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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 solubility abnormal? 24 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 24 reports of Product solubility abnormal have been filed in association with LORATADINE (Curist Allergy Relief). This represents 0.1% of all adverse event reports for LORATADINE.

24
Reports of Product solubility abnormal with LORATADINE
0.1%
of all LORATADINE reports
0
Deaths
0
Hospitalizations

How Dangerous Is Product solubility abnormal From LORATADINE?

Of the 24 reports.

Is Product solubility abnormal Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for LORATADINE. However, 24 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 solubility abnormal?

BUPRENORPHINE (498) BUPRENORPHINE\NALOXONE (274) POLYETHYLENE GLYCOL 3350 (220) CHOLESTYRAMINE (193) PATIROMER (107) LEVOTHYROXINE (100) SOMATROPIN (98) EXENATIDE (97) ESTRADIOL (94) NITROGLYCERIN (81)

Which LORATADINE Alternatives Have Lower Product solubility abnormal Risk?

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

Related Pages

LORATADINE Full Profile All Product solubility abnormal Reports All Drugs Causing Product solubility abnormal LORATADINE Demographics