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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 OXALIPLATIN Cause Performance status decreased? 48 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 48 reports of Performance status decreased have been filed in association with OXALIPLATIN (Oxaliplatin). This represents 0.1% of all adverse event reports for OXALIPLATIN.

48
Reports of Performance status decreased with OXALIPLATIN
0.1%
of all OXALIPLATIN reports
10
Deaths
18
Hospitalizations

How Dangerous Is Performance status decreased From OXALIPLATIN?

Of the 48 reports, 10 (20.8%) resulted in death, 18 (37.5%) required hospitalization, and 6 (12.5%) were considered life-threatening.

Is Performance status decreased Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for OXALIPLATIN. However, 48 reports have been filed with the FAERS database.

What Other Side Effects Does OXALIPLATIN Cause?

Diarrhoea (4,963) Nausea (4,250) Neuropathy peripheral (3,662) Off label use (3,603) Neutropenia (3,391) Vomiting (3,383) Disease progression (3,370) Thrombocytopenia (2,886) Dyspnoea (2,779) Pyrexia (2,269)

What Other Drugs Cause Performance status decreased?

BACLOFEN (156) LENALIDOMIDE (118) PACLITAXEL (112) BEVACIZUMAB (103) SODIUM OXYBATE (103) CARBOPLATIN (100) DEXAMETHASONE (80) CAPECITABINE (75) NIRAPARIB (75) LUMATEPERONE (68)

Which OXALIPLATIN Alternatives Have Lower Performance status decreased Risk?

OXALIPLATIN vs OXAPROZIN OXALIPLATIN vs OXAZEPAM OXALIPLATIN vs OXCARBAZEPINE OXALIPLATIN vs OXITRIPTAN OXALIPLATIN vs OXOMEMAZINE

Related Pages

OXALIPLATIN Full Profile All Performance status decreased Reports All Drugs Causing Performance status decreased OXALIPLATIN Demographics