Sitagliptin: Difference between revisions

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NCLEX nursing pharmacology monographs — batch import
 
Add medication infobox (Drugbox) to monographs
 
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{{Drugbox
| name = Sitagliptin
| brand = Januvia
| therapeutic = Antidiabetic
| pharmacologic = DPP-4 inhibitor
| onset = Peak 1 to 4 hours; once-daily effect.
| halflife = Half-life about 12 hours; no routine level.
| routes = PO (oral)
| highalert = No
| blackbox = None
| antidote = None.
| pregnancy = Limited data; insulin preferred.
}}
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<div style="border-left:4px solid #3f6f5b;background:#f3f6f4;padding:8px 12px;margin-bottom:12px;font-size:0.95em;">
''Nursing pharmacology study reference (NCLEX-style monograph). Numeric values are standard teaching ranges for study and '''must be verified against current manufacturer labeling before clinical use'''. This is educational content, not prescribing guidance.''
''Nursing pharmacology study reference (NCLEX-style monograph). Numeric values are standard teaching ranges for study and '''must be verified against current manufacturer labeling before clinical use'''. This is educational content, not prescribing guidance.''

Latest revision as of 16:09, 17 June 2026

Sitagliptin
Drug monograph · NCLEX study reference
Trade namesJanuvia
Therapeutic classAntidiabetic
Pharmacologic classDPP-4 inhibitor
Onset / peak / durationPeak 1 to 4 hours; once-daily effect.
Half-life / levelHalf-life about 12 hours; no routine level.
RoutesPO (oral)
High-alert (ISMP)No
Black box warningNone
Antidote / reversalNone.
Pregnancy / lactationLimited data; insulin preferred.

Nursing pharmacology study reference (NCLEX-style monograph). Numeric values are standard teaching ranges for study and must be verified against current manufacturer labeling before clinical use. This is educational content, not prescribing guidance.

Sitagliptin (brand name Januvia) — Antidiabetic; DPP-4 inhibitor.

Identification

  • Therapeutic class: Antidiabetic.
  • Pharmacologic class: DPP-4 inhibitor.

Pharmacology

  • Mechanism of action: Inhibits DPP-4, increasing incretin hormones to enhance glucose-dependent insulin release and lower glucagon.
  • Onset / peak / duration: Peak 1 to 4 hours; once-daily effect.
  • Half-life / therapeutic level: Half-life about 12 hours; no routine level.

Clinical use

  • Indications: Type 2 diabetes.
  • Usual dose, route, frequency: 100 mg PO once daily.
  • Maximum dose / adjustments: Reduce dose in renal impairment (50 mg or 25 mg).

Safety

  • Contraindications: Type 1 diabetes, history of serious hypersensitivity.
  • Black box warning: None.
  • Interactions: Few; additive hypoglycemia with insulin or sulfonylureas.
  • Pregnancy / lactation: Limited data; insulin preferred.
  • High-alert: No.

Adverse effects

  • Common side effects: Nasopharyngitis, headache, upper respiratory symptoms.
  • Serious effects to report: Pancreatitis (severe abdominal pain), severe joint pain, hypersensitivity.
  • Antidote / reversal: None.

Nursing process

  • Assessment before administration: Renal function, pancreatitis history.
  • Interventions during therapy: Adjust dose by renal function.
  • Monitor: A1c, renal function.
  • Evaluation / expected outcome: Glycemic control, weight neutral.

Patient teaching

  • Patient teaching: Report severe abdominal or joint pain.
  • Notify provider if: Severe stomach pain, persistent vomiting.
  • Administration tips: With or without food.