Does REGORAFENIB Cause Incorrect product administration duration? 15 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 15 reports of Incorrect product administration duration have been filed in association with REGORAFENIB (Stivarga). This represents 0.2% of all adverse event reports for REGORAFENIB.
15
Reports of Incorrect product administration duration with REGORAFENIB
0.2%
of all REGORAFENIB reports
1
Deaths
4
Hospitalizations
How Dangerous Is Incorrect product administration duration From REGORAFENIB?
Of the 15 reports, 1 (6.7%) resulted in death, 4 (26.7%) required hospitalization.
Is Incorrect product administration duration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for REGORAFENIB. However, 15 reports have been filed with the FAERS database.
What Other Side Effects Does REGORAFENIB Cause?
Off label use (1,906)
Fatigue (1,530)
Palmar-plantar erythrodysaesthesia syndrome (1,230)
Diarrhoea (1,221)
Decreased appetite (941)
Asthenia (825)
Death (813)
Dysphonia (702)
Nausea (688)
Pain in extremity (686)
What Other Drugs Cause Incorrect product administration duration?
ETONOGESTREL (3,974)
POLYETHYLENE GLYCOL 3350 (2,129)
NIRMATRELVIR\RITONAVIR (744)
DOCOSANOL (634)
LANSOPRAZOLE (564)
LOPERAMIDE (543)
NAPROXEN (499)
INSULIN LISPRO (479)
DICLOFENAC (362)
OMEPRAZOLE (302)
Which REGORAFENIB Alternatives Have Lower Incorrect product administration duration Risk?
REGORAFENIB vs REGORAFENIB\REGORAFENIB
REGORAFENIB vs RELATLIMAB
REGORAFENIB vs RELPAX
REGORAFENIB vs RELUGOLIX
REGORAFENIB vs REMDESIVIR