Yasmin 0.03 mg / 3 mg film-coated tablets आयरलैंड - अंग्रेज़ी - HPRA (Health Products Regulatory Authority)

yasmin 0.03 mg / 3 mg film-coated tablets

bayer limited - drospirenone; ethinylestradiol - film-coated tablet - 0.03 mg/3 milligram(s) - progestogens and estrogens, fixed combinations; drospirenone and ethinylestradiol

Loratadine Galpharm 10mg Tablets माल्टा - अंग्रेज़ी - Medicines Authority

loratadine galpharm 10mg tablets

galpharm healthcare limited wrafton, braunton, north devon, ex33 2dl, united kingdom - loratadine - tablet - loratadine 10 milligram(s) - antihistamines for systemic use

DESLORATADINE tablet, film coated संयुक्त राज्य - अंग्रेज़ी - NLM (National Library of Medicine)

desloratadine tablet, film coated

lupin pharmaceuticals, inc. - desloratadine (unii: fvf865388r) (desloratadine - unii:fvf865388r) - desloratadine 5 mg - desloratadine tablets are indicated for the relief of the nasal and non-nasal symptoms of seasonal allergic rhinitis in patients 12 years of age and older. desloratadine tablets are indicated for the relief of the nasal and non-nasal symptoms of perennial allergic rhinitis in patients 12 years of age and older. desloratadine tablets are contraindicated in patients who are hypersensitive to this medication or to any of its ingredients or to loratadine [see warnings and precautions (5.1) and adverse reactions (6.2)]. risk summary   the limited available data with desloratadine in pregnant women are not sufficient to inform a drug-associated risk for major birth defects and miscarriage. there are no adequate and well-controlled studies in pregnant women. desloratadine given during organogenesis to pregnant rats was not teratogenic at the summed area under the concentration-time curve (auc)-based exposures of desloratadine and its metabolite approximately 320 times that at the recommended human daily oral dose (rhd) of 5 mg/day. desloratadine given during organogenesis to pregnant rabbits was not teratogenic at the auc-based exposures of desloratadine approximately 230 times that at the rhd. desloratadine given to pregnant rats during organogenesis through lactation resulted in reduced body weight and slow righting reflex of f1 pups at the summed auc-based exposures of desloratadine and its metabolite approximately 70 times or greater than that at the rhd [see data] . the estimated background risk of major birth defects and miscarriage for the indicated populations 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: desloratadine was given orally during organogenesis to pregnant rats at doses of 6, 24 and 48 mg/kg/day (approximately 50, 200 and 320 times the summed auc-based exposure of desloratadine and its metabolite at the rhd). no fetal malformations were present. reduced fetal weights and skeletal variations noted at doses of 24 and 48 mg/kg/day were likely secondary to the maternal toxicities of reduced body weight gain and food consumption observed at the same doses. desloratadine was also given orally during organogenesis to pregnant rabbits at doses of 15, 30 and 60 mg/kg/day (approximately 30, 70 and 230 times the auc- based exposure of desloratadine at the rhd). no adverse effects to the fetus were noted. reduced maternal body weight gain was noted in rabbits at 60 mg/kg/day. in a peri- and post-natal development study, desloratadine was given to rats orally during the peri- natal (gestation day 6) through lactation periods (postpartum day 21) at doses of 3, 9 and 18 mg/kg/day. reduced body weight and slow righting reflex were reported in f1 pups at doses of 9 mg/kg/day or greater (approximately 70 times or greater than the summed auc-based exposure of desloratadine and its metabolite at the rhd). desloratadine had no effect on f1 pup development at 3 mg/kg/day (approximately 10 times the summed auc-based exposure of desloratadine and its metabolite at the rhd). maternal toxicities including reduced body weight gain and food consumption were noted at 18 mg/kg/day for f0 dams. f1 offspring were subsequently mated and there was no developmental toxicity for f2 pups observed. risk summary desloratadine passes into breast milk. there are not sufficient data on the effects of desloratadine on the breastfed infant or the effects of desloratadine on milk production. the decision should be made whether to discontinue nursing or to discontinue desloratadine, taking into account the developmental and health benefits of breastfeeding, the nursing mother's clinical need, and any potential adverse effects on the breastfed infant from desloratadine or from the underlying maternal condition. infertility there are no data available on human infertility associated with desloratadine. there were no clinically relevant effects of desloratadine on female fertility in rats. a male specific decrease in fertility occurred at an oral desloratadine dose of 12 mg/kg or greater in rats (approximately 65 times the summed auc-based exposure of desloratadine and its metabolite at the rhd). male fertility was unaffected at a desloratadine dose of 3 mg/kg (approximately 10 times the summed auc-based exposure of desloratadine and its metabolite at the rhd). [see nonclinical toxicology (13.1).] the recommended dose of desloratadine oral solution in the pediatric population is based on cross-study comparison of the plasma concentration of desloratadine in adults and pediatric subjects. the safety of desloratadine oral solution has been established in 246 pediatric subjects aged 6 months to 11 years in three placebo-controlled clinical studies. since the course of seasonal and perennial allergic rhinitis and the effects of desloratadine are sufficiently similar in the pediatric and adult populations, it allows extrapolation from the adult efficacy data to pediatric patients. the effectiveness of desloratadine oral solution in these age groups is supported by evidence from adequate and well-controlled studies of desloratadine tablets in adults. the safety and effectiveness of desloratadine tablets or desloratadine oral solution have not been demonstrated in pediatric patients less than 6 months of age. [see clinical pharmacology (12.3)]. clinical studies of desloratadine 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 between the elderly and younger patients. in general, dose selection for an elderly patient should be cautious, reflecting the greater frequency of decreased hepatic, renal, or cardiac function, and of concomitant disease or other drug therapy. [see clinical pharmacology (12.3)]. dosage adjustment for patients with renal impairment is recommended [see dosage and administration (2.5) and clinical pharmacology (12.3)]. dosage adjustment for patients with hepatic impairment is recommended [see dosage and administration (2.5) and clinical pharmacology (12.3)]. there is no information to indicate that abuse or dependency occurs with desloratadine tablets.

APO-IVABRADINE ivabradine (as hydrochloride) 5 mg tablet blister pack ऑस्ट्रेलिया - अंग्रेज़ी - Department of Health (Therapeutic Goods Administration)

apo-ivabradine ivabradine (as hydrochloride) 5 mg tablet blister pack

arrotex pharmaceuticals pty ltd - ivabradine hydrochloride, quantity: 5.39 mg (equivalent: ivabradine, qty 5 mg) - tablet, film coated - excipient ingredients: lactose monohydrate; magnesium stearate; maize starch; colloidal anhydrous silica; maltodextrin; titanium dioxide; hypromellose; iron oxide yellow; iron oxide red; macrogol 4000 - treatment of chronic stable angina symptomatic treatment of chronic stable angina due to atherosclerotic coronary artery disease in patients with normal sinus rhythm and heart rate at or above 70 bpm, who are unable to tolerate or have a contraindication to the use of beta-blockers, or in combination with atenolol 50mg once daily when angina is inadequately controlled.,treatment of chronic heart failure treatment of symptomatic chronic heart failure of nyha classes ii or iii and with documented left ventricular ejection fraction (lvef) ? 35% in adult patients in sinus rhythm and with heart rate at or above 77 bpm, in combination with optimal standard chronic heart failure treatment.

APO-IVABRADINE ivabradine (as hydrochloride) 7.5 mg tablet blister pack ऑस्ट्रेलिया - अंग्रेज़ी - Department of Health (Therapeutic Goods Administration)

apo-ivabradine ivabradine (as hydrochloride) 7.5 mg tablet blister pack

arrotex pharmaceuticals pty ltd - ivabradine hydrochloride, quantity: 8.085 mg (equivalent: ivabradine, qty 7.5 mg) - tablet, film coated - excipient ingredients: magnesium stearate; maize starch; colloidal anhydrous silica; lactose monohydrate; maltodextrin; titanium dioxide; hypromellose; iron oxide yellow; iron oxide red; macrogol 4000 - treatment of chronic stable angina symptomatic treatment of chronic stable angina due to atherosclerotic coronary artery disease in patients with normal sinus rhythm and heart rate at or above 70 bpm, who are unable to tolerate or have a contraindication to the use of beta-blockers, or in combination with atenolol 50mg once daily when angina is inadequately controlled.,treatment of chronic heart failure treatment of symptomatic chronic heart failure of nyha classes ii or iii and with documented left ventricular ejection fraction (lvef) ? 35% in adult patients in sinus rhythm and with heart rate at or above 77 bpm, in combination with optimal standard chronic heart failure treatment.

CYPROHEPTADINE syrup संयुक्त राज्य - अंग्रेज़ी - NLM (National Library of Medicine)

cyproheptadine syrup

pharmaceutical associates, inc. - cyproheptadine (unii: 2yhb6175do) (cyproheptadine - unii:2yhb6175do) - cyproheptadine 2 mg in 5 ml - perennial and seasonal allergic rhinitis vasomotor rhinitis allergic conjunctivitis due to inhalant allergens and foods mild, uncomplicated allergic skin manifestations of urticaria and angioedema amelioration of allergic reactions to blood or plasma cold urticaria dermatographism as therapy for anaphylactic reactions adjunctive to epinephrine and other standard measures after the acute manifestations have been controlled. this drug should not be used in newborn or premature infants. because of the higher risk of antihistamines for infants generally and for newborns and prematures in particular, antihistamine therapy is contraindicated in nursing mothers. hypersensitivity to cyproheptadine and other drugs of similar chemical structure monoamine oxidase inhibitor therapy (see drug interactions) angle-closure glaucoma stenosing peptic ulcer symptomatic prostatic hypertrophy bladder neck obstruction pyloroduodenal obstruction elderly, debilitated patients

Desloratadine ratiopharm यूरोपीय संघ - अंग्रेज़ी - EMA (European Medicines Agency)

desloratadine ratiopharm

ratiopharm gmbh - desloratadine - rhinitis, allergic, perennial; urticaria; rhinitis, allergic, seasonal - antihistamines for systemic use, - desloratadine ratiopharm is indicated in adults for the relief of symptoms associated with:allergic rhinitischronic idiopathic urticaria as initially diagnosed by a physician

Desloratadine Teva यूरोपीय संघ - अंग्रेज़ी - EMA (European Medicines Agency)

desloratadine teva

teva b.v - desloratadine - rhinitis, allergic, perennial; rhinitis, allergic, seasonal - antihistamines for systemic use, - desloratadine teva is indicated for the relief of symptoms associated with:allergic rhinitis;urticaria.

DESLORATADINE tablet संयुक्त राज्य - अंग्रेज़ी - NLM (National Library of Medicine)

desloratadine tablet

avkare - desloratadine (unii: fvf865388r) (desloratadine - unii:fvf865388r) - desloratadine 5 mg - desloratadine tablets are indicated for the relief of the nasal and non-nasal symptoms of seasonal allergic rhinitis in patients 12 years of age and older. desloratadine tablets are indicated for the relief of the nasal and non-nasal symptoms of perennial allergic rhinitis in patients 12 years of age and older. desloratadine tablets are indicated for the symptomatic relief of pruritus, reduction in the number of hives, and size of hives, in patients with chronic idiopathic urticaria 12 years of age and older. - desloratadine tablets are contraindicated in patients who are hypersensitive to this medication or to any of its ingredients or to loratadine [see warnings and precautions ( 5.1) and adverse reactions ( 6.2)]. desloratadine tablets are contraindicated in patients who are hypersensitive to this medication or to any of its ingredients or to loratadine [see warnings and precautions ( 5.1) and

DESLORATADINE- desloratadine tablet संयुक्त राज्य - अंग्रेज़ी - NLM (National Library of Medicine)

desloratadine- desloratadine tablet

avpak - desloratadine (unii: fvf865388r) (desloratadine - unii:fvf865388r) - desloratadine 5 mg - desloratadine tablets are indicated for the relief of the nasal and non-nasal symptoms of seasonal allergic rhinitis in patients 12 years of age and older. desloratadine tablets are indicated for the relief of the nasal and non-nasal symptoms of perennial allergic rhinitis in patients 12 years of age and older. desloratadine tablets are indicated for the symptomatic relief of pruritus, reduction in the number of hives, and size of hives, in patients with chronic idiopathic urticaria 12 years of age and older. - desloratadine tablets are contraindicated in patients who are hypersensitive to this medication or to any of its ingredients or to loratadine [see warnings and precautions ( 5.1) and adverse reactions ( 6.2)]. desloratadine tablets are contraindicated in patients who are hypersensitive to this medication or to any of its ingredients or to loratadine [see warnings and precautions ( 5.1) and adverse reactions ( 6.2)]. pregnancy category c: there are no adequate and well-controlled studies in pregnant