FDA food adverse event report
Consumer gender: Female
Consumer age: 74 year(s)
Product(s):
role: SUSPECT
name_brand: NERVIVE PAIN RELIEVING CREAM
industry_name: Vit/Min/Prot/Unconv Diet(Human/Animal)
role: CONCOMITANT
name_brand: FERROUS SULFATE
industry_name: Vit/Min/Prot/Unconv Diet(Human/Animal)
role: CONCOMITANT
name_brand: VITAMIN C
industry_name: Vit/Min/Prot/Unconv Diet(Human/Animal)
role: CONCOMITANT
name_brand: VITAMIN D
industry_name: Vit/Min/Prot/Unconv Diet(Human/Animal)
Reactions:
Activated partial thromboplastin time prolonged
Application site pain
Blister
Blood creatinine decreased
Blood glucose increased
Blood pressure diastolic increased
Blood pressure systolic increased
Body mass index increased
Carbon dioxide increased
Cellulitis
Dermatitis
Furuncle
Haematocrit decreased
Heart rate decreased
Hyperchloraemia
Hypernatraemia
Hypoaesthesia
Immature granulocyte percentage increased
Leukopenia
Limb injury
Mean cell haemoglobin concentration decreased
Mobility decreased
Muscle hypertrophy
Muscle necrosis
Neutrophil count decreased
Pain in extremity
Peripheral swelling
Protein total decreased
Red cell distribution width increased
Second degree chemical burn of skin
Sepsis
Skin burning sensation
Skin lesion
Skin ulcer
Wound infection
Wound necrosis
Outcomes:
Hospitalization
Other Serious or Important Medical Event