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Zepbound side effects

Nausea tops Zepbound’s label table at 25, 29 and 28 in every 100 people on 5, 10 and 15 mg, against 8 on placebo.

Source for this answer

Source: Read from the Zepbound label, revision 08/2026

Source: Read from the Zepbound label, revision 08/2026

Medically reviewed by Jennifer Montecillo, MD · non-practicing medical reviewerReviewed 2026-08-12every number here is sourced

The two placebo-controlled weight trials, dose by dose

Read the placebo column first. Nearly everything below also happened to some people on placebo. The gap between columns is the part linked to the drug in these trials.

Trial armsPlacebo: n = 958Zepbound 5 mg: n = 630Zepbound 10 mg: n = 948Zepbound 15 mg: n = 941

The two placebo-controlled weight trials, dose by dose
Side effectPlaceboZepbound 5 mgZepbound 10 mgZepbound 15 mg
Nausea8%25%29%28%
DiarrheaGroups diarrhea and frequent bowel movements8%19%21%23%
Vomiting2%8%11%13%
ConstipationGroups constipation and hard stools5%17%14%11%
Belly pain5%9%9%10%
Indigestion4%9%9%10%
Reactions where you injectGroups bruising, redness, itching, pain and rash at the injection site2%6%8%8%
Tiredness3%5%6%7%
Allergic reactions3%5%5%5%
Burping1%4%5%5%
Hair loss1%5%4%5%
Acid reflux2%4%4%5%
Wind2%3%3%4%
Bloating2%3%3%4%
Dizziness2%4%5%4%
Low blood pressureGroups low blood pressure and blood pressure drops on standing0%1%1%2%
Who was in the trials
2,519 adults with obesity or overweight took Zepbound across two trials. The average age was 47 and the average BMI 37.4. A quarter also had type 2 diabetes.
How long
Up to 72 weeks, then 4 weeks off the drug
What made the table
Everything reported by 2 in 100 people or more, and more often than on placebo
Who stopped
4.8, 6.3 and 6.7 in every 100 people stopped for good on 5, 10 and 15 mg, against 3.4 on placebo. Most who stopped did so in the first few months, over stomach and gut problems.

The boxed warning: thyroid tumors in rodents

Zepbound opens with a boxed warning about thyroid C-cell tumors found in rats. It is not known whether tirzepatide does the same in people. The label rules the drug out where medullary thyroid cancer runs in the family, and where someone has the inherited condition MEN 2.

What does the label tell prescribers to watch for?

These warnings sit above the table in the label. They cover uncommon problems that matter most.

Warnings and precautions from the Zepbound FDA label
WarningWhat this label says about it
PancreatitisThe label says to stop if it is suspected.
Gallbladder diseaseReported more often than on placebo in the weight trials.
Severe stomach and gut problemsReported by 1.7, 2.5 and 3.1 in every 100 people on 5, 10 and 15 mg, against 1 on placebo. This is one of the few places the label shows a clean rise with the dose.
Low blood sugarMainly where Zepbound is taken alongside insulin or a sulfonylurea.
Kidney injuryUsually following fluid loss.
Serious allergic reactionsThe label lists these separately from the milder ones in the table.
Diabetic eye diseaseRelevant to the quarter of the trial population who had type 2 diabetes.
Breathing in stomach contents under anestheticThe label tells anesthetists not to assume the stomach is empty.

What matters first

Highest listed reaction
Nausea: 29% in Zepbound 10 mg
Distinct reactions listed
16
Warnings to watch
8
Boxed warning
The boxed warning: thyroid tumors in rodents

What have people actually reported about Zepbound?

70,141 reports naming Zepbound have reached the FDA’s public database. A report is not proof the drug caused anything, and there is no way to know how many people took it.

Most reported terms for Zepbound in openFDA FAERS, retrieved 2026-08-17
Most reportedReportsShare of Zepbound reports
Wrong dose given12,768 reports18% of Zepbound reports
Nausea7,913 reports11% of Zepbound reports
Injection site pain4,792 reports6.8% of Zepbound reports
Drug ineffective4,602 reports6.6% of Zepbound reports
Extra dose given4,527 reports6.5% of Zepbound reports
Diarrhea4,360 reports6.2% of Zepbound reports
Vomiting3,496 reports5.0% of Zepbound reports
Constipation3,026 reports4.3% of Zepbound reports
Accidental underdose2,612 reports3.7% of Zepbound reports
Fatigue2,444 reports3.5% of Zepbound reports

The FDA reports include dosing errors alongside symptoms such as nausea. An error report describes how the product was used; it is not itself a side effect.

These brand-level counts do not isolate a particular device or show why an error happened. They cannot establish that one presentation causes more errors than another.

  • No count of everyone treated. FAERS counts submitted reports, not everyone who used a drug. Each percentage here divides an event count by the drug’s report total. It describes a share of reports, not a share of people treated or their chance of an event.
  • A report is not proof the drug did it. FDA does not require proof that a drug caused an event before accepting a report. The drug, an illness or another factor may be involved. A report naming both a drug and an event does not establish the cause.
  • A bigger number can just mean a more-prescribed drug. More reports can simply mean that more people use the drug, that it is newer, or that it receives more news and legal attention. Raw report totals do not tell you which drug is safer.
  • The same event can be counted twice. One event can reach FAERS through more than one channel — the patient, the prescriber and the manufacturer can all file. FDA does not guarantee that the public files are de-duplicated.
  • Retrieved 2026-08-17 from https://api.fda.gov/drug/event.json. FDA disclaimer: Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.
4Interpret the pageDose patterns, same-drug context, and where the evidence continues

The side effects do not simply rise with the dose

Nausea peaks at 10 mg, not at 15. Constipation runs the other way entirely: 17 in 100 at 5 mg, falling to 11 at 15 mg.

The rows do not all rise with each assigned dose. That does not rule out symptoms after a dose increase for an individual.

The label says nausea, vomiting and diarrhea often occurred while doses increased, then became less common over time. Stopping because of a reaction rose from 4.8 to 6.3 to 6.7 in 100 across the three dose groups.

The sleep apnea trials did not produce a separate table

467 adults with moderate to severe sleep apnea and obesity took part in two more trials, one in people using a breathing machine and one in people who were not.

The label says the safety findings on 10 mg and 15 mg were similar to those in the weight trials. It does not provide a separate common-side-effect table for sleep apnea.

Why do Zepbound and Mounjaro report different numbers for the same drug?

Both are tirzepatide. The percentages differ because the trials behind them differ, not because one product is gentler than the other.

Each label opens its table with the same warning: rates from one drug’s trials cannot be set against another’s. That holds here even though the drug substance is identical. The two sets of trials enrolled different people. They ran to different doses. And they used different cut-offs for what got printed at all.

The Mounjaro side-effect table in full

Where to read next

Two pages carry the parts this one leaves out.

Questions readers ask

Is Zepbound safer than Ozempic?

The cited trials do not establish that Zepbound is safer than Ozempic. SURMOUNT-5 studied weight-management doses, while SURPASS-2 studied adults with type 2 diabetes.

Comparing the two labels directly does not work either. Each set of percentages comes from a different population under a different reporting cut-off.

What not to do when taking Zepbound?

The label says never to share a pen and to tell the care team before anesthesia or deep sedation. It also advises against combining Zepbound with other tirzepatide products or GLP-1 medicines.

Nausea, vomiting and diarrhea often occurred during dose increases in the trials. A group average cannot rule out a dose-related problem for one person.

Are there any long-term side effects from Zepbound?

The main common-side-effect table covers treatment for up to 72 weeks. The label also describes a trial in which some participants continued Zepbound for up to 88 weeks.

These study periods are not yearly risk estimates. The label reports common reactions, serious warnings and later reports separately because each answers a different question.

How much weight can you lose on Zepbound in 3 months?

The trial averages do not predict one person’s weight change after three months. The early months include dose increases, and the label does not require everyone to reach the maximum.

SURMOUNT-5 reported an average loss of 20.2% after 72 weeks with tirzepatide 10 or 15 mg. It studied adults with obesity who did not have type 2 diabetes.

1primary source, each with the day we read it — open the documents used on this page

Zepbound is a registered trademark of its maker. The maker did not write, review or endorse this page. We report figures from a public FDA label and the FDA’s report database. This is not medical advice.

The cross-brand answer is in the GLP-1 hair-loss record.

Beyond the Zepbound reaction table