leflunomide an leflunomide 100mg tablet blister pack
southern cross pharma pty ltd - leflunomide -
leflunomide an leflunomide 20mg tablet bottle
southern cross pharma pty ltd - leflunomide -
leflunomide an leflunomide 10mg tablet bottle
southern cross pharma pty ltd - leflunomide -
leflunomide tablet
alembic pharmaceuticals inc. - leflunomide (unii: g162gk9u4w) (leflunomide - unii:g162gk9u4w) - leflunomide 10 mg - leflunomide tablets usp are indicated for the treatment of adults with active rheumatoid arthritis (ra). leflunomide is contraindicated in: · pregnant women. leflunomide may cause fetal harm. if a woman becomes pregnant while taking this drug, stop leflunomide, apprise the patient of the potential hazard to the fetus, and begin a drug elimination procedure [see warnings and precautions (5.1 and 5.3) and use in specific populations (8.1)]. · patients with severe hepatic impairment [see warnings and precautions (5.2)]. · patients with known hypersensitivity to leflunomide or any of the other components of leflunomide. known reactions include anaphylaxis [see adverse reactions (6.1)]. · patients being treated with teriflunomide [see drug interactions (7)]. pregnancy exposure registry there is a pregnancy exposure registry that monitors pregnancy outcomes in women exposed to leflunomide during pregnancy. health care providers and patients are encouraged to report pr
leflunomide tablet
alembic pharmaceuticals limited - leflunomide (unii: g162gk9u4w) (leflunomide - unii:g162gk9u4w) - leflunomide 10 mg - leflunomide tablets usp are indicated for the treatment of adults with active rheumatoid arthritis (ra). leflunomide is contraindicated in: · pregnant women. leflunomide may cause fetal harm. if a woman becomes pregnant while taking this drug, stop leflunomide, apprise the patient of the potential hazard to the fetus, and begin a drug elimination procedure [see warnings and precautions (5.1 and 5.3) and use in specific populations (8.1)]. · patients with severe hepatic impairment [see warnings and precautions (5.2)]. · patients with known hypersensitivity to leflunomide or any of the other components of leflunomide. known reactions include anaphylaxis [see adverse reactions (6.1)]. · patients being treated with teriflunomide [see drug interactions (7)]. pregnancy exposure registry there is a pregnancy exposure registry that monitors pregnancy outcomes in women exposed to leflunomide during pregnancy. health care providers and patients are encouraged to report pr
leflunomide gh leflunomide 20mg tablet bottle
sanofi-aventis australia pty ltd - leflunomide -
leflunomide tablet
heritage pharmaceuticals inc. d/b/a avet pharmaceuticals inc. - leflunomide (unii: g162gk9u4w) (leflunomide - unii:g162gk9u4w) - leflunomide 10 mg - leflunomide tablets, usp are indicated for the treatment of adults with active rheumatoid arthritis (ra). leflunomide tablets are contraindicated in: •pregnant women. leflunomide may cause fetal harm. if a woman becomes pregnant while taking this drug, stop leflunomide, apprise the patient of the potential hazard to the fetus, and begin a drug elimination procedure [see warnings and precautions (5.1and 5.3) and use in specific populations (8.1)]. •patients with severe hepatic impairment [see warnings and precautions (5.2)] . •patients with known hypersensitivity to leflunomide or any of the other components of leflunomide tablets. known reactions include anaphylaxis [see adverse reactions (6.1)] . •patients being treated with teriflunomide [see drug interactions (7)] . pregnancy exposure registry there is a pregnancy exposure registry that monitors pregnancy outcomes in women exposed to leflunomide during pregnancy. health care providers and patients are encouraged to report pregnancies by calling 1-877-3
leflunomide gh leflunomide 10mg tablet bottle
sanofi-aventis australia pty ltd - leflunomide -
apo-leflunomide tablet
apotex inc - leflunomide - tablet - 10mg - leflunomide 10mg - disease-modifying antirheumatic agents
leflunomide tablet
pro doc limitee - leflunomide - tablet - 20mg - leflunomide 20mg - disease-modifying antirheumatic agents