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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 PEMBROLIZUMAB Cause Product preparation error? 6 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 6 reports of Product preparation error have been filed in association with PEMBROLIZUMAB (KEYTRUDA). This represents 0.0% of all adverse event reports for PEMBROLIZUMAB.

6
Reports of Product preparation error with PEMBROLIZUMAB
0.0%
of all PEMBROLIZUMAB reports
0
Deaths
0
Hospitalizations

How Dangerous Is Product preparation error From PEMBROLIZUMAB?

Of the 6 reports.

Is Product preparation error Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for PEMBROLIZUMAB. However, 6 reports have been filed with the FAERS database.

What Other Side Effects Does PEMBROLIZUMAB Cause?

Malignant neoplasm progression (10,111) Death (4,744) Diarrhoea (4,251) Fatigue (3,833) Off label use (3,416) Product use in unapproved indication (3,191) Pyrexia (3,155) Rash (2,900) Nausea (2,670) Decreased appetite (2,486)

What Other Drugs Cause Product preparation error?

ONABOTULINUMTOXINA (3,593) EVOLOCUMAB (2,785) DUPILUMAB (2,707) BUPRENORPHINE\NALOXONE (777) ABOBOTULINUMTOXINA (751) ALBIGLUTIDE (691) ALBUTEROL (520) PEGFILGRASTIM (473) ALIROCUMAB (402) LEUPROLIDE (400)

Which PEMBROLIZUMAB Alternatives Have Lower Product preparation error Risk?

PEMBROLIZUMAB vs PEMETREXED PEMBROLIZUMAB vs PEMIGATINIB PEMBROLIZUMAB vs PENICILLAMINE PEMBROLIZUMAB vs PENICILLIN PEMBROLIZUMAB vs PENICILLIN G

Related Pages

PEMBROLIZUMAB Full Profile All Product preparation error Reports All Drugs Causing Product preparation error PEMBROLIZUMAB Demographics