Does UNSPECIFIED INGREDIENT Cause Oedema peripheral? 348 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 348 reports of Oedema peripheral have been filed in association with UNSPECIFIED INGREDIENT. This represents 1.3% of all adverse event reports for UNSPECIFIED INGREDIENT.
348
Reports of Oedema peripheral with UNSPECIFIED INGREDIENT
1.3%
of all UNSPECIFIED INGREDIENT reports
113
Deaths
236
Hospitalizations
How Dangerous Is Oedema peripheral From UNSPECIFIED INGREDIENT?
Of the 348 reports, 113 (32.5%) resulted in death, 236 (67.8%) required hospitalization, and 66 (19.0%) were considered life-threatening.
Is Oedema peripheral Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for UNSPECIFIED INGREDIENT. However, 348 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 Oedema peripheral?
AMBRISENTAN (2,959)
TREPROSTINIL (2,816)
ADALIMUMAB (2,356)
LENALIDOMIDE (2,298)
AMLODIPINE (2,076)
PREDNISONE (2,029)
METHOTREXATE (1,939)
MACITENTAN (1,932)
RITUXIMAB (1,698)
TOCILIZUMAB (1,574)
Which UNSPECIFIED INGREDIENT Alternatives Have Lower Oedema peripheral Risk?
UNSPECIFIED INGREDIENT vs UPADACITINIB
UNSPECIFIED INGREDIENT vs URAPIDIL
UNSPECIFIED INGREDIENT vs UREA
UNSPECIFIED INGREDIENT vs URIDINE TRIACETATE
UNSPECIFIED INGREDIENT vs UROFOLLITROPIN