Does LENALIDOMIDE Cause Product dose omission? 1,400 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 1,400 reports of Product dose omission have been filed in association with LENALIDOMIDE (LENALIDOMIDE). This represents 0.4% of all adverse event reports for LENALIDOMIDE.
1,400
Reports of Product dose omission with LENALIDOMIDE
0.4%
of all LENALIDOMIDE reports
2
Deaths
177
Hospitalizations
How Dangerous Is Product dose omission From LENALIDOMIDE?
Of the 1,400 reports, 2 (0.1%) resulted in death, 177 (12.6%) required hospitalization, and 1 (0.1%) were considered life-threatening.
Is Product dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for LENALIDOMIDE. However, 1,400 reports have been filed with the FAERS database.
What Other Side Effects Does LENALIDOMIDE Cause?
Diarrhoea (27,576)
Fatigue (22,956)
Death (19,213)
Off label use (17,017)
Rash (15,794)
Pneumonia (14,807)
Plasma cell myeloma (14,191)
Neuropathy peripheral (10,215)
White blood cell count decreased (9,996)
Constipation (9,635)
What Other Drugs Cause Product dose omission?
APREMILAST (4,567)
DUPILUMAB (2,729)
ALBUTEROL (1,742)
USTEKINUMAB (1,653)
INSULIN GLARGINE (1,500)
ETANERCEPT (1,400)
RUXOLITINIB (1,376)
ALIROCUMAB (1,354)
DIMETHYL (1,248)
TOFACITINIB (1,104)
Which LENALIDOMIDE Alternatives Have Lower Product dose omission Risk?
LENALIDOMIDE vs LENIOLISIB
LENALIDOMIDE vs LENOGRASTIM
LENALIDOMIDE vs LENVATINIB
LENALIDOMIDE vs LEPONEX
LENALIDOMIDE vs LERCANIDIPINE