Australia - engelsk - Department of Health (Therapeutic Goods Administration)

sanofi-aventis australia pty ltd - furosemide, quantity: 40 mg - tablet, uncoated - excipient ingredients: colloidal anhydrous silica; sunset yellow fcf; purified talc; quinoline yellow aluminium lake; lactose monohydrate; maize starch; magnesium stearate - oedema: lasix is indicated in adults, infants and children for the treatment of oedema associated with congestive heart failure, cirrhosis of the liver and renal disease, including the nephrotic syndrome. lasix is particularly useful when an agent with greater diuretic potential than that of those commonly employed is desired. parenteral therapy should be reserved for patients unable to take oral medication or for patients in emergency clinical situations. lasix injection is also indicated as adjunctive therapy in acute pulmonary oedema and cerebral oedema where intense and rapid onset of diuresis is desired. if gastrointestinal absorption is impaired or oral medication is not practical for any reason, lasix is indicated by the intravenous route. parenteral use should be replaced with oral lasix as soon as practical. hypertension. oral lasix may be used in adults for the treatment of hypertension alone or in combination with other antihypertensive agents. hypertensive patients who cannot be adequately control

Australia - engelsk - Department of Health (Therapeutic Goods Administration)

sanofi-aventis australia pty ltd - furosemide, quantity: 10 mg/ml - oral liquid, solution - excipient ingredients: glycerol; purified water; sodium hydroxide; sorbitol solution (70 per cent) (non-crystallising); methyl hydroxybenzoate; ethanol; propyl hydroxybenzoate; sunset yellow fcf; quinoline yellow; flavour - oedema: lasix is indicated in adults, infants and children for the treatment of oedema associated with congestive heart failure, cirrhosis of the liver and renal disease, including the nephrotic syndrome. lasix is particularly useful when an agent with greater diuretic potential than that of those commonly employed is desired. parenteral therapy should be reserved for patients unable to take oral medication or for patients in emergency clinical situations. lasix injection is also indicated as adjunctive therapy in acute pulmonary oedema and cerebral oedema where intense and rapid onset of diuresis is desired. if gastrointestinal absorption is impaired or oral medication is not practical for any reason, lasix is indicated by the intravenous route. parenteral use should be replaced with oral lasix as soon as practical.hypertension. oral lasix may be used in adults for the treatment of hypertension alone or in combination with other antihypertensive agents. hypertensive patients who cannot be adequately controlled with thiazides will probably also not be adequately controlled with lasix alone.

Australia - engelsk - Department of Health (Therapeutic Goods Administration)

sanofi-aventis australia pty ltd - furosemide, quantity: 20 mg - tablet, uncoated - excipient ingredients: colloidal anhydrous silica; lactose monohydrate; purified talc; maize starch; magnesium stearate - oedema: lasix is indicated in adults, infants and children for the treatment of oedema associated with congestive heart failure, cirrhosis of the liver and renal disease, including the nephrotic syndrome. lasix is particularly useful when an agent with greater diuretic potential than that of those commonly employed is desired. parenteral therapy should be reserved for patients unable to take oral medication or for patients in emergency clinical situations. lasix injection is also indicated as adjunctive therapy in acute pulmonary oedema and cerebral oedema where intense and rapid onset of diuresis is desired. if gastrointestinal absorption is impaired or oral medication is not practical for any reason, lasix is indicated by the intravenous route. parenteral use should be replaced with oral lasix as soon as practical. hypertension. oral lasix may be used in adults for the treatment of hypertension alone or in combination with other antihypertensive agents. hypertensive patients who cannot be adequately control

Australia - engelsk - Department of Health (Therapeutic Goods Administration)

sanofi-aventis australia pty ltd - furosemide sodium, quantity: 10.664 mg/ml (equivalent: furosemide, qty 10 mg/ml) - injection, solution - excipient ingredients: sodium hydroxide; sodium chloride; water for injections - oedema: lasix is indicated in adults, infants and children for the treatment of oedema associated with congestive heart failure, cirrhosis of the liver and renal disease including nephrotic syndrome. lasix is particularly useful when an agent with greater diuretic potential than that of those commonly employed is desired. parenteral therapy should be reserved for patients unable to take oral medication, or for patients in emergency clinical situations. lasix injection is also indicated as adjunctive therapy in acute pulmonary and cerebral oedema where intense and rapid onset of diuresis is desired. if gastrointestinal absorption is impaired or oral medication is not practical for any reason, lasix is indicated by the intravenous route. parenteral use should be replaced with oral lasix as soon as practical.

Den europeiske union - bulgarsk - EMA (European Medicines Agency)

l. molteni & c. dei fratelli alitti società di esercizio s.p.a. - Бупренорфина хидрохлорид - Нарушения, свързани с опиоиди - Други лекарства в нервната система - sixmo е показано за заместителна терапия при опиоидной зависимост при клинично стабилни пациенти, възрастни, които се нуждаят от не повече от 8 мг/ден сублингвално бупренорфина, в рамките на медицинска, социална и психологическа помощ.

Den europeiske union - dansk - EMA (European Medicines Agency)

l. molteni & c. dei fratelli alitti società di esercizio s.p.a. - buprenorphin hydrochlorid - opioid-relaterede lidelser - andre narkotika stoffer - sixmo er angivet til substitutionsbehandling for opioidafhængighed i klinisk stabile voksne patienter, der kræver mere end 8 mg/dag af sublingual buprenorphin, inden for en ramme af medicinsk, social og psykologisk behandling.

Den europeiske union - litauisk - EMA (European Medicines Agency)

l. molteni & c. dei fratelli alitti società di esercizio s.p.a. - buprenorfino hidrochloridas - opioidų sutrikimai - kiti nervų sistemos vaistai - sixmo yra nurodyta pakaitinio gydymo nuo opioidų priklausomybės kliniškai stabilios suaugusiems pacientams, kuriems reikia ne daugiau kaip 8 mg/dieną sublingual buprenorfino, pagal programą, medicinos, socialinio ir psichologinio gydymo.

Den europeiske union - tsjekkisk - EMA (European Medicines Agency)

l. molteni & c. dei fratelli alitti società di esercizio s.p.a. - buprenorfin hydrochlorid - poruchy související s opiáty - další léky na nervový systém - sixmo je indikován pro substituční léčbu závislosti na opiátech v klinicky stabilních dospělých pacientů, kteří vyžadují ne více než 8 mg/den sublingvální buprenorfin, v rámci lékařské, sociální a psychologické péče.

Den europeiske union - slovensk - EMA (European Medicines Agency)

l. molteni & c. dei fratelli alitti società di esercizio s.p.a. - buprenorfin hidroklorid - opioidne motnje - druga zdravila na živčnem sistemu - sixmo je primerna za nadomestno zdravljenje odvisnosti od opioidov v klinično stabilno odraslih bolnikih, ki ne zahtevajo več kot 8 mg/dan sublingual buprenorfin, v okviru medicinske, socialne in psihološke obravnave.

Den europeiske union - maltesisk - EMA (European Medicines Agency)

l. molteni & c. dei fratelli alitti società di esercizio s.p.a. - buprenorphine hydrochloride - disturbi relatati ma 'opjojdi - drogi oħra tas-sistema nervuża - sixmo huwa indikat għat-trattament ta 'sostituzzjoni għad-dipendenza opjojd klinikament stabbli pazjenti adulti li jeħtieġu l-ebda aktar minn 8 mg/jum għal taħt l-ilsien ta' buprenorphine, f'qafas mediku, soċjali u psikoloġiku trattament.