Xefo 8 mg pulver og solvens til injektionsvæske, opløsning Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

xefo 8 mg pulver og solvens til injektionsvæske, opløsning

takeda pharma a/s - lornoxicam - pulver og solvens til injektionsvæske, opløsning - 8 mg

Takhzyro Den Europæiske Union - dansk - EMA (European Medicines Agency)

takhzyro

takeda pharmaceuticals international ag ireland branch - lanadelumab - angioødemer, arvelige - other hematological agents - takhzyro is indicated for routine prevention of recurrent attacks of hereditary angioedema (hae) in patients aged 2 years and older.

Alunbrig Den Europæiske Union - dansk - EMA (European Medicines Agency)

alunbrig

takeda pharma a/s - brigatinib - carcinom, ikke-småcellet lunge - antineoplastiske midler - alunbrig is indicated as monotherapy for the treatment of adult patients with anaplastic lymphoma kinase (alk)‑positive advanced non‑small cell lung cancer (nsclc) previously not treated with an alk inhibitor. alunbrig is indicated as monotherapy for the treatment of adult patients with anaplastic lymphoma kinase alkpositive advanced nsclc previously treated with crizotinib.

Rymphysia 1000 mg pulver og solvens til infusionsvæske, opløsning Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

rymphysia 1000 mg pulver og solvens til infusionsvæske, opløsning

takeda manufacturing austria ag - alfa-1 proteinaseinhibitor, humant - pulver og solvens til infusionsvæske, opløsning - 1000 mg

Livtencity Den Europæiske Union - dansk - EMA (European Medicines Agency)

livtencity

takeda pharmaceuticals international ag ireland branch - maribavir - cytomegalovirusinfektioner - antivirale midler til systemisk anvendelse - livtencity is indicated for the treatment of cytomegalovirus (cmv) infection and/or disease that are refractory (with or without resistance) to one or more prior therapies, including ganciclovir, valganciclovir, cidofovir or foscarnet in adult patients who have undergone a haematopoietic stem cell transplant (hsct) or solid organ transplant (sot). det bør overvejes at officielle vejledning om hensigtsmæssig brug af antivirale agenter.

Qdenga Den Europæiske Union - dansk - EMA (European Medicines Agency)

qdenga

takeda gmbh - dengue virus, serotype 2, expressing dengue virus, serotype 1, surface proteins, live, attenuated, dengue virus, serotype 2, expressing dengue virus, serotype 3, surface proteins, live, attenuated, dengue virus, serotype 2, expressing dengue virus, serotype 4, surface proteins, live, attenuated, dengue virus, serotype 2, live, attenuated - dengue - vacciner - qdenga is indicated for the prevention of dengue disease in individuals from 4 years of age. the use of qdenga should be in accordance with official recommendations.

Aduvanz 20 mg kapsler, hårde Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

aduvanz 20 mg kapsler, hårde

takeda pharmaceuticals international ag ireland branch - lisdexamfetamindimesilat - kapsler, hårde - 20 mg

Aduvanz 40 mg kapsler, hårde Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

aduvanz 40 mg kapsler, hårde

takeda pharmaceuticals international ag ireland branch - lisdexamfetamindimesilat - kapsler, hårde - 40 mg

Aduvanz 60 mg kapsler, hårde Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

aduvanz 60 mg kapsler, hårde

takeda pharmaceuticals international ag ireland branch - lisdexamfetamindimesilat - kapsler, hårde - 60 mg

Firazyr Den Europæiske Union - dansk - EMA (European Medicines Agency)

firazyr

takeda pharmaceuticals international ag - icatibant - angioødemer, arvelige - hjertetapi - firazyr er indiceret til symptomatisk behandling af akutte angreb af arvelig angioødem (hae) hos voksne (med c1-esterase-hæmmere mangel).