Does PEMBROLIZUMAB Cause Wrong product administered? 7 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Wrong product administered have been filed in association with PEMBROLIZUMAB (KEYTRUDA). This represents 0.0% of all adverse event reports for PEMBROLIZUMAB.
7
Reports of Wrong product administered with PEMBROLIZUMAB
0.0%
of all PEMBROLIZUMAB reports
1
Deaths
0
Hospitalizations
How Dangerous Is Wrong product administered From PEMBROLIZUMAB?
Of the 7 reports, 1 (14.3%) resulted in death.
Is Wrong product administered Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PEMBROLIZUMAB. However, 7 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 Wrong product administered?
INSULIN LISPRO (337)
INSULIN GLARGINE (226)
RISPERIDONE (141)
QUETIAPINE (137)
ACETAMINOPHEN (133)
INSULIN ASPART (112)
CLOZAPINE (106)
INSULIN HUMAN (104)
TUBERCULIN PURIFIED PROTEIN DERIVATIVE (104)
IBUPROFEN (102)
Which PEMBROLIZUMAB Alternatives Have Lower Wrong product administered Risk?
PEMBROLIZUMAB vs PEMETREXED
PEMBROLIZUMAB vs PEMIGATINIB
PEMBROLIZUMAB vs PENICILLAMINE
PEMBROLIZUMAB vs PENICILLIN
PEMBROLIZUMAB vs PENICILLIN G