Does CLOPIDOGREL BESILATE Cause Product use in unapproved indication? 14 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 14 reports of Product use in unapproved indication have been filed in association with CLOPIDOGREL BESILATE. This represents 6.3% of all adverse event reports for CLOPIDOGREL BESILATE.
14
Reports of Product use in unapproved indication with CLOPIDOGREL BESILATE
6.3%
of all CLOPIDOGREL BESILATE reports
0
Deaths
14
Hospitalizations
How Dangerous Is Product use in unapproved indication From CLOPIDOGREL BESILATE?
Of the 14 reports, 14 (100.0%) required hospitalization.
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 CLOPIDOGREL BESILATE. However, 14 reports have been filed with the FAERS database.
What Other Side Effects Does CLOPIDOGREL BESILATE Cause?
Atrial fibrillation (24)
Dyspnoea (22)
Cardiac failure (20)
Cough (18)
Myocardial infarction (17)
Decreased appetite (16)
Off label use (16)
Dyslipidaemia (15)
Fatigue (13)
Intentional product use issue (13)
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 CLOPIDOGREL BESILATE Alternatives Have Lower Product use in unapproved indication Risk?
CLOPIDOGREL BESILATE vs CLOPIDOGREL BISULFATE
CLOPIDOGREL BESILATE vs CLORAZEPATE
CLOPIDOGREL BESILATE vs CLOSTRIDIUM TETANI TOXOID ANTIGEN
CLOPIDOGREL BESILATE vs CLOTHIAPINE
CLOPIDOGREL BESILATE vs CLOTIAZEPAM