Does DOXYLAMINE Cause Intentional product misuse? 93 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 93 reports of Intentional product misuse have been filed in association with DOXYLAMINE (CareOne Nighttime Sleep Aid). This represents 2.1% of all adverse event reports for DOXYLAMINE.
93
Reports of Intentional product misuse with DOXYLAMINE
2.1%
of all DOXYLAMINE reports
51
Deaths
13
Hospitalizations
How Dangerous Is Intentional product misuse From DOXYLAMINE?
Of the 93 reports, 51 (54.8%) resulted in death, 13 (14.0%) required hospitalization, and 1 (1.1%) were considered life-threatening.
Is Intentional product misuse Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DOXYLAMINE. However, 93 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 misuse?
ETANERCEPT (3,992)
PREGABALIN (3,731)
BUDESONIDE\FORMOTEROL (3,399)
ACETAMINOPHEN (2,924)
ESOMEPRAZOLE (2,852)
MINOXIDIL (2,418)
TOFACITINIB (2,331)
CINACALCET (2,092)
QUETIAPINE (1,855)
ALPRAZOLAM (1,709)
Which DOXYLAMINE Alternatives Have Lower Intentional product misuse Risk?
DOXYLAMINE vs DOXYLAMINE\PYRIDOXINE
DOXYLAMINE vs DRONABINOL
DOXYLAMINE vs DRONEDARONE
DOXYLAMINE vs DROPERIDOL
DOXYLAMINE vs DROSPIRENONE