Welcome to EXIR PHARMACEUTICAL CO. WebSite
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» NEWS
AND EVENTS |
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The gathering was held from 24th August 2008 till 26th August in Tehran...
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Welcome to EXIR PHARMACEUTICAL CO. WebSite
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ARTICLE OF THE DAY |
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Comparison of two treatment regimens in symptomaticaliy homogenous gerd patient
Populations : pantoprazole relieves gastrointestinal symptoms significantily better than omeprazole
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Welcome to EXIR PHARMACEUTICAL CO. WebSite
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EXIR PRODUCTS IN A GLANCE |
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Welcome to EXIR PHARMACEUTICAL CO. WebSite
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EXIR PRODUCTS
» Gastro - Intestinal Agents
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Ranitidine - Exir |
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Generic Name: |
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Ranitidine |
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Dosage: |
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150 mg F.C.Tab/100 s |
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Two human histamine receptors have been cloned and there
is very strong pharmacological evidence for a third, particularly
in brain. Rantac® is a potent histamine H2 antagonist.
Rantac® is four to five times as potent as cimetidine on a
molar basis. It is a potent inhibitor of gastric secretion induced
in response to histamine, pentagastrin, bethanechol, and test
meals.
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Cimetidine - Exir |
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Generic Name: |
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Cimetidine |
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Dosage: |
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200 mg /2ml Amp /10 s |
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Two human histamine receptors have been cloned and there
is very strong pharmacological evidence for a third, particularly
in brain.
Logamet® is a competitive and potent histamine H2 antagonist
inhibiting both basal and stimulated gastric secretion of acid
and with an associated reduction of pepsin output.
Logamet® binds to the heme portion of the cytochrome p450
complex and this is responsible for several drug interactions,
where impairment of excretion of drugs metabolized via this
mechanism occurs. Logamet® binds to androgen receptors
and at high doses antiandrogenic actions, such as decreased
seminal vesicle size, are apparent in animal models.
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Cimetidine - Exir |
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Generic Name: |
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Cimetidine |
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Dosage: |
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200 mg F.C.Tab /100 s |
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Two human histamine receptors have been cloned and there
is very strong pharmacological evidence for a third, particularly
in brain.
Logamet® is a competitive and potent histamine H2 antagonist
inhibiting both basal and stimulated gastric secretion of acid
and with an associated reduction of pepsin output.
Logamet® binds to the heme portion of the cytochrome p450
complex and this is responsible for several drug interactions,
where impairment of excretion of drugs metabolized via this
mechanism occurs. Logamet® binds to androgen receptors
and at high doses antiandrogenic actions, such as decreased
seminal vesicle size, are apparent in animal models.
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