the Creative Commons CC0 1.0 Public Domain Dedication.