Does TIPIRACIL\TRIFLURIDINE Cause Product packaging quantity issue? 24 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 24 reports of Product packaging quantity issue have been filed in association with TIPIRACIL\TRIFLURIDINE. This represents 0.2% of all adverse event reports for TIPIRACIL\TRIFLURIDINE.
24
Reports of Product packaging quantity issue with TIPIRACIL\TRIFLURIDINE
0.2%
of all TIPIRACIL\TRIFLURIDINE reports
3
Deaths
7
Hospitalizations
How Dangerous Is Product packaging quantity issue From TIPIRACIL\TRIFLURIDINE?
Of the 24 reports, 3 (12.5%) resulted in death, 7 (29.2%) required hospitalization.
Is Product packaging quantity issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TIPIRACIL\TRIFLURIDINE. However, 24 reports have been filed with the FAERS database.
What Other Side Effects Does TIPIRACIL\TRIFLURIDINE Cause?
Death (3,017)
Disease progression (1,774)
Fatigue (1,298)
Nausea (1,135)
Diarrhoea (965)
Decreased appetite (659)
Vomiting (628)
White blood cell count decreased (483)
Asthenia (472)
Anaemia (388)
What Other Drugs Cause Product packaging quantity issue?
LEUPROLIDE (523)
ALBUTEROL (431)
BUDESONIDE\FORMOTEROL (301)
FENTANYL (286)
BUPRENORPHINE (225)
CYCLOSPORINE (206)
ESTRADIOL (201)
BIMATOPROST (177)
RIVAROXABAN (174)
EXENATIDE (154)
Which TIPIRACIL\TRIFLURIDINE Alternatives Have Lower Product packaging quantity issue Risk?
TIPIRACIL\TRIFLURIDINE vs TIPRANAVIR
TIPIRACIL\TRIFLURIDINE vs TIRAGOLUMAB
TIPIRACIL\TRIFLURIDINE vs TIRBANIBULIN
TIPIRACIL\TRIFLURIDINE vs TIROFIBAN
TIPIRACIL\TRIFLURIDINE vs TIRZEPATIDE