FDA food adverse event report
Consumer gender: Female
Consumer age: 35 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 WITHOUT IRON
industry_name: Vit/Min/Prot/Unconv Diet(Human/Animal)
Reactions:
CHEST PAIN
CONVULSION
DIZZINESS
DRUG TOXICITY
DYSPNOEA
HEART RATE INCREASED
HYPOAESTHESIA
LETHARGY
NAUSEA
PALPITATIONS
PARALYSIS
Outcomes:
Required Intervention
Visited Emergency Room