Does SODIUM AUROTIOSULFATE Cause Product use issue? 68 Reports in FDA Database
Boost Your Natural Energy & Metabolism
Mitolyn — 6 exotic plants to unlock your body's fat-burning power. 90-day guarantee.
According to the FDA Adverse Event Reporting System (FAERS), 68 reports of Product use issue have been filed in association with SODIUM AUROTIOSULFATE. This represents 68.7% of all adverse event reports for SODIUM AUROTIOSULFATE.
68
Reports of Product use issue with SODIUM AUROTIOSULFATE
68.7%
of all SODIUM AUROTIOSULFATE reports
61
Deaths
44
Hospitalizations
How Dangerous Is Product use issue From SODIUM AUROTIOSULFATE?
Of the 68 reports, 61 (89.7%) resulted in death, 44 (64.7%) required hospitalization, and 37 (54.4%) were considered life-threatening.
Is Product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SODIUM AUROTIOSULFATE. However, 68 reports have been filed with the FAERS database.
What Other Side Effects Does SODIUM AUROTIOSULFATE Cause?
Drug intolerance (76)
Drug ineffective (71)
Synovitis (70)
Hypertension (68)
Intentional product use issue (67)
Treatment failure (67)
Contraindicated product administered (65)
Product use in unapproved indication (65)
Vomiting (65)
Abdominal discomfort (64)
What Other Drugs Cause Product use issue?
INFLIXIMAB (12,752)
DUPILUMAB (10,575)
POLYETHYLENE GLYCOL 3350 (9,432)
METHOTREXATE (8,185)
DICLOFENAC (8,009)
RITUXIMAB (6,948)
ADALIMUMAB (6,379)
ETANERCEPT (6,062)
TOCILIZUMAB (5,944)
ABATACEPT (5,915)