Does DEVICE Cause Hospitalisation? 212 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 212 reports of Hospitalisation have been filed in association with DEVICE. This represents 1.7% of all adverse event reports for DEVICE.
212
Reports of Hospitalisation with DEVICE
1.7%
of all DEVICE reports
15
Deaths
211
Hospitalizations
How Dangerous Is Hospitalisation From DEVICE?
Of the 212 reports, 15 (7.1%) resulted in death, 211 (99.5%) required hospitalization, and 3 (1.4%) were considered life-threatening.
Is Hospitalisation Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DEVICE. However, 212 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 Hospitalisation?
CLOZAPINE (12,144)
CINACALCET (6,997)
DARBEPOETIN ALFA (5,682)
MACITENTAN (3,414)
APIXABAN (3,315)
ADALIMUMAB (3,033)
DUPILUMAB (2,529)
LENALIDOMIDE (2,241)
DENOSUMAB (2,076)
PALIPERIDONE (2,066)
Which DEVICE Alternatives Have Lower Hospitalisation Risk?
DEVICE vs DEXAMETHASONE
DEVICE vs DEXAMETHASONE\DEXAMETHASONE
DEVICE vs DEXAMETHASONE\NEOMYCIN
DEVICE vs DEXAMETHASONE\NEOMYCIN\POLYMYXIN B
DEVICE vs DEXAMETHASONE\TOBRAMYCIN