Sugammadex Piramal Uniunea Europeană - română - EMA (European Medicines Agency)

sugammadex piramal

piramal critical care b.v. - sugammadex sodium - blocaj blocant - sugammadex - reversal of neuromuscular blockade induced by rocuronium or vecuronium in adults.

Sugammadex Mylan Uniunea Europeană - română - EMA (European Medicines Agency)

sugammadex mylan

mylan ireland limited - sugammadex sodium - blocaj blocant - toate celelalte produse terapeutice - reversal of neuromuscular blockade induced by   rocuronium or vecuronium in adults. for the paediatric population: sugammadex is only recommended for routine reversal of rocuronium induced blockade in children and adolescents aged 2 to 17 years.

Sugammadex Fresenius Kabi Uniunea Europeană - română - EMA (European Medicines Agency)

sugammadex fresenius kabi

fresenius kabi deutschland gmbh - sugammadex sodium - blocaj blocant - toate celelalte produse terapeutice - reversal of neuromuscular blockade induced by rocuronium or vecuronium in adults. for the paediatric population: sugammadex is only recommended for routine reversal of rocuronium induced blockade in children and adolescents aged 2 to 17 years.

Sugammadex Amomed Uniunea Europeană - română - EMA (European Medicines Agency)

sugammadex amomed

aop orphan pharmaceuticals gmbh - sugammadex sodium - blocaj blocant - toate celelalte produse terapeutice - inversarea blocadei neuromusculare indusă de rocuroniu sau vecuroniu. for the paediatric population: sugammadex is only recommended for routine reversal of rocuronium induced blockade in children and adolescents aged 2 to 17 years.

Sugammadex Adroiq Uniunea Europeană - română - EMA (European Medicines Agency)

sugammadex adroiq

extrovis eu ltd. - sugammadex sodium - blocaj blocant - toate celelalte produse terapeutice - reversal of neuromuscular blockade induced by rocuronium or vecuronium in adults. for the paediatric population: sugammadex is only recommended for routine reversal of rocuronium induced blockade in children and adolescents aged 2 to 17 years.

ACID IBANDRONIC ALVOGEN 6 mg România - română - ANMDM (Agentia Nationala a Medicamentului si a Dispozitivelor Medicale)

acid ibandronic alvogen 6 mg

synthon bv - olanda - acid ibandronicum - conc. pt. sol. perf. - 6 mg - med. ce influenteaza in structura osoasa si mineralizare bifosfonati

Ibandronic acid Accord Uniunea Europeană - română - EMA (European Medicines Agency)

ibandronic acid accord

accord healthcare s.l.u. - acidul ibandronic - wounds and injuries; breast diseases; neoplastic processes; calcium metabolism disorders; water-electrolyte imbalance - medicamente pentru tratamentul bolilor osoase - acidul ibandronic este indicat la adulți forprevention evenimentelor osoase (fracturi patologice, complicații osoase care necesită radioterapie sau intervenții chirurgicale) la pacienții cu cancer de sân și metastaze osoase. tratamentul hipercalcemiei induse de tumori cu sau fără metastaze. tratamentul osteoporozei la femeile în postmenopauză cu risc crescut de fractură (vezi secțiunea 5. reducerea riscului de fracturi vertebrale a fost demonstrată eficacitatea asupra fracturilor de col femural nu a fost stabilită.