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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does LORATADINE Cause Product use issue? 1,371 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 1,371 reports of Product use issue have been filed in association with LORATADINE (Curist Allergy Relief). This represents 5.4% of all adverse event reports for LORATADINE.

1,371
Reports of Product use issue with LORATADINE
5.4%
of all LORATADINE reports
11
Deaths
8
Hospitalizations

How Dangerous Is Product use issue From LORATADINE?

Of the 1,371 reports, 11 (0.8%) resulted in death, 8 (0.6%) required hospitalization.

Is Product use issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for LORATADINE. However, 1,371 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) 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 Product use issue?

INFLIXIMAB (12,752) DUPILUMAB (10,575) POLYETHYLENE GLYCOL 3350 (9,432) METHOTREXATE (8,185) DICLOFENAC (8,009) RITUXIMAB (6,948) ADALIMUMAB (6,379) ETANERCEPT (6,062) TOCILIZUMAB (5,944) ABATACEPT (5,915)

Which LORATADINE Alternatives Have Lower Product use issue Risk?

LORATADINE vs LORATADINE\PSEUDOEPHEDRINE LORATADINE vs LORAZEPAM LORATADINE vs LORCASERIN LORATADINE vs LORLATINIB LORATADINE vs LORMETAZEPAM

Related Pages

LORATADINE Full Profile All Product use issue Reports All Drugs Causing Product use issue LORATADINE Demographics