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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.

CETIRIZINE\IBUPROFEN\PSEUDOEPHEDRINE: 13 Adverse Event Reports & Safety Profile

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13
Total FAERS Reports
5 (38.5%)
Deaths Reported
9
Hospitalizations
13
As Primary/Secondary Suspect
5
Life-Threatening
9
Disabilities

Active Ingredient: CETIRIZINE HYDROCHLORIDE\IBUPROFEN\PSEUDOEPHEDRINE HYDROCHLORIDE ·

What Are the Most Common CETIRIZINE\IBUPROFEN\PSEUDOEPHEDRINE Side Effects?

#1 Most Reported
Contraindicated product administered
13 reports (100.0%)
#2 Most Reported
Swelling
12 reports (92.3%)
#3 Most Reported
Rheumatoid arthritis
12 reports (92.3%)

All CETIRIZINE\IBUPROFEN\PSEUDOEPHEDRINE Side Effects by Frequency

Side Effect Reports % of Total Deaths Hosp.
Contraindicated product administered 13 100.0% 5 9
Alopecia 12 92.3% 4 8
Arthralgia 12 92.3% 4 8
Arthropathy 12 92.3% 4 8
Blister 12 92.3% 4 8
Discomfort 12 92.3% 4 8
Duodenal ulcer perforation 12 92.3% 4 8
Dyspnoea 12 92.3% 4 8
Fatigue 12 92.3% 4 8
Pericarditis 12 92.3% 4 8
Rash 12 92.3% 4 8
Rheumatoid arthritis 12 92.3% 4 8
Swelling 12 92.3% 4 8
Abdominal discomfort 11 84.6% 3 7
Anti-cyclic citrullinated peptide antibody positive 11 84.6% 4 7
Glossodynia 11 84.6% 3 7
Hand deformity 11 84.6% 3 7
Helicobacter infection 11 84.6% 3 7
Hepatic enzyme increased 11 84.6% 3 7
Infection 11 84.6% 3 7

Who Reports CETIRIZINE\IBUPROFEN\PSEUDOEPHEDRINE Side Effects? Age & Gender Data

Gender: 100.0% female, 0.0% male. Average age: 43.8 years. Most reports from: CA. View detailed demographics →

What Is CETIRIZINE\IBUPROFEN\PSEUDOEPHEDRINE Used For?

IndicationReports
Rheumatoid arthritis 13

Official FDA Label for CETIRIZINE\IBUPROFEN\PSEUDOEPHEDRINE

Official prescribing information from the FDA-approved drug label.