Does CAPMATINIB Cause Blood urea increased? 16 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 16 reports of Blood urea increased have been filed in association with CAPMATINIB (TABRECTA). This represents 0.7% of all adverse event reports for CAPMATINIB.
16
Reports of Blood urea increased with CAPMATINIB
0.7%
of all CAPMATINIB reports
1
Deaths
10
Hospitalizations
How Dangerous Is Blood urea increased From CAPMATINIB?
Of the 16 reports, 1 (6.3%) resulted in death, 10 (62.5%) required hospitalization, and 1 (6.3%) were considered life-threatening.
Is Blood urea increased Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for CAPMATINIB. However, 16 reports have been filed with the FAERS database.
What Other Side Effects Does CAPMATINIB Cause?
Death (411)
Peripheral swelling (283)
Fatigue (257)
Oedema peripheral (247)
Nausea (240)
Malignant neoplasm progression (178)
Dyspnoea (141)
Oedema (130)
Asthenia (113)
Non-small cell lung cancer (96)
What Other Drugs Cause Blood urea increased?
FUROSEMIDE (363)
SACUBITRIL\VALSARTAN (330)
METFORMIN (211)
ECULIZUMAB (197)
ADALIMUMAB (187)
PREDNISONE (186)
ASPIRIN (183)
TACROLIMUS (176)
METHYLPREDNISOLONE (175)
TOLVAPTAN (171)
Which CAPMATINIB Alternatives Have Lower Blood urea increased Risk?
CAPMATINIB vs CAPREOMYCIN
CAPMATINIB vs CAPSAICIN
CAPMATINIB vs CAPTOPRIL
CAPMATINIB vs CARBAMAZEPINE
CAPMATINIB vs CARBETOCIN