30 Day Change Notice Form
Ohio Department of Medicaid
30 Day Change Notice
Effective Date: April 1, 2023
NEW CLINICAL PA REQUIRED PREFERRED DRUGS
| THERAPEUTIC CLASS | CLINICAL CRITERIA REQUIRED PREFERRED |
|---|---|
| Blood Formation, Coagulation, and Thrombosis Agents: Colony Stimulating Factors | Nyvepria |
| Cardiovascular Agents: Pulmonary Arterial Hypertension | Tadliq |
| Endocrine Agents: Osteoporosis – Bone Ossification Enhancers | Forteo |
NEW NON-PREFERRED DRUGS
| THERAPEUTIC CLASS | PA REQUIRED NON-PREFERRED |
|---|---|
| Blood Formation, Coagulation, and Thrombosis Agents: Colony Stimulating Factors | Fylnetra |
| Cardiovascular Agents: Angina, Hypertension, and Heart Failure | Clonidine ER (generic of Nexiclon XR) |
| Central Nervous System (CNS) Agents: Anticonvulsants | Levamlodipine |
| Central Nervous System (CNS) Agents: Antidepressants | Zonisade Susp |
| Genitourinary Agents: Benign Prostatic Hyperplasia | Ztalmy |
| Immunomodulator Agents: Systemic Inflammatory Disease | Auvelity |
| Infectious Disease Agents: Antifungals | Entadfi |
| Respiratory Agents: Nasal Preparations | Sotyktu |
| Topical Agents: Immunomodulators | Ryaltris |
| Zoryve |
REMOVED FROM UPDL
| THERAPEUTIC CLASS | |
|---|---|
| Analgesic Agents: Opioids | Oxaydo |
THERAPEUTIC CATEGORIES WITH CHANGES IN CRITERIA
- Blood Formation, Coagulation, and Thrombosis Agents: Colony Stimulating Factors
- Cardiovascular Agents: Pulmonary Arterial Hypertension
- Endocrine Agents: Osteoporosis – Bone Ossification Enhancers
- Genitourinary Agents: Benign Prostatic Hyperplasia
- Infectious Disease Agents: Antifungals
- Infectious Disease Agents: Hepatitis C Agents
Ohio Department of Medicaid
30 Day Change Notice
Effective Date: April 1, 2023
|
Ohio Department of Medicaid
30 Day Change Notice
Effective Date: April 1, 2023
Infectious Disease Agents: Hepatitis C Agents
OHIO DEPARTMENT OF MEDICAID
PRIOR AUTHORIZATION HEPATITIS C TREATMENT
| Request Date | Review Requested |
|---|---|
| STANDARD URGENT |
| Individual’s Name | Prescriber’s Name |
|---|---|
| Individual’s Medicaid ID Number | Prescriber’s NPI Number |
| Individual’s Date of Birth | Prescriber’s Address |
| Prescriber’s Phone Number | |
| Prescriber’s Fax Number |
Only Hepatitis C treatment PA requests for individuals who meet the following guidelines will be approved. This PA form will cover up to the length authorized by the American Association for the Study of Liver Disease (AASLD) guidelines. Please refer to the APPENDIX which lists the various regimens and the clinical situations for which they will be considered medically necessary according to the Ohio Department of Medicaid (OOM) criteria. The PA must be approved prior to the 1st dose and include appropriate supporting documentation.
APPENDIX
| Treatment naive |
|---|
| No cirrhosis |
| Mayvret 100/40 mg, three (3) tablets daily for 8 weeks (for GT5/6 and/or HIV/HCV co-infection, 12 weeks is recommended) |
| sofosbuvir/velpatasvir 400/100 mg, one tablet daily for 12 weeks |
| Compensated cirrhosis, HIV negative |
| Mayvret 100/40 mg, three (3) tablets daily for 8 weeks (GT4 WITH HIV coinfection, IDSA/AASLD guidelines recommend 12 weeks of therapy) |
| sofosbuvir/velpatasvir 400/100, one tablet daily for 12 weeks (for GT3, add weight based RBV if Y93H positive) |
| Compensated cirrhosis, HIV positive |
| Mayvret 100/40 mg, three (3) tablets daily for 12 weeks |
| sofosbuvir/velpatasvir 400/100 mg, one tablet daily for 12 weeks (for GT2, add weight-based RBV if Y93H positive) |
| Treatment experienced |
| Previously failed a Sofosbuvir-based regimen |
| Mayvret 100/40 mg, three (3) tablets daily for 16 weeks |
| Vosevi 400/100/100 mg, one tablet daily for 12 weeks (e.g. Zepatier) |
| Previously failed a NS3/4 protease inhibitor inclusive regimen (e.g. Zepatier) |
| Vosevi 400/100/100 mg, one tablet daily for 12 weeks (if compensated cirrhosis, add weight-based RBV) |
| Previously failed Mayvret |
| Vosevi 400/100/100 mg, one tablet daily for 12 weeks (if compensated cirrhosis, add weight-based RBV for 24 weeks) |
| Previously failed Vosevi or sofosbuvir + Mayvret |
| Vosevi 400/100/100 mg, one tablet daily + weight-based RBV for 24 weeks |
| Previously failed GT 3 only: sofosbuvir/NS5A (e.g. Harvoni) |
| Vosevi 400/100/100 mg, one tablet daily + weight-based RBV for 12 weeks |
Date of Notice: 3/1/2023
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Review how this policy can be converted into cited criteria, prior authorization checks, and operational automation.