Does UNSPECIFIED INGREDIENT Cause Product dose omission issue? 110 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 110 reports of Product dose omission issue have been filed in association with UNSPECIFIED INGREDIENT. This represents 0.4% of all adverse event reports for UNSPECIFIED INGREDIENT.
110
Reports of Product dose omission issue with UNSPECIFIED INGREDIENT
0.4%
of all UNSPECIFIED INGREDIENT reports
16
Deaths
41
Hospitalizations
How Dangerous Is Product dose omission issue From UNSPECIFIED INGREDIENT?
Of the 110 reports, 16 (14.5%) resulted in death, 41 (37.3%) required hospitalization, and 13 (11.8%) were considered life-threatening.
Is Product dose omission issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for UNSPECIFIED INGREDIENT. However, 110 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 Product dose omission issue?
DUPILUMAB (18,189)
USTEKINUMAB (9,405)
GUSELKUMAB (9,267)
LENALIDOMIDE (8,145)
MEPOLIZUMAB (5,873)
TOFACITINIB (5,646)
VOXELOTOR (5,122)
BELIMUMAB (4,671)
SECUKINUMAB (4,572)
APREMILAST (4,460)
Which UNSPECIFIED INGREDIENT Alternatives Have Lower Product dose omission issue Risk?
UNSPECIFIED INGREDIENT vs UPADACITINIB
UNSPECIFIED INGREDIENT vs URAPIDIL
UNSPECIFIED INGREDIENT vs UREA
UNSPECIFIED INGREDIENT vs URIDINE TRIACETATE
UNSPECIFIED INGREDIENT vs UROFOLLITROPIN