Armenia - English - Դեղերի և բժշկական տեխնոլոգիաների փորձագիտական կենտրոնի գործունեության Հայաստանի Հանրապետությունում

irbitskiy himfarmzavod ojsc - activated charcoal - tablets - 250mg

Tanzania - English - Tanzania Medicinces & Medical Devices Authority

dentopharma supplies limited, tanzania - saliva ejector -

Australia - English - APVMA (Australian Pesticides and Veterinary Medicines Authority)

intervet australia pty limited - inactivated mycoplasma hyopneumoniae strain j - unknown - inactivated mycoplasma hyopneumoniae strain j vaccine - general active 0.0 - immunotherapy

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

bayer healthcare pharmaceuticals inc. - regorafenib (unii: mgn125fs9d) (regorafenib anhydrous - unii:24t2a1doyb) - regorafenib 40 mg - stivarga is indicated for the treatment of patients with metastatic colorectal cancer (crc) who have been previously treated with fluoropyrimidine-, oxaliplatin- and irinotecan-based chemotherapy, an anti-vegf therapy, and, if ras wild- type, an anti-egfr therapy. stivarga is indicated for the treatment of patients with locally advanced, unresectable or metastatic gastrointestinal stromal tumor (gist) who have been previously treated with imatinib mesylate and sunitinib malate. stivarga is indicated for the treatment of patients with hepatocellular carcinoma (hcc) who have been previously treated with sorafenib. none. risk summary based on animal studies and its mechanism of action, stivarga can cause fetal harm when administered to a pregnant woman. there are no available data on stivarga use in pregnant women. administration of regorafenib was embryolethal and teratogenic in rats and rabbits at exposures lower than human exposures at the recommended dose, with increased incidences of cardiovascular, genitourinary, and skeletal malformations [see data ] . advise pregnant women of the potential hazard to a fetus. the estimated background risk of major birth defects and miscarriage for the indicated population is 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. data animal data in embryo-fetal development studies, a total loss of pregnancy (100% resorption of litter) was observed in rats at doses as low as 1 mg/kg (approximately 6% of the recommended human dose, based on body surface area) and in rabbits at doses as low as 1.6 mg/kg (approximately 25% of the human exposure at the clinically recommended dose measured by auc). in a single dose distribution study in pregnant rats, there was increased penetration of regorafenib across the blood-brain barrier in fetuses compared to dams. daily administration of regorafenib to pregnant rats during organogenesis resulted in fetal findings of delayed ossification at doses > 0.8 mg/kg (approximately 5% of the recommended human dose based on body surface area) and dose-dependent increases in skeletal malformations including cleft palate and enlarged fontanelle at doses ≥ 1 mg/kg (approximately 10% of the clinical exposure based on auc). at doses ≥ 1.6 mg/kg (approximately 11% of the recommended human dose based on body surface area), there were dose-dependent increases in the incidence of cardiovascular malformations, external abnormalities, diaphragmatic hernia, and dilation of the renal pelvis. in pregnant rabbits administered regorafenib daily during organogenesis, there were findings of ventricular septal defects evident at the lowest tested dose of 0.4 mg/kg (approximately 7% of the auc in patients at the recommended dose). at doses of ≥ 0.8 mg/kg (approximately 15% of the human exposure at the recommended human dose based on auc), administration of regorafenib resulted in dose-dependent increases in the incidence of additional cardiovascular malformations and skeletal anomalies, as well as significant adverse effects on the urinary system including missing kidney/ureter; small, deformed and malpositioned kidney; and hydronephrosis. the proportion of viable fetuses that were male decreased with increasing dose in two rabbit embryo-fetal toxicity studies. risk summary there are no data on the presence of regorafenib or its metabolites in human milk, the effects of regorafenib on the breastfed infant, or on milk production. in rats, regorafenib and its metabolites are excreted in milk. because of the potential for serious adverse reactions in breastfed infants from stivarga, do not breastfeed during treatment with stivarga and for 2 weeks after the final dose. contraception females use effective contraception during treatment and for 2 months after completion of therapy. males advise male patients with female partners of reproductive potential to use effective contraception during treatment and for 2 months following the final dose of stivarga [see nonclinical toxicology (13.1)] . infertility there are no data on the effect of stivarga on human fertility. results from animal studies indicate that regorafenib can impair male and female fertility [see nonclinical toxicology (13.1)]. the safety and efficacy of  stivarga in pediatric patients less than 18 years of age have not been established. animal data in 28-day repeat-dose studies in rats there were dose-dependent findings of dentin alteration and angiectasis. these findings occurred at regorafenib doses as low as 4 mg/kg (approximately 25% of the auc in humans at the recommended dose). in 13-week repeat-dose studies in dogs there were similar findings of dentin alteration at doses as low as 20 mg/kg (approximately 43% of the auc in humans at the recommended dose). administration of regorafenib in these animals also led to persistent growth and thickening of the femoral epiphyseal growth plate. of the 1142 stivarga-treated patients enrolled in randomized, placebo-controlled trials, 40% were 65 years of age and over, while 10% were 75 and over. no overall differences in efficacy were observed between these patients and younger patients. there was an increased incidence of grade 3 hypertension (18% versus 9%) in the placebo-controlled trials among stivarga-treated patients 65 years of age and older as compared to younger patients. in addition, one grade 4 hypertension event has been reported in the 65 years and older age group and none in the younger age group. no dose adjustment is recommended in patients with mild (total bilirubin ≤uln and ast >uln, or total bilirubin >uln to ≤1.5 times uln) or moderate (total bilirubin >1.5 to ≤3 times uln and any ast) hepatic impairment, [see clinical pharmacology (12.3)] . closely monitor patients with hepatic impairment for adverse reactions [see warnings and precautions (5.1)] . stivarga is not recommended for use in patients with severe hepatic impairment (total bilirubin >3x uln) as stivarga has not been studied in this population. no dose adjustment is recommended for patients with renal impairment. the pharmacokinetics of regorafenib have not been studied in patients who are on dialysis and there is no recommended dose for this patient population [see clinical pharmacology (12.3)] . based on pooled data from three placebo-controlled trials (correct, grid and concur), a higher incidence of hfsr and liver function test abnormalities occurred in asian patients treated with stivarga as compared with whites [see warnings and precautions (5.1, 5.5)] . no starting dose adjustment is necessary based on race.

Australia - English - Department of Health (Therapeutic Goods Administration)

boehringer ingelheim pty ltd - tiotropium bromide monohydrate, quantity: 3.1235 microgram/actuation (equivalent: tiotropium, qty 2.5 microgram/actuation) - inhalation, conventional - excipient ingredients: purified water; hydrochloric acid; disodium edetate; benzalkonium chloride - copd: srivasso respimat is indicated for the long term maintenance treatment of bronchospasm and dyspnoea associated with chronic obstructive pulmonary disease (copd). srivasso respimat is indicated for the prevention of copd exacerbations.,asthma: srivasso respimat is indicated as add-on maintenance bronchodilator treatment in patients aged 6 years and older with moderate to severe asthma.

Australia - English - Department of Health (Therapeutic Goods Administration)

boehringer ingelheim pty ltd - tiotropium bromide monohydrate, quantity: 3.1235 microgram/actuation (equivalent: tiotropium, qty 2.5 microgram/actuation) - inhalation, conventional - excipient ingredients: purified water; hydrochloric acid; disodium edetate; benzalkonium chloride - copd: srivasso respimat is indicated for the long term maintenance treatment of bronchospasm and dyspnoea associated with chronic obstructive pulmonary disease (copd). srivasso respimat is indicated for the prevention of copd exacerbations.,asthma: srivasso respimat is indicated as add-on maintenance bronchodilator treatment in patients aged 6 years and older with moderate to severe asthma.

Australia - English - APVMA (Australian Pesticides and Veterinary Medicines Authority)

zoetis australia pty ltd - inactivated newcastle disease virus antigen - parenteral liquid/solution/suspension - inactivated newcastle disease virus antigen vaccine-viral active 0.0 eid/50 - immunotherapy - poultry - see label | chicken - newcastle disease

European Union - English - EMA (European Medicines Agency)

ceva santé animale - inactivated coxiella burnetii vaccine, strain nine mile - immunologicals for bovidae, inactivated bacterial vaccines (including mycoplasma, toxoid and chlamydia) - goats; cattle - cattle: , for the active immunisation of cattle to lower the risk for non-infected animals vaccinated when non-pregnant to become shedder (5 times lower probability in comparison with animals receiving a placebo), and to reduce shedding of coxiella burnetii in these animals via milk and vaginal mucus., onset of immunity: not established., duration of immunity: 280 days after completion of the primary vaccination course. , goats: , for the active immunisation of goats to reduce abortion caused by coxiella burnetii and to reduce shedding of the organism via milk, vaginal mucus, faeces and placenta., onset of immunity: not established., duration of immunity: one year after completion of the primary vaccination course.

European Union - English - EMA (European Medicines Agency)

laboratorios hipra, s.a. - inactivated rabbit haemorrhagic disease type 2 virus (rhdv2), strainv-1037 - inactivated viral vaccines - rabbits - for active immunisation of rabbits from the age of 30 days to reduce mortality caused by the rabbit haemorrhagic disease type 2 virus (rhdv2)

European Union - English - EMA (European Medicines Agency)

zoetis belgium sa - inactivated recombinant chimeric porcine circovirus type 1 containing the porcine circovirus type 2 orf2 protein, inactivated mycoplasma hyopneumoniae, strain p-5722-3 - inactivated viral and inactivated bacterial vaccines - pigs - for active immunisation of pigs from 3 weeks of age against porcine circovirus type 2 (pcv2) to reduce viral load in blood and lymphoid tissues and fecal shedding caused by infection with pcv2.for active immunisation of pigs over the age of 3 weeks against mycoplasma hyopneumoniae to reduce lung lesions caused by infection with m. hyopneumoniae.