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Gulf Press > Gulf News > UAE > Abu Dhabi Health Alerts on Risks of Peptide Products
UAE

Abu Dhabi Health Alerts on Risks of Peptide Products

Mohamed Mahmoud
Last updated: 2026/09/28 at 12:48 AM
Mohamed Mahmoud
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Abu Dhabi Health Authority’s New Electronic Reporting System for Peptide Products

The Abu Dhabi Health Authority has launched an electronic reporting model to track health problems and side effects individuals may experience after using peptide products. This initiative aims to enhance patient safety and monitor the impacts associated with these products, which are increasingly popular for various health benefits, including weight loss and combating aging.

The new system invites members of the public who have encountered health issues or side effects after using peptide products to complete an electronic form available on its official website. This form includes 13 questions designed to collect details about the usage, experiences, and any associated symptoms of peptide products.

Understanding Peptide Products and Their Uses

Peptide products are medications or substances that contain small proteins known as peptides. They are often marketed for various purposes, such as weight loss, muscle building, and anti-aging effects. With the rise of social media, the promotion and accessibility of these products have surged, sparking considerable discussion among healthcare professionals regarding their safety and efficacy.

Individuals are encouraged to report their experiences using the electronic model, which starts by gathering identifying information like name and contact information. However, the Health Authority assures that details such as name and email are only collected if voluntarily provided by users.

How to Report Health Issues Related to Peptide Usage

The reporting form includes specific questions about the peptide product used, whether users have images of the product, and the intended purpose of use—be it for weight loss, muscle enhancement, anti-aging, or other reasons. Users must specify when they began using the product and describe any health problem or side effect that appeared afterward. Examples of descriptions include phrases like “skin: itchy rash” or “stomach: severe vomiting.”

Additionally, the form seeks information about when the health problem arose, asking users if it occurred on the same day as the dose, within the following days, or weeks later. The users also have the option to report whether they sought medical advice or visited a hospital regarding their issue and their current health status, which can be categorized as “recovered,” “improving,” or “still experiencing issues.”

Regulatory Oversight of Peptide Products in Abu Dhabi

Healthcare facility officials have expressed their concern over the increasing popularity of peptide treatments, especially the marketing strategies that promote them primarily through social media. In response, Abu Dhabi’s health facilities have adopted a risk assessment approach to oversee peptide products. This strategy categorizes them based on risk levels, ranging from low-risk products, such as surface-level cosmetic peptides, to medium and high-risk products that affect one or more organs within the body.

High-risk peptide products are subject to stringent regulatory guidelines to ensure safety and quality. All healthcare providers are mandated to prescribe peptide treatments strictly for clinically appropriate cases supported by available scientific evidence. It is crucial for healthcare professionals to document their clinical evaluations and obtain informed consent from patients before commencing any peptide-based treatment.

Importance of Reporting and Future Steps

The implementation of this electronic reporting model reflects the Health Authority’s commitment to patient safety and evidence-based practices. By encouraging users to share their experiences, the authority aims to better understand the safety profile of peptide products currently on the market and address any emerging health issues.

As the initiative progresses, patients and health professionals should remain vigilant about reporting any adverse effects. The Health Authority is expected to analyze the collected data to inform future guidelines and regulations related to peptide product usage. Keeping track of these developments will allow consumers to make informed choices regarding their health and safety.

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