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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\GUAIFENESIN\PHENIRAMINE Cause Treatment failure? 19 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 19 reports of Treatment failure have been filed in association with CODEINE\GUAIFENESIN\PHENIRAMINE. This represents 70.4% of all adverse event reports for CODEINE\GUAIFENESIN\PHENIRAMINE.

19
Reports of Treatment failure with CODEINE\GUAIFENESIN\PHENIRAMINE
70.4%
of all CODEINE\GUAIFENESIN\PHENIRAMINE reports
19
Deaths
0
Hospitalizations

How Dangerous Is Treatment failure From CODEINE\GUAIFENESIN\PHENIRAMINE?

Of the 19 reports, 19 (100.0%) resulted in death.

Is Treatment failure Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for CODEINE\GUAIFENESIN\PHENIRAMINE. However, 19 reports have been filed with the FAERS database.

What Other Side Effects Does CODEINE\GUAIFENESIN\PHENIRAMINE Cause?

Fatigue (20) Thrombocytopenia (20) Asthma (19) Back pain (19) Bursitis (19) Coeliac disease (19) Constipation (19) Contraindicated product administered (19) Drug hypersensitivity (19) Drug intolerance (19)

What Other Drugs Cause Treatment failure?

METHOTREXATE (14,672) ETANERCEPT (11,893) ADALIMUMAB (9,990) ABATACEPT (9,301) RITUXIMAB (9,217) TOCILIZUMAB (9,097) HYDROXYCHLOROQUINE (8,786) LEFLUNOMIDE (8,686) INFLIXIMAB (8,535) SULFASALAZINE (7,423)

Related Pages

CODEINE\GUAIFENESIN\PHENIRAMINE Full Profile All Treatment failure Reports All Drugs Causing Treatment failure CODEINE\GUAIFENESIN\PHENIRAMINE Demographics