Bupretex 8 mg resoribletter, sublinguale Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

bupretex 8 mg resoribletter, sublinguale

2care4 aps - buprenorphinhydrochlorid - resoribletter, sublinguale - 8 mg

Libroxar 2+0,5 mg resoribletter, sublinguale Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

libroxar 2+0,5 mg resoribletter, sublinguale

laboratoires smb s.a. - buprenorphinhydrochlorid, naloxonhydrochloriddihydrat - resoribletter, sublinguale - 2+0,5 mg

Atropine "Accord" 0,1 mg/ml injektionsvæske, opløsning i fyldt injektionssprøjte Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

atropine "accord" 0,1 mg/ml injektionsvæske, opløsning i fyldt injektionssprøjte

accord healthcare b.v. - atropinsulfat - injektionsvæske, opløsning i fyldt injektionssprøjte - 0,1 mg/ml

Plerixafor Accord Den Europæiske Union - dansk - EMA (European Medicines Agency)

plerixafor accord

accord healthcare s.l.u. - plerixafor - multiple myeloma; hematopoietic stem cell transplantation - immunostimulants, - adult patientsplerixafor accord is indicated in combination with granulocyte-colony stimulating factor (g-csf) to enhance mobilisation of haematopoietic stem cells to the peripheral blood for collection and subsequent autologous transplantation in adult patients with lymphoma or multiple myeloma whose cells mobilise poorly (see section 4. paediatric patients (1 to less than 18 years)plerixafor accord is indicated in combination with g-csf to enhance mobilisation of haematopoietic stem cells to the peripheral blood for collection and subsequent autologous transplantation in children with lymphoma or solid malignant tumours, either:- pre-emptively, when circulating stem cell count on the predicted day of collection after adequate mobilization with g-csf (with or without chemotherapy) is expected to be insufficient with regards to desired hematopoietic stem cells yield, or- who previously failed to collect sufficient haematopoietic stem cells (see section 4.

Plerixafor "Seacross" 20 mg/ml injektionsvæske, opløsning Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

plerixafor "seacross" 20 mg/ml injektionsvæske, opløsning

seacross pharma (europe) limited - plerixafor - injektionsvæske, opløsning - 20 mg/ml

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

bexsero

gsk vaccines s.r.l. - ydre membran vesikler fra neisseria meningitidis gruppe b (stamme nz 98/254), rekombinant neisseria meningitidis gruppe b fhbp fusion protein, rekombinant neisseria meningitidis gruppe b nada protein, rekombinant neisseria meningitidis gruppe b nhba fusion protein - meningitis, meningokok - meningokokvacciner - aktiv immunisering mod invasiv sygdom forårsaget af neisseria meningitidis serogruppe b-stammer.