Duavive Den europeiske union - spansk - EMA (European Medicines Agency)

duavive

pfizer europe ma eeig - los estrógenos conjugados, bazedoxifeno - post menopausia - estrógenos conjugados y bazedoxifeno - duavive está indicado para:tratamiento de los síntomas de la deficiencia de estrógenos en mujeres posmenopáusicas con un útero (con al menos 12 meses desde la última menstruación), para quien el tratamiento con progestágeno que contienen la terapia no es apropiado. la experiencia en el tratamiento de las mujeres mayores de 65 años es limitada.

CYCLOSPORINE capsule, liquid filled USA - engelsk - NLM (National Library of Medicine)

cyclosporine capsule, liquid filled

physicians total care, inc. - cyclosporine (unii: 83hn0gtj6d) (cyclosporine - unii:83hn0gtj6d) - cyclosporine 100 mg - cyclosporine capsules, usp are indicated for the prophylaxis of organ rejection in kidney, liver, and heart allogeneic transplants. it is always to be used with adrenal corticosteroids. the drug may also be used in the treatment of chronic rejection in patients previously treated with other immunosuppressive agents.    cyclosporine capsules are contraindicated in patients with a hypersensitivity to cyclosporine or to any of the ingredients of the formulation.

CYCLOSPORINE injection, solution USA - engelsk - NLM (National Library of Medicine)

cyclosporine injection, solution

padagis us llc - cyclosporine (unii: 83hn0gtj6d) (cyclosporine - unii:83hn0gtj6d) - cyclosporine 50 mg in 1 ml - cyclosporine is indicated for the prophylaxis of organ rejection in kidney, liver, and heart allogeneic transplants. it is always to be used with adrenal corticosteroids. the drug may also be used in the treatment of chronic rejection in patients previously treated with other immunosuppressive agents. because of the risk of anaphylaxis, cyclosporine injection should be reserved for patients who are unable to take the soft gelatin capsules or oral solution. cyclosporine injection is contraindicated in patients with a hypersensitivity to cyclosporine and/or cremophor® el (polyoxyethylated castor oil).

CYCLOSPORINE- cyclosporine capsule USA - engelsk - NLM (National Library of Medicine)

cyclosporine- cyclosporine capsule

eon labs, inc. - cyclosporine (unii: 83hn0gtj6d) (cyclosporine - unii:83hn0gtj6d) - cyclosporine 25 mg - cyclosporine capsules usp (modified) are indicated for the prophylaxis of organ rejection in kidney, liver, and heart allogeneic transplants. cyclosporine capsules usp (modified) have been used in combination with azathioprine and corticosteroids. cyclosporine capsules usp (modified) are indicated for the treatment of patients with severe active, rheumatoid arthritis where the disease has not adequately responded to methotrexate. cyclosporine capsules usp (modified) can be used in combination with methotrexate in rheumatoid arthritis patients who do not respond adequately to methotrexate alone. cyclosporine capsules usp (modified) are indicated for the treatment of adult, nonimmunocompromised patients with severe (i.e., extensive and/or disabling), recalcitrant, plaque psoriasis who have failed to respond to at least one systemic therapy (e.g., puva, retinoids, or methotrexate) or in patients for whom other systemic therapies are contraindicated, or cannot be tolerated. while rebound rarely occurs, most patie

CYCLOSPORINE capsule, gelatin coated USA - engelsk - NLM (National Library of Medicine)

cyclosporine capsule, gelatin coated

american health packaging - cyclosporine (unii: 83hn0gtj6d) (cyclosporine - unii:83hn0gtj6d) - cyclosporine 25 mg - cyclosporine capsules, usp (non-modified) are indicated for the prophylaxis of organ rejection in kidney, liver, and heart allogeneic transplants. it is always to be used with adrenal corticosteroids. the drug may also be used in the treatment of chronic rejection in patients previously treated with other immunosuppressive agents. cyclosporine capsules are contraindicated in patients with a hypersensitivity to cyclosporine or to any of the ingredients of the formulation.

CYCLOSPORINE MODIFIED- cyclosporine capsule, liquid filled USA - engelsk - NLM (National Library of Medicine)

cyclosporine modified- cyclosporine capsule, liquid filled

teva pharmaceuticals usa, inc. - cyclosporine (unii: 83hn0gtj6d) (cyclosporine - unii:83hn0gtj6d) - cyclosporine 25 mg - cyclosporine capsules usp modified are indicated for the prophylaxis of organ rejection in kidney, liver, and heart allogeneic transplants. cyclosporine capsules usp modified have been used in combination with azathioprine and corticosteroids. cyclosporine capsules usp modified are indicated for the treatment of patients with severe active, rheumatoid arthritis where the disease has not adequately responded to methotrexate. cyclosporine capsules usp modified can be used in combination with methotrexate in rheumatoid arthritis patients who do not respond adequately to methotrexate alone. cyclosporine capsules usp modified are indicated for the treatment of adult, nonimmunocompromised patients with severe (i.e., extensive and/or disabling), recalcitrant, plaque psoriasis who have failed to respond to at least one systemic therapy (e.g., puva, retinoids, or methotrexate) or in patients for whom other systemic therapies are contraindicated, or cannot be tolerated. while rebound rarely occurs, most patients will experience relapse with cyclosporine capsules usp modified as with other therapies upon cessation of treatment. cyclosporine capsules usp modified are contraindicated in patients with a hypersensitivity to cyclosporine or to any of the ingredients of the formulation. rheumatoid arthritis patients with abnormal renal function, uncontrolled hypertension, or malignancies should not receive cyclosporine capsules usp modified. psoriasis patients who are treated with cyclosporine capsules usp modified should not receive concomitant puva or uvb therapy, methotrexate or other immunosuppressive agents, coal tar or radiation therapy. psoriasis patients with abnormal renal function, uncontrolled hypertension, or malignancies should not receive cyclosporine capsules usp modified.

CYCLOSPORINE solution USA - engelsk - NLM (National Library of Medicine)

cyclosporine solution

teva pharmaceuticals usa, inc. - cyclosporine (unii: 83hn0gtj6d) (cyclosporine - unii:83hn0gtj6d) - cyclosporine 100 mg in 1 ml - cyclosporine oral solution usp modified is indicated for the prophylaxis of organ rejection in kidney, liver, and heart allogeneic transplants. cyclosporine oral solution usp modified has been used in combination with azathioprine and corticosteroids. cyclosporine oral solution usp modified is indicated for the treatment of patients with severe active, rheumatoid arthritis where the disease has not adequately responded to methotrexate. cyclosporine oral solution usp modified can be used in combination with methotrexate in rheumatoid arthritis patients who do not respond adequately to methotrexate alone. cyclosporine oral solution usp modified is indicated for the treatment of adult, nonimmunocompromised patients with severe (i.e., extensive and/or disabling), recalcitrant, plaque psoriasis who have failed to respond to at least one systemic therapy (e.g., puva, retinoids, or methotrexate) or in patients for whom other systemic therapies are contraindicated, or cannot be tolerated. while rebound rarely occurs

CYCLOSPORINE capsule, gelatin coated USA - engelsk - NLM (National Library of Medicine)

cyclosporine capsule, gelatin coated

apotex corp. - cyclosporine (unii: 83hn0gtj6d) (cyclosporine - unii:83hn0gtj6d) - cyclosporine 25 mg - cyclosporine capsules, (non-modified) are indicated for the prophylaxis of organ rejection in kidney, liver, and heart allogeneic transplants. it is always to be used with adrenal corticosteroids. the drug may also be used in the treatment of chronic rejection in patients previously treated with other immunosuppressive agents.    cyclosporine capsules are contraindicated in patients with a hypersensitivity to cyclosporine or to any of the ingredients of the formulation.

LOSAZIDE F.C.TAB (50+12,5)MG/TAB Hellas - gresk - Εθνικός Οργανισμός Φαρμάκων

losazide f.c.tab (50+12,5)mg/tab

verisfield ΜΟΝΟΠΡΟΣΩΠΗ Α.Ε. Δ.Τ. verisfield Βύρωνος 8 & Γυθείου, Χαλάνδρι 152 31 210.7475196 - losartan potassium; hydrochlorothiazide - f.c.tab (ΕΠΙΚΑΛΥΜΜΕΝΟ ΜΕ ΛΕΠΤΟ ΥΜΕΝΙΟ ΔΙΣΚΙΟ) - (50+12,5)mg/tab - losartan potassium 50mg; hydrochlorothiazide 12,5mg - losartan and diuretics

LOSAZIDE F.C.TAB (100+12,5)MG/TAB Hellas - gresk - Εθνικός Οργανισμός Φαρμάκων

losazide f.c.tab (100+12,5)mg/tab

verisfield ΜΟΝΟΠΡΟΣΩΠΗ Α.Ε. Δ.Τ. verisfield Βύρωνος 8 & Γυθείου, Χαλάνδρι 152 31 210.7475196 - losartan potassium; hydrochlorothiazide - f.c.tab (ΕΠΙΚΑΛΥΜΜΕΝΟ ΜΕ ΛΕΠΤΟ ΥΜΕΝΙΟ ΔΙΣΚΙΟ) - (100+12,5)mg/tab - losartan potassium 100mg; hydrochlorothiazide 12,5mg - losartan and diuretics