Micronase and blood glucose decreased Patient Reports February 12, 2012
Micronase Side Effects Report #5299763-5
Micronase side effect was reported by a Consumer or non-health professional from UNITED STATES on Apr 05, 2007. Female patient, weighting 278.0 lb, was diagnosed with diabetes mellitus non-insulin-dependent and was treated with Micronase. After drug was administered, patient experienced the following side effects: blood glucose decreased, early satiety, feeling abnormal, weight decreased. Micronase dosage: unknown. During the same period patient was treated with BYETTA, GLUCOPHAGE. Patient recovered.
Micronase Side Effects Report #4735197-7
Micronase side effect was reported by a Consumer or non-health professional from UNITED STATES on July 21, 2005. Female patient, 61 years of age, was diagnosed with diabetes mellitus, fibromyalgia and was treated with Micronase. After drug was administered, patient experienced the following side effects: blood glucose decreased, feeling abnormal, muscle spasms, nausea
, stomach discomfort. Micronase dosage: unknown. During the same period patient was treated with VOLTAREN, AVANDIA, TENORMIN, TAGAMET. Patient recovered.Micronase Side Effects Report #6025467-7
Micronase side effect was reported by a Consumer or non-health professional from UNITED STATES on Dec 22, 2008. Female patient, weighting 153.9 lb, was diagnosed with diabetes mellitus and was treated with Micronase. After drug was administered, patient experienced the following side effects: blood glucose decreased, blood glucose increased, cardiac disorder, diarrhoea, flatulence, glycosylated haemoglobin increased, pneumonia
. Micronase dosage: 10 MG, 2X/DAY. During the same period patient was treated with GLIBENCLAMIDE, AVANDIA, GLUCOPHAGE. Patient was hospitalized. Patient recovered.Micronase Side Effects Report #6103145-3
Micronase side effect was reported by a Consumer or non-health professional from UNITED STATES on Feb 20, 2009. Female patient, weighting 140.0 lb, was diagnosed with diabetes mellitus and was treated with Micronase. After drug was administered, patient experienced the following side effects: blood glucose decreased, blood glucose increased, cholecystectomy, transient ischaemic attack. Micronase dosage: 10 MG, 2X/DAY. During the same period patient was treated with GLIBENCLAMIDE, ACTOS, ZETIA, LISINOPRIL, METOPROLOL TARTRATE. Patient was hospitalized. Patient recovered.
Micronase Side Effects Report #6111838-7
Micronase side effect was reported by a Consumer or non-health professional from UNITED STATES on Feb 27, 2009. Female patient, weighting 153.9 lb, was diagnosed with diabetes mellitus, type 2 diabetes mellitus and was treated with Micronase. After drug was administered, patient experienced the following side effects: asthenia, blood glucose decreased, blood glucose increased, body height decreased, cardiac disorder, diarrhoea, dizziness
, flatulence, glycosylated haemoglobin increased. Micronase dosage: 10 MG, 2X/DAY. During the same period patient was treated with GLIBENCLAMIDE, GLIPIZIDE, AVANDIA, GLUCOPHAGE, FOLIC ACID, ACETYLSALICYLIC ACID, POTASSIUM. Patient was hospitalized. Patient recovered.Micronase Side Effects Report #5013794-1
Micronase side effect was reported by a Pharmacist from UNITED STATES on May 26, 2006. Female patient, 82 years of age, was treated with Micronase. After drug was administered, patient experienced the following side effects: blood glucose decreased, cardiac failure, pneumonia aspiration, renal failure. Micronase dosage: unknown. Patient died.
Micronase and blood glucose decreased 