The Pharmacy and Poisons Board (PPB) has issued an alert to Kenyans regarding the use of “Asali ya Wazee”, scientifically known as THEMRA Epimedyumlu Macun.
In a statement, the board cautioned that the product that is promoted for its alleged sexual enhancement properties could be falsified and is not natural.
PPB further noted that it had conducted thorough tests on the honey-based product and detected significant adulteration.
Subsequently, the poisons board said they found high levels of a conventional active pharmaceutical ingredient, known as Sildenafil.
As per PPB, Sildenafil is prescribed for management of erectile dysfunction and pulmonary arterial hypertension.
However, the board warned that it should only be taken under a prescription from an expert as uncontrolled use could lead to health hazards.
“The PPB informs the public that Sildenafil is classified as a Prescription-Only Medicine and its excessive consumption poses serious safety and health hazards,” PPB warned.
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As such, the board cautioned members of the pubic from not only using it but also selling it.
Any person found selling the product, PPB stated, will be liable for legal action when caught.
“In view of the above, the PPB strongly cautions the public against use or involvement in the trade, distribution, wholesale, retail, issuance or dispensing of this product,” the statement added.
Additionally, the poisons board advised members of the public to avoid using products without the approval of experts and authorities.
Kenyans Love for Street Honey
The sight of vendors distributing honey packed in containers is common in Kenya.
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From some quarters, the honey distributed by small-scale vendors is deemed to be natural and hence consumers presume it to have greater benefits to the body.
However, the Pharmacy and Poisons Board has warned against taking such products sold as health products.
In the statement, the poisons board called on members of the public to volunteer any information about products suspected to be in the market without the required approval.
“We encourage both the general public and healthcare providers to promptly report any suspected substandard and falsified medical products,” the statement read in part.
