Canada - English - Health Canada

taro pharmaceuticals inc - epinephrine - solution - 0.3mg - epinephrine 0.3mg - alpha-and beta-adrenergic agonists

Canada - English - Health Canada

taro pharmaceuticals inc - epinephrine - solution - 0.15mg - epinephrine 0.15mg - alpha-and beta-adrenergic agonists

Canada - English - Health Canada

taro pharmaceuticals inc - epinephrine - solution - 0.3mg - epinephrine 0.3mg - alpha-and beta-adrenergic agonists

Canada - English - Health Canada

taro pharmaceuticals inc - epinephrine - solution - 0.15mg - epinephrine 0.15mg - alpha-and beta-adrenergic agonists

Canada - English - Health Canada

rougier pharma division of ratiopharm inc - epinephrine hydrochloride - spray - 3.5% - epinephrine hydrochloride 3.5% - sympathomimetic (adrenergic) agents

Malta - English - Medicines Authority

pfizer hellas s.a. 243 messoghion ave., neo psychiko 15451, athens, greece - norepinephrine - concentrate for solution for infusion - norepinephrine 2 mg/ml - cardiac therapy

Malta - English - Medicines Authority

mercury pharma international limited 4045 kingswood road, city west business park, co, dublin, ireland - epinephrine - solution for injection - epinephrine 1 mg/ml - cardiac therapy

Malta - English - Medicines Authority

pfizer hellas s.a. 243 messoghion ave., neo psychiko 15451, athens, greece - norepinephrine - concentrate for solution for infusion - norepinephrine 2 mg/ml - cardiac therapy

United States - English - NLM (National Library of Medicine)

long grove pharmaceuticals, llc - norepinephrine bitartrate (unii: ify5pe3zrw) (norepinephrine - unii:x4w3enh1cv) - norepinephrine in sodium chloride injection is indicated to raise blood pressure in adult patients with severe, acute hypotension. none. risk summary limited published data consisting of a small number of case reports and multiple small trials involving the use of norepinephrine in pregnant women at the time of delivery have not identified an increased risk of major birth defects, miscarriage or adverse maternal or fetal outcomes. there are risks to the mother and fetus from hypotension associated with septic shock, myocardial infarction and stroke which are medical emergencies in pregnancy and can be fatal if left untreated (see clinical considerations) . in animal reproduction studies, using high doses of intravenous norepinephrine resulted in lowered maternal placental blood flow. clinical relevance to changes in the human fetus is unknown since the average maintenance dose is ten times lower (see data) . increased fetal reabsorptions were observed in pregnant hamsters after receiving daily injections at approximately 2 times the maximum recommended dose on a mg/m2 basis for four days during organogenesis (see data) . the estimated background risk for major birth defects and miscarriage for 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 2-4% and 15-20%, respectively. clinical considerations disease-associated maternal and/or embryo/fetal risk hypotension associated with septic shock, myocardial infarction, and stroke are medical emergencies in pregnancy which can be fatal if left untreated. delaying treatment in pregnant women with hypotension associated with septic shock, myocardial infarction and stroke may increase the risk of maternal and fetal morbidity and mortality. life-sustaining therapy for the pregnant woman should not be withheld due to potential concerns regarding the effects of norepinephrine on the fetus. data animal data a study in pregnant sheep receiving high doses of intravenous norepinephrine (40 mcg/min, at approximately 10 times the average maintenance dose of 2-4 mcg/min in human, on a mg/kg basis) exhibited a significant decrease in maternal placental blood flow. decreases in fetal oxygenation, urine and lung liquid flow were also observed. norepinephrine administration to pregnant rats on gestation day 16 or 17 resulted in cataract production in rat fetuses. in hamsters, an increased number of resorptions (29.1% in study group vs. 3.4% in control group), fetal microscopic liver abnormalities and delayed skeletal ossification were observed at approximately 2 times the maximum recommended intramuscular or subcutaneous dose (on a mg/m2 basis at a maternal subcutaneous dose of 0.5 mg/kg/day from gestation day 7-10). risk summary there are no data on the presence of norepinephrine in either human or animal milk, the effects on the breastfed infant, or the effects on milk production. clinically relevant exposure to the infant is not expected based on the short half-life and poor oral bioavailability of norepinephrine. safety and effectiveness in pediatric patients have not been established. clinical studies of norepinephrine in sodium chloride injection did not include sufficient numbers of subjects aged 65 and over to determine whether they respond differently from younger subjects. other reported clinical experience has not identified differences in responses between the elderly and younger patients. in general, dose selection for an elderly patient should be cautious, usually starting at the low end of the dosing range, reflecting the greater frequency of decreased hepatic, renal, or cardiac function, and of concomitant disease or other drug therapy. avoid administration of norepinephrine in sodium chloride injection into the veins in the leg in elderly patients [see warnings and precautions (5.1)] .

Israel - English - Ministry of Health

trupharm marketing 1985 ltd. - epinephrine - solution for injection - epinephrine 1 mg / 1 ml - epinephrine - epinephrine - epipen is indicated in the emergency treatment of severe allergic reactions (type i) including anaphylaxis to stinging insects (e.g., order hymenoptera, which include bees, wasps, hornets, yellow jackets and fire ants) and biting insects (e.g., triatoma, mosquitoes), allergen immunotherapy, foods, drugs, diagnostic testing substances (e.g., radiocontrast media) and other allergens, as well as idiopathic anaphylaxis or exercise-induced anaphylaxis.epipen is intended for immediate administration in patients who are determined to be at increased risk for anaphylaxis, including individuals with a history of anaphylactic reactions. epipen is intended for immediate administration as emergency supportive therapy only and is not a substitute for immediate medical care.