FDA food adverse event report
Consumer gender: Female
Consumer age: 64 year(s)
Product(s):
role: SUSPECT
name_brand: OCUVITE EYE PLUS MULTI (LUTEIN TABLET)
industry_name: Vit/Min/Prot/Unconv Diet(Human/Animal)
role: CONCOMITANT
name_brand: FOLATE (FOLIC ACID) (800 MICROGRAM)
industry_name: Vit/Min/Prot/Unconv Diet(Human/Animal)
role: CONCOMITANT
name_brand: MULTIPLE VITAMIN
industry_name: Vit/Min/Prot/Unconv Diet(Human/Animal)
role: CONCOMITANT
name_brand: UNSPECIFIED ENZYMES
industry_name: Vit/Min/Prot/Unconv Diet(Human/Animal)
role: CONCOMITANT
name_brand: VITAMIN D3 (CHOLECALCIFEROL) (5000 IU)
industry_name: Vit/Min/Prot/Unconv Diet(Human/Animal)
role: CONCOMITANT
name_brand: WEDGE ULTIMATE EYE FORMULA
industry_name: Vit/Min/Prot/Unconv Diet(Human/Animal)
Reactions:
CHROMATOPSIA
INTRAOCULAR PRESSURE INCREASED
INTRAOCULAR PRESSURE TEST ABNORMAL
VISION BLURRED
VISUAL FIELD DEFECT
Outcomes:
Other Serious or Important Medical Event