Classes
DEA Class; Rx
Common Brand Names; ACTOplus Met, ACTOplus Met XR
- Antidiabetics, Biguanides/Thiazolidinediones
Description
Oral combination of pioglitazone, a thiazolidinedione (TZD), and metformin, a biguanide
Used in adults for type 2 diabetes mellitus; use with caution with insulin
Risk of lactic acidosis due to metformin is low; TZDs may cause or exacerbate heart failure; monitor closely
Indications
Indicated for the treatment of type 2 diabetes mellitus not controlled by diet and exercise.
Contraindications
Hypersensitivity
Severe renal disease: eGFR <30 ml/min/1.73 m²
Acute or chronic metabolic acidosis, including DKA with or without coma
NYHA Class III or IV heart failure
Adverse Effects
- Lower limb edema (2.9-11.3%)
- Upper respiratory infection (12-16)
- Weight gain (2.9-6.7%)
- Diarrhea (4.8-5.8%)
- Nausea (3.6-5.8%)
- Urinary tract infection (5.3-5.8%)
- Dizziness (4.8-5.4%)
- Headache (4.6-5.3%)
- Sinusitis (4.4-5%)
- Edema (3%)
- Hepatitis and hepatic enzyme elevations to >3 XUL, including very rare incidences of hepatic failure with and without fatal outcome
- Cholestatic, hepatocellular, and mixed hepatocellular liver injury
Warnings
Temporarily discontinue in patients undergoing radiologic exams using iodinated contrast agents
Do not initiate in patients aged ≥80 years CrCl demonstrates that renal function is not reduced because these patients are more susceptible to developing lactic acidosis
Withhold metformin in presence of any condition associated with hypoxemia, dehydration, or sepsis
Lactic acidosis should be suspected in any diabetic patient with metabolic acidosis lacking evidence of ketoacidosis (ketonuria and ketonemia); lactic acidosis is a medical emergency that must be treated in a hospital setting
Pioglitazone may cause fluid retention and cause or exacerbate existing heart failure
Edema; thiazolidinediones, which are peroxisome proliferator-activated receptor (PPAR) gamma agonists, can cause dose-related fluid retention, particularly when used in combination with insulin
Pioglitazone exerts its antihyperglycemic effect only in presence of insulin; therefore, do not use in type 1 diabetes mellitus or for treatment of diabetic ketoacidosis
May cause hypoglycemia; patients receiving therapy in combination with insulin or other antidiabetic medications (particularly insulin secretagogues such as sulfonylureas) may be at risk for hypoglycemia; a reduction in dose of the concomitant antidiabetic medication may be necessary to reduce the risk of hypoglycemia; hypoglycemia can also occur when caloric intake is deficient or when strenuous be necessary to reduce the risk of hypoglycemia exercise is not compensated by caloric supplement; hypoglycemia may be difficult to recognize in the elderly, and in people who are taking beta-adrenergic blocking drugs
Rare reports of hepatitis and hepatic enzyme elevations to >3 xULN, including very rare incidences of hepatic failure with and without fatal outcome
In controlled clinical trials of metformin, a decrease to subnormal levels of previously normal serum vitamin B12 levels, without clinical manifestations, reported; certain individuals (those with inadequate vitamin B12 or calcium intake or absorption) appear to be predisposed to developing subnormal vitamin B12 levels; in these patients, routine serum vitamin B12 measurements at two- to three-year intervals may be useful
Metformin is substantially excreted by kidney, and risk of metformin accumulation and lactic acidosis increases with degree of renal impairment
Use of metformin in patients with hepatic impairment has been associated with some cases of lactic acidosis; therapy is not recommended in patients with hepatic impairment
Discuss potential for unintended pregnancy with premenopausal women as therapy with metformin/pioglitazone, may result in ovulation in some anovulatory women
Pregnancy and Lactation
Pregnancy: Limited data with metformin/pioglitazone or pioglitazone in pregnant women are not sufficient to determine a drug-associated risk for major birth defects or miscarriage
Lactation: There is no information regarding the presence of metformin/pioglitazone or pioglitazone in human milk; effects on breastfed infant, or effects on milk production; there is insufficient information on effects of metformin on breastfed infant and no available information on effects of metformin on milk production
Maximum Dosage
45 mg/day PO pioglitazone and 2550 mg/day PO metformin for regular-release tablets; 45 mg/day PO pioglitazone and 2000 mg/day PO metformin for extended-release tablets.
In general do not titrate to the adult maximum dosage.
Safe and effective use has not been established.
Safe and effective use has not been established.
How supplied
Metformin/pioglitazone
tablet
- 500mg/15mg
- 850mg/15mg
tablet, extended-release
- 1,000mg/15mg
- 1,000mg/30mg