upadacitinib
Rinvoq (upadacitinib) is an oral JAK inhibitor approved for rheumatoid arthritis, psoriatic arthritis, ankylosing spondylitis, atopic dermatitis, Crohn's disease, ulcerative colitis, and giant cell arteritis (GCA).
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Rinvoq (upadacitinib) is an oral JAK inhibitor approved for rheumatoid arthritis, psoriatic arthritis, ankylosing spondylitis, atopic dermatitis, Crohn's disease, ulcerative colitis, and giant cell arteritis (GCA).
Rinvoq (upadacitinib) belongs to the JAK Inhibitors class of medications. It was first approved by the FDA in 2019. This medication requires a prescription from a licensed healthcare provider.
This is a summary only. Always read the full prescribing information and consult your healthcare provider for personalized medical advice.
Rinvoq is prescribed for the following conditions. Some uses are FDA-approved indications; others may be evidence-based off-label uses. Consult your healthcare provider for personalized guidance.

The following are general dosing guidelines only. Your actual dose should be determined by your healthcare provider based on your condition, renal/hepatic function, and other medications.
RA/PsA/AS: 15 mg once daily. Atopic dermatitis: 15 mg or 30 mg once daily. Crohn's/UC: 45 mg once daily for 12 weeks (induction), then 15 or 30 mg once daily (maintenance). GCA: 15 mg once daily.
Available Forms
Available Strengths


Always inform your healthcare provider and pharmacist about ALL medications you take, including prescriptions, OTC medicines, vitamins, and supplements.
Strong CYP3A4 inhibitors (ketoconazole, itraconazole, ritonavir)
Increase upadacitinib AUC ~75%, raising immunosuppression and adverse effect risk.
Management: Reduce upadacitinib dose to 15 mg once daily; avoid with strong CYP3A4 inhibitors in higher-dose indications.
Strong CYP3A4 inducers (rifampin, carbamazepine)
Reduce upadacitinib exposure by ~60–75%, risking therapeutic failure.
Management: Avoid combination. If rifampin is essential, consider alternative JAK inhibitor or disease therapy.
Live vaccines
JAK inhibitor immunosuppression may render live vaccines ineffective and poses risk of disseminated infection.
Management: Complete all vaccinations before treatment. Do not give live vaccines during Rinvoq therapy.
Other biologic DMARDs (TNF inhibitors, IL-6 inhibitors, abatacept)
Dual biologic/JAK inhibitor combinations increase infection risk without demonstrated efficacy advantage.
Management: Contraindicated. Use only one immunomodulatory biologic or JAK inhibitor.
Anticoagulants (warfarin) / antiplatelet agents
JAK inhibitors may modestly affect platelet function; warfarin levels may be unpredictably altered.
Management: Monitor INR and bleeding signs when initiating or adjusting Rinvoq.
Methotrexate / azathioprine
Combined immunosuppression increases infection risk and hepatotoxicity potential.
Management: Monitor CBC, LFTs, and signs of infection regularly. Low-dose MTX may be co-prescribed intentionally.
Boxed warning: serious infections, malignancy, major cardiovascular events, thrombosis, and mortality risk — especially in patients ≥50 with at least one cardiovascular risk factor.
Screen for TB, viral hepatitis, and CBC before initiating.
Contraindicated in pregnancy; use effective contraception.

Upadacitinib is a selective JAK1 inhibitor that blocks JAK-STAT signaling pathways involved in the inflammatory cascade driving multiple immune-mediated conditions, including rheumatoid arthritis, atopic dermatitis, and inflammatory bowel disease.
Absorption
Bioavailability ~76%; peak ~2–4 hours (extended-release)
Half-Life
~9–14 hours
Metabolism
Hepatic, primarily CYP3A4
Excretion
Feces (~38%), urine (~24%)

Many medications pass into breast milk in varying amounts. Before using Rinvoqwhile breastfeeding, discuss the benefits and risks with your healthcare provider or pharmacist — they can weigh your dose, your infant's age, and available lactation safety data to find the safest option for you and your baby.

Store at room temperature, 20–25°C (68–77°F). Keep in original container.
Rinvoq (upadacitinib) is an oral JAK1 inhibitor, while Entyvio (vedolizumab) is an injected gut-selective integrin inhibitor. Head-to-head data show Rinvoq achieves higher clinical remission rates in ulcerative colitis. The choice depends on prior treatment history, risk tolerance, and patient preference for oral versus injectable therapy.
Rinvoq selectively inhibits JAK1 (Janus kinase 1), blocking intracellular signaling through the JAK-STAT pathway. This reduces the production and response to multiple pro-inflammatory cytokines including IL-6, IL-12, IL-23, and interferons, which are elevated in RA, atopic dermatitis, IBD, and other conditions Rinvoq treats.
JAK Inhibitors alternatives
Compare all JAK Inhibitors medications — uses, side effects, and cost differences
Rinvoq dosage guide
Adult, pediatric, renal, and hepatic dosing for Rinvoq
Rinvoq side effects
Complete adverse effect profile including common, serious, and rare reactions
Rinvoq drug interactions
Full interaction list with severity ratings for Rinvoq
Rheumatoid Arthritis treatment options
Medications, lifestyle changes, and clinical guidance for Rheumatoid Arthritis
Psoriatic Arthritis treatment options
Medications, lifestyle changes, and clinical guidance for Psoriatic Arthritis
Atopic Dermatitis treatment options
Medications, lifestyle changes, and clinical guidance for Atopic Dermatitis
Rinvoq and Strong CYP3A4 inhibitors (ketoconazole, itraconazole, ritonavir) interaction
Check the clinical significance of combining Rinvoq with Strong CYP3A4 inhibitors (ketoconazole, itraconazole, ritonavir)
Rinvoq and Strong CYP3A4 inducers (rifampin, carbamazepine) interaction
Check the clinical significance of combining Rinvoq with Strong CYP3A4 inducers (rifampin, carbamazepine)
Rinvoq (upadacitinib) is an oral, once-daily extended-release tablet that belongs to the class of drugs called JAK inhibitors. It is one of the most broadly approved medicines in this class, with FDA clearance for rheumatoid arthritis, psoriatic arthritis, ankylosing spondylitis, atopic dermatitis, Crohn's disease, ulcerative colitis, and giant cell arteritis (GCA). As a pill, it offers a convenient alternative to injectable biologics for many patients with these conditions.
Rinvoq belongs to the JAK Inhibitors class of medications. Upadacitinib is a selective JAK1 inhibitor that blocks JAK-STAT signaling pathways involved in the inflammatory cascade driving multiple immune-mediated conditions, including rheumatoid arthritis, atopic dermatitis, and inflammatory bowel disease. Understanding how Rinvoq works helps explain both its benefits and its important safety considerations.
## What Rinvoq is used for
Rinvoq is prescribed for Rheumatoid arthritis, Psoriatic arthritis, Ankylosing spondylitis, Atopic dermatitis, Crohn's disease, Ulcerative colitis, and Giant cell arteritis. In each setting it is generally used when prior standard therapies (including TNF inhibitors for RA and biologics for IBD) have not provided adequate control. Rinvoq is available by prescription only and has been FDA-authorized since 2019.
## Dosage and administration
Typical adult dosing: RA/PsA/AS: 15 mg once daily. Atopic dermatitis: 15 mg or 30 mg once daily. Crohn's/UC: 45 mg once daily for 12 weeks (induction), then 15 or 30 mg once daily (maintenance). GCA: 15 mg once daily.
Rinvoq extended-release tablets are taken once daily with or without food. Tablets are swallowed whole — do not split, crush, or chew them. The induction dose for IBD is higher (45 mg) and is used for the first 12 weeks before stepping down to a maintenance dose. Never change your dose or stop Rinvoq without speaking to your prescriber.
## Side effects
Common side effects include Upper respiratory tract infections, Nausea, Acne, Herpes zoster (shingles), Elevated liver enzymes, and Neutropenia. Serious side effects include Serious infections including opportunistic infections, Blood clots (DVT, pulmonary embolism), Major adverse cardiovascular events (MACE), Malignancy, and Gastrointestinal perforation. Rinvoq carries a boxed warning about serious infections, cancer, cardiovascular events, thrombosis, and mortality — particularly in patients 50 and older with cardiovascular risk factors. These risks must be weighed individually with your prescriber.
## Managing common side effects
## Warnings and precautions
Key precautions: Boxed warning: serious infections, malignancy, MACE, thrombosis, and mortality risk in patients ≥50 with cardiovascular risk factors; Screen for TB, viral hepatitis, and CBC before initiating; Contraindicated in pregnancy. Discuss the complete risk profile with your prescriber before starting Rinvoq, especially if you are over 50, smoke, or have a history of cardiovascular disease or cancer.
## Drug interactions
Rinvoq can interact with Strong CYP3A4 inhibitors (major) — increase upadacitinib exposure; Strong CYP3A4 inducers (major) — decrease upadacitinib exposure; Live vaccines (major) — avoid during therapy. Always inform your prescriber and pharmacist of every medication and supplement you take.
## Cost, coverage, and savings
Rinvoq is a brand-name specialty medication with significant list-price cost. AbbVie offers a myAbbVie Assist savings program and copay cards for eligible patients. Searching for a rinvoq copay card, rinvoq savings card, or rinvoq patient assistance through the official AbbVie website is the best path to cost support. Medicare patients should ask about extra help programs.
## How Rinvoq compares to alternatives
Rinvoq competes with other JAK inhibitors (Xeljanz/tofacitinib, Olumiant/baricitinib) and with injectable biologics (Humira, Entyvio, Skyrizi). For ulcerative colitis, head-to-head data favor Rinvoq over Entyvio in some measures of remission. For atopic dermatitis, Rinvoq and Dupixent represent different mechanism options (JAK inhibition vs. IL-4/13 blockade). The best choice depends on the specific condition, prior treatment, risk tolerance, and preference for oral vs. injectable therapy.
## Monitoring and lifestyle
Before starting Rinvoq, baseline CBC, liver function, lipids, TB screening, and hepatitis B/C testing are standard. During treatment, periodic CBC, liver enzymes, and lipid panels are monitored. Shingles vaccination before starting is recommended where feasible. Avoid live vaccines during treatment.
## What to expect from treatment
Many patients notice improvement in symptoms within 2–4 weeks, with continued gains over the first 3–6 months. For IBD, response is assessed at week 12 of induction. Rinvoq is taken long-term for most conditions — do not stop without your prescriber's guidance.
## Before you start Rinvoq
A complete pre-treatment workup includes TB test, hepatitis screening, CBC, and a thorough medication review. Effective contraception is required throughout treatment due to the contraindication in pregnancy. Update all vaccines before starting if possible, since live vaccines cannot be given during therapy.
## Missed dose and overdose
If you miss a dose of Rinvoq, take it as soon as you remember the same day. If you don't remember until the next day, skip the missed dose and resume your regular schedule. Never take two doses in one day. If overdose is suspected, contact poison control or emergency services.
## Use in specific populations
Pregnancy: Contraindicated — use effective contraception. Breastfeeding: Not recommended. Older adults (≥50): The boxed warning applies most prominently to this group, especially those with cardiovascular risk factors. Kidney/liver impairment: Dose adjustment may be needed for severe impairment.
## When to contact your doctor
Contact your clinician for signs of infection (fever, chills, persistent cough), unexplained weight loss, leg swelling or pain (possible clot), chest pain, or any new skin growth. Do not stop Rinvoq abruptly without guidance.
## Storage and handling
Store at room temperature, 20–25°C (68–77°F). Keep in original container and protect from moisture. Check expiration dates and dispose of expired tablets through a take-back program.
## Clinical evidence and effectiveness
The SELECT program of phase 3 trials demonstrated Rinvoq's efficacy across its approved indications. In SELECT-COMPARE (RA), Rinvoq outperformed adalimumab on ACR50 response. In U-ACHIEVE (UC) and U-EXCEL (Crohn's), robust induction and maintenance remission rates supported approval. The HEADS UP trial showed Rinvoq superior to dupilumab on certain atopic dermatitis endpoints at week 16. Your prescriber can translate these data to your individual situation.
## Key takeaways
## Medical disclaimer
This article about Rinvoq (upadacitinib) is for general education and is not a substitute for professional medical advice, diagnosis, or treatment. Always follow the guidance of your physician or pharmacist and the instructions on your prescription label.
Last reviewed by MedCentralHub Medical Review Board · MedCentralHub Editorial Policy
Medical Disclaimer
The information on this page is for educational purposes only and is not intended as medical advice, diagnosis, or treatment. Always consult your doctor, pharmacist, or qualified healthcare provider before starting, stopping, or changing any medication.