Does DOXYLAMINE Cause Intentional product use issue? 21 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 21 reports of Intentional product use issue have been filed in association with DOXYLAMINE (CareOne Nighttime Sleep Aid). This represents 0.5% of all adverse event reports for DOXYLAMINE.
21
Reports of Intentional product use issue with DOXYLAMINE
0.5%
of all DOXYLAMINE reports
1
Deaths
0
Hospitalizations
How Dangerous Is Intentional product use issue From DOXYLAMINE?
Of the 21 reports, 1 (4.8%) resulted in death, and 4 (19.0%) were considered life-threatening.
Is Intentional product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DOXYLAMINE. However, 21 reports have been filed with the FAERS database.
What Other Side Effects Does DOXYLAMINE Cause?
Drug ineffective (889)
Toxicity to various agents (574)
Somnolence (435)
Drug abuse (427)
Completed suicide (298)
Death (192)
Overdose (179)
Underdose (171)
Maternal exposure during pregnancy (169)
Incorrect dose administered (122)
What Other Drugs Cause Intentional product use issue?
INFLIXIMAB (11,028)
RITUXIMAB (9,602)
INFLIXIMAB-DYYB (7,549)
TOCILIZUMAB (5,078)
METHOTREXATE (4,087)
PREDNISONE (3,961)
ABATACEPT (3,693)
ADALIMUMAB (3,557)
NIVOLUMAB (3,297)
LEFLUNOMIDE (3,280)
Which DOXYLAMINE Alternatives Have Lower Intentional product use issue Risk?
DOXYLAMINE vs DOXYLAMINE\PYRIDOXINE
DOXYLAMINE vs DRONABINOL
DOXYLAMINE vs DRONEDARONE
DOXYLAMINE vs DROPERIDOL
DOXYLAMINE vs DROSPIRENONE