Reconcile 32 mg Chewable Tablets for Dogs Velká Británie - angličtina - VMD (Veterinary Medicines Directorate)

reconcile 32 mg chewable tablets for dogs

forte healthcare ltd - fluoxetine - tablet - neurological agent behavioural - dogs

Reconcile 64 mg Chewable Tablets for Dogs Velká Británie - angličtina - VMD (Veterinary Medicines Directorate)

reconcile 64 mg chewable tablets for dogs

forte healthcare ltd - fluoxetine - tablet - neurological agent behavioural - dogs

PEGASYS PRE-FILLED SYRINGE FOR INJECTION 135 mcg0.5 ml Singapur - angličtina - HSA (Health Sciences Authority)

pegasys pre-filled syringe for injection 135 mcg0.5 ml

dksh singapore pte. ltd. - peginterferon alfa-2a - injection - 135 mcg/0.5 ml - peginterferon alfa-2a 135 mcg/0.5 ml

PEGASYS PRE-FILLED SYRINGE FOR INJECTION 180 mcg0.5 ml Singapur - angličtina - HSA (Health Sciences Authority)

pegasys pre-filled syringe for injection 180 mcg0.5 ml

dksh singapore pte. ltd. - peginterferon alfa-2a - injection - 180 mcg/0.5 ml - peginterferon alfa-2a 180 mcg/0.5 ml

Viraferon Evropská unie - angličtina - EMA (European Medicines Agency)

viraferon

schering-plough europe - interferon alfa-2b - hepatitis c, chronic; hepatitis b, chronic - immunostimulants, - chronic hepatitis b: treatment of adult patients with chronic hepatitis b associated with evidence of hepatitis b viral replication (presence of hbv-dna and hbeag), elevated alanine aminotransferase (alt) and histologically proven active liver inflammation and/or fibrosis.chronic hepatitis c:adult patients:introna is indicated for the treatment of adult patients with chronic hepatitis c who have elevated transaminases without liver decompensation and who are positive for serum hcv-rna or anti-hcv (see section 4.4).the best way to use introna in this indication is in combination with ribavirin.chidren and adolescents:introna is intended for use, in a combination regimen with ribavirin, for the treatment of children and adolescents 3 years of age and older, who have chronic hepatitis c, not previously treated, without liver decompensation, and who are positive for serum hcv-rna. the decision to treat should be made on a case by case basis, taking into account any evidence of disease progression such as hepatic inflammation and fibrosis, as well as prognostic factors for response, hcv genotype and viral load. the expected benefit of treatment should be weighed against the safety findings observed for paediatric subjects in the clinical trials (see sections 4.4, 4.8 and 5.1).

COPEGUS TABLET 200 mg Singapur - angličtina - HSA (Health Sciences Authority)

copegus tablet 200 mg

roche singapore pte. ltd. - ribavirin - tablet, film coated - 200 mg - ribavirin 200 mg

REBETOL CAPSULE 200 mg Singapur - angličtina - HSA (Health Sciences Authority)

rebetol capsule 200 mg

msd pharma (singapore) pte. ltd. - ribavirin - capsule - 200 mg - ribavirin 200 mg

AVELOX TABLET 400 mg Singapur - angličtina - HSA (Health Sciences Authority)

avelox tablet 400 mg

bayer (south east asia) pte ltd - moxifloxacin hcl eqv moxifloxacin - tablet, film coated - 400 mg - moxifloxacin hcl eqv moxifloxacin 400 mg