Kýpur - gríska - Φαρμακευτικών Υπηρεσιών του Υπουργείου Υγείας

delorbis pharmaceuticals ltd (0000009620) 17 athinon street, ergates industrial area, lefkosia, 2081, 28629 - rivastigmine hydrogen tartrate - capsule,hard - 3mg - rivastigmine hydrogen tartrate (8000003317) 4.8mg - rivastigmine

Kýpur - gríska - Φαρμακευτικών Υπηρεσιών του Υπουργείου Υγείας

delorbis pharmaceuticals ltd (0000009620) 17 athinon street, ergates industrial area, lefkosia, 2081, 28629 - galantamine hydrobromide - film coated tablets - 8mg - galantamine hydrobromide (0001953044) 10.253mg - galantamine

Kýpur - gríska - Φαρμακευτικών Υπηρεσιών του Υπουργείου Υγείας

delorbis pharmaceuticals ltd (0000009620) 17 athinon street, ergates industrial area, lefkosia, 2081, 28629 - galantamine hydrobromide - film coated tablets - 12mg - galantamine hydrobromide (0001953044) 15.379mg - galantamine

Kýpur - gríska - Φαρμακευτικών Υπηρεσιών του Υπουργείου Υγείας

delorbis pharmaceuticals ltd (0000009620) 17 athinon street, ergates industrial area, lefkosia, 2081, 28629 - galantamine hydrobromide - film coated tablets - 4mg - galantamine hydrobromide (0001953044) 5.126mg - galantamine

Evrópusambandið - gríska - EMA (European Medicines Agency)

alexion europe sas - ravulizumab - Αιμοσφαιρινουρία, παροξυσμική - Επιλεκτικά ανοσοκατασταλτικά - paroxysmal nocturnal haemoglobinuria (pnh)ultomiris is indicated in the treatment of adult and paediatric patients with a body weight of 10 kg or above with pnh:- in patients with haemolysis with clinical symptom(s) indicative of high disease activity. - in patients who are clinically stable after having been treated with eculizumab for at least the past 6 months (see section 5. atypical haemolytic uremic syndrome (ahus)ultomiris is indicated in the treatment of patients with a body weight of 10 kg or above with ahus who are complement inhibitor treatment-naïve or have received eculizumab for at least 3 months and have evidence of response to eculizumab (see section 5. generalized myasthenia gravis (gmg)ultomiris is indicated as an add-on to standard therapy for the treatment of adult patients with gmg who are anti-acetylcholine receptor (achr) antibody-positive. neuromyelitis optica spectrum disorder (nmosd)ultomiris is indicated in the treatment of adult patients with nmosd who are anti-aquaporin 4 (aqp4) antibody-positive (see section 5. ultomiris is indicated in the treatment of adult patients with paroxysmal nocturnal haemoglobinuria (pnh):- in patients with haemolysis with clinical symptom(s) indicative of high disease activity. - in patients who are clinically stable after having been treated with eculizumab for at least the past 6 months. ultomiris is indicated in the treatment of adult patients with atypical haemolytic uremic syndrome (ahus) who are complement inhibitor treatment-naïve or have received eculizumab for at least 3 months and have evidence of response to eculizumab.

Kýpur - gríska - Φαρμακευτικών Υπηρεσιών του Υπουργείου Υγείας

generics pharma hellas ltd (0000003679) 63, ag. dimitriou str., alimos, athens, 17456 - pantoprazole sodium sesquihydrate - gastro resistant tablet - 40mg - pantoprazole sodium sesquihydrate (8000001653) 45.1mg - pantoprazole

Kýpur - gríska - Φαρμακευτικών Υπηρεσιών του Υπουργείου Υγείας

delorbis pharmaceuticals ltd (0000009620) 17 athinon street, ergates industrial area, lefkosia, 2081, 28629 - pantoprazole sodium sesquihydrate - gastro resistant tablet - 20mg - pantoprazole sodium sesquihydrate (8000001653) 22,575mg - pantoprazole

Kýpur - gríska - Φαρμακευτικών Υπηρεσιών του Υπουργείου Υγείας

delorbis pharmaceuticals ltd (0000009620) 17 athinon street, ergates industrial area, lefkosia, 2081, 28629 - pantoprazole sodium sesquihydrate - gastro resistant tablet - 40mg - pantoprazole sodium sesquihydrate (8000001653) 45,15mg - pantoprazole

Kýpur - gríska - Φαρμακευτικών Υπηρεσιών του Υπουργείου Υγείας

delorbis pharmaceuticals ltd (0000009620) 17 athinon street, ergates industrial area, lefkosia, 2081, 28629 - pantoprazole sodium sesquihydrate - gastro resistant tablet - 20mg - pantoprazole sodium sesquihydrate (8000001653) 22,575mg - pantoprazole

Evrópusambandið - gríska - EMA (European Medicines Agency)

argenx - efgartigimod alfa - myasthenia gravis - Ανοσοκατασταλτικά - vyvgart is indicated as an add on to standard therapy for the treatment of adult patients with generalised myasthenia gravis (gmg) who are anti acetylcholine receptor (achr) antibody positive.