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Working Together To Manage Diabetes: A guide for Pharmacy, Podiatry, Optometry, and Dental professionals


Drug Table Supplement Contents

Diabetes Medications

Table 2. Glucose-Lowering Activity—Oral Diabetes Agent

Medication
Blood Glucose Most Affected
Greatest Risk for Hypoglycemia
Adapted from © 2002, The Diabetes Center, Old Saybrook, CT, used by permission.
SMBG = self-monitoring of blood glucose
Sulfonylureas Fasting and postprandial Nocturnal, fasting, 4–6 hr after meals
Meglitinide or phenylalanine derivative Postprandial 2–3 hr after meals
Biguanide Fasting and postprandial After exercise if prolonged and strenuous
Alpha-glucosidase inhibitor Postprandial None
Thiazolidinedione Fasting and postprandial None
Glucovance™ Fasting and postprandial Nocturnal, fasting, 4–6 hr after meals
Metaglip™ Fasting Nocturnal, fasting, 4–6 hr after meals
Avandamet™ Fasting and postprandial After exercise if prolonged and strenuous
Actoplus Met™ Fasting and postprandial After exercise if prolonged and strenuous
Avandryl™ Fasting and postprandial Nocturnal, fasting, 4–6 hr after meals

 

Table 3. Important Insulin Information*

Insulin
Onset
Peak
Effective Duration
Maximal Duration
Comments
Adapted from © 2006 The Diabetes Center, Old Saybrook, CT. Used with permission.
*Site rotation for injections is necessary for all types of insulin.
Human
Rapid Acting
Lispro (Humalog™)
< 15 min
1–2 hr
2–4 hr
3–5 hr
Should be taken just prior to or just after eating.
Aspart (Novalog™)
< 15 min
1–3 hr
3–5 hr
4–6 hr
Should be taken just prior to or just after eating.
Glulisine (Apidra™)
< 15 min
0.5–1 hr
3 hr
3 hr
Should be taken just prior to or just after eating.
Short Acting
Regular (Novolin R™, Humulin R™)
0.5–1 hr
2–4 hr
3–5 hr
8 hr
Best if taken 30 min before a meal.
Intermediate Acting
Lente (Novolin™, Humulin L™)
3–4 hr
4–12 hr
12–18 hr
16–20 hr
Limited supplies.
NPH (Novolin N™, Humulin N™)
2–4 hr
4–10 hr
10–16 hr
14–18 hr
Bedtime dosing minimizes nocturnal hypoglycemia.
Long Acting
Characterized by a “flat” or “peakless” concentration profile.
Insulin glargine
(Lantus™) analog
4–6 hr
None
24 hr
24 hr
Cannot be mixed with any other insulin. Stress site rotation and not to use same syringe used with other insulins. Not recommended for pre-filling syringes.
Detemir (Levemir™)
3–4 hr
50% in 3–4 hr,
lasting up to 14 hr
5.7–23.2 hr
Dose dependent-
5.7–23.2 hr
Cannot be mixed in same syringe with other insulins.
Duration of action is dose dependent: 6 hrs (0.1U/kg), 12hrs (0.2U/kg), 20 hrs (0.4U/kg), 23 hrs (0.8U/kg and 1.6U/kg).
Ultralente
6–10 hr
Minimal
18–20 hr
20–30 hr
Limited supplies.
Pre-mixed Human
Humalog™ 75/25
Novolog Mix™ 70/30
<15 min
1–2 hr
10–16 hr
14–18 hr
75% NPL, 25% Lispro Should be taken just prior to or just after eating 70% NPH, 30% Aspart because of rapid onset. Caution because of name confusion with Humalog and Novolog.
Humulin™ 70/30
Novolin™ 70/30
0.5–1 hr
2–10 hr
10–16 hr
14–18 hr
Humalin and Novolin are 70% NPH and 30% regular insulin.
Animal Source
Regular
0.5–2 hr
3–4 hr
4–6 hr
6–8 hr
Conversion to human insulin recommended. Dose changes required (usually a 10% reduction in dose when switching to human).
NPH
4–6 hr
8–14 hr
16–20 hr
20–24 hr
Lente
4–6 hr
8–14 hr
16–20 hr
20–24 hr
Inhaled Insulin
Exubera™
10–20 min
30–90 min
2–6 hr
6 hr
Dosed in MG of powder, Available in 1 mg and 3 mg blisters.
1mg approx=3 IU insulin, 3mg approx=8 IU (Inhalation of 1 mg +1 mg +1 mg does not equal 3mg)

 

Table 4. Recommended Insulin Storage

Recommended Insulin Storage
Refrigerated (36°F - 46°F)
Room Temperature (59°F - 86°F)
Adapted from © 2006 The Diabetes Center, Old Saybrook, CT. Used with permission.
*Suggested, not clinically established
Vial
Opened
Unopened
Opened
Unopened
Humalog™, Novolog™, Humulin™, Novolin™, Apidra™
28 days
until expiration date
28 days
28 days
Lantus™ (10 mL)
28 days
until expiration date
28 days
28 days
Detemir (Levemir™)
42 days
until expiration date
42 days
42 days
Pens/Cartridges
Not in use
In use
Humalog™
Until expiration date
28 days
Humulin R™( available in cartridge only)
Until expiration date
28 days
Humulin N™
Until expiration date
14 days
Humulin 70/30™
Until expiration date
10 days
Humalog Mix 75/25™
Until expiration date
10 days
Novolog™
Until expiration date
28 days
Novolog Mix 70/30™
Until expiration date
14 days
Novolin R™ (prefilled and 1.5-mL cartridge)
Until expiration date
30 days
Novolin R™ (3-mL cartridge)
Until expiration date
28 days
Novolin N™ (prefilled and 1.5-mL cartridge)
Until expiration date
7 days
Novolin N™ (3-mL cartridge)
Until expiration date
14 days
Novolin 70/30™ (prefilled and 1.5-mL cartridge)
Until expiration date
7 days
Novolin 70/30™ (3-mL cartridge)
Until expiration date
10 days
Detemir (Levemir™)
Until expiration date
42 days
Apidra™
Until expiration date
28 days
Lantus™
Until expiration date
28 days
Self-filled syringes (Note: not recommended for glargine)
14 days*
7 days*
Inhale Insulin
Not in use (unopened overwrap)
In use (unopened overwrap)
Exubera™ (insulin blisters)
Room Temperature (59° F– 86° F) Until expiration date
Room Temperature (59° F– 86° F) 90days
    Release Unit
Do not refrigerate
Replace every 14 days
    Inhaler & Chamber
ReplaceYearly (Wash Weekly)

 

Table 5. Incretins and Amylins

Agent
Primary Action
How
Supplied/Storage
Typical Dosage
Duration
Action
Side Effects
Precautions
Comments
Adapted from © 2006 The Diabetes Center, Old Saybrook, CT. Used with permission. *DPP-4-dipeptidyl peptidase -4 GIP- glucose dependent insulinotropic polypeptide GLP-glucose like polypeptide ESRD-End Stage Renal Disease TZD-Thiazolidinedione
Exenatide
(Byetta™)
Decreases post-meal glucagon production Delays gastric emptying
Increases satiety, leading to decreased caloric intake.
Degree of response depends on plasma glucose levels
250 mcg/ml:
- 5 mcg/dose prefilled pen
- 10 mcg/dose prefilled pen
If not in use: refrigerate until expiration date.
If in use: stable at room temperature
Discard after 30 days.
5 mcg BID subcutaneous for first 1 month, then 10 mcg BID, injected within 60 minutes before morning and evening meal Peak effects in approx 2 hours with maximal duration of 10 hours. Nausea and hypoglycemia most common; occasional vomiting, diarrhea, jitters, dizziness, headache. Not for use in patients with Type 1 diabetes, severe renal disease or ESRD*, or severe GI disease. Consider lowering dose of sulfonylurea to avoid hypoglycemia when starting.
May reduce the rate of absorption of oral medication.
Medications requiring threshold concentrations should be taken 1 hour prior to injection.
Approved for use with sulfonylureas and/or metformin or in combination with a TZD* alone or with metformin.
Pramlintide
(Symlin™)
Decreases post-meal glucagon production Delays gastric emptying, Increases satiety, leading to decreased caloric intake.
Degree of response depends on plasma glucose levels
5 ml vials containing 0.6 mg/ml. Requires U-100 insulin syringe for injection If not in use: refrigerate until expiration date.
If in use: room temperature Discard after 28 days.
Type 1 diabetes: 15–60 mcg starting with 15 mcg subcutaneously before meals of 30gm or more carbohydrate. Type 2 diabetes: 60–120 mcg starting with 60 mcg subcutaneous before meals. Titrate as directed by prescriber. Maximum effect in 20 minutes with rapid elimination.
Maximum duration of 4 hours
Nausea and hypoglycemia most common. Doses are adjusted based on presentation of these side effects. Occasional vomiting, stomach pain, dizziness, indigestion. Indicated for insulin treated type 2 diabetes or for type 1 diabetes.
Contraindicated in patients with hypoglycemia unawareness, gastroparesis. Or poor adherence Should never be mixed with insulin and should be injected separately. Reduce insulin dose by 50% when starting.
Requires patient testing of blood sugars before and after meals, frequent physician follow up, and thorough understanding of how to adjust doses of insulin and pramlintide.
May reduce the rate of absorption of orally administered medication. Medications requiring threshold concentrations should be taken 1 hour prior to injection.
Sitagliptin
(Januvia™)
DPP-4 inhibitor* Inhibits the DPP-4 enzyme that degrades GLP-1 and GIP resulting in 2-3 fold increased levels of these incretins. Increases insulin secretion in presence of elevated plasma glucose. Reduces postmeal glucagon secretion . 25mg, 50mg, 100mg tablets 100 mg po qD
Moderate renal insufficiency
(CrCl>30 to <50mL/min): 50mg/day
Severe renal insufficiency
(CrCl <30mL/min): 25mg/day
Approximately
24 hours
Low incidence of side effects including hypoglycemia or gastrointestinal symptoms Headache, upper respiratory tract infection, nasopharyngitis Not for use in type 1 diabetes Assessment of renal function is recommended prior to initiation and periodically thereafter. May be used as monotherapy or in combination with metformin or TZDs.
Not associated with weight loss

 

Table 6. Hypoglycemia Treatment

Agent
Primary
Action
How Supplied/Storage
Typical
Dosage
Duration
Action
Side
Effects
Precautions
Comments
Adapted from © 2006 The Diabetes Center, Old Saybrook, CT. Used with permission.
Glucagon Converts liver glycogen to glucose 1 mg vial with diluent; emergency kit, 1 mg vial with prefilled syringe of diluent. Before reconstitution, room temperature until expiration date. After reconstitution, may be stored for up to 48 hours under refrigeration. 0.5–2 mg subcutaneous 15 min, should be followed by carbohydrate snack. Occasional nausea and vomiting Must be reconstituted prior to injection. Should be followed by carbohydrate snack and blood glucose testing every 15 minutes until glucose level returns to acceptable levels. Patient should be instructed to teach colleagues, family, etc. how to give injection. Only use if patient isunconscious or unable to eat or drink. All people taking insulin should receive a prescription for glucagon kit for emergency use.

 

Table 7. Recommended Control Measures

Biochemical Index
Preprandial Peak postprandial A1C (ADA)* Blood pressure LDL TG HDL
Adapted from © 2006 The Diabetes Center, Old Saybrook, CT. Used with permission. LDL=low density lipoprotein TG=triclycerides HDL=high density lipoprotein *ADA—American Diabetes Association
Goal
90–130 mg/dL
<180 mg/dL
<7%
<130/80
<100
<150
>40

 

NDEP-54-S

March 2007

 

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