Evropská unie - angličtina - EMA (European Medicines Agency)

sanofi b.v. - alglucosidase alfa - glycogen storage disease type ii - other alimentary tract and metabolism products, - myozyme is indicated for long-term enzyme-replacement therapy (ert) in patients with a confirmed diagnosis of pompe disease (acid-α-glucosidase deficiency).in patients with late-onset pompe disease the evidence of efficacy is limited.

Malta - angličtina - Medicines Authority

laboratoire aguettant 1 rue alexander fleming, 69007 lyon, france - norepinephrine - concentrate for solution for infusion - norepinephrine 2 mg/ml - cardiac therapy

Malta - angličtina - Medicines Authority

laboratoire aguettant 1 rue alexander fleming, 69007 lyon, france - noradrenaline acid, tartrate - concentrate for solution for infusion - noradrenaline acid tartrate 2 mg/ml - cardiac therapy

Spojené státy - angličtina - NLM (National Library of Medicine)

genzyme corporation - alglucosidase alfa (unii: dti67o9503) (alglucosidase alfa - unii:dti67o9503) - alglucosidase alfa 5 mg in 1 ml - lumizyme® is a hydrolytic lysosomal glycogen-specific enzyme indicated for patients with pompe disease (acid α-glucosidase [gaa] deficiency). none. risk summary data from postmarketing reports and published case reports with alglucosidase alfa use in pregnant women have not identified a lumizyme-associated risk of major birth defects, miscarriage, or adverse maternal or fetal outcomes. the continuation of treatment for pompe disease during pregnancy should be individualized to the pregnant woman. untreated pompe disease may result in worsening disease symptoms in pregnant women [see clinical considerations] . reproduction studies performed in mice and rabbits at doses resulting in exposures up to 0.4 or 0.5 times the human steady-state auc (area under the plasma concentration-time curve), respectively, during the period of organogenesis revealed no evidence of effects on embryo-fetal development. in mice there was an increase in pup mortality during lactation at maternal exposures 0.4 times the human steady-state auc [see data] . the background risk of major birth defects and miscarriage in the indicated population is unknown. all pregnancies have a background risk of birth defect, loss or other adverse outcomes. in the u.s. general population, the estimated background risk of major birth defects and miscarriage in clinically recognized pregnancies is 2% to 4% and 15% to 20%, respectively. pregnant women and women of reproductive potential should be encouraged to enroll in the pompe patient registry. the registry will monitor the effect of lumizyme on pregnant women and their offspring. for more information, visit www.registrynxt.com or call 1-800-745-4447, extension 15500. clinical considerations disease-associated maternal and/or embryo-fetal risk untreated pompe disease has been associated with worsening respiratory and musculoskeletal symptoms in some pregnant women. data animal data all reproductive studies included pretreatment with diphenhydramine to prevent or minimize hypersensitivity reactions. the effects of alglucosidase alfa were evaluated based on comparison to a control group treated with diphenhydramine alone. daily intravenous administration of alglucosidase alfa up to 40 mg/kg in mice and rabbits (0.4 and 0.5 times the human steady-state auc, respectively, at the recommended biweekly dose) during the period of organogenesis had no effects on embryo-fetal development. administration of 40 mg/kg intravenously every other day in mice (0.4 times the human steady-state auc at the recommended biweekly dose) during the period of organogenesis through lactation produced an increase in mortality of offspring during the lactation period. risk summary available published literature suggests the presence of alglucosidase alfa in human milk. there are no reports of adverse effects of alglucosidase alfa on the breastfed infant. there is no information on the effects of alglucosidase alfa on milk production. the developmental and health benefits of breastfeeding should be considered along with the mother's clinical need for lumizyme and any potential adverse effects on the breastfed child from lumizyme or from the underlying maternal condition. lactating women with pompe disease treated with lumizyme should be encouraged to enroll in the pompe disease registry [see use in specific populations (8.1)] . clinical considerations a lactating woman may consider interrupting breastfeeding, pumping and discarding breast milk during treatment and for 24 hours after lumizyme administration in order to minimize drug exposure to a breastfed infant. the safety and effectiveness of alglucosidase alfa have been established in pediatric patients with pompe disease [see adverse reactions (6.2)] . the safety and effectiveness of alglucosidase alfa were assessed in 57 treatment-naive infantile-onset pompe disease patients, aged 0.2 month to 3.5 years at first infusion, in three separate clinical trials [see clinical studies (14.1)] . the safety and effectiveness of alglucosidase alfa were assessed in pediatric patients with late (non-infantile) onset pompe disease in a randomized, double-blind, placebo-controlled study in 90 patients, including 2 patients 16 years of age or less [see clinical studies (14.2)] . anaphylaxis, hypersensitivity reactions, and acute cardiorespiratory failure have occurred in pediatric patients [see boxed warning, warnings and precautions (5.1, 5.3)] . additionally, cardiac arrhythmia and sudden cardiac death have occurred in pediatric patients during general anesthesia for central venous catheter placement [see warnings and precautions (5.4)] . the randomized, double-blind, placebo-controlled study of alglucosidase alfa did not include sufficient numbers (n=4) of patients aged 65 years and over to determine whether they respond differently from younger patients [see clinical studies (14.1)] .

Austrálie - angličtina - Department of Health (Therapeutic Goods Administration)

phebra pty ltd - glucose, quantity: 500 mg/ml - injection, intravenous infusion - excipient ingredients: hydrochloric acid; water for injections; sodium bicarbonate - glucose 50% intravenous infusion is strongly hypertonic and may be used to reduce increased cerebrospinal pressure and/or oedema due to delirium tremens or acute alcoholic intoxication. it may also be used to treat severe hypoglycaemia due to an excess of insulin and to provide concentrated calories in total parenteral nutrition regimes.

Keňa - angličtina - Pharmacy and Poisons Board

questa care inc. c/o surgilinks ltd 4251 s. higuera st. suite 800 san luis obispo ca - glucose iv infusion bp - infusion - glucose iv infusion bp 5%w/v - other i.v. solution additives

Malta - angličtina - Medicines Authority

fresenius medical care deutschland gmbh d-61346 bad homburg, germany - calcium, glucose - solution for peritoneal dialysis - calcium 1.25 mmol/l glucose 1.5 % (w/v) - blood substitutes and perfusion solutions

Malta - angličtina - Medicines Authority

fresenius medical care deutschland gmbh d-61346 bad homburg, germany - calcium, glucose - solution for peritoneal dialysis - calcium 1.25 mmol/l glucose 2.3 % (w/v) - blood substitutes and perfusion solutions

Malta - angličtina - Medicines Authority

fresenius medical care deutschland gmbh d-61346 bad homburg, germany - calcium, glucose - solution for peritoneal dialysis - calcium 1.25 mmol/l glucose 4.25 % (w/v) - blood substitutes and perfusion solutions

Malta - angličtina - Medicines Authority

fresenius medical care deutschland gmbh d-61346 bad homburg, germany - calcium, glucose - solution for peritoneal dialysis - calcium 1.75 mmol/l glucose 1.5 % (w/v) - blood substitutes and perfusion solutions