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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 Contraindicated product administered? 19 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 19 reports of Contraindicated product administered 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 Contraindicated product administered with CODEINE\GUAIFENESIN\PHENIRAMINE
70.4%
of all CODEINE\GUAIFENESIN\PHENIRAMINE reports
19
Deaths
0
Hospitalizations

How Dangerous Is Contraindicated product administered From CODEINE\GUAIFENESIN\PHENIRAMINE?

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

Is Contraindicated product administered 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) Drug hypersensitivity (19) Drug intolerance (19) Fluid retention (19)

What Other Drugs Cause Contraindicated product administered?

ABATACEPT (13,559) METHOTREXATE (13,121) ETANERCEPT (12,062) TOCILIZUMAB (11,547) ADALIMUMAB (11,270) LEFLUNOMIDE (11,206) HYDROXYCHLOROQUINE (10,557) RITUXIMAB (10,479) INFLIXIMAB (9,618) SULFASALAZINE (8,698)

Related Pages

CODEINE\GUAIFENESIN\PHENIRAMINE Full Profile All Contraindicated product administered Reports All Drugs Causing Contraindicated product administered CODEINE\GUAIFENESIN\PHENIRAMINE Demographics