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Sando FDA adverse reports: 1. View All Sando FDA Adverse Reports

Sando FDA safety alerts: No

Reported deaths: 448

Reported hospitalizations: 1183

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Sando Side Effects Report: 4961428-4,Anaemia, Blood Potassium Decreased, Cardiac Arrest, Gastric Haemorrhage, Gastritis, Hepatic Function Abnormal, Hepatic Steatosis, Hyperkalaemia
on Mar 20, 2006 Female patient from UNITED KINGDOM, , 38 years of age, was diagnosed with blood potassium decreased, depression (What is depression?) and was treated with Sando. After Sando was administered, patient had the following side effects: Sando and anaemia, Sando and blood potassium decreased, Sando and cardiac arrest (What is cardiac arrest?), Sando and gastric haemorrhage, Sando and gastritis, Sando and hepatic function abnormal, Sando and hepatic steatosis, Sando and hyperkalaemia. Sando dosage: 2, Bid; Oral. During the same period patient was treated with FLUOXETINE, CITALOPRAM HYDROBROMIDE. Patient died on 06/29/2005.


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Sando Side Effects
Sando and Anaemia
Sando and Blood potassium decreased
Sando and Cardiac arrestWhat is Cardiac arrest?
Sando and Gastric haemorrhage
Sando and Gastritis
Sando and Hepatic function abnormal
Sando and Hepatic steatosis
Sando and Hyperkalaemia

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