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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does CANNABIDIOL Cause Recalled product? 5 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Recalled product have been filed in association with CANNABIDIOL (Epidiolex). This represents 0.0% of all adverse event reports for CANNABIDIOL.

5
Reports of Recalled product with CANNABIDIOL
0.0%
of all CANNABIDIOL reports
0
Deaths
3
Hospitalizations

How Dangerous Is Recalled product From CANNABIDIOL?

Of the 5 reports, 3 (60.0%) required hospitalization.

Is Recalled product Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for CANNABIDIOL. However, 5 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 Recalled product?

PARATHYROID HORMONE (900) ANTIHEMOPHILIC FACTOR, HUMAN RECOMBINANT (80) CALCITRIOL (68) CALCIUM (66) REMDESIVIR (36) LEVOTHYROXINE\LIOTHYRONINE (34) TESTOSTERONE (32) VALSARTAN (32) CHLORHEXIDINE (28) ALCOHOL (26)

Which CANNABIDIOL Alternatives Have Lower Recalled product 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

Related Pages

CANNABIDIOL Full Profile All Recalled product Reports All Drugs Causing Recalled product CANNABIDIOL Demographics