Stelara Solution for Injection in Pre-Filled Syringe 90 mg1 mL Singapore - engelska - HSA (Health Sciences Authority)

stelara solution for injection in pre-filled syringe 90 mg1 ml

johnson & johnson international (singapore) pte ltd - ustekinumab - injection, solution - 90mg/1ml - ustekinumab 90mg/1ml

Mozobil Solution for Injection 20mgml Singapore - engelska - HSA (Health Sciences Authority)

mozobil solution for injection 20mgml

sanofi-aventis singapore pte. ltd. - plerixafor - injection, solution - 20mg/ml - plerixafor 20mg/ml

ALFAXAN 10 mg/ml solution for injection for dogs and cats Irland - engelska - HPRA (Health Products Regulatory Authority)

alfaxan 10 mg/ml solution for injection for dogs and cats

jurox (ireland) limited - alfaxalone - solution for injection - 10 milligram(s)/millilitre - alfaxalone

NUCALA POWDER FOR SOLUTION FOR INJECTION Israel - engelska - Ministry of Health

nucala powder for solution for injection

glaxo smith kline (israel) ltd - mepolizumab - powder for solution for injection - mepolizumab 100 mg - mepolizumab - severe eosinophilic asthmanucala is indicated as an add-on treatment for severe refractory eosinophilic asthma in adult patientschronic rhinosinusitis with nasal polyps (crswnp)nucala is indicated as an add-on therapy with intranasal corticosteroids for the treatment of adult patients with severe crswnp for whom therapy with corticosteroids and surgery in the last 10 years do not provide adequate disease control.eosinophilic granulomatosis with polyangiitis (egpa)nucala is indicated for the treatment of adult patients with eosinophilic granulomatosis with polyangiitis (egpa).hypereosinophilic syndrome (hes)nucala is indicated as an add-on treatment for adult patients with inadequately controlled hypereosinophilic syndrome without an identifiable non-haematologic secondary cause.

Zepraxen 350mg powder for solution for injection/infusion Malta - engelska - Medicines Authority

zepraxen 350mg powder for solution for injection/infusion

vocate pharmaceuticals s.a 150, gounari str, 166 74 glyfada, athens, greece - daptomycin - powder for solution for injection/infusion - daptomycin 350 mg - antibacterials for systemic use

Zepraxen 500mg powder for solution for injection/infusion Malta - engelska - Medicines Authority

zepraxen 500mg powder for solution for injection/infusion

vocate pharmaceuticals s.a 150, gounari str, 166 74 glyfada, athens, greece - daptomycin - powder for solution for injection/infusion - daptomycin 500 mg - antibacterials for systemic use

KIMMTRAK tebentafusp 0.1 mg/0.5 mL concentrated solution for infusion vial Australien - engelska - Department of Health (Therapeutic Goods Administration)

kimmtrak tebentafusp 0.1 mg/0.5 ml concentrated solution for infusion vial

medison pharma australia pty ltd - tebentafusp, quantity: 0.2 mg/ml - injection, concentrated - excipient ingredients: citric acid monohydrate; water for injections; mannitol; trehalose dihydrate; polysorbate 20; dibasic sodium phosphate - kimmtrak is indicated for the treatment of hla-a02 01-positive adult patients with unresectable or metastatic uveal melanoma.

SAIZEN CLICK.EASY 8 Milligram Pdr+Solv for Soln for Inj Irland - engelska - HPRA (Health Products Regulatory Authority)

saizen click.easy 8 milligram pdr+solv for soln for inj

merck serono limited - somatropin, recombinant human growth hormone - pdr+solv for soln for inj - 8 milligram - somatropin and somatropin agonists

LEVETIRACETAM IV ARX levetiracetam 500mg/5mL concentrate solution for IV infusion vial Australien - engelska - Department of Health (Therapeutic Goods Administration)

levetiracetam iv arx levetiracetam 500mg/5ml concentrate solution for iv infusion vial

arrotex pharmaceuticals pty ltd - levetiracetam, quantity: 100 mg/ml - injection, intravenous infusion - excipient ingredients: sodium acetate trihydrate; sodium chloride; water for injections; glacial acetic acid - levetiracetam concentrate solution for iv infusion after dilution is an alternative for patients when oral administration is temporarily not feasible. use in epileptic patients aged 4 years and older, initially as add on therapy, in the treatment of partial onset seizures with or without secondary generalisation; monotherapy in the treatment of partial onset seizures, with or without secondary generalisation, in patients from 16 years of age with newly diagnosed epilepsy; add on therapy in the treatment of myoclonic seizures in adults and adolescents from 12 years of age with juvenile myoclonic epilepsy (jme); and, add on therapy in the treatment of primary generalized tonic-clonic seizures in adults and children from 4 years of age with idiopathic generalized epilepsy (ige).

LEVETIRACETAM-AFT  levetiracetam 500 mg/5 mL concentrate solution for infusion vial Australien - engelska - Department of Health (Therapeutic Goods Administration)

levetiracetam-aft levetiracetam 500 mg/5 ml concentrate solution for infusion vial

aft pharmaceuticals pty ltd - levetiracetam, quantity: 10 % w/v - injection, concentrated - excipient ingredients: glacial acetic acid; sodium chloride; water for injections; sodium acetate trihydrate - levetiracetam-aft oral solution is indicated for:,use in epileptic patients aged 4 years and older, initially as add on therapy, in the treatment of partial onset seizures with or without secondary generalisation,,monotherapy in the treatment of partial onset seizures, with or without secondary generalisation, in patients from 16 years of age with newly diagnosed epilepsy.,add on therapy in the treatment of myoclonic seizures in adults and adolescents from 12 years of age with juvenile myoclonic epilepsy (jme),and,add on therapy in the treatment of primary generalized tonic-clonic seizures in adults and children from 4 years of age with idiopathic generalized epilepsy (ige).,levetiracetam-aft concentrate solution for iv infusion after dilution is an alternative for patients when oral administration is temporarily not feasible.