The National Agency for Food and Drugs Administration and Control (NAFDAC) has issued a public alert cautioning Nigerians against the use of five contaminated syrups imported from Pakistan.
The affected products are Alergo Syrup, Emidone Suspension, Mucorid Syrup, Ulcofin Suspension, and Zincell Syrup.
NAFDAC Director-General, Mojisola Adeyeye, revealed that these syrups have been detected in the Maldives and Pakistan, with 23 batches found to be contaminated with harmful chemicals.
Adeyeye emphasized that the contaminated products have also been identified in Belize, Fiji, and the Lao People’s Democratic Republic.
The manufacturer responsible for these products, Pharmix Laboratories Limited in Pakistan, has been instructed by the Drug Regulatory Authority of Pakistan (DRAP) to cease the production of all oral liquid dosage medicines due to potential contamination issues.
The public alert reads: “In November 2023, samples of five different batches of ALERGO syrup were screened for non-compliance by the quality control laboratory of the Maldives Food and Drug Authority (MFDA) in accordance with the thin layer chromatography (TLC) test for Diethylene Glycol and Ethylene Glycol for inclusion in The International Pharmacopoeia,” the alert reads.
“The routine screening detected potentially unacceptable amounts of diethylene glycol and ethylene glycol as contaminants.
“Laboratory testing conducted by the Therapeutic Goods Administration of Australia (TGA) confirmed that all five batches were contaminated with ethylene glycol at levels ranging from 0.62 to 0.82% w/w relative to the accepted limit of not more than 0.10% w/w.
“A follow-on inspection of PHARMIX LABORATORIES (PVT.) LTD was conducted by the Drug Regulatory Authority of Pakistan (DRAP).
“According to DRAP, a review of the manufacturing facility and manufacturing records suggested that diethylene glycol/ethylene glycol as contaminants may be present in other products and batches manufactured by Pharmix.
“The safety and quality of these products can, therefore, not be guaranteed.
“As a precautionary measure Pharmix has been instructed by DRAP to stop production of all oral liquid dosage medicines and issued a Recall Alert for the five different oral dosage forms manufactured by Pharmix.
“Diethylene glycol and ethylene glycol are toxic to humans when consumed and can prove fatal.
“Toxic effects can include abdominal pain, vomiting, diarrhoea, inability to pass urine, headache, altered mental state, and acute kidney injury which may lead to death.
“These substandard products referenced in this alert are unsafe and their use, especially in children, may result in serious injury or death.
“Although these products are not registered by NAFDAC, they may have been distributed, through formal and informal markets, to other countries or regions, including Nigeria.
“NAFDAC implores importers, distributors, retailers and consumers to exercise caution and increase vigilance within the supply chain to avoid the importation, distribution, sale and use of the substandard cough syrups.
“Members of the public in possession of the above listed products are advised not to sale or use the products, instead they are to submit stock to the nearest NAFDAC office.
“Seek immediate medical advice from a qualified healthcare professional if you have used the product, or suffered an adverse reaction/event having used the products.”
