Slovenia - slovensk - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

teva pharma b.v. - galantamin - kapsula s podaljšanim sproščanjem, trda - galantamin 24 mg / 1 kapsula - galantamin

Slovenia - slovensk - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

teva pharma b.v. - galantamin - kapsula s podaljšanim sproščanjem, trda - galantamin 16 mg / 1 kapsula - galantamin

Frankrike - fransk - ANSM (Agence Nationale de Sécurité du Médicament et des Produits de Santé)

cristers - galantamine 8 mg sous forme de : bromhydrate de galantamine - gélule - 8 mg - pour une gélule > galantamine 8 mg sous forme de : bromhydrate de galantamine - médicaments anti-démentiels - galantamine cristers lp 8 mg, gélule à libération prolongée contient la substance active « galantamine », un médicament anti-démence. il est utilisé chez les adultes pour traiter les symptômes légers à modérément sévères de la maladie d'alzheimer, un type de démence qui altère le fonctionnement cérébral.la maladie d'alzheimer entraîne une perte progressive de la mémoire, une confusion et des modifications du comportement ce qui rend de plus en plus difficile la réalisation des activités de la vie quotidienne.ces effets sont supposés être causés par un déficit en « acétylcholine », une substance responsable d'envoyer des messages entre les cellules du cerveau. galantamine cristers lp augmente la quantité d'acétylcholine dans le cerveau et traite les signes de la maladie.les gélules sont à « libération prolongée ». cela signifie qu'elles libèrent le médicament lentement.

Frankrike - fransk - ANSM (Agence Nationale de Sécurité du Médicament et des Produits de Santé)

cristers - galantamine 16 mg sous forme de : bromhydrate de galantamine - gélule - 16 mg - pour une gélule > galantamine 16 mg sous forme de : bromhydrate de galantamine - médicaments anti-démentiels - galantamine cristers lp 16 mg, gélule à libération prolongée contient la substance active « galantamine », un médicament anti-démence. il est utilisé chez les adultes pour traiter les symptômes légers à modérément sévères de la maladie d'alzheimer, un type de démence qui altère le fonctionnement cérébral.la maladie d'alzheimer entraîne une perte progressive de la mémoire, une confusion et des modifications du comportement ce qui rend de plus en plus difficile la réalisation des activités de la vie quotidienne.ces effets sont supposés être causés par un déficit en « acétylcholine », une substance responsable d'envoyer des messages entre les cellules du cerveau. galantamine cristers lp 16 mg, gélule à libération prolongée augmente la quantité d'acétylcholine dans le cerveau et traite les signes de la maladie.les gélules sont à « libération prolongée ». cela signifie qu'elles libèrent le médicament lentement.

USA - engelsk - NLM (National Library of Medicine)

aphena pharma solutions - tennessee, llc - galantamine hydrobromide (unii: mj4ptd2vvw) (galantamine - unii:0d3q044kca) - galantamine 16 mg - galantamine hydrobromide extended-release capsules are indicated for the treatment of mild to moderate dementia of the alzheimer’s type. galantamine hydrobromide extended-release capsules are contraindicated in patients with known hypersensitivity to galantamine hydrobromide or to any excipients used in the formulation.

USA - engelsk - NLM (National Library of Medicine)

mylan pharmaceuticals inc. - galantamine hydrobromide (unii: mj4ptd2vvw) (galantamine - unii:0d3q044kca) - galantamine 4 mg - galantamine tablets are indicated for the treatment of mild to moderate dementia of the alzheimer’s type. galantamine tablets are contraindicated in patients with known hypersensitivity to galantamine hydrobromide or to any excipients used in the formulation. there are no adequate and well-controlled studies in pregnant women. in studies conducted in animals, administration of galantamine during pregnancy resulted in developmental toxicity (increased incidence of morphological abnormalities and decreased growth in offspring) at doses similar to or greater than those used clinically. galantamine tablets should be used during pregnancy only if the potential benefit justifies the potential risk to the fetus. in rats, administration of galantamine (oral doses of 2 mg/kg/day, 8 mg/kg/day, or 16 mg/kg/day), from day 14 (females) or day 60 (males) prior to mating and continuing in females through the period of organogenesis, resulted in an increased incidence of fetal skeletal variations at the two highest doses. th

USA - engelsk - NLM (National Library of Medicine)

west-ward pharmaceuticals corp. - galantamine hydrobromide (unii: mj4ptd2vvw) (galantamine - unii:0d3q044kca) - galantamine 4 mg - galantamine is indicated for the treatment of mild to moderate dementia of the alzheimer’s type. galantamine is contraindicated in patients with known hypersensitivity to galantamine hydrobromide or to any excipients used in the formulation. pregnancy category c there are no adequate and well-controlled studies in pregnant women. in studies conducted in animals, administration of galantamine during pregnancy resulted in developmental toxicity (increased incidence of morphological abnormalities and decreased growth in offspring) at doses similar to or greater than those used clinically. galantamine should be used during pregnancy only if the potential benefit justifies the potential risk to the fetus. in rats, administration of galantamine (oral doses of 2 mg, 8 mg, or 16 mg/kg/day), from day 14 (females) or day 60 (males) prior to mating and continuing in females through the period of organogenesis, resulted in an increased incidence of fetal skeletal variations at the two highest doses. the no-effect dose fo

USA - engelsk - NLM (National Library of Medicine)

mylan institutional inc. - galantamine hydrobromide (unii: mj4ptd2vvw) (galantamine - unii:0d3q044kca) - galantamine 4 mg - galantamine tablets are indicated for the treatment of mild to moderate dementia of the alzheimer’s type. galantamine tablets are contraindicated in patients with known hypersensitivity to galantamine hydrobromide or to any excipients used in the formulation. there are no adequate and well-controlled studies in pregnant women. in studies conducted in animals, administration of galantamine during pregnancy resulted in developmental toxicity (increased incidence of morphological abnormalities and decreased growth in offspring) at doses similar to or greater than those used clinically. galantamine tablets should be used during pregnancy only if the potential benefit justifies the potential risk to the fetus. in rats, administration of galantamine (oral doses of 2 mg/kg/day, 8 mg/kg/day, or 16 mg/kg/day), from day 14 (females) or day 60 (males) prior to mating and continuing in females through the period of organogenesis, resulted in an increased incidence of fetal skeletal variations at the two highest doses. th

USA - engelsk - NLM (National Library of Medicine)

ncs healthcare of ky, inc dba vangard labs - galantamine hydrobromide (unii: mj4ptd2vvw) (galantamine - unii:0d3q044kca) - galantamine 4 mg - galantamine tablets are indicated for the treatment of mild to moderate dementia of the alzheimer's type. galantamine tablets are contraindicated in patients with known hypersensitivity to galantamine hydrobromide or to any excipients used in the formulation.

Portugal - portugisisk - INFARMED (Autoridade Nacional do Medicamento e Produtos de Saúde)

axone, lda. - galantamina - comprimido revestido por película - 12 mg - galantamina, bromidrato 15.38 mg - galantamine - genérico - duração do tratamento: longa duração