ZOLMITRIPTAN SANOFI 2.5 Milligram Film Coated Tablet Ireland - English - HPRA (Health Products Regulatory Authority)

zolmitriptan sanofi 2.5 milligram film coated tablet

sanofi-aventis ireland limited t/a sanofi - zolmitriptan - film coated tablet - 2.5 milligram

ZOLMITRIPTAN SANOFI 2.5 Milligram Orodispersible Tablet Ireland - English - HPRA (Health Products Regulatory Authority)

zolmitriptan sanofi 2.5 milligram orodispersible tablet

sanofi-aventis ireland limited t/a sanofi - zolmitriptan - orodispersible tablet - 2.5 milligram

ZOLMITRIPTAN TEVA 2.5 Milligram Orodispersible Tablet Ireland - English - HPRA (Health Products Regulatory Authority)

zolmitriptan teva 2.5 milligram orodispersible tablet

teva pharma b.v. - zolmitriptan - orodispersible tablet - 2.5 milligram - selective serotonin (5ht1) agonists

ZOMIG- zolmitriptan tablet
ZOMIG ZMT- zolmitriptan tablet, orally disintegrating United States - English - NLM (National Library of Medicine)

zomig- zolmitriptan tablet zomig zmt- zolmitriptan tablet, orally disintegrating

amneal pharmaceuticals - zolmitriptan (unii: 2fs66th3yw) (zolmitriptan - unii:2fs66th3yw) - zolmitriptan 2.5 mg - zomig is indicated for the acute treatment of migraine with or without aura in adults. limitations of use zomig is contraindicated in patients with: risk summary there are no adequate data on the developmental risk associated with the use of zomig in pregnant women. in reproductive toxicity studies in rats and rabbits, oral administration of zolmitriptan to pregnant animals resulted in embryolethality and fetal abnormalities (malformations and variations) at clinically relevant exposures (see data). in the u.s. general population, the estimated background risk of major birth defects and miscarriage in clinically recognized pregnancies is 2% to 4% and 15% to 20%, respectively. the estimated rates of major birth defects (2.2%-2.9%) and miscarriage (17%) among deliveries to women with migraine are similar to rates reported in women without migraine. clinical considerations disease-associated maternal and/or embryo/fetal risk published data have suggested that women with migraine may be at increased risk of pree

ZOMIG- zolmitriptan spray, metered United States - English - NLM (National Library of Medicine)

zomig- zolmitriptan spray, metered

amneal pharmaceuticals - zolmitriptan (unii: 2fs66th3yw) (zolmitriptan - unii:2fs66th3yw) - zolmitriptan 5 mg - zomig nasal spray is indicated for the acute treatment of migraine with or without aura in adults and pediatric patients 12 years of age and older. limitations of use zomig is contraindicated in patients with: risk summary there are no adequate data on the developmental risk associated with the use of zomig in pregnant women. in reproductive toxicity studies in rats and rabbits, oral administration of zolmitriptan to pregnant animals resulted in embryolethality and fetal abnormalities (malformations and variations) at clinically relevant exposures (see data) . in the u.s. general population, the estimated background risk of major birth defects and miscarriage in clinically recognized pregnancies is 2% to 4% and 15% to 20%, respectively. the estimated rates of major birth defects (2.2%-2.9%) and miscarriage (17%) among deliveries to women with migraine are similar to rates reported in women without migraine. clinical considerations disease-associated maternal and/or embryo/fetal risk published data have sugges