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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does UNSPECIFIED INGREDIENT Cause Sepsis? 434 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 434 reports of Sepsis have been filed in association with UNSPECIFIED INGREDIENT. This represents 1.7% of all adverse event reports for UNSPECIFIED INGREDIENT.

434
Reports of Sepsis with UNSPECIFIED INGREDIENT
1.7%
of all UNSPECIFIED INGREDIENT reports
253
Deaths
333
Hospitalizations

How Dangerous Is Sepsis From UNSPECIFIED INGREDIENT?

Of the 434 reports, 253 (58.3%) resulted in death, 333 (76.7%) required hospitalization, and 152 (35.0%) were considered life-threatening.

Is Sepsis Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for UNSPECIFIED INGREDIENT. However, 434 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 Sepsis?

RITUXIMAB (4,043) CYCLOPHOSPHAMIDE (4,041) METHOTREXATE (3,933) ADALIMUMAB (3,169) DEXAMETHASONE (3,150) LENALIDOMIDE (2,956) VINCRISTINE (2,791) DOXORUBICIN (2,740) PREDNISONE (2,634) PREDNISOLONE (2,281)

Which UNSPECIFIED INGREDIENT Alternatives Have Lower Sepsis Risk?

UNSPECIFIED INGREDIENT vs UPADACITINIB UNSPECIFIED INGREDIENT vs URAPIDIL UNSPECIFIED INGREDIENT vs UREA UNSPECIFIED INGREDIENT vs URIDINE TRIACETATE UNSPECIFIED INGREDIENT vs UROFOLLITROPIN

Related Pages

UNSPECIFIED INGREDIENT Full Profile All Sepsis Reports All Drugs Causing Sepsis UNSPECIFIED INGREDIENT Demographics