AZATHIOPRINE tablet Bandaríkin - enska - NLM (National Library of Medicine)

azathioprine tablet

glenmark pharmaceuticals, inc - azathioprine (unii: mrk240iy2l) (azathioprine - unii:mrk240iy2l) - azathioprine 50 mg - indications and usage: azathioprine tablets are indicated as an adjunct for the prevention of rejection in renal homotransplantation. it is also indicated for the management of active rheumatoid arthritis to reduce signs and symptoms. renal homotransplantation: azathioprine tablets are indicated as an adjunct for the prevention of rejection in renal homotransplantation. experience with over 16,000 transplants shows a 5-year patient survival of 35% to 55%, but this is dependent on donor, match for hla antigens, anti-donor or anti b-cell alloantigen antibody, and other variables. the effect of azathioprine tablets on these variables has not been tested in controlled trials. rheumatoid arthritis: azathioprine istablets are indicated for the treatment of active rheumatoid arthritis (ra) to reduce signs and symptoms. aspirin, non-steroidal anti-inflammatory drugs and/or low dose glucocorticoids may be continued during treatment with azathioprine tablets. the combined use of azathioprine tablets with disease modifying anti-rheumatic drugs (dmards) has not been studied for either added benefit or unexpected adverse effects. the use of azathioprine with these agents cannot be recommended. contraindications: azathioprine tablets should not be given to patients who have shown hypersensitivity to the drug. azathioprine tablets should not be used for treating rheumatoid arthritis in pregnant women. patients with rheumatoid arthritis previously treated with alkylating agents (cyclophosphamide, chlorambucil, melphalan, or others) may have a prohibitive risk of malignancy if treated with azathioprine tablets.

AZATHIOPRINE SODIUM injection, powder, lyophilized, for solution Bandaríkin - enska - NLM (National Library of Medicine)

azathioprine sodium injection, powder, lyophilized, for solution

hikma pharmaceuticals usa inc. - azathioprine sodium (unii: am94r510ms) (azathioprine - unii:mrk240iy2l) - azathioprine 100 mg in 10 ml - azathioprine sodium for injection, usp is indicated as an adjunct for the prevention of rejection in renal homotransplantation. it is also indicated for the management of active rheumatoid arthritis to reduce signs and symptoms. azathioprine is indicated as an adjunct for the prevention of rejection in renal homotransplantation. experience with over 16,000 transplants shows a five-year patient survival of 35% to 55%, but this is dependent on donor, match for hla antigens, anti-donor or anti-b-cell alloantigen antibody and other variables. the effect of azathioprine on these variables has not been tested in controlled trials. azathioprine is indicated for the treatment of active rheumatoid arthritis (ra) to reduce signs and symptoms. aspirin, non-steroidal anti-inflammatory drugs and/or low dose glucocorticoids may be continued during treatment with azathioprine. the combined use of azathioprine with disease modifying anti-rheumatic drugs (dmards) has not been studied for either added benefit or unexpected ad

AZATHIOPRINE GH azathioprine 25mg tablet blister pack Ástralía - enska - Department of Health (Therapeutic Goods Administration)

azathioprine gh azathioprine 25mg tablet blister pack

sandoz pty ltd - azathioprine, quantity: 25 mg - tablet, film coated - excipient ingredients: purified talc; lactose monohydrate; magnesium stearate; maize starch; povidone; colloidal anhydrous silica; titanium dioxide; hypromellose; microcrystalline cellulose; peg-8 stearate - immunosuppressant antimetabolite: either alone, or more commonly, in combination with other agents (usually corticosteroids) and procedures which influence the immune response. therapeutic effect may be evident only after weeks or months and can include a steroid-sparing effect, thereby reducing the toxicity associated with higher dosage and prolonged usage of corticosteroids. azathioprine, in combination with cortocosteroids and/or other immunosuppressive agents and procedures, is indicated in the management of patients receiving organ transplants. azathioprine, either alone or more usually in combination with corticosteroids and/or other procedures, has been used with clinical benefit which may include reduction of dosage or discontinuation of corticosteroids, in a proportion of patients suffering from the following: severe rheumatoid arthritis, systemic lupus erythematosus, dermatomyositis/polymyositis, autoimmune chronic active hepatitis, pemphigus vulgaris, polyarteritis nodosa, autoimmune haemolytic ana

AZATHIOPRINE SODIUM FOR INJECTION POWDER FOR SOLUTION Kanada - enska - Health Canada

azathioprine sodium for injection powder for solution

novopharm limited - azathioprine (azathioprine sodium) - powder for solution - 100mg - azathioprine (azathioprine sodium) 100mg - immunosuppressive agents

AZATHIOPRINE tablet Bandaríkin - enska - NLM (National Library of Medicine)

azathioprine tablet

remedyrepack inc. - azathioprine (unii: mrk240iy2l) (azathioprine - unii:mrk240iy2l) - azathioprine is indicated as an adjunct for the prevention of rejection in renal homotransplantation. it is also indicated for the management of active rheumatoid arthritis to reduce signs and symptoms. renal homotransplantation: azathioprine is indicated as an adjunct for the prevention of rejection in renal homotransplantation. experience with over 16,000 transplants shows a 5-year patient survival of 35% to 55%, but this is dependent on donor, match for hla antigens, anti-donor or anti-b-cell alloantigen antibody, and other variables. the effect of azathioprine on these variables has not been tested in controlled trials. rheumatoid arthritis: azathioprine is indicated for the treatment of active rheumatoid arthritis (ra) to reduce signs and symptoms. aspirin, non-steroidal anti-inflammatory drugs and/or low dose glucocorticoids may be continued during treatment with azathioprine. the combined use of azathioprine with disease modifying anti-rheumatic drugs (dmards) has not been studied for either added benefit or unexpected adverse effects. the use of azathioprine with these agents cannot be recommended. azathioprine should not be given to patients who have shown hypersensitivity to the drug. azathioprin should not be used for treating rheumatoid arthritis in pregnant women. patients with rheumatoid arthritis previously treated with alkylating agents (cyclophosphamide, chlorambucil, melphalan, or others) may have a prohibitive risk of malignancy if treated with azathioprine.

AZATHIOPRINE tablet Bandaríkin - enska - NLM (National Library of Medicine)

azathioprine tablet

ascend laboratories, llc - azathioprine (unii: mrk240iy2l) (azathioprine - unii:mrk240iy2l) - azathioprine is indicated as an adjunct for the prevention of rejection in renal homotransplantation. it is also indicated for the management of active rheumatoid arthritis to reduce signs and symptoms. renal homotransplantation: azathioprine is indicated as an adjunct for the prevention of rejection in renal homotransplantation. experience with over 16,000 transplants shows a 5-year patient survival of 35% to 55%, but this is dependent on donor, match for hla antigens, anti-donor or anti-b-cell alloantigen antibody, and other variables. the effect of azathioprine on these variables has not been tested in controlled trials. rheumatoid arthritis: azathioprine is indicated for the treatment of active rheumatoid arthritis (ra) to reduce signs and symptoms. aspirin, non-steroidal anti-inflammatory drugs and/or low dose glucocorticoids may be continued during treatment with azathioprine. the combined use of azathioprine with disease modifying anti-rheumatic drugs (dmards) has not been studied for either added be

THIOPRINE 50 azathioprine 50 mg film-coated tablet blister pack Ástralía - enska - Department of Health (Therapeutic Goods Administration)

thioprine 50 azathioprine 50 mg film-coated tablet blister pack

sandoz pty ltd - azathioprine, quantity: 50 mg - tablet, film coated - excipient ingredients: magnesium stearate; colloidal anhydrous silica; titanium dioxide; lactose monohydrate; maize starch; purified talc; povidone; hypromellose; microcrystalline cellulose; peg-8 stearate - immunosuppressant antimetabolite: either alone, or more commonly, in combination with other agents (usually corticosteroids) and procedures which influence the immune response. therapeutic effect may be evident only after weeks or months and can include a steroid-sparing effect, thereby reducing the toxicity associated with high dosage and prolonged usage of corticosteroids. azathioprine, in combination with corticosteroids and/or other immunosuppressive agents and procedures, is indicated in the management of patients receiving organ transplants. azathioprine, either alone or more usually in combination with corticosteroids and/or other procedures, has been used with clinical benefit which may include reduction of dosage or discontinuation of corticosteroids, in a proportion of patients suffering from the following: severe rheumatoid arthritis, systemic lupus erythematosus, dermatomyositis/polymyositis, autoimmune chronic active hepatitis, pemphigus vulgaris, polyarteritis nodosa, autoimmune haemolytic anaemia, chronic refractory idiopathic thrombocytopenic purpura.

AZATHIOPRINE TABLET Kanada - enska - Health Canada

azathioprine tablet

sanis health inc - azathioprine - tablet - 50mg - azathioprine 50mg - immunosuppressive agents

AZATHIOPRINE tablet Bandaríkin - enska - NLM (National Library of Medicine)

azathioprine tablet

avera mckennan hospital - azathioprine (unii: mrk240iy2l) (azathioprine - unii:mrk240iy2l) - azathioprine 50

AZATHIOPRINE tablet Bandaríkin - enska - NLM (National Library of Medicine)

azathioprine tablet

bryant ranch prepack - azathioprine (unii: mrk240iy2l) (azathioprine - unii:mrk240iy2l) - azathioprine 50 mg