Inoculate Vaccine

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Vaccinate Hepatitis A Vaccine

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[Function and use] The product can induce immunity against hepatitis A virus in recipients following immunization. It is used to prevent hepatitis A. [Description] The freeze-dried hepatitis A vaccine is a preparation made from the live attenuated strain of hepatitis A virus (HAV) grown in human diploid cell cultures. After cultivation, harvest and extraction of the virus, the virus suspension is lyophilized after adding an appropriate stabilizer to make the vaccine. It looks like a milky-white crisp cake and it turns into a clear liquid after reconstitution. Active constituent: live attenuated Hepatitis A virus. Subsidiary materials: All the components of subsidiary materials approved shall be listed. Diluent:sterile water for injection. [Specifications] 1.0 ml of reconstituted vaccine per container. 1.0 ml per single human dose containing not less than 6.50lg CCID50 of live hepatitis A virus. [Feature] Advantages: 1.Accordance with the trend of biomedicine. 2. Convenient for storage and transportation. 3. The improvement of the stability of the vaccine, 30-months of self life. 4. The extension of the validation.

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Vaccine Of Wild Dog For Humans

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Rabies vaccine(vero cell) for human use, freeze-dried apply fixed bed bio-reactor disks micro-carrier-in high-density culture of vero cell; realize scale production in international standard vaccine industrialization and reach international standard, contributing to early realization of rabies elimination goal. [function and use] the preparation can induce immunity against rabies virus in recipients following immunization. It is used to prevent rabies in human. [specifications] 0.5 ml of reconstituted vaccine per container. 0.5 ml per single human dose. The potency of the vaccine shall be not less than 2.5 iu. [advantages] (1)apply fixed bed bio-reactor disks micro-carrier to realize high-density culture of vero cell and harvest high-titer virus; (2)exclusively obtain the invention patent of rabies vaccine for human use, freeze-dried and its preparation method; (3)export to several countries successively; (4)high potency at least 4.0iudose; (5)great stability, 3-years shelf life; (6)with less clinical reaction, high-level immunogenicity, high conversion rate of serum antibody, high titer of antibody gmt, the vaccine provides ideal protection after injection; (7)5 doses for whole immunization process with standard operation and reliable effect for prevention; (8)lyophilized dosage form for quality guarantee; (9)exclusively apply two dosage forms of pre-filled syringe from american bd company

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Vaccinate Varicella Vaccine For Human

₹ 90.50 / Piece Get Latest Price

[Function and use] The product can induce immunity against varicella-zoster virus in recipients following immunization. It is used to prevent varicella. [Specifications] 0.5ml of reconstituted vaccine per container. 0.5ml per single human dose containing not less than 3.4Lg PFU Oka virus. [Description] The vaccine is a preparation of the Varicella virus strain of Oka grown in human diploid cell cultures. After cultivation and harvest, the virus suspension is lyophilized to make the vaccine by adding in appropriate stabilizer. it looks like a milky-white crisp cake. after reconstitution it turns into a transparent liquid. Indications Varicella virus vaccine, Live attenuated (oka strain) is indicated for : - Theactive immunization against varicella of healthy subjects from 12 months to12 years of age - The active immunization against varicella of susceptible high-risk patients and their susceptible healthy close contacts in the age group of 12 months to12 years .Adverse reactions Common adverse reactions: 1) Redness, swelling, pain. itching etc. at the site of injection within 24 hours following the injection may be found, which couldgenerally be relieved spontaneously within 2 or 3 days. 2) Temporal fever reaction may be found within l to3 weeks after inoculation it is mostly slight (ranging between 37.1 -37.5)and can be relieved spontaneously after ane or two days. No specific treatment is necessary.

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Vaccinate Meningococcal Polysaccharide Vaccine

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1.Group ACYW135 2.Group A+C 3.prevent epidemic cerebrospinal meningitis 4.purified capsular polysaccharide antigens The vaccine is indicated for active immunization against invasive meningococcal disease caused by epidemic Neisseria meningitidis serogroups A, C, Y, W135. [Description]The vaccine is a preparation of preparation polysaccharide antigens extracted from the culture of Neisseria meningitidis group ACYW135 respectively and Iyophilized after addition of an appropriate stabilizer. The final product looks like a white crisp cake. It shall dissolve in the accompanying Phosphate buffered saline (PBS) immediately, and turn into a clear liquid after reconstitution.Active constituent: Neisseria meningitidis group ACYW135 capsular polysaccharides.Subsidiary materials: All the components of subsidiary materials approved shall be listed.Vaccine diluent: Sterile, pyrogen-free PBS. [Vaccination Subjects] At present, the vaccine is only recommended to be used in high-risk population (children and adults) over 2 years of age in the following conditions:(1) Trave

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Trivalent Influenza Vaccine (Split Virion)

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Influenza vaccine (split virion), inactivated apply the most advanced technology in the world to production of influenza vaccine and arrange vaccine production and quality control according to current influenza virus recommended by who. Each quality index of the influenza vaccine is excellent. [eligibles] susceptible individuals and persons liable to be afflicted with the associated complications, such as children, elderly persons and individuals in the epidemic area. [function and use] the product can induce immunity against influenza virus in recipients following immunization. It is used to prevent the infections of the prevalent strains of influenza viruses. [specifications] 0.25 ml or 0.5 ml per container. 0.25 ml per single human dose (used for children aged between 6 months and 3 years) .shall contain 7.5g of influenza haemagglutinin of each influenza virus strain. 0.5 ml per single human dose (used for adult and children aged above 3 years) shall contain 15g of influenza haemagglutinin of each influenza virus strain. [advantages] (1)apply centrifugal purification and column chromatography purification technology to purifying virus and obtainedthe patent certificate of making use of sepharose4ff column chromatography technology for vaccine manufacture. The product quality index is excellent and the purity is high; (2)high-level gmt of conversion rate of serum antibody with safety and reliable effect for prevention

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Human Rabies Vaccine

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Adopted name: rabies vaccine (vero cell) forhuman use, freeze-dried [description] the vaccine is a freeze-dried preparation made fromthe inactivated rabies fixed virus. the virus growsin vero cell cultures. after cultivation andharvest, the virus suspension is concentrated, inactivated, purified, and lyophilized to make thevaccine after the addition of a suitable stabilizer. The product looks like a white crisp cake. Afterreconstitution, it shall turn into a transparentliquid without containing any preservatives. Active constituent : inactivated rabies fixed virus.subsidiary materials: all of the subsidiarymaterials approved shall be listed. Diluent: sterile water for injection [eligibles] if a person is bitten or scratched by a rabid dog orother rabid animals, regardless of age or sex, the wounds shall be cleaned immediately (flush thewounds repeatedly with clean water or soap water and then apply iodine tincture or ethanol repeatedlyto the wounds. ), and the exposed person shall beinoculated with the vaccine according to thepostexposure schedule as soon as possible. The persons at risk of contacting rabies virus (such asveterinarians, animal breeders, forestry workers, workers in slaughterhouse and staffs in rabieslaboratory) shall be immunized following the pre-exposure immunization schedule.

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Vaccinate Influenza Vaccine For Human

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[Drug name] Adopted name: Influenza Vaccine (Split Virion), Inactivated [Description] The influenza vaccine (split virion) is a preparation made from the WHO recommended prevalentstrains of influenza virus type A and type B whichare grown separately in embryonated chicken eggs.After incubation, the virus suspensions in allantoiccavities are harvested. The vaccine is preparedbyinactivation, concentration, purification anddisruption of the virus. It is a slightly milky-whiteliquid, containingthimerosal as a preservative. Active constituent: Influenza haemagglutininderived from each of prevalent influenza virusstrains in that very year. (The name of each ofvirus strains and the content of haemagglutininshall be included. ) Subsidiary materials: All the components of subsidiarymaterials approved shallbe listed. [Eligibles] Suscepitable individuals and persons liable to beafflicted with the associated complications, such aschildren, elderly persons and individuals in theepidemic area. [Action and use] The product can induce immunityagainst influenzavirus in recipients following immunization. It isused to prevent the infections of the prevalentstrains of influenza viruses.

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