Does CENEGERMIN-BKBJ Cause Product storage error? 200 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 200 reports of Product storage error have been filed in association with CENEGERMIN-BKBJ. This represents 1.7% of all adverse event reports for CENEGERMIN-BKBJ.
200
Reports of Product storage error with CENEGERMIN-BKBJ
1.7%
of all CENEGERMIN-BKBJ reports
2
Deaths
16
Hospitalizations
How Dangerous Is Product storage error From CENEGERMIN-BKBJ?
Of the 200 reports, 2 (1.0%) resulted in death, 16 (8.0%) required hospitalization.
Is Product storage error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for CENEGERMIN-BKBJ. However, 200 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 storage error?
INSULIN GLARGINE (7,743)
EVOLOCUMAB (6,606)
ETANERCEPT (3,653)
DENOSUMAB (3,621)
ERENUMAB-AOOE (2,958)
DUPILUMAB (2,631)
ALBUTEROL (2,474)
ABATACEPT (2,101)
DARBEPOETIN ALFA (1,619)
INSULIN LISPRO (1,448)
Which CENEGERMIN-BKBJ Alternatives Have Lower Product storage error Risk?
CENEGERMIN-BKBJ vs CENOBAMATE
CENEGERMIN-BKBJ vs CEPHALEXIN
CENEGERMIN-BKBJ vs CERITINIB
CENEGERMIN-BKBJ vs CERLIPONASE ALFA
CENEGERMIN-BKBJ vs CERTICAN