Foundations

What a doctor checks before prescribing GLP-1 medication

Before GLP-1 medication is prescribed, most of what a doctor asks has little to do with the number on the scale. The thyroid history in your family, whether a pregnancy is planned, whether you have an operation booked. Dr Ong Jin Khang of The Retreat Clinic in Setia Alam sets out what is checked before anything is written, and why in Malaysia this class reaches a patient no other way.

A consulting room desk in morning daylight with an open patient file, a blood pressure cuff and a pen, no patient and no medicine present

The question about your family's thyroid history is not small talk.

Why GLP-1 medication is a prescription and not a purchase

Almost everyone who asks about this medicine has already read about it, and a good number have been offered it by an account on a phone with nobody asking what else they take in the morning. The legal position comes first here, so it goes first.

GLP-1 receptor agonists are classified as Group B poisons under the Poisons Act 1952. The Act sets out what that means: a Group B poison is dispensed against a prescription from a registered medical practitioner, a dentist or a veterinary surgeon. Reported alongside that classification is the consequence, that supplying these medicines outside those conditions is a criminal offence.

The same classification is why this article names no product. The Medicine Advertisements Board does not permit poisons in the First Schedule of the Act to be advertised to the public unless exempted. So the class gets named and nothing else does, which describes how the medicine is meant to move: through an examination rather than a feed. The guide to how clinics here are regulated sets out which law governs which part.

Does the number on the scale decide it?

Partly, and less than most people expect. The Ministry of Health and Malaysian Endocrine and Metabolic Society guideline on obesity sets pharmacotherapy at a body mass index of 30 or above, or 27.5 or above with comorbidities, and only as an adjunct to changes in diet, activity and behaviour. It is not indicated on its own.

The thresholds are Asian ones and sit lower than the figures people quote from overseas: 18.5 to 22.9 normal, 23.0 to 27.4 pre-obese, 27.5 to 32.4 obese class I, 32.5 to 37.4 class II, 37.5 or above class III. Waist circumference sits beside it, at 90 cm for men and 80 cm for women.

Then the guideline is candid about its own tool. BMI does not distinguish muscle from fat and says nothing about where fat sits, so visceral adiposity is the better parameter. Two people reach the same number for opposite reasons, which is where the assessment does work a calculator cannot.

The history that can stop it before it starts

The family thyroid question is not small talk, and it arrives early. At the weight management dose the prescribing information for this class carries a boxed warning about thyroid C-cell tumours seen in rodents, and the medicine is contraindicated in anyone with a personal or family history of medullary thyroid carcinoma, with multiple endocrine neoplasia syndrome type 2, or who has reacted seriously to it before. The Malaysian guideline's drug table carries the same warnings.

Pregnancy is a contraindication, and the label goes further than the word suggests. Weight loss offers no benefit in pregnancy and may cause fetal harm, the medicine is stopped once a pregnancy is recognised, and discontinued at least two months before a planned one because of the long half-life. That is a conversation about the next two years.

The guideline table also warns on acute pancreatitis and gall bladder disease, on hypoglycaemia where the medicine is combined with insulin or an insulin secretagogue, on renal impairment below an eGFR of 15 ml per minute for one agent, and on transient worsening of retinopathy in type 2 diabetes where retinopathy is already present and control improves quickly. None of that is a complete list. It is a class summary from two documents, and whether any item applies to a particular person is decided from a full history in a consultation.

The question about your next anaesthetic

Malaysia's National Pharmaceutical Regulatory Agency has issued a safety alert on this class and anaesthesia, and patients rarely arrive knowing about it. These medicines slow the emptying of the stomach, part of how they work, so a stomach may still hold food at the moment everyone assumes it is empty. The alert states that this may raise the risk of aspiration and aspiration pneumonia during general anaesthesia or deep sedation.

The advice puts the work on the patient as much as the doctor: tell your doctors about any planned procedure requiring anaesthesia, and make the perioperative decision a shared one. That means the dentist offering sedation, the surgeon booking a day case, the endoscopy list.

So it becomes a question at the start, not a discovery later. Anything booked, anything likely this year. A strange thing to be asked at a weight appointment.

What happens next, and the rule for stopping

The guideline sets a review cadence and a stopping rule, and the stopping rule is the more interesting half. Face-to-face review is monthly for three months, then at least three-monthly. If more than 5% weight loss has not been achieved by three months, or there are significant safety or tolerability problems, the guideline says to stop and consider another approach.

A written instruction to stop is unusual in a field where most protocols describe only when to start. A medicine producing nothing still carries its side effect profile.

Loss at any speed brings a second conversation. What happens to skin after a significant loss has a limit no device changes, and it is better raised at the beginning than discovered in a mirror.

The version sold online is a different medicine

In January 2026 the Malaysian Obesity Society issued a public health warning about unregulated GLP-1 and GLP-1 with GIP compounds sold through online platforms, social media and other non-medical channels. Safe use, the society says, depends on proper patient selection, dose titration and monitoring, none of which exists inside that transaction.

Their warning lists what unsupervised use can produce: severe nausea and vomiting, dehydration, hypoglycaemia, pancreatitis or gall bladder disease, worsening of conditions the seller never asked about, and dangerous interactions with medicines nobody reviewed. Products sold this way may carry the wrong dose, contaminants, or a substance entirely different from the label.

Someone buying that way has not found a cheaper version of the same thing. They have bought an unknown.

The check that no examination can do

Everything above is answerable in a room, from a history, an examination and results. The question that decides most of what follows is not on that list.

It is what happens when the medicine stops. The guideline builds stopping into the plan from the start, with a review cadence and a rule for ending it, so that is a scheduled question rather than a failure. What the evidence shows about weight returning once the medicine stops is worth reading before the first prescription rather than after the last one.

A doctor who works through every item above and never asks it has done the safety checking and left the deciding question unasked. It is the slowest part of the appointment and it earns the time.

Common questions

Can I get GLP-1 medication in Malaysia without seeing a doctor?

No. This class is classified as a Group B poison under the Poisons Act 1952, and the Act sets out the mechanism plainly: a Group B poison is dispensed against a prescription from a registered medical practitioner, a dentist or a veterinary surgeon. Supplying it outside those conditions is reported as a criminal offence rather than a technicality. An account offering it without a history, an examination and follow-up is not a cheaper version of the same thing.

What are the main contraindications to GLP-1 medication?

By class, and as a summary rather than a full list: a personal or family history of medullary thyroid carcinoma, multiple endocrine neoplasia syndrome type 2, a previous serious hypersensitivity reaction to the medicine or its excipients, and pregnancy. The label also advises stopping at least two months before a planned pregnancy, because the medicine stays in the body a long time. Warnings sit alongside those for acute pancreatitis, gall bladder disease, hypoglycaemia where it is combined with insulin or an insulin secretagogue, renal impairment, and worsening of existing retinopathy in type 2 diabetes. Whether any of it applies to a particular person is settled from a full history in a consultation.

Do I need to tell my dentist or surgeon that I am taking it?

Yes, and Malaysia's National Pharmaceutical Regulatory Agency has said so in a safety alert. These medicines slow the emptying of the stomach, and a stomach that empties slowly may still hold food when it was assumed to be empty, which the alert links to a raised risk of aspiration and aspiration pneumonia during general anaesthesia or deep sedation. The advice is to tell your doctors about any planned procedure requiring anaesthesia and to decide the perioperative management together.

What weight thresholds do the Malaysian guidelines use?

The Ministry of Health and Malaysian Endocrine and Metabolic Society clinical practice guideline on obesity indicates pharmacotherapy at a body mass index of 30 or above, or 27.5 or above where comorbidities are present, and only as an adjunct to changes in diet, activity and behaviour. The BMI bands it uses are Asian ones: 18.5 to 22.9 normal, 23.0 to 27.4 pre-obese, 27.5 to 32.4 obese class I, 32.5 to 37.4 class II, 37.5 or above class III. Waist circumference thresholds are 90 cm for men and 80 cm for women.

How often would I be seen after starting?

The same guideline sets face-to-face review monthly for the first three months and at least every three months after that. It also sets a stopping rule: if more than 5% weight loss has not been achieved by three months, or there are significant safety or tolerability problems, the medicine is stopped and another approach considered.

Why does this article not name a brand or a product?

Because it cannot. The Medicine Advertisements Board does not permit poisons in the First Schedule of the Poisons Act 1952 to be advertised to the public unless exempted, with narrow exceptions for nicotine replacement therapy and certain press releases about newly registered products. The class can be discussed. A product cannot be promoted on a page anyone can read, and the specifics belong in a consultation after an examination.

Have a question about this?

The honest answer usually depends on your face. A consultation with Dr Ong is in person, and unhurried.