Actoplus and nausea Patient Reports February 12, 2012

Actoplus Side Effects Report #5382858-5
Actoplus side effect was reported by a Consumer or non-health professional from UNITED STATES on June 18, 2007. Female patient, 76 years of age, weighting 210.0 lb, was diagnosed with type 2 diabetes mellitus and was treated with Actoplus. After drug was administered, patient experienced the following side effects: abdominal pain upper, blood glucose increased, eye disorder, fatigue, feeling abnormal, nausea , somnolence, urticaria. Actoplus dosage: 15/850 MG, TWICE DAILY, PER ORAL. During the same period patient was treated with ENABLEX, TRICOR, LISINOPRIL, CENTRUM, PRILOSEC, VITAMIN B6, LEXAPRO, HYDROCHLOROTHIAZIDE. Patient recovered.

Actoplus Side Effects Report #5405829-9
Actoplus side effect was reported by a Health Professional from UNITED STATES on July 26, 2007. Female patient, 76 years of age, weighting 210.0 lb, was diagnosed with type 2 diabetes mellitus and was treated with Actoplus. After drug was administered, patient experienced the following side effects: abdominal pain upper, blood glucose increased, eye disorder, fatigue, feeling abnormal, hypersomnia, nausea , urticaria. Actoplus dosage: 15/850 MG, TWICE DAILY, PER ORAL. During the same period patient was treated with ENABLEX, TRICOR, LISINOPRIL, CENTRUM, PRILOSEC, VITAMIN B6, LEXAPRO, HYDROCHLOROTHIAZIDE. Patient recovered.

Actoplus Side Effects Report #5802528-6
Actoplus side effect was reported by a Consumer or non-health professional from UNITED STATES on May 20, 2008. Female patient, 68 years of age, weighting 140.0 lb, was diagnosed with type 2 diabetes mellitus and was treated with Actoplus. After drug was administered, patient experienced the following side effects: blood glucose decreased, dizziness , nausea , rash pruritic, urticaria. Actoplus dosage: 15 MG/500 MG, 2 IN 1 D WITH MEALS, PER ORAL. During the same period patient was treated with BENICAR, ATENOLOL, LOZOL, LOTREL, CRESTOR, TRICOR. Patient recovered.

Actoplus Side Effects Report #5391817-8
Actoplus side effect was reported by a Consumer or non-health professional from UNITED STATES on June 25, 2007. Female patient, 57 years of age, weighting 148.0 lb, was diagnosed with type 2 diabetes mellitus and was treated with Actoplus. After drug was administered, patient experienced the following side effects: dizziness , dyspepsia, headache , hypersensitivity, nausea , visual disturbance. Actoplus dosage: 15/850 MG BID, AM, 15/500 MG PM DAILY, PER ORAL, 15/850 MG, 3 IN 1 D, PER ORAL. During the same period patient was treated with GLIPIZIDE, VYTORIN, DIOVAN HCT. Patient recovered.