Bretaris Genuair (▼) 322 µg/1 doza prašak za inhaliranje Bosna in Hercegovina - hrvaščina - Agencija za lijekove i medicinska sredstva Bosne i Hercegovine (Агенција за лијекове и медицинска средства Босне и Херцеговине)

bretaris genuair (▼) 322 µg/1 doza prašak za inhaliranje

berlin chemie / menarini bh d.o.o. sarajevo - aklidinijum - prašak za inhaliranje - 322 µg/1 doza - 1 doza praška za inhaliranje sadrži: 322 mcg aklidinijuma (što odgovara 375 mcg aklidinujum bromida)

Bretaris Genuair (▼) 322 µg/1 doza prašak za inhaliranje Bosna in Hercegovina - hrvaščina - Agencija za lijekove i medicinska sredstva Bosne i Hercegovine (Агенција за лијекове и медицинска средства Босне и Херцеговине)

bretaris genuair (▼) 322 µg/1 doza prašak za inhaliranje

berlin chemie / menarini bh d.o.o. sarajevo - aklidinijum - prašak za inhaliranje - 322 µg/1 doza - 1 doza praška za inhaliranje sadrži: 322 mcg aklidinijuma (što odgovara 375 mcg aklidinujum bromida)

Bretaris Genuair (▼) 322 µg/1 doza prašak za inhaliranje Bosna in Hercegovina - hrvaščina - Agencija za lijekove i medicinska sredstva Bosne i Hercegovine (Агенција за лијекове и медицинска средства Босне и Херцеговине)

bretaris genuair (▼) 322 µg/1 doza prašak za inhaliranje

berlin chemie / menarini bh d.o.o. sarajevo - aklidinijum - prašak za inhaliranje - 322 µg/1 doza - 1 doza praška za inhaliranje sadrži: 322 mcg aklidinijuma (što odgovara 375 mcg aklidinujum bromida)

Leqvio Evropska unija - hrvaščina - EMA (European Medicines Agency)

leqvio

novartis europharm limited - inclisiran - hypercholesterolemia; dyslipidemias - sredstva za modifikaciju lipida - leqvio is indicated in adults with primary hypercholesterolaemia (heterozygous familial and non-familial) or mixed dyslipidaemia, as an adjunct to diet:in combination with a statin or statin with other lipid-lowering therapies in patients unable to reach ldl-c goals with the maximum tolerated dose of a statin, oralone or in combination with other lipid-lowering therapies in patients who are statin-intolerant, or for whom a statin is contraindicated.

Ronapreve Evropska unija - hrvaščina - EMA (European Medicines Agency)

ronapreve

roche registration gmbh  - casirivimab, imdevimab - covid-19 virus infection - imuni serumi i homologna, - ronapreve is indicated for:treatment of covid-19 in adults and adolescents aged 12 years and older weighing at least 40 kg who do not require supplemental oxygen and who are at increased risk of progressing to severe covid-19 (see section 4. prevention of covid-19 in adults and adolescents aged 12 years and older weighing at least 40 kg (see section 4. the use of ronapreve should take into account information on the activity of ronapreve against viral variants of concern. pogledajte odjeljke 4. 4 i 5.