Does LETROZOLE\RIBOCICLIB Cause Product dose omission issue? 22 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 22 reports of Product dose omission issue have been filed in association with LETROZOLE\RIBOCICLIB. This represents 3.5% of all adverse event reports for LETROZOLE\RIBOCICLIB.
22
Reports of Product dose omission issue with LETROZOLE\RIBOCICLIB
3.5%
of all LETROZOLE\RIBOCICLIB reports
0
Deaths
5
Hospitalizations
How Dangerous Is Product dose omission issue From LETROZOLE\RIBOCICLIB?
Of the 22 reports, 5 (22.7%) required hospitalization.
Is Product dose omission issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for LETROZOLE\RIBOCICLIB. However, 22 reports have been filed with the FAERS database.
What Other Side Effects Does LETROZOLE\RIBOCICLIB Cause?
Fatigue (69)
Death (66)
Nausea (57)
White blood cell count decreased (39)
Diarrhoea (35)
Rash (27)
Alopecia (25)
Neoplasm malignant (25)
Malaise (24)
Cough (22)
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 LETROZOLE\RIBOCICLIB Alternatives Have Lower Product dose omission issue Risk?
LETROZOLE\RIBOCICLIB vs LEUCOVORIN
LETROZOLE\RIBOCICLIB vs LEUCOVORIN\LEUCOVORIN
LETROZOLE\RIBOCICLIB vs LEUPROLIDE
LETROZOLE\RIBOCICLIB vs LEVALBUTEROL
LETROZOLE\RIBOCICLIB vs LEVAMISOLE