Does CENEGERMIN-BKBJ Cause Product use complaint? 134 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 134 reports of Product use complaint have been filed in association with CENEGERMIN-BKBJ. This represents 1.1% of all adverse event reports for CENEGERMIN-BKBJ.
134
Reports of Product use complaint with CENEGERMIN-BKBJ
1.1%
of all CENEGERMIN-BKBJ reports
1
Deaths
11
Hospitalizations
How Dangerous Is Product use complaint From CENEGERMIN-BKBJ?
Of the 134 reports, 1 (0.7%) resulted in death, 11 (8.2%) required hospitalization.
Is Product use complaint Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for CENEGERMIN-BKBJ. However, 134 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 complaint?
TROFINETIDE (472)
ENZALUTAMIDE (336)
LIFITEGRAST (326)
VOXELOTOR (298)
CLASCOTERONE (285)
NIRMATRELVIR\RITONAVIR (248)
ABALOPARATIDE (224)
ESTRADIOL (208)
MOLNUPIRAVIR (206)
ACETAMINOPHEN (202)
Which CENEGERMIN-BKBJ Alternatives Have Lower Product use complaint Risk?
CENEGERMIN-BKBJ vs CENOBAMATE
CENEGERMIN-BKBJ vs CEPHALEXIN
CENEGERMIN-BKBJ vs CERITINIB
CENEGERMIN-BKBJ vs CERLIPONASE ALFA
CENEGERMIN-BKBJ vs CERTICAN