abemaciclib
Trade Name:Verzenio®
Appearance:tablet
in various strengths, shapes and colours
Monograph Name:abemaciclib
Monograph Body:
Abemaciclib inhibits cyclin-dependent kinases 4 and 6 (CDK4 and CDK6). It blocks retinoblastoma tumor suppressor protein phosphorylation and prevents progression through the cell cycle, resulting in arrest at the G1 phase, leading to suppression of tumour growth.
Bioavailability |
45% (following a single 200 mg oral dose) |
Effects with food |
Cmax increased by 26%; AUC increased by 9%, after a high-fat, high-calorie meal |
Time to reach steady state |
5 days (following repeated twice daily dosing) |
Peak plasma levels |
8 hours |
PPB |
96-98% |
Cross blood brain barrier? |
Yes |
Active metabolites |
Yes |
Inactive metabolites |
Yes |
Feces |
81%, mainly as metabolites |
Urine |
3% |
Half-life |
24.8 hours |
- Breast cancer (HR positive, HER2 negative)
Refer to the product monograph for a full list of approved indications.
Emetogenic Potential:
The following table contains adverse effects from a phase III trial of early breast cancer patients (monarchE) where the incidences in patients receiving abemaciclib in combo with endocrine therapy were ≥2% more than endocrine therapy alone . Adverse effects from the advanced breast cancer clinical trial (Monarch 3) with abemaciclib in combination with anastrozole or letrozole are marked with “†”. Severe adverse events from other studies or post-marketing may also be included.
ORGAN SITE | SIDE EFFECT* (%) | ONSET** | |||
---|---|---|---|---|---|
Cardiovascular | Arterial thromboembolism (rare) | E | |||
Cardiotoxicity (rare) | E | ||||
Hypotension (rare) | E | ||||
Venous thromboembolism (2%) | E | ||||
Dermatological | Alopecia (10%) (≤ Grade 2) | E | |||
Dry skin (10%) † | E | ||||
Hand-foot syndrome (rare) | E | ||||
Nail disorder (5%) | D | ||||
Rash, pruritus (10%) | E | ||||
Gastrointestinal | Anorexia, weight loss (12%) | E | |||
Constipation (10%) | E | ||||
Diarrhea (83%) (8% severe) | E | ||||
Dry mouth (5%) † | E | ||||
Dyspepsia (8%) | E | ||||
Mucositis (13%) | E | ||||
Nausea, vomiting (29%) (Generally mild) | E | ||||
General | Edema - limbs (10%) † | E | |||
Fall (6%) † | E | ||||
Fatigue (39%) | E | ||||
Flu-like symptoms (12%) † | E | ||||
Other - Lymphedema (10%) | E | ||||
Hematological | Myelosuppression (45%) (19% severe, including febrile neutropenia ≤1%) | E D | |||
Hepatobiliary | ↑ LFTs (10%) (severe 2%) | E D | |||
Hypersensitivity | Hypersensitivity (rare) | E | |||
Infection | Infection (48%) (severe 4%) | E | |||
Metabolic / Endocrine | Abnormal electrolyte(s) (9%) † (↓ PO4, ↓ K, ↓ Ca) | E | |||
Musculoskeletal | Musculoskeletal pain (21%) | E | |||
Nervous System | Dizziness (10%) | E | |||
Dysgeusia (5%) | E | ||||
Headache (18%) | E | ||||
Ophthalmic | Dry eye (5%) | E | |||
Watering eyes (5%) † | E | ||||
Renal | Creatinine increased (21%) † | E | |||
Nephrotoxicity (rare) | I E | ||||
Respiratory | Cough, dyspnea (15%) † | E | |||
Pneumonitis (5%) | E |
* "Incidence" may refer to an absolute value or the higher value from a reported range.
"Rare"
may refer to events with < 1% incidence, reported in post-marketing, phase 1 studies,
isolated data or anecdotal
reports.
** I = immediate (onset in hours to days)
E = early (days to weeks)
D = delayed (weeks to months)
L = late (months to years)
The most common side effects for abemaciclib include diarrhea, infection, myelosuppression, fatigue, nausea/vomiting, creatinine increased, musculoskeletal pain, headache, cough/dyspnea and mucositis.
Diarrhea is the most common adverse reaction across clinical studies with a higher incidence during the initial month of treatment. Grade 3 diarrhea has occurred but Grade 4 has not been reported. Diarrhea had been associated with dehydration and infection. The median time to onset of the first diarrhea event was 6 to 8 days and the median duration of grade 2 and 3 diarrhea was 9 to 11 days and 6 to 8 days, respectively.
Myelosuppression was reported in patients receiving abemaciclib. Grade 3 or higher neutropenia has been observed with both monotherapy and combination therapy. The median time to first episode of neutropenia (≥ grade 3) was 29 to 37 days and the median duration of ≥ grade 3 neutropenia was 12 to 15 days. Febrile neutropenia has occurred rarely, and deaths due to neutropenic sepsis have been observed.
Venous thromboembolism (VTE), including deep vein thrombosis (DVT), pulmonary embolism, pelvic venous thrombosis, cerebral venous thrombosis, subclavian and axillary vein thrombosis, and inferior vena cava thrombosis have been reported in up to 6% of patients. Deaths due to VTE have occurred.
Hepatotoxicity and increases in ALT have been reported including Grade 3 or higher events. The median time to onset of ≥ grade 3 ALT elevation was 57 to 87 days and the median time to resolution (to < grade 3) was 13-14 days.
Severe, life threatening and fatal interstitial lung disease (ILD)/pneumonitis has been reported with abemaciclib. Across clinical trials, 3.2% of patients had ILD/pneumonitis of any grade with 0.4% of patients experiencing ≥ grade 3 ILD. The median time to onset was 8.2 months.
A higher rate of infections was reported in patients who received abemaciclib plus endocrine therapy compared to patients treated with placebo plus endocrine therapy. Infections were also reported in patients on single agent abemaciclib. Fatal cases were reported in clinical trials.
Abemaciclib may increase serum creatinine, without affecting glomerular function, by inhibiting renal tubular secretion transporters. It was observed within the first month of abemaciclib clinical trials. Serum creatinine levels remained elevated but stable during treatment, and were reversible at treatment discontinuation. Consider alternative markers that are not based on creatinine (e.g. BUN) for determining renal function.
Refer to protocol by which patient is being treated.
Screen for hepatitis B virus in all cancer patients starting systemic treatment. Refer to the hepatitis B virus screening and management guideline.
Monotherapy:
Oral: 200 mg BID
In combination with endocrine therapy*:
Oral: 150 mg BID
*Pre/perimenopausal women, and men treated with abemaciclib AND an aromatase inhibitor, tamoxifen, or fulvestrant should be treated with a gonadotropin releasing hormone (GnRH) agonist, according to local clinical practice.
Dose Level | Abemaciclib Dose (mg BID) | |
Combination with Endocrine Therapy |
Single Agent | |
0 | 150 | 200 |
-1 | 100 | 150 |
-2 | 50 | 100 |
-3 | Discontinue | 50 |
-4 | Not applicable | Discontinue |
Toxicity |
Grade |
Action |
Hematologic* | Grade 3 | Hold until ≤ grade 2; resume at same dose. |
Grade 4 or recurrent grade 3 | Hold until ≤ grade 2; resume at 1 dose level ↓. | |
Diarrhea** | Grade 2 |
If no resolution to ≤ grade 1 within 24 hours, hold until resolution; resume at same dose. |
Grade 2 that persists/recurs after resumption at the same dose (despite maximal supportive measures) | Hold until ≤ grade 1; resume at 1 dose level ↓. | |
≥ Grade 3 or requires hospitalization | ||
Interstitial lung disease (ILD)/ Pneumonitis | Persistent or recurrent grade 2 toxicity that does not resolve to baseline or grade 1 within 7 days (despite maximal supportive measures) | Hold until recovery to baseline or ≤ grade 1; resume at 1 dose level ↓. |
Grade 3 or 4 | Discontinue | |
Hepatotoxicity | Persistent or recurrent grade 2, or grade 3 (ALT, AST >5 to 20 times ULN), WITHOUT increase in total bilirubin >2 times ULN | Hold until recovery to baseline or grade 1; resume at 1 dose level ↓. |
AST and/or ALT >3 times ULN with total bilirubin >2 times ULN (in the absence of cholestasis) | Discontinue | |
Grade 4 (ALT, AST >20 times ULN) | Discontinue | |
Venous thromboembolism | Grade 1 or 2 |
Early breast cancer: Hold; restart when patient is stable and if clinically appropriate Metastatic breast cancer: No dose modification required |
Grade 3 or 4 | For early or metastatic breast cancer: Hold; restart when patient is stable and if clinically appropriate | |
All other non-hematologic toxicities | Persistent or recurrent grade 2 toxicity that does not resolve to baseline or grade 1 within 7 days (despite maximal supportive measures) | Hold until recovery to baseline or ≤ grade 1; resume at 1 dose level ↓. |
Grade 3 or 4 |
*If blood cell growth factors are required, hold abemaciclib for at least 48 hours after the last growth factor dose and until toxicity resolves to ≤ grade 2; resume at the next lower dose (unless already reduced due to the toxicity that required the growth factor). Growth factor use is as per current local guidelines.
**At the first sign of loose stools, begin management with antidiarrheal agents (i.e. loperamide) and increase oral fluid intake.
Hepatic Impairment | Abemaciclib Dose |
Mild or moderate impairment (Child-Pugh class A or B) | No dosage adjustment necessary. |
Severe impairment (Child-Pugh class C) | Reduce abemaciclib frequency to once daily. |
Renal Impairment | Abemaciclib Dose |
Mild or Moderate (CrCl ≥ 30 mL/min) | No dosage adjustment necessary. |
Severe (CrCl < 30 mL/min); ESRD | Has not been studied |
No dosage adjustment is required. No overall differences in safety or efficacy between patients ≥ 65 years of age and younger. Patients ≥65 years of age reported more hematologic adverse events, hypokalemia (including grade 3), hypocalcemia, grade ≥3 infections, decreased appetite, and increased blood creatinine compared to younger patients in a subgroup analysis from clinical studies.
No dose adjustment based on race is required. Higher incidences of increased ALT and AST and neutropenia have been reported in East Asian patients compared to Caucasian patients in clinical trials.
Safety and efficacy have not been established.
- Abemaciclib tablets should be swallowed whole (do not chew, crush, or split tablets before swallowing). Tablets should not be ingested if they are not intact.
- Abemaciclib doses may be taken with or without food and should be administered at approximately the same times every day.
- Avoid fruit or juice from grapefruit, Seville oranges or starfruit.
- Abemaciclib tablets contain lactose; carefully consider use in patients with hereditary galactose intolerance, severe lactase deficiency or glucose-galactose malabsorption
- If a dose is missed or vomited, the next dose should be taken at the scheduled time. The patient should not take 2 doses at the same time to make up for the missed dose.
- Store at room temperature (15°C to 30°C).
- Patients who are hypersensitive to this drug or to any ingredient in the formulation or component of the container.
- There are no data regarding abemaciclib safety or efficacy in patients with prior exposure to other CDK 4/6 inhibitors.
Other Drug Properties:
-
Carcinogenicity:
No data
-
Genotoxicity:
Unlikely
Not observed in animal studies
-
Teratogenicity:
Yes
-
Embryotoxicity:
Yes
Observed in animal studies.
Abemaciclib is not recommended for use in pregnancy. Adequate contraception should be used by patients and their partners during treatment, and for at least 3 weeks after the last dose.
-
Breastfeeding:
Breastfeeding is not recommended during treatment and for at least 3 weeks after the last dose.
-
Fertility effects:
Probable
Abemaciclib may impair fertility in males.
Abemaciclib inhibits the renal transporters organic cation transporter 2 (OCT2), multidrug and extrusion toxin protein (MATE1), and MATE2.
In vitro, abemaciclib is a substrate of P-glycoprotein (P-gp) and breast cancer resistance protein (BCRP).
AGENT | EFFECT | MECHANISM | MANAGEMENT |
---|---|---|---|
Strong or moderate CYP3A inhibitors (i.e. ketoconazole, clarithromycin, ritonavir, fruit or juice from grapefruit, Seville oranges or starfruit) | ↑ abemaciclib concentration and/or toxicity | ↓ metabolism of abemaciclib | Avoid co-administration with strong CYP3A inhibitors. Use caution when co-administered with moderate CYP3A inhibitors. If co-administration with a CYP3A inhibitor is unavoidable, reduce abemaciclib dose to 50 mg twice daily when combined with strong or moderate CYP3A inhibitors. When combined with ketoconazole, abemaciclib dose should be reduced to 50 mg once daily. When combined with clarithromycin, diltiazem or verapamil, abemaciclib dose should be reduced to 100 mg twice daily. If the CYP3A inhibitor is discontinued, increase the abemaciclib dose (after 3-5 half-lives of the inhibitor) to the dose used before starting the inhibitor. |
Weak CYP3A inhibitors (e.g. ranitidine) | ↑ abemaciclib concentration and/or toxicity | ↓ metabolism of abemaciclib | Use with caution. If co-administration with a weak CYP3A inhibitor is unavoidable, reduce abemaciclib dose to 100 mg twice daily. If the CYP3A inhibitor is discontinued, increase the abemaciclib dose (after 3-5 half-lives of the inhibitor) to the dose used before starting the inhibitor. |
CYP3A inducers (i.e. phenytoin, rifampin, dexamethasone, carbamazepine, phenobarbital, St. John’s Wort, etc) | ↓ abemaciclib concentration and/or efficacy | ↑ metabolism of abemaciclib | Avoid co-administration with strong CYP3A inducers. Consider alternative agents with less CYP3A induction. Use with caution when co-administered with moderate or weak CYP3A inducers. |
OCT2, MATE1, MATE2 substrates (i.e. metformin) | ↑ substrate concentration and/or toxicity | ↓ substrate renal clearance and secretion | Caution |
Treating physicians may decide to monitor more or less frequently for individual patients but should always consider recommendations from the product monograph.
Refer to the hepatitis B virus screening and management guideline for monitoring during and after treatment.
Monitor Type | Monitor Frequency |
---|---|
CBC |
Baseline, every two weeks for the first 2 months, monthly for the next 2 months, and as clinically indicated. |
Liver function tests |
Baseline, every 2 weeks for the first 2 months, monthly for the next 2 months, and as clinically indicated. |
Renal function tests* |
Baseline and as clinically indicated |
Clinical toxicity assessment for signs and symptoms of venous thrombosis, infections, gastrointestinal, respiratory, dermatologic effects and fatigue |
At each visit |
Grade toxicity using the current NCI-CTCAE (Common Terminology Criteria for Adverse Events) version
*Abemaciclib may increase serum creatinine, without affecting glomerular function, by inhibiting renal tubular secretion transporters. Consider alternative markers that are not based on creatinine (e.g. BUN) for determining renal function.
Monitor Type | Monitor Frequency |
---|---|
Electrolytes (including calcium) |
Baseline and as clinically indicated |
Exceptional Access Program (EAP Website)
- abemaciclib - For the adjuvant treatment, in combination with endocrine therapy, of adult patients with HR-positive, HER2-negative, node-positive early breast cancer at high risk of disease recurrence, according to criteria
Dickler MN, Tolaney SM, Rugo HS, et al. MONARCH 1, a phase 2 study of abemaciclib, a CDK4 and CDK6 inhibitor, as a single agent, in patients with refractory HR+/HER2- metastatic breast cancer. Clin Cancer Res. 2017;23(17):5218-24.
Goetz MP, Toi M, Campone M, et al. MONARCH 3: Abemaciclib as initial therapy for advanced breast cancer. J Clin Oncol. 2017 Nov 10;35(32):3638-46.
Johnston SRD, Harbeck N, Hegg R. Abemaciclib Combined With Endocrine Therapy for the Adjuvant Treatment of HR+, HER2-, Node-Positive, High-Risk, Early Breast Cancer (monarchE). J Clin Oncol. 2020 Dec 1;38(34):3987-98.
Sledge GW, Toi M, Neven P, et al. MONARCH 2: Abemaciclib in combination with fulvestrant in women with HR+/HER2- advanced breast cancer who had progressed while receiving endocrine therapy. J Clin Oncol. 2017;35:2875-84.
Verzenio (abemaciclib) product monograph. Toronto, Ontario: Eli Lilly Canada Inc., January 2022.
February 2025 Updated Supplementary Public Funding section
Refer to the New Drug Funding Program or Ontario Public Drug Programs websites for the most up-to-date public funding information.
The information set out in the drug monographs, regimen monographs, appendices and symptom management information (for health professionals) contained in the Drug Formulary (the "Formulary") is intended for healthcare providers and is to be used for informational purposes only. The information is not intended to cover all possible uses, directions, precautions, drug interactions or adverse effects of a particular drug, nor should it be construed to indicate that use of a particular drug is safe, appropriate or effective for a given condition. The information in the Formulary is not intended to constitute or be a substitute for medical advice and should not be relied upon in any such regard. All uses of the Formulary are subject to clinical judgment and actual prescribing patterns may not follow the information provided in the Formulary.
The format and content of the drug monographs, regimen monographs, appendices and symptom management information contained in the Formulary will change as they are reviewed and revised on a periodic basis. The date of last revision will be visible on each page of the monograph and regimen. Since standards of usage are constantly evolving, it is advised that the Formulary not be used as the sole source of information. It is strongly recommended that original references or product monograph be consulted prior to using a chemotherapy regimen for the first time.
Some Formulary documents, such as the medication information sheets, regimen information sheets and symptom management information (for patients), are intended for patients. Patients should always consult with their healthcare provider if they have questions regarding any information set out in the Formulary documents.
While care has been taken in the preparation of the information contained in the Formulary, such information is provided on an “as-is” basis, without any representation, warranty, or condition, whether express, or implied, statutory or otherwise, as to the information’s quality, accuracy, currency, completeness, or reliability.
CCO and the Formulary’s content providers shall have no liability, whether direct, indirect, consequential, contingent, special, or incidental, related to or arising from the information in the Formulary or its use thereof, whether based on breach of contract or tort (including negligence), and even if advised of the possibility thereof. Anyone using the information in the Formulary does so at his or her own risk, and by using such information, agrees to indemnify CCO and its content providers from any and all liability, loss, damages, costs and expenses (including legal fees and expenses) arising from such person’s use of the information in the Formulary.
Dickler MN, Tolaney SM, Rugo HS, et al. MONARCH 1, a phase 2 study of abemaciclib, a CDK4 and CDK6 inhibitor, as a single agent, in patients with refractory HR+/HER2- metastatic breast cancer. Clin Cancer Res. 2017;23(17):5218-24.
Goetz MP, Toi M, Campone M, et al. MONARCH 3: Abemaciclib as initial therapy for advanced breast cancer. J Clin Oncol. 2017 Nov 10;35(32):3638-46.
Johnston SRD, Harbeck N, Hegg R. Abemaciclib Combined With Endocrine Therapy for the Adjuvant Treatment of HR+, HER2-, Node-Positive, High-Risk, Early Breast Cancer (monarchE). J Clin Oncol. 2020 Dec 1;38(34):3987-98.
Sledge GW, Toi M, Neven P, et al. MONARCH 2: Abemaciclib in combination with fulvestrant in women with HR+/HER2- advanced breast cancer who had progressed while receiving endocrine therapy. J Clin Oncol. 2017;35:2875-84.
Verzenio (abemaciclib) product monograph. Toronto, Ontario: Eli Lilly Canada Inc., January 2022.
abemaciclib (patient)
Info Sheet Introduction:For treating certain types of breast cancer
Info Sheet Date: Mercredi, août 23, 2023 Info Sheet body:Other Name: Verzenio®
in various strengths, shapes and colours
For treating certain types of breast cancer
Tell your health care team if you have or had significant medical condition(s), such as:
- lung, liver or kidney problems
- any blood clots or
- any allergies
Abemaciclib tablets contain a small amount of lactose. If you cannot have lactose, talk to your healthcare team.
Remember to:
- Tell your health care team about all of the other medications you are taking.
- Keep taking other medications that have been prescribed for you, unless you have been told not to by your health care team.
You will have a blood test to check for hepatitis B before starting treatment. See the Hepatitis B and Cancer Medications pamphlet for more information.
Talk to your health care team about:
-
How this treatment may affect your sexual health.
-
How this treatment may affect your ability to have a baby, if this applies to you.
This treatment may harm an unborn baby. Tell your health care team if you or your partner are pregnant, become pregnant during treatment, or are breastfeeding.
-
If there is any chance of pregnancy happening, you and your partner together must use 2 effective forms of birth control at the same time until at least 3 weeks after your last treatment dose. Talk to your health care team about which birth control options are best for you.
-
Do not use hormonal birth control (such as birth control pills), unless your health care team told you that they are safe. Talk to your health care team about the safest birth control for you.
-
Do not breastfeed while on this treatment and for 3 weeks after your last dose.
-
This medication is usually taken twice a day by mouth. Talk to your health care team about how and when to take your medication
-
Swallow whole with a glass of water, with or without food.
-
Take the dose at about the same time(s) each day.
-
Do not split, crush or chew the tablets.
-
DO NOT eat or drink grapefruit, starfruit, Seville oranges or their juices (or products that contain these) while taking this drug. They may increase the amount of drug in your blood and increase side effects.
-
If you vomit (throw up) after taking a dose, do not repeat the dose. Take your next dose at your normal time.
-
If you miss a dose, skip it and take your next dose as you normally do. Do not take an extra dose to make up for the missed dose.
To Treat Diarrhea
Abemaciclib can cause diarrhea. Diarrhea is when you have loose bowel movements (watery poo) or you need to go poo (have bowel movements) more often than usual. Diarrhea may start a few days after your treatment.
You may be given a medication called loperamide (Imodium®) to help treat your diarrhea. Take this medication only if you need it. Keep your loperamide with you all the time. When diarrhea starts, take the loperamide right away and drink more fluids.
-
Will this medication interact with other medications or natural health products?
-
This medication can interact with other medications, vitamins, foods and natural health products. Interactions can make the treatment not work as well or cause severe side effects.
-
Tell your health care team about all of your:
-
prescription and over-the-counter (non-prescription) medications and all other drugs, such as cannabis/marijuana (medical or recreational)
-
natural health products such as vitamins, herbal teas, homeopathic medicines, and other supplements
-
-
Check with your health care team before starting or stopping any of them.
-
-
If you take seizure medications (such as phenytoin), your health care team may monitor your blood levels closely and may change your dose.
-
What should I do if I feel unwell, have pain, a headache or a fever?
-
Always check your temperature to see if you have a fever before taking any medications for fever or pain (such as acetaminophen (Tylenol®) or ibuprofen (Advil®)).
-
Fever can be a sign of infection that may need treatment right away.
-
If you take these medications before you check for fever, they may lower your temperature and you may not know you have an infection.
-
How to check for fever:
Keep a digital (electronic) thermometer at home and take your temperature if you feel hot or unwell (for example, chills, headache, mild pain).
- You have a fever if your temperature taken in your mouth (oral temperature) is:
- 38.3°C (100.9°F) or higher at any time
OR
- 38.0°C (100.4°F) or higher for at least one hour.
- 38.3°C (100.9°F) or higher at any time
If you do have a fever:- Try to contact your health care team. If you are not able to talk to them for advice, you MUST get emergency medical help right away.
- Ask your health care team for the Fever pamphlet for more information.
If you do not have a fever but have mild symptoms such as headache or mild pain:
-
Ask your health care team about the right medication for you. Acetaminophen (Tylenol®) is a safe choice for most people.
-
Talk to your health care team before you start taking Ibuprofen (Advil®, Motrin®), naproxen (Aleve®) or ASA (Aspirin®), as they may increase your chance of bleeding or interact with your cancer treatment.
-
Talk to your health care team if you already take low dose aspirin for a medical condition (such as a heart problem). It may still be safe to take.
-
What to DO while on this medication:
-
DO check with your health care team before getting any vaccinations, surgery, dental work or other medical procedures.
What NOT to DO while on this medication:
-
DO NOT eat or drink grapefruit, starfruit, Seville oranges or their juices (or products that contain these) while taking this drug. They may increase the amount of drug in your blood and increase side effects.
-
DO NOT smoke or drink alcohol while on treatment without talking to your health care team first. Smoking and drinking can make side effects worse and make your treatment not work as well.
-
Do not throw out any unused medications at home. Bring them to your pharmacy to be thrown away safely.
-
Keep this medication in the original packaging at room temperature in a dry place, away from heat and light. Keep out of sight and reach of children and pets.
-
How to safely touch oral anti-cancer medications
If you are a patient:
-
Wash your hands before and after touching your oral anti-cancer medication.
-
Swallow each pill whole. Do not crush or chew your pills.
If you are a caregiver:
-
Wear nitrile or latex gloves when touching tablets, capsules or liquids.
-
Wash your hands before putting on your gloves and after taking them off, even if your skin did not touch the oral anti-cancer medication.
-
Throw out your gloves after each use. Do not re-use gloves.
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Do not touch oral anti-cancer medications if you are pregnant or breastfeeding.
-
-
What to do if oral anti-cancer medication gets on your skin or in your eyes
If medication gets on your skin:
-
Wash your skin with a lot of soap and water.
-
If your skin gets red or irritated, talk to your health care team.
If medication gets in your eyes:-
Rinse your eyes with running water right away. Keep water flowing over your open eyes for at least 15 minutes.
-
The following table lists side effects that you may have when taking abemaciclib. The table is set up to list the most common side effects first and the least common last.
It is unlikely that you will have all of the side effects listed and you may have some that are not listed.
Read over the side effect table so that you know what to look for and when to get help. Refer to this table if you experience any side effects while on abemaciclib.
Very Common Side Effects (50 or more out of 100 people) | |
Side effects and what to do | When to contact health care team |
Diarrhea (may be severe) What to look for?
What to do? If you have diarrhea:
|
Talk to your health care team if no improvement after 24 hours of taking diarrhea medication or if severe (more than 7 times in one day) |
Common Side Effects (25 to 49 out of 100 people) | |
Side effects and what to do | When to contact health care team |
Low neutrophils (white blood cells) in the blood (neutropenia) (may be severe) When neutrophils are low, you are at risk of getting an infection more easily. Ask your health care team for the Neutropenia (Low white blood cell count) pamphlet for more information. What to look for?
You have a fever if your temperature taken in your mouth (oral temperature) is:
What to do? If your health care team has told you that you have low neutrophils:
If you have a fever: If you have a fever, try to contact your health care team. If you are unable to talk to the team for advice, you must get emergency medical help right away.
|
If you have a fever, try to contact your health care team. If you are unable to talk to the team for advice, you MUST get emergency medical help right away. |
Low platelets in the blood When your platelets are low, you are at risk for bleeding and bruising. Ask your health care team for the Low Platelet Count pamphlet for more information. What to look for?
What to do? If your health care team has told you that you have low platelets:
If you have signs of bleeding:
If you have bleeding that does not stop or is severe (very heavy), you must get emergency medical help right away.
|
Talk to your health care team if you have any signs of bleeding. If you have bleeding that doesn’t stop or is severe (very heavy), you MUST get emergency help right away. |
Fatigue What to look for?
What to do?
Ask your health care team for the Fatigue pamphlet for more information. |
Talk to your health care team if it does not improve or if it is severe |
Nausea and vomiting (Generally mild) What to look for?
To help prevent nausea:
|
Talk to your health care team if nausea lasts more than 48 hours or vomiting lasts more than 24 hours or if severe |
Less Common Side Effects (10 to 24 out of 100 people) | |
Side effects and what to do | When to contact health care team |
Abnormal kidney lab tests Your health care team may check your kidney function regularly with a blood test. What to look for?
What to do?
|
Talk to your health care team if it does not improve or if it is severe |
Headache; Mild joint, muscle pain or cramps What to look for?
What to do?
Ask your health care team for the Pain pamphlet for more information. |
Talk to your health care team if it does not improve or if it is severe |
Cough and feeling short of breath (May be severe) What to look for?
What to do?
|
Talk to your health care team. If you are not able to talk to your health care team for advice, and you have a fever or severe symptoms, you MUST get emergency medical help right away. |
Mouth sores What to look for?
What to do? To help prevent mouth sores:
|
Talk to your health care team as soon as you notice mouth or lip sores or if it hurts to eat, drink or swallow |
Low appetite; Weight loss What to look for?
Ask your health care team for the Loss of Appetite pamphlet for more information. |
Talk to your health care team if it does not improve or if it is severe |
Liver problems (May be severe) Your health care team may check your liver function with a blood test. The liver changes do not usually cause any symptoms. What to look for?
If you have any symptoms of liver problems, get emergency medical help right away. |
Get emergency medical help right away |
Rash; itchiness, dry, itchy skin What to look for?
What to do? To prevent and treat dry skin:
Rash may be severe in some rare cases and cause your skin to blister or peel. If this happens, get emergency medical help right away. |
Talk to your health care team if it does not improve or if it is severe |
Hair thinning or loss (Generally mild) What to look for?
What to do?
|
Talk to your health care team if this bothers you |
Mild swelling What to look for?
What to do?
|
Talk to your health care team if it does not improve or if it is severe |
Constipation What to look for?
What to do? To help prevent constipation:
To help treat constipation:
Ask your health care team for the Constipation Pamphlet for more information. |
Talk to your health care team if it does not improve or if it is severe |
Dizziness What to look for?
|
Talk to your health care team if it does not improve or if it is severe |
Other rare, but serious side effects are possible.
If you experience ANY of the following, speak to your cancer health care provider or get emergency medical help right away:
-
Irregular heartbeat, chest pain or fainting (passing out).
-
Pain, swelling and hardening of a vein in an arm or leg
- Sudden or severe headache, trouble seeing, speaking, or using your arms and legs.
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Signs of an allergic reaction: Itchiness, rash, swollen lips, face or tongue, chest and throat tightness.
Who do I contact if I have questions or need help?My cancer health care provider is: ______________________________________________ During the day I should contact:________________________________________________ Evenings, weekends and holidays:______________________________________________
|
Other Notes:
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For more links on how to manage your symptoms go to www.cancercareontario.ca/symptoms.
The information set out in the medication information sheets, regimen information sheets, and symptom management information (for patients) contained in the Drug Formulary (the "Formulary") is intended to be used by health professionals and patients for informational purposes only. The information is not intended to cover all possible uses, directions, precautions, drug interactions or side effects of a certain drug, nor should it be used to indicate that use of a particular drug is safe, appropriate or effective for a given condition.
A patient should always consult a healthcare provider if he/she has any questions regarding the information set out in the Formulary. The information in the Formulary is not intended to act as or replace medical advice and should not be relied upon in any such regard. All uses of the Formulary are subject to clinical judgment and actual prescribing patterns may not follow the information provided in the Formulary.



- abemaciclib - For the adjuvant treatment, in combination with endocrine therapy, of adult patients with HR-positive, HER2-negative, node-positive early breast cancer at high risk of disease recurrence, according to criteria
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Cancer Type: Breast Type of Content: Drug Monograph Status: Null Info Sheet Status: Null Global Date: Jeudi, février 27, 2025 Universal Date: 2025-02-27 00:00:00 AddThis: Title URL: abemaciclib Drug Display Status: Active Revision Summary:Drug Monograph: Updated Supplementary Public Funding section