Applies to Medicaid plans.
Covered with requirementsQualification pathways
You can qualify through any one of these.
Step therapy: allergy, contraindication, DDI, side effects, or trial-and-failure of all five preferred agent types
Plus any one of:
- Allergy to all five types of preferred medications (benzphetamine, diethylpropion, orlistat, phendimetrazine, phentermine)
- Contraindication or drug-to-drug interaction with all five types of preferred medications
- History of unacceptable side effects with all five types of preferred medications
- Trial and failure with all five types of preferred agents (at least one orlistat agent, one phentermine product, plus benzphetamine, diethylpropion, and phendimetrazine)
Initial approval — additional medication-specific criteria (all required)
All of:
- Patient age ≥18 years
- Patient has an initial BMI classified as morbidly obese (BMI ≥40 kg/m²)
- Prescriber attests patient will not use more than one weight loss medication in this drug class concurrently
- Prescriber attests documented failure of all other clinically appropriate weight loss interventions
- Prescriber attests use of GLP-1 for weight loss is to avert the need for higher-cost bariatric surgery
- Prescriber attests patient will not use an anti-obesity GLP-1 agonist concurrently with a DPP-4 inhibitor (alogliptin, linagliptin, saxagliptin, or sitagliptin)
- Prescriber attests to absence of contraindications including pregnancy, lactation, personal or family history of medullary thyroid cancer or multiple endocrine neoplasia type II
- Prescriber attests medication therapy is part of a total treatment plan including diet and exercise/activity
- Prescriber attests patient has been informed weight may return with cessation unless lifestyle changes are permanently adopted
- Prescriber attests metabolic or other reasons for obesity/symptoms have been ruled out or diagnosed and treated (e.g., thyroid dysfunction, diabetes, sleep apnea)
- For patients with an eating disorder: prescriber attests treatment has been optimized and confirms safety and appropriateness
Documentation to bring
- Prescriber attestation that patient will not use more than one weight loss medication in this drug class concurrently
- Prescriber attestation of documented failure of all other clinically appropriate weight loss interventions
- Prescriber attestation that use of GLP-1 is to avert the need for higher-cost bariatric surgery
- Prescriber attestation that patient will not use an anti-obesity GLP-1 agonist concurrently with a DPP-4 inhibitor
- Prescriber attestation of absence of contraindications (pregnancy, lactation, personal or family history of medullary thyroid cancer or MEN2)
- Prescriber attestation that medication is part of a total treatment plan including diet and exercise
- Prescriber attestation that patient has been informed about weight return upon cessation
- Prescriber attestation that metabolic or other causes of obesity have been ruled out or treated
- For patients with eating disorder: prescriber attestation that treatment has been optimized
- Documentation of step therapy: allergy, contraindication, DDI, unacceptable side effects, or trial-and-failure of all five preferred agent types (benzphetamine, diethylpropion, orlistat, phendimetrazine, phentermine)
- Baseline BMI documentation (≥40 kg/m²) for patients ≥18 years
- Renewal — patients ≥18: clinical documentation of weight at renewal showing ≥5% weight loss from baseline
Quantity limits
- 2.5 mg/0.5 mL pens/vials — 2 mL (4 pens/vials) per 28 days
- 5 mg/0.5 mL pens/vials — 2 mL (4 pens/vials) per 28 days
- 7.5 mg/0.5 mL pens/vials — 2 mL (4 pens/vials) per 28 days
- 10 mg/0.5 mL pens/vials — 2 mL (4 pens/vials) per 28 days
- 12.5 mg/0.5 mL pens — 2 mL (4 pens) per 28 days
- 15 mg/0.5 mL pens — 2 mL (4 pens) per 28 days
- KwikPen 2.5 mg/dose (10 mg/2.4 mL), KwikPen 5 mg/dose (10 mg/2.4 mL), KwikPen 7.5 mg/dose (10 mg/2.4 mL), KwikPen 10 mg/dose (10 mg/2.4 mL), KwikPen 12.5 mg/dose (10 mg/2.4 mL), KwikPen 15 mg/dose (10 mg/2.4 mL) — 2.4 mL (1 KwikPen) per 28 days
Approval and renewal
- Initial approval: 6 months
- Renewal: every 6 months
- Renewal: For patients ≥18 years: must have maintained weight loss of ≥5% from baseline weight at initiation of therapy. For 1st renewal of established members with initial approval prior to 1/1/2026: prescriber attests to morbid obesity at start, documented failure of all other weight loss interventions, and use was to avert bariatric surgery, plus same weight maintenance requirement.
Not covered when
- Lactation
- Personal or family history of medullary thyroid cancer
- Personal or family history of multiple endocrine neoplasia type II
- Concurrent use of a DPP-4 inhibitor (alogliptin, linagliptin, saxagliptin, sitagliptin)
- Concurrent use of another anti-obesity GLP-1 agonist
- Patients under age 18 (Zepbound minimum age is 18 per this policy)
- Pregnancy
Policy note: This policy applies to 'non-preferred GLP-1s only' for weight loss under Michigan Medicaid PDL. Zepbound (tirzepatide) minimum age per this policy is 18 years. The morbidly obese BMI threshold for adults is ≥40 kg/m²; the policy does not apply the 12-year minimum or pediatric BMI percentile pathway to Zepbound (only to Wegovy and Saxenda/liraglutide). MDHHS recommends prescribers consider the benefits of a diabetes prevention program. A special 1st renewal pathway exists for established members with initial approval prior to 1/1/2026 requiring attestations of morbid obesity at start, documented failure of other interventions, and use to avert bariatric surgery, plus the standard ≥5% weight loss requirement.
Policy effective July 1, 2026 · verified June 4, 2026 · source: Mi Rx Clinical Criteria · View policy document (PDF)