Drug Prior Authorization List — Pharmacy & Medical Benefit PA Requirements
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Defines prior authorization requirements and reviewer routing for pharmacy and medical benefit drugs managed by WPS and partner vendors (ESI, CCUM, eviCore); affects providers submitting PA requests and pharmacies seeking coverage exceptions.
Revised: February 2026 — Effective Date: 2/1/2026 (notice that all listed drugs require a PA and PBM routing guidance added).
Coverage Criteria
General PA approval criteria
Covered when prior authorization is approved by the designated reviewer and medical necessity is met
All drugs listed require PA; if vendor cannot complete review submit to WPS.
General PA requirement
Covered when PA is obtained as required by the plan
Use the reviewer phone numbers listed in each drug entry.
PA approval required
Covered when PA is approved by the designated reviewer
This chunk set lists drugs requiring PA and the reviewer; specific clinical criteria are not included in these chunks.
General PA condition
Covered when prior authorization is obtained and routed to the designated reviewer
This segment lists reviewer assignments and HCPCS codes but does not include specific medical-necessity clinical criteria.
General PA requirement
Covered when prior authorization is obtained and reviewer routing is followed
No clinical eligibility criteria are provided in this part; this section enumerates drugs and routing.
General PA coverage condition
Covered when PA is obtained and processed by the designated reviewer
Applies to all listed drugs
Coverage of services is subject to medical necessity. Services or drugs determined to be experimental, investigational, or unproven under the applicable clinical guidelines will not be covered.
The provided excerpt does not list any clinical exclusions beyond administrative routing instructions; it states that all drugs on the list require prior authorization and includes a PBM routing note that if a PBM other than ESI is used, submit to that PBM.
Chunks include drug-specific context (for example, oncology vs non-oncology routing for certain biologics) but do not define explicit clinical exclusions. The listings indicate intended clinical contexts (e.g., Oncology), which inform reviewer routing rather than serving as coverage exclusions.
The document segments are an administrative list of products that require prior authorization (PA). These chunks provide benefit type, HCPCS/Q-codes where applicable, and the designated reviewer (ESI, CCUM, eviCore or WPS) per drug; they do not specify separate medical exclusions.
No additional coverage exclusions are specified in these sections beyond the uniform requirement that the listed drugs require prior authorization and must be routed to the reviewer shown for that drug.
When submitting prior authorization requests, follow the PBM routing guidance provided for each drug. The document instructs that if an alternate PBM is used (i.e., a PBM other than ESI through WPS), providers should submit to that PBM (including pharmacy drugs that would otherwise be reviewed by ESI or eviCore).
Coverage for drugs listed in this document is contingent on obtaining an approved prior authorization (PA) from the reviewer assigned for that product (ESI, CCUM, eviCore, or WPS when vendors cannot complete review). The chunks do not specify additional clinical exclusions tied to benefit type beyond indicating whether the item is billed under P (Pharmacy) or M (Medical).
Drugs or services that do not meet the payer’s medical necessity criteria, or that are judged to be experimental, investigational, or unproven, will not be covered. The policy emphasizes that PA determinations are made in the context of medical necessity and applicable clinical guidelines.
The chunks provided do not state any specific conditions that would be labeled as ‘not medically necessary’ for individual listed drugs. Decisions about medical necessity are made by the designated reviewer using submitted clinical documentation.
Coding and HCPCS/NDC References
| J0135 | HCPCS Code listed for adalimumab |
| Q5131 | HCPCS Code listed for adalimumab-aacf (biosimilar) |
| J9061 | amivantamab-vmjw (RYBREVANT) |
| G9033 | amantadine hcl (GOCOVRI) - ancillary code listed |
| J7210 | antihem.fviii, sin-chn, b-dm tru (AFSTYLA) |
| J7207 | antihemo.fviii, full length peg (ADYNOVATE) |
| J7205 | antihemoph.fviii rec, fc fusion (ELOCTATE) |
| J7185 | antihemoph.fviii, b-domain del / antihemophilic factor (recombinant) (XYNTHA SOLOFUSE / XYNTHA) |
| J7192 | antihemophilic factor (recombinant) (HELIXATE FS / NOVOEIGHT variants) |
| J7190 | antihemophilic factor (human) (HEMOFIL M / KOATE) |
| J7192 | antihemophil.fviii, full length / antihemophilic factor (recombinant) (various entries) |
| J7190 | antihemophilic factor (human) |
| J7182 | antihemophilic factor (recombinant) NOVOEIGHT |
| J7185 | antihemophilic factor (recombinant) XYNTHA |
| J7211 | antihemophilic factor (recombinant) KOVALTRY |
| J7191 | antihemophilic factor, human / MONOCLATE-P |
| J7183 | antihemophilic factor/vwf WILATE |
| J7186 | antihemophilic factor/vwf ALPHANATE |
| J7187 | antihemophilic factor/vwf HUMATE-P |
| J7188 | antihemophilic fviii, rec porc OBIZUR |
| C9073 | Brexucabtagene autoleucel |
| Q2053 | Brexucabtagene autoleucel |
| J8999 | listed for multiple oral drugs (placeholder HCPCS for oral pharmacy benefit) |
| J8499 | listed for multiple drugs (miscellaneous HCPCS) |
| J3590 | brodalumab HCPCS |
| J0179 | brolucizumab-dbll HCPCS |
| J0584 | burosumab-twza HCPCS |
| J0598 | c1 esterase inhibitor HCPCS |
| J0597 | c1 esterase inhibitor HCPCS |
| J0599 | c1 esterase inhibitor HCPCS |
| J0596 | c1 esterase inhibitor, recomb HCPCS |
| J9043 | cabazitaxel HCPCS |
| J3490 | multiple topical/oral agents (example entries) |
| J9027 | clofarabine |
| J7195 | coagulation factor ix (recombinant) |
| J7189 | coagulation factor viia, recomb |
| J7213 | coagulation factor ix (recombinant) alternate |
| J7212 | coagulation viia, recomb-jncw (SEVENFACT) |
| J7175 | coagulation factor x (COAGADEX) |
| J0775 | collagenase clostridium hist. |
| J7173 | concizumab |
| J0800 | corticotropin (H.P. ACTHAR GEL) |
| J9153 | daunorubicin/cytarabine liposome (VYXEOS LIPOSOME) |
| J0589 | daxibotulinumtoxinA-lanm |
| J0894 | decitabine |
| J0893 | decitabine (sun pharma) |
| J8499 | multiple oral or pharmacy benefit drugs listed (placeholder miscellaneous code) |
| J0897 | denosumab |
| C9399 | denosumab-bbdz |
| J3490 | denosumab-bbdz / miscellaneous J-code uses |
| J9999 | denosumab-bbdz / miscellaneous |
| Q5157 | denosumab-bmwo |
| J1301 | HCPCS code listed for edaravone |
| C9493 | Alternate HCPCS code listed for edaravone |
| J9361 | HCPCS code listed for efbemalenograstim alfa-vuxw |
| J9334 | HCPCS code listed for efgartigimod alfa and hyaluronidase-qvfc |
| J9332 | HCPCS code listed for efgartigimod alfa-fcab |
| J1449 | HCPCS code listed for eflapegrastim-xnst |
| J8999 | Generic J-code used for various oral/other oncology drugs |
| J3490 | Unclassified drug HCPCS code |
| J3590 | Unclassified drug HCPCS code |
| C9399 | C-code used for certain drugs (listed for eladocagene and eplontersen) |
| J1411 | etranacogene dezaparvovec (HEMGENIX) HCPCS |
| J1305 | evinacumab-dgnb (EVKEEZA) HCPCS |
| J3590 | evolocumab (REPATHA) HCPCS |
| J7194 | factor ix cplx(pcc)no4 HCPCS |
| J7203 | factor ix human rec, pegylated HCPCS |
| J7195 | factor ix human recombinant (BENEFIX) HCPCS |
| J7200 | factor ix human recombinant (RIXUBIS) HCPCS |
| J7201 | factor ix rec, fc fusion protn (ALPROLIX) HCPCS |
| J7199 | factor ix recom, albumin fusion HCPCS |
| S0126 | follitropin alfa |
| S0132 | ganirelix acetate (ANTAGON) |
| J8499 | grass pollen-timothy, standard (GRASTEK) |
| J9211 | idarubicin hcl - inj (IDAMYCIN) |
| C9081 | idecabtagene vicleucel (ABECMA) |
| Q2055 | idecabtagene vicleucel (ABECMA) |
| J1743 | idursulfase (ELAPRASE) |
| J9208 | ifosfamide (IFEX, MITOXANA) |
| J1572 | imm glob g (igg)/sorb/iga 0-50 (FLEBOGAMMA) |
| J1562 | imm glob sc/scig/igsc (VIVAGLOBIN) |
| J1557 | immun glob g(igg)/gly/iga 0-50 (GAMMAPLEX) |
| J1555 | immun glob g(igg)/gly/iga ov50 (CUVITRU) |
| J1556 | immun glob g(igg)/gly/iga ov50 (BIVIGAM) |
| J9216 | interferon gamma-1b, recomb. |
| J9153 | liposome-encapsulated combination of daunorubicin and cytarabine (VYXEOS) |
| C9076 | lisocabtagene maraleucel (BREYANZI) |
| C9307 | linvoseltamab-gcpt (LYNOZYFIC) |
| Q2054 | alternate code listed for lisocabtagene maraleucel |
| J9359 | loncastuximab tesirine-lpyl (ZYNLONTA) |
| J8999 | lorlatinib - oral (LORBRENA) / midostaurin - oral (RYDAPT) and other J8999 entries |
| J3394 | lovotibeglogene autotemcel (LYFGENIA) |
| J0224 | lumasiran sodium (OXLUMO) |
| C9074 | lumasiran sodium alternate code |
| J9353 | margetuximab-cmkb (MARGENZA) |
| J9223 | lurbinectedin (ZEPZELCA) |
| J0896 | luspatercept-aamt (REBLOZYL) |
| J7172 | marstacimab-hncq (HYMPAVZI) |
| J1202 | miglustat |
Provider Actions and Submission Instructions
Prior authorization required for all listed drugs
All drugs listed in this policy require prior authorization (PA). Submit the PA to the reviewer specified for the drug (ESI, CCUM, eviCore, or WPS). If the listed reviewer cannot complete the review, submit the request to WPS for evaluation.
- Applies to every drug on the list — PA is required before coverage is approved.
- Use the vendor assignment shown next to each drug entry (ESI, CCUM, eviCore) or WPS if the vendor cannot complete the review.
Submit PA to alternate PBM/vendor when applicable
When the group uses an alternate PBM or vendor (not ESI/CCUM/eviCore), submit prior authorization requests to the applicable PBM/vendor and follow that vendor's precertification process.
- Includes pharmacy drugs reviewed by ESI or eviCore — submit to the other PBM when applicable.
- If the external vendor cannot complete the review, escalate submission to WPS for evaluation.
Obtain PA and submit to designated reviewer
Prior authorization must be obtained for every drug on the list and routed to the reviewer indicated for that specific drug (ESI, CCUM, or eviCore). If the designated PBM cannot complete the review, submit to WPS.
- Use the reviewer contact shown in the drug entry (vendor phone numbers provided).
- Coverage is contingent on PA approval by the designated reviewer.
Follow reviewer routing and use provided contact numbers
Prior authorization is required for each listed drug; the policy shows which reviewer handles each drug and provides reviewer phone numbers for submission. If the vendor cannot complete the review, submit to WPS.
- Reviewer assignments (ESI, CCUM, eviCore or WPS) are provided per drug entry with contact lines.
- Follow the reviewer routing noted in the drug listing when submitting PA requests.
Include HCPCS/CPT codes and route PA to named reviewer
A prior authorization is required for each product listed; the document supplies HCPCS/CPT or miscellaneous codes and identifies the designated reviewer to which the PA must be routed.
- Include the HCPCS/CPT or J-code listed for the product when preparing the PA submission.
- Route the request to the reviewer named in the drug entry (ESI, CCUM, eviCore, or WPS).
Submit PA to the designated reviewer (or WPS if vendor unavailable)
Submit prior authorization requests to the reviewer indicated for the drug. If the indicated reviewer cannot complete the review, submit the PA to WPS for evaluation using the WPS provider contact.
- Use the vendor phone number listed in the drug entry (e.g., 1-800-475-1954 for ESI/CCUM/eviCore).
- If vendor review cannot be completed, submit to WPS at 1-800-333-5003.
Submit PA to the reviewer listed for that drug
Prior authorization must be submitted to the reviewer identified for that drug entry (ESI, CCUM, eviCore or WPS); follow the reviewer assignment shown in the policy.
- Reviewer assignment and the HCPCS/J-code are shown for each drug — submit both as part of the request.
- If the reviewer cannot complete the review, escalate the request to WPS.
Use reviewer assignment and HCPCS codes from drug entry
Each listed drug requires prior authorization; the policy lists reviewer assignments and HCPCS/J-codes per product — submit the PA to the reviewer shown for that code.
- Include benefit type (P or M) and the HCPCS/J-code in the PA submission per the drug entry.
- Route to ESI, CCUM, or eviCore as indicated; if those reviewers cannot complete the review, submit to WPS.
Route PA by benefit type to the reviewer indicated
The policy lists benefit type and the reviewer routing for each drug. Submit PA requests to the reviewer shown (ESI, CCUM, or eviCore) according to the drug’s benefit type and routing instruction.
- Benefit Type indicates Pharmacy (P) or Medical (M) — use this when determining submission process.
- If external reviewer cannot complete review, submit to WPS for evaluation.
If PBM reviewer cannot complete review, submit to WPS
If the PBM for the group is unavailable or unable to complete the review, route the prior authorization request to the appropriate vendor (ESI, CCUM, eviCore) or submit directly to WPS for evaluation.
- Primary vendor phone line for ESI/CCUM/eviCore: 1-800-475-1954.
- WPS provider contact for escalation: 1-800-333-5003.
Contact designated reviewer or submit per routing instructions
All drugs on this list require prior authorization; contact the designated reviewer via the vendor phone number listed in the drug entry or submit per the routing instructions in the policy.
- Use vendor contact 1-800-475-1954 for ESI/CCUM/eviCore.
- If vendor cannot complete the review, submit the PA to WPS at 1-800-333-5003.
Submit PA for listed HCPCS/CPT codes to assigned reviewer
Prior authorization is required for the HCPCS/CPT codes listed with each drug; submit PA to ESI, CCUM, or eviCore as indicated, and use WPS if the PBM cannot complete the review.
- Include the HCPCS/J-code shown in the drug entry when requesting PA.
- Route to the reviewer indicated (CCUM, ESI, eviCore); escalate to WPS if needed.
Submit PA to assigned reviewer; escalate to WPS if needed
Reviewer assignment is indicated for each drug; submit prior authorization requests to the assigned reviewer (ESI, CCUM, eviCore) and use WPS as the escalation path if the reviewer cannot complete the review.
- Reviewer phone numbers for vendors and WPS are provided in the document.
- Follow the per‑drug reviewer assignment when submitting PAs.
Submit to designated reviewer; WPS accepts submissions if PBM cannot complete review
Submit the prior authorization to the reviewer shown for that drug entry; if the PBM reviewer is unable to complete the review, WPS will accept the submission for evaluation.
- Use the reviewer assignment (e.g., CCUM option 2 for certain products) shown next to the drug.
- When vendor review cannot be completed, submit to WPS at 1-800-333-5003.
Submit PA to indicated reviewer; include supporting clinical information
Prior authorization must be submitted to the reviewer indicated for the drug (ESI, CCUM, or eviCore). If those reviewers cannot complete the review, submit the PA to WPS for evaluation.
- Provide the drug name and supporting clinical information with the PA submission.
- Use the vendor phone numbers provided in the policy when contacting external reviewers.
Submit PA with clinical support to designated reviewer or WPS
Submit prior authorization requests to the reviewer identified for the drug; if the PBM cannot complete the review, submit to WPS for evaluation using the WPS contact information provided.
- Include the HCPCS/J-code and clinical justification (medical records, prior treatments, FDA labeling) when submitting PA.
- If using a PBM other than ESI through WPS, submit to that PBM per the group’s arrangement.
Call 1-800-475-1954 for step therapy or PA criteria
Providers may obtain detailed step therapy or prior authorization criteria by calling the prior authorization specialist at 1-800-475-1954 for drugs reviewed by Express Scripts or Care Continuum.
- Call 1-800-475-1954 to speak with a prior authorization specialist for step therapy or PA requirements.
- For eviCore step-therapy/guideline details, consult eviCore’s provider clinical guidelines online.
No step therapy rules specified in this excerpt
The policy does not provide step therapy algorithms or specific step requirements in the listed excerpts.
- No explicit step therapy rules are specified in this document segment; follow PBM/vendor guidance or contact the prior authorization specialist for details.
Note — limited excerpt
(No additional requirements specified in this excerpt.)
Follow oncology vs non‑oncology reviewer routing
Some oncology biologics show different reviewer routing for oncology versus non-oncology use (e.g., CCUM for non-oncology, eviCore for oncology); follow the routing in the drug entry when submitting PAs.
- Check the drug’s comments for routing differences by indication (oncology vs non‑oncology).
- Submit to eviCore for oncology indications when indicated; submit to CCUM/ESI for non‑oncology as shown.
Step therapy not specified — follow vendor guidance
Step therapy is not defined in these chunks; the policy reiterates PA routing instructions without specifying step-therapy steps.
- If step therapy is required, contact the prior authorization specialist or the assigned PBM for details.
- Do not assume step therapy rules from this excerpt; use vendor guidance.
No step therapy rules in this segment
No step therapy rules or additional PA routing beyond reviewer assignments are provided in this segment.
No step therapy rules provided
No step therapy rules are provided in these chunks; the policy focuses on PA requirement and reviewer routing.
Step therapy not specified here
No step therapy rules are specified in these chunks; submit PAs per PBM routing instructions.
Step therapy not specified in provided chunks
No step therapy rules are specified in the provided segments of the policy.
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Follow per‑drug reviewer/program assignment
Reviewer routing and program assignment differ for some products — e.g., certain drugs route to eviCore for oncology reviews and to CCUM or ESI for non‑oncology; follow the routing shown per drug entry.
- Confirm indication in the patient's record to determine correct reviewer routing.
- If the reviewer indicated cannot complete the review, submit to WPS.
Submit PA to other PBM when group does not use ESI through WPS
If the group uses a PBM other than ESI through WPS, submit the PA to that PBM for review (this includes pharmacy drugs that would otherwise be reviewed by ESI or eviCore under WPS arrangements).
- Follow the alternate PBM’s precertification process and contact information.
- If the alternate PBM cannot complete the review, escalate to WPS for evaluation.
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Submit PA to other PBM when applicable
If the sponsor uses a different PBM, submit PA requests to that PBM rather than the ESI/CCUM/eviCore contacts listed in this policy.
Provide medical records and supporting clinical information with PA
Decision-makers use the patient’s medical records, prior treatments, FDA labeling, and peer‑reviewed literature as supporting documentation during PA review — include these when submitting a request.
- Provide relevant medical records and prior treatment history.
- Include FDA labeling and any supporting literature or evidence-based guidelines where applicable.
Submit PA to the listed reviewer or escalate to WPS
Submit PA requests to the reviewer listed in the drug entry using the vendor phone numbers provided; if the vendor cannot complete the review, submit the PA to WPS for evaluation.
- Use vendor contact 1-800-475-1954 for ESI/CCUM/eviCore.
- If vendor review cannot be completed, submit to WPS at 1-800-333-5003.
Escalate to WPS when vendor cannot complete review
When PBMs (ESI, CCUM, eviCore) cannot complete the review, submit the PA to WPS; if the group uses another PBM, submit to that PBM per group arrangement.
- If using another PBM, follow its submission process (e.g., iExchange or fax form per WPS instructions).
- WPS will evaluate requests when external reviewers cannot complete reviews.
Submit PA to listed reviewer or to WPS if PBM cannot complete review
Provide the prior authorization request to the reviewer listed for the drug (ESI, CCUM, or eviCore) or to WPS if the PBM cannot complete the review; reviewer phone numbers are provided in the policy.
- Include the drug name, HCPCS/J-code, benefit type and clinical justification in the submission.
- Use vendor phone numbers or WPS contact for submission and escalation.
Submit PA to designated reviewer or WPS when necessary
Submit PA to the designated reviewer shown for the drug or to WPS if the PBM reviewer cannot complete the review; WPS accepts submissions for evaluation.
- Use the reviewer and escalation contact numbers listed in the drug entry.
- If the group uses an alternate PBM, submit to that PBM per the group's arrangement.
Use ESI/CCUM/eviCore routing; escalate to WPS if required
Submit PA to ESI, CCUM, or eviCore according to the reviewer routing shown for each drug; if those reviewers cannot complete the review, submit the PA to WPS for evaluation.
- Follow the per‑drug reviewer assignment shown in the policy.
- Escalate to WPS using the provided contact when external reviewers cannot complete review.
Submit to WPS when vendor cannot complete review; follow alternate PBM guidance
When external reviewers cannot complete the PA review, submit the prior authorization request to WPS for evaluation; if the group uses another PBM, submit to that PBM as appropriate.
- WPS contact for escalations: 1-800-333-5003.
- For groups not using ESI through WPS, use the alternate PBM’s submission process (iExchange or PA form fax).
Submit PA to designated reviewer; include clinical support
Submit the prior authorization request to the reviewer indicated in the drug entry; if reviewers cannot complete the review, submit to WPS using the WPS contact number provided.
- Provide drug name and supporting clinical documentation when submitting the PA.
- Follow the reviewer phone contacts listed in the policy for initial submission.
Submit PA to WPS if vendor cannot complete review
If a PBM cannot complete the review, submit the PA request to WPS for evaluation using the contact provided in the policy.
- WPS contact for evaluation: 1-800-333-5003.
- If external reviewer cannot complete review, WPS will accept the submission for evaluation.
Submit to vendor reviewers or escalate to WPS
Submit PA requests to the listed reviewer (ESI, CCUM, or eviCore) per the reviewer routing; when reviewers cannot complete review, submit to WPS for evaluation and use the phone contacts provided.
- Use the reviewer phone number 1-800-475-1954 for vendor submissions.
- Escalate to WPS at 1-800-333-5003 if external vendors cannot complete the review.
Provide drug and clinical info and submit PA to reviewer or WPS
Submit the prior authorization to the reviewer shown for the drug or to WPS if the PBM cannot complete the review; reviewer phone numbers and WPS contact are provided in the policy.
- Provide drug name, HCPCS/J-code and supporting clinical information with the PA submission.
- If the group uses an alternate PBM, submit to that PBM per their process.
Submit to assigned vendors; escalate to WPS when needed
Submit PA to ESI, CCUM, or eviCore as listed; if those reviewers cannot complete the review, submit the PA to WPS for evaluation using the contact information supplied.
- Follow per‑drug reviewer routing; include clinical documentation.
- Use WPS contact 1-800-333-5003 for escalations when external reviewers cannot complete review.
Submit PA to listed reviewer or alternate PBM; escalate to WPS if needed
Submit the prior authorization to the listed reviewer (ESI, CCUM, or eviCore) or to WPS if those reviewers cannot complete the review. If the plan uses a PBM other than ESI through WPS, submit to that PBM.
- If using another PBM, follow that PBM’s submission process (iExchange or PA form fax options noted in the policy).
- When vendor reviews cannot be completed, WPS will accept the submission for evaluation.
Submit PA to listed reviewer; escalate to WPS if reviewer cannot complete
Submit PA to the vendor listed for the drug; if the external reviewer is unable to complete the review, submit the PA to WPS for evaluation using the WPS contact number.
- Include HCPCS/J-code and clinical justification in the submission.
- WPS escalation contact: 1-800-333-5003.
Include drug name and supporting clinical documentation with PA
Provide the drug name and supporting clinical information (medical records, prior treatments, FDA labeling, literature) when submitting PA to the listed reviewer (ESI, CCUM, eviCore) or to WPS if the PBM cannot complete review.
- Medical records and prior treatment history should be included.
- Cite FDA labeling or peer‑reviewed literature when relevant to support medical necessity.
Coverage subject to medical necessity; investigational services not covered
Coverage is subject to medical necessity; services deemed experimental, investigational, and/or unproven will not be covered.
- Ensure documentation supports medical necessity and is consistent with evidence‑based guidelines.
- Requests for experimental or investigational uses may be denied.
Denial risk if PA not obtained
Failure to obtain prior authorization for any drug on this list may result in denial of coverage.
- All drugs listed require PA prior to coverage.
- Claims submitted without an approved PA may be denied or processed as non‑authorized.
Claims may be denied without PA
All drugs on this list require prior authorization; claims submitted without PA may be denied.
- PA must be approved by the designated reviewer for coverage to be authorized.
- If the reviewer cannot complete the review, submit to WPS to avoid denial risk.
Claim denial risk if PA not submitted
Failure to submit a prior authorization for any drug on the list may result in denial of coverage because all drugs listed require a PA.
- Submit PA before dispensing or administration to avoid claim denial.
- When in doubt, submit to the designated reviewer or escalate to WPS.
Requests denied if PA not obtained
All drugs on this list require PA; requests will be denied if prior authorization is not obtained.
- Do not administer or dispense listed drugs without PA approval when coverage is sought from WPS.
- Use vendor or WPS submission routes provided to obtain authorization.
Initial Therapy Criteria
Initial therapy PA
Refer to vendor specified for individual drug entry.
Initial therapy PA
Administrative PA required for initiation
Specific clinical initiation criteria not included in these chunks.
Step Therapy
| Step therapy access | Notes |
|---|---|
| Providers may obtain specific step therapy criteria by calling the prior authorization specialist at 1-800-475-1954 | Also consult eviCore clinical guidelines at https://www.evicore.com/provider/clinical-guidelines (select Medical Oncology or Radiation Oncology and search 'WPS Health Insurance') |
| Step therapy | Notes |
|---|---|
| No specific step therapy steps specified in this excerpt | General instruction: follow PBM reviewer routing (ESI, CCUM, eviCore) and submit to WPS if the PBM cannot complete the review |
| Step therapy | Notes |
|---|---|
| Reviewer routing differs by indication and may function operationally as step determination | Example: CCUM for non-oncology (option 2) and eviCore for oncology (option 3); routing noted per drug entry |
| Step therapy | Notes |
|---|---|
| Step therapy rules not specified in these chunks | PA routing and reviewer assignment are provided per drug; follow reviewer indicated (ESI, CCUM, eviCore) and submit to WPS if needed |
| Step therapy | Notes |
|---|---|
| Step therapy not specified in this segment | Document provides PA requirement and reviewer routing (e.g., CCUM or eviCore) but no clinical step algorithm |
| Step therapy | Notes |
|---|---|
| No step therapy rules specified | Only PA requirement and reviewer routing are listed; follow vendor-specific criteria where applicable |
| Step therapy (PBM routing) | Notes |
|---|---|
| If a PBM other than ESI through WPS is used, submit the prior authorization to that PBM | Includes pharmacy drugs reviewed by ESI or eviCore; if external PBM cannot complete review submit to WPS for evaluation |
Site of Care and Benefit Type Notes
Biosimilar and Specific Drug Notes
Background
Prior authorization is used to ensure appropriate use of selected drugs and to confirm medical necessity before coverage. The policy notes that services deemed experimental, investigational, or unproven are not covered and that reviewers use medical records, FDA labeling, and evidence-based literature when making determinations.
Definitions and Key Fields
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