Does LORATADINE Cause Expired product administered? 1,095 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 1,095 reports of Expired product administered have been filed in association with LORATADINE (Curist Allergy Relief). This represents 4.3% of all adverse event reports for LORATADINE.
1,095
Reports of Expired product administered with LORATADINE
4.3%
of all LORATADINE reports
0
Deaths
1
Hospitalizations
How Dangerous Is Expired product administered From LORATADINE?
Of the 1,095 reports, 1 (0.1%) required hospitalization, and 1 (0.1%) were considered life-threatening.
Is Expired product administered Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for LORATADINE. However, 1,095 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)
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 Expired product administered?
POLYETHYLENE GLYCOL 3350 (1,637)
NAPROXEN (1,305)
ALBUTEROL (1,233)
MINOXIDIL (982)
ACETAMINOPHEN (797)
INSULIN LISPRO (770)
FLUTICASONE\SALMETEROL (753)
CETIRIZINE (714)
DICLOFENAC (714)
NICOTINE (704)
Which LORATADINE Alternatives Have Lower Expired product administered Risk?
LORATADINE vs LORATADINE\PSEUDOEPHEDRINE
LORATADINE vs LORAZEPAM
LORATADINE vs LORCASERIN
LORATADINE vs LORLATINIB
LORATADINE vs LORMETAZEPAM