Brimica Genuair Den europeiske union - dansk - EMA (European Medicines Agency)

brimica genuair

covis pharma europe b.v. - formoterol fumarate dihydrate, aclidinium bromide - pulmonal sygdom, kronisk obstruktiv - medicin for obstruktiv sygdomme, - brimica genuair er indiceret som vedligeholdelsesbronkodilatorbehandling for luftstrømningsobstruktion og lindring af symptomer hos voksne patienter med kronisk obstruktiv lungesygdom (copd).

Duaklir Genuair Den europeiske union - dansk - EMA (European Medicines Agency)

duaklir genuair

covis pharma europe b.v. - aclidinium bromid, formoterol fumarate dihydrat - pulmonal sygdom, kronisk obstruktiv - medicin for obstruktiv sygdomme, - duaklir genuair er indiceret som vedligeholdelsesbronkodilatorbehandling for at lindre symptomer hos voksne patienter med kronisk obstruktiv lungesygdom (copd).

Iclusig Den europeiske union - norsk - EMA (European Medicines Agency)

iclusig

incyte biosciences distribution b.v. - ponatinib - leukemia, myeloid; leukemia, lymphoid - antineoplastic agents, protein kinase inhibitors - iclusig is indicated in adult patients withchronic phase, accelerated phase, or blast phase chronic myeloid leukaemia (cml) who are resistant to dasatinib or nilotinib; who are intolerant to dasatinib or nilotinib and for whom subsequent treatment with imatinib is not clinically appropriate; or who have the t315i mutationphiladelphia chromosome positive acute lymphoblastic leukaemia (ph+ all) who are resistant to dasatinib; who are intolerant to dasatinib and for whom subsequent treatment with imatinib is not clinically appropriate; or who have the t315i mutation. se avsnitt 4. 2 assessment of cardiovascular status prior to start of therapy and 4. 4 situations where an alternative treatment may be considered.

Iclusig Den europeiske union - dansk - EMA (European Medicines Agency)

iclusig

incyte biosciences distribution b.v. - ponatinib - leukemia, myeloid; leukemia, lymphoid - antineoplastic agents, protein kinase inhibitors - iclusig is indicated in adult patients withchronic phase, accelerated phase, or blast phase chronic myeloid leukaemia (cml) who are resistant to dasatinib or nilotinib; who are intolerant to dasatinib or nilotinib and for whom subsequent treatment with imatinib is not clinically appropriate; or who have the t315i mutationphiladelphia chromosome positive acute lymphoblastic leukaemia (ph+ all) who are resistant to dasatinib; who are intolerant to dasatinib and for whom subsequent treatment with imatinib is not clinically appropriate; or who have the t315i mutation. se afsnit 4. 2 assessment of cardiovascular status prior to start of therapy and 4. 4 situations where an alternative treatment may be considered.

Buprefarm 10 mikrog/ time Norge - norsk - Statens legemiddelverk

buprefarm 10 mikrog/ time

orifarm generics a/s - buprenorfin - depotplaster - 10 mikrog/ time

Buprefarm 5 mikrog/ time Norge - norsk - Statens legemiddelverk

buprefarm 5 mikrog/ time

orifarm generics a/s - buprenorfin - depotplaster - 5 mikrog/ time

Buprefarm 20 mikrog/ time Norge - norsk - Statens legemiddelverk

buprefarm 20 mikrog/ time

orifarm generics a/s - buprenorfin - depotplaster - 20 mikrog/ time

Benylan 1,4 mg/ml oral opløsning Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

benylan 1,4 mg/ml oral opløsning

mcneil denmark aps - diphenhydraminhydrochlorid - oral opløsning - 1,4 mg/ml

Benylan 2,8 mg/ml oral opløsning Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

benylan 2,8 mg/ml oral opløsning

mcneil denmark aps - diphenhydraminhydrochlorid - oral opløsning - 2,8 mg/ml