Does CAPMATINIB Cause Product use complaint? 31 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 31 reports of Product use complaint have been filed in association with CAPMATINIB (TABRECTA). This represents 1.4% of all adverse event reports for CAPMATINIB.
31
Reports of Product use complaint with CAPMATINIB
1.4%
of all CAPMATINIB reports
6
Deaths
3
Hospitalizations
How Dangerous Is Product use complaint From CAPMATINIB?
Of the 31 reports, 6 (19.4%) resulted in death, 3 (9.7%) required hospitalization, and 1 (3.2%) were considered life-threatening.
Is Product use complaint Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for CAPMATINIB. However, 31 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 Product use complaint?
TROFINETIDE (472)
ENZALUTAMIDE (336)
LIFITEGRAST (326)
VOXELOTOR (298)
CLASCOTERONE (285)
NIRMATRELVIR\RITONAVIR (248)
ABALOPARATIDE (224)
ESTRADIOL (208)
MOLNUPIRAVIR (206)
ACETAMINOPHEN (202)
Which CAPMATINIB Alternatives Have Lower Product use complaint Risk?
CAPMATINIB vs CAPREOMYCIN
CAPMATINIB vs CAPSAICIN
CAPMATINIB vs CAPTOPRIL
CAPMATINIB vs CARBAMAZEPINE
CAPMATINIB vs CARBETOCIN