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Epivir-hbv price

The lower dose of lamivudine in epivir-hbv could make the hiv infection harder to treat.

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Information about Epivir-HBV.

The safety and efficacy of Epivir-HBV have not been established in patients with decompensated hepatic disease or organ transplantand patients dually infected with hepatitis B virusHBVand hepatitis C virusor hepatitis deltaObesity and prolonged nucleoside exposure may be risk factors for hepatotoxicity or lactic acidosis during lamivudine therapyFatalities have been reported with use of antiretroviral agents alone or in combinationincluding lamivudineA majority of these cases occurred in femalesit is unknown if pregnant women are at increased riskClinicians need to be alert for early diagnosis of this syndromePregnant women receiving nucleoside analogs should have LFTs and serum electrolytes assessed more frequently during the last trimester and any new symptoms should be evaluated thoroughlyMost of these reports describe patients receiving lamivudine for HIV treatmentbut there have been reports of lactic acidosis in patients receiving lamivudine for hepatitis BLamivudine should be used with caution in patients with hepatic disease or in those with known risk factors for liver diseasee.galcoholismhowevercases of lactic acidosis or liver problems have been reported in patients with no risk factorsTreatment should be discontinued in any patient who develops clinical or laboratory findings suggestive of lactic acidosis or pronounced hepatotoxicity which may include hepatomegaly and steatosiseven in the absence of marked increases in transaminasesFollowing discontinuation of lamivudine in patients with HBV or HIV infectionsome patients experienced clinical or laboratory evidence of recurrent hepatitiswhich has been fatal in some casesThis reaction may be more severe in patients with decompensated hepatic diseaseThuspatients should be closely monitored for several months after stopping lamivudine therapy for hepatitis B.

A Each subject may be represented in one or more categoryb During treatment phasec Comparable to a Grade 3 toxicity in accordance with modified WHO criteriaULNUpper limit of normal.

The pharmacokinetic properties of lamivudine have been studied as single and multiple oral doses ranging from 5 mg to 600 mg per day administered to HBV-infected subjects.

Follow all directions on your prescription labelDo not take this medicine in larger or smaller amounts or for longer than recommendedYou should not take Epivirfor treating HIVtogether with Epivir-HBVfor treating hepatitis B

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epivir-hbv was developed for patients with chronic hepatitis b.