Does UNSPECIFIED INGREDIENT Cause Febrile neutropenia? 270 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 270 reports of Febrile neutropenia have been filed in association with UNSPECIFIED INGREDIENT. This represents 1.0% of all adverse event reports for UNSPECIFIED INGREDIENT.
270
Reports of Febrile neutropenia with UNSPECIFIED INGREDIENT
1.0%
of all UNSPECIFIED INGREDIENT reports
35
Deaths
203
Hospitalizations
How Dangerous Is Febrile neutropenia From UNSPECIFIED INGREDIENT?
Of the 270 reports, 35 (13.0%) resulted in death, 203 (75.2%) required hospitalization, and 43 (15.9%) were considered life-threatening.
Is Febrile neutropenia Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for UNSPECIFIED INGREDIENT. However, 270 reports have been filed with the FAERS database.
What Other Side Effects Does UNSPECIFIED INGREDIENT Cause?
Death (2,090)
Off label use (1,306)
Drug ineffective (1,227)
Completed suicide (1,190)
Nausea (1,041)
Fatigue (1,020)
Dyspnoea (934)
Pneumonia (903)
Asthenia (894)
Vomiting (877)
What Other Drugs Cause Febrile neutropenia?
CYCLOPHOSPHAMIDE (11,318)
DOXORUBICIN (8,844)
VINCRISTINE (8,676)
RITUXIMAB (6,382)
CYTARABINE (6,142)
METHOTREXATE (6,091)
ETOPOSIDE (5,966)
CARBOPLATIN (4,888)
DEXAMETHASONE (4,382)
PREDNISONE (3,956)
Which UNSPECIFIED INGREDIENT Alternatives Have Lower Febrile neutropenia Risk?
UNSPECIFIED INGREDIENT vs UPADACITINIB
UNSPECIFIED INGREDIENT vs URAPIDIL
UNSPECIFIED INGREDIENT vs UREA
UNSPECIFIED INGREDIENT vs URIDINE TRIACETATE
UNSPECIFIED INGREDIENT vs UROFOLLITROPIN