Does DOXYLAMINE Cause Product use issue? 29 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 29 reports of Product use issue have been filed in association with DOXYLAMINE (CareOne Nighttime Sleep Aid). This represents 0.7% of all adverse event reports for DOXYLAMINE.
29
Reports of Product use issue with DOXYLAMINE
0.7%
of all DOXYLAMINE reports
6
Deaths
5
Hospitalizations
How Dangerous Is Product use issue From DOXYLAMINE?
Of the 29 reports, 6 (20.7%) resulted in death, 5 (17.2%) required hospitalization, and 5 (17.2%) were considered life-threatening.
Is Product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DOXYLAMINE. However, 29 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 Product use issue?
INFLIXIMAB (12,752)
DUPILUMAB (10,575)
POLYETHYLENE GLYCOL 3350 (9,432)
METHOTREXATE (8,185)
DICLOFENAC (8,009)
RITUXIMAB (6,948)
ADALIMUMAB (6,379)
ETANERCEPT (6,062)
TOCILIZUMAB (5,944)
ABATACEPT (5,915)
Which DOXYLAMINE Alternatives Have Lower Product use issue Risk?
DOXYLAMINE vs DOXYLAMINE\PYRIDOXINE
DOXYLAMINE vs DRONABINOL
DOXYLAMINE vs DRONEDARONE
DOXYLAMINE vs DROPERIDOL
DOXYLAMINE vs DROSPIRENONE