أيرلندا - الإنجليزية - HPRA (Health Products Regulatory Authority)

mcdermott laboratories ltd., t/a gerard laboratories - alprazolam - tablet - 500 microgram(s) - benzodiazepine derivatives; alprazolam

أيرلندا - الإنجليزية - HPRA (Health Products Regulatory Authority)

mcdermott laboratories ltd., t/a gerard laboratories - alprazolam - tablet - 250 microgram(s) - benzodiazepine derivatives; alprazolam

أيرلندا - الإنجليزية - HPRA (Health Products Regulatory Authority)

mcdermott laboratories ltd., t/a gerard laboratories - alprazolam - tablet - 1 milligram(s) - benzodiazepine derivatives; alprazolam

أيرلندا - الإنجليزية - HPRA (Health Products Regulatory Authority)

aurobindo pharma (malta) limited - alprazolam - tablet - 1 milligram(s) - benzodiazepine derivatives; alprazolam

أيرلندا - الإنجليزية - HPRA (Health Products Regulatory Authority)

aurobindo pharma (malta) limited - alprazolam - tablet - 250 microgram(s) - benzodiazepine derivatives; alprazolam

أيرلندا - الإنجليزية - HPRA (Health Products Regulatory Authority)

aurobindo pharma (malta) limited - alprazolam - tablet - 500 microgram(s) - benzodiazepine derivatives; alprazolam

الولايات المتحدة - الإنجليزية - NLM (National Library of Medicine)

attix pharmaceuticals - toceranib (unii: 59l7y0530c) (toceranib - unii:59l7y0530c) - toceranib 1 kg in 1 kg

إسرائيل - الإنجليزية - Ministry of Health

pfizer pharmaceuticals israel ltd - taliglucerase alfa - powder for solution for infusion - taliglucerase alfa 200 u/vial - taliglucerase alfa - taliglucerase alfa - elelyso™ (taliglucerase alfa) for injection is a hydrolytic lysosomal glucocerebroside-specific enzyme indicated for long-term enzyme replacement therapy (ert) for adults and pediatric patients with a confirmed diagnosis of type 1 gaucher disease

الولايات المتحدة - الإنجليزية - NLM (National Library of Medicine)

zoetis inc. - toceranib phosphate (unii: 24f9pf7j3r) (toceranib - unii:59l7y0530c) - toceranib 10 mg - palladia tablets are indicated for the treatment of patnaik grade ii or iii, recurrent, cutaneous mast cell tumors with or without regional lymph node involvement in dogs. do not use in dogs used for breeding, or for pregnant or lactating bitches (see clinical pharmacology ).

الولايات المتحدة - الإنجليزية - NLM (National Library of Medicine)

pfizer laboratories div pfizer inc - taliglucerase alfa (unii: 0r4nlx88o4) (taliglucerase alfa - unii:0r4nlx88o4) - taliglucerase alfa 200 u in 5 ml - elelyso is indicated for the treatment of patients 4 years of age and older with a confirmed diagnosis of type 1 gaucher disease. none. risk summary the limited available data on elelyso use in pregnant women are not sufficient to inform a drug-associated risk. however, there are clinical considerations [see clinical considerations] . in animal reproduction studies when pregnant rats and rabbits were administered taliglucerase alfa at intravenous doses up to 5 times the recommended human dose (rhd), there was no evidence of embryo-fetal toxicity [see data] . the estimated background risk of major birth defects and miscarriage for the indicated population(s) are unknown. 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. clinical considerations disease-associated maternal and/or embryo/fetal risk women with type 1 gaucher disease have an increased risk of spontaneous abortion if disease symptoms are not treated and controlled pre-conception and during a pregnancy. pregnancy may exacerbate existing type 1 gaucher disease symptoms or result in new disease manifestations. type 1 gaucher disease manifestations may lead to adverse pregnancy outcomes, including hepatosplenomegaly which can interfere with the normal growth of a fetus and thrombocytopenia which can lead to increased bleeding and possible postpartum hemorrhage requiring transfusion. data animal data reproduction studies have been performed with taliglucerase alfa administered during the period of organogenesis in rats and rabbits. in rats, intravenous doses up to 55 mg/kg/day (about 5 times the rhd of 60 units/kg based on the body surface area) did not cause any adverse effects on embryo-fetal development. in rabbits, intravenous doses up to 27.8 mg/kg/day (about 5 times the rhd of 60 units/kg based on the body surface area) did not show any embryo-fetal toxicity. risk summary there are no data on the presence of taliglucerase alfa in human milk, the effects on the breast fed infant or the effects on milk production. the developmental and health benefits of breastfeeding should be considered along with the mother's clinical need for elelyso and any potential adverse effects on the breastfed child from elelyso or from the underlying maternal condition. the safety and effectiveness of elelyso for the treatment of pediatric patients 4 years of age and older with a confirmed diagnosis of type 1 gaucher disease has been established. the use of elelyso for this indication is supported by evidence of effectiveness from adequate and well-controlled trials of elelyso in adults, with additional pharmacodynamic data from 5 pediatric patients and pharmacokinetic data from 9 pediatric patients who participated in clinical trials [see clinical studies (14.1, 14.2), clinical pharmacology (12.3)]. data from 14 pediatric patients were included in the safety evaluation [see adverse reactions (6.1)]. the safety and effectiveness of elelyso has not been established in patients less than 4 years of age. pediatric patients experienced a higher frequency of vomiting during elelyso treatment (4 of 9 treatment-naïve patients) than adult patients, and this may be a symptom of hypersensitivity reaction. the frequencies of other adverse reactions were similar between pediatric and adult patients treated with elelyso [see adverse reactions (6.1)] . during clinical trials, 8 patients aged 65 or older were treated with elelyso. clinical trials of elelyso did not include sufficient numbers of patients aged 65 and over to determine whether they respond differently from younger patients.