Does UNSPECIFIED INGREDIENT Cause Device breakage? 30 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 30 reports of Device breakage have been filed in association with UNSPECIFIED INGREDIENT. This represents 0.1% of all adverse event reports for UNSPECIFIED INGREDIENT.
30
Reports of Device breakage with UNSPECIFIED INGREDIENT
0.1%
of all UNSPECIFIED INGREDIENT reports
0
Deaths
6
Hospitalizations
How Dangerous Is Device breakage From UNSPECIFIED INGREDIENT?
Of the 30 reports, 6 (20.0%) required hospitalization, and 1 (3.3%) were considered life-threatening.
Is Device breakage Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for UNSPECIFIED INGREDIENT. However, 30 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 Device breakage?
COPPER (9,201)
SOMATROPIN (7,761)
ETONOGESTREL (4,140)
LEVONORGESTREL (2,726)
ETHINYL ESTRADIOL\ETONOGESTREL (741)
CARBIDOPA\LEVODOPA (634)
TREPROSTINIL (396)
ADALIMUMAB (375)
ALBUTEROL (256)
EPOPROSTENOL (240)
Which UNSPECIFIED INGREDIENT Alternatives Have Lower Device breakage Risk?
UNSPECIFIED INGREDIENT vs UPADACITINIB
UNSPECIFIED INGREDIENT vs URAPIDIL
UNSPECIFIED INGREDIENT vs UREA
UNSPECIFIED INGREDIENT vs URIDINE TRIACETATE
UNSPECIFIED INGREDIENT vs UROFOLLITROPIN