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Wegovy (Semaglutide)

Wegovy is an injectable medication manufactured by Novo Nordisk and approved by the FDA in 2021. It helps adults with obesity manage their weight and related health problems. Given as a weekly shot, it is meant to be used alongside a healthy diet and exercise.

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Did you experience serious side effects after taking a diabetes & weight loss drug such as Ozempic or Wegovy?

What Is Wegovy?

Wegovy (semaglutide) has the same main ingredient as Ozempic, but it is used and dosed differently. In studies, people taking Wegovy with lifestyle changes lost about 15% of their body weight over 68 weeks.

An oral version of Wegovy was approved in December 2025. A February 2026 study by Truveta, a group of U.S. health systems that share data, found that many people who previously used GLP-1 medicines switched from shots to pills. Of those starting oral semaglutide for weight loss, about one-fourth had used Wegovy shots and about one-fifth had used Zepbound (tirzepatide) shots. Most people taking the pill had switched from these shots.

Key Wegovy Facts
  • Wegovy was approved by the FDA on June 4, 2021. It was the first new weight-loss drug to be approved since 2014.
  • In clinical trials, people taking Wegovy lost up to 15% of their body weight over 68 weeks, compared to those taking a placebo.
  • Wegovy is given as a weekly shot, with doses up to 2.4 mg.
  • Wegovy contains semaglutide, the same main ingredient in Ozempic. However, the two drugs are used and dosed for different reasons.
  • As of May 19, 2026, the FDA had received 17,009 reports of side effects related to Wegovy, including 107 deaths. However, these reports do not prove that Wegovy caused these events.

How Wegovy Works

Wegovy works similarly to a natural hormone in your body called GLP-1, which helps manage appetite and blood sugar.

What Wegovy Does
  • It helps you feel full after eating.
  • It lowers your appetite by affecting nerve signals.
  • It slows down how quickly food leaves your stomach.
Wegovy has been shown to lower the risk of heart attack and stroke in adults who are overweight or obese and also have heart disease. The FDA approved this new use in March 2024.

Clinical trials have shown significant weight loss compared to not using the drug. Researchers reported that after 68 weeks, a large portion of people taking Wegovy achieved weight loss of 5%, 10% and 15% compared to those not taking the medication.

However, Wegovy can contribute to gastrointestinal side effects, including delayed digestion, nausea, vomiting and stomach paralysis (gastroparesis).

Alternatives to Wegovy

Wegovy belongs to a class of drugs called GLP-1 agonists. There are several medications in this class, and some may work better for you than others. These drugs are typically prescribed for weight management or diabetes.

You should talk with your doctor if you are wondering about the differences between Mounjaro vs. Ozempic. A medical provider can also help you decide which one is better for you when comparing Wegovy vs. Ozempic.

Examples of GLP-1 Medications
MedicationActive IngredientFDA ApprovalPrimary Use
MounjaroTirzepatide2022Type 2 diabetes
OzempicSemaglutide2017Type 2 diabetes and cardiovascular disease
SaxendaLiraglutide2010Weight management
ZepboundTirzepatide2022Weight management

FDA Oversight and Labeling

Wegovy’s original label included a black box warning — the FDA’s most serious alert — about a cancer risk identified in animal studies. The warning states that people with personal or family histories of medullary thyroid cancer (MTC) or multiple endocrine neoplasia syndrome type 2 (MEN 2) should not use Wegovy.

By May 19, 2026, the FDA had received 17,009 reports of adverse events related to Wegovy. Of these, 7,843 were serious, including 107 deaths. However, reports to the FDA Adverse Event Monitoring System do not necessarily mean the drug caused these events.

Latest FDA Regulatory Actions on Wegovy
  • October 14, 2025
    The FDA updated the warning for severe stomach side effects to include potential intestinal obstruction and severe constipation.
  • March 8, 2024
    The FDA approved Wegovy to lower the chances of cardiovascular death, heart attack and stroke in people with cardiovascular disease who are obese or overweight.
  • November 27, 2024
    A warning of severe stomach side effects was added to Wegovy’s label.
  • November 1, 2024
    A warning was added about the risk of pulmonary aspiration during surgeries that require anesthesia or deep sedation. Pulmonary aspiration is the inhalation of food, liquid or stomach content into your trachea and lungs.
  • September 22, 2023
    The FDA added a warning about ileus, or intestinal blockages, to Wegovy’s label.
  • December 23, 2022
    The FDA added warnings about the risk of acute gallbladder disease and increased resting heart rate.
  • June 4, 2021
    Wegovy became the first FDA-approved weight loss drug since 2014.

Side Effects of Wegovy

The most common Wegovy side effects are gastrointestinal, including nausea, diarrhea, vomiting, constipation and stomach pain. The STEP-1 clinical trials found that side effects could affect 10% to 44% of participants. They often occur during a dose increase as the body adjusts.

Common Wegovy Side Effects
  • Gastrointestinal side effects: Nausea (44.2%), diarrhea (31.5%), vomiting (24.8%), constipation (23.4%), indigestion (10.3%), stomach pain (10%), acid reflux, bloating, burping and gas.
  • Blood sugar effects: Low blood sugar can occur in people with Type 2 diabetes.
  • General side effects: Headaches (15.2%), dizziness and fatigue.

Serious but rare side effects include pancreatitis, gastroparesis (stomach paralysis), gallbladder disease and NAION-related vision loss.

The FDA also requires a boxed warning for thyroid C-cell tumor risk based on rodent studies.

Wegovy and Stomach Paralysis (Gastroparesis)

Wegovy slows down the rate at which food leaves your stomach. Research has linked semaglutide drugs (Wegovy, Ozempic and Rybelsus) to a more than three times higher risk of gastroparesis and a 3.5 times higher risk of ileus compared to non-users.

“Wegovy’s delayed gastric emptying may cause or exacerbate gastroparesis in those so predisposed, something I’m seeing with increasing frequency in practice,” Dr. Bharat Pothuri, a board-certified gastroenterologist and founder of GastroDox in Houston, told Drugwatch.

He added that “the gastrointestinal risks aren’t trivial.”

A 2025 study in BMJ Open Gastroenterology discovered that people taking Wegovy, Ozempic or Rybelsus had a higher risk of developing gastroparesis. Their risk was over three times higher than people on a weight loss drug called bupropion-naltrexone and more than six times higher than those who had a sleeve gastrectomy.

A 2023 study in Acta Pharmaceutica Sinica B found that people taking GLP-1 medications experience ileus at a rate 3.5 times higher than those who do not. Ileus is a condition where the intestines act as if they’re blocked, even when there is no physical obstruction.

A warning about ileus was added to the Wegovy label in 2023.

Wegovy and Vision Loss (NAION)

Wegovy contains semaglutide, the same active ingredient as Ozempic, and has been linked in research to an increased risk of NAION (non-arteritic anterior ischemic optic neuropathy). The eye condition is characterized by poor blood flow to the optic nerve. It can cause sudden, typically permanent vision loss in one eye.

As of May 2026, the FDA has not required Novo Nordisk to add a NAION warning to Wegovy’s label.

A 2024 study published in the International Journal of Retina and Vitreous found that using a semaglutide medication like Wegovy more than doubled the risk of NAION over five years. This increased risk was the same regardless of whether or not people had diabetes.

A 2025 study published in JAMA Ophthalmology found a small but increased risk of NAION in people taking semaglutide. The American Academy of Ophthalmology highlighted this study, saying it showed “patients taking semaglutide — the active ingredient in Ozempic and Wegovy — may be at higher risk of developing an eye condition that can cause blindness.”

“For NAION, however, rare though it is, I do believe sight-related side effects should be given a more prominent place on the label. Perception of these drugs as ‘miracle drugs’ may obscure dangerous complications that require more informed consent,” Dr. Pothuri said.

Sudden vision loss is a medical emergency. Anyone experiencing sudden, painless vision loss while taking Wegovy should seek immediate evaluation by an ophthalmologist or emergency physician.

Vision loss and other serious side effects have also sparked GLP-1 lawsuits. Because NAION can be permanent, it’s an especially concerning risk to medical and legal professionals alike. “There are obviously other risks that are warned about with taking Ozempic or Wegovy, but a lot of those risks are temporary in nature,” Danielle Gold told Drugwatch. “If you develop NAION while on this medication, it will likely result in permanent visual impairment.”

 

Vision Changes After GLP-1 Drugs?
If you used GLP-1s like Ozempic, Wegovy, Saxenda or Victoza and were later diagnosed with non-arteritic anterior ischemic optic neuropathy (NAION), you may be eligible for a lawsuit.
See if you qualify

Patients who experienced gastroparesis, ileus or NAION-related vision loss after taking Wegovy have filed lawsuits against Novo Nordisk. Cases are consolidated in MDL 3094 in federal court along with related semaglutide and tirzepatide claims.

Wegovy Lawsuits Claiming Gastroparesis and Stomach Injuries

Wegovy lawsuits claiming gastroparesis, intestinal blockages and other gastrointestinal injuries have been combined in a multidistrict litigation (MDL) in an Eastern Pennsylvania federal court.

MDLs allow several similar lawsuits to be consolidated into a single litigation, expediting the legal process.

As of May 2026, there were 3,636 lawsuits pending in the MDL. The MDL involves lawsuits naming Wegovy along with other GLP-1 drugs.

In November 2025, additional Wegovy lawsuits were combined in a multicounty litigation in New Jersey state court. MCLs function similarly to MDLs by making the judicial process more efficient.

GLP-1 Drugs and Their Manufacturers Named in MDL 3094
MedicationManufacturer
WegovyNovo Nordisk
OzempicNovo Nordisk
RybelsusNovo Nordisk
MounjaroEli Lilly
TrulicityEli Lilly
SaxendaNovo Nordisk

Lawsuits claim that Wegovy and other GLP-1 medications caused “gastroparesis, ileus, intestinal obstruction or pseudo-obstruction or other gastrointestinal injury.”

Each lawsuit alleges that GLP-1 medications may cause stomach injuries. They question whether the manufacturers were aware of these risks and if they adequately informed patients and doctors.

Additionally, the lawsuits raise concerns about the misleading or incomplete safety information.

Wegovy Lawsuits Claiming Vision Loss

Patients who developed NAION after taking Wegovy have filed lawsuits alleging Novo Nordisk failed to warn of vision-loss risks.

In December 2025, Wegovy lawsuits were combined with similar lawsuits into a multidistrict litigation in an Eastern Pennsylvania federal court. Plaintiffs in these lawsuits claimed they received NAION injuries after taking other GLP-1 drugs.

“If you develop NAION while on this medication, it will likely result in permanent visual impairment."
Danielle Gold Attorney at Weitz & Luxenberg

Additional NAION-related Wegovy lawsuits were combined in November 2025 into a multicounty litigation (MCL) in New Jersey state court. MCLs work similarly to MDLs but at the state level.

If you experience severe side effects after taking Wegovy, it’s important to take specific steps. These include getting medical help, consulting with your doctor and talking to an attorney if you’ve been seriously injured.

Should You Stop Taking Wegovy?

You should not stop taking Wegovy or any other prescription medication without talking to your doctor first. Stopping a medication suddenly may cause side effects. Your doctor can recommend a way to stop taking Wegovy safely.

Consider stopping if you experience:
  • Depression or changes in mood
  • Fast heartbeat
  • Gallbladder issues
  • Gastrointestinal complications, including diarrhea, nausea or vomiting
  • Kidney problems
  • Pancreatitis
  • Severe abdominal pain
  • Signs of low blood sugar, including dizziness, sweating or confusion
  • Sudden vision loss in one or both eyes

Seek immediate medical attention if you experience any of these life-threatening side effects after taking Wegovy.

How To Report Side Effects

You can report serious side effects that you experience from Wegovy to the FDA’s MedWatch program. You can also report health issues you have with other medicines, medical devices, dietary supplements, baby formula and cosmetics.

If you or someone in your family has experienced a severe reaction to Wegovy, it’s important to inform your doctor. They can provide important medical information that will help the FDA understand what happened and improve safety for everyone.

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How To File a Wegovy Lawsuit

If you developed NAION, gastroparesis, or another serious injury after taking Wegovy, you can request a free case review. Drugwatch partner attorneys will evaluate your medical records against current MDL criteria to determine your eligibility. Statutes of limitations vary by state, so it’s best to consult a lawyer as soon as possible to preserve your options.

Frequently Asked Questions About Wegovy

What are the most common side effects of Wegovy?
The most common Wegovy side effects are gastrointestinal: nausea, diarrhea, vomiting, constipation and stomach pain. Most occur during dose increases and usually improve within several weeks. Serious, rare side effects include pancreatitis, gallbladder disease, gastroparesis and NAION-related vision loss. The FDA also requires a boxed warning for thyroid C-cell tumor risk based on animal studies.
Is Wegovy the same as Ozempic?
Wegovy and Ozempic contain the same active ingredient, semaglutide, but have different FDA-approved uses and dosing. Wegovy is approved for chronic weight management at doses up to 2.4 mg once weekly. Ozempic is approved for Type 2 diabetes at doses from 0.5 mg to 2 mg once weekly. Both are made by Novo Nordisk.
Can Wegovy cause vision loss?
Wegovy has been linked to a higher risk of NAION (non-arteritic anterior ischemic optic neuropathy), a rare condition causing sudden, usually permanent vision loss in one eye. NAION is uncommon in the general population. However, studies from 2024 and 2025 found an increased risk in semaglutide users. Sudden vision loss requires immediate evaluation by an ophthalmologist or emergency physician.
Is Wegovy covered by insurance?
Wegovy insurance coverage differs by plan. Many commercial insurers cover it for eligible patients, but Medicare, Medicaid and some employer plans may exclude weight-loss drugs or require prior authorization. Without coverage, monthly costs can be several hundred dollars. Novo Nordisk provides patient assistance to help with expenses. Coverage changes frequently, so patients should confirm details directly with their plan before starting treatment.
Please seek the advice of a medical professional before making health care decisions. Thoughts and opinions expressed in personal stories are strictly anecdotal and should not be taken as medical information or advice.