VOCINTI FILM-COATED TABLET 10MG Singapur - angličtina - HSA (Health Sciences Authority)

vocinti film-coated tablet 10mg

takeda pharmaceuticals (asia pacific) pte. ltd. - vonoprazan fumarate 13.36mg eqv vonoprazan - tablet, film coated - vonoprazan fumarate 13.36mg eqv vonoprazan 10mg

VOCINTI FILM-COATED TABLET 20MG Singapur - angličtina - HSA (Health Sciences Authority)

vocinti film-coated tablet 20mg

takeda pharmaceuticals (asia pacific) pte. ltd. - vonoprazan fumarate 26.72mg eqv vonoprazan - tablet, film coated - vonoprazan fumarate 26.72mg eqv vonoprazan 20mg

PREVACID- lansoprazole capsule, delayed release
PREVACID SOLUTAB- lansoprazole tablet, orally disintegrating, delayed release Spojené štáty - angličtina - NLM (National Library of Medicine)

prevacid- lansoprazole capsule, delayed release prevacid solutab- lansoprazole tablet, orally disintegrating, delayed release

takeda pharmaceuticals america, inc. - lansoprazole (unii: 0k5c5t2qpg) (lansoprazole - unii:0k5c5t2qpg) - lansoprazole 15 mg - prevacid and prevacid solutab are indicated in adults for short-term treatment (for four weeks) for healing and symptom relief of active duodenal ulcer [see clinical studies (14.1)] . triple therapy: prevacid or prevacid solutab/amoxicillin/clarithromycin prevacid or prevacid solutab in combination with amoxicillin plus clarithromycin as triple therapy is indicated in adults for the treatment of patients with h. pylori infection and duodenal ulcer disease (active or one year history of a duodenal ulcer) to eradicate h. pylori. eradication of h. pylori has been shown to reduce the risk of duodenal ulcer recurrence [see clinical studies (14.2)] . please refer to the full prescribing information for amoxicillin and clarithromycin. dual therapy: prevacid or prevacid solutab/amoxicillin prevacid or prevacid solutab in combination with amoxicillin as dual therapy is indicated in adults for the treatment of patients with h. pylori infection and duodenal ulcer disease (active or one year history of a duodenal ulc

NINLARO ixazomib (as citrate) 2.3mg capsule blister pack Austrália - angličtina - Department of Health (Therapeutic Goods Administration)

ninlaro ixazomib (as citrate) 2.3mg capsule blister pack

takeda pharmaceuticals australia pty ltd - ixazomib citrate, quantity: 3.29 mg (equivalent: ixazomib, qty 2.3 mg) - capsule - excipient ingredients: microcrystalline cellulose; purified talc; magnesium stearate; gelatin; titanium dioxide; iron oxide red; propylene glycol; ethanol; butan-1-ol; isopropyl alcohol; purified water; shellac; strong ammonia solution; iron oxide black; potassium hydroxide - ninlaro is indicated in combination with lenalidomide and dexamethasone for the treatment of patients with multiple myeloma who have received at least one prior therapy.

NINLARO ixazomib (as citrate) 3mg capsule blister pack Austrália - angličtina - Department of Health (Therapeutic Goods Administration)

ninlaro ixazomib (as citrate) 3mg capsule blister pack

takeda pharmaceuticals australia pty ltd - ixazomib citrate, quantity: 4.3 mg (equivalent: ixazomib, qty 3 mg) - capsule - excipient ingredients: microcrystalline cellulose; purified talc; magnesium stearate; gelatin; titanium dioxide; iron oxide black; propylene glycol; ethanol; butan-1-ol; isopropyl alcohol; purified water; shellac; strong ammonia solution; potassium hydroxide - ninlaro is indicated in combination with lenalidomide and dexamethasone for the treatment of patients with multiple myeloma who have received at least one prior therapy.

NINLARO ixazomib (as citrate) 4mg capsule blister pack Austrália - angličtina - Department of Health (Therapeutic Goods Administration)

ninlaro ixazomib (as citrate) 4mg capsule blister pack

takeda pharmaceuticals australia pty ltd - ixazomib citrate, quantity: 5.7 mg (equivalent: ixazomib, qty 4 mg) - capsule - excipient ingredients: microcrystalline cellulose; purified talc; magnesium stearate; gelatin; titanium dioxide; iron oxide yellow; iron oxide red; propylene glycol; ethanol; butan-1-ol; isopropyl alcohol; purified water; shellac; strong ammonia solution; iron oxide black; potassium hydroxide - ninlaro is indicated in combination with lenalidomide and dexamethasone for the treatment of patients with multiple myeloma who have received at least one prior therapy.

CARBATROL- carbamazepine capsule, extended release Spojené štáty - angličtina - NLM (National Library of Medicine)

carbatrol- carbamazepine capsule, extended release

takeda pharmaceuticals america, inc. - carbamazepine (unii: 33cm23913m) (carbamazepine - unii:33cm23913m) - carbamazepine 100 mg - carbatrol is indicated for use as an anticonvulsant drug. evidence supporting efficacy of carbamazepine as an anticonvulsant was derived from active drug-controlled studies that enrolled patients with the following seizure types:      - partial seizures with complex symptomatology (psychomotor, temporal lobe). patients with these seizures appear to show greater improvements than those with other types. - generalized tonic-clonic seizures (grand mal). - mixed seizure patterns which include the above, or other partial or generalized seizures. absence seizures (petit mal) do not appear to be controlled by carbamazepine (see precautions, general ). carbatrol is indicated in the treatment of the pain associated with true trigeminal neuralgia. beneficial results have also been reported in glossopharyngeal neuralgia. this drug is not a simple analgesic and should not be used for the relief of trivial aches or pains. carbamazepine should not be used in patients with a history of previous bone marrow depression, hyper

DEXILANT 30 MG Izrael - angličtina - Ministry of Health

dexilant 30 mg

takeda israel ltd - dexlansoprazole - modified release capsules - dexlansoprazole 30 mg - dexlansoprazole - dexilant 30 is indicated in adults and in adolescents aged 12 to 17 years for the following:• maintenance of healed erosive reflux oesophagitis and maintenance of relief of heartburn• short-term treatment of heartburn and acid regurgitation associated with symptomatic non-erosive gastro-oesophageal reflux disease (gord).

DEXILANT 60 MG Izrael - angličtina - Ministry of Health

dexilant 60 mg

takeda israel ltd - dexlansoprazole - modified release capsules - dexlansoprazole 60 mg - dexlansoprazole - dexilant 60 is indicated in adults and in adolescents aged 12 to 17 years for the following:• treatment of erosive reflux oesophagitis

TAKHZYRO lanadelumab 300 mg/2 mL solution for injection pre-filled syringe Austrália - angličtina - Department of Health (Therapeutic Goods Administration)

takhzyro lanadelumab 300 mg/2 ml solution for injection pre-filled syringe

takeda pharmaceuticals australia pty ltd - lanadelumab, quantity: 300 mg - injection, solution - excipient ingredients: citric acid monohydrate; water for injections; dibasic sodium phosphate dihydrate; polysorbate 80; histidine; sodium chloride - takhzyro is indicated for routine prevention of recurrent attacks of hereditary angioedema (c1-esterase-inhibitor deficiency or dysfunction) in patients aged 12 years and older.