Anxiety

Active Ingredient: Prazepam

Indication for Prazepam

Population group: only adults (18 years old or older)
Therapeutic intent: Curative procedure

Benzodiazepines are only indicated when the disorder is severe, disabling or subjecting the individual to extreme distress.

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

10-60 mg daily

For:

Dosage regimens

Oral, between 10 milligrams prazepam and 60 milligrams prazepam, divided daily, 1 to 2 doses in total, over the duration of 4 weeks.

Detailed description

The usual dose is 30 mg daily in single or divided doses. The dose should be adjusted within the range 10 mg to 60 mg daily in accordance with response of the patient.

The lowest dose which can control symptoms should be used. It should not be usually continued beyond four weeks.

Treatment should be as short as possible. The patient should be reassessed regularly and the need for continued treatment should be evaluated, especially in case the patient is symptom free. The overall duration of treatment generally should not be more than 4-6 weeks, including a tapering off process.

In certain cases extension beyond the maximum treatment period may be necessary; if so, it should not take place without re-evaluation of the patient’s status with special expertise.

10-15 mg in divided daily doses

For:

Dosage regimens

Oral, between 10 milligrams prazepam and 15 milligrams prazepam, divided daily, over the duration of 4 weeks.

Detailed description

In elderly patients the initial dose should be small, and increments should be made gradually, in accordance with the response of the patient, to preclude ataxia or excessive sedation. Half the normal adult dose is generally sufficient for a therapeutic response in the elderly or debilitated.

The patient should be checked regularly at the start of the treatment and then regularly thereafter, in order to decrease if necessary, the dose or frequency of administration to prevent overdose due to accumulation.

Treatment should be as short as possible. The patient should be reassessed regularly and the need for continued treatment should be evaluated, especially in case the patient is symptom free. The overall duration of treatment generally should not be more than 4-6 weeks, including a tapering off process.

In certain cases extension beyond the maximum treatment period may be necessary; if so, it should not take place without re-evaluation of the patient’s status with special expertise.

Active ingredient

Prazepam

Prazepam is a benzodiazepine derivative and has depressant effects on the central nervous system. Benzodiazepines act at the level of the limbic, thalamic, and hypothalamic regions of the CNS and can produce any level of CNS depression required including sedation, hypnosis, skeletal muscle relaxation, and anticonvulsant activity.

Read more about Prazepam

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