Selegiline 5mg tablets Inggris - Inggris - MHRA (Medicines & Healthcare Products Regulatory Agency)

selegiline 5mg tablets

alliance healthcare (distribution) ltd - selegiline hydrochloride - oral tablet - 5mg

Selegiline 5mg tablets Inggris - Inggris - MHRA (Medicines & Healthcare Products Regulatory Agency)

selegiline 5mg tablets

phoenix healthcare distribution ltd - selegiline hydrochloride - oral tablet - 5mg

Selegiline 5mg tablets Inggris - Inggris - MHRA (Medicines & Healthcare Products Regulatory Agency)

selegiline 5mg tablets

tillomed laboratories ltd - selegiline hydrochloride - oral tablet - 5mg

Selegiline 5mg tablets Inggris - Inggris - MHRA (Medicines & Healthcare Products Regulatory Agency)

selegiline 5mg tablets

mawdsley-brooks & company ltd - selegiline hydrochloride - oral tablet - 5mg

Apo-Selegiline Selandia Baru - Inggris - Medsafe (Medicines Safety Authority)

apo-selegiline

apotex nz ltd - selegiline hydrochloride 5mg;  ;  ;   - tablet - 5 mg - active: selegiline hydrochloride 5mg       excipient: lactose monohydrate magnesium stearate microcrystalline cellulose starch

TRAZODONE HYDROCHLORIDE- trazodone hydrochloride tablet, film coated Amerika Serikat - Inggris - NLM (National Library of Medicine)

trazodone hydrochloride- trazodone hydrochloride tablet, film coated

bryant ranch prepack - trazodone hydrochloride (unii: 6e8zo8lrnm) (trazodone - unii:ybk48bxk30) - trazodone hydrochloride 50 mg - trazodone hydrochloride tablets are indicated for the treatment of major depressive disorder (mdd) in adults. trazodone hydrochloride tablets are contraindicated in: - patients taking, or within 14 days of stopping, monoamine oxidase inhibitors (maois), including maois such as linezolid or intravenous methylene blue, because of an increased risk of serotonin syndrome [see warnings and precautions (5.2), drug interactions (7.1)]. patients taking, or within 14 days of stopping, monoamine oxidase inhibitors (maois), including maois such as linezolid or intravenous methylene blue, because of an increased risk of serotonin syndrome [see warnings and precautions (5.2), drug interactions (7.1)]. teratogenic effects pregnancy category c trazodone hydrochloride has been shown to cause increased fetal resorption and other adverse effects on the fetus in the rat when given at dose levels approximately 6 to 9 times the maximum recommended human dose (mrhd) of 400 mg/day on mg/m2 in adolescents.  there was also an incr

SERTRALINE HYDROCHLORIDE- sertraline hydrochloride tablet, film coated Amerika Serikat - Inggris - NLM (National Library of Medicine)

sertraline hydrochloride- sertraline hydrochloride tablet, film coated

remedyrepack inc. - sertraline hydrochloride (unii: uti8907y6x) (sertraline - unii:quc7nx6wmb) - sertraline 25 mg - sertraline hydrochloride tablets are indicated for the treatment of the following [see clinical studies (14)] : - major depressive disorder (mdd) - obsessive-compulsive disorder (ocd) - panic disorder (pd) - posttraumatic stress disorder (ptsd) - social anxiety disorder (sad) - premenstrual dysphoric disorder (pmdd) sertraline hydrochloride tablets are contraindicated in patients: - taking, or within 14 days of stopping, maois, (including the maois linezolid and intravenous methylene blue) because of an increased risk of serotonin syndrome [see warnings and precautions (5.2), drug interactions (7.1)] . - taking pimozide [see drug interactions (7.1)] . - with known hypersensitivity to sertraline (e.g., anaphylaxis, angioedema) [see adverse reactions (6.1, 6.2)]. risk summary overall, available published epidemiologic studies of pregnant women exposed to sertraline in the first trimester suggest no difference in major birth defect risk compared to the background rate for major birth defects in compar