Opinion

The case for reform: better information, not prohibition alone

In short

About 8 minutes for the short version; 17 with every detail open.

  • This page is our opinion. It is signed, dated and kept apart from the fact pages.
  • Medicines must be tested before they are sold. Thalidomide showed why.
  • People already use peptides that were never tested well. A ban alone leaves them with unknown products.
  • We want public trials, tests for what is in a vial, open harm reports and help from doctors.
  • We do not argue for weaker rules, or that any product is safe to use.
Last reviewed
An empty debating chamber with rows of wooden desks and blue chairs in a half circle, a speaker's desk and a Dutch flag.
The debating hall of the Dutch lower house in The Hague, seen in 2018. Photo: Husky (Wikimedia Commons) CC BY 4.0 Image details

Each section starts with the short answer. The rest is folded under “In detail”.

What is this page?

Our view on how the rules should change. Its facts are sourced like every other page.

Every other page on this site describes. This one argues. We write for people who may already have a peptide in the fridge, and we think some current rules work against the people they are meant to protect. Here is our case, with the case against it.

Our position in brief

What is your position?

Better facts and better access do more good than bans and poor facts.
Six problems with the current situation, and what we would do instead.
What happens nowWhat we propose
Untested peptides are bought and used anyway1,2Public, independent trials of the compounds people actually use
Tests of products keep finding the wrong amount or the wrong substance3,4Testing services for peptides, like drug-checking services
Most harms go unreported, so regulators see few warnings5,6Side-effect reporting that welcomes reports about any product
Products labelled “for research purposes” are sold for use in people, with dosing instructions6Enforcement aimed at sellers and false claims, not at users
Use is often hidden from doctors, as a study of steroid users found7Guidance that helps doctors check on these patients
Promising compounds can wait years for a sponsor, or never get one8,9Faster conditional routes, open to non-commercial sponsors

None of this means weaker rules for sellers. Every proposal keeps the ban on selling and advertising unlicensed medicines. We want to change what happens to people who use these products anyway: whether they can know what they take, whether anyone notices harm, and whether anyone finds out if it works.

The case for caution, taken seriously

Why not just let adults decide for themselves?

Untested medicines can do great harm. Thalidomide is the case most people know.
A black-and-white photo of President John F. Kennedy handing a pen to Frances Kelsey, with men in suits watching.
In 1962, President Kennedy hands a pen to Frances Kelsey. At the FDA she said no to thalidomide. Photo: U.S. Food and Drug Administration (Wikimedia Commons) Public domain Image details

In the late 1950s and early 1960s, thalidomide was widely given to pregnant women for nausea. It caused severe birth defects in thousands of children.10 In the United States, an FDA reviewer, Frances Kelsey, refused to approve it because the company’s evidence was inadequate. It was never sold there.11 The first European medicines directive followed in 1965: medicines must be independently assessed and authorised before they are sold.12

In detail: Why evidence before marketing matters , about 1 minute to read

The rule that came out of thalidomide is simple: the maker must show that a medicine works and is acceptably safe, and an independent body checks, before it is sold. Early results and confident experts are poor guides.

Most drug plans that reach trials in people never end in approval

13.8%

of drug plans that started tests in people were approved in the end: about 1 in 7

What was counted 41,040 industry drug programmes (one drug for one illness) with trials from 2000 to 2015 (Wong 2019) Source Wong et al. (2019)13

Laboratory results often do not hold up either: when scientists at one company tried to confirm 53 “landmark” cancer studies, they succeeded with 6.14 Even approved medicines can reach the market with uncertain benefit. Of 68 cancer uses approved by the EMA from 2009 to 2013, only 24 had shown longer survival at the time of approval; after a median of more than five years, 33 still had no clear evidence of longer or better life.15

In detail: The serious arguments against our position , about 1 minute to read

We take these seriously, and our proposals are shaped by them.

  • Information can look like approval. A careful page about an untested peptide may make it seem normal.
  • Testing can become marketing. A seller could use a test result as a stamp of quality.
  • Help can attract new users. Services for people who already use a product might draw in others.
  • Money is limited. Public money for trials of unlicensed compounds is not spent on care known to work.
  • A regulator’s strength is saying no. Kelsey kept thalidomide off the US market despite constant pressure from its maker.11 Rules that bend to demand lose that strength.
In detail: Thalidomide's second lesson , about 1 minute to read

Thalidomide did not disappear. It later proved useful in leprosy and in multiple myeloma, a blood cancer, and in 2008 it was authorised in the EU for myeloma.10,12 But in rural areas without strong medical surveillance, its use by pregnant women with leprosy has kept causing birth defects.10

The same molecule can harm or help. Information, control and follow-up decide which. We think that lesson applies here too.

People are already using these products

Does the ban stop people using them?

No. Seized goods, warnings and side-effect reports all show that people use them.

Thousands of illegal weight-loss pens were seized in the UK in one year

5,680

weight-loss pens seized in 2025. In all, almost 20 million doses of illegal medicines were seized.

What was counted GLP-1 pens seized by the MHRA, the UK medicines regulator, and its law-enforcement partners in 2025 Source MHRA seizes illegal medicines worth almost £45m in 2025 – disrupting major criminal networks16

Fake weight-loss jabs may show up in EU side-effect reports

234

reports about what may be fake semaglutide. Most side effects in them were serious: 89 in 100

What was counted Reports in EudraVigilance, the EU side-effect database, from 2018 to 2025 (Zinzi 2026) Source Zinzi et al. (2026)17

We found no reliable count of how many people in the Netherlands use peptides from outside pharmacies. But the signs point one way. In 2025 the Dutch inspectorate and medicines board warned that illegal online offers of medicines are increasing.1 In May 2026 the UK regulator raided a site it believed was making retatrutide, tirzepatide and other peptide products.2

In detail: What these numbers do and do not show , about 1 minute to read

Seizures measure enforcement as well as trade, and side-effect reports only what someone chose to report. So these numbers show that use is real; they cannot say how large it is.

Most of the UK’s almost 20 million seized doses were not peptides: they were mainly sedatives, painkillers and erection medicines.16 Of 1,190 doping products seized at the Swiss border, 146 were labelled as peptide hormones or growth factors.3

What a ban without information does

What goes wrong when use is hidden?

People get unknown products, skip check-ups, and harms go unreported. Each problem feeds the next.
Three things that happen when use is hidden, and why each one matters.
What happensWhyWhat follows
The product is unknownNo regulator checks its contents or whether it is free of germsWrong amounts and substances: under 20 in 100 seized doping products held what the label said, in that amount3
Use is hidden from doctorsUsers may doubt what doctors know about these productsNo check-ups: 56 in 100 steroid users in one US study had never told a doctor7
Harms go unreportedThe user stays quiet, and no doctor knowsFew warnings: even for prescribed medicines, a median 94 in 100 side effects went unreported5

Each link makes the next one worse. Someone who hides their use from a doctor will not report a side effect through that doctor. A harm never reported never becomes a warning for the next person.

In detail: Unknown products: what laboratories found , about 1 minute to read
  • Semaglutide bought online without a prescription. A Hungarian university made test purchases, and three vials arrived. The powder was only about 8% to 14% semaglutide, although the labels claimed 99% purity. Yet each vial held about 29% to 39% more semaglutide than its label said.4
  • Products sold as retatrutide, Australia. Three products held 51%, 165% and 190% of the amount on the label.18
  • Falsified peptide medicines, Belgium. A public laboratory tested the ten falsified peptide medicines most often found on the Belgian market, bought from suspected illegal websites. It found amounts that varied widely, low purity, and arsenic and lead in some samples.19

Careful injecting cannot fix any of these. See product risk.

In detail: Hidden from doctors , about 1 minute to read

The US study interviewed 80 weightlifters, 43 of whom used anabolic steroids. The users rated doctors as no more reliable on steroids than friends, websites or their dealers, and 56% had never told a doctor about their use.7

The study is about steroids, not peptides, and is more than 20 years old; we found no comparable study of peptide users. We expect the same pattern, but nobody has measured it: when use is something to hide, people hide it from the person who could help most. In the Netherlands, doctors must keep what you tell them confidential.20 See talking to your doctor.

In detail: Why unreported harm stays invisible , about 1 minute to read

A systematic review of 37 studies from 12 countries found that a median of 94% of side effects of medicines in normal care were not reported to the national reporting systems.5 For products used outside the medical system, the share is unknown. The FDA itself says side effects of compounded GLP-1 medicines are likely under-reported, because ordinary compounding pharmacies are not required to report them to it.6

Reports work when people make them. In EudraVigilance, reports about possibly counterfeit semaglutide mentioned low blood sugar more often than reports about the genuine medicine.17 That fits what regulators found when they tested fake pens: some contained insulin instead of semaglutide.21

The cost of waiting

Is slow regulation harmless?

No. Waiting has real costs. And some compounds may never be tested, because no one will pay.

By one estimate, a new medicine costs about a billion dollars to bring to market

$985 million

the middle estimate of what it costs to make one new medicine, with failed tries counted

What was counted 63 of the 355 new medicines approved by the FDA from 2009 to 2018 for which cost data were public (Wouters 2020) Source Wouters et al. (2020)22

A company spends that kind of money only when it expects to earn it back. For a compound that is cheap to make and already sold widely, that may never happen. The EMA itself has written that companies sometimes lack the incentive to study new uses of old medicines that are no longer protected by a patent or data exclusivity, and that this “could be a wasted opportunity for public health”.8 In public records, the developer’s programme for BPC-157 did not go beyond one small phase 2 trial in the 2000s. That trial found no clear benefit, and it was published only as a short conference summary.9

In detail: Why some compounds may never get a sponsor, and why the picture is not simple , about 1 minute to read

The estimate comes mainly from smaller companies and varies with its assumptions.22 Nor is the incentive problem absolute. Under current EU law, once a medicine is authorised, other companies cannot rely on its trial data to sell copies for 10 years (in some cases 11), whether or not its maker holds a patent.23 The EU agreed a reform of its medicines law in December 2025, with the new rules expected to apply from 2028.24

So the barrier is cost and uncertain return. A compound with weak early evidence, many existing sellers and no clear patient group is unlikely to attract a sponsor, and that is often the kind people buy outside pharmacies. Without public money, “does it work, and what harm does it do?” may never be answered.

In detail: Costs for people now , about 1 minute to read

Wegovy has been authorised in the EU since 2022,25 but in July 2024 the Zorginstituut advised against paying for it from Dutch basic insurance for obesity, citing unclear health gain, unclear long-term effect, no clear way of stopping, and costs of up to €1.3 billion a year.26 Those are real concerns. A new assessment is under way: the Zorginstituut’s scientific advisory council first discussed it on 5 October 2026.27 Meanwhile the CBG reports that these medicines are increasingly used as slimming aids without a prescription.28 Whether the two are linked has not been measured.

Retatrutide shows the gap from the other side. In a phase 3, double-blind, placebo-controlled trial of 2,339 adults with obesity and without diabetes, funded by its maker, average weight loss at 80 weeks was 17.6% to 25.0%, depending on dose, against 3.9% with placebo (Evidence level: Shown in controlled human trials).29 On 5 October 2026 it was not under EMA evaluation,30 while products sold as retatrutide were already being made and seized.2

What we propose

What should change?

Six legal steps. Each gives people better facts. None makes it easier to sell bad products.
Our six ideas. Something like each one is already in place.
ProposalSomething like it already exists
1. Public, independent trials of widely used compoundsIn a pilot started in 2021, EU regulators advised universities and non-profit groups that study older medicines8
2. Testing services for peptidesThe Dutch drug-checking service, possible since the 1990s31
3. Side-effect reporting that welcomes every productLareb accepts reports about products bought online32
4. Enforcement aimed at sellers and false claimsDutch medicines law is written around trade and advertising33,34
5. Guidance for doctors whose patients use these productsThe first Dutch clinic for health problems from anabolic steroids, opened in 201035
6. Faster conditional routes, open to non-commercial sponsorsEU conditional marketing authorisation36

None of these needs new science or weaker rules. Each answers one of the arguments for caution: testing reports problems but never certifies a product; trials replace guesses with evidence; enforcement stays aimed at the people who profit.

In detail: 1. Public trials of the compounds people actually use , about 1 minute to read

Once a substance is widely used, whether it works is a public health question. Most drugs tested in people never reach approval,13 which is why the test is worth paying for: a clear negative result protects people too.

In 2021 the EMA and national regulators started a pilot giving scientific advice to universities and non-profit groups studying new uses of older, off-patent medicines. The aim was evidence strong enough for a company to use in a later application.8 It covered only authorised medicines. We propose extending the idea, with public funding, to the few unauthorised compounds used most widely, chosen openly.

In detail: 2. Testing services for peptides , about 1 minute to read

Since the 1990s the Dutch Ministry of Health has made drug testing possible for people who use drugs, through DIMS at the Trimbos Institute; by 2011 more than 100,000 samples had been handed in.31 A systematic review of 90 studies found that such services appear to influence what people intend to do and do, especially after an unexpected result (Evidence level: Seen in humans in case reports or small uncontrolled studies). Most studies were cross-sectional, so the evidence is limited, and they are about recreational drugs, not peptides.37 Public laboratories already test peptide products that were seized or bought from illegal websites.19,3

To stop testing becoming marketing, a peptide service should report problems, never approval: warnings about dangerous batches, nothing a seller could show as a certificate, and a plain statement that one test describes one sample, not the next vial.

In detail: 3. Side-effect reporting that welcomes every product , about 1 minute to read

In the Netherlands anyone can report a side effect to Lareb, also for products bought online, and Lareb does not pass the report on to your doctor.32 Lareb has said that people who use illegal medicines can come to it too.38

The system exists; what is missing is trust and use. We propose saying clearly and often that such reports are welcome and confidential, and publishing what they show for unlicensed peptides. See if something goes wrong.

In detail: 4. Enforcement aimed at sellers and false claims , about 1 minute to read

Dutch medicines law forbids stocking, offering, selling, supplying and importing a medicine without a licence, and advertising it; breaches can be fined heavily.33,34,39 Using a product is not itself named as an offence, although importing one is, and the ban has no exception for own use.33 See Dutch law.

We support those rules. Enforcement should concentrate on sellers, above all those who make false health claims. In the US, the FDA has warned companies that labelled products “for research purposes” but sold them for use in people, with dosing instructions.6 Users are better reached with information than with fear, because fear keeps them away from doctors and from reporting.

In detail: 5. Guidance for doctors , about 1 minute to read

In 2014 the Endocrine Society, a medical society, noted that most users of performance-enhancing drugs are not athletes but people who lift weights, that their health risks are greatly underappreciated, and that observational studies are needed because trials cannot ethically copy such use.40 In the Netherlands, a first outpatient clinic for people with health problems from anabolic steroids opened in 2010.35

We propose practical guidance from professional bodies on which checks make sense for a patient who uses an unlicensed peptide, and why. A doctor who knows what to look for is someone a patient can tell. See monitoring.

In detail: 6. Clearer, faster conditional routes , about 1 minute to read

A conditional marketing authorisation can be granted on less complete data for a medicine that meets an unmet need, when having it now outweighs the risk of what is unknown. It lasts a year at a time, and the holder must complete agreed studies.36 But it assumes an applicant who will deliver full data later, usually a company. Dutch compassionate-use programmes can also only be started by a manufacturer.41

We propose routes a public body or university can use, with the same duties to keep collecting evidence, and enforced: EU cancer approvals show how long uncertainty can last after a medicine reaches the market.15 See legal routes to treatment.

What we do not argue

Are you saying these products are harmless?

No. We do not argue for weaker rules, or that anyone should use anything.
Six things this page does not say.
We do not argueWhy not
That the rules for selling medicines should be loosenedLicensing protects people from unknown products and false claims
That any compound on this site is free of risk, or that it worksFor most, nobody knows; each compound page says what is known
That anyone should use any productWe inform; the choice is yours
That the ban on advertising should goIt keeps commerce out of health information
That regulators act in bad faithTheir caution has good reasons, set out above
That the US compounding route is a modelIt gives access without trials or required side-effect reporting

We are not anti-regulation and not anti-peptide. We are for knowing more: what is in a product, what it does, and what harm it causes, so that people can act on facts rather than marketing.

In detail: Why the US vote on BPC-157 is not our model , about 2 minutes to read

On 23 July 2026 the FDA’s Pharmacy Compounding Advisory Committee (PCAC) voted 8–6, with one abstention, to recommend BPC-157 for the “503A list” of substances US pharmacies may use to compound medicines on prescription. It considered seven peptides and recommended six: BPC-157, KPV, TB-500, MOTS-c, Semax and epitalon. These results are as reported from the public meeting; the FDA has not posted minutes.42,43 The vote is advisory and non-binding, and it went against FDA staff’s own proposal.42,44 Legal compounding remains prohibited until the FDA formally adopts the recommendation and completes rulemaking.45

None of these peptides is an approved medicine in the EU, the UK or the US; Semax is registered as a medicine in Russia.9,46,47,48 A 503A listing would allow pharmacy compounding on prescription in the US. It is not a marketing authorisation, it says nothing about whether they work, and it changes nothing in the EU or the Netherlands.49,50

The FDA told its committee that a product compounded from a listed substance is not FDA-approved and need not follow the usual manufacturing rules (only the ban on unclean conditions applies).49 The pharmacy also need not report its side effects to the FDA.49 That is access without the evidence and warning signals we argue for.

What would change our mind

Could you be wrong?

Yes. Here is the evidence that would make us change this page.
What we would do if the evidence went against us.
If good evidence showed that…We would…
Clear safety information makes more people start using these productsSay so here, and rethink how such information should be given
Testing services are used mainly to market productsDrop or redesign that proposal
A compound causes serious harm in proper trialsSay so on its page, and support strong action against its sale
Enforcement aimed at users reduces harm more than information doesChange our position on enforcement

When we change this page, the change goes into the corrections log. How we keep opinion apart from the reference pages is in our editorial policy.

Sources

Every claim on this page links to one of these sources. Scholarly sources link to their DOI; regulatory sources to the regulator's own page.

In detail: All 50 sources, numbered as in the text , about 8 minutes to read
  1. Inspectie Gezondheidszorg en Jeugd (IGJ) en College ter Beoordeling van Geneesmiddelen (CBG) (2025). IGJ en CBG waarschuwen voor illegaal online aanbod van medicijnen. Regulator igj.nl (opens an external site) — accessed 22 October 2026 ↩
  2. Medicines and Healthcare products Regulatory Agency (2026). Two arrested during the MHRA's largest ever seizure of unlicensed weight loss medicines. GOV.UK. Regulator gov.uk (opens an external site) — accessed 22 October 2026 ↩
  3. Weber C, Krug O, Kamber M, Thevis M (2017). Qualitative and Semiquantitative Analysis of Doping Products Seized at the Swiss Border. Substance Use & Misuse 52:742-753. Research article doi:10.1080/10826084.2016.1263665 (opens an external site) ↩
  4. Ashraf AR, Mackey TK, Vida RG, Kulcsár G, Schmidt J, Balázs O, Domián BM, Li J, Csákó I, Fittler A (2024). Multifactor Quality and Safety Analysis of Semaglutide Products Sold by Online Sellers Without a Prescription: Market Surveillance, Content Analysis, and Product Purchase Evaluation Study. Journal of Medical Internet Research 26:e65440. Research article doi:10.2196/65440 (opens an external site) ↩
  5. Hazell L, Shakir SA (2006). Under-reporting of adverse drug reactions: a systematic review. Drug Safety 29:385-396. Review doi:10.2165/00002018-200629050-00003 (opens an external site) ↩
  6. U.S. Food and Drug Administration (2026). FDA's concerns with unapproved GLP-1 drugs used for weight loss. Regulator fda.gov (opens an external site) — accessed 20 October 2026 ↩
  7. Pope HG Jr, Kanayama G, Ionescu-Pioggia M, Hudson JI (2004). Anabolic steroid users' attitudes towards physicians. Addiction 99:1189-1194. Research article doi:10.1111/j.1360-0443.2004.00781.x (opens an external site) ↩
  8. European Medicines Agency (2021). Repurposing of authorised medicines: pilot to support not-for-profit organisations and academia. Regulator ema.europa.eu (opens an external site) — accessed 22 October 2026 ↩
  9. U.S. Food and Drug Administration (2026). FDA Briefing Document for BPC-157-Related Bulk Drug Substances (BPC-157 (free base) and BPC-157 acetate), Pharmacy Compounding Advisory Committee meeting, 23–24 July 2026. Regulator fda.gov (opens an external site) — accessed 20 October 2026 ↩
  10. Kim JH, Scialli AR (2011). Thalidomide: the tragedy of birth defects and the effective treatment of disease. Toxicological Sciences 122:1-6. Review doi:10.1093/toxsci/kfr088 (opens an external site) ↩
  11. U.S. Food and Drug Administration (2018). Frances Oldham Kelsey: Medical reviewer famous for averting a public health tragedy. Regulator fda.gov (opens an external site) — accessed 22 October 2026 ↩
  12. European Commission, Directorate-General for Health and Food Safety (2015). 50 years of EU pharmaceutical legislation: milestones (timeline). Regulator ec.europa.eu (opens an external site) — accessed 22 October 2026 ↩
  13. Wong CH, Siah KW, Lo AW (2019). Estimation of clinical trial success rates and related parameters. Biostatistics 20:273-286. Research article doi:10.1093/biostatistics/kxx069 (opens an external site) ↩
  14. Begley CG, Ellis LM (2012). Drug development: Raise standards for preclinical cancer research. Nature 483:531-533. Research article doi:10.1038/483531a (opens an external site) ↩
  15. Davis C, Naci H, Gurpinar E, Poplavska E, Pinto A, Aggarwal A (2017). Availability of evidence of benefits on overall survival and quality of life of cancer drugs approved by European Medicines Agency: retrospective cohort study of drug approvals 2009-13. BMJ 359:j4530. Research article doi:10.1136/bmj.j4530 (opens an external site) ↩
  16. Medicines and Healthcare products Regulatory Agency (2026). MHRA seizes illegal medicines worth almost £45m in 2025 – disrupting major criminal networks. GOV.UK. Regulator gov.uk (opens an external site) — accessed 22 October 2026 ↩
  17. Zinzi A, Gaio M, Ruggiero R, Mascolo A, Riemma MA, Cipriani M, Laino LV, Berrino L, Rossi F, Capuano A (2026). Unmasking counterfeit semaglutide: analysis of real-world safety data from EudraVigilance. Frontiers in Pharmacology 17:1805842. Research article doi:10.3389/fphar.2026.1805842 (opens an external site) ↩
  18. Piatkowski T, Craven A, Cornell S, Ferris J (2026). Composition and Labelling Accuracy of Products Sold as Retatrutide in Australia. Drug and Alcohol Review 45:e70231. Research article doi:10.1111/dar.70231 (opens an external site) ↩
  19. Janvier S, Cheyns K, Canfyn M, Goscinny S, De Spiegeleer B, Vanhee C, Deconinck E (2018). Impurity profiling of the most frequently encountered falsified polypeptide drugs on the Belgian market. Talanta 188:795-807. Research article doi:10.1016/j.talanta.2018.06.023 (opens an external site) ↩
  20. KNMG (Royal Dutch Medical Association) (2024). Medisch beroepsgeheim: wat en waarom. Web page knmg.nl (opens an external site) — accessed 20 October 2026 ↩
  21. Bundesinstitut für Arzneimittel und Medizinprodukte (BfArM) (2024). Fälschung des Arzneimittels Ozempic® (updates 11.10.2023 – 15.02.2024). Regulator bfarm.de (opens an external site) — accessed 20 October 2026 ↩
  22. Wouters OJ, McKee M, Luyten J (2020). Estimated Research and Development Investment Needed to Bring a New Medicine to Market, 2009-2018. JAMA 323:844-853. Research article doi:10.1001/jama.2020.1166 (opens an external site) ↩
  23. European Parliament and Council of the European Union (2001). Directive 2001/83/EC on the Community code relating to medicinal products for human use (consolidated text). Official Journal of the European Communities, L 311. Law eur-lex.europa.eu (opens an external site) — accessed 20 October 2026 ↩
  24. European Medicines Agency (2026). Reform of the EU pharmaceutical legislation. Regulator ema.europa.eu (opens an external site) — accessed 22 October 2026 ↩
  25. European Medicines Agency (2026). Wegovy (semaglutide): EPAR — overview and product information. Official product information ema.europa.eu (opens an external site) — accessed 20 October 2026 ↩
  26. Zorginstituut Nederland (2024). Zorginstituut: geen vergoeding Wegovy voor obesitas wegens onduidelijkheid gezondheidseffecten. Regulator zorginstituutnederland.nl (opens an external site) — accessed 20 October 2026 ↩
  27. Zorginstituut Nederland (2026). Advies — wel of niet vergoeden semaglutide (Wegovy®) voor de behandeling van obesitas (werkagenda). Regulator zorginstituutnederland.nl (opens an external site) — accessed 20 October 2026 ↩
  28. College ter Beoordeling van Geneesmiddelen (CBG-MEB) (2026). Standpunt: Gebruik diabetes- en afslankmedicijnen alleen zoals ze bedoeld zijn. Regulator cbg-meb.nl (opens an external site) — accessed 20 October 2026 ↩
  29. Jastreboff AM, Kaplan LM, Davies MJ, Wilding JPH, Ahmad NN, Murray M, et al. (2026). Retatrutide, a Triple Hormone Receptor Agonist, for Treatment of Obesity. New England Journal of Medicine. Clinical trial doi:10.1056/NEJMoa2604169 (opens an external site) ↩
  30. European Medicines Agency (2026). Applications for new human medicines under evaluation by the CHMP — October 2026 (EMA/222468/2026). Regulator ema.europa.eu (opens an external site) — accessed 20 October 2026 ↩
  31. Brunt TM, Niesink RJ (2011). The Drug Information and Monitoring System (DIMS) in the Netherlands: implementation, results, and international comparison. Drug Testing and Analysis 3:621-634. Review doi:10.1002/dta.323 (opens an external site) ↩
  32. Bijwerkingencentrum Lareb (2026). Alles over bijwerkingen melden. Web page lareb.nl (opens an external site) — accessed 20 October 2026 ↩
  33. Staten-Generaal / Koninkrijk der Nederlanden (2007). Geneesmiddelenwet, artikel 40 (verbod op geneesmiddelen zonder handelsvergunning, en de uitzonderingen). wetten.overheid.nl (BWBR0021505), version in force from 9 September 2025. Law wetten.overheid.nl (opens an external site) — accessed 22 October 2026 ↩
  34. Staten-Generaal / Koninkrijk der Nederlanden (2007). Geneesmiddelenwet, artikelen 84 en 85 (reclame; publieksreclame). wetten.overheid.nl (BWBR0021505), version in force from 9 September 2025. Law wetten.overheid.nl (opens an external site) — accessed 22 October 2026 ↩
  35. Dopingautoriteit (Doping Authority Netherlands) (2025). Pim de Ronde benoemd tot hoogleraar doping en gezondheid aan VU Amsterdam. Web page dopingautoriteit.nl (opens an external site) — accessed 22 October 2026 ↩
  36. European Medicines Agency (2026). Conditional marketing authorisation. Regulator ema.europa.eu (opens an external site) — accessed 22 October 2026 ↩
  37. Maghsoudi N, Tanguay J, Scarfone K, Rammohan I, Ziegler C, Werb D, Scheim AI (2022). Drug checking services for people who use drugs: a systematic review. Addiction 117:532-544. Review doi:10.1111/add.15734 (opens an external site) ↩
  38. Bijwerkingencentrum Lareb (2021). Risico's illegale geneesmiddelen (Medicijnjournaal december 2021). Web page lareb.nl (opens an external site) — accessed 22 October 2026 ↩
  39. Staten-Generaal / Koninkrijk der Nederlanden (2007). Geneesmiddelenwet, artikel 101 (bestuurlijke boete). wetten.overheid.nl (BWBR0021505), version in force from 9 September 2025. Law wetten.overheid.nl (opens an external site) — accessed 22 October 2026 ↩
  40. Pope HG Jr, Wood RI, Rogol A, Nyberg F, Bowers L, Bhasin S (2014). Adverse health consequences of performance-enhancing drugs: an Endocrine Society scientific statement. Endocrine Reviews 35:341-375. Guideline doi:10.1210/er.2013-1058 (opens an external site) ↩
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