ABILIFY- aripiprazole tablet
ABILIFY- aripiprazole solution
ABILIFY- aripiprazole tablet, orally disintegrating
ABILIFY- arip Estados Unidos - inglés - 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

OCUFEN flurbiprofen sodium dihydrate 0.03% eye drops Australia - inglés - Department of Health (Therapeutic Goods Administration)

ocufen flurbiprofen sodium dihydrate 0.03% eye drops

abbvie pty ltd - flurbiprofen sodium dihydrate, quantity: 0.3 mg/ml - eye drops, solution - excipient ingredients: polyvinyl alcohol; potassium chloride; sodium chloride; sodium citrate dihydrate; citric acid monohydrate; disodium edetate; thiomersal; sodium hydroxide; hydrochloric acid; purified water - for the inhibition of intraoperative miosis.

Biphozyl Solution for haemodialysis / haemofiltration Irlanda - inglés - HPRA (Health Products Regulatory Authority)

biphozyl solution for haemodialysis / haemofiltration

baxter holding b.v. - magnesium chloride hexahydrate; sodium chloride; sodium hydrogen carbonate; potassium chloride; disodium phosphate dihydrate - solution for haemodialysis/haemofiltration - hemofiltrates

UNIQUE PH SOLUTION Canadá - inglés - Health Canada

unique ph solution

alcon canada inc - disodium edetate; polyquaternium 1 - solution - 0.01%; 0.0011% - disodium edetate 0.01%; polyquaternium 1 0.0011% - contact lens solutions

Potassium dihydrogen phosphate 1.701% / Potassium hydroxide 0.14% (total potassium 7.5mmol/50ml) / Disodium phosphate dihydrate 667.5mg solution for infusion 50ml pre-filled syringes Reino Unido - inglés - MHRA (Medicines & Healthcare Products Regulatory Agency)

potassium dihydrogen phosphate 1.701% / potassium hydroxide 0.14% (total potassium 7.5mmol/50ml) / disodium phosphate dihydrate 667.5mg solution for infusion 50ml pre-filled syringes

total potassium 7.5mmol/50ml) / disodium phosphate dihydrate 667.5mg solution for infusion 50ml pre-filled syringes (special order - disodium phosphate dihydrate; potassium hydroxide; potassium dihydrogen phosphate - solution for infusion - 13.35mg/1ml ; 1.4mg/1ml ; 17.01mg/1ml

DISODIUM TILUDRONATE Australia - inglés - APVMA (Australian Pesticides and Veterinary Medicines Authority)

disodium tiludronate

ceva animal health pty ltd - disodium tiludronate - unknown - disodium tiludronate biphosphonate active 0.0 - active constituent

DISODIUM METHYLARSONATE Australia - inglés - APVMA (Australian Pesticides and Veterinary Medicines Authority)

disodium methylarsonate

ancom australia pty. limited - disodium methylarsonate = dsma - unknown - disodium methylarsonate = dsma mineral-arsenic active 0.0 - active constituent