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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does LENALIDOMIDE Cause Product formulation issue? 9 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 9 reports of Product formulation issue have been filed in association with LENALIDOMIDE (LENALIDOMIDE). This represents 0.0% of all adverse event reports for LENALIDOMIDE.

9
Reports of Product formulation issue with LENALIDOMIDE
0.0%
of all LENALIDOMIDE reports
0
Deaths
0
Hospitalizations

How Dangerous Is Product formulation issue From LENALIDOMIDE?

Of the 9 reports.

Is Product formulation issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for LENALIDOMIDE. However, 9 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 formulation issue?

MINOXIDIL (1,369) LEVOTHYROXINE (740) AMPHETAMINE ASPARTATE\AMPHETAMINE\DEXTROAMPHETAMINE SACCHARATE\DEXTROAMPHETAMINE (174) OMEPRAZOLE (99) METHYLPHENIDATE (78) OXYCODONE (73) ACETAMINOPHEN\HYDROCODONE (62) ACETAMINOPHEN\OXYCODONE (61) ACETAMINOPHEN (59) BUPROPION (59)

Which LENALIDOMIDE Alternatives Have Lower Product formulation issue Risk?

LENALIDOMIDE vs LENIOLISIB LENALIDOMIDE vs LENOGRASTIM LENALIDOMIDE vs LENVATINIB LENALIDOMIDE vs LEPONEX LENALIDOMIDE vs LERCANIDIPINE

Related Pages

LENALIDOMIDE Full Profile All Product formulation issue Reports All Drugs Causing Product formulation issue LENALIDOMIDE Demographics