Does CAPMATINIB Cause Condition aggravated? 11 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 11 reports of Condition aggravated have been filed in association with CAPMATINIB (TABRECTA). This represents 0.5% of all adverse event reports for CAPMATINIB.
11
Reports of Condition aggravated with CAPMATINIB
0.5%
of all CAPMATINIB reports
2
Deaths
4
Hospitalizations
How Dangerous Is Condition aggravated From CAPMATINIB?
Of the 11 reports, 2 (18.2%) resulted in death, 4 (36.4%) required hospitalization, and 2 (18.2%) were considered life-threatening.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for CAPMATINIB. However, 11 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 Condition aggravated?
TOFACITINIB (16,925)
INFLIXIMAB (16,616)
DUPILUMAB (16,459)
ETANERCEPT (15,897)
METHOTREXATE (14,938)
ADALIMUMAB (13,527)
PREDNISONE (10,751)
INFLIXIMAB-DYYB (10,275)
HYDROXYCHLOROQUINE (8,848)
RITUXIMAB (8,627)
Which CAPMATINIB Alternatives Have Lower Condition aggravated Risk?
CAPMATINIB vs CAPREOMYCIN
CAPMATINIB vs CAPSAICIN
CAPMATINIB vs CAPTOPRIL
CAPMATINIB vs CARBAMAZEPINE
CAPMATINIB vs CARBETOCIN