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The form must be faxed to Caremark at a secure, HIPAA-compliant location.
The requested drug must be prescribed for an FDA-approved indication; otherwise, no further questions are required.
If the participant has failed or is intolerant to generic NSAIDs, documentation of medication trials and reasons for failure must be submitted.
Participants with documented adverse reactions to generic NSAIDs need to provide details and documentation of those reactions.
If there is no formulary agent available for the participant's clinical condition, supporting documentation must be included.
The prescribed drug must fall within the manufacturer’s dosing guidelines or accepted literature; otherwise, it may not be approved.
For any questions regarding prior authorization procedures, Caremark can be contacted at 800-294-5979.