How to take FRUZAQLA^® (fruquintinib)

FRUZAQLA is a convenient, non-chemo pill

FRUZAQLA is a once-daily pill available in 5 mg and 1 mg doses that you can take anywhere. You will not need to visit an infusion center for treatment.

FRUZAQLA is taken as one pill, once a day

Most people take 5 mg of FRUZAQLA orally once daily for the first 21 days, followed by 7 days off treatment—for each 28-day cycle
Swallow FRUZAQLA pill whole
Take each dose at the same time every day. If less than 12 hours have passed since you missed a dose of FRUZAQLA, do take your missed dose. Do not take 2 doses on the same day to make up for a missed dose
Your doctor may change your dose of FRUZAQLA if needed

FRUZAQLA treatment doesn’t have to get in the way of your daily life

It can be taken at home or on the go.
It can be taken with or without food.

Take FRUZAQLA exactly as your doctor tells you. Be sure to talk to your doctor or pharmacist if you have any questions about FRUZAQLA or your dosing.

Create a unique FRUZAQLA Dosing Calendar based on your treatment start date, to help you keep track of your dosing schedule*

Example dosing calendar. Personalize it for your treatment cycle.

Enter the start date of your treatment to download your dosing calendar with the option to email it to yourself

*Please take FRUZAQLA as instructed by your healthcare provider. For more information on how to take FRUZAQLA, please read the Patient Information and full Prescribing Information.

Join Dr. Al Hallak, a GI medical oncologist, to learn about FRUZAQLA's once daily dosing schedule.

FRUZAQLA clinical study

Discover the data from a global clinical trial.

Explore study results

Side effects with FRUZAQLA

Explore the potential common side effects while taking FRUZAQLA.

Read about side effects

Helpful resources and support for people with mCRC

Download FRUZAQLA resources made just for you.

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IMPORTANT SAFETY INFORMATION

FRUZAQLA may cause serious side effects, including:

High blood pressure (hypertension). High blood pressure is common with FRUZAQLA and can also be severe. Your healthcare provider will check your blood pressure before starting treatment with FRUZAQLA,1 time every week for the first month of treatment, and then at least 1 time a month or more often if needed during treatment. Your healthcare provider may prescribe medicine to treat your high blood pressure if needed. Tell your healthcare provider if you get any of the following symptoms of hypertension during treatment: severe headache, lightheadedness or dizziness, confusion, changes in vision, chest pain, trouble breathing, nosebleeds, or vomiting.

Severe bleeding (hemorrhage). FRUZAQLA can cause bleeding that can be serious and may lead to death. Tell your healthcare provider if you get any of the following symptoms of bleeding during treatment:

unusual, severe, or bleeding that will not stop
bruising
lightheadedness
vomiting blood or your vomit looks like coffee grinds
blood in the stool or black stool that looks like tar
blood in the urine or urine that looks red, pink, or brown
coughing up blood or blood clots
menstrual bleeding that is heavier than normal
unusual vaginal bleeding
nose bleeds that happen often

Infections. FRUZAQLA can increase the risk of infections, including serious infections that can lead to death. The most common infections with FRUZAQLA happened in the urinary tract, nose or throat, and lungs. Tell your healthcare provider if you get any of the following symptoms of infection during treatment: fever, severe cough with or without an increase in mucus (sputum) production, severe sore throat, trouble breathing, burning or pain when you urinate, or redness, swelling, or pain in any part of the body.

A tear in your stomach or intestinal wall (gastrointestinal perforation). FRUZAQLA can cause gastrointestinal perforation that can be serious and may lead to death. Tell your healthcare provider right away if you get any of the following symptoms of gastrointestinal perforation during treatment: severe stomach (abdominal) pain or stomach pain that does not go away, vomiting or vomiting blood, blood in the stool or black stool that looks like tar, fever or chills, or nausea.

Liver problems. Increased liver enzymes in your blood are common with FRUZAQLA and can also be severe and may lead to death. Your healthcare provider will do blood tests before and during treatment with FRUZAQLA to check for liver problems. Tell your healthcare provider if you get any of the following symptoms of liver problems during treatment: yellowing of your skin or the white part of your eyes, dark-colored (tea-colored) urine, pain in your right upper stomach area (abdomen), loss of appetite, nausea or vomiting, or bleeding or bruising.

Protein in your urine (proteinuria). Protein in your urine is common with FRUZAQLA and can also be severe. Your healthcare provider will check your urine for protein before starting and during treatment with FRUZAQLA. Tell your healthcare provider if you have to urinate more than usual or if you get swelling of your face, hands, arms, legs, or feet during treatment.

Hand-foot skin reactions (Palmar-Plantar Erythrodysesthesia [PPE]). Hand-foot skin reactions are common with FRUZAQLA and can also be severe. Tell your healthcare provider if you get a severe rash or redness, pain, blisters, bleeding, or swelling on the palms of your hands or soles of your feet during treatment.

Posterior Reversible Encephalopathy Syndrome (PRES). PRES is a serious condition that can happen in your brain during treatment with FRUZAQLA. Tell your healthcare provider right away if you get any of the following symptoms during treatment: headache, seizures, confusion, changes in vision, or problems thinking.

Wound healing problems. Wounds may not heal properly during treatment with FRUZAQLA. Tell your healthcare provider if you plan to have any surgery before starting FRUZAQLA or during treatment. You should stop taking FRUZAQLA at least 2 weeks before planned surgery. Your healthcare provider will tell you when you may start taking FRUZAQLA again after surgery.

Blood clots in your blood vessels (arteries). FRUZAQLA can cause blood clots or blockage in your blood vessels that may lead to heart attack, stroke, or death. Get medical help right away if you get any of the following symptoms during treatment:

severe chest pain or pressure
pain in your arms, legs, back, neck or jaw
shortness of breath
numbness or weakness of your face, arm, or leg, especially on one side of your body
feeling lightheaded or faint
sweating more than usual
sudden confusion, trouble talking or understanding things
trouble walking
sudden severe headache
sudden vision changes in one or both eyes
dizziness or loss of balance or coordination

Allergic reactions to FD&C Yellow No. 5 and FD&C Yellow No. 6. FRUZAQLA 1mg capsules contain the inactive ingredients FD&C Yellow No. 5 (tartrazine) and FD&C Yellow No. 6 (sunset yellow FCF). FD&C Yellow No. 5 (tartrazine) can cause allergic-type reactions (including bronchial asthma) in certain people, especially people who also have an allergy to aspirin. FD&C Yellow No. 6 (sunset yellow FCF) can also cause allergic reactions. Tell your healthcare provider if you get hives, rash, or trouble breathing during treatment with FRUZAQLA.

The most common side effects of FRUZAQLA include:

voice changes or hoarseness

stomach-area (abdominal) pain

diarrhea

weakness, lack of strength and energy, and feeling very tired or sleepy (asthenia)

These are not all of the possible side effects of FRUZAQLA. Call your doctor for medical advice about side effects. You may report side effects to Takeda at 1-844-662-8532 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch.

Before taking FRUZAQLA, tell your healthcare provider about all your medical conditions, including if you:

Have high blood pressure.

Have bleeding problems

Have an infection

Have liver or kidney problems

Plan to have surgery or have had recent surgery. You should stop taking FRUZAQLA at least 2 weeks before your planned surgery. Your healthcare provider will tell you when you can start FRUZAQLA again after your surgery

Have recently had a blood clot, stroke, or heart attack

Are allergic to FD&C Yellow No. 5 (tartrazine) or FD&C Yellow No. 6 (sunset yellow FCF)

Are pregnant or plan to become pregnant. FRUZAQLA can harm your unborn baby. You should not become pregnant during treatment with FRUZAQLA.

Females who can become pregnant:

Your healthcare provider will do a pregnancy test before you start treatment with FRUZAQLA.
Use effective birth control (contraception) during treatment and for 2 weeks after your last dose of FRUZAQLA.
Tell your healthcare provider right away if you become pregnant during treatment with FRUZAQLA.

Males with female partners who can become pregnant:

Use effective birth control during treatment and for 2 weeks after your last dose of FRUZAQLA.
Tell your healthcare provider right away if your partner becomes pregnant during your treatment with FRUZAQLA.

Are breastfeeding or plan to breastfeed. It is not known if FRUZAQLA passes into your breast milk. Do not breastfeed during treatment and for 2 weeks after your last dose of FRUZAQLA.

Tell your healthcare provider about all the medicines you take, including prescription and over-the-counter medicines, vitamins, and herbal supplements. FRUZAQLA may affect the way other medicines work, and other medicines may affect how FRUZAQLA works.

Especially tell your healthcare provider if you take blood thinners (anticoagulants).

Know the medicines you take. Keep a list of your medicines to show to your healthcare provider and pharmacist when you get a new medicine.

Please see Patient Information in the FRUZAQLA (fruquintinib) full Prescribing Information.