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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 CETIRIZINE Cause Product administration interrupted? 7 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Product administration interrupted have been filed in association with CETIRIZINE (Cetirizine). This represents 0.0% of all adverse event reports for CETIRIZINE.

7
Reports of Product administration interrupted with CETIRIZINE
0.0%
of all CETIRIZINE reports
0
Deaths
1
Hospitalizations

How Dangerous Is Product administration interrupted From CETIRIZINE?

Of the 7 reports, 1 (14.3%) required hospitalization, and 1 (14.3%) were considered life-threatening.

Is Product administration interrupted Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for CETIRIZINE. However, 7 reports have been filed with the FAERS database.

What Other Side Effects Does CETIRIZINE Cause?

Drug ineffective (13,819) Fatigue (9,476) Pain (9,377) Abdominal discomfort (8,413) Alopecia (8,412) Systemic lupus erythematosus (8,196) Pemphigus (8,063) Rheumatoid arthritis (7,891) Off label use (7,790) Glossodynia (7,407)

What Other Drugs Cause Product administration interrupted?

CALCIUM OXYBATE\MAGNESIUM OXYBATE\POTASSIUM OXYBATE\SODIUM OXYBATE (1,446) SODIUM OXYBATE (1,272) CANNABIDIOL (511) ISOTRETINOIN (503) APREMILAST (314) TREPROSTINIL (295) EPOPROSTENOL (205) LENALIDOMIDE (146) ETANERCEPT (142) INTERFERON BETA-1A (115)

Which CETIRIZINE Alternatives Have Lower Product administration interrupted Risk?

CETIRIZINE vs CETIRIZINE\PSEUDOEPHEDRINE CETIRIZINE vs CETRIMIDE CETIRIZINE vs CETRORELIX CETIRIZINE vs CETUXIMAB CETIRIZINE vs CETYLPYRIDINIUM

Related Pages

CETIRIZINE Full Profile All Product administration interrupted Reports All Drugs Causing Product administration interrupted CETIRIZINE Demographics