Does UNSPECIFIED INGREDIENT Cause Condition aggravated? 475 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 475 reports of Condition aggravated have been filed in association with UNSPECIFIED INGREDIENT. This represents 1.8% of all adverse event reports for UNSPECIFIED INGREDIENT.
475
Reports of Condition aggravated with UNSPECIFIED INGREDIENT
1.8%
of all UNSPECIFIED INGREDIENT reports
222
Deaths
287
Hospitalizations
How Dangerous Is Condition aggravated From UNSPECIFIED INGREDIENT?
Of the 475 reports, 222 (46.7%) resulted in death, 287 (60.4%) required hospitalization, and 168 (35.4%) were considered life-threatening.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for UNSPECIFIED INGREDIENT. However, 475 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 Condition aggravated?
TOFACITINIB (16,925)
INFLIXIMAB (16,616)
DUPILUMAB (16,459)
ETANERCEPT (15,897)
METHOTREXATE (14,938)
ADALIMUMAB (13,527)
PREDNISONE (10,751)
INFLIXIMAB-DYYB (10,275)
HYDROXYCHLOROQUINE (8,848)
RITUXIMAB (8,627)
Which UNSPECIFIED INGREDIENT Alternatives Have Lower Condition aggravated Risk?
UNSPECIFIED INGREDIENT vs UPADACITINIB
UNSPECIFIED INGREDIENT vs URAPIDIL
UNSPECIFIED INGREDIENT vs UREA
UNSPECIFIED INGREDIENT vs URIDINE TRIACETATE
UNSPECIFIED INGREDIENT vs UROFOLLITROPIN