Actoplus and blood glucose increased 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 #5929602-8
Actoplus side effect was reported by a Physician from UNITED STATES on June 19, 2008. Female patient, 70 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: asthenia, blood glucose increased, decreased appetite, fatigue, jaundice , vein disorder, weight decreased. Actoplus dosage: 15 MG/500 MG, 1 IN 1 D, PER ORAL ; 15 MG/500 MG, 2 IN 1 D, PER ORAL. During the same period patient was treated with ACTOPLUS MET, METFORMIN, AMARYL, THYROID, PREMPRO, DIOVAN, METOPROLOL TARTRATE, CELEBREX. Patient recovered.

Actoplus Side Effects Report #5692565-7
Actoplus side effect was reported by a Consumer or non-health professional from UNITED STATES on Mar 21, 2008. Male patient, 65 years of age, weighting 220.0 lb, was diagnosed with type 2 diabetes mellitus and was treated with Actoplus. After drug was administered, patient experienced the following side effects: arthralgia, blood glucose increased, glycosylated haemoglobin increased, meniscus lesion, precancerous skin lesion. Actoplus dosage: 15 MG/850 MG, 1 IN 1 D, PER ORAL; 15 MG/850 MG, 2 IN 1 D, PER ORAL. During the same period patient was treated with ACTOPLUS MET, ACTOS, TAZTIA XT, AVALIDE, METFORMIN. Patient recovered.


Actoplus Side Effects Report #6130491-X
Actoplus side effect was reported by a Consumer or non-health professional from UNITED STATES on Mar 10, 2009. Female patient, 49 years of age, weighting 278.0 lb, was diagnosed with type 2 diabetes mellitus and was treated with Actoplus. After drug was administered, patient experienced the following side effects: abasia, blood glucose increased, blood iron decreased, dizziness , myocardial strain, nasopharyngitis, pneumonia , pulmonary thrombosis. Actoplus dosage: 15/500 MG, 1 IN 1 D, PER ORAL,. During the same period patient was treated with SYNTHROID, FUROSEMIDE, ALPRAZOLAM, GLUCOTROL, LANTUS, HUMALOG. Patient was hospitalized. Patient recovered.

Actoplus Side Effects Report #5049458-8
Actoplus side effect was reported by a Pharmacist from UNITED STATES on July 11, 2006. Male patient, 49 years of age, weighting 190.0 lb, was diagnosed with diabetes mellitus non-insulin-dependent and was treated with Actoplus. After drug was administered, patient experienced the following side effects: blood glucose increased. Actoplus dosage: unknown. Patient recovered.

Actoplus Side Effects Report #5095125-4
Actoplus side effect was reported by a Physician from UNITED STATES on Aug 25, 2006. Male patient, 39 years of age, weighting 334.0 lb, was diagnosed with diabetes mellitus non-insulin-dependent and was treated with Actoplus. After drug was administered, patient experienced the following side effects: blood glucose increased, chest pain , coronary artery disease . Actoplus dosage: 15/850 MG, Q12H PER ORAL. During the same period patient was treated with TOPROL, DEPAKOTE ER, ALDACTONE, SEROQUEL, CELEBREX, COZAAR, VYTORIN, WELLBURTIN. Patient was hospitalized. Patient recovered.

Actoplus Side Effects Report #4915688-6
Actoplus side effect was reported by a Consumer or non-health professional from UNITED STATES on Feb 07, 2006. Male patient, 39 years of age, weighting 312.0 lb, was diagnosed with diabetes mellitus non-insulin-dependent and was treated with Actoplus. After drug was administered, patient experienced the following side effects: blood glucose increased, chest pain , coronary artery disease . Actoplus dosage: 15/850 MG, Q12H, PER ORAL. During the same period patient was treated with TOPROL, DEPAKOTE ER, ALDACTONE, SEROQUEL, CELEBREX, COZAAR, VYTORIN, WELLBUTRIN. Patient was hospitalized. Patient recovered.