Does LORATADINE Cause Off label use? 1,386 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 1,386 reports of Off label use have been filed in association with LORATADINE (Curist Allergy Relief). This represents 5.5% of all adverse event reports for LORATADINE.
1,386
Reports of Off label use with LORATADINE
5.5%
of all LORATADINE reports
13
Deaths
73
Hospitalizations
How Dangerous Is Off label use From LORATADINE?
Of the 1,386 reports, 13 (0.9%) resulted in death, 73 (5.3%) required hospitalization, and 11 (0.8%) were considered life-threatening.
Is Off label use Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for LORATADINE. However, 1,386 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)
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)
Headache (654)
What Other Drugs Cause Off label use?
RITUXIMAB (39,751)
INFLIXIMAB (34,801)
DENOSUMAB (34,612)
METHOTREXATE (24,020)
VEDOLIZUMAB (21,017)
ETANERCEPT (20,178)
TOCILIZUMAB (18,256)
PREDNISONE (17,867)
LENALIDOMIDE (17,017)
ADALIMUMAB (16,417)
Which LORATADINE Alternatives Have Lower Off label use Risk?
LORATADINE vs LORATADINE\PSEUDOEPHEDRINE
LORATADINE vs LORAZEPAM
LORATADINE vs LORCASERIN
LORATADINE vs LORLATINIB
LORATADINE vs LORMETAZEPAM