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What percent of people have bad side effects from Ozempic?

2 min read

According to clinical trial data, a significant percentage of patients experience side effects from Ozempic, primarily affecting the gastrointestinal system. These reactions, which can range from mild to severe, are a key factor in understanding what percent of people have bad side effects from Ozempic.

Quick Summary

A significant percentage of Ozempic users experience adverse reactions, predominantly gastrointestinal issues like nausea, vomiting, and diarrhea. The frequency and intensity of side effects increase with higher doses but often decrease over time for many users. While most reactions are mild, rare but serious complications can occur, leading some patients to discontinue the medication.

Key Points

  • Prevalence: A significant percentage of Ozempic users, potentially close to half in some studies, experience adverse reactions, predominantly affecting the digestive system.

  • Common Side Effects: The most common adverse reactions include nausea, vomiting, diarrhea, abdominal pain, and constipation, all of which occur more frequently than with a placebo.

  • Dosage Matters: The frequency and intensity of side effects are often linked to the dosage, with higher doses typically associated with more frequent gastrointestinal issues.

  • Temporary Nature: For many, the common side effects are temporary and tend to decrease over several weeks as the body adjusts to the medication, especially when the dose is increased gradually.

  • Discontinuation: A small but notable percentage of patients discontinue Ozempic specifically due to gastrointestinal side effects, while other reports suggest overall discontinuation rates can be much higher due to various factors.

  • Rare but Serious Risks: Less common but serious side effects include pancreatitis, gallbladder disease, diabetic retinopathy complications, and a boxed warning for potential thyroid C-cell tumors.

In This Article

Ozempic side effects: Frequency from clinical trials

Clinical trials for Ozempic (semaglutide) indicate that a notable percentage of patients experience adverse reactions, especially when starting treatment or increasing the dose. Gastrointestinal issues are particularly common. For more details on side effect percentages from clinical trials, including common gastrointestinal adverse reactions by dose, please refer to {Link: novomedlink.com https://www.novomedlink.com/diabetes/products/treatments/ozempic/efficacy-safety/safety-profile.html}.

Discontinuation rates due to side effects

While many side effects are manageable, some patients discontinue treatment due to intolerable symptoms. Clinical trial data shows that discontinuation rates due to gastrointestinal issues were 3.1% for the 0.5 mg dose and 3.8% for the 1 mg dose of Ozempic. However, some studies indicate higher overall discontinuation rates for semaglutide, particularly when used for weight loss, with reasons extending beyond side effects to include factors like cost.

Less common and serious adverse reactions

In addition to common digestive issues, Ozempic carries risks of less frequent but more serious side effects. These can include pancreatitis, gallbladder disease, and complications related to diabetic retinopathy. There is also a boxed warning about a potential risk of thyroid C-cell tumors based on rodent studies, though the human relevance is under investigation. Severe gastrointestinal side effects leading to dehydration can also result in acute kidney injury.

Comparison of Ozempic side effects vs. placebo

The table below illustrates the difference in reported side effect rates from placebo-controlled clinical trials, highlighting that gastrointestinal symptoms are significantly more common with Ozempic use. More information is available on {Link: novomedlink.com https://www.novomedlink.com/diabetes/products/treatments/ozempic/efficacy-safety/safety-profile.html}.

Adverse Reaction Placebo (N=262) % Ozempic 0.5 mg (N=260) % Ozempic 1 mg (N=261) %
Nausea 6.1% 15.8% 20.3%
Vomiting 2.3% 5.0% 9.2%
Diarrhea 1.9% 8.5% 8.8%
Abdominal pain 4.6% 7.3% 5.7%
Constipation 1.5% 5.0% 3.1%

Conclusion

Clinical trial data suggests that a significant number of individuals may experience gastrointestinal side effects while taking Ozempic. While most of these effects are mild and temporary, a smaller percentage of patients stop the medication due to symptom severity. Less common but serious complications are also possible. The likelihood and intensity of side effects are individual and dose-dependent. Patients should discuss potential risks and management strategies with their healthcare provider before starting Ozempic. Further information is available on the manufacturer's website.

Frequently Asked Questions

Clinical trial data from type 2 diabetes studies indicates that between 30% and 40% of patients experienced gastrointestinal side effects on standard Ozempic doses. In some studies involving higher doses (semaglutide for weight loss), the percentage of people with gastrointestinal side effects could be higher. However, most of these side effects are considered mild to moderate.

The most common side effects reported in clinical trials are gastrointestinal and include nausea (15.8–20.3%), vomiting (5–9.2%), diarrhea (8.5–8.8%), abdominal pain (5.7–7.3%), and constipation (3.1–5%).

Yes, for most people, the common gastrointestinal side effects like nausea and vomiting are temporary. They are most likely to occur when starting the medication or increasing the dose and typically lessen or resolve within a few weeks to a few months as the body acclimates.

Serious side effects are less common but can include pancreatitis (inflammation of the pancreas), gallbladder disease (including gallstones), complications related to diabetic retinopathy, and a potential risk of thyroid tumors. Acute kidney injury due to dehydration from severe vomiting and diarrhea has also been reported.

The frequency and severity of gastrointestinal side effects generally increase with higher doses of Ozempic. Clinical trial data shows a higher percentage of patients reporting adverse reactions at the 1 mg dose compared to the 0.5 mg dose.

In clinical trials, 3.1% and 3.8% of patients on the 0.5 mg and 1 mg Ozempic doses, respectively, discontinued treatment due to gastrointestinal side effects. Other studies have reported higher overall discontinuation rates for semaglutide, with reasons often including a mix of side effects and other factors like cost or insurance coverage.

Ozempic's side effect profile is similar to other GLP-1 receptor agonists, with common reactions being gastrointestinal issues like nausea, vomiting, and diarrhea. Specific frequency rates can vary between different drugs and dosages, so a healthcare provider can help determine the best option for a patient's tolerability.

References

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Medical Disclaimer

This content is for informational purposes only and should not replace professional medical advice.