Does PEMETREXED Cause Intentional product use issue? 35 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 35 reports of Intentional product use issue have been filed in association with PEMETREXED (Pemetrexed). This represents 0.2% of all adverse event reports for PEMETREXED.
35
Reports of Intentional product use issue with PEMETREXED
0.2%
of all PEMETREXED reports
9
Deaths
11
Hospitalizations
How Dangerous Is Intentional product use issue From PEMETREXED?
Of the 35 reports, 9 (25.7%) resulted in death, 11 (31.4%) required hospitalization, and 1 (2.9%) were considered life-threatening.
Is Intentional product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PEMETREXED. However, 35 reports have been filed with the FAERS database.
What Other Side Effects Does PEMETREXED Cause?
Malignant neoplasm progression (2,149)
Off label use (1,663)
Anaemia (1,430)
Pancytopenia (1,236)
Neutropenia (1,200)
Nausea (1,195)
Diarrhoea (1,165)
Acute kidney injury (1,105)
Thrombocytopenia (1,059)
Disease progression (969)
What Other Drugs Cause Intentional product use issue?
INFLIXIMAB (11,028)
RITUXIMAB (9,602)
INFLIXIMAB-DYYB (7,549)
TOCILIZUMAB (5,078)
METHOTREXATE (4,087)
PREDNISONE (3,961)
ABATACEPT (3,693)
ADALIMUMAB (3,557)
NIVOLUMAB (3,297)
LEFLUNOMIDE (3,280)
Which PEMETREXED Alternatives Have Lower Intentional product use issue Risk?
PEMETREXED vs PEMIGATINIB
PEMETREXED vs PENICILLAMINE
PEMETREXED vs PENICILLIN
PEMETREXED vs PENICILLIN G
PEMETREXED vs PENICILLIN G BENZATHINE