Does TETRAHYDROZOLINE Cause Product use in unapproved indication? 38 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 38 reports of Product use in unapproved indication have been filed in association with TETRAHYDROZOLINE (Foster and Thrive Original Formula Eye Drops). This represents 5.3% of all adverse event reports for TETRAHYDROZOLINE.
38
Reports of Product use in unapproved indication with TETRAHYDROZOLINE
5.3%
of all TETRAHYDROZOLINE reports
0
Deaths
3
Hospitalizations
How Dangerous Is Product use in unapproved indication From TETRAHYDROZOLINE?
Of the 38 reports, 3 (7.9%) required hospitalization, and 1 (2.6%) were considered life-threatening.
Is Product use in unapproved indication Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TETRAHYDROZOLINE. However, 38 reports have been filed with the FAERS database.
What Other Side Effects Does TETRAHYDROZOLINE Cause?
Drug ineffective (201)
Eye irritation (83)
Ocular hyperaemia (59)
Product use issue (59)
Therapeutic response unexpected (39)
Accidental exposure to product (38)
Intentional product misuse (38)
Off label use (36)
Drug effect incomplete (25)
Drug ineffective for unapproved indication (25)
What Other Drugs Cause Product use in unapproved indication?
DUPILUMAB (33,452)
DICLOFENAC (12,197)
METHOTREXATE (8,930)
PREDNISONE (7,625)
RITUXIMAB (7,519)
MYCOPHENOLATE MOFETIL (5,910)
ACETAMINOPHEN (5,819)
CYCLOPHOSPHAMIDE (5,750)
RISPERIDONE (5,551)
TACROLIMUS (5,057)
Which TETRAHYDROZOLINE Alternatives Have Lower Product use in unapproved indication Risk?
TETRAHYDROZOLINE vs TETRAZEPAM
TETRAHYDROZOLINE vs TEZEPELUMAB
TETRAHYDROZOLINE vs TEZEPELUMAB-EKKO
TETRAHYDROZOLINE vs THALIDOMIDE
TETRAHYDROZOLINE vs THALOMID