Does SODIUM AUROTIOSULFATE Cause Dyspnoea? 10 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 10 reports of Dyspnoea have been filed in association with SODIUM AUROTIOSULFATE. This represents 10.1% of all adverse event reports for SODIUM AUROTIOSULFATE.
10
Reports of Dyspnoea with SODIUM AUROTIOSULFATE
10.1%
of all SODIUM AUROTIOSULFATE reports
10
Deaths
10
Hospitalizations
How Dangerous Is Dyspnoea From SODIUM AUROTIOSULFATE?
Of the 10 reports, 10 (100.0%) resulted in death, 10 (100.0%) required hospitalization, and 10 (100.0%) were considered life-threatening.
Is Dyspnoea Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SODIUM AUROTIOSULFATE. However, 10 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)
Product use issue (68)
Intentional product use issue (67)
Treatment failure (67)
Contraindicated product administered (65)
Product use in unapproved indication (65)
Vomiting (65)
What Other Drugs Cause Dyspnoea?
ALBUTEROL (21,856)
TREPROSTINIL (16,348)
AMBRISENTAN (13,367)
PREDNISONE (12,830)
BUDESONIDE\FORMOTEROL (11,158)
TIOTROPIUM (10,863)
ADALIMUMAB (10,547)
DUPILUMAB (10,310)
FLUTICASONE\SALMETEROL (9,783)
MEPOLIZUMAB (9,192)