Acetylcysteine ​​reduces the hepatotoxic effect of paracetamol.

Allopurinol also enhances its hepatotoxic effects.

Inductors of microsomal oxidation, isoniazid, and hepatotoxic drugs increase the hepatotoxic effects of paracetamol.

Also disclosed are pharmaceutical compositions comprising a hepatotoxic agent and an alginate composition and uses thereof for treating medical conditions treatable by the hepatotoxic agent.

As mentioned, It is hepatotoxic, so using it alongside another hepatotoxic compound exacerbates the potential for liver damage.

with inducers of liver microsomal enzymes, agents with a hepatotoxic effect, there is a risk of enhancing the hepatotoxic effect of paracetamol.

With simultaneous use with inducers of liver microsomal enzymes, agents that have a hepatotoxic effect, there is a risk of an increase in the hepatotoxic effect of paracetamol.

As mentioned earlier, Dianabol is hepatotoxic, so it increases the potential for liver damage in addition to another hepatotoxic compound.

Oxandrolone, as with other 17-alkylated steroids, is hepatotoxic.

Oxandrolone, as with other 17-alkylated steroids, is hepatotoxic.

Anavar, like other 17-alkylated steroids, is unfortunately hepatotoxic.

6-mercaptopurine is hepatotoxic in animals and man.

Do not affect the digestive tract, do not have a hepatotoxic effect.

Due to its 17a-alkylated arrangement, Anadrol-Oxymetholone is extremely hepatotoxic.

6-mercaptopurine is hepatotoxic in animals and man.