No evidence of safety, quality issues with dermal filler in case of woman going blind after jab: HSA

HSA said its probe into the dermal filler AestheFill has found no evidence of product-related safety and quality issues. PHOTO: REGEN BIOTECH

SINGAPORE – A Health Sciences Authority (HSA) investigation into the dermal filler AestheFill has found no evidence of product-related safety and quality issues, after a woman lost her vision in the first reported case of its kind in Singapore.

HSA on Thursday said it had concluded its probe into AestheFill, a dermal filler from South Korea that temporarily reduces wrinkles and folds in the skin.

This came a month after The Straits Times broke the news that a woman went blind in July from being injected with the dermal filler at a Redhill clinic. HSA was alerted to the incident on July 29.

HSA said in a statement on Thursday that to mitigate the risk of blood vessel blockage, which can cause blindness, Parvus – the Singapore distributor of AestheFill – will strengthen its training of healthcare professionals, and retrain its existing providers.

It will also develop an information leaflet for healthcare professionals to explain the risks of the procedure to patients.

ST first reported in September that the woman had apparently suffered sudden blindness after she was injected with AestheFill at the clinic. It is understood that both her eyes were affected.

On Thursday, HSA said that as part of its investigations, it reviewed device history records for the specific lot of AestheFill that was injected into the woman. The records contain details about the manufacturing process, including quality checks and the results of these tests.

The results of the chemical and microbiological tests were within specifications, indicating that the product had been manufactured according to required standards and is safe for use, it said.

Parvus earlier told ST that the outcome of its own investigations indicated that the accidental injection of AestheFill into the woman’s bloodstream had led to her losing her vision.

HSA classifies dermal fillers as Class D medical devices, which carry the highest risk. AestheFill has been registered in Singapore since Oct 1, 2021.

Blindness due to blood vessel blockage is a known risk for dermal fillers, and consumers should be aware of this and other risks, the authority said.

Such risks are typically explained in the instructions for use given to healthcare practitioners. The instructions for AestheFill caution against injecting it into blood vessels as it may cause blockage.

Other common complications that may arise from the use of dermal fillers include swelling, redness, raised bumps in or under the skin (nodules or granulomas) and temporary blurring of vision. Injection into blood vessels may also cause skin blanching, or the paling of skin.

To minimise the risks associated with dermal fillers, HSA advised consumers to discuss the procedure with healthcare practitioners before undergoing treatment.

The Ministry of Health’s investigations into the case are under way.

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