FDA food adverse event report
Consumer gender: Female
Consumer age: 73 year(s)
Product(s):
role: SUSPECT
name_brand: UQORA DEFEND PART 2
industry_name: Vit/Min/Prot/Unconv Diet(Human/Animal)
role: SUSPECT
name_brand: UQORA PROMOTE PART 3
industry_name: Vit/Min/Prot/Unconv Diet(Human/Animal)
role: SUSPECT
name_brand: UQORA URIARY CARE FLUSH PROACTIVE REGIMEN PART 1
industry_name: Vit/Min/Prot/Unconv Diet(Human/Animal)
role: CONCOMITANT
name_brand: FISH OIL
industry_name: Vit/Min/Prot/Unconv Diet(Human/Animal)
role: CONCOMITANT
name_brand: MULTIVITAMIN
industry_name: Vit/Min/Prot/Unconv Diet(Human/Animal)
role: CONCOMITANT
name_brand: VITAMIN D3
industry_name: Vit/Min/Prot/Unconv Diet(Human/Animal)
Reactions:
Abdominal pain
Anal incontinence
Blood glucose increased
Blood pressure increased
Cerebrovascular accident
Cystitis
Death
Decreased appetite
Delirium
Duodenal ulcer
Gait inability
Hospitalisation
Kidney infection
Malaise
Oxygen saturation decreased
Pancreatic carcinoma metastatic
Pyrexia
Sepsis
Urinary incontinence
Urinary tract infection
Outcomes:
Death
Life Threatening
Hospitalization
Other Serious or Important Medical Event