Linagliptin prescribing information for the UK

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Linagliptin 

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Safety Profile

Common and very common adverse events only listed here - please refer to SmPC for complete table of adverse events.

System organ class / Adverse reactionFrequency of adverse reaction*
Metabolism and nutrition disorders
Hypoglycaemia†Very common
Investigations
Lipase increased‡Common
  • *
    The adverse reactions are listed by absolute frequency. Frequencies are defined as very common (≥1/10), common (≥1/100 to <1/10), uncommon (≥1/1,000 to <1/100), rare (≥1/10,000 to <1/1,000), very rare (<1/10,000) or not known (cannot be estimated from the available data).
  • †
    Adverse reaction observed in combination with metformin plus sulphonylurea.
  • ‡
    Based on lipase elevations >3 x upper limit of normal observed in clinical trials.

Linagliptin

Linagliptin

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  • Mechanism of Action
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  • Dose & Administration

The most frequently reported adverse reaction was hypoglycaemia when Linagliptin was used in combination with metformin and sulphonylurea. Linagliptin alone had a comparable incidence of hypoglycaemia to placebo.1 Caution is advised when linagliptin is used in combination with a sulphonylurea and/or insulin. A dose reduction of the sulphonylurea or insulin may be considered to reduce the risk of hypoglycaemia.

Patients should be informed of the characteristic symptoms of acute pancreatitis. If pancreatitis is suspected, Linagliptin should be discontinued; if acute pancreatitis is confirmed, Linagliptin should not be restarted. Caution should be exercised in patients with a history of pancreatitis.1 The incidence of pancreatitis with Linagliptin is rare (≥1/10,000 - < 1/1000).

Bullous pemphigoid has been observed in patients taking linagliptin. If bullous pemphigoid is suspected, Linagliptin should be discontinued.1 The incidence of bullous pemphigoid with Linagliptin is rare (≥1/10,000 - 1/1,000).

Pharmacokinetic studies suggest that no dose adjustment is required for patients with hepatic impairment but clinical experience in such patients is lacking.1

Avoid use during pregnancy. A decision must be made whether to discontinue breast-feeding or to discontinue/abstain from Linagliptin therapy taking into account the benefit of breast-feeding for the child and the benefit of therapy for the woman. A risk to the breast-fed child cannot be excluded.1

Refer to the SmPC for a full list of adverse effects, warnings and precautions.1

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One Dose. Always.

Helping a broad range of adult patients

With its simple dosing and suitability for all stages of renal function, Linagliptin is suitable for most adult patients with type 2 diabetes (T2D), independent of age, BMI and ethnicity.1
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Mechanism of Action

How does Linagliptin work?

Linagliptin inhibits the enzyme dipeptidyl peptidase-4 (DPP-4), which is involved in the inactivation of incretin hormones, which are involved in the physiological regulation of glucose homeostasis.1
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Carmelina® Carolina®

The long-term cardiovascular (CV) and kidney safety profile

Linagliptin has been comprehensively assessed via prespecified CARMELINA® and CAROLINA® subgroup analyses in >2,000 patients with T2D aged 65 years and older.2,3,#
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Abbreviations:

3P-MACE: 3-point major cardiac events; CV: cardiovascular; MI: myocardial infarction; SmPC: Summary of Product Characteristics; T2D: type 2 diabetes.

Footnotes

  • #
    Primary endpoint for CARMELINA® and CAROLINA®: Time to first occurrence of any of the following CV components: CV death (including fatal stroke and fatal MI), non-fatal MI (excluding silent MI), or non-fatal stroke (3P-MACE).

References

  1. Linagliptin Summary of Product Characteristics. SmPC available at EMC.
  2. Cooper ME, et al. Diabetes Obes Metab 2020;22:1062–1073
  3. Espeland MA, et al. Diabetes Obes Metab 2021;23(2):569-580

Linagliptin is indicated in adults with type 2 diabetes mellitus as an adjunct to diet and exercise to improve glycaemic control as:

  • monotherapy when metformin is inappropriate due to intolerance, or contraindicated due to renal impairment

  • in combination with other medicinal products for the treatment of diabetes, including insulin, when these do not provide adequate glycaemic control

PC-GB-112453 | May 2026

Reporting adverse events

Adverse events should be reported. Reporting forms and information can be found at www.mhra.gov.uk/yellowcard. Adverse events should also be reported to Boehringer Ingelheim Drug Safety on 0800 328 1627 (freephone).

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