Victoza Side Effects: What the FDA Label Lists
[Side effects · Victoza]

Victoza side effects

liraglutide · once-daily injection · Label checked

Short answer: In the label's placebo-controlled trials in adults, nausea was the most common side effect of Victoza: 18% on 1.2 mg and 20% on 1.8 mg, against 5% on placebo. Diarrhea, headache, vomiting and decreased appetite followed. Withdrawals for stomach side effects happened mainly in the first 2 to 3 months. The label carries a boxed warning about thyroid C-cell tumors seen in rodents.

What Victoza is approved for: The label says Victoza is approved, along with diet and exercise, to improve blood sugar control in adults and children 10 years and older with type 2 diabetes. It is also approved to lower the risk of major heart events (heart death, non-fatal heart attack or non-fatal stroke) in adults with type 2 diabetes and established heart disease.

Source
VICTOZA (liraglutide) injection, for subcutaneous use, prescribing information and Medication Guide. Novo Nordisk. DailyMed, version published November 17, 2025. DailyMed setid 5a9ef4ea-c76a-4d34-a604-27c5b505f5a4

Does Victoza have a boxed warning?

Boxed warning

WARNING: RISK OF THYROID C-CELL TUMORS

Liraglutide caused thyroid C-cell tumors in rats and mice, and it is not known whether Victoza causes these tumors, including medullary thyroid carcinoma (MTC), in people. Victoza must not be used by people with a personal or family history of MTC or with Multiple Endocrine Neoplasia syndrome type 2 (MEN 2). The label lists a lump in the neck, trouble swallowing, shortness of breath and lasting hoarseness as possible thyroid tumor symptoms.

What are the most common Victoza side effects?

These are the label's own numbers from the Adverse Reactions section. Where the label compares with placebo (a dummy treatment), both columns are shown, so you can see how much more often a reaction happened on Victoza.

Table 1. Adverse reactions reported in ≥5% of Adult Patients Treated with VICTOZA for Type 2 Diabetes Mellitus [Section 6.1]
Adverse reactionPlacebo N=661 (%)Liraglutide 1.2 mg N= 645 (%)Liraglutide 1.8 mg N= 1024 (%)
Nausea51820
Diarrhea41012
Headache71110
Nasopharyngitis8910
Vomiting269
Decreased appetite1109
Dyspepsia147
Upper Respiratory Tract Infection676
Constipation155
Back Pain345

Pooled from 5 placebo-controlled blood sugar trials in adults: 1,673 adults took Victoza for a mean of 37.3 weeks. Low blood sugar is not included in this table. The label says side effects in children 10 and older were comparable.

Table 2. Adult Incidence (%) and Rate (episodes/patient year) of Hypoglycemia in 26-Week Combination Therapy Placebo-controlled Trials [Section 6.1]
Trial and event typePlacebo comparatorVictoza treatment
Add-on to Metformin (N=121 placebo, N=724 Victoza): Patient not able to self-treat00.1 (0.001)
Add-on to Metformin: Patient able to self-treat2.5 (0.06)3.6 (0.05)
Add-on to Glimepiride (N=114 placebo, N=695 Victoza): Patient not able to self-treat00.1 (0.003)
Add-on to Glimepiride: Patient able to self-treat2.6 (0.17)7.5 (0.38)
Add-on to Glimepiride: Not classified00.9 (0.05)
Add-on to Metformin + Rosiglitazone (N=175 placebo, N=355 Victoza): Patient not able to self-treat00
Add-on to Metformin + Rosiglitazone: Patient able to self-treat4.6 (0.15)7.9 (0.49)
Add-on to Metformin + Rosiglitazone: Not classified1.1 (0.03)0.6 (0.01)
Add-on to Metformin + Glimepiride (N=114 placebo, N=230 Victoza): Patient not able to self-treat02.2 (0.06)
Add-on to Metformin + Glimepiride: Patient able to self-treat16.7 (0.95)27.4 (1.16)
Add-on to Metformin + Glimepiride: Not classified00

Four 26-week add-on trials in adults. Each cell is the percent of patients, with episodes per patient year in brackets. "Patient not able to self-treat" means an event that needed another person's help.

Other numbers in the Adverse Reactions section

  • Section 6.1

    Withdrawals because of stomach and gut side effects: 4.3% on Victoza and 0.5% on placebo, mainly in the first 2 to 3 months. Severe stomach and gut side effects: 4.4% on 1.2 mg, 4.2% on 1.8 mg and 1.1% on placebo.

  • Section 6.1

    Injection site reactions (such as rash or redness) were reported in about 2% of adults on Victoza; less than 0.2% stopped because of them.

  • Section 6.1

    In children 10 and older, 21.2% on Victoza had blood sugar below 54 mg/dL, with no severe low blood sugar episodes in the Victoza group.

  • Section 6.1

    Pancreatitis: 13 cases on Victoza versus 1 on a comparator (2.7 vs 0.5 cases per 1,000 patient-years). Papillary thyroid cancer: 7 cases versus 1 (1.5 vs 0.5 per 1,000 patient-years).

  • Section 6.1

    Heart rate rose by a mean of 2 to 3 beats per minute versus placebo; the label says Victoza did not have adverse effects on blood pressure.

What serious risks does the Victoza label warn about?

The Warnings and Precautions part of the label lists these. Each line gives the label's heading and what it means in plain words.

  • Section 5.1

    Risk of thyroid C-cell tumors. Liraglutide caused thyroid C-cell tumors in rats and mice, and cases of MTC have been reported after marketing. People with a personal or family history of MTC or with MEN 2 must not use Victoza.

  • Section 5.2

    Acute pancreatitis. Inflammation of the pancreas, including fatal cases, has been seen with GLP-1 drugs including liraglutide. The label says to stop Victoza if pancreatitis is suspected.

  • Section 5.3

    Never share a pen. Victoza pens must never be shared between people, even if the needle is changed, because of the risk of passing on blood-borne infections.

  • Section 5.4

    Low blood sugar. Adults using Victoza with a sulfonylurea or insulin may have a higher risk of low blood sugar. In children 10 and older, the risk was higher with Victoza regardless of insulin or metformin use.

  • Section 5.5

    Kidney injury from fluid loss. Acute kidney injury, sometimes needing dialysis, has been reported, mostly in people who became dehydrated from nausea, vomiting or diarrhea. The label says to monitor kidney function in these people, especially when starting or raising the dose.

  • Section 5.6

    Severe stomach and gut side effects. Severe stomach and gut side effects were reported in 4.4% on 1.2 mg and 4.2% on 1.8 mg, against 1.1% on placebo. Victoza is not recommended in people with severe gastroparesis.

  • Section 5.7

    Allergic reactions. Serious allergic reactions such as anaphylaxis and angioedema have been reported after marketing. The label says to stop Victoza if one occurs.

  • Section 5.8

    Gallbladder disease. In the LEADER trial, 3.1% on Victoza versus 1.9% on placebo had an acute gallbladder event such as gallstones or gallbladder inflammation.

  • Section 5.9

    Food or liquid in the lungs during anesthesia. Victoza slows stomach emptying. Rare reports describe food entering the lungs during procedures with general anesthesia or deep sedation. The label says to tell your providers you take Victoza before any planned procedure.

When does the label say to call your doctor?

From the Medication Guide that comes with Victoza:

  • A lump or swelling in the neck, hoarseness, trouble swallowing or shortness of breath: tell your healthcare provider (possible thyroid tumor symptoms).
  • Severe stomach pain that will not go away, with or without vomiting, sometimes felt through to the back: stop using Victoza and call your healthcare provider right away.
  • Signs of low blood sugar such as dizziness, sweating, confusion, shakiness, fast heartbeat or hunger: the guide lists these as warning signs, and says the risk may be higher with a sulfonylurea or insulin, and in children 10 and older.
  • Nausea, vomiting or diarrhea that does not go away: tell your healthcare provider right away, because fluid loss can cause kidney problems.
  • Stomach problems that are severe or will not go away: tell your healthcare provider.
  • Swelling of the face, lips, tongue or throat, trouble breathing or swallowing, severe rash or itching, fainting or a very rapid heartbeat: stop using Victoza and get medical help right away.
  • Pain in the upper stomach, fever, yellowing of the skin or eyes, or clay-colored stools: tell your healthcare provider right away (possible gallbladder problems).
  • A planned surgery or procedure with anesthesia or deep sedation: tell all your healthcare providers you take Victoza beforehand.

How do I keep track of side effects in Dose Track?

Dose Track has a side-effect log. Each entry records the symptom, a severity (none, mild, moderate, severe or life-threatening), the date and an optional note, and can be tied to a specific dose or logged on its own. The history screen shows what you logged over time, which makes it easier to tell your prescriber when a reaction started and whether it is easing. The app records what you enter; it does not judge whether a symptom is serious. For anything on the label's call-your-doctor list, call your doctor.

This page is what the FDA label says, in plain words. It is not medical advice. Follow your prescriber, and ask them or your pharmacist about anything here.

Side effects for similar medicines

Frequently asked questions

What is the most common side effect of Victoza?+
Nausea. In the label's placebo-controlled trials in adults, nausea was reported by 18% on 1.2 mg and 20% on 1.8 mg, compared with 5% on placebo. Diarrhea was next at 10% and 12%, versus 4% on placebo.
Does Victoza reduce appetite?+
Decreased appetite is listed as a common side effect. In the placebo-controlled trials it was reported by 10% on 1.2 mg and 9% on 1.8 mg, compared with 1% on placebo.
Does Victoza cause low blood sugar?+
The risk depends on the other medicines used. In the add-on to metformin and glimepiride trial, 2.2% on Victoza had an episode they could not treat themselves, versus 0% on placebo. In children 10 and older, 21.2% had blood sugar below 54 mg/dL.
When do stomach side effects usually happen on Victoza?+
The label says withdrawals because of stomach and gut side effects mainly occurred during the first 2 to 3 months of the trials. Overall, 4.3% of people on Victoza withdrew for these reasons, compared with 0.5% on placebo.
What side effects were reported after Victoza went on the market?+
The label lists postmarketing reports including pancreatitis (sometimes fatal), bowel blockage, dehydration from stomach side effects, liver enzyme rises, gallbladder problems, allergic reactions, MTC, taste changes, kidney failure, a skin condition called cutaneous amyloidosis, and hair loss. Their frequency cannot be reliably estimated.