Does CANNABIDIOL Cause Product dose omission? 301 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 301 reports of Product dose omission have been filed in association with CANNABIDIOL (Epidiolex). This represents 1.7% of all adverse event reports for CANNABIDIOL.
301
Reports of Product dose omission with CANNABIDIOL
1.7%
of all CANNABIDIOL reports
1
Deaths
56
Hospitalizations
How Dangerous Is Product dose omission From CANNABIDIOL?
Of the 301 reports, 1 (0.3%) resulted in death, 56 (18.6%) required hospitalization, and 1 (0.3%) were considered life-threatening.
Is Product dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for CANNABIDIOL. However, 301 reports have been filed with the FAERS database.
What Other Side Effects Does CANNABIDIOL Cause?
Seizure (4,980)
Hospitalisation (1,840)
Off label use (1,636)
Product use in unapproved indication (1,585)
Diarrhoea (1,356)
Death (1,115)
Somnolence (1,005)
Product dose omission issue (895)
Drug ineffective (859)
Fatigue (715)
What Other Drugs Cause Product dose omission?
APREMILAST (4,567)
DUPILUMAB (2,729)
ALBUTEROL (1,742)
USTEKINUMAB (1,653)
INSULIN GLARGINE (1,500)
ETANERCEPT (1,400)
LENALIDOMIDE (1,400)
RUXOLITINIB (1,376)
ALIROCUMAB (1,354)
DIMETHYL (1,248)
Which CANNABIDIOL Alternatives Have Lower Product dose omission Risk?
CANNABIDIOL vs CANNABIDIOL\HERBALS
CANNABIDIOL vs CANNABIS SATIVA FLOWERING TOP
CANNABIDIOL vs CANNABIS SATIVA SUBSP. INDICA TOP
CANNABIDIOL vs CANRENOATE
CANNABIDIOL vs CANRENOIC ACID