International Tobacco Harm Reduction Advocates Urge Bangladesh to Reconsider Ban Proposal

Aug.22.2022
International Tobacco Harm Reduction Advocates Urge Bangladesh to Reconsider Ban Proposal
International tobacco harm reduction advocates urge Bangladesh authorities to reconsider proposed ban on e-cigarettes and smokeless nicotine products.

A group of international advocates for harm reduction in tobacco have written a letter to the Ministry of Health, calling on the authorities in Bangladesh to reconsider their proposed ban on electronic cigarettes and other smokeless nicotine alternatives.


The letter points out that smokeless nicotine products have the potential to help people quit smoking, and urges the Bangladesh government to ban less harmful cigarette alternatives.


The Bangladeshi government should encourage a shift from traditional cigarettes to e-cigarettes on a large scale and take swift action to minimize illnesses related to smoking, in order to protect smokers. This is according to a statement released.


According to the letter, the authorities in Bangladesh should establish a science-based tobacco control and harm reduction policy, which would "result in public health benefits.


This letter is a response to the recent discussions around the 2013 revision of the 2005 Smoking and Tobacco Products (Control) Act, which includes a new "ban on electronic cigarettes.


The author of this letter believes that the proposed ban would have an impact on protecting the major tobacco companies' cigarette trade and existing commercial interests, even as these companies are attempting to shift towards marketing lower-risk products.


The letter requests that the government of Bangladesh "accept reduced-harm tobacco products as a part of tobacco control in Bangladesh," stating that this "will meet the needs of those who cannot or are unwilling to quit smoking altogether.


The author warned that banning or excessively regulating e-cigarettes without considering the impact on smoking, could easily exacerbate the harm to public health by either sustaining smoking or stimulating black market activity.


The letter urges government authorities to adopt a proportionate approach in regulating electronic cigarettes to address the health issues caused by traditional tobacco cigarettes.


It is suggested that electronic cigarettes should be used to reduce smoking, which is the primary form of tobacco use in Bangladesh. The article emphasizes that electronic cigarettes should be seen as an opportunity rather than a risk.


The letter also provides several pieces of scientific evidence indicating that the harm caused by electronic cigarettes is far less than that of smoking.


In 2018, independent experts from the UK Public Health Department reviewed biomarker data and came to the conclusion that vaping only poses a small fraction of the risk of smoking, and completely switching from smoking to vaping can bring significant health benefits. Based on current knowledge, highlighting that vaping is at least 95% less harmful than smoking is an effective way to communicate the large differences in relative risk, and can encourage more smokers to make the switch to vaping, the letter states.


The letter urges Bangladesh to establish adequate regulations in line with the risks associated with tobacco, emphasizing that the primary objective of the country's tobacco policy should be to prevent and control the high rates of mortality and morbidity associated with tobacco.


The new regulatory system can set age limits, product standards, labeling, marketing and usage restrictions at its discretion, rather than imposing outright bans. The letter suggests that Bangladesh has the opportunity to learn from the experiences of the UK, EU and other places where there are valuable lessons to be learned.


Experts emphasize that in the proportional risk approach, products with the highest risk face the strictest regulations, while substitutes with lower risk face fewer and lighter restrictions.


Prohibition is the worst policy choice as it deprives law-abiding smokers of safer options, creates a black market, increases crime and corruption, ultimately burdening law enforcement agencies.


The main form of tobacco use in Bangladesh is through the use of e-cigarettes, which should be used as a means to reduce smoking, according to a letter. The letter indicates that e-cigarettes should be viewed as an opportunity rather than a risk.


The letter was signed by 17 individuals, including Dr. Delon Human, a former advisor to both the Director-General of the World Health Organization and the United Nations Secretary-General Ban Ki-moon.


Other signatories include Dr. Andres Milton, President of the European Red Cross and Red Crescent Network on HIV/AIDS and Tuberculosis, as well as scholars from Sweden, New Zealand, and Germany such as Professor Marewa Glover of Public Health at the University of Auckland and Professor Heino Stöver of Social Science Addiction Research at Frankfurt University of Applied Sciences.


Statement:


This article is compiled from third-party information and is intended for industry professionals for exchange and learning purposes only.


This article does not represent the views of 2FIRSTS, and 2FIRSTS cannot confirm the authenticity and accuracy of the article's content. The translation of this article is solely for internal communication and research within the industry.


Due to limitations in our translation skills, the translated article may not fully convey the meaning of the original text. Please refer to the original article for accuracy.


2FIRSTS maintains complete alignment with the Chinese government on any domestic, Hong Kong, Macao, Taiwan, or foreign related issues and positions.


The copyright of the compiled information belongs to the original media and author, and if there is any infringement, please contact us for deletion.



Disclaimer

This article is provided solely for professional research, industry discussion, and informational purposes. Any references to brands, companies, products, technologies, or policies are made for factual reporting and analytical purposes only, and do not constitute endorsement, recommendation, promotion, or advertising by 2Firsts.

Nicotine-containing products, including but not limited to cigarettes, e-cigarettes, heated tobacco products, and nicotine pouches, carry significant health risks. Readers are responsible for complying with all applicable laws and regulations in their respective jurisdictions, including age restrictions and access limitations.

The information contained in this article should not be regarded as investment, legal, medical, regulatory, or commercial advice. While 2Firsts strives to ensure the accuracy and reliability of its content, it does not assume liability for any direct or indirect loss arising from errors, omissions, inaccuracies, or reliance on the information contained herein.

This article is not intended for individuals below the legal age for accessing tobacco or nicotine-related information in their jurisdiction.

 

Copyright Notice

This article is either original content produced by 2Firsts or content reproduced, translated, summarized, or adapted from third-party sources with attribution where applicable. The intellectual property rights of the original content remain with 2Firsts or the respective original rights holders.

No individual or organization may copy, reproduce, distribute, republish, modify, translate, or otherwise use this content without prior authorization. Any unauthorized use may result in legal action.

For copyright-related inquiries, corrections, or removal requests, please contact: info@2firsts.com.

 

AI-Assisted Translation and Editing Notice

Portions of this article may have been translated, edited, or reviewed with the assistance of artificial intelligence tools to improve efficiency and readability. Due to the limitations of AI-assisted translation and editing, discrepancies, omissions, or inaccuracies may exist when compared with the original source.

Where applicable, readers are advised to refer to the original source for the most complete and accurate information. If you identify any errors or believe that any content infringes upon your rights, please contact us at info@2firsts.com, and we will review and address the matter promptly.

U.S. Judge Stays Helix, NJOY Challenge to FDA PMTA Rule Pending New Rulemaking Court Stays Altria's Helix, NJOY Challenge to PMTA Rule as FDA Prepares New Rulemaking
U.S. Judge Stays Helix, NJOY Challenge to FDA PMTA Rule Pending New Rulemaking Court Stays Altria's Helix, NJOY Challenge to PMTA Rule as FDA Prepares New Rulemaking
A federal judge in Texas on Oct. 8 granted a joint request by the FDA and plaintiffs including Altria subsidiaries Helix Innovations and NJOY to stay litigation challenging the agency's 2021 PMTA rule. The court cited FDA's anticipated rulemaking concerning the regulation at issue. FDA announced on Sept. 28 that it intends to reassess the PMTA framework and could initiate new rulemaking to replace it. The parties must file a joint status report within 45 days and every 45 days thereafter. A motion by three Reynolds American companies to intervene remains pending.
Regulations
Oct.10
Australia Adds 6-Methylnicotine to Schedule 9 Prohibited Substances, Effective October 1
Australia Adds 6-Methylnicotine to Schedule 9 Prohibited Substances, Effective October 1
Australia's Therapeutic Goods Administration published a final decision on September 25 to classify 6-methylnicotine as a Schedule 9 prohibited substance under the Poisons Standard, effective October 1, 2026. TGA said the chemical has been reported in e-cigarette liquids sold in Australia and marketed as nicotine-free or nicotine alternatives, while evidence also indicates its use in preparations such as oral pouches. The government originally proposed a Schedule 7 classification but ultimately adopted the stricter Schedule 9 designation, citing acute toxicity, dependence risk, use in unapproved consumer products and misleading marketing.
News
Sep.29 by 2Firsts Perspectives
FDA Authorizes JUUL2, Cites Adult Switching Amid Efforts to Speed PMTA Reviews
FDA Authorizes JUUL2, Cites Adult Switching Amid Efforts to Speed PMTA Reviews
The FDA authorized the JUUL2 device and tobacco- and menthol-flavored pods on Aug. 28, bringing the number of authorized e-cigarette products to 48. The agency highlighted complete switching among adult smokers, with six-week switching rates reaching 28.4%–49.3% for the menthol pod. The decision comes as FDA works to speed PMTA reviews, reduce application backlogs and expand authorized e-cigarette and nicotine-pouch products while maintaining enforcement priorities for unauthorized products.
Regulations
Aug.29
Altria Showcases Ploom, Marlboro Heated Tobacco Sticks and Non-Nicotine Energy Products at NACS Show 2026
Altria Showcases Ploom, Marlboro Heated Tobacco Sticks and Non-Nicotine Energy Products at NACS Show 2026
At the 2026 NACS Show, Altria displayed Ploom devices alongside imagery of Marlboro-branded heated tobacco sticks, while also featuring RIOT Energy and Proper Wild non-nicotine products. The booth showcased on! PLUS nicotine pouches, including 12 mg variants not listed among FDA-authorized products as of October 9, and NJOY e-cigarettes. Altria also presented convenience-store traffic figures highlighting its retail presence. 2Firsts examines the company's expanded product portfolio, non-nicotine business activities and the regulatory status of products displayed at the show.
EXPO
Oct.10
UK Extends Age-18 Rules to Zero-Nicotine Vapes and Nicotine Pouches From Oct. 29, Bans Vending Machines and Promotional Giveaways
UK Extends Age-18 Rules to Zero-Nicotine Vapes and Nicotine Pouches From Oct. 29, Bans Vending Machines and Promotional Giveaways
Key provisions of the UK's Tobacco and Vapes Act 2026 will take effect on Oct. 29, extending an age-18 sales restriction to all vaping and non-medicinal nicotine products. In England, Wales and Northern Ireland, the change brings zero-nicotine vapes within statutory age-of-sale rules and also covers products including nicotine pouches, strips and pearls. The law will also prohibit proxy purchasing for under-18s, consumer-facing vending machines, promotional giveaways and substantial discounts intended to promote vaping and nicotine products.
Regulations
Oct.10
Former Roche Neuroscience and Rare Diseases Communications Director Ria Kioupritzi Joins PMI as Scientific Affairs Director
Former Roche Neuroscience and Rare Diseases Communications Director Ria Kioupritzi Joins PMI as Scientific Affairs Director
Eleftheria (Ria) Kioupritzi, a biopharmaceutical professional with more than 15 years of experience, has joined Philip Morris International as Director Scientific Affairs within Corporate Affairs. She previously served at Roche as Senior Scientific Communications Director for Neuroscience and Rare Diseases and worked extensively in spinal muscular atrophy. Her earlier career also covered competitive intelligence, clinical and regulatory monitoring, pipeline development and launch preparation. During her time working in Roche's SMA field, Evrysdi passed through several U.S. FDA milestones, including its initial approval, an expanded indication for younger infants and approval of a tablet formulation. Public records do not show that Kioupritzi herself led the FDA submissions.
Sep.22