Does PENTAMIDINE Cause Product use in unapproved indication? 17 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 17 reports of Product use in unapproved indication have been filed in association with PENTAMIDINE. This represents 4.4% of all adverse event reports for PENTAMIDINE.
17
Reports of Product use in unapproved indication with PENTAMIDINE
4.4%
of all PENTAMIDINE reports
3
Deaths
9
Hospitalizations
How Dangerous Is Product use in unapproved indication From PENTAMIDINE?
Of the 17 reports, 3 (17.6%) resulted in death, 9 (52.9%) 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 PENTAMIDINE. However, 17 reports have been filed with the FAERS database.
What Other Side Effects Does PENTAMIDINE Cause?
Drug ineffective (71)
Off label use (56)
Pneumocystis jirovecii pneumonia (43)
Pyrexia (42)
Condition aggravated (29)
Acute kidney injury (25)
Renal failure (23)
Respiratory failure (21)
Drug ineffective for unapproved indication (20)
Graft versus host disease (19)
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 PENTAMIDINE Alternatives Have Lower Product use in unapproved indication Risk?
PENTAMIDINE vs PENTAMIDINE ISETHIONATE
PENTAMIDINE vs PENTAZOCINE
PENTAMIDINE vs PENTOBARBITAL
PENTAMIDINE vs PENTOSAN POLYSULFATE
PENTAMIDINE vs PENTOSTATIN