Does RAMUCIRUMAB Cause Hyperammonaemia? 7 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Hyperammonaemia have been filed in association with RAMUCIRUMAB (CYRAMZA). This represents 0.1% of all adverse event reports for RAMUCIRUMAB.
7
Reports of Hyperammonaemia with RAMUCIRUMAB
0.1%
of all RAMUCIRUMAB reports
1
Deaths
6
Hospitalizations
How Dangerous Is Hyperammonaemia From RAMUCIRUMAB?
Of the 7 reports, 1 (14.3%) resulted in death, 6 (85.7%) required hospitalization.
Is Hyperammonaemia Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for RAMUCIRUMAB. However, 7 reports have been filed with the FAERS database.
What Other Side Effects Does RAMUCIRUMAB Cause?
Malignant neoplasm progression (743)
Death (492)
Interstitial lung disease (269)
Febrile neutropenia (229)
Neutropenia (229)
Decreased appetite (187)
Diarrhoea (186)
Hypertension (175)
Pyrexia (161)
Nausea (160)
What Other Drugs Cause Hyperammonaemia?
VALPROIC ACID (581)
VALPROATE (328)
FLUOROURACIL (263)
DIVALPROEX (256)
LEVETIRACETAM (192)
TACROLIMUS (181)
ACETAMINOPHEN (177)
OXALIPLATIN (160)
TOPIRAMATE (156)
GLYCEROL PHENYLBUTYRATE (147)
Which RAMUCIRUMAB Alternatives Have Lower Hyperammonaemia Risk?
RAMUCIRUMAB vs RANEXA
RAMUCIRUMAB vs RANIBIZUMAB
RAMUCIRUMAB vs RANIMUSTINE
RAMUCIRUMAB vs RANITIDINE
RAMUCIRUMAB vs RANITIDINE\RANITIDINE