Accolate and hepatic function abnormal Patient Reports February 13, 2012

Accolate Side Effects Report #4662621-0
Accolate side effect was reported by a Physician from on Apr 25, 2005. Female patient, 77 years of age, was diagnosed with asthma  and was treated with Accolate. After drug was administered, patient experienced the following side effects: blood bilirubin increased, decreased appetite, hepatic function abnormal, jaundice . Accolate dosage: unknown. During the same period patient was treated with NORVASC, TOYOFAROL, MUCODYNE, SILECE, HALCION. Patient died on 04/29/2005.

Accolate Side Effects Report #4690467-6
Accolate side effect was reported by a Health Professional from on Jan 18, 2002. Female patient, weighting 114.6 lb, was diagnosed with asthma  and was treated with Accolate. After drug was administered, patient experienced the following side effects: ageusia, alanine aminotransferase increased, aspartate aminotransferase increased, eye haemorrhage, hepatic function abnormal, malaise, platelet count decreased, tremor. Accolate dosage: unknown. During the same period patient was treated with SPIROPENT, PROGRAF, THEOLONG, FLUTIDE, BIOFERMIN R, SELBEX, MEDROL. Patient was hospitalized. Patient recovered.

Accolate Side Effects Report #4551744-2
Accolate side effect was reported by a Consumer or non-health professional from on Dec 29, 2004. Male patient, 79 years of age, was treated with Accolate. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, chronic obstructive pulmonary disease, hepatic function abnormal, ileus paralytic, shock, skin ulcer, urinary tract infection . Accolate dosage: unknown. Patient died on 05/09/2002.

Accolate Side Effects Report #4553335-6
Accolate side effect was reported by a Consumer or non-health professional from on Dec 29, 2004. Male patient, 71 years of age, was treated with Accolate. After drug was administered, patient experienced the following side effects: hepatic function abnormal, lung neoplasm malignant, metastases to bone, metastases to bone marrow, peptic ulcer , rheumatoid arthritis . Accolate dosage: 20 MG DAILY PO. Patient died on 11/12/2002.


Accolate Side Effects Report #4551742-9
Accolate side effect was reported by a Health Professional from on Dec 29, 2004. Male patient, 69 years of age, was treated with Accolate. After drug was administered, patient experienced the following side effects: acute myocardial infarction, cerebral haemorrhage, hepatic function abnormal, obstructive chronic bronchitis with acute exacerbation, shock. Accolate dosage: 40 MG DAILY PO. Patient died on 12/16/2002.

Accolate Side Effects Report #4551516-9
Accolate side effect was reported by a Consumer or non-health professional from on Dec 29, 2004. Male patient, 67 years of age, was treated with Accolate. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, bronchial carcinoma, congestive cardiomyopathy, hepatic function abnormal, metastases to lung, pleurisy, pneumonia . Accolate dosage: 40 MG DAILY PO. Patient died on 11/24/2001.

Accolate Side Effects Report #4551747-8
Accolate side effect was reported by a Health Professional from on Dec 29, 2004. Female patient, 66 years of age, was treated with Accolate. After drug was administered, patient experienced the following side effects: bacteraemia, disseminated intravascular coagulation, hepatic function abnormal, injury, lung disorder, pneumonia , post procedural complication, septic shock. Accolate dosage: 40 MG DAILY PO. Patient died on 08/29/2002.

Accolate Side Effects Report #4551756-9
Accolate side effect was reported by a Health Professional from on Dec 29, 2004. Female patient, 64 years of age, was treated with Accolate. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, chronic obstructive pulmonary disease, depressed level of consciousness, hepatic function abnormal, renal failure acute, septic shock. Accolate dosage: 2 X 20 MG TABLETS DISPENSED FOR SEVEN DAYS TREATMENT. Patient died on 04/28/2002.