Panama - English - Ministerio de Salud (Dirección Nacional de Farmacia Y Drogas)

laboratorios vijosa s.a. de c.v. - extracto de echinacea (echinacea purpurea) (hierba) - extracto de echinacea (echinacea purpurea) (hierba)....177.76 mg.

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

stat rx usa - alfuzosin hydrochloride (unii: 75046a1xtn) (alfuzosin - unii:90347ytw5f) - alfuzosin hydrochloride 10 mg - uroxatral is indicated for the treatment of signs and symptoms of benign prostatic hyperplasia. uroxatral is not indicated for the treatment of hypertension. the recommended dosage is one 10 mg uroxatral (alfuzosin hcl) extended-release tablet once daily. the extent of absorption of uroxatral is 50% lower under fasting conditions. therefore, uroxatral should be taken immediately after the same meal each day. the tablets should not be chewed or crushed. uroxatral (alfuzosin hcl) extended-release tablet 10 mg is available as a round, three-layer tablet: one white layer between two yellow layers, debossed with x10. uroxatral is contraindicated for use in patients with moderate or severe hepatic impairment (childs-pugh categories b and c), since alfuzosin blood levels are increased in these patients. [see clinical pharmacology (12.3)]. uroxatral is contraindicated for use with potent cyp3a4 inhibitors such as ketoconazole, itraconazole, and ritonavir, since alfuzosin blood levels are increased. [see

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

physicians total care, inc. - alfuzosin hydrochloride (unii: 75046a1xtn) (alfuzosin - unii:90347ytw5f) - alfuzosin hydrochloride 10 mg - uroxatral is indicated for the treatment of signs and symptoms of benign prostatic hyperplasia. uroxatral is not indicated for the treatment of hypertension. uroxatral is not indicated for use in the pediatric population. uroxatral is contraindicated for use: - in patients with moderate or severe hepatic impairment (childs-pugh categories b and c), since alfuzosin blood levels are increased in these patients [see use in specific populations (8.7) and clinical pharmacology (12.3)]. - with potent cyp3a4 inhibitors such as ketoconazole, itraconazole, and ritonavir, since alfuzosin blood levels are increased [see drug interactions (7.1) and clinical pharmacology (12.3)] . - in patients with known hypersensitivity, such as urticaria and angioedema, to alfuzosin hydrochloride or any component of uroxatral tablets [see adverse reactions (6.2)] pregnancy category b. uroxatral is not indicated for use in women, and there are no studies of alfuzosin in pregnant women alfuzosin was not teratogenic, embryotoxic or

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

concordia pharmaceuticals inc. - alfuzosin hydrochloride (unii: 75046a1xtn) (alfuzosin - unii:90347ytw5f) - alfuzosin hydrochloride 10 mg - uroxatral is indicated for the treatment of signs and symptoms of benign prostatic hyperplasia. uroxatral is not indicated for the treatment of hypertension. uroxatral is not indicated for use in the pediatric population. uroxatral is contraindicated for use: - in patients with moderate or severe hepatic impairment (childs-pugh categories b and c), since alfuzosin blood levels are increased in these patients [see use in specific populations (8.7) and clinical pharmacology (12.3)]. - with potent cyp3a4 inhibitors such as ketoconazole, itraconazole, and ritonavir, since alfuzosin blood levels are increased [see drug interactions (7.1) and clinical pharmacology (12.3)] . - in patients with known hypersensitivity, such as urticaria and angioedema, to alfuzosin hydrochloride or any component of uroxatral tablets [see adverse reactions (6.2)] risk summary uroxatral is not indicated for use in women. there are no adequate data on the developmental risk associated with use of uroxatral in pregnant women. b

Israel - English - Ministry of Health

trupharm marketing 1985 ltd. - food extract - solution for injection - food extract - allergen extracts - skin testing and immunotherapy.

New Zealand - English - Medsafe (Medicines Safety Authority)

stallergenes greer new zealand ltd - allergen extracts 0.1 ir/ml (dermatophagoides farinae body extract); allergen extracts 1 ir/ml (dermatophagoides farinae body extract); allergen extracts 10 ir/ml (dermatophagoides farinae body extract) - solution for injection - active: allergen extracts 0.1 ir/ml (dermatophagoides farinae body extract) excipient: aluminium hydroxide gel mannitol phenol sodium chloride water active: allergen extracts 1 ir/ml (dermatophagoides farinae body extract) excipient: aluminium hydroxide gel mannitol phenol sodium chloride water active: allergen extracts 10 ir/ml (dermatophagoides farinae body extract) excipient: aluminium hydroxide gel mannitol phenol sodium chloride water

New Zealand - English - Medsafe (Medicines Safety Authority)

stallergenes greer new zealand ltd - allergen extracts 10 ir/ml (dermatophagoides farinae body extract) - solution for injection - 10 ir/ml - active: allergen extracts 10 ir/ml (dermatophagoides farinae body extract) excipient: aluminium hydroxide gel mannitol phenol sodium chloride water

New Zealand - English - Medsafe (Medicines Safety Authority)

stallergenes greer new zealand ltd - allergen extracts 0.1 ir/ml (betula alba pollen extract); allergen extracts 1 ir/ml (betula alba pollen extract); allergen extracts 10 ir/ml (betula alba pollen extract) - solution for injection - active: allergen extracts 0.1 ir/ml (betula alba pollen extract) excipient: aluminium hydroxide gel mannitol phenol sodium chloride water active: allergen extracts 1 ir/ml (betula alba pollen extract) excipient: aluminium hydroxide gel mannitol phenol sodium chloride water active: allergen extracts 10 ir/ml (betula alba pollen extract) excipient: aluminium hydroxide gel mannitol phenol sodium chloride water

New Zealand - English - Medsafe (Medicines Safety Authority)

stallergenes greer new zealand ltd - allergen extracts 10 ir/ml (betula alba pollen extract) - solution for injection - 10 ir/ml - active: allergen extracts 10 ir/ml (betula alba pollen extract) excipient: aluminium hydroxide gel mannitol phenol sodium chloride water

New Zealand - English - Medsafe (Medicines Safety Authority)

stallergenes greer new zealand ltd - allergen extracts 0.1 ir/ml (feline epithelium extract); allergen extracts 1 ir/ml (feline epithelium extract); allergen extracts 10 ir/ml (feline epithelium extract) - solution for injection - active: allergen extracts 0.1 ir/ml (feline epithelium extract) excipient: aluminium hydroxide gel mannitol phenol sodium chloride water active: allergen extracts 1 ir/ml (feline epithelium extract) excipient: aluminium hydroxide gel mannitol phenol sodium chloride water active: allergen extracts 10 ir/ml (feline epithelium extract) excipient: aluminium hydroxide gel mannitol phenol sodium chloride water