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Get the free Drug Requested: (tofacitinib) / XR (tofacitinib xr)

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OPTIMA HEALTH PLAN PHARMACY PRIOR AUTHORIZATION/STEPPED REQUEST* Directions: The prescribing physician must sign and clearly print name (preprinted stamps not valid) on this request. All other information
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01
Step 1: Read the drug information leaflet and familiarize yourself with the dosage instructions.
02
Step 2: Wash your hands thoroughly before handling the medication.
03
Step 3: Take one tofacitinib XR tablet orally, with or without food, as directed by your healthcare provider.
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Step 4: Swallow the tablet whole and do not crush, chew, or split it.
05
Step 5: If you forget to take a dose, take it as soon as you remember. If it is close to the time for your next dose, skip the missed dose and resume your regular dosing schedule.
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Step 6: Store the medication in a cool, dry place away from direct sunlight and out of reach of children.
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Step 7: Follow up with your healthcare provider for any questions or concerns about the medication.

Who needs drug requested tofacitinib xr?

01
Tofacitinib XR is a prescription medication typically used to treat rheumatoid arthritis and psoriatic arthritis in adults.
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It may also be prescribed for other conditions as determined by a healthcare provider.
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Only individuals who have been diagnosed with these specific conditions and have been prescribed Tofacitinib XR by a healthcare provider need this medication.
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Tofacitinib XR is an extended-release medication used to treat conditions such as rheumatoid arthritis, psoriatic arthritis, and ulcerative colitis.
Pharmaceutical manufacturers or sponsors who are seeking approval to market tofacitinib XR must file the necessary documentation.
The request form for tofacitinib XR should be completed with detailed information about the drug's formulation, intended use, clinical data, and manufacturing process.
The purpose of requesting tofacitinib XR is to obtain regulatory approval for marketing the drug as a treatment option for specified medical conditions.
The request must include the drug's chemical composition, clinical trial results, manufacturing details, labeling information, and safety data.
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