Does DESLORATADINE Cause Product use in unapproved indication? 121 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 121 reports of Product use in unapproved indication have been filed in association with DESLORATADINE (Desloratadine). This represents 3.9% of all adverse event reports for DESLORATADINE.
121
Reports of Product use in unapproved indication with DESLORATADINE
3.9%
of all DESLORATADINE reports
2
Deaths
44
Hospitalizations
How Dangerous Is Product use in unapproved indication From DESLORATADINE?
Of the 121 reports, 2 (1.7%) resulted in death, 44 (36.4%) required hospitalization, and 19 (15.7%) were considered life-threatening.
Is Product use in unapproved indication Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DESLORATADINE. However, 121 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)
Fall (118)
Vomiting (113)
Hypotension (111)
What Other Drugs Cause Product use in unapproved indication?
DUPILUMAB (33,452)
DICLOFENAC (12,197)
METHOTREXATE (8,930)
PREDNISONE (7,625)
RITUXIMAB (7,519)
MYCOPHENOLATE MOFETIL (5,910)
ACETAMINOPHEN (5,819)
CYCLOPHOSPHAMIDE (5,750)
RISPERIDONE (5,551)
TACROLIMUS (5,057)
Which DESLORATADINE Alternatives Have Lower Product use in unapproved indication Risk?
DESLORATADINE vs DESMOPRESSIN
DESLORATADINE vs DESOGESTREL
DESLORATADINE vs DESOGESTREL\ETHINYL ESTRADIOL
DESLORATADINE vs DESONIDE
DESLORATADINE vs DESOXIMETASONE