LEVOCETIRIZINE DIHYDROCHLORIDE tablet, film coated ABD - İngilizce - NLM (National Library of Medicine)

levocetirizine dihydrochloride tablet, film coated

aidarex pharmaceuticals llc - levocetirizine dihydrochloride (unii: sod6a38aga) (levocetirizine - unii:6u5ea9rt2o) - levocetirizine dihydrochloride 5 mg - levocetirizine dihydrochloride tablets are indicated for the treatment of the uncomplicated skin manifestations of chronic idiopathic urticaria in adults and children 6 years of age and older.   pediatric use information in pediatric patients (age 6 months to 5 years) is approved for ucb inc.’s levocetirizine dihydrochloride drug product labeling. however, due to ucb inc.’s marketing exclusivity rights; this drug product is not labeled for such use in those pediatric patients. the use of levocetirizine dihydrochloride tablet is contraindicated in: patients with known hypersensitivity to levocetirizine or any of the ingredients of levocetirizine dihydrochloride tablet, or to cetirizine. observed reactions range from urticaria to anaphylaxis [see adverse reactions (6.2)]. patients with end-stage renal disease (clcr < 10 ml/min) and patients undergoing hemodialysis. children 6 months to 11 years of age with impaired renal function pregnancy category b   there are no adequate and well-controlled studies i

LEVOCETIRIZINE DIHYDROCHLORIDE tablet, film coated ABD - İngilizce - NLM (National Library of Medicine)

levocetirizine dihydrochloride tablet, film coated

dispensing solutions, inc. - levocetirizine dihydrochloride (unii: sod6a38aga) (levocetirizine - unii:6u5ea9rt2o) - levocetirizine dihydrochloride 5 mg - levocetirizine dihydrochloride tablets are indicated for the treatment of the uncomplicated skin manifestations of chronic idiopathic urticaria in adults and children 6 years of age and older. pediatric use information in pediatric patients (age 6 months to 5 years) is approved for ucb inc.'s levocetirizine dihydrochloride drug product labeling. however, due to ucb inc.'s marketing exclusivity rights; this drug product is not labeled for such use in those pediatric patients. the use of levocetirizine dihydrochloride tablets is contraindicated in: patients with known hypersensitivity to levocetirizine or any of the ingredients of levocetirizine dihydrochloride tablets, or to cetirizine. observed reactions range from urticaria to anaphylaxis [see adverse reactions ( 6.2) ]. patients with end-stage renal disease (clcr < 10 ml/min) and patients undergoing hemodialysis. children 6 months to 11 years of age with impaired renal function. pregnancy category b there are no adequate and well-controlled studies in preg

LEVOCETIRIZINE DIHYDROCHLORIDE tablet ABD - İngilizce - NLM (National Library of Medicine)

levocetirizine dihydrochloride tablet

proficient rx lp - levocetirizine dihydrochloride (unii: sod6a38aga) (levocetirizine - unii:6u5ea9rt2o) - levocetirizine dihydrochloride 5 mg - levocetirizine dihydrochloride tablets are indicated for the relief of symptoms associated with perennial allergic rhinitis in children 6 months to 2 years of age. levocetirizine dihydrochloride tablets are indicated for the treatment of the uncomplicated skin manifestations of chronic idiopathic urticaria in adults and children 6 months of age and older. the use of levocetirizine dihydrochloride tablets is contraindicated in: patients with known hypersensitivity to levocetirizine or any of the ingredients of levocetirizine dihydrochloride tablets, or to cetirizine. observed reactions range from urticaria to anaphylaxis [see adverse reactions (6.2) ]. patients with end-stage renal disease (clcr < 10 ml/min) and patients undergoing hemodialysis. children 6 months to 11 years of age with impaired renal function. pregnancy category b there are no adequate and well-controlled studies in pregnant women. because animal reproduction studies are not always predictive of human response, levocetirizine dihydrochloride

LEVOCETIRIZINE DIHYDROCHLORIDE tablet ABD - İngilizce - NLM (National Library of Medicine)

levocetirizine dihydrochloride tablet

remedyrepack inc. - levocetirizine dihydrochloride (unii: sod6a38aga) (levocetirizine - unii:6u5ea9rt2o) - levocetirizine dihydrochloride 5 mg - levocetirizine dihydrochloride tablets are indicated for the treatment of the uncomplicated skin manifestations of chronic idiopathic urticaria in adults and children 6 years of age and older. the use of levocetirizine dihydrochloride tablets are contraindicated in: patients with known hypersensitivity to levocetirizine or any of the ingredients of levocetirizine dihydrochloride tablets, or to cetirizine. observed reactions range from urticaria to anaphylaxis [ see adverse reactions ( 6.2) ]. patients with end-stage renal disease (cl cr <10 ml/min) and patients undergoing hemodialysis.  children 6 months to 11 years of age with impaired renal function risk summary available data from published literature and postmarketing experience with levocetirizine use in pregnant women are insufficient to identify any drug-associated risks of miscarriage, birth defects, or adverse maternal or fetal outcomes. in animal reproduction studies, there was no evid

LEVOCETIRIZINE DIHYDROCHLORIDE tablet ABD - İngilizce - NLM (National Library of Medicine)

levocetirizine dihydrochloride tablet

pd-rx pharmaceuticals, inc. - levocetirizine dihydrochloride (unii: sod6a38aga) (levocetirizine - unii:6u5ea9rt2o) - levocetirizine dihydrochloride 5 mg - levocetirizine dihydrochloride tablets are indicated for the relief of symptoms associated with perennial allergic rhinitis in children 6 months to 2 years of age. levocetirizine dihydrochloride tablets are indicated for the treatment of the uncomplicated skin manifestations of chronic idiopathic urticaria in adults and children 6 months of age and older. the use of levocetirizine dihydrochloride tablets is contraindicated in: patients with known hypersensitivity to levocetirizine or any of the ingredients of levocetirizine dihydrochloride tablets, or to cetirizine. observed reactions range from urticaria to anaphylaxis [see adverse reactions (6.2) ]. patients with end-stage renal disease (cl cr < 10 ml/min) and patients undergoing hemodialysis. children 6 months to 11 years of age with impaired renal function. risk summary available data from published literature and postmarketing experience with levocetirizine use in pregnant women are insufficient to identify any drug-associat

LEVOCETIRIZINE DIHYDROCHLORIDE tablet, film coated ABD - İngilizce - NLM (National Library of Medicine)

levocetirizine dihydrochloride tablet, film coated

carlsbad technology, inc. - levocetirizine dihydrochloride (unii: sod6a38aga) (levocetirizine - unii:6u5ea9rt2o) - levocetirizine dihydrochloride 5 mg - levocetirizine dihydrochloride tablets are indicated for the relief of symptoms associated with seasonal allergic rhinitis in adults and children 6 years of age and older. levocetirizine dihydrochloride tablets are indicated for the relief of symptoms associated with perennial allergic rhinitis in adults and children 6 years of age and older. levocetirizine dihydrochloride tablets are indicated for the treatment of the uncomplicated skin manifestations of chronic idiopathic urticaria in adults and children 6 years of age and older. the use of levocetirizine dihydrochloride tablets is contraindicated in: patients with known hypersensitivity to levocetirizine or any of the ingredients of levocetirizine dihydrochloride tablets, or to cetirizine. observed reactions range from urticaria to anaphylaxis [see adverse reactions ( 6.2) ]. patients with end-stage renal disease (cl cr < 10 ml/min)

CHEMISTS' OWN CHILDREN'S C-ZINE ANTI ALLERGY ORAL LIQUID cetirizine hydrochloride 1 mg/mL oral liquid bottle Avustralya - İngilizce - Department of Health (Therapeutic Goods Administration)

chemists' own children's c-zine anti allergy oral liquid cetirizine hydrochloride 1 mg/ml oral liquid bottle

arrotex pharmaceuticals pty ltd - cetirizine hydrochloride, quantity: 1 mg/ml - oral liquid - excipient ingredients: glacial acetic acid; glycerol; propylene glycol; purified water; saccharin sodium; sodium acetate trihydrate; sodium methyl hydroxybenzoate; sodium propyl hydroxybenzoate; sorbitol solution (70 per cent) (non-crystallising); flavour - seasonal allergic rhinitis: cetirizine is indicated for the relief of symptoms associated with season allergic rhinitis (hayfever) in adults and children aged 2-12 years. symptoms treated effectively include sneezing, rhinorrhoea, post-nasal discharge, nasal pruritus, occular pruritus and tearing and redness of the eyes. ,perennial allergic rhinitis: cetirizine is indicated for the relief of,symptoms associated with perennial allergic rhinitis in adults and children aged 2-12 years. symptoms treated effectively include sneezing, rhinorrhoea, post-nasal discharge, nasal pruritus, ocular pruritus and tearing. ,chronic idiopathic urticaria: cetirizine is indicated for the treatment of the uncomplicated skin manifestations of chronic idiopathic urticaria in adults and children aged 2-12 years. it significantly reduces the occurrence, severity and duration of hives and markedly reduces pruritus.

ZYRTEC Cetirizine hydrochloride 5mg/5mL oral liquid bottle Avustralya - İngilizce - Department of Health (Therapeutic Goods Administration)

zyrtec cetirizine hydrochloride 5mg/5ml oral liquid bottle

johnson & johnson pacific pty ltd - cetirizine hydrochloride, quantity: 1 mg/ml - oral liquid - excipient ingredients: sodium acetate; saccharin sodium; glacial acetic acid; propylene glycol; sorbitol solution (70 per cent) (non-crystallising); propyl hydroxybenzoate; glycerol; purified water; methyl hydroxybenzoate; flavour - seasonal allergic rhinitis: cetirizine is indicated for the relief of symptoms associated with seasonal allergic rhinitis (hay fever) in adults and children aged 1-12 years. symptoms treated effectively include sneezing, rhinorrhoea, post-nasal discharge, nasal pruritus, ocular pruritus and tearing and redness of the eyes. perennial allergic rhinitis: cetirizine is indicated for the relief of symptoms associated with perennial allergic rhinitis in adults and children aged 1-12 years. symptoms treated effectively include sneezing, rhinorrhoea, post-nasal discharge, nasal pruritus, ocular pruritus and tearing. chronic idiopathic urticaria: cetirizine is indicated for the treatment of the uncomplicated skin manifestations of chronic idiopathic urticaria in adults and children aged 1-12 years. it significantly reduces the occurence, severity and duration of hives and markedly reduces pruritus. as with other antihistamines, patients should be advised to seek medical advice about the possibility that their urticaria is associated with ingestion of certain foods.

ZYRTEC Cetirizine hydrochloride 10mg/mL oral liquid bottle Avustralya - İngilizce - Department of Health (Therapeutic Goods Administration)

zyrtec cetirizine hydrochloride 10mg/ml oral liquid bottle

johnson & johnson pacific pty ltd - cetirizine hydrochloride, quantity: 10 mg/ml - oral liquid - excipient ingredients: propyl hydroxybenzoate; sodium acetate; glycerol; saccharin sodium; propylene glycol; glacial acetic acid; methyl hydroxybenzoate; purified water - seasonal allergic rhinitis: cetirizine is indicated for the relief of symptoms associated with seasonal allergic rhinitis (hay fever) in adults and children aged 1-12 years. symptoms treated effectively include sneezing, rhinorrhoea, post-nasal discharge, nasal pruritus, orcular pruritus and tearing and redness of the eyes. perennial allergic rhinitis: cetirizine is indicated for the relief of symptoms associated with perennial allergic rhinitis in adults and children aged 1-12 years. symptoms treated effectively include sneezing, rhinorrhoea, post-nasal discharge, nasal pruritus, ocular pruritus and tearing. chronic idiopathic urticaria: cetirizine is indicated for the treatment of the uncomplicated skin manifestations of chronic idiopathic urticaria in adults and children aged 1-12 years. it significantly reduces the occurence, severity and duration of hives and markedly reduces pruritus. as with other antihistamines, patients should be advised to seek medical advice about the possibility that their urticaria is associated with ingestion of certain foods.

TRUST FOR KIDS CETIRIZINE ANTIHISTAMINE LIQUID cetirizine hydrochloride 5mg/5mL oral solution bottle Avustralya - İngilizce - Department of Health (Therapeutic Goods Administration)

trust for kids cetirizine antihistamine liquid cetirizine hydrochloride 5mg/5ml oral solution bottle

pharmacor pty ltd - cetirizine hydrochloride, quantity: 1 mg/ml - oral liquid, solution - excipient ingredients: sorbitol solution (70 per cent) (non-crystallising); saccharin sodium; purified water; methyl hydroxybenzoate; propyl hydroxybenzoate; sodium acetate; propylene glycol; glycerol; glacial acetic acid; flavour - seasonal allergic rhinitis: cetirizine is indicated for the relief of symptoms associated with seasonal allergic rhinitis (hay fever) in adults and children 1-12 years. symptoms treated effectively include sneezing, rhinorrhoea, post-nasal discharge, nasal pruritus, ocular pruritus and tearing and redness of the eyes. ,perennial allergic rhinitis: cetirizine is indicated for the relief of symptoms associated with perennial allergic rhinitis in adults and children aged 1-12 years. symptoms treated effectively include sneezing, rhinorrhoea, post-nasal discharge, nasal pruritus, ocular pruritus and tearing. ,chronic idiopathic urticaria: cetirizine is indicated for the treatment of the uncomplicated skin manifestations of chronic idiopathic urticaria in adults and children aged 1-12 years. it significantly reduces the occurrence, severity and duration of hives and markedly reduces pruritus. as with other antihistamines, patients should be advised to seek medical advice about the possibility that their urticaria is associated with ingestion of certain foods.