FDA food adverse event report
Consumer gender: Female
Consumer age: 57 year(s)
Product(s):
role: SUSPECT
name_brand: WOMENS ULTRA MEGA ACTIVE VITAPAK PACKET - CALCIUM 600
industry_name: Vit/Min/Prot/Unconv Diet(Human/Animal)
role: SUSPECT
name_brand: WOMENS ULTRA MEGA ACTIVE VITAPAK PACKET - CONJUGATED LINOLEIC ACID (CLA)
industry_name: Vit/Min/Prot/Unconv Diet(Human/Animal)
role: SUSPECT
name_brand: WOMENS ULTRA MEGA ACTIVE VITAPAK PACKET - ENERGY ENHANCER
industry_name: Vit/Min/Prot/Unconv Diet(Human/Animal)
role: SUSPECT
name_brand: WOMENS ULTRA MEGA ACTIVE VITAPAK PACKET - L-CARNITINE
industry_name: Vit/Min/Prot/Unconv Diet(Human/Animal)
role: SUSPECT
name_brand: WOMENS ULTRA MEGA ACTIVE WITHOUT IRON
industry_name: Vit/Min/Prot/Unconv Diet(Human/Animal)
Reactions:
ABDOMINAL PAIN UPPER
ASTHENIA
DYSARTHRIA
HYPERSENSITIVITY
INSOMNIA
LOSS OF CONSCIOUSNESS
URINARY TRACT INFECTION
Outcomes:
Other Serious or Important Medical Event
Visited Emergency Room