Prozac one of 30 antidepressants probed by UK watchdog over links to suicide

More than 30 of the most common antidepressants used in the UK are to be reviewed by the UK’s medicines regulator, as figures point to hundreds of deaths linked to suicide and self-harm.

The drugs, which include Prozac and are prescribed to millions of patients, will all be looked at by the Medicines and Healthcare products Regulation Authority (MHRA).

It follows concerns raised by families in Britain over what safety measures are in place for those taking the drugs, such as clear warnings of potential side effects.

The regulator will look into the effectiveness of current warnings, according to a letter from mental health minister Maria Caulfield and seen by The Independent.

There has been a huge rise in the use of antidepressants in England with 85 million prescriptions issued in 2022-23, up from 58 million in 2015-16, according to NHS figures.

Lord Nigel Crisp, peer and chair of the Beyond Pills All-Party Parliamentary Group, told The Independent: “Overprescribing of antidepressants has an enormous cost in terms of human suffering because so many people become dependent and then struggle to get off them – and wastes vital NHS resources.”

The review comes as:

:: More than 515 death alerts linked to these drugs, involving suicidal ideation and self harm, have been made to the MHRA since 2000. These alerts don’t directly confirm the cause.

:: Side effects of many antidepressants can include suicidal thoughts and anxiety, according to the National Insitute for Clinical Excellence.

:: One mother Liz Richardson, called on the regulator via The Independent to review safety measures around mirtazapine after her daughter took her own life two weeks after being prescribed the antidepressant.

:: Some antidepressants have been given to children as young as four and the total cost of the medication to the NHS in 2022-23 was more than £231 million

The regulator confirmed to The Independent that the expert working group will look at 30 different medications. Drugs include fluoxetine, the brand name of which is Prozac, lithium, and citalopram.

According to MHRA data, fluoxetine has prompted 9,237 serious and fatal alerts over adverse reactions since 2000 . Of those, 438 were related to “suicidal and self-injurious behaviours” and 286 were linked to anxiety symptoms.

Data suggests there have been 73 fatalities linked to suicidal and self-injurious behaviours in the last two decades. The data does not confirm the drugs are a direct cause of death.

Last week The Independent reported on calls from Ms Richardson for the regulator to review safety measures around mirtazapine after her daughter Rebecca Kruza took her own life two weeks after being prescribed the medication.

Mirtazapine, which was given a “black box” alert in the USA due to its side effects, has had 59 alerts linked to suicidal and self-injurious behaviours. This led to the US regulator placing clearer warnings on the packaging.

It will be included in the MHRA’s wider review.

In a letter to Ms Richardson, Ms Caulfield said the MHRA’s review will look into the effectiveness of the warnings about suicide relating to antidepressants.

As the use of antidepressants soars, the most recent NHS data from March 2023 to December 2023 shows 331,000 10 to 19 year olds were prescribed an antidepressant – up from 240,000 during the same period in 2015-16.

Last year, the Beyond Pills APPG called for government action to reverse the increase in prescriptions of these drugs.

Professor James Davies, associate professor of Psychology at University of Roehampton and member of the Beyond Pills APPG, warned there were “insufficient” provision of social and psychological alternatives to medication.

While 8.5 million people were prescribed anti-depressants in 2022-23, only 1.2 million people started talking threapy treatment.

“We have over 85 million prescriptions of these drugs each year in England, and that figure grows yearly,” he said.

“Another concern is not only are we seeing vaulted rates of prescribing to the general population, we’re seeing the average duration of time a given person spends on these drugs increasing as well…

“One of the reasons for this is that there’s still insufficient provision for social and psychological alternatives in the NHS.”

He warned patients are not being adequately followed up once they have been prescribed these medications.

Professor Davies added: “We should not be prescribing these psychotropics to young people. We should be providing young people with the psychological and social support necessary to enable them to overcome the difficulties that they’re encountering.”

The MHRA said it could not confirm the scope of the review or what actions could be taken as a result as it was still convening its panel of experts.

It told The Independent: “We are currently finalising the core membership of the expert working group considering risk minimisation measures for antidepressants and anticipate that their first meeting will take place in July. The group will be considering all antidepressants on the UK market.”

Professor Davies highlighted concerns over the regulator’s ability to conduct the review.

He said: “The MHRA is far too close with the industry to be objective for this review, in my view. It is 100 per cent funded by the pharmaceutical industry. There are serious concerns about what we call regulatory capture which is when it is far too close to the industry it is purporting to independently regulate.”

An MHRA spokesperson said it had “robust conflict of interest mechanisms covering MHRA staff, board members and those who give independent, expert advice on MHRA committees. These mitigate any potential conflicts of interest effectively”.

Dr Amit Aggarwal, from the Association of the British Pharmaceutical Industry (ABPI), said companies support “ethical and evidence-based prescribing”, and wants to help healthcare professionals and patients reach sensible decisions on best treatment.

A Department of Health and Social Care spokesperson said Talking Therapies was the recommended first line treatment and that the scheme is expanding to include 384,000 more people over the next five years.

It added: “The decision to prescribe a particular product is a clinical one and should be based on the patient’s medical need, taking into account NICE guidelines, which recommend not routinely offering antidepressant medication as a first-line treatment for less severe depression.”

Eli Lilly, which owns Prozac, told The Independent: “There is nothing more important to Lilly than the safety of our medicines. For decades, Lilly has been submitting fluoxetine safety data, to regulatory authorities around the world, including the MHRA and FDA.

“Fluoxetine is approved by the MHRA and FDA and continues to be considered to have a positive benefit-risk profile by regulatory authorities, physicians and patients around the world.”