DULOXETINE- duloxetine hydrochloride capsule, delayed release 미국 - 영어 - NLM (National Library of Medicine)

duloxetine- duloxetine hydrochloride capsule, delayed release

preferred pharmaceuticals, inc. - duloxetine hydrochloride (unii: 9044sc542w) (duloxetine - unii:o5tnm5n07u) - duloxetine 60 mg - duloxetine delayed-release capsules are indicated for the treatment of: monoamine oxidase inhibitors (maois) — the use of maois intended to treat psychiatric disorders with duloxetine delayed-release capsules or within 5 days of stopping treatment with duloxetine delayed-release capsules is contraindicated because of an increased risk of serotonin syndrome. the use of duloxetine delayed-release capsules within 14 days of stopping an maoi intended to treat psychiatric disorders is also contraindicated [see dosage and administration (2.8) and warnings and precautions (5.4)] . starting duloxetine delayed-release capsules in a patient who is being treated with maois such as linezolid or intravenous methylene blue is also contraindicated because of an increased risk of serotonin syndrome [see dosage and administration (2.9) and warnings and precautions (5.4)] . teratogenic effects pregnancy category c risk summary — there are no adequate and well-controlled studies of duloxetine delayed-release capsules administr

DULOXETINE capsule, delayed release 미국 - 영어 - NLM (National Library of Medicine)

duloxetine capsule, delayed release

preferred pharmaceuticals inc. - duloxetine hydrochloride (unii: 9044sc542w) (duloxetine - unii:o5tnm5n07u) - duloxetine 30 mg - duloxetine is indicated for the treatment of: monoamine oxidase inhibitors (maois) -the use of maois intended to treat psychiatric disorders with duloxetine or within 5 days of stopping treatment with duloxetine is contraindicated because of an increased risk of serotonin syndrome. the use of duloxetine within 14 days of stopping an maoi intended to treat psychiatric disorders is also contraindicated [see dosage and administration (2.8) and warnings and precautions (5.4)] . starting duloxetine in a patient who is being treated with maois such as linezolid or intravenous methylene blue is also contraindicated because of an increased risk of serotonin syndrome [see dosage and administration (2.9) and warnings and precautions (5.4)]. pregnancy category c risk summary — there are no adequate and well-controlled studies of duloxetine administration in pregnant women. in animal studies with duloxetine, fetal weights were decreased but there was no evidence of teratogenicity in pregnant rats and rabbits at oral do

DULOXETINE HYDROCHLORIDE capsule, delayed release 미국 - 영어 - NLM (National Library of Medicine)

duloxetine hydrochloride capsule, delayed release

preferred pharmaceuticals, inc. - duloxetine hydrochloride (unii: 9044sc542w) (duloxetine - unii:o5tnm5n07u) - duloxetine 20 mg - duloxetine delayed-release capsules are indicated for the treatment of: monoamine oxidase inhibitors (maois) the use of maois intended to treat psychiatric disorders with duloxetine delayed-release capsules or within 5 days of stopping treatment with duloxetine delayed-release capsules is contraindicated because of an increased risk of serotonin syndrome. the use of duloxetine delayed-release capsules within 14 days of stopping an maoi intended to treat psychiatric disorders is also contraindicated [see dosage and administration (2.8) and warnings and precautions (5.4)]. starting duloxetine delayed-release capsules in a patient who is being treated with maois such as linezolid or intravenous methylene blue is also contraindicated because of an increased risk of serotonin syndrome [see dosage and administration (2.9) and warnings and precautions (5.4)] . pregnancy category c   risk summary there are no adequate and well-controlled studies of duloxetine administration in pregnant women. in animal studie

DULOXETINE capsule, delayed release 미국 - 영어 - NLM (National Library of Medicine)

duloxetine capsule, delayed release

heritage pharmaceuticals inc. - duloxetine hydrochloride (unii: 9044sc542w) (duloxetine - unii:o5tnm5n07u) - duloxetine is indicated for the treatment of: - major depressive disorder [see clinical studies (14.1)] - generalized anxiety disorder [see clinical studies (14.2)] - diabetic peripheral neuropathy [see clinical studies (14.3)] - chronic musculoskeletal pain [see clinical studies (14.5)]         monoamine oxidase inhibitors (maois) -the use of maois intended to treat psychiatric disorders with duloxetine or within 5 days of stopping treatment with duloxetine is contraindicated because of an increased risk of serotonin syndrome. the use of duloxetine within 14 days of stopping an maoi intended to treat psychiatric disorders is also contraindicated [see dosage and administration (2.8) and warnings and precautions (5.4)] .         starting duloxetine in a patient who is being treated with maois such as linezolid or intravenous methylene blue is also contraindicated because of an increased risk of serotonin syndrome [see dosage and administration (2.9) and warnings and precautions (5.4)].         pregnancy

Unbranded 5 mg Softgel Capsule 필리핀 - 영어 - FDA (Food And Drug Administration)

unbranded 5 mg softgel capsule

ambica international corporation; distributor: international pharmaceuticals, inc. - nifedipine - softgel capsule - 5 mg

None 10 mg Film-Coated Tablet 필리핀 - 영어 - FDA (Food And Drug Administration)

none 10 mg film-coated tablet

ambica international corp.; distributor: international pharmaceuticals, inc. - atorvastatin (as calcium) - film-coated tablet - 10 mg

None 5mg Chewable Tablet 필리핀 - 영어 - FDA (Food And Drug Administration)

none 5mg chewable tablet

ambica international crop.; distributor: international pharmaceuticals, inc. - montelukast (as sodium) - chewable tablet - 5mg

None 500 mg Film-Coated Tablet 필리핀 - 영어 - FDA (Food And Drug Administration)

none 500 mg film-coated tablet

ambica international corporation; distributor: international pharmaceuticals, inc. - levofloxacin (as hemihydrate) - film-coated tablet - 500 mg

None 5mg Film-Coated Tablet 필리핀 - 영어 - FDA (Food And Drug Administration)

none 5mg film-coated tablet

ambica international corporation; distributor: international pharmaceuticals, inc. - levocetirizine - film-coated tablet - 5mg

None 200mg Film-Coated Tablet 필리핀 - 영어 - FDA (Food And Drug Administration)

none 200mg film-coated tablet

ambica international corp.; distributor: international pharmaceuticals, inc. - cefixime (as trihydrate) - film-coated tablet - 200mg