Does DEVICE Cause Product quality issue? 567 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 567 reports of Product quality issue have been filed in association with DEVICE. This represents 4.5% of all adverse event reports for DEVICE.
567
Reports of Product quality issue with DEVICE
4.5%
of all DEVICE reports
2
Deaths
9
Hospitalizations
How Dangerous Is Product quality issue From DEVICE?
Of the 567 reports, 2 (0.4%) resulted in death, 9 (1.6%) required hospitalization, and 2 (0.4%) were considered life-threatening.
Is Product quality issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DEVICE. However, 567 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)
Drug ineffective (488)
Dyspnoea (482)
What Other Drugs Cause Product quality issue?
ETONOGESTREL (4,651)
ALBUTEROL (4,466)
TIOTROPIUM (3,821)
MOMETASONE FUROATE (3,406)
LIDOCAINE (3,126)
FLUTICASONE\SALMETEROL (2,986)
FORMOTEROL\MOMETASONE FUROATE (2,458)
FENTANYL (2,450)
NICOTINE (1,987)
EXENATIDE (1,839)
Which DEVICE Alternatives Have Lower Product quality issue Risk?
DEVICE vs DEXAMETHASONE
DEVICE vs DEXAMETHASONE\DEXAMETHASONE
DEVICE vs DEXAMETHASONE\NEOMYCIN
DEVICE vs DEXAMETHASONE\NEOMYCIN\POLYMYXIN B
DEVICE vs DEXAMETHASONE\TOBRAMYCIN