Does UNSPECIFIED INGREDIENT Cause Complication associated with device? 31 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 31 reports of Complication associated with device have been filed in association with UNSPECIFIED INGREDIENT. This represents 0.1% of all adverse event reports for UNSPECIFIED INGREDIENT.
31
Reports of Complication associated with device with UNSPECIFIED INGREDIENT
0.1%
of all UNSPECIFIED INGREDIENT reports
1
Deaths
15
Hospitalizations
How Dangerous Is Complication associated with device From UNSPECIFIED INGREDIENT?
Of the 31 reports, 1 (3.2%) resulted in death, 15 (48.4%) required hospitalization, and 4 (12.9%) were considered life-threatening.
Is Complication associated with device Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for UNSPECIFIED INGREDIENT. However, 31 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 Complication associated with device?
ETONOGESTREL (6,047)
COPPER (1,083)
BACLOFEN (525)
TREPROSTINIL (422)
EPOPROSTENOL (399)
LEVONORGESTREL (344)
ADALIMUMAB (269)
CARBIDOPA\LEVODOPA (169)
MACITENTAN (169)
TEDUGLUTIDE (133)
Which UNSPECIFIED INGREDIENT Alternatives Have Lower Complication associated with device Risk?
UNSPECIFIED INGREDIENT vs UPADACITINIB
UNSPECIFIED INGREDIENT vs URAPIDIL
UNSPECIFIED INGREDIENT vs UREA
UNSPECIFIED INGREDIENT vs URIDINE TRIACETATE
UNSPECIFIED INGREDIENT vs UROFOLLITROPIN