Does UNSPECIFIED INGREDIENT Cause Drug dose omission? 121 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 121 reports of Drug dose omission have been filed in association with UNSPECIFIED INGREDIENT. This represents 0.5% of all adverse event reports for UNSPECIFIED INGREDIENT.
121
Reports of Drug dose omission with UNSPECIFIED INGREDIENT
0.5%
of all UNSPECIFIED INGREDIENT reports
0
Deaths
46
Hospitalizations
How Dangerous Is Drug dose omission From UNSPECIFIED INGREDIENT?
Of the 121 reports, 46 (38.0%) required hospitalization, and 4 (3.3%) were considered life-threatening.
Is Drug dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for UNSPECIFIED INGREDIENT. However, 121 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 Drug dose omission?
ETANERCEPT (10,871)
CINACALCET (8,683)
EVOLOCUMAB (4,914)
ADALIMUMAB (3,993)
INSULIN LISPRO (3,063)
GOLIMUMAB (2,652)
TERIPARATIDE (2,616)
APREMILAST (2,466)
ALBUTEROL (2,309)
FLUTICASONE\SALMETEROL (2,153)
Which UNSPECIFIED INGREDIENT Alternatives Have Lower Drug dose omission Risk?
UNSPECIFIED INGREDIENT vs UPADACITINIB
UNSPECIFIED INGREDIENT vs URAPIDIL
UNSPECIFIED INGREDIENT vs UREA
UNSPECIFIED INGREDIENT vs URIDINE TRIACETATE
UNSPECIFIED INGREDIENT vs UROFOLLITROPIN