The dangers of mixing drugs Celine Valery
Which of these three people
is doing something risky?
Is it the one who takes their cholesterol
medication with grapefruit juice?
The one who takes Acetaminophen pain
relievers
for a sore ankle before
going out for drinks?
Or the one who’s on a blood-thinning
medication
and takes an aspirin for a headache?
Actually, all of them are.
Each has inadvertently created a drug
interaction that could, in extreme cases,
lead to kidney failure; liver damage;
or internal bleeding.
Drug interactions happen
when the combination of a drug
with another substance
causes different effects than either
would individually.
Foods, herbal supplements, legal drugs,
and illicit substances
can all cause drug interactions.
Most drug interactions
fall into two categories.
Some take place when two substances’
effects influence each other directly.
In other cases, one substance effects
how the body processes another,
like how it is absorbed, metabolized,
or transported around the body.
Blood thinners and aspirin, for example,
have similar effects that become
dangerous when combined.
Both prevent blood clots from forming—
blood thinners by preventing the formation
of the clotting factors
that hold clots together,
and aspirin by preventing blood cells
from clumping into groups
that become clots.
Individually, these effects
are usually safe,
but taken together, they can prevent blood
clotting to a dangerous extent,
possibly causing internal bleeding.
While blood thinners and aspirin are
generally harmless
when taken individually,
interactions where one substance
exacerbates the effects of another
can also take place between drugs that
are independently harmful.
Cocaine and heroin are each dangerous,
and those dangers compound when the
two drugs are combined—
even though their behavioral effects may
feel like they cancel each other out.
Cocaine is a stimulant, and many of its
effects, like increased heart rate,
cause the body to need more oxygen.
But heroin, a depressant,
slows breathing—
reducing the body’s oxygen supply just
when it needs more.
This combination strains the organs and
can cause respiratory failure and death.
The interaction between grapefruit juice
and certain medications
in class of cholesterol-lowering drugs
called statins,
has to do with drug metabolism.
The liver produces enzymes, molecules that
facilitate the breakdown of substances
that enter the body.
Enzymes can both activate drugs,
by breaking them down into their
therapeutic ingredients
from more complex molecules,
and deactivate them,
by breaking harmful compounds down
into harmless metabolites.
There are many, many different enzymes,
each of which has a binding site that
fits a specific molecule.
Grapefruit binds to the same enzyme
as statins,
making less of that enzyme available
to break down statins.
So combining the two means that a
greater concentration of the drug
stays in the bloodstream for a longer
period of time,
potentially causing kidney failure.
Alcohol can also alter the function of the
enzyme that breaks down Acetaminophen,
the active ingredient in pain relievers
like Tylenol and paracetamol.
When someone takes Acetaminophen, some
of it is converted into a toxic substance.
At the recommended dose,
there isn’t usually enough of this toxic
byproduct to cause harm.
But heavy drinking can alter enzyme
activity
so more of that byproduct is produced,
potentially causing liver damage
even with what’s usually a safe dose of
acetominophen.
Meanwhile, the herbal remedy Saint John’s
Wort increases the liver’s production
of a particular enzyme.
That means the drugs this enzyme is
responsible for breaking down
get metabolized faster—
sometimes too fast, before they can
have their therapeutic effects.
In spite of the dizzying number of
possible interactions,
most of the dangerous interactions
with commonly used drugs are well known.
And new developments in science are
helping us keep better track
of drug interactions than ever.
Some researchers are developing AI
programs that can predict the side effects
of drug interactions before they occur,
using information about the landscape
of protein interactions within your body.
For the new drugs that are being developed
all the time,
supercomputers are being used to find
potential interactions
while those drugs
are still in development.