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GLP-1 side effects: how common they are, how long they last and which are serious

Nausea, diarrhea, vomiting and constipation are the side effects most people on Wegovy or Zepbound get, mostly while the dose is going up. The serious ones are rarer and listed on the label. Hair loss, alcohol and vision questions come from trials and health-record studies, not the label. The numbers, side by side.

Most people who take a GLP-1 drug for weight get at least one stomach side effect. In the trials behind the Wegovy label, 44% of people on the 2.4 mg dose had nausea, against 16% on placebo [1]. In the Zepbound trials it was 25% to 29%, against 8% [2]. Diarrhea, vomiting and constipation follow the same pattern. These effects are most common while the dose is being raised, which is why both labels start low and step up every four weeks.

The serious side effects, such as pancreatitis, gallbladder disease and kidney injury from dehydration, are much rarer and are spelled out in the label's warnings. This page sets out both, from the FDA labels for Wegovy (semaglutide) and Zepbound (tirzepatide), then covers three questions the labels answer only partly or not at all: hair loss, alcohol and eyesight.

The common ones, in numbers

The table puts the two labels side by side. The Wegovy column is the 2.4 mg weekly dose; the Zepbound column gives the range across its 5, 10 and 15 mg maintenance doses. Each figure is the share of people who reported the effect at any point in trials that ran 68 to 72 weeks.

Side effectWegovy 2.4 mgPlaceboZepbound 5 to 15 mgPlacebo
Nausea44%16%25% to 29%8%
Diarrhea30%16%19% to 23%8%
Vomiting24%6%8% to 13%2%
Constipation24%11%11% to 17%5%
Abdominal pain20%10%9% to 10%5%
Fatigue11%5%5% to 7%3%
Hair loss3%1%4% to 5%1%

Sources: Wegovy label Table 3 [1]; Zepbound label Table 1 [2]. Zepbound also lists injection-site reactions, in 6% to 8% against 2% [2].

Two cautions in reading it. The labels themselves say rates from different drugs' trials cannot be compared directly, because the trials differed [1][2]. And a "yes" in a trial means the effect happened at least once, not that it lasted the whole time.

Wegovy tablets, taken daily, produced the same kinds of side effects at similar rates in their trial [1]. The new 7.2 mg Wegovy dose added more of them: 39% nausea, 22% vomiting and, unusually, 22% dysesthesia, a burning or tingling feeling on the skin, against 6% on 2.4 mg [1].

When they happen, and how many people stop

Both drugs slow the stomach and act on appetite centers in the brain, so the stomach effects come with the mechanism. They are worst when the dose goes up. That is the stated reason for the escalation schedules: Wegovy starts at 0.25 mg and Zepbound at 2.5 mg, and neither starting dose is meant to be the long-term one [1][2].

Most people stay on treatment. In the Wegovy trials, 6.8% stopped because of side effects, against 3.2% on placebo; nausea, vomiting and diarrhea were the main reasons [1]. In the Zepbound trials it was 4.8% to 6.7% by dose, against 3.4%, and most of those stopped in the first few months [2].

The serious ones on the label

These are the warnings both labels carry, in plain terms [1][2]:

  • Thyroid C-cell tumors. A boxed warning. Both drugs caused these tumors in rodents; whether they do in people is not known. Neither drug is for anyone with a personal or family history of medullary thyroid cancer or MEN 2.
  • Pancreatitis. Severe stomach pain that will not go away, sometimes spreading to the back, is a reason to stop and call a doctor. Since approval, necrotizing and fatal cases have been reported [1][2].
  • Gallbladder disease. Gallstones and inflammation, which can need surgery. Fast weight loss raises the risk, but the Wegovy label notes it was more common than on placebo even after allowing for weight lost [1].
  • Kidney injury from dehydration. Vomiting and diarrhea can dry you out enough to hurt the kidneys. Since approval, some Zepbound cases have needed dialysis [2].
  • Severe stomach problems. Including, since approval, bowel obstruction, ileus and fecal impaction [1][2].
  • Low blood sugar. Mainly in people who also take insulin or a sulfonylurea.
  • Allergic reactions. Including anaphylaxis and swelling of the face or throat.
  • Diabetic eye disease. People with type 2 diabetes and retinopathy should be watched, because fast drops in blood sugar can worsen it.
  • Food in the lungs under anesthesia. Because the stomach empties slowly, tell anyone sedating you that you take one of these drugs.
  • Heart rate. Wegovy can raise resting heart rate [1].

One warning has gone. The Wegovy label carried a section on suicidal behavior and ideation; it was removed in February 2026 [1].

A large health-record study of people with type 2 diabetes compared the severe stomach outcomes (pancreatitis, gallbladder disease, bowel obstruction, gastroparesis and severe constipation) across semaglutide, tirzepatide and the older dulaglutide. The risk was about the same for all three [5].

Hair loss

Hair loss is on both labels. In the Zepbound trials it was 4% to 5% against 1% on placebo, and the label ties it to weight loss: it was reported by 7.1% of women and 0.5% of men, and nobody stopped Zepbound because of it [2]. On Wegovy it was 3% at 2.4 mg and 6% at 7.2 mg [1].

Studies outside the label point the same way. A 2026 meta-analysis of nine trials with 4,114 GLP-1 users found hair loss about three times as often as on placebo, with an overall rate of 3.9% [3]. In a health-record study of people with type 2 diabetes, starting a GLP-1 drug carried a higher risk of new hair loss than starting an SGLT-2 or DPP-4 drug, though the absolute risk was low [4]. The increase was in non-scarring hair loss.

Alcohol

Neither label has a warning about alcohol. What exists is research on whether these drugs reduce drinking.

Three randomized trials have tested semaglutide in alcohol use disorder:

  • 48 adults on low weekly doses for nine weeks drank less in a supervised lab session and had fewer drinks on the days they drank, but no fewer drinks per day overall [7].
  • 108 adults with obesity on 2.4 mg weekly for 26 weeks cut their heavy drinking days by 13.7 percentage points more than placebo [8].
  • 50 adults on oral semaglutide for eight weeks had fewer heavy drinking days, with no change in drinks per day [9].

None of this is an approved use. In practice, the overlap that matters is dehydration: alcohol on top of vomiting or diarrhea adds to the kidney risk in § 03, and in people taking insulin or a sulfonylurea, both alcohol and the drug can lower blood sugar.

Eyesight

Reports have linked semaglutide to NAION, a sudden loss of vision from poor blood flow to the optic nerve. It is not among the warnings on the US labels for Wegovy or Ozempic [1]. A 2026 meta-analysis of six observational studies covering 4.8 million people did not find a consistent overall increase. The certainty was low: the risk looked raised in type 2 diabetes and not in obesity, and the authors could not separate the drug from the disease [6]. Sudden vision loss on any drug needs urgent care.

Is a GLP-1 safe?

For the approved drugs, the side effects are known in unusual detail because tens of thousands of people took them in trials. Most are stomach effects that are worst early. The serious ones are uncommon, and most have warning signs: lasting stomach pain, signs of dehydration, swelling of the face or throat.

That knowledge belongs to the approved products. A compounded or sublingual version uses the same molecule but has not been through those trials, and its dose depends on the pharmacy that made it. What the drugs do for weight, and how they compare, is on our pages for semaglutide, tirzepatide and the GLP-1 class.

Frequently asked

What is the most common GLP-1 side effect?

Nausea. It affected 44% of people on Wegovy 2.4 mg and 25% to 29% on Zepbound in the trials behind the labels, against 16% and 8% on placebo [1][2].

How long do GLP-1 side effects last?

They are most common while the dose is going up, which is why both labels raise it in four-week steps. Most people who stopped because of them did so in the first months [2]. If they do not ease, a prescriber can hold the dose or step back down.

Does Zepbound or Wegovy cause hair loss?

Both labels list it: 4% to 5% on Zepbound and 3% on Wegovy 2.4 mg, against 1% on placebo. The Zepbound label links it to weight loss and reports it far more often in women [1][2].

Can you drink alcohol on a GLP-1?

The labels carry no alcohol warning. Trials of semaglutide in alcohol use disorder found less heavy drinking. Alcohol does add to dehydration, and to low blood sugar in people on insulin or a sulfonylurea [7][8][9].

What are the serious side effects of GLP-1 drugs?

Pancreatitis, gallbladder disease, kidney injury from dehydration, severe stomach problems including bowel obstruction, allergic reactions and a boxed warning for thyroid C-cell tumors seen in rodents [1][2].

Does semaglutide cause vision loss?

A link to NAION has been reported but not confirmed. A 2026 meta-analysis rated the evidence low certainty, and the US labels do not list it as a warning [1][6].

References

  1. FDA. Wegovy (semaglutide) injection and tablets, prescribing information, revised June 2026: sections 5, 6.1 (Tables 3 and 4) and 6.2. DailyMed, read 10 November 2026.
  2. FDA. Zepbound (tirzepatide) injection, prescribing information, effective 28 August 2026: sections 5, 6.1 (Table 1) and 6.2. DailyMed, read 10 November 2026.
  3. Cheng PL, et al. Glucagon-like peptide-1 receptor agonists and hair loss: a systematic review and meta-analysis. Diabetes Res Clin Pract. 2026. PMID 42155605.
  4. Tang H, et al. Risk of hair loss associated with glucagon-like peptide-1 receptor agonists in adults with type 2 diabetes: target trial emulation. BMJ. 2026. PMID 42486607.
  5. Crisafulli S, et al. Comparative gastrointestinal safety of dulaglutide, semaglutide, and tirzepatide in adults with type 2 diabetes. Ann Intern Med. 2026. PMID 41183330.
  6. Abdelaal A, et al. Semaglutide and the risk of nonarteritic ischemic optic neuropathy: a systematic review and certainty of evidence meta-analysis. Ophthalmology. 2026. PMID 41692115.
  7. Hendershot CS, et al. Once-weekly semaglutide in adults with alcohol use disorder: a randomized clinical trial. JAMA Psychiatry. 2025. PMID 39937469.
  8. Klausen MK, et al. Once-weekly semaglutide versus placebo in patients with alcohol use disorder and comorbid obesity: a randomised, double-blind, placebo-controlled trial. Lancet. 2026. PMID 42070571.
  9. Schacht JP, et al. Oral semaglutide for alcohol use disorder: a randomized clinical trial. Am J Psychiatry. 2026. PMID 42522065.

Editorial note: Informational only — not medical advice. The figures come from the FDA labels and the published studies listed above. A side effect that is severe, or does not ease, is a question for the prescriber.