Does LORATADINE Cause Product prescribing issue? 122 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 122 reports of Product prescribing issue have been filed in association with LORATADINE (Curist Allergy Relief). This represents 0.5% of all adverse event reports for LORATADINE.
122
Reports of Product prescribing issue with LORATADINE
0.5%
of all LORATADINE reports
2
Deaths
1
Hospitalizations
How Dangerous Is Product prescribing issue From LORATADINE?
Of the 122 reports, 2 (1.6%) resulted in death, 1 (0.8%) required hospitalization.
Is Product prescribing issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for LORATADINE. However, 122 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 prescribing issue?
DUPILUMAB (1,715)
POLYETHYLENE GLYCOL 3350 (1,439)
LENALIDOMIDE (948)
OXYCODONE (646)
RIVAROXABAN (359)
ACETAMINOPHEN\OXYCODONE (347)
ETONOGESTREL (311)
ACETAMINOPHEN\HYDROCODONE (298)
CERTOLIZUMAB PEGOL (297)
CABOZANTINIB S-MALATE (294)
Which LORATADINE Alternatives Have Lower Product prescribing issue Risk?
LORATADINE vs LORATADINE\PSEUDOEPHEDRINE
LORATADINE vs LORAZEPAM
LORATADINE vs LORCASERIN
LORATADINE vs LORLATINIB
LORATADINE vs LORMETAZEPAM