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

Saridon FDA safety alerts: No

Reported deaths: 1

Reported hospitalizations: 1

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Saridon Side Effects Report: 4653486-1,Blood Alkaline Phosphatase Increased, Gamma-glutamyltransferase Increased, Gastrointestinal Haemorrhage, Haematemesis, Prothrombin Time Prolonged
on Apr 05, 2005 Female patient from , , 86 years of age, was diagnosed with back pain (What is back pain?), chronic obstructive pulmonary disease, condition aggravated and was treated with Saridon. After Saridon was administered, patient had the following side effects: Saridon and blood alkaline phosphatase increased, Saridon and gamma-glutamyltransferase increased, Saridon and gastrointestinal haemorrhage, Saridon and haematemesis, Saridon and prothrombin time prolonged. Saridon dosage: 2400 Mg Qday Po. During the same period patient was treated with AMOXI, CAPTOPRIL, TORSEMIDE. Patient was hospitalized. Patient died on 03/13/2005.


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Comments to date: 3. Page 1 of 1.

simranjeet singh   India

11:21am on Wednesday, April 6th, 2011

inflammation in oesophagus

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10:27am on Saturday, March 12th, 2011

What's on Your cvbgfazdxCdsxZCvgtyb uhja Mind?

santanu   kolkata

5:32am on Monday, December 27th, 2010

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Saridon Side Effects
Saridon and Blood alkaline phosphatase increased
Saridon and Gamma-glutamyltransferase increased
Saridon and Gastrointestinal haemorrhage
Saridon and Haematemesis
Saridon and Prothrombin time prolonged

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