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Molecule

Pramlintide

Also known as pramlintide acetate
Available on requestCold chainDiabetes
Presentations
2
Brands
1
Manufacturers
1
Available from stock
0

Pramlintide is an amylin analog indicated as an adjunctive treatment in patients with type 1 or type 2 diabetes who use mealtime insulin therapy and who have failed to achieve desired glucose control despite optimal insulin therapy. MedsAcross supplies Pramlintide for export from India to licensed hospitals, importers and physicians acting for named patients, with the documents each country requires.

Information from the US FDA prescribing information, retrieved 12 November 2026. Not yet medically reviewed.How we review

Key facts

Pharmacological class
Amylin Analog, Amylin Agonists
ATC classification
A10BX05 Pramlintide · Diabetes medicines, subgroup A10B, subgroup A10BX
US FDA first approval
16 March 2005
EU status
Not recorded
Orphan designation
Not recorded
WHO essential medicine
Not recorded
India (CDSCO)
Not yet confirmed against CDSCO approval lists
Routes
Subcutaneous
Dosage forms
Injection
Identifiers
UNII 726I6TE06GRxCUI 139953CAS 151126-32-8DrugBank DB01278Q2062094

Clinical information

From the regulator-approved product information. Each section names its source.

Uses

SYMLIN is indicated as an adjunctive treatment in patients with type 1 or type 2 diabetes who use mealtime insulin therapy and who have failed to achieve desired glucose control despite optimal insulin therapy. SYMLIN is an amylin analog indicated for patients with type 1 or type 2 diabetes who use mealtime insulin and have failed to achieve desired glycemic control despite optimal insulin therapy.

Source: US FDA prescribing information

How it works

Pramlintide is an analog of human amylin. Amylin is colocated with insulin in secretory granules and cosecreted 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). Figure 1: Secretion Profile of Amylin and Insulin in Healthy Adults In patients with type 1 and type 2 diabetes, there is reduced secretion from pancreatic beta cells of both insulin and amylin in response to food. Amylin affects the rate of postprandial glucose appearance through a variety of mechanisms, as determined by nonclinical studies. 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.

Source: US FDA prescribing information

Dosing overview

• Upon initiation of SYMLIN, reduce mealtime insulin dose by 50%. Monitor glucoses frequently and individualize subsequent insulin dose adjustments. • Type 1 Diabetes: Start at 15 mcg subcutaneously before major meals. Increase in 15 mcg increments to a maximum premeal dose of 30 or 60 mcg, if not tolerated, reduce to 30 mcg, as tolerated. • Type 2 Diabetes: Start at 60 mcg subcutaneously before major meals then increase to 120 mcg before meals, as tolerated. • Wait at least 3 days between dose titrations to minimize nausea.

Source: US FDA prescribing information

Contraindications

SYMLIN is contraindicated in patients with any of the following: • serious hypersensitivity reaction to SYMLIN or to any of its product components. • hypoglycemia unawareness. • confirmed gastroparesis. • Prior serious hypersensitivity reaction to SYMLIN or its ingredients. • Hypoglycemia unawareness. • Confirmed gastroparesis

Source: US FDA prescribing information

Warnings and precautions

Boxed warning (severe hypoglycemia symlin): use with insulin increases the risk of severe hypoglycemia, particularly in patients with type 1 diabetes. When severe hypoglycemia occurs, it is seen within 3 hours following a SYMLIN injection. Serious injuries may occur if severe hypoglycemia occurs while operating a motor vehicle, heavy machinery, or while engaging in other high-risk activities. • Severe hypoglycemia: Increased risk particularly for type 1 diabetes. Upon initiation of SYMLIN, reduce mealtime insulin dose by 50% and frequently monitor blood glucoses. • Never share a SymlinPen between patients, even if the needle is changed. • Do not mix SYMLIN and insulin: Mixing can alter the pharmacokinetics of both products. Administer as separate injections.

Source: US FDA prescribing information

Side effects

Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in practice. • Most common adverse reactions (incidence ≥5% and higher incidence than placebo): nausea, vomiting, anorexia, headache.

Source: US FDA prescribing information

Interactions

Insulin The pharmacokinetic parameters of pramlintide are altered when SYMLIN is mixed in the same syringe with regular, NPH, and 70/30 premixed formulations of recombinant human insulin. SYMLIN and insulin must not be mixed and must be administered as separate injections.

Source: US FDA prescribing information

Storage

Table 9: Storage Conditions Dosage Form Unopened (not in use) Refrigerated Open (in use) Refrigerated or Temperature up to 86°F (30°C) 1.5 mL pen-injector Until Expiration Date Use Within 30 Days 2.7 mL pen-injector Storage conditions are summarized in Table 9.

Source: US FDA prescribing information

For healthcare professionals and buyers. This is not medical advice. Treatment decisions belong to the prescriber.

All presentations

2 presentations of Pramlintide, sorted by availability.

MedicineManufacturerRegisterAvailability
SymlinPen 1500 mcg/1.5 mL injectionSubcutaneous Cold chainAstraZeneca PharmaceuticalsUS FDAAvailable on request
SymlinPen 2700 mcg/2.7 mL injectionSubcutaneous Cold chainAstraZeneca PharmaceuticalsUS FDAAvailable on request

Brands by market

1 brand names across 1 markets.

Brand names by country

United States

Manufacturers

Regulatory status

Approval facts from US FDA, EMA and CDSCO data, and registration status by country where we hold register data.

RegisterStatusSource
US FDAFirst approved 16 March 2005Drugs@FDA
EU (EMA)Not recorded—
India (CDSCO)Not yet confirmed against CDSCO approval lists—
United StatesRegisteredUS FDA (NDC directory, openFDA)Checked 12 November 2026

Conditions

Conditions linked to Pramlintide in public data. This is not a list of approved uses, see the clinical information.

Questions and answers

Is Pramlintide available for export from India?

Yes, on request. MedsAcross lists 2 presentations of Pramlintide and sources them for licensed hospitals, importers and physicians against valid import documents.

What brand names does Pramlintide have?

The catalogue lists 1 brand names for Pramlintide, including SymlinPen.

Is Pramlintide approved by the US FDA?

Yes. The US FDA first approved Pramlintide on 16 March 2005, according to Drugs@FDA.

Does Pramlintide need cold chain shipping?

At least one listed presentation of Pramlintide must be kept cold, so it is shipped in temperature-controlled packaging. Check the storage line on each presentation.

Which ATC class is Pramlintide in?

Pramlintide is classified under ATC code A10BX05 (Pramlintide).

References

  1. SymlinPen prescribing information (AstraZeneca Pharmaceuticals). U.S. National Library of Medicine, DailyMed. Retrieved 18 December 2019

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