Alogliptin
Brand names: Vipidia, Nesina
Alogliptin is an oral dipeptidyl peptidase-4 (DPP-4) inhibitor used to improve glycaemic control in adults with type 2 diabetes mellitus.
ClinCalc Pro is rebuilding its dose data from primary open sources — the manufacturer SmPC (eMC), the WHO Model Formulary and other official references — under clinician review. This drug's structured dose is not yet published here. Confirm all doses against the product SmPC and your local formulary before prescribing.
Clinical monograph
How it works
It inhibits DPP-4, prolonging the action of incretin hormones such as GLP-1 and GIP, which enhances glucose-dependent insulin secretion and suppresses glucagon release.
Prescribing in practice
- Acute pancreatitis has been reported with DPP-4 inhibitors, so it should be stopped if pancreatitis is suspected and avoided in those with a history of it.
- The dose should be reduced in renal impairment, requiring assessment of renal function before and during treatment.
- It is weight-neutral and carries a low risk of hypoglycaemia alone, but this risk rises when combined with a sulfonylurea or insulin.
Monitoring
Monitor glycaemic control (including HbA1c) and renal function, and remain alert for symptoms of pancreatitis or hypersensitivity reactions.
Counselling the patient
- A daily tablet that lowers blood sugar in type 2 diabetes.
- Seek urgent advice for severe, persistent abdominal pain, which could indicate pancreatitis.
- Continue diet, exercise and blood glucose monitoring as advised.
Evidence & guidelines
Alogliptin is an established DPP-4 inhibitor for type 2 diabetes, with its pancreatitis and renal precautions reflected in NICE guidance and the SPC.
Reference: SmPC Vipidia; EXAMINE trial NEJM 2013; 369:1327-35; NICE NG28 (T2DM 2022); ADA Standards of Care 2024; Drug verified in RxNorm (NLM); confirm dosing against the manufacturer SPC (eMC). Verify against your local formulary and current prescribing references before prescribing. Monograph status: clinician-reviewed (2026-07-04).
Related
Curated clinical cross-links plus same-class fallbacks.
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