TAGRISSO is an FDA-approved oral targeted therapy used when your non-small cell lung cancer (NSCLC) with certain abnormal EGFR gene(s)* has spread to nearby tissues (locally advanced) and is unable to be removed (unresectable) by surgery and has responded or stabilized following chemotherapy and radiation treatment.

*For tumors with EGFR exon 19 deletions or exon 21 L858R mutations.

Clinical Trial Results

TAGRISSO helped adults with locally advanced, unresectable stage 3 EGFR+ NSCLC have more time without their cancer growing or spreading after CRT

More than
3 years
without EGFR+ NSCLC
growing
or spreading

Median progression-free survival was

~39


months for adults taking
TAGRISSO after CRT

VS

~6


months for adults taking
placebo
(no active medicine)
after CRT

Median progression-free survival measures the median amount of time that half of the people enrolled in the study were on treatment before their cancer started growing or spreading.

Median progression-free
survival was

18.9


months for adults taking TAGRISSO alone

versus

10.2


months for adults taking erlotinib or gefitinib

 

Median progression-free survival measures the median amount of time that half of the people enrolled in the study were on treatment before their cancer started growing or spreading. In the clinical trial, half the adults who took TAGRISSO alone lived at least 18.9 months without their cancer growing or spreading and half the adults who took erlotinib or gefitinib lived at least 10.2 months without their cancer growing or spreading.

More time without EGFR+ NSCLC growing or spreading

Median progression-free survival measures the amount of time that half of the people enrolled in the study were on treatment before their cancer started growing or spreading. In the clinical trial, half the adults who took TAGRISSO lived at least 39.1 months without their cancer growing or spreading and half the adults who took no active medicine lived at least 5.6 months without their cancer growing or spreading.

TAGRISSO may not work for everyone. Individual results may vary.

Median is the middle number in a group of numbers arranged from lowest to highest.

“Inspirational patient
quote to come”

—Name X.

Learn more about the clinical trial

Clock Icon

The clinical trial studying TAGRISSO after CRT included 216 adults with locally advanced unresectable (stage 3) EGFR+ NSCLC that couldn’t be removed by surgery and has responded or stabilized during or following platinum-based chemotherapy and radiation treatment (CRT).

They were given either TAGRISSO (143 patients) or a placebo (no active medicine) (73 patients) within six weeks of completing CRT. Patients continued treatment with TAGRISSO until their doctor told them to stop.

The main goal of the clinical trial was to measure the length of time adults were on treatment before their cancer started growing or spreading. This is called progression-free survival (PFS). For adults taking TAGRISSO, it took significantly longer for cancer to grow or spread than it did for those taking no active medicine.

TAGRISSO helped protect from new tumors
in the body and brain

Of adults taking TAGRISSO, 22% had a new tumor(s) in the body

compared to

68% of those who took no active medicine.

Of adults taking TAGRISSO, 8% had a new tumor(s) in the brain

compared to

29% of those who took no active medicine.

“Inspirational patient
quote to come”

—Name X.

The clinical trial included 216 adults with locally advanced (stage 3) EGFR+ NSCLC that couldn’t be removed by surgery and had not progressed during or after chemoradiation. They were given either TAGRISSO or a placebo (no active medicine) within six weeks of completing chemoradiation. Patients continued treatment with TAGRISSO until their doctor told them to stop.

The main goal of the clinical trial was to measure the time adults were on treatment before their cancer started growing or spreading. This is called progression-free survival (PFS). For adults taking TAGRISSO, it took significantly longer (7 times longer) for cancer to grow or spread than it did for those taking no active medicine.

Fewer people who took TAGRISSO after chemoradiation had progression to the brain compared to those who took no medicine

About 20% of adults (29 out of 143) taking TAGRISSO after chemoradiation had progression to the brain compared to 41% of adults (30 out of 73) who took no medicine.

Nearly 8 in 10 adults responded to treatment with TAGRISSO alone

About 8 out of 10 adults (77% or 215 out of 279 patients) taking TAGRISSO alone saw their tumors shrink; about 7 out of 10 adults (69% or 191 out of 277 patients) treated with other EGFR-targeted therapies, erlotinib or gefitinib, saw their tumors shrink.

Learn more about how to take TAGRISSO

Dosing Information

How to take TAGRISSO after CRT

Dosing that may conveniently fit into your daily routine

TAGRISSO After CRTRadiation Image

CRT treatment as prescribed

 

TAGRISSO Tablet

once-a-day pill (80-mg tablet)

Fork and Spoon Icon

may be taken with or without food, and can be taken at home

TAGRISSO + chemotherapy should be taken as prescribed by your doctor
Follow your treatment plan as prescribed by your doctor

What if I’m having trouble swallowing TAGRISSO whole?

Water Icon

Place your TAGRISSO pill in a glass or container. Pour in 2 ounces (60 mL) of water. Don’t use carbonated water or any other liquids

Drinking Water Icon

Drink the TAGRISSO and water mixture right away

TAGRISSO Pills with Water

Stir the TAGRISSO tablet and water until the TAGRISSO tablet is in small pieces (the tablet will not completely dissolve). Do not crush, heat, or use ultrasound to prepare the mixture

Water Jug Icon

Add 4 to 8 ounces (120 to 240 mL) of water into the container and drink to make sure that you take your full dose of TAGRISSO

What if I miss a dose?

Calendar Time

What if I miss a dose?

If you miss a dose of TAGRISSO, do not make up for the missed dose. Take your next dose at your regular time.

Your doctor may change your dose, temporarily stop, or permanently stop treatment with TAGRISSO if you have side effects.

It’s important to follow your doctor’s instructions for staying on track with your treatment. Always take TAGRISSO exactly as directed by your doctor.

Take TAGRISSO once a day, every day, as prescribed by your doctor

Safety Considerations

You may experience side effects with TAGRISSO

It’s important to talk to your healthcare team right away if you experience side effects.

Be sure to talk to your doctor about any side effect you are experiencing. Your doctor may change your dose, temporarily stop, or permanently stop treatment with TAGRISSO if you have side effects.

Your doctor may change your dose, temporarily stop, or permanently stop treatment with TAGRISSO if you have side effects.

TAGRISSO may cause serious side effects, including: 

  • Lung problems. TAGRISSO may cause severe lung problems that may lead to death. Symptoms may be similar to those symptoms from lung cancer. Tell your healthcare provider right away if you have any new or worsening lung symptoms, including trouble breathing, shortness of breath, cough, or fever
  • Heart problems, including heart failure. TAGRISSO may cause heart problems that may lead to death. Your healthcare provider should check your heart function before you start taking TAGRISSO and during treatment as needed. Tell your healthcare provider right away if you have any of the following signs and symptoms of a heart problem: feeling like your heart is pounding or racing, shortness of breath, swelling of your ankles and feet, dizziness, feeling lightheaded, or feeling faint
  • Eye problems. TAGRISSO may cause eye problems. Tell your healthcare provider right away if you have symptoms of eye problems which may include watery eyes, sensitivity to light, eye pain, eye redness, or vision changes. Your healthcare provider may send you to see an eye specialist (ophthalmologist) if you get eye problems with TAGRISSO
  • Skin problems. TAGRISSO may cause skin problems. Tell your healthcare provider right away if you develop skin reactions that look like rings (target lesions), severe blistering or peeling of the skin
  • Inflammation of the blood vessels in your skin. TAGRISSO may cause blood vessel problems in your skin. Tell your healthcare provider right away if you develop purple spots or redness of the skin that does not fade in color when pressed (non-blanching) on your lower arms, lower legs, or buttocks or large hives on the main part of your body (trunk) that do not go away within 24 hours and look bruised
  • Blood and bone marrow problems. TAGRISSO may cause a condition where your bone marrow cannot make enough new blood cells (aplastic anemia), and which may lead to death. Your healthcare provider will monitor your blood cell counts before you start and during treatment with TAGRISSO. Tell your healthcare provider right away if you develop any signs and symptoms of blood and bone marrow problems, including a new fever or fever that does not go away (100.4 °F), easy bruising or bleeding that will not stop, unusually pale skin, infection, tiredness, or weakness

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

  • have lung or breathing problems other than your lung cancer
  • have heart problems, including a condition called long QTc syndrome
  • have problems with your electrolytes, such as sodium, potassium, calcium or magnesium
  • have a history of eye problems
  • are pregnant or plan to become pregnant. TAGRISSO can harm your unborn baby. Tell your healthcare provider right away if you become pregnant during treatment with TAGRISSO or think you may be pregnant
  • Females who are able to become pregnant should have a pregnancy test before starting treatment with TAGRISSO. You should use effective birth control (contraception) during treatment with TAGRISSO and for 6 weeks after the last dose of TAGRISSO
  • Males who have female partners that are able to become pregnant should use effective birth control during treatment with TAGRISSO and for 4 months after the last dose of TAGRISSO
  • females who are breastfeeding or plan to breastfeed. It is not known if TAGRISSO passes into your breast milk. Do not breastfeed during treatment with TAGRISSO and for 2 weeks after your last dose of TAGRISSO. Talk to your healthcare provider about the best way to feed your baby during this time

Tell your healthcare provider about all the medicines you take, including prescription and over-the-counter medicines, vitamins, or herbal supplements. Especially tell your healthcare provider if you take a heart or blood pressure medicine

The most common side effects of TAGRISSO when given alone include:

  • low white blood cell counts
  • low platelet counts
  • low red blood cell counts (anemia)
  • diarrhea
  • rash
  • muscle, bone, or joint pain
  • changes in your nails, including: redness, tenderness, pain, inflammation, brittleness, separation from the nailbed, and shedding of nail
  • dry skin
  • mouth sores
  • tiredness
  • low white blood cell counts
  • low platelet counts
  • low red blood cell counts (anemia)
  • diarrhea
  • rash
  • muscle, bone, or joint pain
  • changes in your nails, including: redness, tenderness, pain, inflammation, brittleness, separation from the nailbed, and shedding of nail
  • dry skin
  • mouth sores
  • tiredness

The most common side effects of TAGRISSO when given alone after treatment with platinum-based chemotherapy and radiation treatment include:

  • low white blood cell counts
  • lung problems
  • low platelet counts
  • rash
  • diarrhea
  • changes in your nails, including: redness, tenderness, pain, inflammation, brittleness, separation from the nailbed, and shedding of nail
  • cough
  • COVID-19
  • low white blood cell counts
  • lung problems
  • low platelet counts
  • rash
  • diarrhea
  • changes in your nails, including: redness, tenderness, pain, inflammation, brittleness, separation from the nailbed, and shedding of nail
  • cough
  • COVID-19

The most common side effects of TAGRISSO in combination with pemetrexed and platinum-based chemotherapy include:

  • low white blood cell counts
  • low platelet counts
  • rash
  • diarrhea
  • mouth sores
  • changes in your nails, including: redness, tenderness, pain, inflammation, brittleness, separation from the nailbed, and shedding of nail
  • dry skin
  • increase of a substance in the blood called creatinine
  • low white blood cell counts
  • low platelet counts
  • rash
  • diarrhea
  • mouth sores
  • changes in your nails, including: redness, tenderness, pain, inflammation, brittleness, separation from the nailbed, and shedding of nail
  • dry skin
  • increase of a substance in the blood called creatinine

Tell your healthcare provider if you have any side effect that bothers you or that does not go away.

These are not all the possible side effects of TAGRISSO. For more information, ask your healthcare provider or pharmacist.

TAGRISSO is a prescription medicine used to treat adults with non-small cell lung cancer (NSCLC) that has certain abnormal epidermal growth factor receptor (EGFR) gene(s):

  • to help prevent your lung cancer from coming back after your tumor(s) has been removed by surgery, or
  • when your lung cancer has spread to nearby tissues (locally advanced), that is unable to be removed (unresectable) by surgery and has responded or stabilized following chemotherapy and radiation treatment, or
  • as your first treatment when your lung cancer has spread to other parts of the body (metastatic), or
  • in combination with pemetrexed and platinum-based chemotherapy, as your first treatment when your lung cancer has spread to nearby tissues (locally advanced) or to other parts of the body (metastatic), or
  • when your lung cancer has spread to other parts of the body (metastatic) and you have had previous treatment with an EGFR tyrosine kinase inhibitor (TKI) medicine that did not work or is no longer working.

Your healthcare provider will perform a test to make sure that TAGRISSO is right for you.
It is not known if TAGRISSO is safe and effective in children.

Please see complete Prescribing Information, including Patient Information for TAGRISSO.

Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.

  • Take TAGRISSO exactly as your healthcare provider tells you to take it
  • Your healthcare provider may change your dose, temporarily stop, or permanently stop treatment with TAGRISSO if you have side effects
  • Take TAGRISSO 1 time each day
  • You can take TAGRISSO with or without food
  • If you miss a dose of TAGRISSO, do not make up for the missed dose. Take your next dose at your regular time
  • If you cannot swallow TAGRISSO tablets whole:
    • Place your dose of TAGRISSO in a container that contains 60 mL (2 ounces) of water. Do not use carbonated water or any other liquids
    • Stir the TAGRISSO tablet and water until the TAGRISSO tablet is in small pieces (the tablet will not completely dissolve). Do not crush, heat, or use ultrasound to prepare the mixture
    • Drink the TAGRISSO and water mixture right away
    • Add 120 mL to 240 mL (4 to 8 ounces) of water into the container and drink to make sure that you take your full dose of TAGRISSO
  • If you have a nasogastric (NG) tube:
    • Follow the same instructions for mixing TAGRISSO tablets in a container that contains 15 mL of water. Do not use carbonated water or any other liquids
    • Stir the TAGRISSO tablets and water until the TAGRISSO tablets are in small pieces (the tablets will not completely dissolve). Do not crush, heat, or use ultrasound to prepare the mixture
    • Add another 15 mL of water into the container to make sure no pieces of TAGRISSO tablet remain
    • Give the TAGRISSO tablet and water mixture using the NG tube manufacturer instructions within 30 minutes
    • Add another 30 mL of water into the syringe and give the water and any remaining TAGRISSO through the NG tube to make sure that all of the medicine is given. Repeat this step until no pieces remain in the syringe. This will help to ensure that the full prescribed dose of the TAGRISSO is given
Be sure to revisit How to take TAGRISSO
for more information

Adding chemotherapy to TAGRISSO may increase the risk of certain side effects

These are not all the possible side effects of TAGRISSO or TAGRISSO + chemotherapy. For more information, ask your healthcare provider or pharmacist.

Keep your healthcare team informed of all the side effects you may be feeling as they can change over time.

Your healthcare team can find out the cause of your side effects and adjust your TAGRISSO + chemotherapy or TAGRISSO-only treatment plan to help.

In the clinical trial of TAGRISSO + chemotherapy, side effects changed over time

TAGRISSO Side Effect

How to discuss side effects with your doctor 

If you’ve been diagnosed with stage 3 EGFR+ NSCLC that has spread to nearby tissues and can’t be removed by surgery and are getting ready to start treatment with TAGRISSO after CRT, download our TAGRISSO brochure.

If you’ve been diagnosed with locally advanced or metastatic EGFR+ NSCLC and are getting ready to start treatment with TAGRISSO + chemotherapy, download our brochure.

  • Store TAGRISSO at room temperature between 68 °F and 77 °F (20 °C to 25 °C)
  • Safely throw away medicine that is out of date or that you no longer need
  • Keep TAGRISSO and all medicines out of the reach of children

General information about the safe and effective use of TAGRISSO.

  • Medicines are sometimes prescribed for purposes other than those listed in a Patient Information leaflet. Do not use TAGRISSO for a condition for which it was not prescribed. Do not give TAGRISSO to other people, even if they have the same symptoms you have. It may harm them. You can ask your pharmacist or healthcare provider for information about TAGRISSO that is written for health professionals

 

  • Active ingredient: osimertinib
  • Inactive ingredients: mannitol, microcrystalline cellulose, low-substituted hydroxypropyl cellulose, and sodium stearyl fumarate. Tablet coating contains: polyvinyl alcohol, titanium dioxide, macrogol 3350, talc, ferric oxide yellow, ferric oxide red and ferric oxide black

 

Before your next office visit,
see common questions about
TAGRISSO and locally advanced stage 3 EGFR+ NSCLC that cannot be removed by surgery

Support is available for patients who may need help accessing TAGRISSO

If you’ve been diagnosed with stage 3 EGFR+ NSCLC that can’t be removed by surgery and are getting ready to start treatment with TAGRISSO after chemotherapy and radiation treatment, download our TAGRISSO brochure.

If you’ve been diagnosed with locally advanced or metastatic EGFR+ NSCLC and are getting ready to start treatment with TAGRISSO + chemotherapy, download our brochure.

IMPORTANT SAFETY INFORMATION

TAGRISSO may cause serious side effects, including:

  • Lung problems. TAGRISSO may cause severe lung problems that may lead to death. Symptoms may be similar to those symptoms from lung cancer. Tell your healthcare provider right away if you have any new or worsening lung symptoms, including trouble breathing, shortness of breath, cough, or fever
  • Heart problems, including heart failure. TAGRISSO may cause heart problems that may lead to death. Your healthcare provider should check your heart function before you start taking TAGRISSO and during treatment as needed. Tell your healthcare provider right away if you have any of the following signs and symptoms of a heart problem: feeling like your heart is pounding or racing, shortness of breath, swelling of your ankles and feet, dizziness, feeling lightheaded, or feeling faint
  • Eye problems. TAGRISSO may cause eye problems. Tell your healthcare provider right away if you have symptoms of eye problems which may include watery eyes, sensitivity to light, eye pain, eye redness, or vision changes. Your healthcare provider may send you to see an eye specialist (ophthalmologist) if you get eye problems with TAGRISSO
  • Skin problems. TAGRISSO may cause skin problems. Tell your healthcare provider right away if you develop skin reactions that look like rings (target lesions), severe blistering or peeling of the skin
  • Inflammation of the blood vessels in your skin. TAGRISSO may cause blood vessel problems in your skin. Tell your healthcare provider right away if you develop purple spots or redness of the skin that does not fade in color when pressed (non-blanching) on your lower arms, lower legs, or buttocks or large hives on the main part of your body (trunk) that do not go away within 24 hours and look bruised
  • Blood and bone marrow problems. TAGRISSO may cause a condition where your bone marrow cannot make enough new blood cells (aplastic anemia), and which may lead to death. Your healthcare provider will monitor your blood cell counts before you start and during treatment with TAGRISSO. Tell your healthcare provider right away if you develop any signs and symptoms of blood and bone marrow problems, including a new fever or fever that does not go away (100.4 °F), easy bruising or bleeding that will not stop, unusually pale skin, infection, tiredness, or weakness

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

  • have lung or breathing problems other than your lung cancer
  • have heart problems, including a condition called long QTc syndrome
  • have problems with your electrolytes, such as sodium, potassium, calcium or magnesium
  • have a history of eye problems
  • are pregnant or plan to become pregnant. TAGRISSO can harm your unborn baby. Tell your healthcare provider right away if you become pregnant during treatment with TAGRISSO or think you may be pregnant
  • Females who are able to become pregnant should have a pregnancy test before starting treatment with TAGRISSO. You should use effective birth control (contraception) during treatment with TAGRISSO and for 6 weeks after the last dose of TAGRISSO
  • Males who have female partners that are able to become pregnant should use effective birth control during treatment with TAGRISSO and for 4 months after the last dose of TAGRISSO
  • females who are breastfeeding or plan to breastfeed. It is not known if TAGRISSO passes into your breast milk. Do not breastfeed during treatment with TAGRISSO and for 2 weeks after your last dose of TAGRISSO. Talk to your healthcare provider about the best way to feed your baby during this time

Tell your healthcare provider about all the medicines you take, including prescription and over-the-counter medicines, vitamins, or herbal supplements. Especially tell your healthcare provider if you take a heart or blood pressure medicine

The most common side effects of TAGRISSO when given alone include:

  • low white blood cell counts
  • low platelet counts
  • low red blood cell counts (anemia)
  • diarrhea
  • rash
  • muscle, bone, or joint pain
  • changes in your nails, including: redness, tenderness, pain, inflammation, brittleness, separation from the nailbed, and shedding of nail
  • dry skin
  • mouth sores
  • tiredness
  • low white blood cell counts
  • low platelet counts
  • low red blood cell counts (anemia)
  • diarrhea
  • rash
  • muscle, bone, or joint pain
  • changes in your nails, including: redness, tenderness, pain, inflammation, brittleness, separation from the nailbed, and shedding of nail
  • dry skin
  • mouth sores
  • tiredness

The most common side effects of TAGRISSO when given alone after treatment with platinum-based chemotherapy and radiation treatment include:

  • low white blood cell counts
  • lung problems
  • low platelet counts
  • rash
  • diarrhea
  • changes in your nails, including: redness, tenderness, pain, inflammation, brittleness, separation from the nailbed, and shedding of nail
  • cough
  • COVID-19
  • low white blood cell counts
  • lung problems
  • low platelet counts
  • rash
  • diarrhea
  • changes in your nails, including: redness, tenderness, pain, inflammation, brittleness, separation from the nailbed, and shedding of nail
  • cough
  • COVID-19

The most common side effects of TAGRISSO in combination with pemetrexed and platinum-based chemotherapy include:

  • low white blood cell counts
  • low platelet counts
  • rash
  • diarrhea
  • mouth sores
  • changes in your nails, including: redness, tenderness, pain, inflammation, brittleness, separation from the nailbed, and shedding of nail
  • dry skin
  • increase of a substance in the blood called creatinine
  • low white blood cell counts
  • low platelet counts
  • rash
  • diarrhea
  • mouth sores
  • changes in your nails, including: redness, tenderness, pain, inflammation, brittleness, separation from the nailbed, and shedding of nail
  • dry skin
  • increase of a substance in the blood called creatinine

Tell your healthcare provider if you have any side effect that bothers you or that does not go away.

These are not all the possible side effects of TAGRISSO. For more information, ask your healthcare provider or pharmacist.

What is TAGRISSO?

TAGRISSO is a prescription medicine used to treat adults with non-small cell lung cancer (NSCLC) that has certain abnormal epidermal growth factor receptor (EGFR) gene(s):

  • to help prevent your lung cancer from coming back after your tumor(s) has been removed by surgery, or
  • when your lung cancer has spread to nearby tissues (locally advanced), that is unable to be removed (unresectable) by surgery and has responded or stabilized following chemotherapy and radiation treatment, or
  • as your first treatment when your lung cancer has spread to other parts of the body (metastatic), or
  • in combination with pemetrexed and platinum-based chemotherapy, as your first treatment when your lung cancer has spread to nearby tissues (locally advanced) or to other parts of the body (metastatic), or
  • when your lung cancer has spread to other parts of the body (metastatic) and you have had previous treatment with an EGFR tyrosine kinase inhibitor (TKI) medicine that did not work or is no longer working.

Your healthcare provider will perform a test to make sure that TAGRISSO is right for you.
It is not known if TAGRISSO is safe and effective in children.

Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.

EGFR is epidermal growth factor receptor; EGFR+ is epidermal growth factor receptor mutation-positive; NSCLC is non-small cell lung cancer.

EGFR+ is epidermal growth factor receptor mutation-positive; NSCLC is non-small cell lung cancer.

IMPORTANT SAFETY INFORMATION

see-more