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Showing posts with label iatrogenic suicide. Show all posts
Showing posts with label iatrogenic suicide. Show all posts

Thursday, 16 October 2014

Non-psychiatric drugs linked to suicidal behaviour and depression in new study

Adverse side effects of medicines can be underestimated and often not recognised as such. 110 drugs prescribed on the NHS have been linked to depression, self-harm and suicidal behaviour in a scientific study of patient Yellow Cards drug reaction reports sent to the Medicine’s Regulatory agency, the MHRA.

The paper published this September 2014 in the journal BMC Pharmacology & Toxicology is believed to be the first UK systematic review of psychiatric side-effects. Researchers found reports of 11,000 cases of depression, self injurious and suicidal behaviour following prescribed drug use between 1964 and 2011. This number covered 1.65% of all reports received in this time period.

Anti-depressants, acne, smoking cessation and weight-loss drugs were most frequently linked with serious psychiatric adverse drug reactions (ADRs). Clozapine, the anti-psychotic drug, had the highest reporting rate of suicide, with 78 reports between 1998 and 2011 linking the fatality to the drug.

Both nervous system and non-nervous system drugs met the study’s thresholds of at least 20 reports for depression, 10 for non-fatal suicide and 5 for fatal suicide between 1998 and 2011. Topping the charts with most frequent reports of depression were smoking cessation medicine, varenicline (Champix / Chantix) and bupriopion (Wellbutrin / Zyban), followed by paroxetine (Seroxat or Paxil), the SSRI antidepressant. Also high on the list of drugs linked to depression were the acne treatment, isotretinoin (Roaccutane / Accutane), and rimonabant (Acomplia), a drug for weight loss. For suicidal and self injurious behaviour, SSRIs, varenicline and clozapine occurred most often.

Figures found in the study are likely to underrepresent the true count of iatrogenic effects (drug-induced side effects) as the Yellow Card reporting system remains relatively underused by both patients and healthcare professionals.

The paper recommends the drugs most commonly arising in patient reports for grave psychiatric conditions need further analysis to understand the reasons why these drugs might be causing undue harm.

When a drug is licensed for prescription, pre-market trials do not undergo full powered studies into adverse drug reactions (ADRs) as this would require larger numbers of participants. Post-marketing pharmacovigilance using the Yellow Card reporting system and its careful analysis is therefore one of the main ways we can achieve a fuller picture into the neglected area of patient experience with medication.
Due to poor publicity and the underpowered studies of iatrogenic effects, psychiatric drug reactions and withdrawal effects are neither sufficiently well recognised nor analysed in the medical community. A study published in 2004 found that fewer than half of pharmacy programmes and medical schools provided students with a guide to reporting ADRs. Yet NHS Education for Scotland (NES), in a press release published in June 2014, stated that 7% of acute hospital admissions were due to ADRs. The NES have thus launched six new e-learning modules to support healthcare professionals identifying and reporting iatrogenic symptoms. Clinical pharmacologist Dr Simon Maxwell published an article reporting that undergraduate study is in urgent need of review to improve the safe and effective use of drugs in patients. 74% of medical students felt the amount of teaching in this area of safe prescribing  was ‘too little’ or ‘far too little’, and most disagreed that their assessment ‘thoroughly tested knowledge and skills’.

If we are to reduce the effect of ADRs on the population, and their economic impact that costs the NHS an estimated £2 billion each year, healthcare professionals and pharmaceutical companies need to make best use of new information made available by patient reporting.

Jacqueline Bond blogging for APRIL

Saturday, 17 March 2012

David Healy Pharmageddon & Suicide Prevention

David Healy has used Charles Medawar's research and his own experience and research for his new book
Pharmageddon. Not yet available in UK but can be purchased from Amazon. Also sections available to read on Amazon web site. An important contribution to creating awareness of psychiatric adverse reactions to medicines and suicide risk for some people who take SSRI antidepressants and other drugs.
With added information about the way medicines are licensed and the secrecy that covers up deception.


Patients are entitled to know the risk and be allowed to decide for themselves whether the benefits outweigh the possible harm of accepting any treatment offered by doctors who may have no knowledge of how drugs work. (Pharmacology was removed from curriculum requirement in 1993 by the GMC in their guidelines called 'Tomorrow's Doctors'.

Unfortunately in the UK a senior policy maker at the head of D of H Mental Health,  Professor Louis Appleby,  has decided not to inform doctors to be aware that akathisia (extreme agitation) an adverse side-effect, can lead to suicide. He believes information about medication induced suicide may cause harm.
To whom I wonder? See blog: http://davidhealy.org/platonic-lies http://davidhealy.org/

The Suicide Prevention Strategy for England

The Suicide Prevention Strategy for England contains no mention of suicide triggered by adverse drug reactions (ADR) or the adverse side-effect caused by many psychotropic medicines including SSRI and similar antidepressants  akathisia. The current consultation being reviewed now, was under the auspices of a person who was sympathetic to this being included. He has been removed from his post!

http://davidhealy.org/