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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 Product prescribing issue? 13 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 13 reports of Product prescribing issue have been filed in association with CODEINE (Codeine-Guaifenesin). This represents 0.1% of all adverse event reports for CODEINE.

13
Reports of Product prescribing issue with CODEINE
0.1%
of all CODEINE reports
5
Deaths
6
Hospitalizations

How Dangerous Is Product prescribing issue From CODEINE?

Of the 13 reports, 5 (38.5%) resulted in death, 6 (46.2%) required hospitalization, and 3 (23.1%) were considered life-threatening.

Is Product prescribing issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for CODEINE. However, 13 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)