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Exception Drug Status (EDS) Request Form, Oral Anti-Diabetic Medications

This form reaches you when a patient with type 2 diabetes needs an SGLT2 inhibitor or DPP-4 inhibitor covered by Manitoba Pharmacare. Coverage depends on the patient's earlier trials of metformin and a sulfonylurea, or for empagliflozin on established cardiovascular disease, and it can't start before the request reaches the EDS office.

At a glance

Checked October 2026

Issued by
Manitoba Health, Seniors and Long-Term Care
Where
Manitoba
Completed by
Prescriber
Format
Fillable PDF
Language
English

What the form is for

Manitoba covers several oral diabetes drugs only through Exception Drug Status, which means the patient has to meet the criteria in the EDS listing before Pharmacare pays. This form covers five of them: canagliflozin, empagliflozin, linagliptin, saxagliptin, and sitagliptin. Approval is granted only when you show the patient meets those criteria, and Manitoba Health can ask for more documentation.

For combination products, such as empagliflozin with metformin or sitagliptin with metformin, use the general EDS request form instead. Other drugs have their own Manitoba EDS forms.

Who completes it

The prescriber completes and signs the whole form. There’s no patient section, and you confirm on the form that you’ve told the patient their information is going to Manitoba Health to obtain EDS coverage.

How to fill it in

Prescriber, patient, and medication

Enter your name, address, phone, fax, and licence number, not your billing number. Give the patient’s name, date of birth, PHIN, and Manitoba Health registration number (MHSC). Check the medication requested and enter the strength and regimen.

Diagnosis and indication

Mark type 2 diabetes, or for empagliflozin only, the cardiovascular indication: an adjunct to diet, exercise, and standard care to reduce cardiovascular death in type 2 diabetes. Use “other” only for an indication you can support from the criteria notice.

The three statements

Answer yes or no to all three: the patient had a trial of metformin that led to intolerance or inadequate control, had a trial of a sulfonylurea with the same result, and insulin isn’t an option. If you answer no to any of them, give your rationale in the space provided. For canagliflozin and the DPP-4 inhibitors, the criteria in the EDS notice rest on inadequate control on, or intolerance to, metformin and a sulfonylurea when insulin isn’t an option, so explain any no with the specific clinical reason.

Established cardiovascular disease, for empagliflozin

For the cardiovascular indication, check the condition that applies: previous MI, multi-vessel coronary artery disease, single-vessel disease with significant stenosis and a positive stress test or an unstable angina admission within 12 months, unstable angina more than 2 months ago with confirmed coronary disease, ischemic or hemorrhagic stroke, or occlusive peripheral artery disease. The criteria also need inadequate glycemic control despite an adequate trial of metformin.

Additional clinical information and signature

Add the A1C values, the doses and dates of the metformin and sulfonylurea trials, and the reason for any intolerance. Check the consent box, then date and sign.

Common reasons it’s delayed

  • A “no” to the metformin, sulfonylurea, or insulin statements with no rationale.
  • Empagliflozin requested for cardiovascular protection with no qualifying condition checked.
  • A combination product requested on this form instead of the general one.
  • A billing number entered in place of the licence number.
  • No doses, dates, or A1C values to show the earlier trials failed.

Submitting and who pays

Fax the form to the EDS office at (204) 942-2030 or 1-877-208-3588, which are for health professionals only. Diabetes drugs are triaged as chronic requests, with a turnaround of 5 to 10 business days. Coverage starts from the date the request is received, and drugs bought before that aren’t covered, so send it before the patient fills the prescription. Once approved, Pharmacare pays after the patient’s deductible is met.

Get the official form

Download the current version from Manitoba Health, Seniors and Long-Term Care each time. Forms change without notice, and an old edition can be returned.

Official page ↗ PDF ↗

Medulla Forms

Fill Exception Drug Status (EDS) Request Form, Oral Anti-Diabetic Medications from the visit and the chart.

Upload the fillable PDF to your practice's forms once. Medulla fills it from the visit and the chart open in your EMR, leaves blank anything the record doesn't support, and opens the form for your review. When it's done, save it to the patient's chart in one click.

Free 1-month trial. No credit card required.

Sources for this guide

Questions

Questions we hear a lot.

Can I use this form for Synjardy or Janumet?

No. The form says to use the general EDS request form for combination products such as empagliflozin/metformin, sitagliptin/metformin, and saxagliptin/metformin. The EDS notice covers Synjardy for patients stable for at least 3 months on the separate components, who must also meet the empagliflozin criteria.

What are Manitoba's EDS criteria for empagliflozin?

For reducing cardiovascular death, the patient must have type 2 diabetes with inadequate glycemic control despite an adequate trial of metformin, and established cardiovascular disease as defined in the EMPA-REG OUTCOME trial, such as a previous MI, multi-vessel coronary disease, stroke, or occlusive peripheral artery disease.

How long does an EDS request for a diabetes drug take?

Manitoba classes medications for chronic conditions such as type 2 diabetes as chronic requests, with a turnaround of 5 to 10 business days from when the EDS office receives a complete application.

What if the patient hasn't tried a sulfonylurea?

Answer no to that statement and give your rationale in the space below the questions. The form asks for a rationale whenever you answer no to any of the metformin, sulfonylurea, or insulin statements.

Is patient information secure?

Yes. Medulla has a SOC 2 Type II report from an independent auditor, is HIPAA, PIPEDA, and PHIPA compliant, and is built and hosted in Canada, so patient data stays in the country and never gets pasted into consumer AI tools. Everything is encrypted in transit and at rest. See how we protect patient data.

More questions? Browse help.medulla.ca.