OLBETAM CAPSULE 250 mg Singapore - English - HSA (Health Sciences Authority)

olbetam capsule 250 mg

pfizer private limited - acipimox - capsule - 250 mg - acipimox 250 mg

Xalkori Capsules 200mg Singapore - English - HSA (Health Sciences Authority)

xalkori capsules 200mg

pfizer private limited - crizotinib - capsule - 200 mg - crizotinib 200 mg

Xalkori Capsules 250mg Singapore - English - HSA (Health Sciences Authority)

xalkori capsules 250mg

pfizer private limited - crizotinib - capsule - 250 mg - crizotinib 250 mg

Sutent Capsule 37.5mg Singapore - English - HSA (Health Sciences Authority)

sutent capsule 37.5mg

pfizer private limited - sunitinib malate 50.100mg eqv sunitinib - capsule - 37.5mg - sunitinib malate 50.100mg eqv sunitinib 37.5mg

PFIZER-BIONTECH COVID-19 VACCINE- bnt162b2 injection, suspension United States - English - NLM (National Library of Medicine)

pfizer-biontech covid-19 vaccine- bnt162b2 injection, suspension

pfizer manufacturing belgium nv - tozinameran (unii: 5085zfp6sj) (tozinameran - unii:5085zfp6sj) - pfizer-biontech covid-19 vaccine is authorized for use under an emergency use authorization (eua) for active immunization to prevent coronavirus disease 2019 (covid-19) caused by severe acute respiratory syndrome coronavirus 2 (sars-cov-2) in individuals 6 months of age and older. this eua prescribing information pertains only to pfizer-biontech covid-19 vaccine supplied in a multiple dose vial with a purple cap, which is authorized for use in individuals 12 years of age and older. do not administer pfizer-biontech covid-19 vaccine to individuals with known history of a severe allergic reaction (e.g., anaphylaxis) to any component of the pfizer-biontech covid-19 vaccine [see description (13)] . risk summary all pregnancies have a risk of birth defect, loss, or other adverse outcomes. in the us 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. available data on pfizer-biontech covid-19 vaccine

PFIZER-BIONTECH COVID-19 VACCINE- bnt162b2 injection, suspension United States - English - NLM (National Library of Medicine)

pfizer-biontech covid-19 vaccine- bnt162b2 injection, suspension

pfizer manufacturing belgium nv - tozinameran (unii: 5085zfp6sj) (tozinameran - unii:5085zfp6sj) - pfizer-biontech covid-19 vaccine is authorized for use under an emergency use authorization (eua) for active immunization to prevent coronavirus disease 2019 (covid-19) caused by severe acute respiratory syndrome coronavirus 2 (sars-cov-2) in individuals 6 months of age and older. this eua prescribing information pertains only to pfizer-biontech covid-19 vaccine supplied in a multiple dose vial with a gray cap and label with a gray border, which is authorized for use in individuals 12 years of age and older. do not administer pfizer-biontech covid-19 vaccine to individuals with known history of a severe allergic reaction (e.g., anaphylaxis) to any component of the pfizer-biontech covid-19 vaccine [see description (13)] . risk summary all pregnancies have a risk of birth defect, loss, or other adverse outcomes. in the us 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. available data on pfizer