Elaprase New Zealand - English - Medsafe (Medicines Safety Authority)

elaprase

pharmacy retailing (nz) ltd t/a healthcare logistics - idursulfase 2 mg/ml;   - concentrate for infusion - 2 mg/ml - active: idursulfase 2 mg/ml   excipient: dibasic sodium phosphate heptahydrate monobasic sodium phosphate monohydrate polysorbate 20 sodium chloride water for injection - elaprase is indicated for the long term treatment of patients with hunter syndrome (mucopolysaccharidosis ii, mps ii).

NAGLAZYME Israel - English - Ministry of Health

naglazyme

medison pharma ltd - galsulfase - concentrate for solution for infusion - galsulfase 1 mg/ml - galsulfase - galsulfase - naglazyme is indicated for long-term enzyme replacement therapy in patients with a confirmed diagnosis of mpsvi (n-acetylglactosamine 4 sulfatase deficiency maroteaux-lamy syndrome).

Anbinex Powder For Injection 1000 I.U. Singapore - English - HSA (Health Sciences Authority)

anbinex powder for injection 1000 i.u.

grifols asia pacific pte. ltd. - human antithrombin - injection, powder, lyophilized, for solution - 1000 i.u. per 20ml - human antithrombin 1000 i.u. per 20ml

Anbinex Powder For Injection 500 I.U. Singapore - English - HSA (Health Sciences Authority)

anbinex powder for injection 500 i.u.

grifols asia pacific pte. ltd. - human antithrombin - injection, powder, lyophilized, for solution - 500 i.u. per 10ml - human antithrombin 500 i.u. per 10ml

ALDURAZYME Singapore - English - HSA (Health Sciences Authority)

aldurazyme

sanofi-aventis singapore pte. ltd. - laronidase - injection, solution - 2.9mg - laronidase 2.9mg

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

vimizim

biomarin international limited - recombinant human n-acetylgalactosamine-6-sulfatase - mucopolysaccharidosis iv - other alimentary tract and metabolism products, - vimizim is indicated for the treatment of mucopolysaccharidosis, type iva (morquio a syndrome, mps iva) in patients of all ages.

Naglazyme New Zealand - English - Medsafe (Medicines Safety Authority)

naglazyme

pharmacy retailing (nz) ltd t/a healthcare logistics - galsulfase 1 mg/ml - concentrate for infusion - 1 mg/ml - active: galsulfase 1 mg/ml excipient: polysorbate 80 sodium chloride sodium phosphate water for injection - naglazyme is indicated as long term enzyme replacement therapy in patients with mucopolysaccharidosis vi (mps vi, n-acetylgalactosamine 4-sulfatase deficiency, maroteaux-lamy syndrome).

IALURIL Procedure pack - Bladder instillation, barrier Australia - English - Department of Health (Therapeutic Goods Administration)

ialuril procedure pack - bladder instillation, barrier

juno pharmaceuticals pty ltd - 44670 - bladder instillation, barrier - procedure pack consisting of a clear plastic pre-filled syringe containing a sterile aqueous solution of hyaluronic acid sodium salt (1.6%), sodium chondroitin sulphate (2%) and calcium chloride administered as a bladder instillation via connection to a catheter using the leur lock adaptor and the ialuadapter included in the pack. the ialuadapter allows for administration by either the patient or healthcare professional. ialuril is indicated to re-establish the glycosaminoglycan layers (gags) of the urothelial vesical tissue in cases in which their loss can cause frequent and recurring problems such as painful bladder syndrome (pbs), interstitial cystitis, treatment and prevention of recurrent urinary tract infection, cystitis as a result of bacillus calmette ? guerin therapy, or chemical and radiation therapy. ialuril is also indicated in the cases where the loss of the glycosaminoglycan layers (gags) is associated with forms of chronic inflammation, in which their composition and integrity appears compromis

IALURIL Prefill - Bladder instillation, barrier Australia - English - Department of Health (Therapeutic Goods Administration)

ialuril prefill - bladder instillation, barrier

juno pharmaceuticals pty ltd - 44670 - bladder instillation, barrier - clear plastic pre-filled syringe containing a sterile aqueous solution of hyaluronic acid sodium salt (1.6%), sodium chondroitin sulphate (2%) and calcium chloride administered as a bladder instillation via a catheter. ialuril prefill is indicated to re-establish the glycosaminoglycan layers (gags) of the urothelial vesical tissue in cases in which their loss can cause frequent and recurring problems such as painful bladder syndrome (pbs), interstitial cystitis, treatment and prevention of recurrent urinary tract infection, cystitis as a result of bacillus calmette ? guerin therapy, or chemical and radiation therapy. ialuril prefill is also indicated in the cases where the loss of the glycosaminoglycan layers (gags) is associated with forms of chronic inflammation, in which their composition and integrity appears compromised in different ways.

NAGLAZYME galsulfase-rch 5mg/5mL concentrated solution for injection vial Australia - English - Department of Health (Therapeutic Goods Administration)

naglazyme galsulfase-rch 5mg/5ml concentrated solution for injection vial

biomarin pharmaceutical australia pty ltd - galsulfase, quantity: 5 mg - injection, concentrated - excipient ingredients: monobasic sodium phosphate monohydrate; water for injections; dibasic sodium phosphate heptahydrate; polysorbate 80; sodium chloride - for the long-term enzyme replacement therapy in patients with mucopolysaccharidosis vi (mps vi - n acetylgalactosamine 4-sulfatase deficiency)