Europese Unie -
Nederlands -
EMA (European Medicines Agency)
artesunate amivas
amivas ireland ltd - artesunate - malaria - antiprotozoaire - artesunate amivas is indicated for the initial treatment of severe malaria in adults and children. aandacht moet worden gegeven aan de officiële richtlijnen betreffende het juiste gebruik van antimalaria agenten.
Europese Unie -
Nederlands -
EMA (European Medicines Agency)
skytrofa (previously lonapegsomatropin ascendis pharma)
ascendis pharma endocrinology division a/s - lonapegsomatropin - growth and development - hypofyse en hypothalamische hormonen en analogen - growth failure in children and adolescents aged from 3 years up to 18 years due to insufficient endogenous growth hormone secretion (growth hormone deficiency [ghd]),.
Europese Unie -
Nederlands -
EMA (European Medicines Agency)
zenalpha
vetcare oy - medetomidine hydrochloride, vatinoxan hydrochloride - psycholeptica, hypnotica en kalmerende middelen - honden - to provide restraint, sedation and analgesia during conduct of non-invasive, non-painful or mildly painful procedures and examinations intended to last no more than 30 minutes.
Nederland -
Nederlands -
myHealthbox
roundup® dynamic
bayer ag - waterige oplossing - 500 g/l glyfosaat
Europese Unie -
Nederlands -
EMA (European Medicines Agency)
lutetium (177lu) chloride billev (previously illuzyce)
billev pharma aps - lutetium (177lu) chloride - radionuclide-beeldvorming - therapeutische radiofarmaca - lutetium (177lu) chloride billev is a radiopharmaceutical precursor, and it is not intended for direct use in patients. it is to be used only for the radiolabelling of carrier molecules that have been specifically developed and authorised for radiolabelling with lutetium (177lu) chloride.
Europese Unie -
Nederlands -
EMA (European Medicines Agency)
livtencity
takeda pharmaceuticals international ag ireland branch - maribavir - cytomegalovirus-infecties - antivirale middelen voor systemisch gebruik - 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). aandacht moet worden gegeven aan de officiële richtlijnen betreffende het juiste gebruik van antivirale middelen.
Nederland -
Nederlands -
CBG-MEB (College ter Beoordeling van Geneesmiddelen)
venfalex xr 150 mg, capsules met verlengde afgifte, hard
medochemie limited constantinopelstreet 1-10 3011 limassol (cyprus) - venlafaxinehydrochloride 169,7 mg/stuk samenstelling overeenkomend met ; venlafaxine 150 mg/stuk - capsule met verlengde afgifte, hard - chinolinegeel (e 104) ; dibutylsebacaat ; ethylcellulose (e 462) ; gelatine (e 441) ; hyprolose (e 463) ; hypromellose (e 464) ; maÏszetmeel ; natriumlaurilsulfaat (e 487) ; oliezuur ; patentblauw v (e131) ; saccharose ; siliciumdioxide (e 551) ; suikermaÏsbolletjes ; talk (e 553 b) ; titaandioxide (e 171) ; zonnegeel fcf (e 110), chinolinegeel (e 104) ; dibutylsebacaat ; ethylcellulose (e 462) ; gelatine (e 441) ; hyprolose (e 463) ; hypromellose (e 464) ; maÏszetmeel ; natriumlaurilsulfaat (e 487) ; oliezuur ; patentblauw v (e131) ; saccharose ; siliciumdioxide (e 551) ; sugar spheres ; talk (e 553 b) ; titaandioxide (e 171) ; zonnegeel fcf (e 110), - venlafaxine