Does LORATADINE Cause Product administration error? 16 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 16 reports of Product administration error have been filed in association with LORATADINE (Curist Allergy Relief). This represents 0.1% of all adverse event reports for LORATADINE.
16
Reports of Product administration error with LORATADINE
0.1%
of all LORATADINE reports
1
Deaths
1
Hospitalizations
How Dangerous Is Product administration error From LORATADINE?
Of the 16 reports, 1 (6.3%) resulted in death, 1 (6.3%) required hospitalization, and 1 (6.3%) were considered life-threatening.
Is Product administration error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for LORATADINE. However, 16 reports have been filed with the FAERS database.
What Other Side Effects Does LORATADINE Cause?
Drug ineffective (7,516)
Extra dose administered (1,556)
Somnolence (1,391)
Off label use (1,386)
Product use issue (1,371)
Expired product administered (1,095)
Product use in unapproved indication (902)
Accidental exposure to product by child (830)
Drug effect incomplete (679)
Dizziness (674)
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 LORATADINE Alternatives Have Lower Product administration error Risk?
LORATADINE vs LORATADINE\PSEUDOEPHEDRINE
LORATADINE vs LORAZEPAM
LORATADINE vs LORCASERIN
LORATADINE vs LORLATINIB
LORATADINE vs LORMETAZEPAM