FDA food adverse event report
Consumer gender: Female
Consumer age: 63 year(s)
Product(s):
role: SUSPECT
name_brand: SUNDOWN NIACIN 500MG TIME RELEASE
industry_name: Vit/Min/Prot/Unconv Diet(Human/Animal)
role: CONCOMITANT
name_brand: CALCIUM
industry_name: Vit/Min/Prot/Unconv Diet(Human/Animal)
role: CONCOMITANT
name_brand: EVENING PRIMROSE OIL
industry_name: Vit/Min/Prot/Unconv Diet(Human/Animal)
role: CONCOMITANT
name_brand: GARLIC
industry_name: Vit/Min/Prot/Unconv Diet(Human/Animal)
role: CONCOMITANT
name_brand: VITAMIN D
industry_name: Vit/Min/Prot/Unconv Diet(Human/Animal)
role: CONCOMITANT
name_brand: VITAMIN E
industry_name: Vit/Min/Prot/Unconv Diet(Human/Animal)
Reactions:
BURNING SENSATION
GENERALISED ERYTHEMA
PAIN
RASH
Outcomes:
Hospitalization
Required Intervention
Other Serious or Important Medical Event
Visited a Health Care Provider