Samospharma Limited has categorically denied any links to Aveo Pharmaceutical Pvt. Ltd and Westfin Pharmaceutical Pvt. Ltd, the two firms recently implicated in a BBC investigation into the illicit sale of opioid pills in West Africa.
The BBC Africa Eye exposé revealed that Aveo Pharmaceuticals, through Westfin International, allegedly exported unapproved opioid-based medications, including tapentadol and carisoprodol, to Ghana, Nigeria, and Côte d’Ivoire.
These substances, which are highly addictive, pose serious health risks such as respiratory failure and death.
Following these revelations, the Food and Drugs Authority (FDA) revoked Aveo Pharmaceuticals’ Good Manufacturing Practices (GMP) certification. Additionally, it instructed Samospharma, a Ghanaian importer, to immediately cease all dealings with Aveo Pharmaceuticals and Westfin International.
However, Samospharma has pushed back against these claims, asserting that it has no association with the accused companies. The company is demanding a public retraction from the FDA, arguing that the allegations are unfounded and damaging to its reputation.
“We do not, and never have, engaged in any fraudulent practices as alleged in the BBC report, nor do we associate with entities such as Aveo Pharmaceutical Pvt. Ltd and Westfin Pharmaceutical Pvt. Ltd that engage in such activities.”
Beyond rejecting any links to Aveo and Westfin, Samospharma also took issue with inaccuracies in the FDA’s statement concerning the manufacturer of Timonidin Eye Drops, an FDA-approved product.
The company disputed the FDA’s claim that Indiana Ophthalmics LLP was responsible for producing Timonidin Eye Drops, clarifying that this information was incorrect. According to Samospharma, Indiana Ophthalmics LLP has never played a role in the manufacturing of the product. While acknowledging the firm as a respected name in ophthalmic care, Samospharma urged the FDA to review its records and correct the error immediately.
To support its position, Samospharma provided several documents, including confirmation from Kilitch Drugs (India) Ltd, which stated that it is the actual manufacturer and exporter of Timonidin Eye Drops and Samocef Injection.
The company also submitted commercial invoices and FDA consignment documents verifying the importation of these products in 2022 and 2023. Additionally, an export invoice and customs bill of entry from Sudarshan Pharma Industries Ltd and the GRA Customs Division confirmed the 2023 importation of Prolatan (Latanoprost) Eye Drops.
Samospharma has called on the FDA to take immediate steps to correct what it describes as a serious misrepresentation and ensure accurate information is provided to the public.
In a strongly worded statement, Samospharma has called on the FDA to either present concrete evidence supporting its claims or withdraw them entirely.