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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\PSEUDOEPHEDRINE\TRIPROLIDINE Cause Product use issue? 8 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 8 reports of Product use issue have been filed in association with CODEINE\PSEUDOEPHEDRINE\TRIPROLIDINE. This represents 40.0% of all adverse event reports for CODEINE\PSEUDOEPHEDRINE\TRIPROLIDINE.

8
Reports of Product use issue with CODEINE\PSEUDOEPHEDRINE\TRIPROLIDINE
40.0%
of all CODEINE\PSEUDOEPHEDRINE\TRIPROLIDINE reports
0
Deaths
5
Hospitalizations

How Dangerous Is Product use issue From CODEINE\PSEUDOEPHEDRINE\TRIPROLIDINE?

Of the 8 reports, 5 (62.5%) required hospitalization, and 5 (62.5%) were considered life-threatening.

Is Product use issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for CODEINE\PSEUDOEPHEDRINE\TRIPROLIDINE. However, 8 reports have been filed with the FAERS database.

What Other Side Effects Does CODEINE\PSEUDOEPHEDRINE\TRIPROLIDINE Cause?

Off label use (8) Drug ineffective (7) Headache (7) Joint swelling (7) Musculoskeletal stiffness (7) Pain (7) Product use in unapproved indication (7) Pruritus (7) Drug dependence (5) Helicobacter infection (5)

What Other Drugs Cause Product use issue?

INFLIXIMAB (12,752) DUPILUMAB (10,575) POLYETHYLENE GLYCOL 3350 (9,432) METHOTREXATE (8,185) DICLOFENAC (8,009) RITUXIMAB (6,948) ADALIMUMAB (6,379) ETANERCEPT (6,062) TOCILIZUMAB (5,944) ABATACEPT (5,915)

Related Pages

CODEINE\PSEUDOEPHEDRINE\TRIPROLIDINE Full Profile All Product use issue Reports All Drugs Causing Product use issue CODEINE\PSEUDOEPHEDRINE\TRIPROLIDINE Demographics