Does LORATADINE Cause Wrong technique in product usage process? 348 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 348 reports of Wrong technique in product usage process have been filed in association with LORATADINE (Curist Allergy Relief). This represents 1.4% of all adverse event reports for LORATADINE.
348
Reports of Wrong technique in product usage process with LORATADINE
1.4%
of all LORATADINE reports
0
Deaths
0
Hospitalizations
How Dangerous Is Wrong technique in product usage process From LORATADINE?
Of the 348 reports.
Is Wrong technique in product usage process Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for LORATADINE. However, 348 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 Wrong technique in product usage process?
EVOLOCUMAB (21,664)
ALBUTEROL (17,114)
ADALIMUMAB (11,766)
PEGFILGRASTIM (10,217)
ETANERCEPT (9,835)
ERENUMAB-AOOE (9,359)
SACUBITRIL\VALSARTAN (8,022)
LEUPROLIDE (5,062)
FENTANYL (2,812)
SEMAGLUTIDE (2,538)
Which LORATADINE Alternatives Have Lower Wrong technique in product usage process Risk?
LORATADINE vs LORATADINE\PSEUDOEPHEDRINE
LORATADINE vs LORAZEPAM
LORATADINE vs LORCASERIN
LORATADINE vs LORLATINIB
LORATADINE vs LORMETAZEPAM