The US Food and Drug Administration (FDA) has sent warning letters to eight companies for unauthorised manufacturing or marketing of unapproved eye drugs.
The companies must respond with steps to correct violations within 15 days of receiving warnings. Failing to comply could lead to the FDA pursuing legal action, including product seizure and/or a court order to the company to stop unapproved product manufacturing and distribution. The FDA has already placed an import alert on some of the eight companies, stopping the entry of these drugs into the US.
The illegal eye products were marketed for varied ocular conditions, including conjunctivitis (pink eye), cataracts, and glaucoma. Some of the eight companies had product sterility issues, as per the FDA.
The heightened risk of harm is of particular concern to the FDA, as the topical eye application of these drugs can “bypass some of the body’s natural defences” and cause adverse reactions. Furthermore, some of the drugs contain silver compounds, namely silver sulphate, silver sulphate or argentum. Long-term use of silver can cause discolouration of the eye (argyria), causing it to turn grey or blue-grey.
The FDA noted that the investigation into the eye products is ongoing and may result in additional regulatory or enforcement actions. The agency also advised that the customers using the drugs should seek medical advice and report any adverse reactions on the FDA’s MedWatch program.
How well do you really know your competitors?
Access the most comprehensive Company Profiles on the market, powered by GlobalData. Save hours of research. Gain competitive edge.
Your download email will arrive shortly
Not ready to buy yet? Download a free sample
We are confident about the unique quality of our Company Profiles. However, we want you to make the most beneficial decision for your business, so we offer a free sample that you can download by submitting the below formBy GlobalData
In January, the FDA issued a warning letter to online pharmacy pharmahealthonline.com for selling unapproved and misbranded drugs, including opioids and benzodiazepines.
US pharmacies including CVS Health and Walgreens Boots Alliance have taken steps to maximise profits. In August, CVS Health partnered with Sandoz for the commercial launch of Humira biosimilar, Hyrimoz, in Q1 2024. Meanwhile, Walgreens Boots Alliance has instituted a cost management programme to save $3.5bn to $4.1bn.