Actoplus and blood glucose decreased Patient Reports February 12, 2012

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 #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 #5008128-2
Actoplus side effect was reported by a Consumer or non-health professional from UNITED STATES on Dec 21, 2005. Female patient, 81 years of age, weighting 150.0 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. Actoplus dosage: 15/850 MG, 1 IN 1 D, PER ORAL. During the same period patient was treated with HUMALOG. Patient recovered.

Actoplus Side Effects Report #5281316-6
Actoplus side effect was reported by a Physician from UNITED STATES on Sept 07, 2006. Female patient, 75 years of age, weighting 264.6 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, 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 #5281317-8
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, 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 #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 #5034559-0
Actoplus side effect was reported by a Pharmacist from UNITED STATES on June 01, 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, loss of consciousness, malaise, thanatophobia. 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.