Does UNSPECIFIED INGREDIENT Cause Extremity necrosis? 8 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 8 reports of Extremity necrosis have been filed in association with UNSPECIFIED INGREDIENT. This represents 0.0% of all adverse event reports for UNSPECIFIED INGREDIENT.
8
Reports of Extremity necrosis with UNSPECIFIED INGREDIENT
0.0%
of all UNSPECIFIED INGREDIENT reports
1
Deaths
6
Hospitalizations
How Dangerous Is Extremity necrosis From UNSPECIFIED INGREDIENT?
Of the 8 reports, 1 (12.5%) resulted in death, 6 (75.0%) required hospitalization.
Is Extremity necrosis Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for UNSPECIFIED INGREDIENT. However, 8 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 Extremity necrosis?
CANAGLIFLOZIN (95)
CALCIUM\DEXTROSE\MAGNESIUM\SODIUM\SODIUM (84)
CARBOPLATIN (46)
PEMETREXED (45)
ADALIMUMAB (42)
GEMCITABINE (40)
METHYLPREDNISOLONE (40)
EPINEPHRINE (39)
PEMBROLIZUMAB (37)
NOREPINEPHRINE (34)
Which UNSPECIFIED INGREDIENT Alternatives Have Lower Extremity necrosis Risk?
UNSPECIFIED INGREDIENT vs UPADACITINIB
UNSPECIFIED INGREDIENT vs URAPIDIL
UNSPECIFIED INGREDIENT vs UREA
UNSPECIFIED INGREDIENT vs URIDINE TRIACETATE
UNSPECIFIED INGREDIENT vs UROFOLLITROPIN