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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 PEMETREXED Cause Incorrect product administration duration? 11 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 11 reports of Incorrect product administration duration have been filed in association with PEMETREXED (Pemetrexed). This represents 0.1% of all adverse event reports for PEMETREXED.

11
Reports of Incorrect product administration duration with PEMETREXED
0.1%
of all PEMETREXED reports
0
Deaths
7
Hospitalizations

How Dangerous Is Incorrect product administration duration From PEMETREXED?

Of the 11 reports, 7 (63.6%) required hospitalization.

Is Incorrect product administration duration Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for PEMETREXED. However, 11 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 Incorrect product administration duration?

ETONOGESTREL (3,974) POLYETHYLENE GLYCOL 3350 (2,129) NIRMATRELVIR\RITONAVIR (744) DOCOSANOL (634) LANSOPRAZOLE (564) LOPERAMIDE (543) NAPROXEN (499) INSULIN LISPRO (479) DICLOFENAC (362) OMEPRAZOLE (302)

Which PEMETREXED Alternatives Have Lower Incorrect product administration duration Risk?

PEMETREXED vs PEMIGATINIB PEMETREXED vs PENICILLAMINE PEMETREXED vs PENICILLIN PEMETREXED vs PENICILLIN G PEMETREXED vs PENICILLIN G BENZATHINE

Related Pages

PEMETREXED Full Profile All Incorrect product administration duration Reports All Drugs Causing Incorrect product administration duration PEMETREXED Demographics