Does UNSPECIFIED INGREDIENT Cause Complication of device removal? 14 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 14 reports of Complication of device removal have been filed in association with UNSPECIFIED INGREDIENT. This represents 0.1% of all adverse event reports for UNSPECIFIED INGREDIENT.
14
Reports of Complication of device removal with UNSPECIFIED INGREDIENT
0.1%
of all UNSPECIFIED INGREDIENT reports
0
Deaths
1
Hospitalizations
How Dangerous Is Complication of device removal From UNSPECIFIED INGREDIENT?
Of the 14 reports, 1 (7.1%) required hospitalization.
Is Complication of device removal Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for UNSPECIFIED INGREDIENT. However, 14 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 of device removal?
COPPER (7,895)
ETONOGESTREL (3,578)
LEVONORGESTREL (2,039)
MIRENA (44)
INTERFERON BETA-1A (37)
TREPROSTINIL (24)
IMPLANON (21)
ETHINYL ESTRADIOL\ETONOGESTREL (15)
BUPRENORPHINE (11)
DEVICE (11)
Which UNSPECIFIED INGREDIENT Alternatives Have Lower Complication of device removal Risk?
UNSPECIFIED INGREDIENT vs UPADACITINIB
UNSPECIFIED INGREDIENT vs URAPIDIL
UNSPECIFIED INGREDIENT vs UREA
UNSPECIFIED INGREDIENT vs URIDINE TRIACETATE
UNSPECIFIED INGREDIENT vs UROFOLLITROPIN