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Symlin Injection (Amylin)
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SYMLIN® (pramlintide acetate) Injection is an antihyperglycemic drug for use in patients with diabetes treated with insulin. Pramlintide is a synthetic analog of human amylin, a naturally occurring neuroendocrine hormone synthesized by pancreatic beta cells that contributes to glucose control during the postprandial period. Pramlintide is provided as an acetate salt of the synthetic 37-amino acid polypeptide, which differs in amino acid sequence from human amylin by replacement with proline at positions 25 (alanine), 28 (serine), and 29 (serine).
The structural formula of pramlintide acetate is as shown:
Pramlintide acetate is a white powder that has a molecular formula of C 171 H 267 N 51 O 53 S 2 · × C 2 H 4 O 2 (3</= × </=8); the molecular weight is 3949.4. Pramlintide acetate is soluble in water.
SYMLIN is formulated as a clear, isotonic, sterile solution for subcutaneous (SC) administration. SYMLIN vials contain 0.6 mg/mL of pramlintide (as acetate), 2.25 mg/mL of metacresol as a preservative, D-mannitol as a tonicity modifier, and acetic acid and sodium acetate as pH modifiers. SYMLIN has a pH of approximately 4.0.
Amylin is co-located with insulin in secretory granules and co-secreted with insulin by pancreatic beta cells in response to food intake. Amylin and insulin show similar fasting and postprandial patterns in healthy individuals ( Figure 1 ).
Amylin affects the rate of postprandial glucose appearance through a variety of mechanisms. Amylin slows gastric emptying (i.e., the rate at which food is released from the stomach to the small intestine) without altering the overall absorption of nutrients. In addition, amylin suppresses glucagon secretion (not normalized by insulin alone), which leads to suppression of endogenous glucose output from the liver. Amylin also regulates food intake due to centrally-mediated modulation of appetite.
In patients with insulin-using type 2 or type 1 diabetes, the pancreatic beta cells are dysfunctional or damaged, resulting in reduced secretion of both insulin and amylin in response to food.
Mechanism of Action
SYMLIN, by acting as an amylinomimetic agent, has the following effects: 1) modulation of gastric emptying; 2) prevention of the postprandial rise in plasma glucagon; and 3) satiety leading to decreased caloric intake and potential weight loss.
Gastric Emptying. The gastric-emptying rate is an important determinant of the postprandial rise in plasma glucose. SYMLIN slows the rate at which food is released from the stomach to the small intestine following a meal and, thus, it reduces the initial postprandial increase in plasma glucose. This effect lasts for approximately 3 hours following SYMLIN administration. SYMLIN does not alter the net absorption of ingested carbohydrate or other nutrients.
Postprandial Glucagon Secretion. In patients with diabetes, glucagon concentrations are abnormally elevated during the postprandial period, contributing to hyperglycemia. SYMLIN has been shown to decrease postprandial glucagon concentrations in insulin-using patients with diabetes.
Satiety. SYMLIN administered prior to a meal has been shown to reduce total caloric intake. This effect appears to be independent of the nausea that can accompany SYMLIN treatment.
Absorption. The absolute bioavailability of a single SC dose of SYMLIN is approximately 30 to 40%. Subcutaneous administration of different doses of SYMLIN into the abdominal area or thigh of healthy subjects resulted in dose-proportionate maximum plasma concentrations (C max ) and overall exposure (expressed as area under the plasma concentration curve or (AUC)) ( Table 1 ).
Injection of SYMLIN into the arm showed higher exposure with greater variability, compared with exposure after injection of SYMLIN into the abdominal area or thigh.
There was no strong correlation between the degree of adiposity as assessed by BMI or skin fold thickness measurements and relative bioavailability. Injections administered with 6.0-mm and 12.7-mm needles yielded similar bioavailability.
Distribution. SYMLIN does not extensively bind to blood cells or albumin (approximately 40% of the drug is unbound in plasma), and thus SYMLIN's pharmacokinetics should be insensitive to changes in binding sites.
Metabolism and Elimination. In healthy subjects, the half-life of SYMLIN is approximately 48 minutes. SYMLIN is metabolized primarily by the kidneys. Des-lys 1 pramlintide (2-37 pramlintide), the primary metabolite, has a similar half-life and is biologically active both in vitro and in vivo in rats. AUC values are relatively constant with repeat dosing, indicating no bioaccumulation.
Renal Insufficiency : Patients with moderate or severe renal impairment (Cl Cr >20 to </=50 mL/min) did not show increased SYMLIN exposure or reduced SYMLIN clearance, compared to subjects with normal renal function. No studies have been done in dialysis patients.
Hepatic Insufficiency : Pharmacokinetic studies have not been conducted in patients with hepatic insufficiency. However, based on the large degree of renal metabolism (see Metabolism and Elimination ), hepatic dysfunction is not expected to affect blood concentrations of SYMLIN.
Geriatric : Pharmacokinetic studies have not been conducted in the geriatric population. SYMLIN should only be used in patients known to fully understand and adhere to proper insulin adjustments and glucose monitoring. No consistent age-related differences in the activity of SYMLIN have been observed in the geriatric population (n=539 for patients 65 years of age or older in the clinical trials).
Pediatric : SYMLIN has not been evaluated in the pediatric population.
Gender : No study has been conducted to evaluate possible gender effects on SYMLIN pharmacokinetics. However, no consistent gender-related differences in the activity of SYMLIN have been observed in the clinical trials (n=2799 for male and n=2085 for female).
Race/Ethnicity : No study has been conducted to evaluate the effect of ethnicity on SYMLIN pharmacokinetics. However, no consistent differences in the activity of SYMLIN have been observed among patients of differing race/ethnicity in the clinical trials (n=4257 for white, n=229 for black, n=337 for Hispanic, and n=61 for other ethnic origins).
Drug Interactions : The effect of SYMLIN (120 µg) on acetaminophen (1000 mg) pharmacokinetics as a marker of gastric-emptying was evaluated in patients with type 2 diabetes (n=24). SYMLIN did not significantly alter the AUC of acetaminophen. However, SYMLIN decreased acetaminophen C max (about 29% with simultaneous co-administration) and increased the time to maximum plasma concentration or t max (ranging from 48 to 72 minutes) dependent on the time of acetaminophen administration relative to SYMLIN injection. SYMLIN did not significantly affect acetaminophen t max when acetaminophen was administered 1 to 2 hours before SYMLIN injection. However, the t max of acetaminophen was significantly increased when acetaminophen was administered simultaneously with or up to 2 hours following SYMLIN injection (see PRECAUTIONS , Drug Interactions ).
In clinical studies in patients with insulin-using type 2 and type 1 diabetes, SYMLIN administration resulted in a reduction in mean postprandial glucose concentrations, reduced glucose fluctuations, and reduced food intake. SYMLIN doses differ for insulin-using type 2 and type 1 patients (see DOSAGE AND ADMINISTRATION ).
Reduction in Postprandial Glucose Concentrations. SYMLIN administered subcutaneously immediately prior to a meal reduced plasma glucose concentrations following the meal when used with regular insulin or rapid-acting insulin analogs ( Figure 2 ). This reduction in postprandial glucose decreased the amount of short-acting insulin required and limited glucose fluctuations based upon 24-hour glucose monitoring. When rapid-acting analog insulins were used, plasma glucose concentrations tended to rise during the interval between 150 minutes following SYMLIN injection and the next meal (see DOSAGE AND ADMINISTRATION ).
Reduced Food Intake. A single, subcutaneous dose of SYMLIN 120 µg (type 2) or 30 µg (type 1) administered 1 hour prior to an unlimited buffet meal was associated with reductions in total caloric intake (placebo-subtracted mean changes of ~23% and 21%, respectively), which occurred without decreases in meal duration.
A total of 5325 patients and healthy volunteers received SYMLIN in clinical studies. This includes 1688 with type 2 diabetes and 2375 with type 1 diabetes in short- and long-term controlled clinical trials, long-term uncontrolled clinical trials, and an open-label study in the clinical practice setting.
Clinical Studies in Type 2 Diabetes
The efficacy of a range of SYMLIN doses was evaluated in several placebo-controlled and open-label clinical trials in insulin-using patients with type 2 diabetes. Based on results obtained in these studies, the recommended dose of SYMLIN for patients with insulin-using type 2 diabetes is 120 µg administered immediately prior to major meals.
Two, long-term (26 to 52 week), randomized, double-blind, placebo-controlled studies of SYMLIN were conducted in patients with type 2 diabetes using fixed dose insulin to isolate the SYMLIN effect. Demographic and baseline characteristics for the 871 SYMLIN-treated patients are as follows: mean baseline HbA1c ranged from 9.0 to 9.4%, mean age was 56.4 to 59.1 years, mean duration of diabetes ranged from 11.5 to 14.4 years, and mean BMI ranged from 30.1 to 34.4 kg/m 2 . In both of these studies, SYMLIN or placebo was added to the participants' existing diabetes therapies, which included insulin with or without a sulfonylurea agent and/or metformin.
Table 2 summarizes the composite results across both studies for patients assigned to the 120-µg dose after 6 months of treatment.
In a cohort of 145 patients who completed two years of SYMLIN treatment the baseline subtracted HbA1c and weight reductions were: -0.40% and -0.36 kg, respectively.
Open-Label Study in the Clinical Practice Setting. An open-label study of SYMLIN was conducted at the recommended dose of 120 µg in 166 patients with insulin-using type 2 diabetes who were unable to achieve glycemic targets using insulin alone. A flexible-dose insulin regimen was employed in these patients (see DOSAGE and ADMINISTRATION ). In this study, patients adjusted their insulin regimen based on pre-and post-meal glucose monitoring. At baseline, mean HbA1c was 8.3%, mean age was 54.4 years, mean duration of diabetes was 13.3 years, and mean BMI was 38.6 kg/m 2 . SYMLIN was administered with major meals. SYMLIN plus insulin treatment for 6 months resulted in a baseline-subtracted mean HbA1c reduction of -0.56 ± 0.15% and a baseline-subtracted mean weight reduction of -2.76 ± 0.34 kg. These changes were accomplished with reductions in doses of total, short-acting, and long-acting insulin (-6.4 ± 2.66, -10.3 ± 4.84, and -4.20 ± 2.42 %, respectively).
Clinical Studies in Type 1 Diabetes
The efficacy of a range of SYMLIN doses was evaluated in several placebo-controlled and open-label clinical trials conducted in patients with type 1 diabetes. Based on results obtained in these studies, the recommended dose of SYMLIN for patients with type 1 diabetes is 30 µg or 60 µg administered immediately prior to major meals.
Three, long-term (26 to 52 week), randomized, double-blind, placebo-controlled studies of SYMLIN were conducted in patients with type 1 diabetes (N=1717). Two of these studies allowed only minimal insulin adjustments in order to isolate the SYMLIN effect; in the third study, insulin adjustments were made according to standard medical practice. Demographic and baseline characteristics for the 1179 SYMLIN-treated patients were as follows: mean baseline HbA1c range was 8.7 to 9.0%, mean age range was 37.3 to 41.9 years, mean duration of diabetes range was 15.5 to 19.2 years, and mean BMI range was 25.0 to 26.8 kg/m 2 . SYMLIN or placebo was added to existing insulin therapies.
Table 3 summarizes the composite results across these studies for patients assigned to the 30 or 60 µg dose after 6 months of treatment.
In a cohort of 73 patients who completed two years of SYMLIN treatment the baseline subtracted HbA1c and weight changes were: -0.35% and 0.60 kg, respectively.
SYMLIN Dose-Titration Trial. A dose-titration study of SYMLIN was conducted in patients with type 1 diabetes. Patients with relatively good baseline glycemic control (mean HbA1c = 8.1%) were randomized to receive either insulin plus placebo or insulin plus SYMLIN. Other baseline and demographics characteristics were: mean age of 41 years, mean duration of diabetes of 20 years, mean BMI of 28 kg/m 2 . SYMLIN was initiated at a dose of 15 µg and titrated upward at weekly intervals by 15-µg increments to doses of 30 µg or 60 µg, based on whether patients experienced nausea. Once a tolerated dose of either 30 µg or 60 µg was reached, the SYMLIN dose was maintained for the remainder of the study (SYMLIN was administered before major meals). During SYMLIN titration, the insulin dose (mostly the short/rapid acting insulin) was reduced by 30-50% in order to reduce the occurrence of hypoglycemia. Once a tolerated SYMLIN dose was reached, insulin dose adjustments were made according to standard clinical practice, based on pre- and post-meal blood glucose monitoring. By 6 months of treatment, patients treated with SYMLIN and insulin and patients treated with insulin and placebo had equivalent reductions in mean HbA1c (-0.47 ± 0.07% vs. -0.49 ± 0.07%, respectively); patients on SYMLIN lost weight (-1.33 ± 0.31 kg relative to baseline and -2.6 kg relative to placebo plus insulin-treated patients). SYMLIN-treated patients used less total insulin (-11.7% relative to baseline) and less short/rapid-acting insulin (-22.8%) relative to baseline.
Open-Label Study in the Clinical Practice Setting. An open-label study of SYMLIN was conducted in patients with type 1 diabetes who were unable to achieve glycemic targets using insulin alone. A flexible-dose insulin regimen was employed in these patients after SYMLIN titration was completed (see DOSAGE and ADMINISTRATION ). In this study, patients adjusted their insulin regimen based on pre-and post-meal glucose monitoring. At baseline, mean HbA1c was 8.0%, mean age was 42.7 years, mean duration of diabetes was 21.2 years, and mean BMI was 28.6 kg/m 2 . SYMLIN daily dosage was 30 µg or 60 µg with major meals.
SYMLIN plus insulin reduced HbA1c and body weight from baseline at 6 months by a mean of 0.18% and 3.0 kg, respectively. These changes in glycemic control and body weight were achieved with reductions in doses of total, short-acting, and long-acting insulin (-12.0 ± 1.36, -21.7 ± 2.81, and -0.4 ± 1.59%, respectively).
INDICATIONS AND USAGE
SYMLIN is given at mealtimes and is indicated for:
SYMLIN is contraindicated in patients with any of the following:
Proper patient selection is critical to safe and effective use of SYMLIN. Before initiation of therapy, the patient's HbA1c, recent blood glucose monitoring data, history of insulin-induced hypoglycemia, current insulin regimen, and body weight should be reviewed. SYMLIN therapy should only be considered in patients with insulin-using type 2 or type 1 diabetes who fulfill the following criteria:
Patients meeting any of the following criteria should NOT be considered for SYMLIN therapy:
Hypoglycemia. SYMLIN alone does not cause hypoglycemia. However, SYMLIN is indicated to be co-administered with insulin therapy and in this setting SYMLIN increases the risk of insulin-induced severe hypoglycemia, particularly in patients with type 1 diabetes. Severe hypoglycemia associated with SYMLIN occurs within the first 3 hours following a SYMLIN injection. If severe hypoglycemia occurs while operating a motor vehicle, heavy machinery, or while engaging in other high-risk activities, serious injuries may occur. Therefore, when introducing SYMLIN therapy, appropriate precautions need to be taken to avoid increasing the risk for insulin-induced severe hypoglycemia. These precautions include frequent pre- and post-meal glucose monitoring combined with an initial 50% reduction in pre-meal doses of short-acting insulin (see DOSAGE and ADMINISTRATION ).
Symptoms of hypoglycemia may include hunger, headache, sweating, tremor, irritability, or difficulty concentrating. Rapid reductions in blood glucose concentrations may induce such symptoms regardless of glucose values. More severe symptoms of hypoglycemia include loss of consciousness, coma, or seizure.
Early warning symptoms of hypoglycemia may be different or less pronounced under certain conditions, such as long duration of diabetes; diabetic nerve disease; use of medications such as beta-blockers, clonidine, guanethidine, or reserpine; or intensified diabetes control.
The addition of any antihyperglycemic agent such as SYMLIN to an existing regimen of one or more anti-hyperglycemic agents (e.g., insulin, sulfonylurea), or other agents that can increase the risk of hypoglycemia may necessitate further insulin dose adjustments and particularly close monitoring of blood glucose.
The following are examples of substances that may increase the blood glucose-lowering effect and susceptibility to hypoglycemia: oral anti-diabetic products, ACE inhibitors, diisopyramide, fibrates, fluoxetine, MAO inhibitors, pentoxifylline, propoxyphene, salicylates, and sulfonamide antibiotics.
Clinical studies employing a controlled hypoglycemic challenge have demonstrated that SYMLIN does not alter the counter-regulatory hormonal response to insulin-induced hypoglycemia. Likewise, in SYMLIN-treated patients, the perception of hypoglycemic symptoms was not altered with plasma glucose concentrations as low as 45 mg/dL.
Hypoglycemia (See WARNINGS ).
Information for Patients: Health care providers should inform patients of the potential risks and advantages of SYMLIN therapy. Health care providers should also inform patients about self-management practices including glucose monitoring, proper injection technique, timing of dosing, and proper storage of SYMLIN. In addition, the importance of adherence to meal planning, physical activity, recognition and management of hypoglycemia and hyperglycemia, and assessment of diabetes complications. Refer patients to the SYMLIN Medication Guide for additional information.
Instruct patients on handling of special situations such as intercurrent conditions (illness or stress), an inadequate or omitted insulin dose, inadvertent administration of increased insulin or SYMLIN dose, inadequate food intake or missed meals.
SYMLIN and insulin should always be administered as separate injections and never be mixed.
Women with diabetes should be advised to inform their healthcare professional if they are pregnant or contemplating pregnancy.
Renal Impairment: The dosing requirements for SYMLIN are not altered in patients with moderate or severe renal impairment (Cl Cr >20 to </=50 mL/min). No studies have been done in dialysis patients (see CLINICAL PHARMACOLOGY ; Special Populations ).
Hepatic Impairment: Studies have not been performed in patients with hepatic impairment. However, hepatic dysfunction is not expected to affect blood concentrations of SYMLIN (see CLINICAL PHARMACOLOGY ; Special Populations ).
Allergy: Local allergy. Patients may experience redness, swelling, or itching at the site of injection. These minor reactions usually resolve in a few days to a few weeks. In some instances, these reactions may be related to factors other than SYMLIN, such as irritants in a skin cleansing agent or improper injection technique.
Systemic Allergy. In controlled clinical trials up to 12 months, potential systemic allergic reactions were reported in 65 (5%) of type 2 patients and 59 (5%) of type 1 SYMLIN-treated patients. Similar reactions were reported by 18 (4%) and 28 (5%) of placebo-treated type 2 and type 1 patients, respectively. No patient receiving SYMLIN was withdrawn from a trial due to a potential systemic allergic reaction.
Due to its effects on gastric emptying, SYMLIN therapy should not be considered for patients taking drugs that alter gastrointestinal motility (e.g., anticholinergic agents such as atropine) and agents that slow the intestinal absorption of nutrients (e.g., (alpha)-glucosidase inhibitors). Patients using these drugs have not been studied in clinical trials.
SYMLIN has the potential to delay the absorption of concomitantly administered oral medications. When the rapid onset of a concomitant orally administered agent is a critical determinant of effectiveness (such as analgesics), the agent should be administered at least 1 hour prior to or 2 hours after SYMLIN injection.
In clinical trials, the concomitant use of sulfonylureas or biguanides did not alter the adverse event profile of SYMLIN. No formal interaction studies have been performed to assess the effect of SYMLIN on the kinetics of oral antidiabetic agents.
Mixing SYMLIN and Insulin
The pharmacokinetic parameters of SYMLIN were altered when mixed with regular, NPH, and 70/30 premixed formulations of recombinant human insulin immediately prior to injection. Thus, SYMLIN and insulin should not be mixed and must be administered separately.
Carcinogenesis, Mutagenesis, Impairment of Fertility
Carcinogenesis. A two-year carcinogenicity study was conducted in CD-1 mice with doses of 0.2, 0.5, and 1.2 mg/kg/day of SYMLIN (32, 67, and 159 times the exposure resulting from the maximum recommended human dose based on area under the plasma concentration curve or AUC, respectively). No drug-induced tumors were observed. A two-year carcinogenicity study was conducted in Sprague-Dawley rats with doses of 0.04, 0.2, and 0.5 mg/kg/day of SYMLIN (3, 9, and 25 times the exposure resulting from the maximum recommended human dose based on AUC, respectively). No drug-induced tumors were observed in any organ.
Mutagenesis. SYMLIN was not mutagenic in the Ames test and did not increase chromosomal aberration in the human lymphocytes assay. SYMLIN was not clastogenic in the in vivo mouse micronucleus test or in the chromosomal aberration assay utilizing Chinese hamster ovary cells.
Impairment of Fertility. Administration of 0.3, 1, or 3 mg/kg/day of SYMLIN (8, 17, and 82 times the exposure resulting from the maximum recommended human dose based on body surface area) had no significant effects on fertility in male or female rats. The highest dose of 3 mg/kg/day resulted in dystocia in 8/12 female rats secondary to significant decreases in serum calcium levels.
Teratogenic Effects: Pregnancy Category C. No adequate and well-controlled studies have been conducted in pregnant women. Studies in perfused human placenta indicate that SYMLIN has low potential to cross the maternal/fetal placental barrier. Embryofetal toxicity studies with SYMLIN have been performed in rats and rabbits. Increases in congenital abnormalities (neural tube defect, cleft palate, exencephaly) were observed in fetuses of rats treated during organogenesis with 0.3 and 1.0 mg/kg/day (10 and 47 times the exposure resulting from the maximum recommended human dose based on AUC, respectively). Administration of doses up to 0.3 mg/kg/day SYMLIN (9 times maximum recommended dose based on AUC) to pregnant rabbits had no adverse effects in embryofetal development; however, animal reproduction studies are not always predictive of human response. SYMLIN should be used during pregnancy only if it is determined by the healthcare professional that the potential benefit justifies the potential risk to the fetus.
It is unknown whether SYMLIN is excreted in human milk. Many drugs, including peptide drugs, are excreted in human milk. Therefore, SYMLIN should be administered to nursing women only if it is determined by the health care professional that the potential benefit outweighs the potential risk to the infant.
Safety and effectiveness of SYMLIN in pediatric patients have not been established.
SYMLIN has been studied in patients ranging in age from 15 to 84 years of age, including 539 patients 65 years of age or older. The change in HbA1c values and hypoglycemia frequencies did not differ by age, but greater sensitivity in some older individuals cannot be ruled out. Thus, both SYMLIN and insulin regimens should be carefully managed to obviate an increased risk of severe hypoglycemia.
Adverse events (excluding hypoglycemia, discussed below) commonly associated with SYMLIN when co-administered with a fixed dose of insulin in the long-term, placebo-controlled trials in insulin-using type 2 patients and type 1 patients are presented in Table 4 and Table 5 , respectively. The same adverse events were also shown in the open-label clinical practice study, which employed flexible insulin dosing.
Most adverse events were gastrointestinal in nature. In patients with type 2 or type 1 diabetes, the incidence of nausea was higher at the beginning of SYMLIN treatment and decreased with time in most patients. The incidence and severity of nausea are reduced when SYMLIN is gradually titrated to the recommended doses (see DOSAGE and ADMINISTRATION ).
SYMLIN alone (without the concomitant administration of insulin) does not cause hypoglycemia. However, SYMLIN is indicated as an adjunct treatment in patients who use mealtime insulin therapy and co-administration of SYMLIN with insulin can increase the risk of insulin-induced hypoglycemia, particularly in patients with type 1 diabetes (see Boxed Warning). The incidence of severe hypoglycemia during the SYMLIN clinical development program is summarized in Table 6 and Table 7 .
Single 10 mg doses of SYMLIN (83 times the maximum dose of 120 µg) were administered to three healthy volunteers. Severe nausea was reported in all three individuals and was associated with vomiting, diarrhea, vasodilatation, and dizziness. No hypoglycemia was reported. SYMLIN has a short half-life and in the case of overdose, supportive measures are indicated.
DOSAGE AND ADMINISTRATION
SYMLIN dosage differs depending on whether the patient has type 2 or type 1 diabetes (see below). When initiating therapy with SYMLIN, initial insulin dose reduction is required in all patients (both type 2 and type 1) to reduce the risk of insulin-induced hypoglycemia. As this reduction in insulin can lead to glucose elevations, patients should be monitored at regular intervals to assess SYMLIN tolerability and the effect on blood glucose, so that individualized insulin adjustments can be initiated. If SYMLIN therapy is discontinued for any reason (e.g., surgery or illnesses), the same initiation protocol should be followed when SYMLIN therapy is re-instituted (see below).
Initiation of SYMLIN therapy
Patients With Insulin-using Type 2 Diabetes
In patients with insulin-using type 2 diabetes, SYMLIN should be initiated at a dose of 60 µg and increased to a dose of 120 µg as tolerated.
Patients should be instructed to:
Patients With Type 1 Diabetes
In patients with type 1 diabetes, SYMLIN should be initiated at a dose of 15 µg and titrated at 15-µg increments to a maintenance dose of 30 µg or 60 µg as tolerated.
Patients should be instructed to:
Once Target Dose of SYMLIN Is Achieved in Type 2 or Type 1 Patients
After a maintenance dose of SYMLIN is achieved, both insulin-using patients with type 2 diabetes and patients with type 1 diabetes should be instructed to:
SYMLIN should be administered subcutaneously immediately prior to each major meal (>/=250 kcal or containing >/=30 g of carbohydrate).
To administer SYMLIN from vials, use a U-100 insulin syringe (preferably a 0.3 mL [0.3 cc] size) for optimal accuracy. If using a syringe calibrated for use with U-100 insulin, use the chart below ( Table 8 ) to measure the microgram dosage in unit increments. Do not mix SYMLIN with insulin.
Each SYMLIN dose should be administered subcutaneously into the abdomen or thigh. Injection sites should be rotated so that the same site is not used repeatedly. The injection site selected should also be distinct from the site chosen for any concomitant insulin injection. Each SYMLIN injection should be administered subcutaneously to abdomen or thigh (administered into the arm is not recommended because of variable absorption).
Discontinuation of Therapy
SYMLIN therapy should be discontinued if any of the following occur:
Preparation and Handling
SYMLIN should be inspected visually for particulate matter or discoloration prior to administration whenever the solution and the container permit.
SYMLIN is supplied as a sterile injection in 5 mL vials, containing 0.6 mg/mL pramlintide (as acetate), for use with a syringe. To administer SYMLIN from vials, use a U-100 insulin syringe (preferably a 0.3 mL [0.3 cc] size). If using a syringe calibrated for use with U-100 insulin, use the chart ( Table 8 ) in the DOSAGE AND ADMINISTRATION section to measure the microgram dosage in unit increments. Do not mix SYMLIN with insulin.
SYMLIN Injection is available in the following package size:
5 mL vials (NDC 66780-110-01)
Unopened (not in-use) Vials: Before use, SYMLIN vials should be refrigerated, 36°F to 46°F (2°C to 8°C), and protected from light. Do not freeze. If a vial has been frozen or overheated, throw it away.
Opened (in-use) Vials: Opened vials in use (punctured) can be kept either refrigerated or at room temperature for up to 28 days as long as the temperature is not greater than 77°F (25°C). Opened vials, whether or not refrigerated, must be used within 28 days. Discard after 28 days.
Storage conditions and stability are summarized in Table 9 :
Vials are manufactured for:
Amylin Pharmaceuticals, Inc.
San Diego, CA 92121 USA