ribociclib
Trade Name:Kisqali™
Other Names:Kisqali™
Appearance:Tablet
Monograph Name:ribociclib
Monograph Body:
Ribociclib is an inhibitor of cyclin-dependent kinase (CDK) 4 and 6. The cyclin D-CDK4/6 complex regulates cell cycle progression through phosphorylation of the retinoblastoma protein (pRb). Inhibition of pRb phosphorylation arrests the cell cycle in the G1 phase, suppressing DNA synthesis and inhibiting cancer cell growth.
Effects with food |
No clinically significant effect on Cmax and AUC when administered with a high-fat, high-calorie meal |
Peak plasma levels |
1 to 4 hours |
Time to reach steady state |
8 days |
Bioavailability |
66% (after a single dose) |
PPB |
70% |
Distribution Sites |
Equally distributed between red blood cells and plasma |
Cross blood brain barrier? |
Relatively low brain penetration observed in animals with intact blood brain barriers. |
- Ribociclib undergoes extensive hepatic metabolism mainly via CYP3A4.
- No major metabolite was considered to have clinically relevant contribution to efficacy and safety.
Active metabolites |
No |
Inactive metabolites |
Yes |
Ribociclib is eliminated mainly via the feces, with a small contribution from the renal route.
Half-life |
32 hours |
Feces |
69% (total dose); 17% unchanged |
Urine |
23% (total dose); 12% unchanged |
- Breast cancer
Refer to the product monograph for a full list and details of approved indications.
Emetogenic Potential:
The adverse effects reported below were based on a phase III study of postmenopausal women with breast cancer, receiving ribociclib plus letrozole or placebo plus letrozole, where the incidence was > 2% more than placebo. Severe or life-threatening adverse effects from other sources and post-marketing are also included.
ORGAN SITE | SIDE EFFECT* (%) | ONSET** | |||
---|---|---|---|---|---|
Cardiovascular | QT interval prolonged (5%) (1% severe) | E | |||
Venous thromboembolism (4%) (may be severe) | E | ||||
Dermatological | Alopecia (35%) | E | |||
Rash, pruritus (24%) (may be severe) | I E | ||||
Toxic epidermal necrolysis (rare) | E | ||||
Gastrointestinal | Abdominal pain (21%) | E | |||
Anorexia, weight loss (22%) | E | ||||
Constipation (30%) | E | ||||
Diarrhea (41%) (2% severe) | E | ||||
Dry mouth (14%) | E | ||||
Dyspepsia (11%) | I E | ||||
Mucositis (16%) | E | ||||
Nausea, vomiting (55%) (3% severe) | I | ||||
General | Edema - limbs (19%) | E | |||
Fatigue (43%) | E | ||||
Hematological | Myelosuppression ± infection, bleeding (77%) (64% severe) | E | |||
Hepatobiliary | ↑ LFTs (23%) (12% severe; <1% hepatotoxicity) | D | |||
Metabolic / Endocrine | Abnormal electrolyte(s) (5%) (↓ Ca, ↓ K, ↓ PO4; 4% severe) | E | |||
Musculoskeletal | Musculoskeletal pain (27%) | E | |||
Nervous System | Dysgeusia (10%) | E | |||
Headache (29%) | E | ||||
Insomnia (17%) | E | ||||
Syncope (2%) | E | ||||
Ophthalmic | Dry eye (6%) | E | |||
Watering eyes (12%) | E | ||||
Renal | Creatinine increased (11%) (< 1% severe) | E | |||
Respiratory | Dyspnea (16%) | E | |||
Pneumonitis (rare) (may be severe) | E D |
* "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 ribociclib include myelosuppression ± infection, bleeding, nausea, vomiting, fatigue, diarrhea, alopecia, constipation, headache, musculoskeletal pain, rash, pruritus, and ↑ LFTs.
Neutropenia was the most frequently reported side effect in patients treated with ribociclib plus any combination. The median time to onset for Grade > 2 neutropenia was 17 days, while the median time to resolution to Grade < 3 was 12 days.
Drug induced liver injury [ALT or AST > 3 x upper limit of normal (ULN) and total bilirubin > 2 x ULN, without cholestasis] or Hy’s Law has been reported with ribociclib combination therapy. In patients treated with ribociclib plus letrozole or fulvestrant, recovery to normal levels occurred within 154 days or within 121 to 532 days, respectively, after ribociclib discontinuation.
Median time to onset of QTcF > 480 msec was 15 days regardless of combination and these changes were reversible upon withholding the dose or modification. QTc prolongation is expected to be maximal between days 8 to 21 of the 28-day cycle during steady state treatment.
Refer to protocol by which the 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.
Hypokalemia, hypomagnesemia and hypocalcemia should be corrected prior to starting or continuing ribociclib.
Ribociclib should be started only in patients with QTcF < 450 msec.
Pre/perimenopausal women, and men, treated with ribociclib and an aromatase inhibitor or fulvestrant should also be treated with luteinizing hormone-releasing hormone (LHRH) agonists according to local clinical practice.
Advanced or Metastatic Breast Cancer:
Oral: 600 mg/day on Days 1 to 21, followed by 7 days off treatment, in 28-day cycles
In combination with an aromatase inhibitor (e.g., letrozole) or fulvestrant. Refer to regimen monographs for dosing details.
Early Breast Cancer:
Refer to the product monograph for details.
Advanced or Metastatic Breast Cancer:
Dose Level | Ribociclib Dose (mg/day) (21 days on, 7 days off) |
0 | 600 |
-1 | 400 |
-2 | 200 |
-3 | Discontinue |
Toxicity | Severity | Ribociclib Dose | |
Neutropenia |
Grade 3 |
Hold dose until ANC > 1 x 109/L, then restart at the same dose level. If recurs, hold dose until ANC > 1 x 109/L, then restart with 1 dose level ↓. |
|
Grade 4 |
Hold dose until ANC > 1 x 109/L, then restart with 1 dose level ↓. |
||
QTcF | > 480 msec |
Hold dose until QTcF resolves to < 480 msec, then restart with 1 dose level ↓. If recurs, hold dose until QTcF resolves to < 480 msec, then restart with 1 dose level ↓. |
|
> 500 msec | Hold dose until QTcF resolves to < 480 msec, then restart with 1 dose level ↓. | ||
Torsade de Pointes, or polymorphic ventricular tachycardia, unexplained syncope or Signs/symptoms of serious arrhythmia |
Any | Discontinue. | |
Bilirubin ≤ 2 x ULN | and |
AST and/or ALT >3 to 5 x ULN (Grade 2) |
If Baseline Grade 2: continue at current dose. If Baseline Grade 0-1: hold dose until ≤ baseline, then restart at the same dose. If recurs, hold dose until ≤ baseline, then restart with 1 dose level ↓. |
and |
AST and/or ALT >5 to 20 x ULN (Grade 3) |
Hold dose until ≤ baseline, then restart with 1 dose level ↓. If recurs, discontinue. |
|
and |
AST and/or ALT >20 x ULN (Grade 4) |
Discontinue. | |
Bilirubin > 2 x ULN, in the absence of cholestasis |
and |
AST and/or ALT >3 x ULN (Grade > 2) irrespective of baseline |
Discontinue. |
Interstitial lung disease (ILD)/pneumonitis | Grade 2 (symptomatic) | Hold dose until recovery to Grade < 1, then restart with 1 dose level ↓. | |
Grade 3 or 4 | Discontinue. | ||
Severe cutaneous reactions (e.g. progressive widespread skin rash often with blisters or mucosal lesions) | Any | Discontinue. | |
Other related toxicity | Grade 3 |
Hold dose until Grade ≤ 1, then restart at same dose. If recurs, hold dose until Grade ≤ 1, then restart with 1 dose level ↓. |
|
Grade 4 | Discontinue. |
Ribociclib has not been studied in patients with moderate or severe hepatic impairment (ALT or AST > 5 x ULN or total serum bilirubin > ULN [except documented Gilbert’s syndrome]).
Advanced or Metastatic Breast Cancer:
Hepatic Impairment | Ribociclib Starting Dose |
Mild (Child-Pugh class A) | No dose adjustment recommended |
Moderate (Child-Pugh class B) | 400 mg once daily; initiate treatment only if benefit outweighs risk |
Severe (Child-Pugh class C) | 400 mg once daily; initiate treatment only if benefit outweighs risk |
Advanced or Metastatic Breast Cancer:
Creatinine Clearance† | Ribociclib Starting Dose |
≥ 30 | No dose adjustment recommended. |
15 to < 30 |
200 mg daily*; initiate treatment only if benefit outweighs risk. |
< 15 | No data available. |
†Reported as eGFR (mL/min/1.73m2)
*No data in breast cancer patients; data from healthy or non-cancer patients with severe renal impairment.
No adjustment of the starting dose is required. No overall difference in safety was observed between patients over 65 years of age and younger patients.
No clinically relevant effects of gender on ribociclib pharmacokinetics parameters.
No clinically relevant effects of race on ribociclib pharmacokinetics parameters.
The safety and efficacy of ribociclib in pediatric patients have not been established.
-
Administer ribociclib with or without food, approximately at the same time each day, preferably in the morning.
-
Tablets should be swallowed whole and not chewed, crushed or split prior to swallowing. Tablets that are broken, cracked, or otherwise not intact should not be ingested.
-
If the patient vomits after taking ribociclib, do not give an extra dose; give the next dose at the usual time.
-
If a dose is missed, it should be skipped and the next dose given at the usual time, the next day. Patients should not take extra doses to make up for a missed dose.
-
Grapefruit, starfruit, Seville oranges, their juices or products should be avoided during ribociclib treatment.
-
Confirm the storage information that is listed on the product packaging. There is a new ribociclib supply that requires storage in a refrigerator between 2-8°C. Once dispensed, patients should store ribociclib between 20-25°C for up to 2 months. Keep in the original package to protect from moisture.
- Patients with hypersensitivity to this drug or to any ingredient in the formulation.
- Patients with untreated congenital long QT syndrome, a QTcF interval of ≥ 450 msec at baseline, and those who are at significant risk of developing QTc prolongation (for example, uncontrolled or significant cardiac disease including recent myocardial infarction, congestive heart failure, unstable angina and bradyarrhythmia).
- Ribociclib is associated with concentration-dependent QTc prolongation, with expected maximal QTc prolongation during steady state treatment between days 8 and 21 of the 28-day cycle.
- Exercise caution in patients who are suspected to be at an increased risk of Torsades de Pointes during treatment with a QT-prolonging drug.
- Avoid use in patients with uncorrected hypokalemia, hypomagnesemia, or hypocalcemia and other risk factors.
- Use in caution in patients at risk of thromboembolic events.
- Patients should exercise caution when driving or operating machinery due to syncope.
Other Drug Properties:
-
Carcinogenicity:
Unknown
-
Phototoxicity:
Unlikely
-
Genotoxicity:
No
-
Embryotoxicity:
Documented in animals
-
Fetotoxicity:
Documented in animals
-
Teratogenicity:
Documented in animals
-
Pregnancy:
Ribociclib is not recommended for use in pregnancy. Adequate contraception should be used by patients and their partners during treatment, and for at least 21 days after the last dose.
-
Excretion into breast milk:
Documented in animals
-
Breastfeeding:
Breastfeeding is not recommended during treatment and for at least 21 days after the last dose.
-
Fertility effects:
Probable
Documented in animal studies in male animals
- Ribociclib is primarily metabolized by CYP3A is a time-dependent inhibitor of CYP3A. Therefore, medicinal products which can influence CYP3A enzyme activity may alter the pharmacokinetics of ribociclib and ribociclib can affect the pharmacokinetics of co-administered CYP3A substrates. Ribociclib has weak inhibitory effects on CYP1A2 substrates though no induction of CYP1A2, CYP2B6, CYP2C9 or CYP3A4 was observed in vitro.
- Ribociclib may inhibit BCRP, OCT2, Multidrug and Toxic Compound Extrusion Protein-1 (MATE1) and human Bile Salt Export Pump (BSEP). Monitor patients closely when co-administering ribociclib and substrates of these transporters.
- There is no clinically relevant interaction with letrozole, exemestane, anastrozole or fulvestrant.
- There is no expected interaction with goserelin.
AGENT | EFFECT | MECHANISM | MANAGEMENT |
---|---|---|---|
CYP3A4 inhibitors (e.g. ketoconazole, clarithromycin, ritonavir, fruit or juice from grapefruit, Seville oranges or starfruit) | ↑ ribociclib exposure (e.g. ritonavir ↑ ribociclib exposure by 3.2-fold) | ↓ metabolism of ribociclib | Avoid strong CYP3A4 inhibitors. If unavoidable, ↓ ribociclib dose by 200mg (i.e. from 600mg to 400mg). After discontinuation of strong CYP3A4 inhibitor, resume ribociclib dose used prior to initiating the CYP3A4 inhibitor (after a washout period of at least 5 half-lives). Monitor closely. |
CYP3A4 inducers (e.g. phenytoin, rifampin, dexamethasone, carbamazepine, phenobarbital, St. John’s Wort, etc) | ↓ ribociclib exposure (e.g. rifampin ↓ ribociclib exposure by 89%) | ↑ metabolism of ribociclib | Avoid strong CYP3A4 inducers. |
CYP3A4 substrates with narrow therapeutic index (e.g. alfentanil, cyclosporine, dihydroergotamine, ergotamine, everolimus, fentanyl, midazolam, pimozide, quinidine, sirolimus and tacrolimus) | ↑ CYP3A4 Substrate exposure (e.g. ribociclib ↑ midazolam exposure by 280%) | ↓ metabolism of CYP3A4 Substrate | Avoid CYP3A4 substrates with a narrow therapeutic index. If unavoidable, consider reducing dose of substrate. |
Drugs that may prolong QT (e.g. amiodarone, procainamide, sotalol, venlafaxine, amitriptyline, sunitinib, methadone, chloroquine, clarithromycin, haloperidol, fluconazole, moxifloxacin, domperidone, ondansetron, etc) | ↑ risk of QT prolongation | Additive | Avoid concomitant use. If must co-administer, monitor as clinically indicated. |
Drugs that disrupt electrolyte levels (e.g. loop/thiazide diuretics, laxatives, amphotericin B, high dose corticosteroids) | serum electrolyte imbalance | ↓ electrolyte levels | Avoid to the extent possible. |
Drugs that reduce heart rate (e.g. beta blockers, calcium channel blockers, digoxin) | ↑ risk of arrhythmia | Avoid to the extent possible. | |
Tamoxifen | ↑ risk of QT prolongation | ↑ tamoxifen exposure by 2-fold with co-administration | Combined use is not recommended. |
Statins | ↑ risk of rhabdomyolysis | CDK inhibitors may ↑ statin exposure (Health Canada, 2025) | Consider close monitoring |
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 2 weeks for the first 2 cycles, at the beginning of each subsequent 4 cycles and as clinically indicated |
Liver function tests |
Baseline, every 2 weeks for the first 2 cycles, at the beginning of each subsequent 4 cycles and as clinically indicated (more frequent monitoring required in patients with ≥ Grade 2 LFTs) |
Electrolytes, including potassium, magnesium, calcium, and phosphorous |
Baseline, at regular intervals during steady-state treatment in later cycles and as clinically indicated (for example, patients with QTc prolongation) |
ECG |
Baseline, repeat on day 14 of cycle 1, and then as clinically indicated (more frequent monitoring in patients at risk) |
Renal function tests |
Baseline and as clinically indicated |
Clinical toxicity assessment of infection, bleeding, thromboembolism (close monitoring in patients at risk), pneumonitis, gastrointestinal and skin effects, and fatigue |
At each visit |
Grade toxicity using the current NCI-CTCAE (Common Terminology Criteria for Adverse Events) version
Exceptional Access Program (EAP Website )
- ribociclib - For the treatment of patients with estrogen receptor (ER)-positive, human epidermal growth factor receptor 2 (HER 2)-negative, unresectable locally advanced or metastatic breast cancer in combination with an aromatase inhibitor or fulvestrant according to clinical criteria
Hortobagyi, G. N. et al. Ribociclib as first-line therapy for HR-positive, advanced breast cancer. New Engl. J. Med. 375, 1738–1748 (2016).
Product monograph: Kasqali (ribociclib). Novartis Pharmaceuticals. June 12, 2025.
Summary Safety Review - Cyclin-dependent Kinase Inhibitors (abemaciclib, palbociclib and ribociclib) and HMG-CoA Reductase Inhibitors (atorvastatin, fluvastatin, lovastatin, pravastatin, rosuvastatin and simvastatin) (Statins) - Assessing the Potential Risk of Rhabdomyolysis Due to Drug Interaction. Health Canada. Accessed April 25, 2025.
September 2025 Updated Pharmacokinetics, Adverse Effects, Dosing, Administration Guidelines, Pregnancy/Lactation, Interactions, and Monitoring sections
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.
Hortobagyi, G. N. et al. Ribociclib as first-line therapy for HR-positive, advanced breast cancer. New Engl. J. Med. 375, 1738–1748 (2016).
Product monograph: Kasqali (ribociclib). Novartis Pharmaceuticals. June 12, 2025.
Summary Safety Review - Cyclin-dependent Kinase Inhibitors (abemaciclib, palbociclib and ribociclib) and HMG-CoA Reductase Inhibitors (atorvastatin, fluvastatin, lovastatin, pravastatin, rosuvastatin and simvastatin) (Statins) - Assessing the Potential Risk of Rhabdomyolysis Due to Drug Interaction. Health Canada. Accessed April 25, 2025.
ribociclib (patient)
Info Sheet Introduction:- For treating a certain type of breast cancer. Ribociclib is given together with another medication.
ribociclib
Pronunciation:
rye-boe-SYE-klib
Other Name(s):
Kisqali™
Appearance:
Tablet
This handout gives general information about this cancer medication.
You will learn:
-
who to contact for help
-
what the medication is
-
how it is given
-
what to expect while on medication
This handout was created by Ontario Health (Cancer Care Ontario) together with patients and their caregivers who have also gone through cancer treatment. It is meant to help support you through your cancer treatment and answer some of your questions.
This information does not replace the advice of your health care team. Always talk to your health care team about your treatment.
My cancer health care provider is: _____________________________________________
During the day I should contact: _______________________________________________
Evenings, weekends and holidays: _____________________________________________
This page gives general information about this cancer medication.
You will learn:
-
who to contact for help
-
what the medication is
-
how it is given
-
what to expect while on this medication
This information was created by Ontario Health (Cancer Care Ontario) together with patients and their caregivers who have also gone through cancer treatment. It is meant to help support you through your cancer treatment and answer some of your questions.
This information does not replace the advice of your health care team. Always talk to your health care team about your treatment.
- For treating a certain type of breast cancer. Ribociclib is given together with another medication.
Tell your health care team if you have or had significant medical condition(s), especially if you have / had:
-
heart problems (including irregular heartbeat or heart rate),
-
a family history of severe heart problems,
-
low salt levels in your blood (such as low calcium, magnesium, phosphorous, or potassium),
-
liver, kidney problems, or
- any allergies.
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.
- This medication is usually taken once a day by mouth for 21 days followed by a 7 day break with no ribociclib treatment. Talk to your health care team about how and when to take your medication.
-
Take the dose at about the same time each day, preferably in the morning.
-
Swallow whole with a glass of water, with or without food.
-
Do not crush, chew or split the tablets.
-
If you miss a dose, skip this and take your next dose as you normally do. Do not take an extra dose to make up for the missed dose.
-
If you vomit (throw up) after taking your medication, do not take an extra dose. Take your next dose at the normal time.
Warning: If you take too much of this medication by accident, or if you think a child or a pet may have swallowed your medication, you must call the Ontario Poison Control Center right away at: 1-800-268-9017.
-
DO check with your health care team before getting any vaccinations, surgery, dental work or other medical procedures.
-
DO NOT take any other medications, such as vitamins, over-the-counter (non-prescription) drugs or substances, or natural health products without checking with your health care team.
-
DO NOT start any complementary or alternative therapies, such as acupuncture or homeopathic products, without checking with your health care team.
-
DO NOT use tobacco products (such as smoking cigarettes or vaping) 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 eat or drink grapefruit, starfruit, Seville oranges or their juices (or products that contain these) while on this treatment. These may increase the quantity of the medication in your blood and increase the side effects.
-
DO NOT drive, operate machinery or do any tasks that need you to be alert if you feel faint.
-
DO check with your health care team before getting any vaccinations, surgery, dental work or other medical procedures.
-
DO NOT take any other medications, such as vitamins, over-the-counter (non-prescription) drugs or substances, or natural health products without checking with your health care team.
-
DO NOT start any complementary or alternative therapies, such as acupuncture or homeopathic products, without checking with your health care team.
-
DO NOT use tobacco products (such as smoking cigarettes or vaping) 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 eat or drink grapefruit, starfruit, Seville oranges or their juices (or products that contain these) while on this treatment. These may increase the quantity of the medication in your blood and increase the side effects.
-
DO NOT drive, operate machinery or do any tasks that need you to be alert if you feel faint.
Yes, this medication can interact with other medications, vitamins, foods, traditional medicines and natural health products. Interactions can make this medication 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
- other drugs and substances, such as cannabis/marijuana (medical or recreational)
- natural health products such as vitamins, herbal teas, homeopathic medicines, and other supplements, or traditional medicines
Check with your health care team before starting or stopping any of them.
- Anti-inflammatory medications such as ibuprofen (Advil® or Motrin®), naproxen (Aleve®) or Aspirin®.
- Over-the-counter products such as dimenhydrinate (Gravol®)
- Natural health products such as St. John’s Wort
- Traditional medicines
- Supplements such as vitamin C
- Grapefruit juice
- Alcoholic drinks
- Tobacco
- All other drugs or substances, such as marijuana or cannabis (medical or recreational)
-
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.
-
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.
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 21 days 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 at least 21 days after your last dose.
-
Check with your pharmacist about whether you should store your ribociclib tablets at room temperature or in the refrigerator.
-
Keep the tablets in the original packaging.
-
Keep out of sight and reach of children and pets.
-
Do not throw out any unused ribociclib tablets at home. Bring them to your pharmacy to be thrown away safely.
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.
-
Do not touch oral anti-cancer medications if you are pregnant or breastfeeding.
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 getting ribociclib. 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 ribociclib.
Very Common Side Effects (50 or more 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 (May be severe) 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. |
Nausea and vomiting (Generally mild) What to look for?
What to do? To help prevent nausea:
|
Talk to your healthcare team if nausea lasts more than 48 hours or vomiting lasts more than 24 hours or if it is severe. |
Common Side Effects (25 to 49 out of 100 people) | |
Side effects and what to do | When to contact health care team |
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. |
Diarrhea What to look for?
What to do? If you have diarrhea:
Ask your health care team for the Diarrhea pamphlet for more information. |
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). |
Hair thinning or loss (Generally mild) What to look for?
What to do?
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Talk to your health care team if this bothers you. |
Constipation What to look for?
What to do? To help prevent 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. |
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. |
Less Common Side Effects (10 to 24 out of 100 people) | |
Side effects and what to do | When to contact health care team |
Rash; dry, itchy skin (May be severe) 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. |
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.
If you have any symptoms of liver problems, get emergency medical help right away. |
Get emergency medical help right away. |
Low appetite What to look for?
What to do?
|
Talk to your health care team if it does not improve or if it is severe. |
Mild swelling What to look for?
What to do?
If you have swelling:
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Talk to your health care team if it does not improve or if it is severe. |
Trouble Sleeping Your medications may cause trouble sleeping. It may get better once your body gets used to the medication or when your treatment ends. What to look for?
What to do? Talk to your health care team if it does not improve or if it is severe. |
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?
To help prevent mouth sores:
If you have mouth sores:
Ask your health care team for the Oral Care (Mouth Care) pamphlet for more information. |
Talk to your health care team as soon as you notice mouth or lip sores or if it hurts to eat, drink or swallow. |
Dry mouth What to look for?
What to do?
See our Mouth Care pamphlet for more information. Talk to your health care team if your dry mouth does not improve or if it is severe.
|
Talk to your health care team if it does not improve or if it is severe. |
Eye problems What to look for?
What to do?
|
Contact your health care team as soon as possible. |
Heartburn; stomach upset; bloating What to look for?
What to do?
|
Talk to your health care team if it does not improve or if it is severe. |
Taste changes What to look for?
What to do?
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Talk to your health care team if it does not improve or if it is severe. |
Other rare, but serious side effects are possible with this treatment.
If you have any of the following, talk to your cancer health care team or get emergency medical help right away:
- irregular heartbeat, shortness of breath, chest pain, fainting spells or swelling in your legs, ankles and belly
- pain, swelling and hardening of the vein in an arm or leg
- muscle spasms, cramping, weakness, twitching, seizures, confusion or blood pressure changes
For more information on how to manage your symptoms ask your health care provider, or visit: https://www.cancercareontario.ca/symptoms.
September 2025 Updated/Revised drug information sheet
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.



- ribociclib - For the treatment of patients with estrogen receptor (ER)-positive, human epidermal growth factor receptor 2 (HER 2)-negative, unresectable locally advanced or metastatic breast cancer in combination with an aromatase inhibitor or fulvestrant according to clinical criteria
rye-boe-SYE-klib
Cancer Type: Breast Type of Content: Drug Monograph Status: Null Info Sheet Status: Null Global Date: Friday, September 12, 2025 Universal Date: 2025-09-12 00:00:00 AddThis: Title URL: ribociclib Drug Display Status: Active Revision Summary:Drug Monograph: Updated Pharmacokinetics, Adverse Effects, Dosing, Administration Guidelines, Pregnancy/Lactation, Interactions, and Monitoring sections
Patient Info Sheet EN: Updated/Revised drug information sheet