MERCK SHARP & DOHME STERILE DILUENT for live virus vaccines  injection prefilled syringe Australia - English - Department of Health (Therapeutic Goods Administration)

merck sharp & dohme sterile diluent for live virus vaccines injection prefilled syringe

merck sharp & dohme (australia) pty ltd - water for injections, quantity: 0.75 ml - diluent, not applicable - excipient ingredients: - for use as a diluent for merck, sharp & dohme live virus vaccines.

BAVENCIO Israel - English - Ministry of Health

bavencio

merck serono ltd - avelumab - concentrate for solution for infusion - avelumab 20 mg / 1 ml - metastatic merkel cell carcinomabavencio is indicated for the treatment of adult patients with metastatic merkel cell carcinoma (mcc).locally advanced or metastatic urothelial carcinomafirst-line maintenance treatment of urothelial carcinomabavencio is indicated for the maintenance treatment of patients with locally advanced or metastatic urothelial carcinoma (uc) that has not progressed with first-line platinum-containing chemotherapy.previously-treated urothelial carcinomabavencio is indicated for the treatment of patients with locally advanced or metastatic urothelial carcinoma (uc) who:• have disease progression during or following platinum-containing chemotherapy• have disease progression within 12 months of neoadjuvant or adjuvant treatment with platinum-containing chemotherapy advanced renal cell carcinomabavencio in combination with axitinib is indicated for the first-line treatment of patients with advanced renal cell carcinoma (rcc).

PROQUAD Israel - English - Ministry of Health

proquad

merck sharp & dohme (israel - 1996) company ltd, israel - measles virus enders edmonston strain (live, attenuated); mumps virus jeryl lynn™ (level b) strain (live, attenuated); rubella virus wistar ra 27/3 strain (live, attenuated); varicella virus oka/merck strain (live, attenuated) - powder and solvent for suspension for injection - measles virus enders edmonston strain (live, attenuated); varicella virus oka/merck strain (live, attenuated); rubella virus wistar ra 27/3 strain (live, attenuated); mumps virus jeryl lynn™ (level b) strain (live, attenuated) - measles, combinations with mumps, rubella and varicella, live attenuated - proquad is indicated for simultaneous vaccination against measles, mumps, rubella, and varicella in individuals from 12 months of age to 12 years of age.proquad can be administered to individuals from 9 months of age under special circumstances: outbreak situations, or travel to a region with high prevalence of measles.

CUBICIN 500 MG Israel - English - Ministry of Health

cubicin 500 mg

merck sharp & dohme (israel - 1996) company ltd, israel - daptomycin - lyophilized powder for solution for injection - daptomycin 500 mg/vial - daptomycin - cubicin is indicated for the treatment of the infections listed below. * complicated skin and skin structure infectionscomplicated skin and skin structure infections (csssi) caused by susceptible isolates of the following gram-positive bacteria: staphylococcus aureus (including methicillin-resistant isolates), streptococcus pyogenes, streptococcus agalactiae, streptococcus dysgalactiae subsp. equisimilis, and enterococcus faecalis (vancomycin-susceptible isolates only).* staphylococcus aureus bloodstream infections (bacteremia), including those with right-sided infective endocarditis, caused by methicillin-susceptible and methicillin-resistant isolatesstaphylococcus aureus bloodstream infections (bacteremia), including those with right-sided infective endocarditis, caused by methicillin-susceptible and methicillin-resistant isolates.* combination therapy may be clinically indicated if the documented or presumed pathogens include gram negative or anaerobic organisms

TEPMETKO Israel - English - Ministry of Health

tepmetko

merck serono ltd - tepotinib as hydrochloride hydrate - film coated tablets - tepotinib as hydrochloride hydrate 225 mg - tepotinib - tepmetko is indicated for the treatment of adult patients with metastatic non-small cell lung cancer (nsclc) harbouring a met tyrosine kinase receptor exon 14 (metex14) skipping mutation.

Vildagliptin/Metformin HCl Merck 50mg/850mg film-coated Tablets Malta - English - Medicines Authority

vildagliptin/metformin hcl merck 50mg/850mg film-coated tablets

merck healthcare kgaa frankfurter strasse 250, 64293 darmstadt, germany - vildagliptin, metformin hydrochloride - film-coated tablet - metformin hydrochloride 850 mg vildagliptin 50 mg - drugs used in diabetes

Vildagliptin/Metformin HCl Merck  50mg/1000mg film-coated Tablets Malta - English - Medicines Authority

vildagliptin/metformin hcl merck 50mg/1000mg film-coated tablets

merck healthcare kgaa frankfurter strasse 250, 64293 darmstadt, germany - vildagliptin, metformin hydrochloride - film-coated tablet - vildagliptin 50 mg metformin hydrochloride 1000 mg - drugs used in diabetes

GLUCOVANCE TABLET 500 mg5 mg Singapore - English - HSA (Health Sciences Authority)

glucovance tablet 500 mg5 mg

merck pte. ltd. - glibenclamide; metformin hcl - tablet, film coated - 5 mg - glibenclamide 5 mg; metformin hcl 500 mg

PegIntron European Union - English - EMA (European Medicines Agency)

pegintron

merck sharp & dohme b.v. - peginterferon alfa-2b - hepatitis c, chronic - immunostimulants, - adults (tritherapy)pegintron in combination with ribavirin and boceprevir (tritherapy) is indicated for the treatment of chronic-hepatitis-c (chc) genotype-1 infection in adult patients (18 years of age and older) with compensated liver disease who are previously untreated or who have failed previous therapy.please refer to the ribavirin and boceprevir summaries of product characteristics (smpcs) when pegintron is to be used in combination with these medicines.adults (bitherapy and monotherapy)pegintron is indicated for the treatment of adult patients (18 years of age and older) with chc who are positive for hepatitis-c-virus rna (hcv-rna), including patients with compensated cirrhosis and / or co-infected with clinically stable hiv.pegintron in combination with ribavirin (bitherapy) is indicated for the treatment of chc infection in adult patients who are previously untreated including patients with clinically stable hiv co-infection and in adult patients who have failed previous treatment with interferon-alpha (pegylated or non-pegylated) and ribavirin combination therapy or interferon-alpha monotherapy.interferon monotherapy, including pegintron, is indicated mainly in case of intolerance or contraindication to ribavirin.please refer to the ribavirin smpc when pegintron is to be used in combination with ribavirin.paediatric population (bitherapy)pegintron is indicated in a combination regimen with ribavirin for the treatment of children three years of age and older and adolescents who have chc, previously untreated, without liver decompensation, and who are positive for hcv-rna.when deciding not to defer treatment until adulthood, it is important to consider that the combination therapy induced a growth inhibition that may be irreversible in some patients. the decision to treat should be made on a case-by-case basis.please refer to the ribavirin smpc for capsules or oral solution when pegintron is to be used in combination with ribavirin.

VARIVAX- varicella virus vaccine live injection, powder, lyophilized, for suspension United States - English - NLM (National Library of Medicine)

varivax- varicella virus vaccine live injection, powder, lyophilized, for suspension

merck sharp & dohme llc - varicella-zoster virus strain oka/merck live antigen (unii: gpv39zgd8c) (varicella-zoster virus strain oka/merck live antigen - unii:gpv39zgd8c) - varicella-zoster virus strain oka/merck live antigen 1350 [pfu] in 0.5 ml - varivax is a vaccine indicated for active immunization for the prevention of varicella in individuals 12 months of age and older. do not administer varivax to individuals with a history of anaphylactic or severe allergic reaction to any component of the vaccine (including neomycin and gelatin) or to a previous dose of a varicella-containing vaccine. do not administer varivax to individuals who are immunodeficient or immunosuppressed due to disease or medical therapy. disseminated varicella disease and extensive vaccine-associated rash have been reported in individuals who are immunosuppressed or immunodeficient who were inadvertently vaccinated with a varicella-containing vaccine. do not administer varivax to individuals with an active febrile illness with fever >101.3°f (>38.5°c). do not administer varivax to individuals with active, untreated tuberculosis (tb). do not administer varivax to individuals who are pregnant or planning on becoming pregnant in the next 3 months. wild-type varicella is known to cau