Does PEMBROLIZUMAB Cause Physical deconditioning? 72 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 72 reports of Physical deconditioning have been filed in association with PEMBROLIZUMAB (KEYTRUDA). This represents 0.1% of all adverse event reports for PEMBROLIZUMAB.
72
Reports of Physical deconditioning with PEMBROLIZUMAB
0.1%
of all PEMBROLIZUMAB reports
19
Deaths
53
Hospitalizations
How Dangerous Is Physical deconditioning From PEMBROLIZUMAB?
Of the 72 reports, 19 (26.4%) resulted in death, 53 (73.6%) required hospitalization, and 8 (11.1%) were considered life-threatening.
Is Physical deconditioning Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PEMBROLIZUMAB. However, 72 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 Physical deconditioning?
ACETAMINOPHEN (193)
ESOMEPRAZOLE (189)
AMLODIPINE (186)
FLUOXETINE (184)
TOFACITINIB (182)
ESCITALOPRAM OXALATE (181)
MOCLOBEMIDE (178)
VALSARTAN (176)
VENLAFAXINE (176)
TRAMADOL (173)
Which PEMBROLIZUMAB Alternatives Have Lower Physical deconditioning Risk?
PEMBROLIZUMAB vs PEMETREXED
PEMBROLIZUMAB vs PEMIGATINIB
PEMBROLIZUMAB vs PENICILLAMINE
PEMBROLIZUMAB vs PENICILLIN
PEMBROLIZUMAB vs PENICILLIN G