International reference: 1 US FDA recall for this ingredient

TEMPERATURE ABUSE: Products were exposed to temperatures outside of the products labeled storage conditions (dulaglutide)

US-market enforcement records (OpenFDA), shown for reference - not specific to this product in Kenya.

Registered Kenya · PPB

TRULICITY 1.5MG/0.5ML

DULAGLUTIDE

H2019/CTD4517/1210ER 1.5MG/0.5ML NEW/INNOVATOR alimentary tract and metabolism INN generic

What it does

Dulaglutide is a medication used to help manage blood sugar levels in people with diabetes.

Commonly used for: type 2 diabetes, diabetes mellitus

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Plain-language summary for general understanding - not medical advice. Always follow your pharmacist/doctor.

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Registration & product details

Registration no.
H2019/CTD4517/1210ER
Registration date
2019-04-30 00:00:00
Expiry date
-
Status
Registered
Active ingredient
DULAGLUTIDE
Dosage form
1.5MG/0.5ML
Strength
-
Pack size
PACK OF 4 SINGLE DOSE PENS
Therapeutic class
NEW/INNOVATOR
ATC class (WHO)
A10BJ - Glucagon-like peptide-1 (GLP-1) analogues
RxNorm RxCUI
1551291
Manufacturer / MAH
Statim Pharmaceuticals
Applicant / LTR
ELI LILLY AND COMPANY
Country of origin
FOREIGN
Manufacturer location
23, Omega Business Park, Off Baba Dogo Rd, Nairobi, Kenya

Source: Pharmacy and Poisons Board · fetched 2026-01-28 19:51:27 · updated 2026-08-03 03:09:07

Disclaimer: This information is sourced from Pharmacy and Poisons Board (Kenya). Always consult a qualified healthcare professional before using any medication.

About this medicine

Dulaglutide is a medication used to help manage blood sugar levels in people with diabetes.

What it treats

  • type 2 diabetes
  • diabetes mellitus

How it works

Dulaglutide helps the body produce more insulin when blood sugar is high and lowers the amount of sugar released from the liver.

Who it's for

This medicine is for adults with type 2 diabetes, usually in combination with other diabetes medications.

Cautions

  • • Use with caution if you are taking other antidiabetic drugs.

AI-assisted summary grounded in BNF data - general information only, not medical advice. Always confirm with your pharmacist or doctor.

Clinical monograph: Dulaglutide

BNF-referenced

Dulaglutide is a long-acting glucagon-like peptide-1 (GLP-1) receptor agonist used in the management of type 2 diabetes mellitus. It enhances glucose-dependent insulin secretion, inhibits glucagon release, and slows gastric emptying, leading to improved glycemic control. This medication is administered via subcutaneous injection and is typically prescribed when diet and exercise alone do not provide adequate glucose control.

Indications

  • Type 2 diabetes mellitus as monotherapy when metformin is inappropriate
  • Type 2 diabetes mellitus in combination with other antidiabetic drugs, including insulin, when existing treatment fails to achieve adequate glycemic control

Dosage

Adults: 0.75 mg once weekly; may be increased to 1.5 mg once weekly after at least 4 weeks, with a maximum dose of 4.5 mg once weekly if needed.

Mechanism of action

Dulaglutide mimics the action of GLP-1, a hormone that regulates glucose levels. It increases insulin secretion in a glucose-dependent manner, suppresses glucagon secretion from the alpha cells of the pancreas, and slows gastric emptying, which contributes to a reduction in appetite and food intake.

Pharmacodynamics

Dulaglutide's pharmacodynamic effects include increased insulin secretion in response to elevated blood glucose levels, decreased glucagon secretion, and delayed gastric emptying. This results in a decrease in postprandial blood glucose levels and contributes to weight loss in some patients. The glucose-lowering effect is associated with lower HbA1c levels and improved overall glycemic control.

Pharmacokinetics

Dulaglutide is administered subcutaneously and has a half-life of approximately 5 days, allowing for once-weekly dosing. It is predominantly eliminated via the lymphatic system and does not undergo significant hepatic metabolism. The peak plasma concentration occurs about 24 to 72 hours after administration. It is important to note that renal impairment may affect the pharmacokinetics of dulaglutide, but no specific dose adjustments are recommended based solely on renal function.

Contra-indications

  • Hypersensitivity to dulaglutide or any of its excipients
  • Personal or family history of medullary thyroid carcinoma
  • Multiple endocrine neoplasia syndrome type 2
  • Severe gastrointestinal disease
  • Acute pancreatitis or a history of pancreatitis

Adverse effects

  • Nausea
  • Diarrhea
  • Vomiting
  • Decreased appetite
  • Abdominal pain
  • Fatigue
  • Hypoglycemia when used with other antidiabetic medications
  • Liver dysfunction (rare reports)

Interactions

  • Insulin secretagogues or insulin may require dose adjustment to avoid hypoglycemia
  • Concomitant use with other GLP-1 receptor agonists is not recommended
  • Medications that slow gastric emptying may enhance dulaglutide's effects

Precautions

  • Monitor for signs of pancreatitis
  • Assess renal function prior to use
  • Exercise caution in patients with a history of gastrointestinal disease
  • Discontinue if signs of liver dysfunction occur, such as jaundice

Pregnancy

Avoid use during pregnancy due to potential toxicity observed in animal studies.

Breast-feeding

Avoid use during breastfeeding; dulaglutide is present in milk in animal studies.

Storage

Store in a refrigerator (2°C to 8°C). Do not freeze. Once in use, can be stored at room temperature for up to 14 days.

Formulations

  • Dulaglutide 0.75 mg / 1.5 mg / 3 mg / 4.5 mg solution for injection in a prefilled pen
BNF 85 (British National Formulary) p.797 PubChem / pathway

AI-synthesized from BNF references - general information only, not a substitute for professional medical advice or the current BNF. Verify doses with a pharmacist.

This drug in other countries

The same active ingredient registered across other registries we cover - including different brands.

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