Does BIFIDOBACTERIUM LONGUM Cause Product administration error? 5 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Product administration error have been filed in association with BIFIDOBACTERIUM LONGUM. This represents 3.6% of all adverse event reports for BIFIDOBACTERIUM LONGUM.
5
Reports of Product administration error with BIFIDOBACTERIUM LONGUM
3.6%
of all BIFIDOBACTERIUM LONGUM reports
0
Deaths
5
Hospitalizations
How Dangerous Is Product administration error From BIFIDOBACTERIUM LONGUM?
Of the 5 reports, 5 (100.0%) 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 BIFIDOBACTERIUM LONGUM. However, 5 reports have been filed with the FAERS database.
What Other Side Effects Does BIFIDOBACTERIUM LONGUM Cause?
Off label use (93)
Abdominal pain (58)
Malaise (58)
Anaemia (57)
Chronic sinusitis (57)
Colitis (57)
Constipation (57)
Drug ineffective (57)
Erythema (57)
Female genital tract fistula (57)
What Other Drugs Cause Product administration error?
HYDROXYPROGESTERONE CAPROATE (972)
ACETAMINOPHEN (666)
CENEGERMIN-BKBJ (613)
LEUPROLIDE (595)
EVOLOCUMAB (565)
ADALIMUMAB (543)
METHYLPHENIDATE (414)
OLMESARTAN MEDOXOMIL (314)
ASPIRIN (241)
SECUKINUMAB (225)
Which BIFIDOBACTERIUM LONGUM Alternatives Have Lower Product administration error Risk?
BIFIDOBACTERIUM LONGUM vs BIFIDOBACTERIUM LONGUM SUBSP. INFANTIS
BIFIDOBACTERIUM LONGUM vs BILASTINE
BIFIDOBACTERIUM LONGUM vs BIMATOPROST
BIFIDOBACTERIUM LONGUM vs BIMATOPROST\TIMOLOL
BIFIDOBACTERIUM LONGUM vs BIMEKIZUMAB