FDA food adverse event report
Consumer gender: Female
Consumer age: 30 year(s)
Product(s):
role: SUSPECT
name_brand: OXYELITE PRO
industry_name: Vit/Min/Prot/Unconv Diet(Human/Animal)
role: CONCOMITANT
name_brand: PRENATAL
industry_name: Vit/Min/Prot/Unconv Diet(Human/Animal)
role: CONCOMITANT
name_brand: UNSPECIFIED HERBAL
industry_name: Vit/Min/Prot/Unconv Diet(Human/Animal)
Reactions:
ALANINE AMINOTRANSFERASE INCREASED
ALPHA-1 ANTI-TRYPSIN INCREASED
ANOREXIA
ASPARTATE AMINOTRANSFERASE INCREASED
BLOOD BILIRUBIN INCREASED
BLOOD IRON INCREASED
CERULOPLASMIN DECREASED
CHROMATURIA
FATIGUE
GALLBLADDER DISORDER
HEPATITIS
HEPATOMEGALY
JAUNDICE
LIVER INJURY
NAUSEA
NEUTROPHIL COUNT INCREASED
PRURITUS
RASH
SERUM FERRITIN INCREASED
TRANSFERRIN INCREASED
VOMITING
Outcomes:
Hospitalization