Cimetidine
Class:Antipeptic ulcerants
Mechanism of action
Competitive
inhibition of histamine at H2 receptors of the gastric parietal cells resulting
in reduced gastric acid secretion,gastric volume and hydrogen ion concentration
reduced.
Pharmacokinetics
Onset of action:1
hour.peak serum concentration:1 hour after oral dose.Duration 6 hours.Distribution:crosses
the placenta;appears in breast milk.Protein binding 20
percent.Bioavailability:60 to 70 percent.Elimination :principally as unchanged
drug by the kidney;some excretion in bile and feces.
Indications
Treatment of acute
gastritis,which can manifest as heartburn,epigastric
pain,hyperacidity,dyspepsia or acute aggravation of chronic gastritis.
Precautions
Exclude malignancy in
gastric ulcer.use in pregnancy should be avoided unless essential for patient's
benefit.Dosage to be reduced in patients with severely impaired renal funtion.
Side effects
Diarrhea,dizziness,rash,tiredness;reversible
gynecomastia has been reported;reversible liver damage,acute
pancreatitis,thrombocytopenia,agranulocytosis,headache,myalgia,arthralgia,dysrhythmias
and anaphylaxis;also aplastic anemia,very rarely alopecia,isolated increases of
plasma creatinine and serum transamine.
Pregnancy
Pregnancy risk factor
B
Drug interactions
Cimetidine may
prolong the clearance of warfarin-type anticoagulants,phenytoin,theophylline
and nifedipin.Patient receiving such drugs should be monitored ,as dosage
reduction may be necessary.
Dosage
200 mg (10 ml) twice
a day after breakfast and at bed time.
Brands
Tabs.Cimet 400
mg,Tabs.Tagamet 200 mg.
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