Does EXEMESTANE Cause Product dose omission? 17 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 17 reports of Product dose omission have been filed in association with EXEMESTANE (Exemestane). This represents 0.2% of all adverse event reports for EXEMESTANE.
17
Reports of Product dose omission with EXEMESTANE
0.2%
of all EXEMESTANE reports
0
Deaths
5
Hospitalizations
How Dangerous Is Product dose omission From EXEMESTANE?
Of the 17 reports, 5 (29.4%) required hospitalization.
Is Product dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for EXEMESTANE. However, 17 reports have been filed with the FAERS database.
What Other Side Effects Does EXEMESTANE Cause?
Fatigue (1,122)
Malignant neoplasm progression (1,025)
Arthralgia (943)
Diarrhoea (941)
Nausea (913)
Neoplasm progression (692)
Dyspnoea (673)
Malaise (620)
Headache (606)
Asthenia (597)
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)
LENALIDOMIDE (1,400)
RUXOLITINIB (1,376)
ALIROCUMAB (1,354)
DIMETHYL (1,248)
Which EXEMESTANE Alternatives Have Lower Product dose omission Risk?
EXEMESTANE vs EXENATIDE
EXEMESTANE vs EXFORGE
EXEMESTANE vs EXJADE
EXEMESTANE vs EXTAVIA
EXEMESTANE vs EXTRANEAL