IDACIO SOLUTION FOR INJECTION FOR PAEDIATRIC USE 40MG0.8ML VIAL Սինգապուր - անգլերեն - HSA (Health Sciences Authority)

idacio solution for injection for paediatric use 40mg0.8ml vial

fresenius kabi (singapore) pte ltd - adalimumab - injection, solution - adalimumab 40mg/0.8ml

IDACIO SOLUTION FOR INJECTION IN PRE-FILLED PEN 40MG0.8ML Սինգապուր - անգլերեն - HSA (Health Sciences Authority)

idacio solution for injection in pre-filled pen 40mg0.8ml

fresenius kabi (singapore) pte ltd - adalimumab - injection, solution - adalimumab 40mg/0.8ml

IDACIO SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE 40MG0.8ML Սինգապուր - անգլերեն - HSA (Health Sciences Authority)

idacio solution for injection in pre-filled syringe 40mg0.8ml

fresenius kabi (singapore) pte ltd - adalimumab - injection, solution - adalimumab 40mg/0.8ml

Cyltezo Եվրոպական Միություն - անգլերեն - EMA (European Medicines Agency)

cyltezo

boehringer ingelheim international gmbh - adalimumab - hidradenitis suppurativa; arthritis, psoriatic; psoriasis; crohn disease; arthritis, juvenile rheumatoid; uveitis; arthritis, rheumatoid; colitis, ulcerative; spondylitis, ankylosing - immunosuppressants - please refer to section 4.1 of the summary of product characteristics in the product information document.,

Solymbic Եվրոպական Միություն - անգլերեն - EMA (European Medicines Agency)

solymbic

amgen europe b.v. - adalimumab - arthritis, psoriatic; spondylitis, ankylosing; crohn disease; colitis, ulcerative; hidradenitis suppurativa; psoriasis; arthritis, rheumatoid - immunosuppressants - please refer to section 4.1 of the summary of product characteristics in the product information document. ,

Humira Նոր Զելանդիա - անգլերեն - Medsafe (Medicines Safety Authority)

humira

abbvie limited - adalimumab 50 mg/ml;  ;   - solution for injection - 20mg/0.4ml - active: adalimumab 50 mg/ml     excipient: citric acid monohydrate dibasic sodium phosphate dihydrate mannitol monobasic sodium phosphate dihydrate polysorbate 80 sodium chloride sodium citrate sodium hydroxide water for injection - humira in combination with methotrexate is indicated for reducing the signs and symptoms of moderately to severely active polyarticular juvenile idiopathic arthritis in patients aged 2 years of age and older. humira can be given as monotherapy in case of intolerance to methotrexate or when continued treatment with methotrexate is inappropriate.

Humira Նոր Զելանդիա - անգլերեն - Medsafe (Medicines Safety Authority)

humira

abbvie limited - adalimumab 50 mg/ml;  ;   - solution for injection - 40 mg/0.8ml - active: adalimumab 50 mg/ml     excipient: citric acid monohydrate dibasic sodium phosphate dihydrate dimeticone mannitol monobasic sodium phosphate dihydrate polysorbate 80 sodium chloride sodium citrate dihydrate sodium hydroxide water for injection - rheumatoid arthritis humira is indicated for reducing signs and symptoms, as well as inhibiting the progression of structural damage in adult patients with moderate to severely active rheumatoid arthritis. this includes the treatment of patients with recently diagnosed moderate to severely active disease who have not received methotrexate. humira can be used alone or in combination with methotrexate.