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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 CODEINE Cause Maternal exposure timing unspecified? 73 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 73 reports of Maternal exposure timing unspecified have been filed in association with CODEINE (Codeine-Guaifenesin). This represents 0.3% of all adverse event reports for CODEINE.

73
Reports of Maternal exposure timing unspecified with CODEINE
0.3%
of all CODEINE reports
73
Deaths
73
Hospitalizations

How Dangerous Is Maternal exposure timing unspecified From CODEINE?

Of the 73 reports, 73 (100.0%) resulted in death, 73 (100.0%) required hospitalization, and 73 (100.0%) 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 CODEINE. However, 73 reports have been filed with the FAERS database.

What Other Side Effects Does CODEINE Cause?

Drug hypersensitivity (7,479) Toxicity to various agents (2,951) Drug ineffective (2,632) Drug abuse (2,122) Pain (2,024) Rash (1,931) Nausea (1,907) Rheumatoid arthritis (1,861) Headache (1,701) Off label use (1,662)

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 CODEINE Alternatives Have Lower Maternal exposure timing unspecified Risk?

CODEINE vs CODEINE\GUAIFENESIN CODEINE vs CODEINE\IBUPROFEN CODEINE vs CODEINE\PROMETHAZINE CODEINE vs COLCHICINE CODEINE vs COLCHICINE\DICYCLOMINE

Related Pages

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