Does DEVICE Cause Pulmonary function test decreased? 8 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 8 reports of Pulmonary function test decreased have been filed in association with DEVICE. This represents 0.1% of all adverse event reports for DEVICE.
8
Reports of Pulmonary function test decreased with DEVICE
0.1%
of all DEVICE reports
0
Deaths
6
Hospitalizations
How Dangerous Is Pulmonary function test decreased From DEVICE?
Of the 8 reports, 6 (75.0%) required hospitalization.
Is Pulmonary function test decreased Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DEVICE. However, 8 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 Pulmonary function test decreased?
IVACAFTOR\LUMACAFTOR (378)
ALBUTEROL (325)
BUDESONIDE\FORMOTEROL (304)
OMALIZUMAB (288)
PREDNISONE (275)
AZTREONAM LYSINE (252)
TIOTROPIUM (223)
PIRFENIDONE (207)
ELEXACAFTOR\IVACAFTOR\TEZACAFTOR (192)
TOBRAMYCIN (190)
Which DEVICE Alternatives Have Lower Pulmonary function test decreased Risk?
DEVICE vs DEXAMETHASONE
DEVICE vs DEXAMETHASONE\DEXAMETHASONE
DEVICE vs DEXAMETHASONE\NEOMYCIN
DEVICE vs DEXAMETHASONE\NEOMYCIN\POLYMYXIN B
DEVICE vs DEXAMETHASONE\TOBRAMYCIN