Does LORATADINE Cause Incorrect product administration duration? 32 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 32 reports of Incorrect product administration duration have been filed in association with LORATADINE (Curist Allergy Relief). This represents 0.1% of all adverse event reports for LORATADINE.
32
Reports of Incorrect product administration duration with LORATADINE
0.1%
of all LORATADINE reports
0
Deaths
0
Hospitalizations
How Dangerous Is Incorrect product administration duration From LORATADINE?
Of the 32 reports.
Is Incorrect product administration duration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for LORATADINE. However, 32 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 Incorrect product administration duration?
ETONOGESTREL (3,974)
POLYETHYLENE GLYCOL 3350 (2,129)
NIRMATRELVIR\RITONAVIR (744)
DOCOSANOL (634)
LANSOPRAZOLE (564)
LOPERAMIDE (543)
NAPROXEN (499)
INSULIN LISPRO (479)
DICLOFENAC (362)
OMEPRAZOLE (302)
Which LORATADINE Alternatives Have Lower Incorrect product administration duration Risk?
LORATADINE vs LORATADINE\PSEUDOEPHEDRINE
LORATADINE vs LORAZEPAM
LORATADINE vs LORCASERIN
LORATADINE vs LORLATINIB
LORATADINE vs LORMETAZEPAM