Does UNSPECIFIED INGREDIENT Cause Peripheral venous disease? 46 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 46 reports of Peripheral venous disease have been filed in association with UNSPECIFIED INGREDIENT. This represents 0.2% of all adverse event reports for UNSPECIFIED INGREDIENT.
46
Reports of Peripheral venous disease with UNSPECIFIED INGREDIENT
0.2%
of all UNSPECIFIED INGREDIENT reports
41
Deaths
44
Hospitalizations
How Dangerous Is Peripheral venous disease From UNSPECIFIED INGREDIENT?
Of the 46 reports, 41 (89.1%) resulted in death, 44 (95.7%) required hospitalization, and 41 (89.1%) were considered life-threatening.
Is Peripheral venous disease Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for UNSPECIFIED INGREDIENT. However, 46 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 Peripheral venous disease?
RITUXIMAB (1,281)
ADALIMUMAB (1,249)
METHOTREXATE (1,246)
SECUKINUMAB (1,186)
ABATACEPT (1,168)
DICLOFENAC (1,168)
LEFLUNOMIDE (1,154)
TOCILIZUMAB (1,137)
PREDNISONE (1,101)
ALENDRONATE (1,097)
Which UNSPECIFIED INGREDIENT Alternatives Have Lower Peripheral venous disease Risk?
UNSPECIFIED INGREDIENT vs UPADACITINIB
UNSPECIFIED INGREDIENT vs URAPIDIL
UNSPECIFIED INGREDIENT vs UREA
UNSPECIFIED INGREDIENT vs URIDINE TRIACETATE
UNSPECIFIED INGREDIENT vs UROFOLLITROPIN