Does TEMOCILLIN Cause Product use in unapproved indication? 7 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Product use in unapproved indication have been filed in association with TEMOCILLIN. This represents 9.1% of all adverse event reports for TEMOCILLIN.
7
Reports of Product use in unapproved indication with TEMOCILLIN
9.1%
of all TEMOCILLIN reports
1
Deaths
3
Hospitalizations
How Dangerous Is Product use in unapproved indication From TEMOCILLIN?
Of the 7 reports, 1 (14.3%) resulted in death, 3 (42.9%) 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 TEMOCILLIN. However, 7 reports have been filed with the FAERS database.
What Other Side Effects Does TEMOCILLIN Cause?
Toxicity to various agents (15)
Confusional state (13)
Liver injury (12)
Cholestasis (9)
Acute kidney injury (8)
Off label use (8)
Clostridium difficile infection (7)
Drug ineffective (7)
Encephalopathy (7)
Hallucination, visual (6)
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)