Psychoses, mental subnormality, nausea and vomiting

Active Ingredient: Trifluoperazine

Indication for Trifluoperazine

Population group: only children (1 year - 12 years old) , adolescents (12 years - 18 years old) , adults (18 years old or older)

Low dosage: Trifluoperazine is indicated as an adjunct in the short-term management of anxiety states, depressive symptoms secondary to anxiety and agitation. Orally it is also indicated in the symptomatic treatment of nausea and vomiting.

High dosage: Trifluoperazine is intended for the treatment of symptoms and prevention of relapse in schizophrenia and in other psychoses, especially of the paranoid type, but not in depressive psychoses. It may also be used as an adjunct in short-term management of severe psychomotor agitation and of dangerously impulsive behaviour in, for example, mental subnormality.

For this indication, competent medicine agencies globally authorize below treatments:

2-4 mg a day in divided doses or 10 mg a day, increased to 15 mg after a week and thereafter further increases of 5 mg at three-day intervals

For:

Dosage regimens

Regimen A: Oral, between 2 milligrams trifluoperazine and 4 milligrams trifluoperazine, divided daily.

Regimen B: Oral, 5 milligrams trifluoperazine, 2 times daily, over the duration of 1 week. Afterwards, oral, between 10 milligrams trifluoperazine and 15 milligrams trifluoperazine, divided daily.

Detailed description

Low dosage: 2-4 mg a day given in divided doses, according to the severity of the patient’s condition. If necessary, dosage may be increased to 6 mg a day, but above this level extrapyramidal symptoms are more likely to occur in some patients.

High dosage: The recommended starting dosage for physically fit adults is 5 mg twice a day after a week this may be increased to 15 mg a day. If necessary, further increases of 5 mg may be made at three-day intervals, but not more often. When satisfactory control has been achieved, dosage should be reduced gradually until an effective maintenance level has been established.

As with all major tranquillisers, clinical improvement may not be evident for several weeks after starting treatment, and there may be delay before recurrence of symptoms after stopping treatment. Gradual withdrawal from high dosage treatment is advisable.

1-5 mg daily given in divided doses

For:

Dosage regimens

Oral, between 1 milligrams trifluoperazine and 5 milligrams trifluoperazine, divided daily.

Detailed description

Low dosage: For children 3-5 years, up to 1 mg a day given in divided doses.

For children aged 6-12 years, the dosage may be increased to a maximum of 4 mg a day.

High dosage: For children aged 6-12 years, the initial oral dosage should not exceed 5 mg a day, given in divided doses. Any subsequent increase should be made with caution, at intervals of not less than three days, and taking into account age, body weight and severity of symptoms.

1-2 mg a day in divided doses or 5 mg a day, increased to 10 mg after a week and thereafter further increases of 5 mg at three-day intervals

For:

Dosage regimens

Regimen A: Oral, between 1 milligrams trifluoperazine and 2 milligrams trifluoperazine, divided daily.

Regimen B: Oral, 5 milligrams trifluoperazine, once daily, over the duration of 1 week. Afterwards, oral, between 10 milligrams trifluoperazine and 15 milligrams trifluoperazine, divided daily.

Detailed description

Reduce starting dose in elderly or frail patients by at least half.

Active ingredient

Trifluoperazine

Trifluoperazine is one of the phenothiazine class of compounds and as such has many pharmacodynamic effects which relate to its therapeutic actions and side effects. The most notable action of phenothiazines is antagonism at dopamine receptors in the CNS.

Read more about Trifluoperazine

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