Does DESLORATADINE Cause Product administration error? 10 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 10 reports of Product administration error have been filed in association with DESLORATADINE (Desloratadine). This represents 0.3% of all adverse event reports for DESLORATADINE.
10
Reports of Product administration error with DESLORATADINE
0.3%
of all DESLORATADINE reports
0
Deaths
1
Hospitalizations
How Dangerous Is Product administration error From DESLORATADINE?
Of the 10 reports, 1 (10.0%) required hospitalization.
Is Product administration error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DESLORATADINE. However, 10 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 administration error?
HYDROXYPROGESTERONE CAPROATE (972)
ACETAMINOPHEN (666)
CENEGERMIN-BKBJ (613)
LEUPROLIDE (595)
EVOLOCUMAB (565)
ADALIMUMAB (543)
METHYLPHENIDATE (414)
OLMESARTAN MEDOXOMIL (314)
ASPIRIN (241)
SECUKINUMAB (225)
Which DESLORATADINE Alternatives Have Lower Product administration error Risk?
DESLORATADINE vs DESMOPRESSIN
DESLORATADINE vs DESOGESTREL
DESLORATADINE vs DESOGESTREL\ETHINYL ESTRADIOL
DESLORATADINE vs DESONIDE
DESLORATADINE vs DESOXIMETASONE