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Ozempic side effects

Ozempic’s label reports nausea in 20.3 of every 100 people on the 1 mg dose, and 15.8 on 0.5 mg, against 6.1 on placebo.

Source for this answer

Source: Read from the Ozempic label, revision 05/2026

Source: Read from the Ozempic label, revision 05/2026

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

The two placebo-controlled diabetes trials

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 = 262Ozempic 0.5 mg: n = 260Ozempic 1 mg: n = 261

The two placebo-controlled diabetes trials
Side effectPlaceboOzempic 0.5 mgOzempic 1 mg
Nausea6.1%15.8%20.3%
Vomiting2.3%5%9.2%
Diarrhea1.9%8.5%8.8%
Belly pain4.6%7.3%5.7%
Constipation1.5%5%3.1%
Who was in the trials
521 adults with type 2 diabetes took Ozempic across two trials, one on its own and one alongside background insulin. The average age was 56 and people had had diabetes for about 9 years.
How long
An average of 32.9 weeks on the drug
What made the table
Everything reported by 5 in 100 people or more, and more often than on placebo. Low blood sugar is counted separately.
Who stopped
The label reports that in the wider pool of seven trials, and in the two-year heart outcomes trial, the kinds and rates of common side effects looked like the table above.

The boxed warning: thyroid tumors in rodents

Ozempic carries the same boxed warning as every product in this family. Rats and mice given semaglutide grew thyroid C-cell tumors, and nobody knows whether people do. The label says the drug is not for anyone whose family has had medullary thyroid cancer, or who 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 Ozempic FDA label
WarningWhat this label says about it
PancreatitisThe label lists it among the reasons to stop.
Diabetic eye diseaseThis gets its own warning here, because the trial population had diabetes and 8.9 in 100 already had eye damage at the start.
Low blood sugarThe risk rises when Ozempic is taken with insulin or a sulfonylurea, and the label says those doses may need cutting.
Kidney injuryUsually after fluid loss from being sick or having diarrhea.
Severe stomach and gut problemsAdded to the label in October 2025.
Gallbladder diseaseIncluding gallstones and inflammation.
Serious allergic reactionsIncluding swelling of the face and throat.
Breathing in stomach contents under anestheticThe label warns anesthetists that the stomach may not be empty.
Sharing a penThe label warns that an Ozempic pen must never be shared, even with the needle changed, because of infection risk.

What matters first

Highest listed reaction
Nausea: 20.3% in Ozempic 1 mg
Distinct reactions listed
5
Warnings to watch
9
Boxed warning
The boxed warning: thyroid tumors in rodents

What have people actually reported about Ozempic?

66,161 reports naming Ozempic 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 Ozempic in openFDA FAERS, retrieved 2026-08-17
Most reportedReportsShare of Ozempic reports
Nausea9,751 reports15% of Ozempic reports
Off label use6,949 reports11% of Ozempic reports
Vomiting6,341 reports9.6% of Ozempic reports
Diarrhea5,980 reports9.0% of Ozempic reports
Decreased appetite4,507 reports6.8% of Ozempic reports
Constipation4,406 reports6.7% of Ozempic reports
Weight decreased4,157 reports6.3% of Ozempic reports
Impaired gastric emptying3,431 reports5.2% of Ozempic reports
Product used for an unapproved purpose3,294 reports5.0% of Ozempic reports
Blood glucose increased2,962 reports4.5% of Ozempic reports

FDA reports include how a drug was used as well as symptoms reported afterward. Entries about use outside the label do not identify the reason for use on their own.

The counts cannot show whether Ozempic is safer than another product. They reflect reports filed, without a matching count of everyone exposed to each drug.

  • 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 2 mg dose has separate findings

The main common-side-effect table covers 0.5 mg and 1 mg. The label reports separate findings from a 40-week trial comparing 1 mg and 2 mg.

That trial enrolled 959 people using metformin, with or without a sulfonylurea. Stomach and bowel reactions affected 34 in 100 on 2 mg and 30.8 in 100 on 1 mg.

The label reports no new safety concerns in that trial. Side effects still occurred, as the trial percentages show.

Why Ozempic’s numbers look lower than Wegovy’s

The labels’ main tables come from different studies. They cannot establish that one product is easier to take than the other.

The doses differ: Ozempic’s main table covers 0.5 mg and 1 mg; Wegovy’s main weight-trial table covers 2.4 mg. Ozempic’s participants had type 2 diabetes. Wegovy’s weight trials enrolled people with obesity or overweight.

The cut-off differs as well. Ozempic prints everything at 5 in 100 and above. Wegovy prints everything at 2 and above. So an effect landing between those two lines shows up on one label and not the other.

The labels themselves open with the warning that rates from one drug’s trials cannot be lined up against another’s. That applies here even though the drug substance is the same.

Why do Ozempic and Wegovy report different numbers for the same drug?

Both are semaglutide. 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 Wegovy side-effect table in full

Where to read next

Two pages carry the parts this one leaves out.

Questions readers ask

What are the long-term side effects of taking Ozempic?

The main side-effect table comes from two diabetes trials averaging 32.9 weeks on Ozempic. The label also includes longer heart and kidney trials with different safety reporting.

The common table is not a yearly risk estimate. Later FDA reports can describe concerns after treatment starts, but they do not measure how often users experience them.

Can I just stop taking Ozempic?

The label does not give a gradual dose-reduction schedule for stopping Ozempic. That does not mean stopping has no effect on blood sugar or other treatment goals.

It lists reasons to stop, including suspected pancreatitis. A prescriber can explain whether to stop and how the rest of the treatment plan would change.

What I wish I knew before taking Ozempic?

The 0.25 mg dose is a starting step, not a maintenance dose. The main common-side-effect table covers 0.5 mg and 1 mg. The label reports separate findings for 2 mg.

Those figures come from adults with type 2 diabetes. They are not a direct comparison with weight-management doses or with another drug’s trials.

How do you feel after an Ozempic injection?

The label’s common-side-effect table does not predict how someone will feel in the hours after an injection. It counts reports over the trial.

What it does record is how often. Nausea reached 20.3 in every 100 people on 1 mg and 15.8 on 0.5 mg, against 6.1 on placebo. Vomiting, diarrhea, belly pain and constipation follow below it.

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

Ozempic 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.

Beyond the Ozempic reaction table