Does CANNABIDIOL Cause Product administration interrupted? 511 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 511 reports of Product administration interrupted have been filed in association with CANNABIDIOL (Epidiolex). This represents 2.8% of all adverse event reports for CANNABIDIOL.
511
Reports of Product administration interrupted with CANNABIDIOL
2.8%
of all CANNABIDIOL reports
10
Deaths
208
Hospitalizations
How Dangerous Is Product administration interrupted From CANNABIDIOL?
Of the 511 reports, 10 (2.0%) resulted in death, 208 (40.7%) required hospitalization, and 3 (0.6%) were considered life-threatening.
Is Product administration interrupted Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for CANNABIDIOL. However, 511 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 administration interrupted?
CALCIUM OXYBATE\MAGNESIUM OXYBATE\POTASSIUM OXYBATE\SODIUM OXYBATE (1,446)
SODIUM OXYBATE (1,272)
ISOTRETINOIN (503)
APREMILAST (314)
TREPROSTINIL (295)
EPOPROSTENOL (205)
LENALIDOMIDE (146)
ETANERCEPT (142)
INTERFERON BETA-1A (115)
ADALIMUMAB (86)
Which CANNABIDIOL Alternatives Have Lower Product administration interrupted 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