Tantum Verde z okusom mentola 3 mg pastile Slovenia - Slovenian - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

tantum verde z okusom mentola 3 mg pastile

angelini pharma Ősterreich gmbh - benzidamin - pastila - benzidamin 2,68 mg / 1 pastila - benzidamin

Omacor 1000 mg mehke kapsule Slovenia - Slovenian - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

omacor 1000 mg mehke kapsule

pronova biopharma - omega-3-kislinski etilestri 90 - kapsula, mehka - omega-3-kislinski etilestri 90 1000 mg / 1 kapsula - omega-3-trigliceridi z drugimi estri in kislinami

Omacor 1000 mg mehke kapsule Slovenia - Slovenian - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

omacor 1000 mg mehke kapsule

pronova biopharma - omega-3-kislinski etilestri 90 - kapsula, mehka - omega-3-kislinski etilestri 90 1000 mg / 1 kapsula - omega-3-trigliceridi z drugimi estri in kislinami

Impulsor European Union - Slovenian - EMA (European Medicines Agency)

impulsor

pierre fabre medicament - milnacipran - fibromialgija

Braftovi European Union - Slovenian - EMA (European Medicines Agency)

braftovi

pierre fabre medicament - encorafenib - melanoma; colorectal neoplasms - antineoplastična sredstva - encorafenib is indicated:in combination with binimetinib is indicated for the treatment of adult patients with unresectable or metastatic melanoma with a braf v600 mutationin combination with cetuximab, for the treatment of adult patients with metastatic colorectal cancer (crc) with a braf v600e mutation, who have received prior systemic therapy.

Mektovi European Union - Slovenian - EMA (European Medicines Agency)

mektovi

pierre fabre medicament - binimetinib - melanoma - antineoplastična sredstva - binimetinib v kombinaciji z encorafenib je indiciran za zdravljenje odraslih bolnikov z unresectable ali metastatskega melanoma z braf v600 mutacija.

Busilvex European Union - Slovenian - EMA (European Medicines Agency)

busilvex

pierre fabre medicament - busulfan - hematopoetična presaditev izvornih celic - antineoplastična sredstva - busilvex sledi ciklofosfamid (bucy2) je navedena kot kondicioniranje zdravljenje pred konvencionalne krvotvornih matičnih celic presaditev (hpct) pri odraslih bolnikih, ko kombinacija se šteje na voljo možnost. busilvex naslednje fludarabine (fb) je označena kot naprava za zdravljenje pred haematopoietic progenitor cell presaditev (hpct) pri odraslih bolniki, ki so kandidati za zmanjšane intenzivnosti naprava (ric) režim. busilvex sledi ciklofosfamid (bucy4) ali melphalan (bumel) je označena kot naprava za zdravljenje pred konvencionalnimi haematopoietic progenitor cell presaditev v pediatričnih bolnikih.

Nerlynx European Union - Slovenian - EMA (European Medicines Agency)

nerlynx

pierre fabre medicament - neratinib - neoplazme dojke - antineoplastična sredstva - nerlynx je označen za podaljšano adjuvant zdravljenje odraslih bolnikov z zgodnji fazi hormon receptor her2 pozitiven-overexpressed/dopolniti rak dojke, ki so manj kot eno leto od zaključka pred adjuvant trastuzumab, ki temelji terapija.

Ebvallo European Union - Slovenian - EMA (European Medicines Agency)

ebvallo

pierre fabre medicament - tabelecleucel - lymphoproliferative disorders - ebvallo is indicated as monotherapy for treatment of adult and paediatric patients 2 years of age and older with relapsed or refractory epstein-barr virus positive post-transplant lymphoproliferative disease (ebv+ ptld) who have received at least one prior therapy. for solid organ transplant patients, prior therapy includes chemotherapy unless chemotherapy is inappropriate.

Hemangiol European Union - Slovenian - EMA (European Medicines Agency)

hemangiol

pierre fabre medicament - propranolol hidroklorid - hemangioma - beta blokatorji - hemangiol is indicated in the treatment of proliferating infantile haemangioma requiring systemic therapy: , life- or function-threatening haemangioma,, ulcerated haemangioma with pain and/or lack of response to simple wound care measures,, haemangioma with a risk of permanent scars or disfigurement. , it is to be initiated in infants aged 5 weeks to 5 months.