Does PENTAMIDINE ISETHIONATE Cause Intentional product use issue? 22 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 22 reports of Intentional product use issue have been filed in association with PENTAMIDINE ISETHIONATE (Pentam 300). This represents 5.8% of all adverse event reports for PENTAMIDINE ISETHIONATE.
22
Reports of Intentional product use issue with PENTAMIDINE ISETHIONATE
5.8%
of all PENTAMIDINE ISETHIONATE reports
15
Deaths
17
Hospitalizations
How Dangerous Is Intentional product use issue From PENTAMIDINE ISETHIONATE?
Of the 22 reports, 15 (68.2%) resulted in death, 17 (77.3%) required hospitalization, and 16 (72.7%) were considered life-threatening.
Is Intentional product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PENTAMIDINE ISETHIONATE. However, 22 reports have been filed with the FAERS database.
What Other Side Effects Does PENTAMIDINE ISETHIONATE Cause?
Off label use (56)
Neutropenia (27)
Pneumocystis jirovecii pneumonia (27)
Pancreatitis acute (26)
Febrile neutropenia (25)
Dyspnoea (24)
Pyrexia (22)
Stenotrophomonas infection (22)
Product use in unapproved indication (20)
Rash (20)
What Other Drugs Cause Intentional product use issue?
INFLIXIMAB (11,028)
RITUXIMAB (9,602)
INFLIXIMAB-DYYB (7,549)
TOCILIZUMAB (5,078)
METHOTREXATE (4,087)
PREDNISONE (3,961)
ABATACEPT (3,693)
ADALIMUMAB (3,557)
NIVOLUMAB (3,297)
LEFLUNOMIDE (3,280)
Which PENTAMIDINE ISETHIONATE Alternatives Have Lower Intentional product use issue Risk?
PENTAMIDINE ISETHIONATE vs PENTAZOCINE
PENTAMIDINE ISETHIONATE vs PENTOBARBITAL
PENTAMIDINE ISETHIONATE vs PENTOSAN POLYSULFATE
PENTAMIDINE ISETHIONATE vs PENTOSTATIN
PENTAMIDINE ISETHIONATE vs PENTOXIFYLLINE