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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 CAPMATINIB Cause Product storage error? 6 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 6 reports of Product storage error have been filed in association with CAPMATINIB (TABRECTA). This represents 0.3% of all adverse event reports for CAPMATINIB.

6
Reports of Product storage error with CAPMATINIB
0.3%
of all CAPMATINIB reports
0
Deaths
0
Hospitalizations

How Dangerous Is Product storage error From CAPMATINIB?

Of the 6 reports.

Is Product storage error Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for CAPMATINIB. However, 6 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 storage error?

INSULIN GLARGINE (7,743) EVOLOCUMAB (6,606) ETANERCEPT (3,653) DENOSUMAB (3,621) ERENUMAB-AOOE (2,958) DUPILUMAB (2,631) ALBUTEROL (2,474) ABATACEPT (2,101) DARBEPOETIN ALFA (1,619) INSULIN LISPRO (1,448)

Which CAPMATINIB Alternatives Have Lower Product storage error Risk?

CAPMATINIB vs CAPREOMYCIN CAPMATINIB vs CAPSAICIN CAPMATINIB vs CAPTOPRIL CAPMATINIB vs CARBAMAZEPINE CAPMATINIB vs CARBETOCIN

Related Pages

CAPMATINIB Full Profile All Product storage error Reports All Drugs Causing Product storage error CAPMATINIB Demographics