Does IVERMECTIN Cause Product use in unapproved indication? 366 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 366 reports of Product use in unapproved indication have been filed in association with IVERMECTIN (Ivermectin). This represents 12.1% of all adverse event reports for IVERMECTIN.
366
Reports of Product use in unapproved indication with IVERMECTIN
12.1%
of all IVERMECTIN reports
8
Deaths
38
Hospitalizations
How Dangerous Is Product use in unapproved indication From IVERMECTIN?
Of the 366 reports, 8 (2.2%) resulted in death, 38 (10.4%) required hospitalization, and 3 (0.8%) 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 IVERMECTIN. However, 366 reports have been filed with the FAERS database.
What Other Side Effects Does IVERMECTIN Cause?
Drug ineffective (538)
Off label use (288)
Pruritus (217)
Erythema (204)
Rosacea (131)
Skin burning sensation (113)
Headache (112)
Rash (105)
Condition aggravated (89)
Skin irritation (82)
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 IVERMECTIN Alternatives Have Lower Product use in unapproved indication Risk?
IVERMECTIN vs IVOSIDENIB
IVERMECTIN vs IXABEPILONE
IVERMECTIN vs IXAZOMIB
IVERMECTIN vs IXEKIZUMAB
IVERMECTIN vs JAKAFI