Does UNSPECIFIED INGREDIENT Cause Concomitant disease aggravated? 9 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 9 reports of Concomitant disease aggravated have been filed in association with UNSPECIFIED INGREDIENT. This represents 0.0% of all adverse event reports for UNSPECIFIED INGREDIENT.
9
Reports of Concomitant disease aggravated with UNSPECIFIED INGREDIENT
0.0%
of all UNSPECIFIED INGREDIENT reports
0
Deaths
6
Hospitalizations
How Dangerous Is Concomitant disease aggravated From UNSPECIFIED INGREDIENT?
Of the 9 reports, 6 (66.7%) required hospitalization, and 1 (11.1%) were considered life-threatening.
Is Concomitant disease aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for UNSPECIFIED INGREDIENT. However, 9 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 Concomitant disease aggravated?
SACUBITRIL\VALSARTAN (533)
SECUKINUMAB (461)
FINGOLIMOD (425)
MACITENTAN (286)
OMALIZUMAB (186)
SELEXIPAG (166)
METHOTREXATE (150)
RUXOLITINIB (142)
OCTREOTIDE (125)
BOSENTAN (123)
Which UNSPECIFIED INGREDIENT Alternatives Have Lower Concomitant disease aggravated Risk?
UNSPECIFIED INGREDIENT vs UPADACITINIB
UNSPECIFIED INGREDIENT vs URAPIDIL
UNSPECIFIED INGREDIENT vs UREA
UNSPECIFIED INGREDIENT vs URIDINE TRIACETATE
UNSPECIFIED INGREDIENT vs UROFOLLITROPIN