Does DEVICE Cause Dyspnoea? 482 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 482 reports of Dyspnoea have been filed in association with DEVICE. This represents 3.8% of all adverse event reports for DEVICE.
482
Reports of Dyspnoea with DEVICE
3.8%
of all DEVICE reports
28
Deaths
135
Hospitalizations
How Dangerous Is Dyspnoea From DEVICE?
Of the 482 reports, 28 (5.8%) resulted in death, 135 (28.0%) required hospitalization, and 21 (4.4%) 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 DEVICE. However, 482 reports have been filed with the FAERS database.
What Other Side Effects Does DEVICE Cause?
Blood glucose increased (2,114)
Device issue (1,417)
Product use issue (1,076)
Intercepted product preparation error (1,033)
Wrong technique in product usage process (935)
Device leakage (795)
Injection site pain (751)
Syringe issue (634)
Product quality issue (567)
Drug ineffective (488)
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)
Which DEVICE Alternatives Have Lower Dyspnoea Risk?
DEVICE vs DEXAMETHASONE
DEVICE vs DEXAMETHASONE\DEXAMETHASONE
DEVICE vs DEXAMETHASONE\NEOMYCIN
DEVICE vs DEXAMETHASONE\NEOMYCIN\POLYMYXIN B
DEVICE vs DEXAMETHASONE\TOBRAMYCIN