Does POLATUZUMAB VEDOTIN Cause Hypomagnesaemia? 46 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 46 reports of Hypomagnesaemia have been filed in association with POLATUZUMAB VEDOTIN (POLIVY). This represents 1.0% of all adverse event reports for POLATUZUMAB VEDOTIN.
46
Reports of Hypomagnesaemia with POLATUZUMAB VEDOTIN
1.0%
of all POLATUZUMAB VEDOTIN reports
5
Deaths
17
Hospitalizations
How Dangerous Is Hypomagnesaemia From POLATUZUMAB VEDOTIN?
Of the 46 reports, 5 (10.9%) resulted in death, 17 (37.0%) required hospitalization, and 4 (8.7%) were considered life-threatening.
Is Hypomagnesaemia Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for POLATUZUMAB VEDOTIN. However, 46 reports have been filed with the FAERS database.
What Other Side Effects Does POLATUZUMAB VEDOTIN Cause?
Disease progression (1,131)
Off label use (692)
Anaemia (344)
Blood lactate dehydrogenase increased (307)
Drug ineffective (305)
Neutropenia (303)
Death (295)
Covid-19 (286)
Febrile neutropenia (286)
Pyrexia (285)
What Other Drugs Cause Hypomagnesaemia?
OMEPRAZOLE (1,766)
PANTOPRAZOLE (1,246)
PANITUMUMAB (611)
ESOMEPRAZOLE (591)
CARBOPLATIN (586)
LANSOPRAZOLE (504)
FUROSEMIDE (501)
FLUOROURACIL (477)
METFORMIN (415)
CISPLATIN (395)
Which POLATUZUMAB VEDOTIN Alternatives Have Lower Hypomagnesaemia Risk?
POLATUZUMAB VEDOTIN vs POLATUZUMAB VEDOTIN-PIIQ
POLATUZUMAB VEDOTIN vs POLIDOCANOL
POLATUZUMAB VEDOTIN vs POLYETHYLENE GLYCOL
POLATUZUMAB VEDOTIN vs POLYETHYLENE GLYCOL 3350
POLATUZUMAB VEDOTIN vs POLYETHYLENE GLYCOL 3350\POTASSIUM\SODIUM BICARBONATE\SODIUM