Rituzena (previously Tuxella) European Union - English - EMA (European Medicines Agency)

rituzena (previously tuxella)

celltrion healthcare hungary kft. - rituximab - lymphoma, non-hodgkin; microscopic polyangiitis; leukemia, lymphocytic, chronic, b-cell; wegener granulomatosis - antineoplastic agents - rituzena is indicated in adults for the following indications:non-hodgkin’s lymphoma (nhl)rituzena is indicated for the treatment of previously untreated patients with stage iii iv follicular lymphoma in combination with chemotherapy.rituzena monotherapy is indicated for treatment of patients with stage iii iv follicular lymphoma who are chemo resistant or are in their second or subsequent relapse after chemotherapy.rituzena is indicated for the treatment of patients with cd20 positive diffuse large b cell non hodgkin’s lymphoma in combination with chop (cyclophosphamide, doxorubicin, vincristine, prednisolone) chemotherapy.chronic lymphocytic leukaemia (cll)rituzena in combination with chemotherapy is indicated for the treatment of patients with previously untreated and relapsed/refractory cll. only limited data are available on efficacy and safety for patients previously treated with monoclonal antibodies including rituzenaor patients refractory to previous rituzena plus chemotherapy.granulomatosis with polyangiitis and microscopic polyangiitisrituzena, in combination with glucocorticoids, is indicated for the induction of remission in adult patients with severe, active granulomatosis with polyangiitis (wegener’s) (gpa) and microscopic polyangiitis (mpa).

Rasitrio European Union - English - EMA (European Medicines Agency)

rasitrio

novartis europharm ltd. - aliskiren, amlodipine, hydrochlorothiazide - hypertension - cardiovascular system - rasitrio is indicated for the treatment of essential hypertension as substitution therapy in adult patients whose blood pressure is adequately controlled on the combination of aliskiren, amlodipine and hydrochlorothiazide given concurrently at the same dose level as in the combination.

Zoledronic acid Teva Generics European Union - English - EMA (European Medicines Agency)

zoledronic acid teva generics

teva generics b.v - zoledronic acid monohydrate - osteoporosis; osteitis deformans - bisphosphonates - treatment of osteoporosisin post-menopausal womenin adult menat increased risk of fracture, including those with recent low-trauma hip fracture.treatment of osteoporosis associated with long-term systemic glucocorticoid therapyin post-menopausal womenin adult menat increased risk of fracture.treatment of paget's disease of the bone in adults.

Zoledronic acid Teva Pharma European Union - English - EMA (European Medicines Agency)

zoledronic acid teva pharma

teva b.v. - zoledronic acid - osteoporosis; osteitis deformans; osteoporosis, postmenopausal - drugs for treatment of bone diseases - treatment of osteoporosis: , in post-menopausal women;, in men; , at increased risk of fracture including those with a recent low-trauma hip fracture. treatment of osteoporosis associated with long-term systemic glucocorticoid therapy: , in post-menopausal women;, in men; , at increased risk of fracture. treatment of paget’s disease of the bone in adults.,

Imprida HCT European Union - English - EMA (European Medicines Agency)

imprida hct

novartis europharm ltd. - amlodipine, valsartan, hydrochlorothiazide - hypertension - angiotensin ii antagonists, plain, angiotensin ii antagonists, combinations - treatment of essential hypertension as substitution therapy in adult patients whose blood pressure is adequately controlled on the combination of amlodipine, valsartan and hydrochlorothiazide (hct), taken either as three single-component formulations or as a dual-component and a single-component formulation.

Rasilamlo European Union - English - EMA (European Medicines Agency)

rasilamlo

novartis europharm ltd - aliskiren, amlodipine - hypertension - agents acting on the renin-angiotensin system - rasilamlo is indicated for the treatment of essential hypertension in adult patients whose blood pressure is not adequately controlled with aliskiren or amlodipine used alone.

STONEWALL HERBICIDE Australia - English - APVMA (Australian Pesticides and Veterinary Medicines Authority)

stonewall herbicide

amgrow pty ltd - oryzalin - suspension concentrate - oryzalin anilide/aniline-dinitro active 500.0 g/l - herbicide - almond | amenity plantings | apple | apricot | banana | cherry | conifer - seedling stage | grape | grapefruit | macadamia nut | - barnyard grass or water grass | barnyard or water grass | blackberry nightshade | caltrop or yellow vine | deadnettle | fat hen | fumitory | guinea grass | lovegrass | paddy melon | paradoxa grass | pigeon grass | pigweed spp. | silverleaf nightshade | sow or milk thistle | spiny burrgrass, innocent weed | summer or crab grass | wireweed, knotweed or hogweed | annual lovegrass | annual phalaris | annual pigweed | annual summer grass | barnyard grass | bindy-eye | black nightshade | bullhead | bull's head | caltrop burr | canary grass | cathead | cat's-head | common sowthistle | fallopia aviculare | gentle annie | goat's-head | gooseberry melon | hedgehog grass | henbit deadnettle | munyeroo | nightshade | pigeon weed | pink weed | portulaca oleracea | prickly paddy melon | puncture vine | purple pigeon grass | purslane | setaria gracilis | setaria pallidefusca | setaria porphyrantha | setaria pumila | setaria verticillata | setaria viridis | silver-leaf nightshade | sow thistle | sowthistle | stingless nettle

CETILSAN 3 mg Sugar free lozenges Malta - English - Medicines Authority

cetilsan 3 mg sugar free lozenges

lab. chimico farmaceutico a sella s.r.l via vicenza 67, schio, italy - cetylpyridinium chloride - lozenge - cetylpyridinium chloride 3 mg - throat preparations

Agenerase European Union - English - EMA (European Medicines Agency)

agenerase

glaxo group ltd. - amprenavir - hiv infections - antivirals for systemic use - agenerase, in combination with other antiretroviral agents, is indicated for the treatment of protease inhibitor (pi) experienced hiv-1 infected adults and children above the age of 4 years. agenerase capsules should normally be administered with low dose ritonavir as a pharmacokinetic enhancer of amprenavir (see sections 4.2 and 4.5). the choice of amprenavir should be based on individual viral resistance testing and treatment history of patients (see section 5.1).the benefit of agenerase boosted with ritonavir has not been demonstrated in pi nave patients (see section 5.1)