Does DEVICE Cause Application site haemorrhage? 5 Reports in FDA Database
Boost Your Natural Energy & Metabolism
Mitolyn — 6 exotic plants to unlock your body's fat-burning power. 90-day guarantee.
According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Application site haemorrhage have been filed in association with DEVICE. This represents 0.0% of all adverse event reports for DEVICE.
5
Reports of Application site haemorrhage with DEVICE
0.0%
of all DEVICE reports
0
Deaths
2
Hospitalizations
How Dangerous Is Application site haemorrhage From DEVICE?
Of the 5 reports, 2 (40.0%) required hospitalization.
Is Application site haemorrhage Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DEVICE. However, 5 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 Application site haemorrhage?
PEGFILGRASTIM (1,394)
MINOXIDIL (78)
BUPRENORPHINE (68)
ESTRADIOL (64)
DOCOSANOL (62)
BECAPLERMIN (60)
INGENOL MEBUTATE (50)
FENTANYL (47)
EVOLOCUMAB (45)
NICOTINE (37)
Which DEVICE Alternatives Have Lower Application site haemorrhage Risk?
DEVICE vs DEXAMETHASONE
DEVICE vs DEXAMETHASONE\DEXAMETHASONE
DEVICE vs DEXAMETHASONE\NEOMYCIN
DEVICE vs DEXAMETHASONE\NEOMYCIN\POLYMYXIN B
DEVICE vs DEXAMETHASONE\TOBRAMYCIN