Sulpiride: Difference between revisions

From SEHK Wiki
Helen (talk | contribs)
Helen (talk | contribs)
No edit summary
Line 66: Line 66:
Most serious and/or frequently occurring adverse effects of sulpiride include the following:
Most serious and/or frequently occurring adverse effects of sulpiride include the following:
{| class = "wikitable"
{| class = "wikitable"
!Endocrine disorders
!style="text-align: left"| Endocrine disorders
|  
|  
*Common: hyperprolactinaemia (elevated plasma levels of the hormone prolactin, which in turn lead to galactonrrhea, amornorrhea, gynecomastia etc)
*Common: hyperprolactinaemia (elevated plasma levels of the hormone prolactin, which in turn lead to galactonrrhea, amornorrhea, gynecomastia etc)
|-
|-
!Nervous system
!style="text-align: left"| Nervous system
|
|
Common:
Common:
Line 96: Line 96:
*Tardive dyskinesia
*Tardive dyskinesia
|-
|-
!Metabolism disorders
!style="text-align: left"| Metabolism disorders
|
|
Not known:
Not known:
Line 102: Line 102:
*Syndrome of inappropriate antidiuretic hormone secretion (SIADH)
*Syndrome of inappropriate antidiuretic hormone secretion (SIADH)
|-
|-
!Cardiac disorders
!style="text-align: left"| Cardiac disorders
|
|
Rare:
Rare:
Line 110: Line 110:
*Electrocardiogram QT prolonged
*Electrocardiogram QT prolonged
|-
|-
!Vascular disorder
!style="text-align: left"| Vascular disorder
|Uncommon: orthostatic hypotension
|Uncommon: orthostatic hypotension
|-
|-
Line 118: Line 118:
Uncommon: saliva hypersecretion
Uncommon: saliva hypersecretion
|-
|-
!Breast disorder
!style="text-align: left"| Breast disorder
|Common: breast pain, galactorrhoea
|Common: breast pain, galactorrhoea
|-
|-
!
!style="text-align: left"|
|
|
Common:  
Common:  
*weight gain
*weight gain
|}
==Pharmacokinetics==
{|class="wikitable"
!style="text-align: left"| Oral bioavailability
|Sulpiride is readily absorbed after oral doses.
|-
!style="text-align: left"| Onset of action
|Peak plasma concentrations are reached 3 – 6 hours after an oral dose.
|-
!style="text-align: left"| Metabolism
|It is metabolized in the liver
|-
!style="text-align: left"| Elimination half-life
|
It is excreted in the urine and faeces.
The elimination half-life is approximately 8 hours.
|}
|}

Revision as of 23:15, 26 October 2020

Drug Class: Antipsychotics, typical ; Antipsychotics, 1st Generation Sulpiride (中文:[[ ]])is a typical antipsychotic or 1st Generation antipsychotic medication. It is used in the treatment of psychosis associated with schizophrenia and major depressive disorder. In low dosage, it is used for anxiety and mild depression.

Pronunciation

Sulpiride 200mg

Sulpiride 50mg

Drug Names

Generic Name 藥名 HA Code 藥物代碼 Classification藥物分類
Sulpiride Cap 50 mg SULP19 P1S1S3
Sulpiride Tab 200 mg SULP20 P1S1S3

Mechanism of Action

Sulpiride is a selective antagonist at dopamine D2, D3 and 5-HT1A receptors. The presumed effectiveness of antipsychotic drugs relied on their ability to block dopamine receptors. This assumption arose from the dopamine hypothesis that maintains that both schizophrenia and bipolar disorder are a result of excessive dopamine activity.

Dosage

Indication Dose

Schizophrenia with predominantly negative

symptoms(flattening of affect, poverty of

speech, apathy, as well as depression)

By mouth

ADULT:

  • 200 – 400 mg twice daily.
  • Maximum 800 mg per day

ELDERLY or debilitated patients:

  • Lower initial dose to be given
  • Increased gradually according to response

Schizophrenia with mainly positive

symptoms(hallucinations, delusions,

incongruity of speech) Respond to higher doses

By mouth

ADULT:

  • 200 – 400 mg twice daily
  • Maximum 2.4 g per day

ELDERLY or debilitated patients:

  • Lower initial dose to be given
  • Increased gradually according to response

Side Effects

Most serious and/or frequently occurring adverse effects of sulpiride include the following:

Endocrine disorders
  • Common: hyperprolactinaemia (elevated plasma levels of the hormone prolactin, which in turn lead to galactonrrhea, amornorrhea, gynecomastia etc)
Nervous system

Common:

  • Sedation or drowsiness
  • Extrapyramidal side effects

-Tremor

-Akathisia – a sense of inner restlessness that cannot stay still

-Parkinsonism

  • Anticholinergic side-effects such as:

-Dry mouth

-Constipation

-Blurred vision Uncommon:

  • Hypertonia
  • Dyskinesia

Rare:

  • Oculogyric crisis

Not known:

  • Neuroleptic malignant syndrome
  • Convulsion
  • Tardive dyskinesia
Metabolism disorders

Not known:

  • Hyponatraemia
  • Syndrome of inappropriate antidiuretic hormone secretion (SIADH)
Cardiac disorders

Rare:

  • Ventricular arrhythmia
  • Ventricular fibrillation, or tachycardia

Not known:

  • Electrocardiogram QT prolonged
Vascular disorder Uncommon: orthostatic hypotension
Gastrointestinal disorder

Common: constipation Uncommon: saliva hypersecretion

Breast disorder Common: breast pain, galactorrhoea

Common:

  • weight gain

Pharmacokinetics

Oral bioavailability Sulpiride is readily absorbed after oral doses.
Onset of action Peak plasma concentrations are reached 3 – 6 hours after an oral dose.
Metabolism It is metabolized in the liver
Elimination half-life

It is excreted in the urine and faeces.

The elimination half-life is approximately 8 hours.