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PACK IN HAND · ONE-PAGE CHECK

Medicine pack check sheet

Print this sheet or fill it in before speaking with a pharmacist or clinician. Copy only what is printed on the pack in hand. The published fields below are starting points from this record, not proof that your pack is the same product.

Published record starting point

Record display name
ONGLYZA
Generic name / active ingredient
saxagliptin
Dosage-form class
Dosage form and presentation as documented in the linked primary label
Route
Oral
Record reviewed
2026-08-31

Copy from the pack in hand

Source-linked reading points

  • 2.5 mg and 5 mg are amounts per tablet, not tablet counts. Kidney function and strong CYP3A4/5 inhibitors may affect professional decisions, but the site does not convert test results or medicine names into a strength.
  • Severe persistent abdominal pain that may radiate to the back, with or without vomiting, may signal pancreatitis and needs timely clinical contact as directed by the label.
  • Shortness of breath, orthopnoea, ankle or leg swelling, unusually rapid weight gain or unusual fatigue may signal heart failure, especially with prior heart failure or kidney problems.
  • ONGLYZA, KOMBIGLYZE XR, QTERN and QTERNMET XR may share saxagliptin; do not combine from brand names. Hypoglycaemia risk may rise with insulin or a sulfonylurea.

Reviewed presentation examples — compare every field

  • Equivalent to saxagliptin 2.5 mg per tablet; not an individual's tablet countNDC 0310-6100-30 / NDA 022350
  • Equivalent to saxagliptin 5 mg per tablet; not an individual's tablet countNDC 0310-6105-30 / NDA 022350
  • Equivalent to saxagliptin 2.5 mg per tablet; not an individual's tablet countDIN 02375842
  • Equivalent to saxagliptin 5 mg per tablet; not an individual's tablet countDIN 02333554

EDITORIAL RECORD

Who prepared and checked this page

Byline
OriginDrug Content Editorial
Review role
Public primary-source verification
Last reviewed
2026-08-31
Source record
5 clickable primary-source entry points are listed with this dossier.

The review role checks source traceability, stated market, document version and product-identity fields. It is not a claim of clinical licensure, prescribing authority or individual pharmacy service. Read the editorial policy.

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