Does CENEGERMIN-BKBJ Cause Product use issue? 164 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 164 reports of Product use issue have been filed in association with CENEGERMIN-BKBJ. This represents 1.4% of all adverse event reports for CENEGERMIN-BKBJ.
164
Reports of Product use issue with CENEGERMIN-BKBJ
1.4%
of all CENEGERMIN-BKBJ reports
3
Deaths
7
Hospitalizations
How Dangerous Is Product use issue From CENEGERMIN-BKBJ?
Of the 164 reports, 3 (1.8%) resulted in death, 7 (4.3%) required hospitalization.
Is Product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for CENEGERMIN-BKBJ. However, 164 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 use issue?
INFLIXIMAB (12,752)
DUPILUMAB (10,575)
POLYETHYLENE GLYCOL 3350 (9,432)
METHOTREXATE (8,185)
DICLOFENAC (8,009)
RITUXIMAB (6,948)
ADALIMUMAB (6,379)
ETANERCEPT (6,062)
TOCILIZUMAB (5,944)
ABATACEPT (5,915)
Which CENEGERMIN-BKBJ Alternatives Have Lower Product use issue Risk?
CENEGERMIN-BKBJ vs CENOBAMATE
CENEGERMIN-BKBJ vs CEPHALEXIN
CENEGERMIN-BKBJ vs CERITINIB
CENEGERMIN-BKBJ vs CERLIPONASE ALFA
CENEGERMIN-BKBJ vs CERTICAN