Actoplus and incorrect dose administered 
Actoplus and incorrect dose administered Patient Reports February 12, 2012
Actoplus Side Effects Report #5683454-2
Actoplus side effect was reported by a Pharmacist from UNITED STATES on Mar 14, 2008. Female patient, 54 years of age, 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, incorrect dose administered. Actoplus dosage: 15 MG/850 MG, 2 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. Patient recovered.
Actoplus Side Effects Report #5107285-7
Actoplus side effect was reported by a Physician from UNITED STATES on Sept 07, 2006. Female patient, 75 years of age, weighting 120.0 lb, was diagnosed with diabetes mellitus non-insulin-dependent and was treated with Actoplus. After drug was administered, patient experienced the following side effects: anxiety
, blood glucose decreased, depressed level of consciousness, feeling hot, incorrect dose administered, malaise. Actoplus dosage: 15/500 MG, BID OR TID, PER ORAL. During the same period patient was treated with GLYBURIDE, DYAZIDE, PRAVACHOL, EVISTA, ATENOLOL, ACTONEL, CALCIUM, ASPIRIN. Patient recovered.Actoplus Side Effects Report #5011521-5
Actoplus side effect was reported by a Pharmacist from UNITED STATES on May 15, 2006. Female patient, 75 years of age, weighting 120.0 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 decreased, feeling hot, incorrect dose administered, loss of consciousness, malaise. Actoplus dosage: 15/500 MG, 2 IN 1 D, PER ORAL. During the same period patient was treated with GLYBURIDE, HCTZ, PRAVACHOL, EVISTA. Patient recovered.
Actoplus Side Effects Report #5105817-6
Actoplus side effect was reported by a Pharmacist from UNITED STATES on Sept 01, 2006. Female patient, 70 years of age, weighting 203.0 lb, was diagnosed with diabetes mellitus non-insulin-dependent and was treated with Actoplus. After drug was administered, patient experienced the following side effects: anxiety
, blood glucose decreased, incorrect dose administered, myocardial infarction, somnolence. Actoplus dosage: unknown. During the same period patient was treated with ZETIA, ASPIRIN, FUROSEMIDE, VITAMIN E, ASCORBIC ACID, CALCIUM PLUS, GLUCOSAMINE PLUS, FISH OIL. Patient was hospitalized. Patient recovered.Actoplus Side Effects Report #5141662-3
Actoplus side effect was reported by a Pharmacist from UNITED STATES on Oct 05, 2006. Female patient, 70 years of age, weighting 203.0 lb, was diagnosed with diabetes mellitus non-insulin-dependent and was treated with Actoplus. After drug was administered, patient experienced the following side effects: anxiety
, blood glucose decreased, incorrect dose administered, myocardial infarction, somnolence. Actoplus dosage: unknown. During the same period patient was treated with ZETIA, ASPIRIN, FUROSEMIDE, VITAMIN E, ASCORBIC ACID, CALCIUM PLUS, GLUCOSAMINE PLUS, FISH OIL. Patient was hospitalized. Patient recovered.Actoplus Side Effects Report #5199444-2
Actoplus side effect was reported by a Pharmacist from UNITED STATES on Dec 14, 2006. Female patient, 70 years of age, weighting 203.0 lb, was diagnosed with diabetes mellitus non-insulin-dependent and was treated with Actoplus. After drug was administered, patient experienced the following side effects: anxiety
, blood glucose decreased, incorrect dose administered, myocardial infarction, somnolence. Actoplus dosage: unknown. During the same period patient was treated with ZETIA, ASPIRIN, FUROSEMIDE, VITAMIN E, ASCORBIC ACID, CALCIUM PLUS, GLUCOSAMINE PLUS, FISH OIL. Patient was hospitalized. Patient recovered.Actoplus Side Effects Report #5448530-8
Actoplus side effect was reported by a Consumer or non-health professional from UNITED STATES on Aug 24, 2007. Female patient, 70 years of age, was diagnosed with diabetes mellitus and was treated with Actoplus. After drug was administered, patient experienced the following side effects: incorrect dose administered, treatment noncompliance. Actoplus dosage: 15/850 MG, PER ORAL; 15/500 MG, PER ORAL. Patient recovered.
Actoplus Side Effects Report #5193889-2
Actoplus side effect was reported by a Pharmacist from UNITED STATES on Dec 07, 2006. Female patient, 67 years of age, was treated with Actoplus. After drug was administered, patient experienced the following side effects: incorrect dose administered. Actoplus dosage: 15/850 MG, 1 IN 1 D, PER ORAL. Patient recovered.
Actoplus Side Effects Report #5225102-1
Actoplus side effect was reported by a Pharmacist from UNITED STATES on Jan 16, 2007. Female patient was treated with Actoplus. After drug was administered, patient experienced the following side effects: incorrect dose administered. Actoplus dosage: 15/500 MG TWICE DAILY, PER ORAL. Patient recovered.