ABILIFY- aripiprazole tablet
ABILIFY- aripiprazole solution
ABILIFY- aripiprazole tablet, orally disintegrating
ABILIFY- arip United States - English - NLM (National Library of Medicine)

abilify- aripiprazole tablet abilify- aripiprazole solution abilify- aripiprazole tablet, orally disintegrating abilify- arip

otsuka america pharmaceutical, inc. - aripiprazole (unii: 82vfr53i78) (aripiprazole - unii:82vfr53i78) - aripiprazole 2 mg - abilify (aripiprazole) oral tablets, orally-disintegrating tablets, and oral solution are indicated for the treatment of: - schizophrenia - acute treatment of manic and mixed episodes associated with bipolar i disorder - adjunctive treatment of major depressive disorder - irritability associated with autistic disorder - treatment of tourette's disorder abilify injection is indicated for the treatment of: - agitation associated with schizophrenia or bipolar mania abilify is contraindicated in patients with a history of a hypersensitivity reaction to aripiprazole. reactions have ranged from pruritus/urticaria to anaphylaxis [see adverse reactions (6.2)] . pregnancy exposure registry there is a pregnancy exposure registry that monitors pregnancy outcomes in women exposed to atypical antipsychotics, including abilify, during pregnancy. healthcare providers are encouraged to register patients by contacting the national pregnancy registry for atypical antipsychotics at 1-866-961-2388 or visit http://womensmentalhea

BIOLOGICAL THERAPIES DISODIUM EDETATE SOLUTION 3g/100mL injection vial Australia - English - Department of Health (Therapeutic Goods Administration)

biological therapies disodium edetate solution 3g/100ml injection vial

orthomolecular medisearch laboratories pty ltd trading as biological therapies - disodium edetate, quantity: 30 mg/ml - injection, concentrated - excipient ingredients: water for injections - this product accepted for registration/listing as 'currently supplied' at the time of commencement of the act. indications held in artg paper records. (old code) 1. disodium edetate is particularly effective in treating lead accumulation and lead poisoning. this is especially so where there is a concomitant hypercalcaemic problem (refer "indications (2)"). however it must be noted that disodium edetate is equally effective with calcium disodium edetate in removing heavy metals, even in the absence of hypercalcaemia. for patients with elevated serum calcium or hypermobility of their body pools of calcium where there may be transiently or prolonged raised serum calcium (see "indications (2)"), the edta of choice for removing heavy metals may be disodium edetate. there are no recognised safe limits for lead intoxication. lead poisoning may occur by ingestion or inhalation of lead dust or fumes. poisoning is manifested by a metallic taste, anorexia, irritability, apathy, abdominal colic, vomiting, diarrhoea, cons

Cleansil New Zealand - English - Medsafe (Medicines Safety Authority)

cleansil

bausch & lomb (nz) ltd - disodium edetate dihydrate 0.01%; thiomersal 0.004% - contact lens solution - 0.01%/0.004% - active: disodium edetate dihydrate 0.01% thiomersal 0.004%

Crystal New Zealand - English - Medsafe (Medicines Safety Authority)

crystal

morgan and hall ltd - disodium edetate dihydrate 0.01%{relative}; poloxamer 1.3%{relative}; thiomersal 0.004%{relative} - contact lens solution - 0.01/1.3/0.004%w/v - active: disodium edetate dihydrate 0.01%{relative} poloxamer 1.3%{relative} thiomersal 0.004%{relative}

Flexigel New Zealand - English - Medsafe (Medicines Safety Authority)

flexigel

morgan and hall ltd - disodium edetate dihydrate 0.01%{relative}; miranol 2mca 0.2%{relative}; thiomersal 0.004%{relative} - contact lens solution - 0.01%/0.2%/0.004% - active: disodium edetate dihydrate 0.01%{relative} miranol 2mca 0.2%{relative} thiomersal 0.004%{relative}

Sil New Zealand - English - Medsafe (Medicines Safety Authority)

sil

bausch & lomb (nz) ltd - disodium edetate dihydrate 0.01%; thiomersal 0.004% - contact lens solution - 0.01%/0.004% - active: disodium edetate dihydrate 0.01% thiomersal 0.004%

BIOLOGICAL THERAPIES DISODIUM EDETATE 3g + SODIUM ASCORBATE 5g 50mL injection vial Australia - English - Department of Health (Therapeutic Goods Administration)

biological therapies disodium edetate 3g + sodium ascorbate 5g 50ml injection vial

orthomolecular medisearch laboratories pty ltd trading as biological therapies - sodium ascorbate, quantity: 100 mg/ml; disodium edetate, quantity: 60 mg/ml - injection, concentrated - excipient ingredients: water for injections; sodium hydroxide - 1. disodium edetate is particularly effective in treating lead accumulation and lead poisoning. this is especially so where there is a concomitant hypercalcaemic problem (refer "indications (2)"). however it must be noted that disodium edetate is equally effective with calcium disodium edetate in removing heavy metals, even in the absence of hypercalcaemia. for patients with elevated serum calcium or hypermobility of their body pools of calcium where there may be transiently or prolonged raised serum calcium (see "indications (2)"), the edta of choice for removing heavy metals may be disodium edetate. there are no recognised safe limits for lead intoxication. lead poisoning may occur by ingestion or inhalation of lead dust or fumes. poisoning is manifested by a metallic taste, anorexia, irritability, apathy, abdominal colic, vomiting, diarrhoea, constipation, headache, leg cramps, black stools, oliguria, stupor, convulsions, palsies and coma. chronic lead poisoning causes variable involvement of the central n

Allergan Preserved Saline New Zealand - English - Medsafe (Medicines Safety Authority)

allergan preserved saline

amo australia pty limited (nz) - disodium edetate dihydrate 0.01%; sodium chloride 0.9%;  ;  ; thiomersal 0.00115% - contact lens solution - active: disodium edetate dihydrate 0.01% sodium chloride 0.9%     thiomersal 0.00115%

Hydrocare Preserved Saline New Zealand - English - Medsafe (Medicines Safety Authority)

hydrocare preserved saline

amo australia pty limited (nz) - disodium edetate dihydrate 0.01%; sodium chloride 0.9%;  ;  ; sodium polymetaphosphate 0.2%;  ; thiomersal 0.001% - contact lens solution - active: disodium edetate dihydrate 0.01% sodium chloride 0.9%     sodium polymetaphosphate 0.2%   thiomersal 0.001%

Soflet New Zealand - English - Medsafe (Medicines Safety Authority)

soflet

morgan and hall ltd - dibasic sodium phosphate 0.018%{relative}; disodium edetate dihydrate 0.01%{relative}; monobasic sodium phosphate dihydrate 0.33%{relative}; sodium chloride 0.827%{relative}; thiomersal 0.002%{relative} - contact lens solution - active: dibasic sodium phosphate 0.018%{relative} disodium edetate dihydrate 0.01%{relative} monobasic sodium phosphate dihydrate 0.33%{relative} sodium chloride 0.827%{relative} thiomersal 0.002%{relative}