Actoplus and asthenia Patient Reports February 12, 2012

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 #5469679-X
Actoplus side effect was reported by a Physician from UNITED STATES on Sept 05, 2007. Female patient, 65 years of age, weighting 240.0 lb, was diagnosed with type 2 diabetes mellitus and was treated with Actoplus. After drug was administered, patient experienced the following side effects: asthenia, disease progression, myopathy, pain in extremity, paraesthesia, rash pruritic. Actoplus dosage: 15 MG/850 MG BID, PER ORAL. During the same period patient was treated with LIPITOR, FOSAMAX, ENALAPRIL MALEATE, ASPIRIN, VITAMIN D, DETROL LA. Patient recovered.

Actoplus Side Effects Report #5118484-2
Actoplus side effect was reported by a Health Professional from UNITED STATES on Sept 18, 2006. Female patient, 61 years of age, weighting 235.0 lb, was diagnosed with diabetes mellitus non-insulin-dependent and was treated with Actoplus. After drug was administered, patient experienced the following side effects: asthenia, dyspnoea, hyperaesthesia, movement disorder , muscular weakness, myalgia. Actoplus dosage: 15/500 MG, TWICE DAILY, PER ORAL. During the same period patient was treated with ACE INHIBITOR, TRICOR, AVANDAMET. Patient recovered.

Actoplus Side Effects Report #5419570-X
Actoplus side effect was reported by a Consumer or non-health professional from UNITED STATES on Aug 15, 2007. Male patient, 42 years of age, weighting 192.0 lb, was diagnosed with blood glucose increased and was treated with Actoplus. After drug was administered, patient experienced the following side effects: abdominal distension, asthenia, dyspnoea, fluid retention. Actoplus dosage: unknown. Patient recovered.