Valovir (Valaciclovir Tablet 500mg)

国家: 马来西亚

语言: 英文

来源: NPRA (National Pharmaceutical Regulatory Agency, Bahagian Regulatori Farmasi Negara)

现在购买

产品特点 产品特点 (SPC)
08-07-2021

有效成分:

VALACICLOVIR HYDROCHLORIDE

可用日期:

CAMBER LABORATORIES SDN. BHD.

INN(国际名称):

VALACICLOVIR HYDROCHLORIDE

每包单位数:

100Tablet Tablets; 100Tablet Tablets; 100Tablet Tablets

厂商:

Hetero Labs Limited

产品特点

                                VALOVIR
Valaciclovir Tablet 500 mg
DESCRIPTION AND COMPOSITION:
White to off-white, film coated, caplet shaped tablets,
debossed with 'V' on one side and '500' on other side.
Each film coated tablet contains: Valaciclovir Hydor-
chloride 556mg equivalent to Valaciclovir 500mg
PHARMACODYNAMIC PROPERTIES:
Valaclovir an antiviral, is the L-valine ester of acyclovir.
Aciclovir is a purine (guanine) nucleoside analogue.
MODE OF ACTION:
Valaciclovir is rapidly and almost completely converted
in man to acyclovir and valine, probably by the enzyme
referred to as valaciclovir hydrolase.
Aciclovir is a specific inhibitor of the herpes viruses with in vitro
activity against herpes simplex viruses (HSV) type 1 and type 2,
varicella zoster virus (VZV), cytomegalvorus (CMV), Epstein-
Bair Virus (EBV) and human herpes virus 6 (HHV-6). Aciclovir
inhibits herpes virus DNA synthesis once it has been
phosphorylated to the active triphosphate form. The first stage of
phosphorylation requires the activity of a virus-specific enzyme.
In the case of HSV, VZV and EBV this enzyme is the viral
thymidine kinase (TK), which is only present in virus infected
cells. Selectivity is maintained in CMV with phosphorylation,
at least in part, being mediated through the phosphotransferase
gene product of UL97.
This requirement for activation of acyclovir by a virus specific
enzyme largely explains its selectivity. The phosphorylation
process is completed conversion from mono to triphosphate by
cellular kinases. Aciclovir triphosphate competitively inhibits the
virus DNA polymerase and incorporation of this nucleoside
analogue results in obligate chain termination, halting virus DNA
synthesis and this blocking virus replication. Extensive monitoring
of clinical HSV and VZV isolates
from patients receiving
acyclovir therapy or prophylaxis has revealed that virus with
reduced sensitivity to acyclovir is extremely rare in the
immunocomptetent and is only found infrequently in severely
immuno compromised individuals e.g. organ or bone marrow
transplant 
                                
                                阅读完整的文件
                                
                            

其他语言的文件

资料单张 资料单张 马来文 09-07-2021

搜索与此产品相关的警报