Rumänien - rumänska - ANMDM (Agentia Nationala a Medicamentului si a Dispozitivelor Medicale)

sanofi-aventis deutschland gmbh - germania - levofloxacinum - sol. perf. - 5mg/ml - chinolone antibacteriene fluorochinolone

Europeiska unionen - rumänska - EMA (European Medicines Agency)

novartis europharm limited  - indacaterol acetate, mometasone furoate - astm - medicamente pentru afecțiuni obstructive ale căilor respiratorii, - atectura breezhaler is indicated as a maintenance treatment of asthma in adults and adolescents 12 years of age and older not adequately controlled with inhaled corticosteroids and inhaled short acting beta2-agonists.

Europeiska unionen - rumänska - EMA (European Medicines Agency)

aimmune therapeutics ireland limited - defatted powder of arachis hypogaea l., semen (peanuts) - peanut hypersensitivity - allergens - palforzia is indicated for the treatment of patients aged 4 to 17 years with a confirmed diagnosis of peanut allergy. palforzia may be continued in patients 18 years of age and older. palforzia should be used in conjunction with a peanut-avoidant diet.

Europeiska unionen - rumänska - EMA (European Medicines Agency)

mylan ireland limited - fingolimod clorhidrat de - scleroză multiplă, scleroză multiplă recurent-remisivă - imunosupresoare - indicated as single disease modifying therapy in highly active relapsing remitting multiple sclerosis for the following groups of adult and paediatric patients aged 10 years and older:patients with highly active disease despite a full and adequate course of treatment with at least one disease modifying therapy (for exceptions and information about washout periods see sections 4. 4 și 5. 1)orpatients cu evoluție rapidă severă scleroză multiplă recurentă remisivă definită prin 2 sau mai multe recidive care produc invaliditate într-un an și cu 1 sau mai multe leziuni evidențiate cu gadoliniu la irm craniană sau o creștere semnificativă a încărcării leziunilor t2 comparativ cu o irm anterioară recentă.

Europeiska unionen - rumänska - EMA (European Medicines Agency)

mylan ireland limited - fingolimod clorhidrat de - scleroză multiplă, scleroză multiplă recurent-remisivă - imunosupresoare - indicated as single disease modifying therapy in highly active relapsing remitting multiple sclerosis for the following groups of adult and paediatric patients aged 10 years and older: patients with highly active disease despite a full and adequate course of treatment with at least one disease modifying therapy (for exceptions and information about washout periods see sections 4. 4 și 5. 1) or patients with rapidly evolving severe relapsing remitting multiple sclerosis defined by 2 or more disabling relapses in one year, and with 1 or more gadolinium enhancing lesions on brain mri or a significant increase in t2 lesion load as compared to a previous recent mri.

Europeiska unionen - rumänska - EMA (European Medicines Agency)

eigerbio europe limited - lonafarnib - progeria; laminopathies - alte medicamente pentru tractul digestiv și metabolism, - zokinvy is indicated for the treatment of patients 12 months of age and older with a genetically confirmed diagnosis of hutchinson-gilford progeria syndrome or a processing-deficient progeroid laminopathy associated with either a heterozygous lmna mutation with progerin-like protein accumulation or a homozygous or compound heterozygous zmpste24 mutation.

Europeiska unionen - rumänska - EMA (European Medicines Agency)

marinus pharmaceuticals emerald limited - ganaxolone - epileptic syndromes; spasms, infantile - alte antiepileptice - ztalmy is indicated for the adjunctive treatment of epileptic seizures associated with cyclin-dependent kinase-like 5 (cdkl5) deficiency disorder (cdd) in patients 2 to 17 years of age. ztalmy may be continued in patients 18 years of age and older.

Europeiska unionen - rumänska - EMA (European Medicines Agency)

jazz pharmaceuticals ireland limited - crisantaspase - leucemia limfoblastică limfoblastică a celulelor precursoare - agenți antineoplazici - enrylaze is indicated as a component of a multi-agent chemotherapeutic regimen for the treatment of acute lymphoblastic leukaemia (all) and lymphoblastic lymphoma (lbl) in adult and paediatric patients (1 month and older) who developed hypersensitivity or silent inactivation to e. coli-derived asparaginase.

Rumänien - rumänska - ANMDM (Agentia Nationala a Medicamentului si a Dispozitivelor Medicale)

madaus sa - spania - plante - pulb. eff. - 3500mg - laxative laxative de volum

Rumänien - rumänska - ANMDM (Agentia Nationala a Medicamentului si a Dispozitivelor Medicale)

dr. b. scheffler nachf. gmbh & co. kg - germania - acid ascorbicum - compr. eff. - 1000mg - acid ascorbic (vitamina c) (incl. combinatii) acid ascorbic (vitamina c)