Varilrix inj. sol. (pwdr. + solv.) s.c./i.m. pre-filled syr. vial Belgien - engelska - AFMPS (Agence Fédérale des Médicaments et des Produits de Santé)

varilrix inj. sol. (pwdr. + solv.) s.c./i.m. pre-filled syr. vial

glaxosmithkline biologicals sa-nv - varicella-zoster virus (live, attenuated) >= 2000 pfu - powder and solvent for solution for injection - varicella virus - varicella, live attenuated

Varivax inj. susp. (pwdr. + solv.) s.c./i.m. pre-filled syr. vial Belgien - engelska - AFMPS (Agence Fédérale des Médicaments et des Produits de Santé)

varivax inj. susp. (pwdr. + solv.) s.c./i.m. pre-filled syr. vial

msd belgium bv-srl - varicella-zoster virus (live, attenuated) - powder and solvent for suspension for injection - varicella virus - varicella, live attenuated

Varilrix inj. sol. (pwdr. + solv.) s.c./i.m. amp. vial Belgien - engelska - AFMPS (Agence Fédérale des Médicaments et des Produits de Santé)

varilrix inj. sol. (pwdr. + solv.) s.c./i.m. amp. vial

glaxosmithkline biologicals sa-nv - varicella-zoster virus (live, attenuated) >= 2000 pfu - powder and solvent for solution for injection - varicella virus - varicella, live attenuated

Varilrix™ (Vial + Ampoule) Varicella vaccine - live not less than 10^3.3 PFU/ Vial Injection Förenade Arabemiraten - engelska - MOHAP (Ministry of Health & Prevention) - وزارة الصحة ووقاية المجتمع.الإمارات

varilrix™ (vial + ampoule) varicella vaccine - live not less than 10^3.3 pfu/ vial injection

gulf drug llc dubai-street no 10 - varicella virus - injection - varicella vaccine - live not less than 10^3.3 pfu/ vial - immunologicals , vaccines-vaccines , antisera

PROQUAD POWDER FOR SOLUTION Kanada - engelska - Health Canada

proquad powder for solution

merck canada inc - measles virus vaccine live attenuated (edmonston b strain); mumps virus vaccine live attenuated (jeryl lynn strain); rubella virus vaccine live attenuated (wistar ra27/3 strain); varicella-zoster virus vaccine live attenuated (oka/merck strain) - powder for solution - 3.00log10 tcid50; 4.30log10 tcid50; 3.00log10 tcid50; 3.99log10 pfu - measles virus vaccine live attenuated (edmonston b strain) 3.00log10 tcid50; mumps virus vaccine live attenuated (jeryl lynn strain) 4.30log10 tcid50; rubella virus vaccine live attenuated (wistar ra27/3 strain) 3.00log10 tcid50; varicella-zoster virus vaccine live attenuated (oka/merck strain) 3.99log10 pfu - vaccines

VARIZIG- human varicella-zoster immune globulin solution USA - engelska - NLM (National Library of Medicine)

varizig- human varicella-zoster immune globulin solution

saol therapeutics - human varicella-zoster immune globulin (unii: 33t61iwl27) (human varicella-zoster immune globulin - unii:33t61iwl27) - varizig® [varicella zoster immune globulin (human)] is indicated for post-exposure prophylaxis of varicella in high risk individuals. high risk groups include: - immunocompromised children and adults, - newborns of mothers with varicella shortly before or after delivery, - premature infants, - neonates and infants less than one year of age, - adults without evidence of immunity, - pregnant women. varizig administration is intended to reduce the severity of varicella. administer varizig as soon as possible following varicella zoster virus (vzv) exposure, ideally within 96 hours for greatest effectiveness. - there is no convincing evidence that varizig reduces the incidence of chickenpox infection after exposure to vzv. - there is no convincing evidence that established infections with vzv can be modified by varizig administration. - there is no indication for the prophylactic use of varizig in immunodeficient children or adults when there is a past history of varicella, unless the patient is undergoing bone m

VARIZIG- human varicella-zoster immune globulin injection, solution USA - engelska - NLM (National Library of Medicine)

varizig- human varicella-zoster immune globulin injection, solution

kamada ltd. - human varicella-zoster immune globulin (unii: 33t61iwl27) (human varicella-zoster immune globulin - unii:33t61iwl27) - varizig ® [varicella zoster immune globulin (human)] is indicated for post-exposure prophylaxis of varicella in high risk individuals. high risk groups include: - immunocompromised children and adults, - newborns of mothers with varicella shortly before or after delivery, - premature infants, - neonates and infants less than one year of age, - adults without evidence of immunity, - pregnant women. varizig administration is intended to reduce the severity of varicella. administer varizig as soon as possible following varicella zoster virus (vzv) exposure, ideally within 96 hours for greatest effectiveness. - there is no convincing evidence that varizig reduces the incidence of chickenpox infection after exposure to vzv. - there is no convincing evidence that established infections with vzv can be modified by varizig administration. - there is no indication for the prophylactic use of varizig in immunodeficient children or adults when there is a past history of varicella, unless the patient is undergoing bone marrow transplantation. - individuals known to have anaphylactic or severe systemic (hypersensitivity) reactions to human immune globulin preparations should not receive varizig. - iga-deficient patients with antibodies against iga and a history of hypersensitivity may have an anaphylactoid reaction. - varizig contains less than 40 micrograms per milliliter of iga. animal reproduction studies have not been conducted with varizig. it also is not known whether varizig can cause fetal harm when administered to a pregnant woman or can affect reproduction capacity. varizig should be given to a pregnant woman only if clearly needed. the safety and effectiveness of varizig have been evaluated for post-exposure prophylaxis in clinical trials in 166 pregnant women [see 6adverse reactions and 14clinical studies ]. it is not known whether varizig is excreted in human milk. because many drugs are excreted in human milk, caution should be exercised when varizig is administered to a nursing mother. the dosing recommendations in the treatment of pediatric patients are by body weight [see 2dosage and administration ]. the safety and effectiveness of varizig have been evaluated for post-exposure prophylaxis in the varizig expanded access clinical trial in 374 pediatric patients, including immunocompromised pediatric patients: - 94 preterm newborns and infants, - 53 term newborns, - 45 infants and toddlers, - 176 children and, - 43 adolescents. in the eap, follow up data were available for 110 varizig treatments in infants (including newborns, pre-term infants, and infants less than 1 year old). three severe infections were reported, all three with pox count greater than 100, one of which also had pneumonia and another one also developed probable varicella encephalitis. clinical studies of varizig administered intramuscularly for post-exposure prophylaxis did not include sufficient numbers of geriatric subjects (aged 65 and over) to determine whether they respond differently from younger subjects. use caution when administering varizig to patients aged 65 and over who are judged to be at increased risk of thrombotic events [see 5warnings and precautions ]. do not exceed recommended doses and administer varizig intramuscularly only. in the eap, both adult (n=37) and pediatric immunocompromised subjects (n=235) were treated. twelve immunocompromised subjects developed clinical varicella and none developed varicella pneumonitis; however at least five are reported to have received concomitant acyclovir and due to incomplete reporting, it is not known if others also received acyclovir.

ProQuad Europeiska unionen - engelska - EMA (European Medicines Agency)

proquad

merck sharp & dohme b.v. - virus, live attenuated, measles, virus, live attenuated, mumps, virus, live attenuated, rubella, virus, live attenuated, varicella - chickenpox; rubella; measles; mumps; immunization - vaccines - proquad is indicated for simultaneous vaccination against measles, mumps, rubella and varicella in individuals from 12 months of age. proquad can be administered to individuals from 9 months of age under special circumstances (e.g., to conform with national vaccination schedules, outbreak situations, or travel to a region with high prevalence of measles.,

PRIORIX-TETRA POWDER FOR SOLUTION Kanada - engelska - Health Canada

priorix-tetra powder for solution

glaxosmithkline inc - mumps virus vaccine live attenuated (jeryl lynn strain); measles virus vaccine live attenuated; rubella virus vaccine live attenuated (wistar ra27/3 strain); varicella-zoster virus vaccine live attenuated (oka-strain) - powder for solution - 25118.9ccid50; 1000ccid50; 1000ccid50; 1995.2623ccid50 - mumps virus vaccine live attenuated (jeryl lynn strain) 25118.9ccid50; measles virus vaccine live attenuated 1000ccid50; rubella virus vaccine live attenuated (wistar ra27/3 strain) 1000ccid50; varicella-zoster virus vaccine live attenuated (oka-strain) 1995.2623ccid50 - vaccines