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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 DOXYLAMINE Cause Maternal exposure timing unspecified? 5 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Maternal exposure timing unspecified have been filed in association with DOXYLAMINE (CareOne Nighttime Sleep Aid). This represents 0.1% of all adverse event reports for DOXYLAMINE.

5
Reports of Maternal exposure timing unspecified with DOXYLAMINE
0.1%
of all DOXYLAMINE reports
0
Deaths
4
Hospitalizations

How Dangerous Is Maternal exposure timing unspecified From DOXYLAMINE?

Of the 5 reports, 4 (80.0%) required hospitalization, and 1 (20.0%) were considered life-threatening.

Is Maternal exposure timing unspecified Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for DOXYLAMINE. However, 5 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 Maternal exposure timing unspecified?

RITUXIMAB (402) METHOTREXATE (350) ADALIMUMAB (343) DICLOFENAC (331) TOCILIZUMAB (327) HYDROXYCHLOROQUINE (309) FOLIC ACID (304) INFLIXIMAB (303) LEFLUNOMIDE (302) SECUKINUMAB (301)

Which DOXYLAMINE Alternatives Have Lower Maternal exposure timing unspecified Risk?

DOXYLAMINE vs DOXYLAMINE\PYRIDOXINE DOXYLAMINE vs DRONABINOL DOXYLAMINE vs DRONEDARONE DOXYLAMINE vs DROPERIDOL DOXYLAMINE vs DROSPIRENONE

Related Pages

DOXYLAMINE Full Profile All Maternal exposure timing unspecified Reports All Drugs Causing Maternal exposure timing unspecified DOXYLAMINE Demographics