FDA food adverse event report
Consumer gender: Female
Consumer age: 43 year(s)
Product(s):
role: SUSPECT
name_brand: WOMENS ULTRA MEGA ACTIVE VITAPAK CALCIUM 600
industry_name: Vit/Min/Prot/Unconv Diet(Human/Animal)
role: SUSPECT
name_brand: WOMENS ULTRA MEGA ACTIVE VITAPAK CLA 1000
industry_name: Vit/Min/Prot/Unconv Diet(Human/Animal)
role: SUSPECT
name_brand: WOMENS ULTRA MEGA ACTIVE VITAPAK ENERGY ENHANCER
industry_name: Vit/Min/Prot/Unconv Diet(Human/Animal)
role: SUSPECT
name_brand: WOMENS ULTRA MEGA ACTIVE VITAPAK L CARNITINE
industry_name: Vit/Min/Prot/Unconv Diet(Human/Animal)
role: SUSPECT
name_brand: WOMENS ULTRA MEGA ACTIVE VITAPAK WOMENS ULTRA MEGA ACTIVE WITHOUT IRON
industry_name: Vit/Min/Prot/Unconv Diet(Human/Animal)
Reactions:
APHASIA
BLOOD GLUCOSE DECREASED
BLOOD PRESSURE INCREASED
DIZZINESS
FEELING COLD
HEADACHE
HYPOAESTHESIA
MENTAL IMPAIRMENT
TREMOR
Outcomes:
Other Serious or Important Medical Event