Hyftor Umoja wa Ulaya - Kiaisilandi - EMA (European Medicines Agency)

hyftor

plusultra pharma gmbh - sirolimus - angiofibroma; tuberous sclerosis - hyftor is indicated for the treatment of facial angiofibroma associated with tuberous sclerosis complex in adults and paediatric patients aged 6 years and older.

Pioglitazone Teva Pharma Umoja wa Ulaya - Kiaisilandi - EMA (European Medicines Agency)

pioglitazone teva pharma

teva pharma b.v. - pioglitazón hýdróklóríð - sykursýki, tegund 2 - lyf notuð við sykursýki - pioglitazone is indicated in the treatment of type-2 diabetes mellitus as monotherapy: , in adult patients (particularly overweight patients) inadequately controlled by diet and exercise for whom metformin is inappropriate because of contraindications or intolerance. , pioglitazone is also indicated for combination with insulin in type 2 diabetes mellitus adult patients with insufficient glycaemic control on insulin for whom metformin is inappropriate because of contraindications or intolerance. eftir hafin með lyfleysu, sjúklingar ætti að vera metið eftir 3 til 6 mánuði að meta fullnægjandi að bregðast við meðferð (e. lækkun í hba1c). Í sjúklingum sem ekki að sýna nægilegt svar, engar upplýsingar ætti að hætta. Í ljósi væntanlegra áhættu með langvarandi meðferð, ávísun ætti að staðfesta á síðari lífi umsagnir að njóta góðs af lyfleysu er viðhaldið.

Axura Umoja wa Ulaya - Kiaisilandi - EMA (European Medicines Agency)

axura

merz pharmaceuticals gmbh - memantínhýdróklóríð - alzheimer sjúkdómur - Önnur lyf gegn vitglöpum - meðferð sjúklinga með miðlungsmikla til alvarlega alzheimerssjúkdóma.

Pirfenidone axunio (previously Pirfenidone AET) Umoja wa Ulaya - Kiaisilandi - EMA (European Medicines Agency)

pirfenidone axunio (previously pirfenidone aet)

axunio pharma gmbh - pirfenidone - idiopathic lungvefi - Ónæmisbælandi lyf - pirfenidone aet is indicated in adults for the treatment of mild to moderate idiopathic pulmonary fibrosis (ipf).

Prialt Umoja wa Ulaya - Kiaisilandi - EMA (European Medicines Agency)

prialt

esteve pharmaceuticals gmbh - zícónótíð - injections, spinal; pain - verkjalyf - zícónótíð er ætlað til meðferðar við alvarlegum langvarandi sársauka hjá sjúklingum sem þarfnast verkjastillingar.

Ranivisio Umoja wa Ulaya - Kiaisilandi - EMA (European Medicines Agency)

ranivisio

midas pharma gmbh - ranibizumab - wet macular degeneration; macular edema; diabetic retinopathy; diabetes complications - augnlækningar - ranivisio is indicated in adults for:• the treatment of neovascular (wet) age-related macular degeneration (amd)• the treatment of visual impairment due to diabetic macular oedema (dme)• the treatment of proliferative diabetic retinopathy (pdr)• the treatment of visual impairment due to macular oedema secondary to retinal vein occlusion (branch rvo or central rvo)• the treatment of visual impairment due to choroidal neovascularisation (cnv).

Vancomycin-MIP Innrennslisstofn, lausn 1000 mg Aislandi - Kiaisilandi - LYFJASTOFNUN (Icelandic Medicines Agency)

vancomycin-mip innrennslisstofn, lausn 1000 mg

mip pharma gmbh - vancomycin hydrochloride - innrennslisstofn, lausn - 1000 mg

Vancomycin-MIP Innrennslisstofn, lausn 500 mg Aislandi - Kiaisilandi - LYFJASTOFNUN (Icelandic Medicines Agency)

vancomycin-mip innrennslisstofn, lausn 500 mg

mip pharma gmbh - vancomycin hydrochloride - innrennslisstofn, lausn - 500 mg