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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 Wrong patient received product? 27 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 27 reports of Wrong patient received product have been filed in association with DESLORATADINE (Desloratadine). This represents 0.9% of all adverse event reports for DESLORATADINE.

27
Reports of Wrong patient received product with DESLORATADINE
0.9%
of all DESLORATADINE reports
0
Deaths
0
Hospitalizations

How Dangerous Is Wrong patient received product From DESLORATADINE?

Of the 27 reports.

Is Wrong patient received product Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for DESLORATADINE. However, 27 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 Wrong patient received product?

INSULIN LISPRO (334) CLOZAPINE (198) RISPERIDONE (176) OXAZEPAM (152) BISOPROLOL (150) LEVETIRACETAM (126) ACETAMINOPHEN (123) METFORMIN (116) INSULIN GLARGINE (114) CLONAZEPAM (112)

Which DESLORATADINE Alternatives Have Lower Wrong patient received product Risk?

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

Related Pages

DESLORATADINE Full Profile All Wrong patient received product Reports All Drugs Causing Wrong patient received product DESLORATADINE Demographics