FDA food adverse event report
Consumer gender: Female
Consumer age: 42 year(s)
Product(s):
role: SUSPECT
name_brand: WOMEN'S ULTRA MEGA ACTIVE VITAPAK CALCIUM 600
industry_name: Vit/Min/Prot/Unconv Diet(Human/Animal)
role: SUSPECT
name_brand: WOMEN'S ULTRA MEGA ACTIVE VITAPAK CLA 1000
industry_name: Vit/Min/Prot/Unconv Diet(Human/Animal)
role: SUSPECT
name_brand: WOMEN'S ULTRA MEGA ACTIVE VITAPAK ENERGY ENHANCER
industry_name: Vit/Min/Prot/Unconv Diet(Human/Animal)
role: SUSPECT
name_brand: WOMEN'S ULTRA MEGA ACTIVE VITAPAK L-CARNITINE
industry_name: Vit/Min/Prot/Unconv Diet(Human/Animal)
role: SUSPECT
name_brand: WOMEN'S ULTRA MEGA ACTIVE VITAPAK WOMEN'S ULTRA MEGA ACTIVE WITHOUT IRON
industry_name: Vit/Min/Prot/Unconv Diet(Human/Animal)
Reactions:
BLOOD PRESSURE INCREASED
DIZZINESS
DYSPNOEA
FEELING ABNORMAL
FEELING JITTERY
HEART RATE INCREASED
MALAISE
NAUSEA
VERTIGO
Outcomes:
Required Intervention
Visited Emergency Room