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More than 11 percent of Americans take antidepressants, including rising numbers of kids and adolescents and even pregnant women.
The majority of Americans believe that depression is linked to a chemical imbalance in the brain, and that drugs can fix this imbalance—just as someone with Type 1 diabetes might take insulin. But that’s not true, according to board-certified psychiatrist Josef Witt-Doerring.
“There's never been any evidence that there's been a chemical imbalance,” Witt-Doerring says. “There is no way to differentiate patients who are depressed from those who are not depressed using any objective markers.”
Instead of fixing a chemical balance, what antidepressants really do is mask symptoms, he says.
A former FDA officer and now director of TaperClinic, Witt-Doerring helps people safely get off of psychiatric medications.
In this episode, we dive into the realities of antidepressant drug use, what most patients often aren’t told by their doctors, and how a patient can be weaned off of psychiatric drugs safely and avoid devastating withdrawal symptoms.
How do these drugs affect people long-term? Are they really safe for pregnant women? And what kinds of potential side effects do they have?
And we dig into perhaps the most taboo subject of all: Is there a link between antidepressants and mass shootings?
A lot of people have this idea that
anti-depressants, they're fixing
something, you know, kind of like a type
1 diabetic takes insulin, restoring them
to a normal state.
That's not true. Over 35 million people
in America take anti-depressants, but
many are not being told about the
long-term side effects of these drugs,
says psychiatrist Dr. Yseph Wit During.
He's the founder of the Taper Clinic,
which treats severe withdrawal symptoms
and helps people safely get off of
psychiatric medications.
>> There is a group of people that when you
bring them off that medication over 2
months, that's what I would say is a
fast taper. They will actually develop
very severe withdrawal symptoms that do
not get better. They get back on the
drug, but the symptoms don't go away.
How do anti-depressants actually work
and what kinds of side effects can they
have? What we know is that many of the
mass shooters are exposed to
anti-depressants. In the case of um some
who are trans, there's also hormone
medications as well which can have a
mood destabilizing effect. This is
American thought leaders and I'm Ya
Kell.
[Music]
Dr. Yseph Whit During such a pleasure to
have you back on American thought
leaders.
>> Glad to be back. So, what's the bottom
line? We keep hearing about SSRIs. We
keep hearing about anti-depressants that
they're maybe not effective, not
working. But then there's lots of
studies that show that they do have a
positive effect. What's the bottom line?
So,
it really comes down to the definition.
What does it really mean to say that
this medication works? And I think to
answer that question, you really have to
look at the chemical imbalance theory
because a lot of people have this idea
that anti-depressants, they're they're
fixing something, you know, kind of like
a type 1 diabetic takes insulin. So, if
it's okay, I'd like to talk a little bit
about that.
>> Yeah, please.
>> So, uh, back in the 1950s, uh,
anti-depressants emerged onto the market
for the first time. And the way they
were discovered was in tuberculosis
patients. there was a new drug
calledizit and they noticed that when
they gave it to those TB patients they
they looked less depressed they they
started to appear more energized and so
someone noticed this and said well let's
try this with patients who have
depression and they noticed that that
effect translated these depressed
patients became more lively now as they
discovered more about this drug and
other anti-depressants that were
emerging at the time they found that
they were actually increasing um monoam
amines, which is a name that we give to
serotonin, norepinephrine, and dopamine.
And so what the original researchers um
reasoned was that maybe depression is
actually caused by deficits of those
chemicals and the and the reason these
drugs are working is that they're
correcting that. Now, I don't really buy
that because I think the alternative
explanation is that you're giving
someone a drug that's having a drug
effect and it's masking it. You you
don't have to postulate that the person
is depressed because they were lacking
those chemicals, but that ended up being
a very um commercially important
narrative for drug companies. And so
they kind of ran with this idea that the
anti-depressants were fixing an
underlying thing because it's it's
better PR to say that they're fixing a
medical condition that you have than to
actually confront the other side which
is that you are taking a drug that has a
drug effect that is masking your
symptoms. Most people feel uncomfortable
about that because they start to think
well I don't want to mask symptoms. I
don't want to sweep real problems under
the rug. And so that's where this idea
of the chemical imbalance comes from.
Now coming back to your original
question about like do they work? So
a lot of people think that they work in
that they are fixing this imbalance.
They are restoring them to a normal
state.
That's not true. We we've there's never
been any evidence that there's been a
chemical imbalance. I mean we've looked
at um the CSF which is the cerebral
spinal fluid. We've looked at
metabolites for serotonin. We've done
post-mortem autopsies on the brains to
look at receptors for serotonin. Um, and
we've also done brain scans. We we've
never found a chemical imbalance. And
so,
>> so we've never found depression
connected with a chemical imbalance in
the brain. That's the bottom line.
>> That is the bottom line. Yeah. There is
no way to differentiate patients who are
depressed from those who are not
depressed using any objective markers.
And that's why when you go and see a
psychiatrist or a family medicine
doctor, they're not doing blood tests.
They're not scanning your brain. Um
they're essentially just doing a
checklist. The these are not
biologically grounded conditions. And so
the idea that you're taking a drug that
is going to fix that chemical imbalance,
that has no legs underneath it because
we we can't we haven't even found it.
There's nothing there. Mhm.
>> But what the drugs are doing and what
they are doing fairly consistently for
people is um inducing a drug effect. And
if we're going to go with the most
common class of anti-depressants, which
is the SSRI, what that effect typically
is is one of emotional numbing or uh
emotional constriction we say.
>> Mhm.
>> And that can be experienced as very
therapeutic for some people. If you are
in a state where you're having a lot of
anxiety and you take a drug and it kind
of constricts that that in it sort of
numbs that out, you're going to feel
better. And if you're highly suicidal,
you might even say that that drug saved
your life.
>> Um and so
I think that yes, these drugs do work.
they consistently um produce this effect
and that can be experienced as
therapeutic for some people, but for
others and and this is why oftent times
you'll never hear psychiatrists or the
media kind of talk about them as having
a drug effect. But but for some issues,
numbing someone out and masking those
problems is actually going to make them
worse. Um because they they need to
actually focus on why they're unhappy
instead of just like masking them with
the drug. So the bottom line is
basically it's complicated.
>> Yeah. Yeah. It's a lot easier of a
narrative to kind of sell like you have
a chemical imbalance, you have a
problem, take this drug, it's going to
kind of pick it up to a place um that
that's normal. Nothing to see here. But
the truth is is that depression is so
much more complicated than that. You
know, you can have problems with your
relationships, uh with work, your
physical health can sometimes result in
depression. And if you're not addressing
those things and you're just kind of
masking the symptoms for the drug, sure,
you're going to feel better. You could
say that it's working. You could say
that it's helping, but it's not actually
getting to the underlying reasons.
>> And this is really important because uh
over time, these drugs actually wear
off. People become tolerant to them
>> and then so you can get into a situation
where you're sort of maxed out on the
dose of the drug.
>> It's wearing off. You're not
experiencing that therapeutic effect
anymore. you still have all of those
problems that led you to getting on the
drug in the first place. And this is
what drives polyarm pharmacy, the
tolerance. They need to start another
drug. It wears off and they start
another one. And this is why you hear
that some people are on four, five, six
medications. Now they're going for
things like ECT and TMS. It's not it's
not really a sustainable long-term
strategy for many people.
>> So polyfarm pharmacy, that's uh taking
multiple drugs to deal with a condition.
And you're saying to often that's
because of tolerance that's developed.
What about uh ECT and the other acronym
you mentioned?
>> Yes. So ECT electrocomvulsive therapy
which is shock therapy. TMS is uh
transcranial magnetic stimulation and
these are psychiatric interventions
um that are they're kind of the end of
the line treatments after you you've
used the medications. Um they're they're
sort of like this advanced therapy. ECT
has a lot more side effects. There's
cognitive damage that can emerge from
it. Um, and but ultimately people will
end up there after, you know, they've
been on five different medications and
and they've worn off. And one of the
really sad things uh about what I'm
seeing in my field right now is that
there's some dishonesty when it comes to
explaining to patients why all of these
medications aren't working. Because I
think an honest response would be yes,
this is the understandable and
predictable outcome of of masking
symptoms with a drug effect that your
body is adapting to and here we are. But
many patients are told that well you
have treatment resistant depression your
mental illness is evolving you know you
you've developed a new condition and so
they don't really tell the patients
honestly what's happened and and then
they just keep on stacking on treatments
>> um when the solution might actually be
to come off of them and find another
approach. Mhm.
>> So, right now, probably the last thing
you want to be seeing is a pitch from
Yan. But I want to encourage you to
subscribe to the Epoch Times. It is how
we keep the lights on. It is how we keep
these interviews coming. Just hit the
link below and subscribe to the Epoch
Times.
Just a little bit about uh
electrocompulsive therapy and uh TMS.
>> From what I understand, there are
campaigns to get rid of
electrocompulsive therapy itself. Is is
is it something that actually helps
people? This is basically the same the
same question as with SSRIs for and I
guess is it for depression? Is it for
other conditions?
>> Yes. So there's there's two ma main
areas where people use ECT. So the first
one is depression. Um and the second one
is catatonia. And catatonia is a state
of um it's a very severe psychiatric
state where people can sometimes stop
moving, they stop eating and they and
they enter kind of a frozen state. Now
for catatonia, ECT can be very effective
in breaking people out of that. So I
want to put that aside. I do think there
is a use for ECT for patients with
catatonia that don't respond to other
things.
But where it's used mostly is in
depression um in treatment resistant
depression. And the reason that it's so
controversial is that it can cause um it
can cause a lot of memory impairment. Um
after you get ECT, you can forget kind
of large portions of your life. They
call it retrograde amnesia
>> and that can be very devastating for
some people. Uh some people even report
that they have difficulty remembering
things going forward. Um and the the
issue and why this has become so
controversial is that it's often
downplayed. Uh the the psychiatric
establishment has said, you know, ECT
it's it's well tolerated. There's not a
lot of side effects. But there's
actually a very large group of people
out there who are saying, "No, I'm I
actually have enduring problems with my
memory after this."
Um, now coming back to the question of
does it work? It does work for some
people. Um, and it will kind of break
them out of the depressive cycle.
The issue is is that it's being used on
a lot of patients
whose problems aren't actually, you
know, this depression or this treatment
resistant depression. Their issues are
really drug induced. You know, they're
on a cocktail of five different
medications that are that have worn off.
They're causing side effects. And
instead of the doctors kind of looking
at that and and seeing it in that
context, they're very quick to say, "No,
you just have severe depression." They
don't look at the medications and start
taking them off and and seeing if the
person gets better.
>> And so that's that's what I think is
going on with ECT.
>> Mhm.
>> And before I ask you about TMS, because
I'm also that's one that I'm not
familiar with. Actually, a very
influential book in my childhood or or
or I guess ear young adult years was a
book called Zen and the Art of
Motorcycle Maintenance
>> which is a book where it's precisely a
guy is with his son and he's had ECT
done and he has retrograde amnesia and
he's trying to figure out who he was
right and on this trip. So, I'm very
familiar with this with this. It was
actually quite an influential book in a
lot of ways for me. But what about this
TMS? TMS is like baby ECT. It's it's
actually a lot less harmful on average.
Um, and there's less controversy about
it. It's essentially a a a large magnet
that sends pulses into the brain that
disrupt um
>> um the the magnetic fields
>> as opposed to electric shocks, right?
>> As opposed to, you know, sending a
direct current through the brain um and
inducing a seizure because that's what
happens in ECT.
>> Uh patients are awake when they get TMS.
um it's less effective than ECT uh but
it also causes less side effects and I'd
say there's much less controversy around
that treatment.
>> I want to come back to you know your
work. So your work is focused a lot on
helping people come off of these
psychiatric drug cocktails and I think
as we're starting to talk about that I
want to mention that it's incredibly
important for people to do it properly
with help. It needs to be done slowly.
It needs to be done with support because
sometimes cutting them off very quickly
which some people might be tempted to do
if they realize that those drugs might
be actually the now the problem uh it
can cause its own suite of problems.
>> Yes.
>> If you could just speak to that a little
bit.
>> Yeah. So it's an area where there is
uh some nuances needed. Now um so I work
in it's a specialty practice. People
come and find me after they've had
difficulty coming off their medications.
Now,
I want you to imagine that let's say
you've been on an anti-depressant or
something like Xanax or Clonopin for
several years. You know, that's that's a
lot of Americans. Um
quite a large group of them can actually
stop these drugs pretty quickly within a
couple of months. They they have really
nasty withdrawal, but then they kind of
pull through it and and things normalize
for them. they move on with their life
and withdrawal is never really a big
issue for them. I would say that they
have very healthy elastic brains.
There's something just about them that
allowed them to adapt to coming off that
drug really quickly, readapt. Um, now
what I focus on in my work is a smaller
piece of that pie that there is a group
of people that when you bring them off
that medication over two months, that's
what I would say is a fast taper. And
that's really common for a lot of family
doctors and psychiatrists. They will
actually develop very severe withdrawal
symptoms that do not get better. Um
well, they'll develop very serious
withdrawal symptoms that don't get
better in that time frame. Now, there's
two really important things that most
people need to be aware of here. The
first thing is that if that happens to
you and you don't have one of these very
elastic brains that can readapt quickly
and you you get through it, your doctor
will tell you will tell you sometimes
that well this is unexpected. Uh, I've
been taught that this that you can taper
people in two months, that the
withdrawal is mild, that it's going to
go away. And because that hasn't
happened with you, this is proof that
your underlying condition is coming
back. And this means that you need the
drug. And so they'll put the patient
back on the drug. And this person
essentially ends up on an unwanted
medication potentially indefinitely,
afraid that they're unable to come off.
And so that's happening with a lot of
people. Now the other area which is even
less common but it's very important is
that some patients when you pull them
off the medications too quickly
particularly anti-depressants and benzo
they develop a condition called
protracted withdrawal and probably the
best way to describe this is just to
tell you what it's like for a patient.
So you go in and see your doctor and
you're coming off Xanax or clonopin.
These are really common sedatives.
you your your doctor pulls you off
pretty quickly or maybe you do it
yourself and you you end up with a lot
of withdrawal. You're you're anxious.
You can't sleep. Um your ears are
ringing. All pretty normal stuff.
One month goes by, two months go by and
you're still feeling unwell and and you
and you're white knuckling it. You say,
you know, if I just hang on long enough,
I'm going to get through this and I
don't want to give up. 3 months goes by.
It's still there. and then you say, "You
know what? This is too much. I want to
get back on the drug. I can't deal with
this. I'm gonna figure out another way
off." They get back on the drug, but the
symptoms don't go away. Um, and
so then you have a person who, you know,
is essentially has severe anxiety, brain
fog, ear ringing, kind of a whole host
of neurological problems. That person's
actually experienced a form of brain
damage. Um, and that's really what I
focus on in my practice is this small
group of people who come off whose
nervous systems become incredibly
sensitized. Um, and for them it usually
takes them about 18 months to two years
to recover. Sometimes it's even years
after it's like you've had a concussion.
And that has been really important for
me because it's actually changed the way
I practice. I now recommend to anyone
that I talk about that I talk to that
you have to come off these medications
in a controlled way. You need to do it
gradually because that because severe
withdrawal for some people and and we
cannot predict who they are can actually
cause this type of injury which which is
very disruptive to their lives. M
>> what percentage of people are not the
sort of the neuroplastic type that can
you know come off these common sedatives
in a couple of months?
>> No one has ever studied that. But I will
say I think it is a small fraction of
people. I think it's probably it's
probably five 5% of people 5 to 10% who
who have the protracted withdrawal.
Maybe it's maybe it's like um
I think 40% of people will will have a
lot of difficulty and may not be able to
to come off that quickly without severe
symptoms. But the people who actually
get hurt that's really small.
>> Um now I don't want to diminish the
problem because even if I say it's a
small fraction of them, there's millions
of people dealing with this problem. you
know, when we have 15% of the American
population taking anti-depressants and
worldwide, that's that's an enormous
amount. Um, and when you go online, you
can go to places like surviving
anti-depressants, different online
forums, uh, Facebook groups, that's
where these these these folks are. And
there's hundreds of thousands of people
in these forums supporting each other as
they're going through this. So it's it's
not common but it is a big public health
issue.
>> The other dimension that we haven't
talked about yet is the kind of is the
side effects which I understand often
people coming into using these drugs are
not aware of. And I'm I'm not talking
about the sedatives but I'm talking
about the SSRI
>> sure
>> uh anti-depressants.
So,
the side effect issue, if I were to list
the ones that I'm I'm most concerned
about, and there's a lot, so I'm going
to move fairly quickly on this.
>> The first one is something that everyone
should be aware of, and that is the risk
of actually not dealing with the real
problem.
>> Because if you go and see a doctor and
they're just like, "Hey, Jan, you have
major depressive disorder. Take this
medication." But actually maybe there
was some issue um with your
relationships or your work or something
like that.
You're distracted. You you now think I'm
going to understand these problems. It's
coming from my brain and you miss the
opportunity of actually addressing real
issues in your life and so they fester.
That's the main thing that I really
worry about. Mhm.
>> Now there's some other issues which are
um less common uh but important and and
so one of them is behavioral changes.
And so the the ways these are uh have
turned up in the media is really the
issue of drug induced suicide
>> and drug induced homicide. Um, and so
that is, you know, I'm not going to say
that that's a common issue, but it's
something that people need to be aware
of. And they kind of have similar
mechanisms, which I want to go into. So
you know as I mentioned before these
these drugs the SSRIs generally have
like a blunting and constricting effect
but all drugs you know recreational and
otherwise
um there can be a group of people who
will have a paradoxical um it'll have a
paradoxical effect on you know the
example I like to use is you could have
10 people sitting around smoking smoking
some cannabis nine people are giggling
and having a good time and you get one
person who becomes paranoid you know
there's just something unique about that
person's, you know, their brain and
their genetics that they have that bad
reaction. Now, if we're talking about
suicide,
if you get someone who is already
depressed and then you expose them to a
medication and they have one of these
paradoxical reactions, you can actually
make them worse. You can kind of tip
them into actually acting on those
behaviors. So, so not only are they
depressed and suicidal in the first
place, now they they become more
depressed, more agitated, more
impulsive, very blunted and
disconnected. They're not having a
therapeutic experience on it. And so,
they may impulsively end up taking their
life uh because of the medication. And
this actually happened uh recently in a
case I read about a young man called
Bryson Burks. He was um 20 years old. He
had a football injury. Now, he was never
depressed before, but his doctor put him
on three anti-depressants for pain. And
he took them for several months while he
was recovering. And when he healed, he
he came off of them. And during that
withdrawal process, he became unstable
and he actually took his life. And and
his his mom has been now speaking out
about the risks of coming off these
medications because it was a completely
avoidable death.
So in this case, if he had come off them
slower or he had supervision, what I'm
getting at is it's avoidable. How
>> it's Yeah. So
>> the symptoms have to do with coming off
the medication too quickly. If if you do
a staggered approach off these these
these meds, uh you know, you you drop
10% or 15% and then you wait a short
period of time, then you do it again,
you'll be much more in control. Um, and
so some withdrawal is inevitable when
you're coming off these medications, but
you want to keep it in that mild to
moderate range of symptoms where you're
still functioning well. You need to
avoid severe withdrawal symptoms where
you can become unstable. Now, what I
read about this case, and I don't have
all the details, is that he came off
three medications in 3 weeks.
>> And that is a lot even if you've only
been on the medications for several
months.
>> And so it was likely he was pulled off
rapidly.
um and essentially went into severe
withdrawal and it did something he never
would have done um if he wasn't in that
state. And then what about homicide?
>> Now this is a very controversial area
that does not get a lot of coverage. So,
and this has turned up in a lot of um a
lot of discussions about school
shootings actually that that you know
they notice that school shooters are
taking SSRIs. And so I want to unpack
that. But I want to start by saying
this. I'm not trying to say that you
know every single school shooter or mass
shooting event is due to SSRIs. I think
clearly it's a multiffactorial problem.
I think we have issues with um social
contagion that that spurs this on. I
also think we have to be real. We we
have a lot of firearms in this country
and because of that if someone's having
a adverse behavioral reaction to a
medication, you can grab a gun. You
know, you if if there's not guns around,
you grab a knife, but obviously a gun is
a more deadly weapon and it can cause
more harm. That said, the role that
these anti-depressants play has to be
considered. Um,
and I want to talk a little bit about
the drug labels quickly before I go on
to this because I know some people they
hear this and they go, "This is
quackery." You know, there is there
can't be a link here. If you just look
at the drug labels for aderall and rolin
in the warnings and precautions, it
already lists aggression and hostility.
This is where they put the most
important risks. If you look at SSRIs,
it already lists there in the label that
they increase the risk of suicidal
behavior. It lists hostility, agitation,
and violence. If you look at abilify,
which is an antiscychotic, homicidal
ideiation is already in there. And so
what I want people to be aware of who
are listening to this is this. These
risks are actually already in the drug
labels from the manufacturers.
Now the question is okay sure maybe
there's some violence maybe you can have
homicidal ideiation but can this
actually you know has this been linked
to actual homicides
and time and time again we've seen this
go through the court system and judges
and juries have have found that this has
been involved and perhaps the most
well-known case of this was a case in
Wyoming and it involved a gentleman
called uh Don Shell um he was an older
man and he had been exposed to Prozac in
the past an SSRI and he had an agitated
response to it and they stopped it
quickly. His next doctor who did not
know that he had that history in the
past gave him a drug called Paxel which
is an SSRI. Now this shouldn't have
happened given he already had a bad
experience to the same drug class. And
so they so so Don's new doctor put him
on Paxel and within a week he killed his
wife, he killed his daughter and he
killed his granddaughter and then he
shot himself. I mean an unspeakable
tragedy uh for the family. Now the
surviving son-in-law um um his
daughter's husband and the and the
father of um the grandchild that he lost
um brought suit against Smith Klein uh
Smith Klein. This is before GSK had
formed and this was heard out before a
jury um in Wyoming and they ruled in
favor of Tobin. That was the name of the
son-in-law who survived. He was given a
million-dollar verdict. It was for
failure to warn. Um uh Smith Klein
appealed it. Um it did not change the
verdict. And so we already have court
cases where judges juries have heard the
information and said, you know, if not
for the drug, this wouldn't have
happened. The same thing happened in
Australia. A man uh strangled and killed
his wife during a a bad reaction to
Paxel again. Um and the judge ruled
there as well. Uh if um if not for the
drug, this wouldn't have happened. And
there's been many other cases uh that
have been described in a paper by David
Healey who really is the big expert on
this called uh anti-depressants and
violence uh intersection um with the
law. Um and and so this is already
happening. I I know we don't like to
talk about it in the media. It's
something that's very suppressed.
>> Uh but the courts are already dealing
with this and and they are finding that
these drugs are playing a role.
>> I often hear about um po possible SSRI
involvement in shootings, but typically
we hear about this in with respect to
mass shootings. Mhm.
>> Right. And so these I is this is there
any relationship that's been drawn
there?
>> So perhaps the most well-known case uh
when it comes to mass shootings was a
case that was in Louisville, Kentucky
that involved a gentleman called I think
it was uh West Becker was his name. and
um he went into his um his place of
work. I think it was a paper printing
factory and he killed several people
with a firearm. Um
this case is a little bit complicated
though. It was uh there were multiple
lawsuits about u Prozac and violence at
the time and this was the first one that
went forward but before it got to get
before it went to verdict it was settled
um out of court. So, we never really had
a jury rule on it, but many people
thought that the drug was involved. What
we know is that many of the mass
shooters are exposed to
anti-depressants. Um, in the case of um
some who are trans, there's also hormone
medications as well, which can have a
mood destabilizing effect. And so there
is potential there that you you get
someone who is already unhappy and you
put them on a medication that's known in
rare instances to cause these issues
that can lead to or precipitate
violence. Now the problem is that is
that we're really not looking at it and
and it's very rare to evaluate someone
um who's had
um who does something like this because
they usually take their life. Mhm. The
>> the only case that I've really heard of
recently where we were able to interview
someone where it looked like there was a
relationship was the Aurora shooting, I
think I think may have been 12 people
were killed in in Colorado. It was the
Batman shooting where James Holmes
dressed up as the Joker, I believe, and
and and he murdered a lot of people
there. Now, so there were multiple
forensic experts that ended up
interviewing him and one of them, David
Healey, he believed that if not for the
Zoloft, this would not have happened.
And the way that he kind of pieced that
together was that he noticed that when
James went up on the dose, which is
commonly the time that people become
destabilized,
>> he had a clear behavioral change. He
started to send um flirtatious messages
to his roommates, which was a very big
change from a very reserved, quiet, sort
of nerdy guy. Um he ends up dying his
hair red as well. And his his behavior
marketkedly changes and then three uh 3
weeks later he ends up doing this
terrible mash shooting. And so what
happened there? Well, it looks like it
induced a manic episode. Mhm.
>> Um, now the defense actually chose not
to run with that story. Not really sure
why, but I think it has to do again with
the death penalty was on the table if
there was a whiff that we're trying to
look for something exculpatory. Um, that
might not go down that well. And so they
actually didn't use it. But the whole
case was described really well in the
BBC documentary, A Prescription for
Murder. and they actually go through all
of the details. If someone's really
interested in that, it's a great watch.
You can just Google it. Um, but to me, I
thought that was a very compelling
temporal relationship between increasing
the dose, having a clear behavioral
change, and then shortly thereafter
committing a um a mass shooting. The
reason why it's actually so important to
look at this is because people are
afraid to um and I'm going to posit a
little bit about the psychology of this.
Um, so
if if you're involved and if you're the
surviving family member in um and a
school shooting has happened in your
town and several people have died, I
actually think there is tremendous
pressure on you to just want this to go
away. I mean, it's such an unspeakable
tragedy that to start saying, "Hey, you
know, I think a drug was involved. I
actually don't think the person did
this, you know, on purpose. I think they
were under the influence." people aren't
going to go there. I mean, it's it's it
might be right, but I can see that there
is a lot of pressure on them. And this
is why it's so important for governments
to start looking into this because it
can actually change things.
>> Now, I want to unpack that a little bit.
If we started looking into these mass uh
these mass shooting events and actually
kind of even if the family doesn't want
to talk about it, investigating it,
talking to the the surviving family
members, okay, were they on a
medication? Had they had any dose
changes? Did you notice any changes in
their behavior recently? Uh you know, if
if yes, were there any alternative
explanations? Were they using drugs or
or anything otherwise? Um because if
we're finding that these rare events
that happen on these medications are
actually a part of this as a country we
might decide that when we put someone on
an SSRI we say hey I really want a
spouse a family member or a friend here
so I could say in very rare instances
these may lead to behavioral changes
that can sometimes result in violence
over the next month I just want you to
check in on this person if you if you
think that there's any changes call me
immediately and let's talk about it.
>> Because these drugs are often given out
almost in like these fiveminute
appointments with family medicine
doctors and you don't know if that
person's really being monitored.
>> And so it can really it can lead to
better informed consent. It can lead to
having important conversations with
family members about uh about
supervision. Um, and that's
and that's really what I'm I hope is
going to happen because in Tennessee,
um, the governor, Bill Lee, actually
with bipartisan support was able to get
a bill through recently to look into the
role of psychotropics in mass shootings.
>> And so they're they're actually finally
going to investigate this instead of
just trying to move on um from these
tragedies. You know, you can imagine
there's a lot of, you know, there's, I
think, a lot of reasons why in the past
people may have wanted to move on.
Sometimes it's family members not
wanting to go there. Then there's, you
know, the potential for abusing that
family member could also not want to
believe that their uh son or daughter
could do this at all. So, they may want
to blame the drug. The opposite Yeah.
>> situation. And then, of course, there's
the, you know, kind of corporate
interest of not being implicated in in
anything like this. So there's a whole
lot of let's there's a whole lot of
strong interests um at at play here.
>> And then there's this intimidation that
I see happen just in general when it
comes to criticizing psychiatric
medications.
um uh media companies, they're not going
to want to talk about it because when
they do, uh you get groups like um you
get these these these faux grassroots
patient organizations like NAMI
Depression Bipolar Support Alliance,
these these groups that are essentially
propped up by pharmaceutical funding,
you know, and people don't realize this,
the these patient advocacy groups.
Anytime the media comes out with a
critical story, they get calls, hey, you
know, this is stigmatizing our patient
population. You know, you're being
harmful. You're scaring people away from
life-saving drugs. That, you know, they
reach out to other reporters. They say,
you know, Epoch Times or whoever is
picking this up, they're so dangerous
and they don't want that kind of
pressure. And so it creates this feeling
as if
you know this is this is what we
believe. You know these drugs could
never do it and to even bring it up is
actually dangerous. You're a dangerous
person.
>> But that is clearly serving a commercial
uh a commercial interest there and and
and that intimidation for a long time
has actually worked. media companies are
not interested in in covering the other
side of the story because they think
it's compassionate and it in some way to
to to the people who take the
medications, but that's really uh I
think it's really a cover for a
commercial motive that that is shaping
things
>> there. Presumably there's all sorts of
patient advocacy organizations, right?
Not necessarily ones that are all say
fund pharma involved. Yeah.
>> Right.
>> So, what about the other ones?
>> Yeah. Yeah. Like,
>> well, it it comes down to money and like
how big your microphone is. So, you can
have like mental illness is so
complicated, right? Like imagine a
spectrum. On the one hand, you have some
people who are just like these these
drugs, they're always safe and they
never have any risks and we really ought
to use them. And then on the other side
is, you know, we ought to be really
careful about these medications. There's
there's a lot that can go wrong. I think
about the pharmaceutical company as
almost like a gardener with like a water
spigot with a watering spigot. You get
to just kind of survey all of the
different people out there and their
opinions and you can say these guys,
these are the people who align with my
opinion or this celebrity with this
story or, you know, this group. We're
just going to pour water on them. We're
we're going to help them grow. We're
going to develop them. We're going to
um you know, help them with their PR.
we're going to connect them with with
journalists. They use their financial
resources to platform a certain
perspective which helps them because
you're right there there are there are
other groups out there but you never
hear about them
>> because they're not financially
resourced
>> in the same way as as a group that goes
along with the agenda of of these
companies.
>> Interesting.
>> Yeah.
>> So you used to be in the FDA. Um tell me
what you did. So I was a medical officer
in the division of psychiatry and so my
role was to um review clinical trial
dossier to to get drugs onto the market
and it was also to review um uh emerging
safety problems
and so what made you
leave? Yeah,
>> presumably you took a pay cut
>> when I
>> when you went solo. I mean, so I, you
know, I actually it was it was the
opposite. I was actually seduced into
the pharmaceutical industry, which is
another uh big issue. And so I I
actually tripled my salary when I left
the FDA. I I was still kind of confused
>> um in my career. And so I I was at the
FDA
and I mean we can talk about the
problems there, but but I ended up going
into the pharmaceutical industry uh as a
drug safety person and that was my last
stop. I I kind of made it there for
about a year and eventually I said I
can't be a part of this. You know, I was
able to sort of suspend my suspicions
that there were problems with
psychiatric medications up until this
point. But then when you it's like going
into the factory and seeing how the
sausage is made. When I actually got to
see the evidence base underlying the
these medications, I realized that I
believe I'm participating in one of the
biggest scams of the 21st century when
it comes to just the overprescribing of
these medications. And so I had to I had
to get out. I I could not be there
anymore.
>> Okay. Fascinating. Um because because
you said overprescribing again, you're
not saying that they don't work at all.
You're saying that they're used way too
much.
>> Correct. Yeah.
>> And we tell people incorrect things
about the medications. For instance,
something I was always told as a medical
student and trainee is don't worry about
the anti-depressants. They're safe and
effective. You know, they're approved by
the FDA. These things work. When I went
there, what I learned was they were
actually leaving out a really important
piece of information, which was uh yeah,
for the 12 weeks that they studied for.
Um, and I mean, that's a whopper. I
mean, if you think that half of the
people on anti-depressants are on them
for 5 years or longer, um, that's
important for people to know that these
drugs really aren't studied, uh, that
long. And so I learned that when I went
there that that there's never been a
randomized placeboc control trial that
has gone longer than 12 months. And I
was also learning about all these all
these other side effects. You know,
things I talked to you about before like
postsri sexual dysfunction.
>> Um the fact that these medications
actually make some people worse in the
long run. They cause something called
tardy dysphoria. It's where you're
fatigued and you have brain fog and you
have low motivation. Um and so if people
actually knew that the drugs were none
of none of them the SSRIs have been
studied longer than a year that it's
quite easy to see that people develop
tolerance to them and they wear off over
time and that there's actually these you
know they're uncommon but they're
extremely important side effects that
can have lifechanging ramifications.
I believe that 90 90% plus people would
say you know I don't want to take that
risk. this doesn't seem like a great
strategy. And then they would start
looking for other ways of uh working on
their mental health.
>> Well, and maybe I think going back to
something you mentioned, they might feel
compelled to deal with the underlying
problem. Correct. Potentially in their
life and address that or something. I
think that's what you're alluding to
here, right?
>> Exactly. Yeah. Yeah.
>> You went back to the FDA recently. You
were on a panel. uh what was it like?
So
it was really heartwarming um and it it
made me very happy. Now let me unpack
that a little. So the I was there to
talk about uh the risks to children
exposed to SSRI and anti-depressant
medications in uterero. So when the mom
is pregnant with them and quick summary
of that is that most women are told that
there's nothing to worry about when you
uh take a medication when the baby is
growing uh when you're pregnant with the
child.
That is not the case. We actually have
12 different MRI studies that show
structural and functional changes uh in
the babies who are exposed. Um, we have
some quite concerning animal studies
that show that there's a higher rate of
um, autistic- like behaviors and also
decreased sexual interest in in rodents
who are exposed growing up. And really
the message when we went there is that
moms should hear this. They they should
hear that there are some signals that
there could be changes. We're seeing it
in the animal studies. It's something
that you need to be aware of. Make sure
you really need these drugs before you
get on them.
Um, and so that was the message. We got
slaughtered by the mainstream media
afterwards, uh, essentially for
again, you know, the same thing. I mean,
we're scaring people away from
medications, but they never really
engaged with any of the evidence or the
points that we made. Now, the reason why
I was so happy
about this was it signaled a real change
at the FDA. Um the last time I was there
in 2020 when I was working, I felt like
the agency was acting more like
advocates for psychiatric medications.
Um
psychiatrists
before really they had become so
fixed on this idea that if you if you
talk about the risks of these
medications, you're going to scare
people away. And that had really
permeated the the FDA. The reason why
this was so different was that we were
invited there by Marty Mccari and his
leadership team to actually address a
serious issue. And so it felt like
there's, you know, with the Maha
movement and Bobby and him putting in
people that are in line with his agenda
that the agency is actually taking some
of these serious risks. They're taking
them seriously again. They're and and
they're wanting to talk about them. It
was a really positive experience for me.
M
>> um what about in the aftermath? Yes, you
were criticized in a number of legacy
media. What about in terms of you know
patients or uh patient advocates or what
was the reaction?
>> I mean the reaction has been amazing. uh
you know myself and other panel members
like Adam Ur we've been making our way
through alternative media sources where
it's been whether it's been podcasts
um where people are interested in
getting this message out and so it it
put this issue on the map and people
have been very interested in it and more
people are talking about it. Over the
last few decades, the use of these drugs
has
grown massively, I think, would be fair
to say.
>> Um, is that still continuing?
Does it make sense to continue that?
>> Um, you know, where where do you think
things should go from here given what we
know today?
>> I think we need to really question what
we're doing. I mean, the use of
anti-depressants has gone up uh fivefold
since the early 90s. That that's when
Prozac entered the market. Since then,
teen suicide, suicide, disability um
from mental health diagnoses has all
gone up about 50%. We are not heading in
the right direction with the way we are
treating uh mental health problems. M
>> I think we need to look at that and
notice it. Now in my psychiatry circles,
what people say is, "Well, mental health
is getting worse for other reasons and
these drugs are a damn sort of stemming
the tide of overflowing mental health
problems instead of actually considering
that maybe this strategy doesn't work.
You know, maybe treating everyone with
anxiety and depression with these
medications and and and this is this is
80% of mental health visits. It's for
depression and anxiety, not bipolar and
schizophrenia. Most people are coming
with these these issues.
>> Maybe we need to look at does this
really work when people come in with
these problems to give them medications
instead of really understanding their
lives and helping them fix it. I mean, I
would love to see people dive into that
problem more because I don't think what
we're doing is leading to better mental
health outcomes.
>> So, as we finish up,
>> Yeah. Um, what do psychiatrists that you
think are on the right track do? Um,
like what's in their sort of arsenal of
tools? Sure.
>> When someone comes in in this situation?
>> Well, I want to talk about what I think
things should be like because because
right now most psychiatric meds are
handed out by family medicine doctors,
gynecologists,
um,
and people on the front lines. So, uh,
these professionals because of our
insurance system, which really pushes
people towards, uh, shorter visits,
that's how we're incentivized to kind of
turn through people. We're not
incentivized to get people better. The
more people we see in the in the less
amount of time,
>> the more the more we the more we make.
>> Um, and so I I do I feel for my
colleagues who are in this system and
they want genuinely to help people and
they think they're helping people
because that's what they've heard. We
need to find a way to change the system
so that we can actually help people in
more sustainable ways. Now, what might
that look like? And and and these are
the things that I think about a lot.
Embedded in primary care, we need to
have a curriculum and also some groups
about satisfying relationships, about
finding meaning, whether it's through
work, your faith, or your community. We
need to have um education about physical
health whether it's you know moving your
body good nutrition as well and also uh
on substance use disorder. I think those
four things are the main areas and I
think if we can have a a curriculum
around that where people can they can
watch um they can become educated on
some basic knowledge of these four major
pillars that really drive a lot of
anxiety and depression and then they can
meet in groups to to kind of go through
this content and to talk to the
professionals.
we can actually start to really fix some
of these major problems. And I would
love to see a a family medicine doctor
talk with a patient and they say, "Well,
you know, I'm having relationship
problems. I'm having um some health
issues." And they go, "Well, don't
worry. We've got something for you for
you. I want you to do this assessment."
And then on Tuesday night, you can come
in here and you can meet with one of our
professionals. We're going to start
teaching you about this. And that will
take the pressure off the family doctor
to say, "Hey, take this medication."
Because they actually have something to
offer them
>> in that case. And to me, it's just
bananas that in this country, we haven't
done something like that.
>> And that places like the NIMH have not
been conducting research on helping
people with these these enduring
problems. The these aren't new problems.
These are things that all people have
suffered from for a really long time. We
need to get more research and more of an
emphasis on on helping people with these
issues
so we can eventually give it to um
insurance companies and get this funded.
Um up until now, NIMH has just been
doing like biological targets for drug
development. We need to refocus on
non-drug therapies for anxiety and
depression so we can back up our family
doctors and the OBGYNS. And then
presumably another thing I think you
mentioned this earlier is if a doctor is
going to be recommend a mech medication
to explain the possible side effects in
more detail.
>> Yes, absolutely. Yeah, I think I mean I
I've got some ideas about this. I think
I think the FDA should should make drug
companies put a QR code um on the top of
prescription bottles. And so when you
get a prescription, you see something
there and it says, "Watch me." And the
FDA develops a 5-minute patientfriendly
video where you just look at it on your
phone and they say, "Hey,
these are the risks. Uh this is what you
need to know about the drug." Because
many doctors, they they're not taking
the time to fully inform people. And and
there there is a scalable way of getting
that information out there. I don't know
why we don't do these things. Um I I
think there's so much space for
improvement. um in in healthcare.
>> Well, Dr. Yseph Whit During, it's such a
pleasure to have had you on.
>> Thank you for having me again.
>> Thank you all for joining Dr. Yseph Wit
During and me on this episode of
American Thought Leaders. I'm your host,
Yana Kellik.
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