Domperidone
Description
Don A is a dopamine antagonist that principally blocks the dopamine receptors
located in the chemoreceptor trigger zone and stomach its gastro prokinetic
action is based on its blocking effect of dopamine receptors that have an
influence on the motility of gastro intestinal tract due to its weak
penetration across the blood brain barrier Don
A has almost no effect on the dopaminergic receptors in the brain therefore
excluding psychotropic and neurologic side effects Don A restores normal motility and tone of the upper gastro
intestinal tract facilitates gastric emptying enhances antral and duodenal
peristalsis and regulates contraction of the pylorus Don A also increases esophageal peristalisis and lower esophageal
sphincter pressure and thus prevents regurgitation of gastric content
Indications
Stimulation of gut
mobility
a) Non ulcer dyspepsia
b) Esophageal reflux, reflux esophagitis
and gastritis
c) Diabetic gastro paresis
d) Functional dyspepsia
e) Speeding barium transit in follow
through radiological studies.
Dosage and administration
Dose and frequency of
administration should be adjusted according to severity and duration of
symptoms Don A tablet suspension and
paediatric drops should be taken minutes before meal.
Contraindications
Domperidone is contraindicated to the
patients with known hypersensitivity to this drug and in case of neonates
Precautions
Domperidone should be used with absolute
caution in case of children because there may be increased risk of extra
pyramidal reactions in young children because of an incompletely developed
blood brain barrier since Domperidone is highly metabolized in liver it should
be used with caution in patients with hepatic impairment
Side effect
The common side effect of Domperidone
is hyperprolactinemia which may result in galactorrhea breast enlargement
soreness and reduced libido other side effects are dry mouth thirst headache
nervoudness drowsiness diarrhea skin rash and itching which may occur during
treatment with Domperidone extra pyramidal reactions are seen in 0.05% of
patients in clinical studies.
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