Before you consider a peptide: who should not, and why

In short

About 11 minutes for the short version; 16 with every detail open.

  • Some people should not use these products at all. This page says who, and why.
  • Pregnancy, breastfeeding and being under 18 rule them out. So does cancer, for healing and growth peptides.
  • With insulin or some diabetes tablets, GLP-1 type products can make blood sugar fall too low.
  • Never share needles, vials or pens. Never stop a medicine your doctor prescribed.
  • Tell your doctor what you plan. A doctor can check these risks with you.
Last reviewed
A stethoscope with black tubing and a silver chest piece lying on a plain grey surface.
Talk to a doctor before you start. Photo: Jacek Halicki (Wikimedia Commons) CC BY-SA 4.0 Image details

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

Who should not use these products?

People who are pregnant, breastfeeding or under 18. Cancer and some other illnesses rule out some products.
Who should not use which kind of product, and the main reason why
SituationWhich productsMain reason
Pregnant, breastfeeding or trying to conceiveAllHarm to an unborn baby seen in animals for GLP-1 medicines; no human data for the others
Under 18AllThe body is still growing; long-term effects in young people are unknown
Cancer now or in the pastHealing and growth peptides (BPC-157, TB-500, growth hormone boosters)They push blood vessel growth, cell movement or growth hormone, which could help a tumour grow
Insulin or sulfonylurea tabletsGLP-1 type products (semaglutide, tirzepatide, retatrutide)Together they can push blood sugar dangerously low
Heart disease or high blood pressureMelanocortin peptides (melanotan II, PT-141)PT-141 briefly raises blood pressure after each dose; one case report of a racing heart after melanotan II
Eating disorder, now or in the pastAppetite-lowering products (GLP-1 type)Less hunger can make restriction worse
Kidney diseaseAll, especially GLP-1 typeKidneys clear many peptides; vomiting and diarrhoea can harm the kidneys
Pancreatitis in the pastGLP-1 typeThey are linked to an inflamed pancreas
Medullary thyroid cancer or MEN 2 in you or your familyGLP-1 typeThyroid tumours in rodents; US labels forbid use
Weak immune systemAll injectionsHigher risk of infection and sepsis
Blood thinnersAll injections, and some products directlyMore bleeding and bruising; some products change clotting
Competitive sportMost unapproved peptidesBanned at all times; you are responsible for what is in your body

This is not a full list for any one product. A doctor who knows you can check what applies to you. See talking to your doctor.

In detail: Why we made this list ourselves , about 1 minute to read

An authorised medicine comes with a list of people who must not use it. Doctors call these contraindications. The list exists because the medicine was tested and the risks were written down.

Most peptides sold online have no such list. They were never tested well enough in people.1,2,3 So we work from what each substance does in the body. If a substance pushes growth, it is a worry for someone with cancer. If it lowers blood sugar, it is a worry for someone on insulin. This page explains these situations one by one.

Pregnancy and breastfeeding

Can I use them if I am pregnant or breastfeeding?

No. Animal tests showed harm to the unborn young with GLP-1 medicines. For others, nobody knows.
Labels say to stop one or two months before a planned pregnancy. Other peptides have no human data. How long before a planned pregnancy the EU labels say to stop.
  • Wegovy (semaglutide)

    stop at least 2 months before

  • Mounjaro (tirzepatide)

    stop at least 1 month before

  • Experimental peptides (BPC-157, TB-500, KPV)

    Not known: no human pregnancy data at all

Sources Wegovy (semaglutide); Mounjaro (tirzepatide); 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; FDA Briefing Document for TB-500-Related Bulk Drug Substances (TB-500 (free base) and TB-500 acetate), Pharmacy Compounding Advisory Committee meeting, 23–24 July 2026; FDA Briefing Document for KPV-Related Bulk Drug Substances (KPV (free base) and KPV acetate), Pharmacy Compounding Advisory Committee meeting, 23-24 July 20264,5,1,2,3

An unborn baby grows very fast. A substance that changes growth, blood vessels, hormones or appetite could disturb that growth. “No data” does not mean “safe”. It means nobody knows.

In detail: What the labels and the animal studies say , about 1 minute to read

For GLP-1 medicines, animal studies showed harm to the unborn young. The EU label for Wegovy says not to use it in pregnancy or while breastfeeding. It says to stop at least 2 months before a planned pregnancy. The reason is that the medicine stays in the body for a long time. For Mounjaro the label says to stop at least 1 month before.4,5

For experimental peptides there are no human pregnancy data at all. BPC-157 has one study in pregnant rats. It found no birth defects in the young rats. But it did not test fertility, or how the young grew up after birth. TB-500 and KPV have no such studies.1,2,3

Under 18

Can teenagers use them?

We advise against unapproved peptides under 18. Nobody has studied what they do to a growing body.
Even a teen medicine has open questions. For unapproved peptides there is nothing to go on.
Authorised medicine with a use in teenagers (for example Wegovy)Unapproved peptide
Authorised for teenagers?Yes Wegovy from age 12, on prescription4No Not an approved medicine
Long-term effects in teenagers known?Unknown Effects on bones, fertility and mental health are still uncertain6Unknown There is nothing to go on

Teenagers are still growing. The teenage years are the key time for building strong bones.6

In detail: Growth signals, and what is known about authorised medicines , about 1 minute to read

Some peptides raise growth hormone, which is a growth signal.7 What extra growth signals do to a body that is still growing has not been studied.

Some authorised medicines are allowed for teenagers. Wegovy, for example, is authorised from age 12, on prescription.4 Even for these, the long-term effects on bones, fertility and mental health in teenagers are still uncertain.6 For unapproved peptides, there is nothing to go on. We advise against them for anyone under 18.

Cancer, now or in the past

Can I use them if I have, or had, cancer?

Not healing or growth peptides. They push growth signals that could help a tumour grow.
Some push blood vessel growth or growth signals. What they do to a tumour in people is unknown.
BPC-157TB-500Growth hormone boosters (CJC-1295, ipamorelin, tesamorelin)
Pushes blood vessel growth or growth signals?Yes More blood vessel growth in cells, chick eggs and rats8Unknown TB-500 itself was not tested. In mice, melanoma cells with extra thymosin beta-4, the protein it is based on, spread further9,2Yes Tesamorelin raises growth hormone and IGF-1, which are growth factors7. Anti-doping rules class CJC-1295 and ipamorelin as growth hormone releasing factors10
Could it feed a tumour in people?Unknown Never studiedUnknown Never studiedUnknown Never studied. The tesamorelin label forbids its use in active cancer7

A tumour needs a blood supply to grow. Making new blood vessels is one of the basic tools of cancer.11

If you have had cancer, or have an unexplained lump, do not use them. See BPC-157, TB-500, CJC-1295, ipamorelin and tesamorelin.

In detail: What the lab and animal studies found, and what nobody knows , about 1 minute to read

Several “healing” peptides act on exactly this. In studies in cells, chick eggs and rats, BPC-157 increased blood vessel growth (Evidence level: Shown in animal studies).8 In a study in mice, melanoma cells that made extra thymosin beta-4 spread further and grew more blood vessels (Evidence level: Shown in animal studies).9 Thymosin beta-4 is the natural protein that TB-500 is based on. TB-500 itself was not tested in that study.2 Tesamorelin, an authorised growth hormone booster, raises growth hormone and IGF-1, which are growth factors. Its label forbids its use in active cancer.7 Anti-doping rules class CJC-1295 and ipamorelin as growth hormone releasing factors too.10

Whether these peptides could feed a hidden or treated tumour in people has never been studied. (Evidence level: Proposed, not demonstrated in any experiment) Nobody can tell you the risk is low.

In detail: Tanning peptides after melanoma , about 1 minute to read

Tanning peptides are a separate worry for anyone who has had melanoma. In one case report, a man with past melanoma injected an alpha-MSH peptide. New, abnormal-looking moles appeared, and old moles grew darker.12 See melanotan II.

Diabetes treated with insulin or sulfonylurea tablets

Can I use them with insulin or diabetes tablets?

Not without your doctor. Together with a GLP-1 type product, blood sugar can fall dangerously low.

The short animation shows why the combination can push blood sugar too low.

Animation · 25 seconds GLP-1-type medicines (such as semaglutide or tirzepatide) with insulin or a sulfonylurea: the risk of low blood sugar

Your device asks for less motion, so this animation does not play. The picture shows the end result and the list explains every step.

  1. Alone, a GLP-1-type medicine lowers high sugar. Near normal, it works less. Sugar rarely gets too low.

    Evidence: In humans

  2. Insulin lowers sugar too. So do tablets called sulfonylureas. They still work when sugar is normal or low.

    Evidence: In humans

  3. Used together, they can push blood sugar too low. This is called hypoglycaemia.

    Evidence: In humans

  4. So the prescriber may lower the insulin or tablet dose. The labels suggest this.

    Evidence: In humans

  5. Shaking, sweating or confused? Take sugar if the person can swallow. If not, call your local emergency number.

    Evidence: In humans

In short: On its own, a GLP-1-type medicine such as semaglutide or tirzepatide rarely makes blood sugar too low. With insulin or a sulfonylurea tablet it can, so the prescriber may lower the insulin or tablet dose. Know the signs and take sugar at once. If the person cannot swallow, call your local emergency number.

Lines: solid = shown in people

Based on: Mounjaro (tirzepatide)5; Ozempic (semaglutide)13; Sola et al. (2015)14; American Diabetes Association Professional Practice Committee for Diabetes (2026)15

Never use a GLP-1 type product instead of insulin. See semaglutide, tirzepatide and retatrutide.

In detail: Why the combination is the problem, and what the labels say , about 1 minute to read

GLP-1 type products (semaglutide, tirzepatide, retatrutide) make the pancreas release more insulin, but mainly when blood sugar is high. On their own, they rarely push blood sugar too low.4

Insulin and sulfonylurea tablets (such as gliclazide) work differently. They lower blood sugar whatever its level. Together with a GLP-1 type product, blood sugar can fall dangerously low. The EU labels warn about this, and a doctor may need to lower the insulin or tablet dose.4,5,14

The Wegovy label says semaglutide is not a substitute for insulin, and that it was not studied in type 1 diabetes.4

Heart disease or high blood pressure

Can I use them with heart disease or high blood pressure?

Do not use PT-141 or melanotan II. PT-141 raises blood pressure for some hours after each dose.
PT-141 raises blood pressure. For melanotan II, there is one case report of a racing heart.
Bremelanotide (PT-141)Melanotan II
An authorised medicine?Yes In the US, as Vyleesi16No Not in the EU17
Raises blood pressure or heart rate?Yes Blood pressure rises for some hours after each dose16Unknown One case report of a racing heart18
Label warning about heart disease?Yes Not with uncontrolled high blood pressure or known heart disease16No No EU label, because it is not authorised17

See PT-141 and melanotan II.

In detail: What the label and the case report say , about 1 minute to read

Bremelanotide (PT-141) is a melanocortin peptide. It is authorised in the US as Vyleesi. Its label says it raises blood pressure for some hours after each dose. It must not be used with uncontrolled high blood pressure or known heart disease.16

Melanotan II is a close relative of bremelanotide.18 It is not an authorised medicine in the EU.17 In one case report, a man had a racing heart, muscle breakdown and kidney problems after injecting it.18

Eating disorders

Can I use them if I have had an eating disorder?

Not products that lower hunger, unless your treatment team agrees. Less hunger can make restriction worse.
Why less hunger can be a danger for someone who restricts food
  1. GLP-1 type products make you less hungry and full sooner.4,6
  2. For someone who restricts food, less hunger can make the restriction deeper.
  3. Experts are concerned about misuse by people with eating disorders.19

If you have, or had, an eating disorder, do not use appetite-lowering products without your treatment team.

In detail: What the studies show, and their limits , about 1 minute to read

A 2025 review looked at 25 studies in people with obesity or type 2 diabetes. Eating behaviour mostly improved or stayed the same. The data were limited.20

One case report describes misuse of semaglutide by a person with atypical anorexia.21

Kidney disease

Can I use them with kidney disease?

Ask a doctor first. A product may stay in you longer, and fluid loss can harm the kidneys.
For semaglutide, the effect of weak kidneys was measured. For unapproved peptides, it was not.
Semaglutide (Wegovy)Unapproved peptides
Measured in people with kidney disease?Yes Kidney disease did not change the amount in the blood in a way that matters4No Nobody has measured it
More side effects with kidney disease?Yes People with moderate kidney disease may get more stomach and gut side effects4Unknown Not studied
Advised with severe kidney disease?No Not recommended4Unknown Not studied

The kidneys filter many peptides out of the blood and break them down.22 If your kidneys work less well, a product may stay in your body longer than expected.

In detail: Fluid loss, and what the semaglutide label says , about 1 minute to read

This is not true for every peptide. For semaglutide, kidney disease did not change the amount in the blood in a way that matters.4 For unapproved peptides, nobody has measured it.

GLP-1 type products often cause vomiting and diarrhoea at first. Losing a lot of fluid can, in rare cases, damage the kidneys.5,4 People with moderate kidney disease may get more stomach and gut side effects on semaglutide. It is not recommended with severe kidney disease.4

Pancreatitis, or thyroid cancer in the family

What if I had pancreatitis, or thyroid cancer runs in my family?

Talk to a doctor first. Labels warn about pancreatitis. The US label also warns about thyroid cancer.
The US label forbids use with a family risk of medullary thyroid cancer. The EU label does not. Medullary thyroid cancer (MTC) or MEN 2, in you or your family.
EU label (Wegovy)US label (Ozempic)
Thyroid tumours in rodents?Yes GLP-1 medicines caused thyroid tumours in rodents4Yes The same finding23
Shown to happen in people?Unknown The risk for people is thought to be low, but it cannot be ruled out4Unknown Unknown23
Use forbidden with MTC or MEN 2 in you or your family?No Not a formal contraindication, so discuss it with a doctor4Yes The US label forbids use in this group23
  • Pancreatitis in the past: GLP-1 medicines are linked to acute pancreatitis. The labels advise caution if you have had it.4,5
In detail: The thyroid warning in full , about 1 minute to read
  • Medullary thyroid cancer or MEN 2, in you or your family: GLP-1 medicines caused thyroid tumours in rodents. Whether this happens in people is unknown. The EU label says the risk for people is thought to be low, but it cannot be ruled out. The US label forbids use in this group. In the EU it is not a formal contraindication, so discuss it with a doctor.23,4

A weak immune system

What if my immune system is weak?

Each injection is more likely to cause an infection. Talk to your own doctor first.
Why a weak immune system makes each injection riskier
  1. Some illnesses and medicines weaken the immune system. Examples are HIV, chemotherapy, steroids and other medicines that suppress the immune system.
  2. A weak immune system makes skin infections and sepsis more likely.24,25,26
  3. Every injection is a small wound, so the risk of each injection is higher.

Talk to the doctor who treats your condition first.

Blood thinners

Can I use them with blood thinners?

Talk to your doctor first. Injections bruise more, and some products may change clotting.
Two ways a product can add to the effect of a blood thinner
  1. Through the injection. Blood thinners (anticoagulants) make it take longer for blood to clot. You bruise and bleed more easily.27 So injections can bruise more.
  2. Through the product itself. Some products may also act on clotting directly. In 28-day studies in rats and dogs, BPC-157 changed a blood clotting test.1
In detail: The INR test, and semaglutide with blood thinners , about 1 minute to read

The INR is the blood test for warfarin-type blood thinners. A lower INR has been reported in people who took semaglutide with acenocoumarol, a blood thinner of this type. So the label advises frequent INR checks when someone on these blood thinners starts semaglutide.4

Competitive sport

Can I use them if I compete in sport?

Most are banned at all times. A positive test counts, even if you did not mean it.
Most unapproved peptides and growth hormone boosters are banned in sport at all times.
Unapproved peptides (for example BPC-157)Growth hormone boosters (CJC-1295, ipamorelin, tesamorelin)
Banned in sport?Yes At all times. WADA bans any substance with no approval for human use, and names BPC-15710,28Yes At all times10,28
A violation even if you did not mean to take it?Yes Strict liability: what is found in your body counts29,30Yes The same rule applies29,30

A product with the wrong contents can end a career. See sport and doping.

In detail: What the anti-doping rules say , about 1 minute to read

Most unapproved peptides are banned in sport at all times. The World Anti-Doping Agency (WADA) bans any substance with no approval for human use, and names BPC-157. It also bans growth hormone boosters such as CJC-1295, ipamorelin and tesamorelin.10,28

Anti-doping rules use strict liability. If a banned substance is found in your body, that is a rule violation. This is true even if you did not mean to take it.29,30

Rules for everyone

What applies to everyone?

Never share equipment. Never use a product that looks wrong. Never stop a prescribed medicine.
Three rules for everyone, and the main reason for each
RuleWhy
Never share needles, syringes, vials or pensBlood on them can pass on HIV and hepatitis B or C. A shared vial or pen can do this even with a new needle.31,23
Never use a product that looks wrong4,7,32It may be spoiled or contaminated.
Never stop a medicine your doctor prescribed33The condition it treats can come back or get worse.
In detail: Why sharing is dangerous, even with a new needle , about 1 minute to read

A used needle can carry a tiny amount of blood into a vial or a pen. The next person can then get HIV or hepatitis B or C, even with a new needle. Blood does not need to be visible to pass on these viruses.31,23 Never share a pen, even if you change the needle. Never share a vial, water or other equipment.23,4,34,35

In detail: What a product that looks wrong can mean , about 1 minute to read

A liquid that should be clear but is cloudy, coloured or has bits in it may be spoiled or contaminated. So may a vial with a broken seal. Do not use it.4,7,32 See sterile technique and product risk.

In detail: Why not to stop a prescribed medicine , about 1 minute to read

Do not stop or change a prescribed medicine on your own.33 The condition it treats can come back or get worse. If you think a peptide could replace a medicine, discuss it with your doctor first.

If you go ahead: check the product

What should I check before I use a product?

The seal, the label, how it looks and how it was kept. Keep the vial.

If your product did not come from a pharmacy: check before you use it

These checks can show that something is wrong. None of them can show that a product is good or free of germs.36,37,38

Tick each box when you have checked it.

  • The seal and the vial are whole

    A broken cap or seal, or a cracked vial, can let germs in. Then do not use it.39,32,31

  • The label shows the name, amount, batch number and expiry date

    In the EU, a medicine must show all four, even on a small vial. If one is missing, or the date has passed, that is a warning sign. Take a photo of the label.40,39

  • It looks right

    A liquid, or a powder after mixing, should be clear and colourless, with no bits. Is it cloudy, has it changed colour, or do you see bits? Then do not use it.7,4

  • A lab report proves little if:

    • its batch number is not the one on your vial;
    • it does not name the lab, or has no date or signature;
    • it shows only purity (HPLC), with no test of what it is, such as mass spectrometry;
    • it has no test for germs (sterility) or for toxins from germs (endotoxin).

    Even a full report covers only one sample. A report from the seller comes from someone who gains if it looks good. It cannot show that your vial is clean.41,42,1,2,43

  • It was kept as the label says

    Heat, freezing and sunlight can damage a peptide. Did it arrive warm, or was it frozen? Then do not use it. Often nobody can tell you how it was kept on the way. If you cannot know, you cannot rule out damage. When in doubt, throw it out.4,44,45,31

  • Clean steps, and a new sterile needle and syringe every time

    Wash your hands and wipe the rubber top with alcohol. Never share a needle, a syringe or a vial.31,46,44

  • Keep the vial, its label and any papers

    Keep them, even when the vial is empty, until you know you feel well. If you need a doctor, bring them. A lab can test what was inside.47,48

  • Tell a doctor, and agree which checks fit you

    A doctor can help you choose blood tests that fit what you use. In the Netherlands, your doctor must keep what you say private.49,50,51

  • Know the warning signs before you start

    Spreading redness, fever, a swollen face or hard breathing need help fast. If it is severe, call your local emergency number.24,25,52

Tell your doctor

Should I tell my doctor?

Yes. A doctor can check these risks with you. In the Netherlands, doctors must keep it private.

A doctor can check for the risks on this page. Many need only a conversation or a simple test. In the Netherlands, your doctor must keep what you say private.51

  • Are you pregnant, breastfeeding or trying to conceive?
  • Are you under 18?
  • Have you ever had cancer, or do you have an unexplained lump?
  • Do you use insulin or diabetes tablets?
  • Do you have heart disease or high blood pressure?
  • Have you ever had an eating disorder?
  • Do you have kidney disease, or have you had pancreatitis?
  • Has anyone in your family had medullary thyroid cancer or MEN 2?
  • Do you have a weak immune system, or take blood thinners?
  • Do you compete in a sport with doping tests?

If you answer yes to any of these, talk to a doctor before you start. Then read the warning signs, so you know when to get help.

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 52 sources, numbered as in the text , about 8 minutes to read
  1. 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 ↩
  2. U.S. Food and Drug Administration (2026). FDA Briefing Document for TB-500-Related Bulk Drug Substances (TB-500 (free base) and TB-500 acetate), Pharmacy Compounding Advisory Committee meeting, 23–24 July 2026. Regulator fda.gov (opens an external site) — accessed 20 October 2026 ↩
  3. U.S. Food and Drug Administration (2026). FDA Briefing Document for KPV-Related Bulk Drug Substances (KPV (free base) and KPV acetate), Pharmacy Compounding Advisory Committee meeting, 23-24 July 2026. Regulator fda.gov (opens an external site) — accessed 20 October 2026 ↩
  4. 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 ↩
  5. European Medicines Agency (2026). Mounjaro (tirzepatide): EPAR — overview and product information. Official product information ema.europa.eu (opens an external site) — accessed 20 October 2026 ↩
  6. Haider MA, Javed H (2026). GLP-1 Receptor Agonists in Adolescents: Emerging Endocrine, Reproductive, and Psychosocial Concerns. Journal of Pediatric and Adolescent Gynecology. Research article doi:10.1016/j.jpag.2026.06.017 (opens an external site) ↩
  7. U.S. Food and Drug Administration / DailyMed (National Library of Medicine) (2026). EGRIFTA SV (tesamorelin for injection): prescribing information and instructions for use. Official product information dailymed.nlm.nih.gov (opens an external site) — accessed 20 October 2026 ↩
  8. Hsieh MJ, Liu HT, Wang CN, Huang HY, Lin Y, et al. (2017). Therapeutic potential of pro-angiogenic BPC157 is associated with VEGFR2 activation and up-regulation. Journal of Molecular Medicine 95:323-333. Research article doi:10.1007/s00109-016-1488-y (opens an external site) ↩
  9. Cha HJ, Jeong MJ, Kleinman HK (2003). Role of thymosin beta4 in tumor metastasis and angiogenesis. Journal of the National Cancer Institute 95:1674-1680. Research article doi:10.1093/jnci/djg100 (opens an external site) ↩
  10. World Anti-Doping Agency (2025). World Anti-Doping Code International Standard: Prohibited List 2026. Regulator wada-ama.org (opens an external site) — accessed 20 October 2026 ↩
  11. Hanahan D, Weinberg RA (2011). Hallmarks of cancer: the next generation. Cell 144:646-674. Review doi:10.1016/j.cell.2011.02.013 (opens an external site) ↩
  12. Cardones AR, Grichnik JM (2009). alpha-Melanocyte-stimulating hormone-induced eruptive nevi. Archives of Dermatology 145:441-444. Research article doi:10.1001/archdermatol.2008.623 (opens an external site) ↩
  13. European Medicines Agency (2026). Ozempic (semaglutide): EPAR — overview and product information. Official product information ema.europa.eu (opens an external site) — accessed 20 October 2026 ↩
  14. Sola D, Rossi L, Schianca GP, Maffioli P, Bigliocca M, Mella R, Corlianò F, Fra GP, Bartoli E, Derosa G (2015). Sulfonylureas and their use in clinical practice. Archives of Medical Science 11:840-848. Review doi:10.5114/aoms.2015.53304 (opens an external site) ↩
  15. American Diabetes Association Professional Practice Committee for Diabetes (2026). 6. Glycemic Goals, Hypoglycemia, and Hyperglycemic Crises: Standards of Care in Diabetes—2026. Diabetes Care 49:S132-S149. Guideline doi:10.2337/dc26-S006 (opens an external site) ↩
  16. U.S. Food and Drug Administration / DailyMed (National Library of Medicine) (2025). VYLEESI (bremelanotide injection): prescribing information. Official product information dailymed.nlm.nih.gov (opens an external site) — accessed 20 October 2026 ↩
  17. European Medicines Agency (2026). Medicines (search of centrally authorised medicines and EPARs). Regulator ema.europa.eu (opens an external site) — accessed 20 October 2026 ↩
  18. Nelson ME, Bryant SM, Aks SE (2012). Melanotan II injection resulting in systemic toxicity and rhabdomyolysis. Clinical Toxicology 50:1169-1173. Research article doi:10.3109/15563650.2012.740637 (opens an external site) ↩
  19. Schaefer LM, Kerver GA, Allison KC, Kohoutek B, Steffen KJ (2025). Use (and Potential for Abuse) of Glucagon-Like Peptide-1 Medications Among Individuals with Eating Disorders: Empirical Review and Clinical Guidance. The Psychiatric Clinics of North America 49:183-202. Review doi:10.1016/j.psc.2025.08.013 (opens an external site) ↩
  20. Jebeile H, Danielsen YS, Sumithran P, Lorien S, Jardine IR, Baur LA, Lister NB (2025). GLP-1 Receptor Agonist Medications for Obesity and Type 2 Diabetes Treatment: A Rapid Review of Changes in Eating Behaviors and Eating Disorder Risk. Obesity Reviews 27:e70049. Review doi:10.1111/obr.70049 (opens an external site) ↩
  21. Guerdjikova AI, Ward A, Ontiveros M, McElroy SL (2024). Semaglutide Misuse in Atypical Anorexia Nervosa-A Case Report. Journal of Clinical Psychopharmacology 44:179-180. Research article doi:10.1097/JCP.0000000000001820 (opens an external site) ↩
  22. Diao L, Meibohm B (2013). Pharmacokinetics and pharmacokinetic-pharmacodynamic correlations of therapeutic peptides. Clinical Pharmacokinetics 52:855-868. Review doi:10.1007/s40262-013-0079-0 (opens an external site) ↩
  23. U.S. Food and Drug Administration / Novo Nordisk (2026). OZEMPIC (semaglutide) injection — prescribing information (revised 05/2026). Official product information accessdata.fda.gov (opens an external site) — accessed 20 October 2026 ↩
  24. NHS (England) (2024). Cellulitis. Web page nhs.uk (opens an external site) — accessed 20 October 2026 ↩
  25. NHS (England) (2026). Sepsis. Web page nhs.uk (opens an external site) — accessed 20 October 2026 ↩
  26. NHS (England) (2023). Boils. Web page nhs.uk (opens an external site) — accessed 20 October 2026 ↩
  27. NHS (England) (2024). Anticoagulant medicines: side effects. Web page nhs.uk (opens an external site) — accessed 20 October 2026 ↩
  28. World Anti-Doping Agency (2026). World Anti-Doping Code International Standard: Prohibited List 2027 (in effect 1 January 2027). Regulator wada-ama.org (opens an external site) — accessed 20 October 2026 ↩
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