Tag: NAFDAC

  • Manufacturers‘ to register with NAFDAC

    Manufacturers‘ to register with NAFDAC

    Lagos State Consumer Protection Agency (LASCOPA) has said manufacturers must register their products with National Agency for Food and Drugs Administrative Control (NAFDAC).

    It also said comprehensive and genuine product information must be placed strategically for easy accessibility.

    General Manager of LASCOPA, Afolabi Solebo, spoke during a monitoring visit to supermarkets and grocery stores.

    Solebo noted growing concerns about proliferation of unregistered consumables, as well as lack of product information on most.

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    He said unregistered products  pose significant risks to public health and safety.

    Solebo called on supermarkets, restaurants, grocery stores, and other establishments selling dairy, baking and containerised products to  register them with NAFDAC, containing information as production and expiry dates.

    He added: “LASCOPA is pleased with the growth of businesses in Lagos but frowns at products  disastrous to consumers’ health.

    ‘’The agency does not intend to witch-hunt anyone, but will protect the  public.

    “Manufacturers and others in the consumable goods chain should ensure goods are registered with NAFDAC, with information placed for easy access.”

  • Drug abuse: NAFDAC begins tracking, tracing of tramadol, codeine, others

    Drug abuse: NAFDAC begins tracking, tracing of tramadol, codeine, others

    The National Agency for Food and Drug Administration and Control (NAFDAC) has launched narcotic drug serialization to track and trace narcotic products from the source of production to the consumer.

    The agency said the move became imperative to combat the menace of drug and substance abuse in Nigeria, particularly among the youth population.

    Emphasizing the seriousness of the issue of substance abuse, the agency’s Director-General, Prof. Mojisola Adeyeye, at the commissioning of the narcotic drugs serialization pilot project in Lagos on Friday, said: ‘’The abuse of drug substances is global. We have realized our issue in Nigeria, and we are ready to address it.’’

    Adeyeye, in a statement on Sunday, January 21, by NAFDAC’s Resident Media Consultant, Sayo Akintola, noted that narcotics were chosen amongst other classes of drugs to make sure drug or substance abuse in Nigeria is eliminated or mitigated.

    Adeyeye who attributed the challenge of substandard and falsified medicines, along with disorderly drug distribution by unscrupulous entities in the sector, however, revealed plans to implement serialization for all other NAFDAC-regulated drug products.

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    The statement reads: “In its renewed efforts to combat the menace of drug and substance abuse in Nigeria, particularly amongst the teeming youth population, the National Agency for Food and Drug Administration and Control NAFDAC has put in place effective mechanisms to track and trace narcotic products right from the very source of production, the manufacturing plant, to the end user, the patient through narcotic drugs serialization

    “Prof Adeyeye noted that narcotics were chosen amongst other classes of drugs to make sure that we do not have drug or substance abuse in Nigeria or to mitigate it, adding that this will be replicated for all other NAFDAC-regulated drug products.

    “Going down memory lane, Prof Adeyeye recalled the ubiquitous misuse of Tramadol and Codeine all over the country when she got to NAFDAC in 2017 with their adverse effects on the mental health of young adults, children, and women that were selling codeine or tramadol.

    “For the first six months of my tenure, I was running after tramadol or codeine at that time”.

    “As a regulatory Agency saddled with the responsibility of ensuring the safety and quality of medicines, she stated that NAFDAC places utmost importance on good distribution practices as a core mandate of the agency is to ensure that the distribution of medical products along the pharmaceutical supply chain reflects best global practices.

    “She however regretted that one of the greatest challenges that we face today in the healthcare sector is the occurrence of substandard and falsified medicines.

    “She added that in Nigeria, this problem is further compounded by the chaotic drug distribution practices of unscrupulous elements of society who do not place premium on human lives.

    ‘’These are the sharp practices that the Traceability project (Track and Trace) seeks to stop.’’, she maintained as she enthused that Track and Trace (Traceability) is indeed a game changer.

    “With this technology, she said medicines can now be tracked and traced right from the very source of production, the manufacturing plant, to the end user, the patient.

    “Through the scanning device on an Android phone, the NAFDAC boss said consumers can now verify the authenticity of the drug product they consume and be assured of the quality of medicines.

    “More importantly, she said the track and trace technology is a veritable tool to be deployed in the event of medication recalls.

    ‘’The commissioning event of the project is a crystallization of a series of activities that the Agency embarked upon since May 2018, when we attended the very first GS1 Africa healthcare conference in Addis Ababa, Ethiopia.

    “This led to the development and formulation of the Traceability Strategy Document, a five-year implementation roadmap for pharmaceutical products that was launched by the then Honourable Minister for Health in October 2020’’.

    “She said the narcotic drugs serialization pilot project symbolizes a significant milestone in the Agency’s commitment to delivering quality, efficacious, and easily verifiable medical products to the Nigerian consumer by adequately securing the drug distribution network.

    “She explained that the need to commence the track and trace of pharmaceutical products with narcotic medicines is a very strategic one, noting that Narcotic drugs occupy a very prime place in healthcare, and due to the very high propensity for abuse and diversion of this group of essential medicines cannot always be overruled.

    “The DG disclosed that the pilot project will be on for about one year, during which ‘’we expect to have been familiar with all that will be necessary to enhance the deployment and full implementation of the track and trace project for other drug classes in scalable phases.’’

    “Prof Adeyeye further stated that manufacturers must first commission the products they are registered to distribute into the NAFDAC Traceability System, and when it gets to the distributors or the wholesalers, they will also scan the products using a 2D Data Matrix barcode scanner to capture the event related to the movement of the product.

    “The NAFDAC boss said that all this will be captured in the Agency’s Information Traceability System so that if something goes off the track within the supply chain it would be easily traced and tracked and help in no small measure to reduce drug abuse.

    “The Managing Director of the technical partner, GS1 Nigeria, Mr. Tunde Odunlami, described the occasion as a very significant day in the history of traceability in Nigeria.

    “For GS1, he said that it has been a journey that started over ten years ago when the company started preaching the importance of traceability. He, however, commended NAFDAC for identifying the importance of this standard in transforming the way we do things in the country and enabling traceability and a good distribution system for the country.

    ‘’NAFDAC has taken the mantle as you can see today where we are now doing serialization of a very important class of medication which is Narcotics.’’, he said, as he explained the GSI standard and the role it will play in the system.

    “Mr. Odunlami further explained that GS1 provided the standard while Newsoft Nigeria Plc is the solution provider saddled with the responsibility of developing the solution and carrying out the implementation.”

  • Adulterated oil: NAFDAC moves against Olonka rubber oil

    Adulterated oil: NAFDAC moves against Olonka rubber oil

    The National Agency for Food and Drug Administration and Control (NAFDAC) has said that it will investigate the reported conversion of polyethylene into edible oil.

    Emphasizing its commitment to safeguarding the health of Nigerians as a responsible, science-based regulatory agency, yesterday, it noted that the investigation became imperative following a viral social media report regarding the conversion of polyethylene into edible oil.

    A statement by the agency’s Resident Media Consultant, Tayo Akintola reads in part: ” The attention of the Management of NAFDAC has been drawn to viral posts making the rounds on social media where an individual was reporting the alleged frying of plantain chips by a woman who “before she grated the plantain into the hot oil she melted about five of the white polythene what we call ‘olonka rubber’ into the oil.”

    “It is important to mention that the viral post began circulating on a date predating the day it was said to have been observed and that it did not give any indication of geographical location (country) of where the practice was observed.

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    “NAFDAC is a responsible and responsive regulatory authority guided by science.

    “In this regard, the agency is taking a science-based approach in response to the alleged claim and will conduct a necessary laboratory investigation into the claim.”

    The agency, however, urged the public to be vigilant and observant of the foods and beverages they consume, stating, “In the meantime, our advice to the public who consume NAFDAC regulated food products remains the same and centres around being vigilant as a consumer:

    “Purchase from a reputable source.

    “Check for the NAFDAC Registration Number of the product on the label/package as a sign that it is approved by NAFDAC.

    “Stay away from the product if the packaging looks suspect or compromised.

    “Stay away from the product if there is any objectionable smell or colour.

    “Exercise caution if the price at which the product is being offered for sale is much cheaper than similar products.

    “We use this medium to reassure the public that the Agency is proactive and remains alive to her responsibilities of safeguarding the health of the public and that thorough investigation of the alleged claim will be conducted.”

  • Adulterated oil: NAFDAC moves against Olonka rubber oil

    Adulterated oil: NAFDAC moves against Olonka rubber oil

    The National Agency for Food and Drug Administration and Control (NAFDAC) will investigate the reported conversion of polyethylene into edible oil, it emerged on Saturday.

    Emphasizing its commitment to safeguarding the health of Nigerians as a responsible, science-based regulatory agency, it noted that the investigation becomes imperative following a viral social media report regarding the conversion of polyethylene into edible oil.

    A statement by the agency’s resident media consultant, Tayo Akintola reads in part: ” The attention of the management of NAFDAC has been drawn to viral posts making the rounds on social media where an individual was reporting the alleged frying of plantain chips by a woman who, before she grated the plantain into the hot oil, she melted about 5 of the white polyethylene what we call ‘Olonka rubber’ into the oil.

    “It is important to mention that the viral post began circulating on a date pre-dating the day it was said to have been observed and that it did not give any indication of the geographical location (country) of where the practice was observed.

    “NAFDAC is a responsible and responsive regulatory authority guided by science. In this regard, the Agency is taking a science-based approach in her response to the alleged claim and will conduct necessary laboratory investigation into the claim”.

    The agency, however, urged the public to be vigilant and observant of the foods and beverages they consume, stating, “In the meantime, our advice to the public who consume NAFDAC-regulated food products remains the same and centres around being vigilant as a consumer:

    Read Also: NAFDAC to conduct tests on ‘under-dosed paracetamol’

    “Purchase from a reputable source. Check for the NAFDAC Registration Number of the product on the label/package as a sign that it is approved by NAFDAC.

    “Stay away from the product if the packaging looks suspect or compromised. Stay away from the product if there is any objectionable smell or colour.

    “Exercise caution if the price at which the product is being offered for sale is much cheaper than similar products. We use this medium to reassure the public that the Agency is proactive and remains alive to her responsibilities of safeguarding the health of the public and that a thorough investigation of the alleged claim will be conducted.”

  • NAFDAC to conduct tests on ‘under-dosed paracetamol’

    NAFDAC to conduct tests on ‘under-dosed paracetamol’

    The National Agency for Food and Drug Administration (NAFDAC) is set to conduct tests on some paracetamol tablets sold in Nigeria.

    The agency’s move followed social media reports that some of the drugs were under-dosed.

    In a statement in Abuja, the NAFDAC Director General, Prof. Mojisola Adeyeye, assured Nigerians that the agency, being recognised by the World Health Organisation (WHO) as a stable, well-functioning agency, and by other international partners as an organisation that places a premium on the quality, safety and efficacy of medicines, food, and other regulated products, its capacity to carry out a comprehensive test is not in doubt.

    She said: “NAFDAC is aware of a recent story presently being circulated on social media alleging that nearly all paracetamol tablets sold in Nigeria are under-dosed.

    “We have received a copy of the publication of the research finding of the subject and we wish to state categorically that the report is misleading and the science is questionable. 

    “As the quality culture of NAFDAC demands, as soon as the agency became aware of the news, the director general had meetings with the respective directors and gave a directive that a survey of the market should be done to sample and test.

    “This was followed up with the DG’s meeting with the leadership of the Pharmaceutical Manufacturing Group of the Manufacturing Association of Nigeria (MAN) to inform them of the agency’s intent. 

    “NAFDAC’s laboratories are ISO 17025-certified every year to ensure that the procedures used for testing are based on international standards and the equipment or instruments used are qualified similarly. 

    “We do yearly post-marketing survey of medicines to ensure that the quality and safety are maintained.”

    “Where there is a deviation from this, that is, whenever we find any regulated product to be substandard or falsified, NAFDAC regularly issues public alerts or do recalls.

    “In the last two years, we have issued 88 public alerts and ordered 32 recalls for medicines and foods.

    Read Also: NAFDAC conducts test on underdosed paracetamol

    “We are using this medium to assure the public that NAFDAC is using international standards and scientific methods to survey the paracetamol product where samples are collected from different parts of the country in the right amount and will be tested using well calibrated, and qualified state-of-the-art equipment or instruments. 

    “This is part of our routine regulatory post-marketing surveillance, among others, throughout the life cycle of a medicine.

    “We want to reiterate that NAFDAC has five ISO-17025 laboratories across the country, and a WHO Prequalified Laboratory at Yaba, Lagos, where medicines are tested for quality and safety. 

    “The laboratories test medicines using official monographs of British Pharmacopeia, United States Pharmacopoeia, and International Pharmacopoeia.

    “As soon as we finish the laboratory testing, we will update the public.

    “NAFDAC wishes to reassure the public that the agency is very vigilant in her responsibilities in safeguarding the health of the nation. 

    “It is on this basis that NAFDAC has been recognised by WHO as a stable, well-functioning agency, and by other international partners as an organisation that places premium on the quality, safety and efficacy of medicines, food, and other regulated products.”

  • NAFDAC conducts test on underdosed paracetamol

    NAFDAC conducts test on underdosed paracetamol

    The National Agency for Food and Drug Administration and Control (NAFDAC) is set to conduct paracetamol tablets sold in Nigeria following social media reports that the drugs are underdosed, it emerged on Monday.

    The agency said it will deppoy international standards and scientific method to survey the paracetamol product where samples are collected from different parts of the country in the right amount and will be tested using well calibrated, and qualified state-of-the-art equipment or instruments.

    Prof. Mojisola Adeyeye, the agency’s Director General (DG) said the test is part of NAFDAC’s routine regulatory post marketing surveillance among others throughout the life cycle of a medicine.

    Adeyeye, in a statement assured Nigerians that NAFDAC, being recognized by WHO as a stable, well-functioning agency, and by other international partners as an organisation that places premium on the quality, safety and efficacy of medicines, food, and other regulated products, its capacity to carry out a comprehensive test is not in doubt.

    She said: “NAFDAC is aware of a recent story presently being circulated on social media alleging that nearly all paracetamol tablets sold in Nigeria are under dosed.

    “We have received a copy of the publication of the research finding of the subject and we wish to state categorically that the report is misleading, and the science is questionable.

    “As the quality culture of NAFDAC demands, as soon as the Agency became aware of the news, the Director General, had meetings with the respective Directors and gave a directive that a survey of the market should be done to sample and test”.

    This was followed up with the DG meeting with the leadership of the Pharmaceutical Manufacturing Group of the Manufacturing Association of Nigeria to inform them of the Agency’s intent.

    “NAFDAC’s laboratories are ISO 17025-certified every year to ensure that the procedures used for testing are based on international standards and the equipment or instruments used are qualified similarly.

    “We do yearly post-marketing survey of medicines to ensure that the quality and safety are maintained.

    “Where there is a deviation from this, i.e., whenever we find any regulated product to be substandard or falsified, NAFDAC regularly issues public alerts or do recalls.

    “In the last two years we have issued eighty-eight (88) public alerts and ordered thirty-two (32) recalls for medicines and foods.

    “We are using this medium to assure the public that NAFDAC is using international standards and scientific method to survey the paracetamol product where samples are collected from different parts of the country in the right amount and will be tested using well calibrated, and qualified state-of-the-art equipment or instruments.

    “This is part of our routine regulatory post marketing surveillance among others throughout the life cycle of a medicine.

    Read Also: NAFDAC seeks stiffer counterfeiting law without fine option

    “We want to reiterate that NAFDAC has five ISO-17025 Laboratories across the country, and a WHO Prequalified Laboratory at Yaba Lagos where medicines are tested for quality and safety.

    “The laboratories test medicines using official monographs of British Pharmacopeia, United States Pharmacopoeia, and International Pharmacopoeia.

    “As soon as we finish the laboratory testing, we will update the public.

    “NAFDAC wishes to reassure the public that the Agency is very vigilant in her responsibilities in safeguarding the health of the nation.

    “It is on this basis that NAFDAC has been recognized by WHO as a stable, well-functioning agency, and by other international partners as an organisation that places premium on the quality, safety and efficacy of medicines, food, and other regulated products”, the DG added.

  • How NAFDAC’s price review will lift MSMEs

    How NAFDAC’s price review will lift MSMEs

    For micro small and medium enterprises (MSMEs) they are starting the year on a very sound note thanks to the largesse from the National Agency for Food and Drug Administration and Control (NAFDAC). 

    Rising from its meeting, the Council of NAFDAC has rolled out a new set of palliatives to help MSMEs survive the temporary economic fallouts of fuel subsidy removal and enhance the ease of doing business in Nigeria.

    To this end, the Agency has reviewed downward, the present administrative charges for late renewal of NAFDAC-regulated products to make the business environment more investment-friendly in a quick response to the realities of the time.

    This translates to a 65 per cent decrease in processing fees for the renewal of registration for locally manufactured products (which will be N44, 200) as against what is currently charged and 45 per cent of the processing fee for foreign products (which will be $ 450) as against what is currently charged.

    In addition, the Director General, Prof Mojisola Adeyeye disclosed that the Agency has also granted a 10 per cent review of tariff structure for facility and inspection fees for Special Economic Zones (SEZs)

    This is contained in a press statement signed by the Agency’s resident media consultant, Mr. Sayo Akintola.

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    According to the Press release, “As businesses across the world confront the disruptions caused by the global economic meltdown, Prof Adeyeye noted that NAFDAC would continue to adopt and implement practical measures to ensure that the projected growth in the micro, small and medium enterprises (MSMEs) sector is not seriously affected by the development.”

    She further explained that the response of the Agency was not just to give succour and assistance to existing MSMEs, but also ensure that there is practical and active fillip to new MSMEs so that the growth of this sector is not discouraged by the current economic trauma.

    “This is our moment and NAFDAC as a regulatory agency is prepared to back MSMEs and other businesses that are prepared for the innovative and interesting times that lie ahead of us,” she added.

    “We have no excuse not to be one of the most productive and prolific economies in the world. We hope to achieve this aim in the incredible numbers of MSMEs that we have,” she said, as she described NAFDAC palliatives for MSMEs as a thoughtful and strategic response to the realities of the present time.

    “These are all indicators of the new spirit of NAFDAC and foretaste of the support MSMEs stand to enjoy in wading through these trying times. But this is not a new undertaking for us. It is merely an extension or intensification of the Federal Government’s long-standing commitment to MSMEs.”

    However, reacting to NAFDAC’S gesture, Engineer John Okodu, manufacturer of Star table and sachet water said that NAFDAC needs to do more if they sincerely want to encourage the MSMEs.

    “NAFDAC should reduce their charges further to at least augment what manufacturers are spending on energy. Electricity is almost nonexistent resulting in manufacturers depending on generators. Currently a liter of diesel is about N1,150-N1,300 while fuel is about N650 per liter.”

    Meanwhile, NAFDAC has reaffirmed its commitment to eradicating the menace of counterfeit drugs and unwholesome products from the Nigerian market.

    In response to recent negative press concerning the activities of fake drug manufacturers and sellers of substandard food and beverages, NAFDAC is intensifying efforts to ensure the safety of drugs and food consumed by Nigerians.

    The agency, led by Director-General Prof. Mojisola Adeyeye, stands resolute against a campaign of calumny launched by those who seek to profit at the expense of the well-being of fellow citizens. The recent exposure of a cartel involved in the production of fake wines and soft drinks in Aba, Abia State, underscores the gravity of the situation.

    Prof. Adeyeye clarified that NAFDAC brought the activities of these nefarious individuals to the public’s attention to safeguard citizens during the Yuletide festivities, cautioning against consuming potentially harmful substances disguised as cheap wines and soft drinks.

    The Director-General expressed dismay at the uncomplimentary commentaries in the media, highlighting the interception of counterfeiters in Eziukwu Market, Aba, as an example of NAFDAC’s commitment.

    She emphasised that the agency would not be deterred by unfounded allegations, urging the public to be vigilant and report any suspicious activities.

    Despite numerous life-threatening encounters and attacks on NAFDAC officers, Prof. Adeyeye assured that the agency remains undeterred in its mission to  safeguard the health of Nigerians. She urged citizens to assist by providing useful information on the activities of counterfeiters, emphasising, “They live and operate in our midst. We should say something when we see something.”

    Calling for the support of the 10th National Assembly, Prof. Adeyeye appealed for the expedited review of penalties against counterfeiting. She argued that stiff penalties, without an option of a fine, would discourage perpetrators from engaging in such illicit trades.

    NAFDAC, having achieved ISO 9001:2015 certification and World Health Organisation (WHO) Maturity Level 3, continues in its efforts to combat the scourge of substandard medicines. Prof. Adeyeye pledged that the agency would persist with sensitisation activities across the country in the New Year, ensuring Nigerians are aware of the threats posed by counterfeit products.

    Prof. Adeyeye urged consumers to scrutinize branded drinks or drugs before consumption. NAFDAC advises the public to consider the “4 Ps” before purchasing drugs, food, drinks, or alcohol.

  • NAFDAC seeks stiffer counterfeiting law without fine option

    NAFDAC seeks stiffer counterfeiting law without fine option

    The National Agency for Food and Drug Administration and Control (NAFDAC) has promised to remain resolute in its commitment to rid the country of counterfeit drugs and unwholesome products.

    It affirmed that threats to the lives of its officers as well as the recent negative press concerning the activities of fake drug manufacturers and sellers of substandard food and beverages would not discourage its efforts at ensuring the safety of drugs and food consumed in Nigeria.

    NAFDAC’s Director General, Prof. Mojisola Adeyeye, who restated the agency’s commitment to safeguarding the nation’s health, noted that an urgent review of the nation’s law on counterfeiting would address the issue.

    Adeyeye said the support of the National Assembly for the review of the extant law for stiff penalties without an option of fine for the offenders had become expedient.

    The NAFDAC boss said this would deter the audacious stance of perpetrators in the illicit trade, who appeared unfazed by existing penalties.

    Section 3 (1) (a) of the Counterfeiting and Fake Drugs and Unwholesome Processed Foods (Miscellaneous Provisions) Act, 2004, states that ‘Any person who commits an offence under (a) Section 1 of this Act, is liable on conviction to a fine not exceeding N500,000 or imprisonment for a term of not less than five years or more than fifteen years or to both such fine and imprisonment’.

    Section 3 (2) states: ‘Where an offence under Section 1 or 2 of this Act has been committed by a body corporate, every person who at the time of the commission of the offence was a proprietor, director, general manager, secretary or other similar officer, servant or agent of the body corporate (or a person purporting to act in any such capacity), he, as well as the body corporate, shall be deemed to be guilty of the offence and may be proceeded against and punished accordingly’.

    Though she did spell out details of the agency’s proposed penalties, Adeyeye stressed that stiffer penalties without an option of a fine would discourage perpetrators from engaging in such illicit trades.

    According to her, the recent exposure of a cartel involved in the production of fake wines and soft drinks in Aba, Abia State, underscores the gravity of the situation.

    Adeyeye assured Nigerians that NAFDAC remained steadfast to battle those aiming to profit at the expense of the well-being of their fellow citizens.

    Read Also: Counterfeiting law: NAFDAC seeks stiffer penalties, no option of fine for offenders

    In a statement yesterday in Abuja by the agency’s Resident Media Consultant, Sayo Akintola, the director general expressed dismay at uncomplimentary commentaries in a section of the media.

    She cited the interception of counterfeiters in Eziukwu Market in Aba, Abia State, as an example of the agency’s commitment to fighting counterfeiting.

    The NAFDAC boss said the agency would not be deterred by unfounded allegations, urging the public to be vigilant and report any suspicious activities.

    Adeyeye said officers from the Investigation and Enforcement (I&E) as well as Pharmacovigilance and Post-Marketing Surveillance directorates had been empowered to apprehend those involved in the production and distribution of counterfeit drugs and substandard food items.

    According to her, despite numerous life-threatening encounters and attacks on NAFDAC officers, the agency remains undeterred in its mission to safeguard the health of Nigerians.

    Adeyeye urged fellow Nigerians to provide useful information on the activities of counterfeiters, saying: “They live and operate in our midst. We should say something when we see something.”

    The NAFDAC boss promised that the agency would persist with its sensitisation activities across the country in the new year, ensure that Nigerians were aware of the threats posed by counterfeit products.

  • Counterfeiting law: NAFDAC seeks stiffer penalties, no option of fine for offenders

    Counterfeiting law: NAFDAC seeks stiffer penalties, no option of fine for offenders

    The National Agency for Food and Drug Administration and Control (NAFDAC) has vowed to remain resolute in its commitment to rid the nation of the menace of counterfeit drugs and unwholesome products.

    This is as the agency affirmed that threats to the lives of its officers as well as the recent negative press concerning the activities of fake drug manufacturers and sellers of substandard food and beverages are not enough to discourage its efforts to ensure the safety of drugs and food consumed by Nigerians.

    The agency’s director general, Prof Mojisola Adeyeye has however declared that an expedited review of the nation’s law on counterfeiting would go a long way in addressing the issue. 

    Adeyeye said the support of the lawmakers for the review of the extant law for stiff penalties without an option of fine for the offenders was crucial, given the audacious stance of perpetrators in the illicit trade, seemingly undeterred by existing penalties.

    Section 3 (1) (a) of the Counterfieing and Fake Drugs and Unwholesome Processed Foods (Miscellaneous Provisions) Act, 2004 states that ‘Any person who commits an offence under (a) Section 1 of this Act, is liable on conviction to a fine not exceeding N500,000 or imprisonment for a term of not less than five years or more than fifteen years or to both such fine and imprisonment’.

    Section 3 (2) states ‘Where an offence under section 1 or 2 of this Act has been committed by a body corporate, every person who at the time of the commission of the offence was a proprietor, director, general manager, secretary or other similar officer, servant or agent of the body corporate (or a person purporting to act in any such capacity), he, as well as the body corporate, shall be deemed tobe guilty of the offence and may be proceeded against and punished accordingly’.

    Though her proposed penalties were not disclosed, Adeyeye however asserted that stiffer penalties, without an option of a fine, would discourage perpetrators from engaging in such illicit trades.

    According to her, the recent exposure of a cartel involved in the production of fake wines and soft drinks in Aba, Abia State, underscores the gravity of the situation.

    However, she assured that NAFDAC remains steadfast against the slanderous campaign initiated by those aiming to profit at the expense of the well-being of their fellow citizens.

    She said NAFDAC brought the nefarious activities of the individuals involved to the public’s attention to safeguard citizens during the Yuletide festivities, as a caution against consuming potentially harmful substances disguised as cheap wines and soft drinks.

    In a statement on Tuesday, January 9, by the agency’s Resident Media Consultant, Sayo Akintola, the DG expressed dismay at uncomplimentary commentaries in the media, citing the interception of counterfeiters in Eziukwu Market in Aba, Abia State as an example of the agency’s commitment.

    She said the agency would not be deterred by unfounded allegations while urging the public to be vigilant and report any suspicious activities.

    She assured that officers from the Investigation and Enforcement (I&E) and Pharmacovigilance and Post-Marketing Surveillance Directorates have been empowered to apprehend those involved in the production and distribution of counterfeit drugs and substandard food items.

    According to her, despite numerous life-threatening encounters and attacks on NAFDAC officers, the agency remains undeterred in its mission to safeguard the health of Nigerians. 

    Read Also: NAFDAC alerts Nigerians to substandard, contaminated syrup

    She urged citizens to assist by providing useful information on the activities of counterfeiters, emphasizing, “They live and operate in our midst. We should say something when we see something.”

    Adeyeye pledged that the agency would persist with sensitization activities across the country in the New Year, ensuring Nigerians are aware of the threats posed by counterfeit products.

    According to her, NAFDAC remains steadfast in its mission to minimize the circulation of counterfeit products, ensuring that Nigerians consume only healthy and safe products. 

    She said: “The agency encourages the public to report any suspicious activities or illegal production of adulterated products to the nearest NAFDAC office nationwide. 

    “NAFDAC, having achieved ISO 9001:2015 certification and World Health Organization (WHO) Maturity Level 3, continues in its efforts to combat the scourge of substandard medicines.”

  • NAFDAC alerts Nigerians to substandard, contaminated syrup

    NAFDAC alerts Nigerians to substandard, contaminated syrup

    The National Agency for Food and Drug Administration and Control (NAFDAC) has notified the public about five contaminated syrups allegedly going round in World Health Organisation (WHO) regions.

    The notification is contained in a public alert number 037/2023, signed by the agency’s Director General, Prof. Mojisola Adeyeye, a copy of which was obtained by the News Agency of Nigeria (NAN) yesterday in Abuja.

    The agency listed the WHO regions to include: America, Eastern Mediterranean, Southeast Asia, and Western Pacific.

    It said the five oral liquid dosage forms (syrup and suspension) were also detected in the Maldives and Pakistan, adding that some of the affected products have also been detected in Belize, Fiji, and Lao People’s Democratic Republic.

    NAFDAC listed the syrups as: ALERGO Syrup, EMIDONE Suspension, MUCORID Syrup, ULCOFIN Suspension, and ZINCELL Syrup.

    The agency stated that “a total of 23 batches of the products are affected and named the manufacturer as PHARMIX LABORATORIES (PVT.) LTD (Pakistan)”.

    It added: “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).

    “This is in accordance with the Thin Layer Chromatography (TLC) test for Diethylene Glycol and Ethylene Glycol for inclusion in the International Pharmacopoeia.

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    “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 per cent w/w relative to the accepted limit of not more than 0.10 per cent w/w.

    “A follow-on inspection of PHARMIX LABORATORIES (PVT.) LTD was conducted by the Drug Regulatory Authority of Pakistan (DRAP).

    “The DRAP 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 LABORATORIES (PVT.) LTD.

    “The safety and quality of these products can, therefore, not be guaranteed,” Adeyeye quoted DRAP as saying.

    The NAFDAC boss explained that as precautionary measure, DRAP had instructed PHARMIX LABORATORIES to stop production of all oral liquid dosage medicines and issued a Recall Alert for the five different oral dosage manufactured by the company.

    She added that Diethylene Glycol and Ethylene Glycol are toxic to humans when consumed and can prove fatal.