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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 DESLORATADINE Cause Product prescribing error? 11 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 11 reports of Product prescribing error have been filed in association with DESLORATADINE (Desloratadine). This represents 0.4% of all adverse event reports for DESLORATADINE.

11
Reports of Product prescribing error with DESLORATADINE
0.4%
of all DESLORATADINE reports
4
Deaths
4
Hospitalizations

How Dangerous Is Product prescribing error From DESLORATADINE?

Of the 11 reports, 4 (36.4%) resulted in death, 4 (36.4%) required hospitalization, and 2 (18.2%) were considered life-threatening.

Is Product prescribing error Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for DESLORATADINE. However, 11 reports have been filed with the FAERS database.

What Other Side Effects Does DESLORATADINE Cause?

Intentional overdose (182) Drug ineffective (179) Somnolence (143) Urticaria (142) Dizziness (132) Fatigue (131) Pruritus (130) Product use in unapproved indication (121) Fall (118) Vomiting (113)

What Other Drugs Cause Product prescribing error?

SOMATROPIN (1,123) SACUBITRIL\VALSARTAN (1,023) SECUKINUMAB (821) TOFACITINIB (805) DUPILUMAB (725) NIRMATRELVIR\RITONAVIR (611) PREGABALIN (476) METHOTREXATE (434) TORSEMIDE (352) METOPROLOL (325)

Which DESLORATADINE Alternatives Have Lower Product prescribing error Risk?

DESLORATADINE vs DESMOPRESSIN DESLORATADINE vs DESOGESTREL DESLORATADINE vs DESOGESTREL\ETHINYL ESTRADIOL DESLORATADINE vs DESONIDE DESLORATADINE vs DESOXIMETASONE

Related Pages

DESLORATADINE Full Profile All Product prescribing error Reports All Drugs Causing Product prescribing error DESLORATADINE Demographics