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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.

ZANIDATAMAB for Gastrooesophageal reflux disease: Side Effects & Safety Data

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There are 7 adverse event reports in the FDA FAERS database where ZANIDATAMAB was used for Gastrooesophageal reflux disease.

Most Reported Side Effects for ZANIDATAMAB

Side Effect Reports % Deaths Hosp.
Diarrhoea 49 34.5% 5 45
Infusion related reaction 17 12.0% 0 14
Sepsis 9 6.3% 2 9
Hypokalaemia 8 5.6% 4 5
Pneumonia 8 5.6% 1 8
Cerebrovascular accident 7 4.9% 0 7
Decreased appetite 7 4.9% 0 7
Pneumonitis 7 4.9% 1 4
Acute kidney injury 6 4.2% 1 4
Vomiting 6 4.2% 1 6
Asthenia 5 3.5% 0 5
Nausea 5 3.5% 1 5

Other Indications for ZANIDATAMAB

Adenocarcinoma gastric (78) Oesophageal adenocarcinoma (42) Product used for unknown indication (7) Prophylaxis (6)

Other Drugs Used for Gastrooesophageal reflux disease

RANITIDINE (141,291) OMEPRAZOLE (28,339) ESOMEPRAZOLE (27,743) PANTOPRAZOLE (18,706) LANSOPRAZOLE (17,671) DEXLANSOPRAZOLE (5,185) RABEPRAZOLE (1,689) NEXIUM (1,209) FAMOTIDINE (1,099) VONOPRAZAN (766)

Related Pages

ZANIDATAMAB Full Profile All Gastrooesophageal reflux disease Drugs ZANIDATAMAB Demographics ZANIDATAMAB Timeline