Does ATOVAQUONE Cause Product use in unapproved indication? 83 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 83 reports of Product use in unapproved indication have been filed in association with ATOVAQUONE (Atovaquone). This represents 3.7% of all adverse event reports for ATOVAQUONE.
83
Reports of Product use in unapproved indication with ATOVAQUONE
3.7%
of all ATOVAQUONE reports
18
Deaths
38
Hospitalizations
How Dangerous Is Product use in unapproved indication From ATOVAQUONE?
Of the 83 reports, 18 (21.7%) resulted in death, 38 (45.8%) required hospitalization, and 5 (6.0%) 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 ATOVAQUONE. However, 83 reports have been filed with the FAERS database.
What Other Side Effects Does ATOVAQUONE Cause?
Off label use (176)
Drug ineffective (164)
Condition aggravated (145)
Thrombocytopenia (127)
Pyrexia (117)
Rash (108)
Neutropenia (89)
Diarrhoea (86)
Pneumocystis jirovecii pneumonia (83)
Pancytopenia (76)
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 ATOVAQUONE Alternatives Have Lower Product use in unapproved indication Risk?
ATOVAQUONE vs ATOVAQUONE\PROGUANIL
ATOVAQUONE vs ATRACURIUM
ATOVAQUONE vs ATRIPLA
ATOVAQUONE vs ATROPINE
ATOVAQUONE vs ATROPINE\ATROPINE