Does DOXYLAMINE Cause Wrong technique in product usage process? 53 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 53 reports of Wrong technique in product usage process have been filed in association with DOXYLAMINE (CareOne Nighttime Sleep Aid). This represents 1.2% of all adverse event reports for DOXYLAMINE.
53
Reports of Wrong technique in product usage process with DOXYLAMINE
1.2%
of all DOXYLAMINE reports
0
Deaths
0
Hospitalizations
How Dangerous Is Wrong technique in product usage process From DOXYLAMINE?
Of the 53 reports, and 4 (7.5%) were considered life-threatening.
Is Wrong technique in product usage process Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DOXYLAMINE. However, 53 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 Wrong technique in product usage process?
EVOLOCUMAB (21,664)
ALBUTEROL (17,114)
ADALIMUMAB (11,766)
PEGFILGRASTIM (10,217)
ETANERCEPT (9,835)
ERENUMAB-AOOE (9,359)
SACUBITRIL\VALSARTAN (8,022)
LEUPROLIDE (5,062)
FENTANYL (2,812)
SEMAGLUTIDE (2,538)
Which DOXYLAMINE Alternatives Have Lower Wrong technique in product usage process Risk?
DOXYLAMINE vs DOXYLAMINE\PYRIDOXINE
DOXYLAMINE vs DRONABINOL
DOXYLAMINE vs DRONEDARONE
DOXYLAMINE vs DROPERIDOL
DOXYLAMINE vs DROSPIRENONE