Does CABAZITAXEL Cause Product preparation error? 6 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 6 reports of Product preparation error have been filed in association with CABAZITAXEL (Jevtana). This represents 0.2% of all adverse event reports for CABAZITAXEL.
6
Reports of Product preparation error with CABAZITAXEL
0.2%
of all CABAZITAXEL reports
1
Deaths
3
Hospitalizations
How Dangerous Is Product preparation error From CABAZITAXEL?
Of the 6 reports, 1 (16.7%) resulted in death, 3 (50.0%) required hospitalization, and 1 (16.7%) were considered life-threatening.
Is Product preparation error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for CABAZITAXEL. However, 6 reports have been filed with the FAERS database.
What Other Side Effects Does CABAZITAXEL Cause?
Febrile neutropenia (197)
Malignant neoplasm progression (172)
Fatigue (160)
Prostatic specific antigen increased (148)
Pyrexia (145)
Disease progression (143)
Diarrhoea (142)
Anaemia (127)
Neutropenia (126)
Drug ineffective (125)
What Other Drugs Cause Product preparation error?
ONABOTULINUMTOXINA (3,593)
EVOLOCUMAB (2,785)
DUPILUMAB (2,707)
BUPRENORPHINE\NALOXONE (777)
ABOBOTULINUMTOXINA (751)
ALBIGLUTIDE (691)
ALBUTEROL (520)
PEGFILGRASTIM (473)
ALIROCUMAB (402)
LEUPROLIDE (400)
Which CABAZITAXEL Alternatives Have Lower Product preparation error Risk?
CABAZITAXEL vs CABERGOLINE
CABAZITAXEL vs CABOTEGRAVIR
CABAZITAXEL vs CABOTEGRAVIR\RILPIVIRINE
CABAZITAXEL vs CABOZANTINIB
CABAZITAXEL vs CABOZANTINIB S-MALATE