Kanada - enska - Health Canada

novartis pharmaceuticals canada inc - inclisiran (inclisiran sodium) - solution - 284mg - inclisiran (inclisiran sodium) 284mg

Bandaríkin - enska - NLM (National Library of Medicine)

watson laboratories, inc - citalopram hydrobromide (unii: i1e9d14f36) (citalopram - unii:0dhu5b8d6v) - tablet - 10 mg - citalopram hbr is indicated for the treatment of depression. the efficacy of citalopram hbr in the treatment of depression was established in 4-6 week controlled trials of outpatients whose diagnosis corresponded most closely to the dsm-iii and dsm-iii-r category of major depressive disorder (see clinical pharmacology). a major depressive episode (dsm-iv) implies a prominent and relatively persistent (nearly every day for at least 2 weeks) depressed or dysphoric mood that usually interferes with daily functioning, and includes at least five of the following nine symptoms: depressed mood, loss of interest in usual activities, significant change in weight and/or appetite, insomnia or hypersomnia, psychomotor agitation or retardation, increased fatigue, feelings of guilt or worthlessness, slowed thinking or impaired concentration, a suicide attempt or suicidal ideation. the antidepressant action of citalopram in hospitalized depressed patients has not been adequately studied. the efficacy of citalopram in mainta

Bandaríkin - enska - NLM (National Library of Medicine)

paradocs all natural inc. - avena sativa flowering top (unii: ma9cqj3f7f) (avena sativa flowering top - unii:ma9cqj3f7f), equisetum hyemale (unii: 59677rxh25) (equisetum hyemale - unii:59677rxh25), hypericum perforatum (unii: xk4iux8mnb) (hypericum perforatum - unii:xk4iux8mnb), ulmus rubra bark (unii: 91qy4pxu8q) (ulmus rubra bark - unii:91qy4pxu8q), glycyrrhiza glabra (unii: 2788z9758h) (glycyrrhiza glabra - unii:2788z9758h), pueraria montana var. lobata whole (unii: d295ofk7e1) (pueraria montana var. lobata whole - unii:d295o - avena sativa flowering top 3 [hp_x] in 1 ml - to aid with proper hydration. to aid with proper hydration.

Bandaríkin - enska - NLM (National Library of Medicine)

babo botanicals, inc. - zinc oxide 16.0% - purpose: sunscreen stop use and ask doctor if rash occurs. helps prevent sunburn. • if used as directed with other sun protection measures (see directions), decreases the risk of skin cancer and early skin aging caused by the sun.

Ástralía - enska - Department of Health (Therapeutic Goods Administration)

novartis pharmaceuticals australia pty ltd - inclisiran, quantity: 284 mg - injection, solution - excipient ingredients: sodium hydroxide; phosphoric acid; water for injections - leqvio is indicated as an adjunct to diet and exercise to reduce low-density lipoprotein cholesterol (ldl-c) in adults with heterozygous familial hypercholesterolaemia, atherosclerotic cardiovascular disease, or at high risk of a cardiovascular event:,? in combination with a statin or statin with other lipid-lowering therapies in patients unable to reach ldl-c goals with the maximum tolerated dose of a statin or,,? alone or in combination with other lipid-lowering therapies in patients who are statin-intolerant.

Bandaríkin - enska - NLM (National Library of Medicine)

global blood therapeutics, inc, a subsidiary of pfizer inc. - voxelotor (unii: 3zo554a4q8) (voxelotor - unii:3zo554a4q8) - oxbryta is indicated for the treatment of sickle cell disease (scd) in adults and pediatric patients 4 years of age and older. this indication is approved under accelerated approval based on increase in hemoglobin (hb) [see clinical studies (14)] . continued approval for this indication may be contingent upon verification and description of clinical benefit in confirmatory trial(s). oxbryta is contraindicated in patients with a history of serious drug hypersensitivity reaction to voxelotor or excipients. clinical manifestations may include generalized rash, urticaria, mild shortness of breath, mild facial swelling, and eosinophilia [see warnings and precautions (5.1) and adverse reactions (6.1)]. risk summary there are no available data on oxbryta use in pregnant women to evaluate for a drug-associated risk of major birth defects, miscarriage, or adverse maternal or fetal outcomes. in animal reproduction studies, oral administration of voxelotor to pregnant rats and rabbits during organogenesis at exposures up to 2.8-times (rats) and 0.3-times (rabbits) the exposure at the maximum recommended human dose resulted in no adverse developmental effects (see data). the estimated background risk of major birth defects and miscarriage for the indicated population is approximately 14% and up to 43%, respectively. all pregnancies have a background risk of birth defect, loss, or other adverse outcomes. there are adverse effects on maternal and fetal outcomes associated with scd in pregnancy (see clinical considerations). oxbryta should only be used during pregnancy if the benefit of the drug outweighs the potential risk. clinical considerations disease-associated maternal and/or embryo/fetal risk women with scd have an increased risk of adverse pregnancy outcomes for the mother and the fetus. pregnant women are at greater risk for vasoocclusive crises, pre-eclampsia, eclampsia, and maternal mortality. for the fetus, there is an increased risk for intrauterine growth restriction, preterm delivery, low birth weight, and perinatal mortality. data animal data in embryo-fetal development studies, voxelotor was administered orally to pregnant rats at 15, 50, and 250 mg/kg/day (gestation days 7 through 17) and rabbits at 25, 75, and 150 mg/kg/day (gestation days 7 through 19) through organogenesis. maternal toxicity was observed at the highest dose levels in these studies equivalent to 2.8-times (rats) and 0.3-times (rabbits) the exposures in patients receiving oxbryta at the recommended daily dose. there was no evidence of adverse developmental outcomes in rats or rabbits. in a pre- and postnatal development study, voxelotor was administered orally to pregnant rats at 15, 50 and 250 mg/kg/day (gestation day 6 through lactation day 20). maternal gestational body weights were decreased at 250 mg/kg/day, which continued to the end of lactation. the findings in offspring included reduced survival and reduced body weights throughout lactation, weaning and maturation. the effects in offspring were observed at the maternal dose of 250 mg/kg/day with an exposure approximately 2.8-times the exposure in patients at the recommended dose. risk summary there are no data on the presence of voxelotor in human milk, the effects on the breastfed child, or the effects on milk production. voxelotor was detected in milk in lactating rats. plasma concentrations of voxelotor in pregnant rats were higher than the concentration in milk. when a drug is present in animal milk, it is likely that the drug will be present in human milk. the concentration of voxelotor in animal milk does not necessarily predict the concentration of drug in human milk. because of the potential for serious adverse reactions in the breastfed child, including changes in the hematopoietic system, advise patients that breastfeeding is not recommended during treatment with oxbryta, and for at least 2 weeks after the last dose. the safety and effectiveness of oxbryta for scd have been established in pediatric patients aged 4 years and older. the safety and efficacy of oxbryta in pediatric patients with scd below the age of 4 years have not been established. use of oxbryta in pediatric patients 12 to <17 years for scd is supported by evidence from an adequate and well-controlled study in adults and pediatric patients (hope trial). the hope trial enrolled 26 pediatric patients aged 12 to <17 years, in which 12 pediatric patients received oxbryta 1,500 mg once daily and 14 pediatric patients received oxbryta 900 mg once daily [see adverse reactions (6.1), clinical pharmacology (12.3), and clinical studies (14.1)] . use of oxbryta in pediatric patients 4 to <12 years for scd is supported by evidence from an open-label, phase 2 study. the study enrolled 45 pediatric patients aged 4 to <12 years and 11 patients aged 12 to <17 years with scd. patients 12 to <17 years received oxbryta 1,500 mg once daily. patients 4 to <12 years were administered oxbryta based on body weight. oxbryta doses of 600 mg, 900 mg, or 1,500 mg once daily were administered to patients weighing 10 kg to <20 kg, 20 kg to <40 kg, or ≥40 kg, respectively [see adverse reactions (6.1), clinical pharmacology (12.3), and clinical studies (14.2)] . pharmacokinetics, safety and efficacy were similar across the pediatric age groups and across pediatric and adult patients [see dosage and administration (2) , clinical pharmacology (12.3) and clinical studies (14)]. the adverse reactions observed were similar across the pediatric age groups and across pediatric and adult patients [see adverse reactions (6.1)]. clinical studies of oxbryta did not include sufficient numbers of subjects aged 65 and over to determine whether they respond differently from younger subjects. severe hepatic impairment increases voxelotor exposures [see clinical pharmacology (12.3)] . reduce oxbryta dose [see dosage and administration (2.3, 2.4)]. this instructions for use has been approved by the u.s. food and drug administration. revised: 08/2023 instructions for use oxbryta® [ox brye ta] (voxelotor) tablets for oral suspension 300 mg this instructions for use contains information on how to take oxbryta tablets for oral suspension. read this instructions for use before you or your child start taking oxbryta tablets for oral suspension for the first time and each time you or your child get a refill. there may be new information. this information does not take the place of talking to your healthcare provider about your or your child's medical condition or treatment. talk to your healthcare provider or pharmacist if you have questions about how to take or give the prescribed dose of oxbryta tablets for oral suspension. important information you need to know before taking oxbryta tablets for oral suspension: gather supplies you will need the following items to prepare the dose of oxbryta tablets for oral suspension (not included with oxbryta tablets for oral suspension): you will also need: preparing a dose of oxbryta tablets for oral suspension step 1. wash and dry your hands well before preparing the dose. step 2. pour room temperature clear drink into the cup. the table below shows the amount of clear drink needed for your prescribed dose. you may add more clear drink if needed to mix the tablets. number of oxbryta tablets for oral suspension amount of clear drink 1 1 teaspoon (5 ml) 2 2 teaspoons (10 ml) 3 3 teaspoons (15 ml) 4 4 teaspoons (20 ml) 5 5 teaspoons (25 ml) 7 7 teaspoons (35 ml) 8 8 teaspoons (40 ml)         step 3. add the prescribed number of oxbryta tablets for oral suspension into the cup. step 4. swirl the cup until the tablet(s) break apart (disperse) in the drink. be careful not to spill the mixture. step 5. wait for 1 to 5 minutes. giving the dose step 6. swirl the cup again. take or give all of the prepared medicine right away. step 7. add 1 or 2 teaspoons of room temperature clear drink to the cup to make sure the full dose is taken. swirl the cup until the remaining medicine is mixed and take or give it right away. step 8. wash the teaspoon and cup with warm soap and water. storing oxbryta keep oxbryta and all medicines out of the reach of children. disposing of oxbryta when all the tablets in the bottle have been taken, throw away the bottle. safely dispose of (throw away) oxbryta that is out of date or no longer needed using your local household waste guidelines. distributed by global blood therapeutics, inc a subsidiary of pfizer inc. south san francisco, ca 94080 lab-1568-1.0 for more information, go to www.pfizer.com or call 1-800-438-1985.

Ísrael - enska - Ministry of Health

novartis israel ltd - inclisiran as sodium - solution for injection - inclisiran as sodium 189 mg/ml - inclisiran - leqvio is indicated in adults with primary hypercholesterolaemia (heterozygous familial and non familial) or mixed dyslipidaemia, as an adjunct to diet:• in combination with a statin or statin with other lipid lowering therapies in patients unable to reach ldl c goals with the maximum tolerated dose of a statin, or• alone or in combination with other lipid lowering therapies in patients who are statin intolerant, or for whom a statin is contraindicated.

Ástralía - enska - Department of Health (Therapeutic Goods Administration)

we are feel good global pty ltd - bemotrizinol, quantity: 30 mg/g; octocrylene, quantity: 20 mg/g; zinc oxide, quantity: 200 mg/g; diethylamino hydroxybenzoyl hexyl benzoate, quantity: 40 mg/g - lotion - excipient ingredients: iron oxide black; allantoin; purified water; disodium edetate; cyclomethicone; carnauba wax; aloe vera; iron oxide yellow; triacontanyl pvp; iron oxide red; white beeswax; glycerol; white soft paraffin; caprylyl glycol; octanohydroxamic acid; magnesium sulfate heptahydrate; butylated hydroxytoluene; dl-alpha-tocopheryl acetate; peg-30 dipolyhydroxystearate; alkyl (c12-15) benzoate; isopropyl palmitate; nicotinamide; dexpanthenol; calcium stearate; glyceryl monooleate - may assist in preventing some skin cancers (sunscreen) ; may reduce the risk of some skin cancers (sunscreen) ; spf 50 plus broad spectrum very high protection sunscreen ; can aid in the prevention of premature skin ageing (sunscreen) ; can aid in the prevention of solar keratosis (sunscreen) ; can aid in the prevention of sunspots (sunscreen)

Írland - enska - HPRA (Health Products Regulatory Authority)

global vet health sl - amoxicillin trihydrate - powder for use in drinking water - 500 milligram(s)/gram - amoxicillin - chickens, ducks, pigs, turkeys - antibacterial

Bandaríkin - enska - NLM (National Library of Medicine)

gowoonsesang cosmetics co., ltd. - zinc oxide (unii: soi2loh54z) (zinc oxide - unii:soi2loh54z) - zinc oxide 5 mg in 100 mg