Riddhi Siddhi Medical Services Rajaji Puram, Lucknow, Uttar Pradesh

triple antigenrndiphtheria, tetanus and pertussis vaccine (adsorbed) i.p indicationrnindicated for infants above the age of six weeks and of pre-school children against diphtheria, tetanus and pertussis (whooping cough). Route of administrationrnintramuscular injection immunization schedulernfirst 3 doses should be given 4 weeks apart at 6, 10 and 14 weeks. a booster dose can be given at the age of 15-18 months and also between the ages of 4 to 6 years. Compositionrneach single 0.5 ml dose containsrndiphtheria toxoid � 25 lf (� 30 iu)rntetanus toxoid � 5 lf (� 40 iu)rnb. Pertussis � 16 ou (� 4 iu)rnadsorbed on aluminium phosphate, al+++ � 1.25 mgrnpreservative: 0.005% thiomersalrnpresentation:rnbox of 10 ampoules of 0.5 ml eachrnbox of 10 md vials of 5 ml eachrnhomernabout usrnproductsrnproducts for overseasrnproducts for indiarnproduct listrnproduct pipeline

tresivacrnmeasles, mumps and rubella vaccine (live) i.p. (freeze-dried) indicationrnfor active immunization against measles, mumps and rubella in infants & children, adolescents and young adults at risk. Route of administrationrnsubcutaneous injection immunization schedulernfirst dose of mmr is given at 9 months of agernsecond dose of mmr is given anytime between 15-18 months rnthird dose of mmr is given anytime between 4-6 years of age. Compositionrnthe reconstituted vaccine contains in each single human dose of 0.5 ml:rnnot less than 1000 ccid50 of measles virusrnnot less than 5000 ccid50 of mumps virusrnnot less than 1000 ccid50 of rubella virusrnpresentation:rnbox of 10 single dose vials. box of 10 ampoules of 0.5 ml diluent provided separately

synflorix injection iconrnglaxo smithkline pharmaceuticals ltd composition for synflorix injectionrnpneumococcal polysaccharide vaccine (1mcg) primary uses of synflorix injectionrnpneumonia.

Rabipur injectionicon glaxo smithkline pharmaceuticals ltd composition for rabipur injection rabies vaccine (2.5iu) primary uses of rabipur injection rabies.

pentavac sd/pfsrndiphtheria, tetanus, pertussis (whole cell), hepatitis b (rdna) and haemophilus type b conjugate vaccine (adsorbed) i.p. Indicationrnfor the prevention of serious childhood diseases: diphtheria, tetanus, pertussis (whooping cough), hepatitis b and haemophilus influenzae type b. Route of administrationrnintramuscular injection. Immunization schedulernfirst dose is given at 6 weeks or 10 weeks or 14 weeks of age second dose is given anytime between 12-18 months of age compositionrneach dose of 0.5 ml containsrndiphtheria toxoid � 25 lf (� 30 iu)rntetanus toxoid � 2.5 lf (� 40 iu)rnb. Pertussis (whole cell) � 16 ou (� 4.0 iu)*rnhbsag (rdna) � 10 mcgrnpurified capsular hib polysaccharide (prp)rnconjugated to tetanus toxoid (carrier protein) 10 mcgrn+++ adsorbed on aluminium phosphate, al � 1.25 mgrnpreservative: thiomersal 0.005% *the lower fiducial limit (p=0.95) of the estimated potency is not less than 2.0 iu. Adsorbed can be given at the age of 15-18 months. presentation:rnpentavac sd: 1 dose vial of 0.5 mlrnpentavac pfs: 1 x 0.5 ml - 1 dose pre-filled syringe

menactraâ®rnmeningococcal (groups a, c, y and w-135) polysacchariderndiphtheria toxoid conjugate vaccinernsolution for intramuscular injection menactra is indicated for active immunization to prevent invasive meningococcalrndisease caused by neisseria meningitidis serogroups a, c, y and w-135. Menactra isrnapproved for use in individuals 9 months through 55 years of age. Menactra does notrnprevent n meningitidis serogroup b disease. (1) single-dose vial, 0.5 ml

hexaximrndtpa-hepb-ipv-hibrndiphtheria, tetanus, pertussis (acellular, component), hepatitis b (rdna), poliomyelitis (inactivated) and haemophilus influenzae type b conjugate vaccine (adsorbed).

easy six vaccine icon panacea biotech ltd composition for easy six vaccine diphtheria immune globulin (30iu), hemophiliacs b conjugate vaccine (10mcg), pertussis toxoid (4iu), tetanus toxoid (60iu), poliomyelitis virus type 1 (40d antigen unit), poliomyelitis virus type 2 (8d antigen unit), poliomyelitis virus type 3 (8d antigen unit) icon prescription required primary uses of easy six vaccine infections, hemophiliacs influenza type b disease, pertussis 23930.5 ml in 1 vial.

Cervarix VaccineiconrnGlaxo SmithKline Pharmaceuticals LtdrnComposition for Cervarix VaccinernHuman Papillomavirus Bivalent (Types 16 and 18) Vaccine, Recombinant (NA) Primary uses of Cervarix VaccinernPrevention of HPV-Associated CancersrnMRP₹2405rn₹2405/Suspension for Injectionrn0.5 ml in 1 prefilled syringe

Boostrix vaccineiconrnglaxo smithkline pharmaceuticals ltdrncomposition for boostrix vaccinerndiphtheria toxoid (2iu) + tetanus toxoid (20iu) + pertussis toxoid (8mcg) + pertactin (2.5mcg)rnprimary uses of boostrix vaccinerntetanus, pertussis, diphtheriarnmrp₹1098rn0.5 ml in 1 prefilled syringe.

Biovac v vaccineiconrnwockhardt ltdrncomposition for biovac v vaccinernvaricella vaccine (0.5ml)rnprimary uses of biovac v vaccinernvaricella (viral infection which causes an itchy and blister like rash on the skin)rnmrp₹1799rn0.5 ml in 1 vial.

Biovac a vaccineiconrnwockhardt ltdrncomposition for biovac a vaccinernhepatitis a (6.5ccid50)rnprimary uses of biovac a vaccinernhepatitis a prophylaxisrnmrp₹1395rn0.5 ml in 1 vial.

Hemalb 20% is produced from pooled human plasma for fractionation conforming to the highest standards setrnforth by regulatory authorities. In addition, the plasma donor units and the production plasma pool are testedrnnegative using nat approved by regulatory authorities for hiv1& 2, hcv and hbv. For i.v. Infusion. manufactured by: hemarus therapeutics limited.

Human albumin 20% is a nonpyrogenic, sterile aqueous solution of human albumin i.p. For intravenous administration and isrnpurified from pooled human venous plasma using a series of chromatography steps. Each 100 ml vial contains 20 g ofrnalbumin stabilized with n- acetyl tryptophan (0.016 m) and sodium caprylate (0.016 m) in a solution that has beenrnadjusted to physiological ph with sodium hydroxide. The sodium content in the solution is 145 ± 15 meq/l and thernpotassium content is not more than 2meq/l. The aluminium content is nmt 200 µg/l. It is clear, slightly viscous andrnstraw yellow in colour and do not contain preservative or antimicrobial agent.

Human normal immunoglobulin for intravenous use i.p. (ivig) is a sterile, 5% liquid preparation ofrnimmunoglobulin g (igg) purified from a large pool of human plasma for fractionation. The product is manufacturedrnby a series of chromatography based purification process. The manufacturing process includes dedicated viralrninactivation and removal steps such as treatment with tnbp and triton x-100, low ph treatment andrnnanofiltration.

Human normal immunoglobulin for intravenous use i.p. (ivig) is a sterile, 5% liquid preparation ofrnimmunoglobulin g (igg) purified from a large pool of human plasma for fractionation. The product is manufacturedrnby a series of chromatography based purification process. The manufacturing process includes dedicated viralrninactivation and removal steps such as treatment with tnbp and triton x-100, low ph treatment andrnnanofiltration.

Indicationrnfor the prevention of tuberculosis route of administrationrnintradermal injection dosagernthe vaccine should be administered in the dose of: 0.05 ml, intradermal for infants under one year of age 0.1 ml, intradermal for children over one year of age and adult. Immunization schedulerntubervac (bcg) vaccine should be administered very early in infancy at birth: 0.05 ml, intradermal for infants under one year of agern0.1 ml, intradermal for children over one year of age and adultsrnpresentation:rn20 dose vial (0.05ml) with diluent rn10 dose vial (0.1 ml) with diluent