Severe pain

Active Ingredient: Levomepromazine

Indication for Levomepromazine

Population group: only adults (18 years old or older)

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

37.5-1000 mg in 3 divided doses daily

Route of admnistration

Oral

Defined daily dose

37.5 - 1,000 mg

Dosage regimen

From 12.5 To 333.333 mg 3 time(s) per day every day

Detailed description

Ambulant patients: initially the total daily oral dose should not exceed 25 mg to 50 mg usually divided into 3 doses; a larger portion of the dosage may be taken at bedtime to minimise diurnal sedation. The dosage is then gradually increased to the most effective level compatible with sedation and other side effects.

Bed patients: initially the total daily oral dosage may be 100 mg to 200 mg, usually divided into 3 doses, gradually increased to 1g daily if necessary. When the patient is stable attempts should be made to reduce the dosage to an adequate maintenance level.

37.5-150 mg in 3 divided doses daily

Route of admnistration

Intravenous

Defined daily dose

37.5 - 150 mg

Dosage regimen

From 12.5 To 50 mg 3 time(s) per day every day

37.5-150 mg in 3 divided doses daily

Route of admnistration

Intramuscular

Defined daily dose

37.5 - 150 mg

Dosage regimen

From 12.5 To 50 mg 3 time(s) per day every day

Active ingredient

Levomepromazine

Levomepromazine resembles chlorpromazine and promethazine in the pattern of its pharmacology. It possesses anti-emetic, antihistamine and anti-adrenaline activity and exhibits a strong sedative effect.

Read more about Levomepromazine

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