How is amoxapine metabolized?

How is amoxapine metabolized?

Amoxapine is almost completely metabolized in the liver, with less than 5% of the drug being excreted in the urine and feces unchanged Dollery (1999).

What is amoxapine used for?

Amoxapine is a tricyclic antidepressant that is used to treat symptoms of depression, anxiety, or agitation. Amoxapine may also be used for purposes not listed in this medication guide.

How long does amoxapine stay in your system?

Aromatic hydroxylation in the liver produces two major metabolites, which are excreted in the urine primarily but also in the feces. Amoxapine’s elimination half-life is eight hours; one of the metabolites has a long half-life (30 hours).

Is amoxapine a TCA?

Amoxapine is a tricyclic antidepressant used in the treatment of neurotic or reactive depressive disorders and endogenous or psychotic depression. Amoxapine, the N-demethylated derivative of the antipsychotic agent loxapine, is a dibenzoxazepine-derivative tricyclic antidepressant (TCA).

Is amoxapine an antagonist?

Amoxapine, an antidepressant structurally related to the antipsychotic agent, loxapine, has dopamine antagonist activity and is a marked stimulator (three to four times basal) of PRL secretion [37].

What symptoms does amoxapine treat?

Amoxapine is a tricyclic antidepressant that is used to treat symptoms of depression, anxiety, or agitation.

Does Amoxapine cause weight gain?

Some people (less than 1%) in clinical trials had weight gain from amoxapine. Amoxapine can also increase your appetite, which may cause you to eat more and lead to weight gain.

Is amoxapine an antipsychotic drug?

Amoxapine is marketed as an antidepressant. However, its in-vitro profile, receptor occupancy and preclinical effects are very similar to atypical antipsychotics. Amoxapine has also shown efficacy as an atypical antipsychotic in open trials.

Is amoxapine an antipsychotic?

How does nesiritide work in the body?

Nesiritide works by facilitating cardiovascular homeostasis through the negative regulation of the renin-angiotensin-aldosterone system. This regulation will in order stimulate cyclic guanosine monophosphate and smooth muscle cell relaxation. In simpler terms, it promotes vasodilation, natriuresis, and diuresis.


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