Actoplus and cardio-respiratory arrest Patient Reports February 12, 2012

Actoplus Side Effects Report #4901302-2
Actoplus side effect was reported by a Health Professional from UNITED STATES on Jan 30, 2006. Female patient, 26 years of age, weighting 329.0 lb, was treated with Actoplus. After drug was administered, patient experienced the following side effects: cardio-respiratory arrest, glycosylated haemoglobin increased. Actoplus dosage: 15/500 MG, 2 IN 1 D, PER ORAL. During the same period patient was treated with AVANDIA, NORTREL. Patient died on 01/29/2006.

Actoplus Side Effects Report #4907230-0
Actoplus side effect was reported by a Health Professional from UNITED STATES on Feb 02, 2006. Female patient, 26 years of age, weighting 329.0 lb, was diagnosed with uterine haemorrhage and was treated with Actoplus. After drug was administered, patient experienced the following side effects: cardio-respiratory arrest, glycosylated haemoglobin increased, pulmonary embolism . Actoplus dosage: 15/500 MG, 2 IN 1 D, PER ORAL. During the same period patient was treated with NORTREL, AVANDIA. Patient died on 01/29/2006.

Actoplus Side Effects Report #4976969-3
Actoplus side effect was reported by a Health Professional from UNITED STATES on Apr 07, 2006. Female patient, 26 years of age, weighting 329.0 lb, was diagnosed with uterine haemorrhage and was treated with Actoplus. After drug was administered, patient experienced the following side effects: arteriosclerosis, arteriosclerosis coronary artery, cardio-respiratory arrest, hepatic steatosis, pulmonary congestion, pulmonary embolism , pulmonary infarction. Actoplus dosage: 15/500 MG, 2 IN 1 D, PER ORAL. During the same period patient was treated with NORTREL, AVANDIA. Patient died on 01/29/2006.