Does CENEGERMIN-BKBJ Cause Product administration error? 613 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 613 reports of Product administration error have been filed in association with CENEGERMIN-BKBJ. This represents 5.1% of all adverse event reports for CENEGERMIN-BKBJ.
613
Reports of Product administration error with CENEGERMIN-BKBJ
5.1%
of all CENEGERMIN-BKBJ reports
1
Deaths
41
Hospitalizations
How Dangerous Is Product administration error From CENEGERMIN-BKBJ?
Of the 613 reports, 1 (0.2%) resulted in death, 41 (6.7%) required hospitalization.
Is Product administration error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for CENEGERMIN-BKBJ. However, 613 reports have been filed with the FAERS database.
What Other Side Effects Does CENEGERMIN-BKBJ Cause?
Eye pain (5,847)
Eye irritation (1,871)
Product dose omission issue (1,335)
Ocular hyperaemia (1,226)
Photophobia (1,065)
Vision blurred (944)
Wrong technique in product usage process (899)
Eye swelling (847)
Ocular discomfort (797)
Lacrimation increased (737)
What Other Drugs Cause Product administration error?
HYDROXYPROGESTERONE CAPROATE (972)
ACETAMINOPHEN (666)
LEUPROLIDE (595)
EVOLOCUMAB (565)
ADALIMUMAB (543)
METHYLPHENIDATE (414)
OLMESARTAN MEDOXOMIL (314)
ASPIRIN (241)
SECUKINUMAB (225)
HYDROCHLOROTHIAZIDE\OLMESARTAN MEDOXOMIL (222)
Which CENEGERMIN-BKBJ Alternatives Have Lower Product administration error Risk?
CENEGERMIN-BKBJ vs CENOBAMATE
CENEGERMIN-BKBJ vs CEPHALEXIN
CENEGERMIN-BKBJ vs CERITINIB
CENEGERMIN-BKBJ vs CERLIPONASE ALFA
CENEGERMIN-BKBJ vs CERTICAN