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    Home»Health»Stop-Smoking Drug Chantix Does Not Increase Risk of Psychiatric Problems
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    Stop-Smoking Drug Chantix Does Not Increase Risk of Psychiatric Problems

    By Society for the Study of AddictionApril 21, 20211 Comment3 Mins Read
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    Stop Smoking
    A new analysis of data shows varenicline does not increase the risk of psychiatric problems.

    A new analysis confirms varenicline does not increase psychiatric risk, supporting its safe use to help smokers quit.

    A new analysis of data from a randomized controlled trial of the stop-smoking drug varenicline (brand name Chantix in the US and Champix elsewhere), has provided clear evidence that varenicline does not increase the risk of psychiatric problems. The study also assessed the risk of psychiatric problems associated with bupropion and the nicotine patch. It similarly found moderate to strong evidence for no increased risk of neuropsychiatric adverse events relative to use of a placebo.

    Varenicline is very effective at helping smokers to stop, mainly by reducing cigarette cravings. However, concerns were raised soon after its launch that it might lead a small proportion of users to experience psychiatric problems such as suicidal thoughts, mood disturbance, and increased aggression.

    This led the US Food and Drug Administration and the European Medicines Agency to require the manufacturer, Pfizer, to run a very large clinical trial to assess the safety of the drug. The results were published in 2016 and they were interpreted as giving varenicline a clean bill of health. The analysis conducted at the time showed that there was no ‘statistically significant’ difference between the rate of psychiatric adverse events in people given varenicline and those given an inactive placebo. However, did not mean there was no effect of the drug, just that there was no strong evidence that there was an effect — which is not the same thing at all.

    Bayesian Analysis Offers Direct, Clear Answers on Risk

    When assessing drug side effects we need to be able to judge what the likelihood is of it causing side effects. The study team has today published a new analysis of the trial data directly addressing that question. It used a method similar to that used by codebreakers during the Second World War, called Bayesian analysis, to directly estimate the strength of evidence that varenicline causes psychiatric problems. The analysis provided strong evidence that in people without a psychiatric history, varenicline does not increase the risk of psychiatric problems. In people with a psychiatric history, it found that it probably did not lead to psychiatric problems but with less certainty. When it came to causing serious psychiatric problems, even in this group it provided strong evidence of no adverse effect of the drug.

    Dr. Emma Beard (UCL Behavioural Science and Health), who led the analysis, commented “The shadow of psychiatric problems has arguably cost thousands of lives by putting people off using varenicline to help them stop, and doctors off prescribing it. This analysis should provide further reassurance to smokers and clinicians that this is a safe, life-saving drug.”

    Professor Robert West, (also UCL), who was senior author on the paper, said “In my view, this kind of Bayesian analysis should be standard for assessing all drug side effects, including for example, COVID-19 vaccines. It directly answers the question we want answered: what is the strength of evidence that the drug has side effects? I’d like to see all studies of side effects use this approach in the future.”

    Reference: “Estimation of risk of neuropsychiatric adverse events from varenicline, bupropion and nicotine patch versus placebo: secondary analysis of results from the EAGLES trial using Bayes factors” by Emma Beard, Sarah E. Jackson, Robert M. Anthenelli, Neal L. Benowitz, Lisa St. Aubin, Thomas McRae, David Lawrence, Cristina Russ, Alok Krishen, A. Eden Evins and Robert West, 22 April 2021, Addiction.
    DOI: 10.1111/add.15440

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    1 Comment

    1. Pasi Toropainen on June 10, 2021 4:24 pm

      Could you please find out and answer to me ??I have find out amazing numbers from FDA ADVERSE EVENTS REPORTING SYSTEM (FAERS). I don`t know why Varenicline-cases and Chantix-cases has been reported as separate there?? Chantix/Champix and varenicline are the same ? Isn`t it so ?
      How is the real numbers in FDA and EMA ?? Chantix/Champix is top secret and most dangerous drug on the market.

      Numbers of adverse events :

      FDA (USA):

      Varenicline : total cases 75 841 serious cases 33 758 death cases 1525

      Chantix : total cases 66 037 serious cases 24 256 death cases 1170

      In EMA (Europe ) adverse drug reports the numbers don`t tell how many death cases ?

      Varenicline : total cases 22 968

      Champix : total cases 13 926

      We all know that those numbers in FDA,TGA and EMA are only tip of the iceberg.
      Just wondering what is the truth behind those numbers and why they had to be reported as separate? How many death cases in USA and Europe are the real one?
      Somehow I feel there is corruption between Pfizer and EMA /FDA/TGA ??

      Pfizer don`t even know how Chantix works……how it can be still on the market? So many death cases and permanent side effects….internet is full of horror stories about side effects and suicides….and no-one do anything?
      Someone need to tell the truth about this…..could you please help with this?

      Best,

      Pasi Toropainen

      Reply
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