thyrogen poudre versare soluzione iniettabile
sanofi-aventis (suisse) sa - thyrotropinum alfa - poudre versare soluzione iniettabile - praeparatio cryodesiccata: thyrotropinum alfa 0.9 mg, mannitolum, natrii dihydrogenophosphas monohydricus, dinatrii phosphas heptahydricus, natrii chloridum, pro vitro corresp. natrium 1.19 mg. - il cancro della tiroide - biotechnologika
thyrogen
sanofi b.v. - tireotropina alfa - neoplasie della tiroide - dell'ipofisi anteriore del lobo ormoni e farmaceutici, l'ipofisi e l'ipotalamo gli ormoni e farmaceutici - thyrogen is indicated for use with serum thyroglobulin (tg) testing with or without radioiodine imaging for the detection of thyroid remnants and well-differentiated thyroid cancer in post thyroidectomy patients maintained on hormone suppression therapy (thst). low risk patients with well-differentiated thyroid carcinoma who have undetectable serum tg levels on thst and no rh (recombinant human) tsh-stimulated increase of tg levels may be followed-up by assaying rh tsh-stimulated tg levels. thyrogen is indicated for pre-therapeutic stimulation in combination with a range of 30 mci (1. 1 gbq) to 100 mci (3. 7 gbq) radioiodine for ablation of thyroid tissue remnants in patients who have undergone a near-total or total thyroidectomy for well-differentiated thyroid cancer and who do not have evidence of distant metastatic thyroid cancer (see section 4.
oroxine
aspen pharma trading limited - levotiroxina sodica - levotiroxina sodica
sandostatin 0,05 mg/ml soluzione iniettabile
novartis pharma schweiz ag - octreotidum - soluzione iniettabile - octreotidum 0.05 mg ut octreotidi acetas, mannitolum, acidum lacticum, natrii hydrogenocarbonas q.s. ad ph, aqua ad iniectabile ad solutionem pro 1 ml. - la somatostatina-analogon - synthetika
sandostatin 0,1 mg/ml soluzione iniettabile
novartis pharma schweiz ag - octreotidum - soluzione iniettabile - octreotidum 0.1 mg ut octreotidi acetas, mannitolum, acidum lacticum, natrii hydrogenocarbonas q.s. ad ph, aqua ad iniectabile ad solutionem pro 1 ml. - la somatostatina-analogon - synthetika
sandostatin 0,2 mg/ml soluzione iniettabile
novartis pharma schweiz ag - octreotidum - soluzione iniettabile - octreotidum 0.2 mg ut octreotidi acetas, mannitolum, phenolum, acidum lacticum, natrii hydrogenocarbonas q.s. ad ph, aqua ad iniectabile ad solutionem pro 1 ml. - la somatostatina-analogon - biotechnologika
sandostatin 0,5 mg/ml soluzione iniettabile
novartis pharma schweiz ag - octreotidum - soluzione iniettabile - octreotidum 0.5 mg ut octreotidi acetas, mannitolum, acidum lacticum, natrii hydrogenocarbonas q.s. ad ph, aqua ad iniectabile ad solutionem pro 1 ml. - la somatostatina-analogon - synthetika
sandostatin lar 10 mg fertigspritzen injektionspräparat
novartis pharma schweiz ag - octreotidum - injektionspräparat - praeparatio sicca: octreotidum 10 mg ut octreotidi acetas 11.2 mg, poly(lactidum-co-glycolidum), mannitolum, pro vitro. solvens: carmellosum natricum corresp. natrium 1.512 mg, mannitolum, poloxamerum 188, aqua ad iniectabile q.s. ad solutionem pro 2.0 ml. - la somatostatina-analogon - synthetika
sandostatin lar 20 mg fertigspritzen injektionspräparat
novartis pharma schweiz ag - octreotidum - injektionspräparat - praeparatio sicca: octreotidum 20 mg ut octreotidi acetas 22.4 mg, poly(lactidum-co-glycolidum), mannitolum, pro vitro. solvens: carmellosum natricum corresp. natrium 1.512 mg, mannitolum, poloxamerum 188, aqua ad iniectabile q.s. ad solutionem pro 2.0 ml. - la somatostatina-analogon - synthetika
sandostatin lar 30 mg fertigspritzen injektionspräparat
novartis pharma schweiz ag - octreotidum - injektionspräparat - praeparatio sicca: octreotidum 30 mg ut octreotidi acetas 33.6 mg, poly(lactidum-co-glycolidum), mannitolum, pro vitro. solvens: carmellosum natricum corresp. natrium 1.512 mg, mannitolum, poloxamerum 188, aqua ad iniectabile q.s. ad solutionem pro 2.0 ml. - la somatostatina-analogon - synthetika