Does LENALIDOMIDE Cause Product dose omission in error? 618 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 618 reports of Product dose omission in error have been filed in association with LENALIDOMIDE (LENALIDOMIDE). This represents 0.2% of all adverse event reports for LENALIDOMIDE.
618
Reports of Product dose omission in error with LENALIDOMIDE
0.2%
of all LENALIDOMIDE reports
2
Deaths
37
Hospitalizations
How Dangerous Is Product dose omission in error From LENALIDOMIDE?
Of the 618 reports, 2 (0.3%) resulted in death, 37 (6.0%) required hospitalization.
Is Product dose omission in error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for LENALIDOMIDE. However, 618 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 in error?
DUPILUMAB (7,586)
TOFACITINIB (2,461)
PALBOCICLIB (592)
DIROXIMEL (481)
ABALOPARATIDE (457)
NIRAPARIB (428)
RUXOLITINIB (425)
TERIFLUNOMIDE (371)
DIMETHYL (308)
RELUGOLIX (293)
Which LENALIDOMIDE Alternatives Have Lower Product dose omission in error Risk?
LENALIDOMIDE vs LENIOLISIB
LENALIDOMIDE vs LENOGRASTIM
LENALIDOMIDE vs LENVATINIB
LENALIDOMIDE vs LEPONEX
LENALIDOMIDE vs LERCANIDIPINE