Does ACTIVATED CHARCOAL Cause Product administration error? 6 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 6 reports of Product administration error have been filed in association with ACTIVATED CHARCOAL (THE FLOWER REMEDY Get Up and Go). This represents 2.0% of all adverse event reports for ACTIVATED CHARCOAL.
6
Reports of Product administration error with ACTIVATED CHARCOAL
2.0%
of all ACTIVATED CHARCOAL reports
0
Deaths
6
Hospitalizations
How Dangerous Is Product administration error From ACTIVATED CHARCOAL?
Of the 6 reports, 6 (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 ACTIVATED CHARCOAL. However, 6 reports have been filed with the FAERS database.
What Other Side Effects Does ACTIVATED CHARCOAL Cause?
Overdose (73)
Toxicity to various agents (69)
Off label use (62)
Drug ineffective (59)
Drug abuse (50)
Intentional product misuse (49)
Completed suicide (48)
Rash (45)
Abdominal discomfort (44)
Arthropathy (43)
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 ACTIVATED CHARCOAL Alternatives Have Lower Product administration error Risk?
ACTIVATED CHARCOAL vs ACTONEL
ACTIVATED CHARCOAL vs ACYCLOVIR
ACTIVATED CHARCOAL vs AD26.COV2.S
ACTIVATED CHARCOAL vs ADAGRASIB
ACTIVATED CHARCOAL vs ADALIMUMAB