Details for: LATUDA
Company: SUNOVION PHARMACEUTICALS CANADA INC
DIN | DIN name | Active Ingredient(s) | Strength | Dosage Form | Route of Administration |
---|---|---|---|---|---|
02422050 | LATUDA | LURASIDONE HYDROCHLORIDE | 20 MG | TABLET | ORAL |
02387751 | LATUDA | LURASIDONE HYDROCHLORIDE | 40 MG | TABLET | ORAL |
02413361 | LATUDA | LURASIDONE HYDROCHLORIDE | 60 MG | TABLET | ORAL |
02387778 | LATUDA | LURASIDONE HYDROCHLORIDE | 80 MG | TABLET | ORAL |
02387786 | LATUDA | LURASIDONE HYDROCHLORIDE | 120 MG | TABLET | ORAL |
Summary Reports
Regulatory Decision Summary
Regulatory Decision Summary
Summary Safety Review - Atypical antipsychotics - Assessing the Potential Risk of Sleep Apnoea
Summary Safety Review - Atypical antipsychotics - Assessing the Potential Risk of Urinary Retention
Summary Safety Review - Atypical Antipsychotics - Liver failure
Summary Safety Review - Atypical antipsychotics - Assessing the potential risk of sleep walking and sleep-related eating disorder
Summary Safety Review - Atypical antipsychotics - Assessing the potential risk of Drug Reaction with Eosinophilia and Systemic Symptoms (DRESS)
Consumer Information
This information was provided by the drug’s manufacturer when this drug product was approved for sale in Canada. It is designed for consumers and care givers. It is a summary of information about the drug and will not tell you everything about the drug. Contact your doctor or pharmacist if you have any questions about the drug.
What the medication is used for
LATUDA is used to treat the symptoms of schizophrenia in adults
and in adolescents (15-17 years of age).
Schizophrenia is characterized by symptoms such as:
People with this condition may also feel depressed, guilty, anxious, or tense.
LATUDA is also used to treat the symptoms of depression associated with bipolar disorder in adults and adolescents (13-17 years of age) such as:
LATUDA is not a cure for your condition, but it can help manage your symptoms.
Your doctor may have prescribed LATUDA for another reason. Ask your doctor if you have any questions about why LATUDA has been prescribed for you.
A Reminder: This medicine has been prescribed only for you. Never give it to anyone else.
What it does
LATUDA belongs to a group of medicines called atypical
antipsychotics.
Antipsychotic medications affect the chemicals (neurotransmitters)
that allow nerve cells to talk to each other. Two of the chemicals in
the brain, called dopamine and serotonin, may be out of balance in
schizophrenia or bipolar depression. It is not known exactly how
LATUDA works. However, it seems to help keep the right balance
of dopamine and serotonin in your brain.
When it should not be used
Do not take LATUDA if you:
What the medicinal ingredient is
lurasidone hydrochloride
What the non-medicinal ingredients are
LATUDA contains the following nonmedicinal ingredients: carnauba wax, croscarmellose sodium, hypromellose, magnesium stearate, mannitol, Opadry® (hypromellose, polyethylene glycol, and titanium dioxide), pregelatinized starch; 80 mg tablet also contains: FD&C Blue No.2 Aluminum Lake and yellow ferric oxide
What dosage form it comes in
20 mg, 40 mg, 60 mg, 80 mg, and 120 mg tablets
Warnings and precautions
Various medicines of the group to which LATUDA belongs have been associated with an increased rate of death when used in elderly patients with dementia. LATUDA is not approved for use in elderly patients with dementia.
BEFORE you use LATUDA, talk to your doctor or pharmacist if you:
- are taking any other medicines (prescriptions or over the counter medicines)
- are pregnant, think you are pregnant, or plan to become pregnant
- are breastfeeding or plan to breastfeed
- are an elderly patient suffering from dementia (loss of memory and other mental abilities)
- exercise vigorously or work in hot or sunny places
- have high blood sugar or a history of diabetes
- have a history of kidney or liver problems
- have involuntary, irregular muscle movements, especially in the face or tongue
- have high blood pressure or rapid heartbeats and a drop in pressure when getting up
- have low blood pressure
- suffer from heart disease or have a family history of heart disease, stroke, or "mini" stroke
- have had problems with the way your heart beats (arrhythmias) or are taking medications that affect how your heart beats
- have heart problems including “QT prolongation”
- are at risk for developing blood clots. Risks include:
- a family history of blood clots
- being over age over 65
- smoking
- being over weight
- a recent major surgery (such as hip or knee replacement)
- not being able to move due to air travel or other reason
- take birth control ("The Pill")
- have or have had breast cancer
- have pituitary tumours
- drink alcohol or use street drugs
- have ever had fainting, blackouts, or seizures
- work with hazardous machinery or drive a motorized vehicle
- have or have had low levels of white blood cells
Driving and using machines: LATUDA may make you feel drowsy. Do not drive a car or operate machinery until you know how LATUDA affects you.
Low Blood Pressure: When taking LATUDA, some people may faint, feel lightheaded or dizzy, especially when getting up from a lying or sitting position. This is more likely to happen if you are elderly and also at the start of treatment or when the dose is increased. This will usually go away on its own but if it does not, tell your doctor.
Dehydration and overheating: When taking LATUDA, it is important not to become too hot or dehydrated. Do not exercise too much and try to avoid extreme heat.
Falls: Feeling sleepy, a fall in blood pressure when you stand up from sitting or lying down, vision or speech problems have been reported with the use of antipsychotic drugs. This can lead to falls that may cause fractures or other fall-related injuries. Certain medications, diseases or conditions can make this worse.
Interactions with this medication
Tell all doctors, dentists, and pharmacists who are treating you that
you are taking LATUDA.
As well, be sure to tell them about any other medications you take,
including any drugs, vitamins, minerals, natural supplements or
alternative medicines.
Inform your doctor if you start or stop taking any of the following
medications as they may interact with LATUDA:
The effects of alcohol could be made worse while taking LATUDA. It is recommended that you do not drink alcohol while taking LATUDA.
You should avoid consuming grapefruit, grapefruit juice, or products containing grapefruit extract while receiving LATUDA.
Proper use of this medication
Usual Adult and Adolescent (15-17 years old) Dose:
Schizophrenia:
Usual starting dose: 40 mg once a day. The highest recommended
dose for adolescents is 80 mg.
Usual Adult and Adolescent (13-17 years old) Dose:
Depression Associated with Bipolar Disorder:
Usual starting dose: 20 mg once a day alone or in combination with
lithium or valproate.
Take LATUDA exactly the way your doctor has prescribed it,
every day and at the same time. You should check with your doctor
or pharmacist if you are not sure. Your doctor has decided on the
best dose for you based on your individual situation. Your doctor
may increase or decrease your dose depending on your response.
Take LATUDA with food (at least 350 calories) and swallow
whole with water.
If you have moderate liver problems, your daily dose of LATUDA
should not be more than 80 mg. If you have severe liver problems,
your daily dose of LATUDA should not be more than 40 mg.
If you have moderate or severe kidney problems, your daily dose
of LATUDA should not be more than 80 mg.
LATUDA is not for use in children under 15 years of age with
symptoms of schizophrenia. LATUDA is not for use in children
under 13 years of age being treated for the symptoms of depression
associated with bipolar disorder.
Missed Dose:
If you miss a dose by a few hours, take it as soon as possible. If you
are close to your next dose, just skip the missed dose and take your
next dose at your regular time. DO NOT TAKE 2 DOSES OF
LATUDA AT THE SAME TIME TO MAKE UP FOR A MISSED
DOSE.
Overdose:
Side effects and what to do about them
Like other medicines, LATUDA can cause some side effects. These
side effects are likely to be minor and temporary. However, some
may be serious and need medical attention.
The most common side effects of LATUDA in adult patients with
schizophrenia are:
The most common side effects of LATUDA in adolescent patients (15-17 years) with schizophrenia are:
The most common side effects of LATUDA in adult patients with depression associated with bipolar disorder are:
The most common side effects of LATUDA in adolescent patients (13-17 years) with depression associated with bipolar disorder are:
Other side effects of LATUDA include:
The following may also occur with LATUDA, and may be seen in routine blood testing:
If you have high levels of prolactin (measured with a blood test) and a condition called hypogonadism you may be at an increased risk of breaking a bone due to osteoporosis. This occurs in both men and women.
Your doctor should check your body weight before starting LATUDA and continue to monitor it for as long as you are being treated.
Your doctor should take blood tests before starting LATUDA. They will monitor blood sugar and the number of infection fighting white blood cells. Your doctor should continue to monitor your blood for as long as you are being treated.
You should tell your doctor if you notice any symptoms that worry you, even if you think the problems are not connected with the medicine or are not listed here.
Symptom / effect | Talk with your doctor or pharmacist Only if severe | Talk with your doctor or pharmacist In all cases | Stop taking drug and seek immediate medical emergency help |
---|---|---|---|
Common | |||
New or worsening constipation | ✔ | ||
Uncommon | |||
Involuntary movements mainly of your face or tongue (tardive dyskinesia) | ✔ | ||
Sudden weakness or numbness of the face, arms, or legs and slurred speech or vision problems, even if for a short period of time | ✔ | ||
Feeling faint, or dizzy, or lose consciousness, or feel a change in the way your heart beats (palpitations) | ✔ | ||
Difficulty swallowing | ✔ | ||
Rare | |||
Pronounced muscle stiffness or inflexibility with high fever, rapid or irregular heartbeat, sweating, state of confusion, or reduced consciousness (Neuroleptic Malignant Syndrome) | ✔ | ||
Seizure (loss of consciousness with uncontrollable shaking) | ✔ | ||
Symptoms of a severe allergic reaction such as swelling of the mouth, face, lips, or tongue, and may include difficulty breathing | ✔ | ||
Blood clots: swelling, pain and redness in an arm or leg that can be warm to touch. You may develop sudden chest pain, difficulty breathing, and heart palpitations. | ✔ | ||
Very dark (“tea coloured”) urine, muscle tenderness, and/or aching (rhabdomyolysis) | ✔ | ||
Long-lasting (greater than 4 hours in duration) and painful erection of the penis | ✔ | ||
Unknown | |||
Drug Reaction with Eosinophilia and Systemic Symptoms (DRESS) (serious skin reaction that may affect more than one or more organs): fever, severe rash, swollen lymph glands, flulike feeling, yellow skin or eyes, shortness of breath, dry cough, chest pain or discomfort, feel thirsty, urinate less often, less urine | ✔ |
How to store
Store at room temperature (15 – 30°C).
The expiry date of this medicine is printed on the package label.
Do not use the medicine after this date. Keep out of the reach and
sight of children.
Reporting side effects
You can report any suspected side effects associated with the use of health products to Health Canada by:
- Visiting the Web page on Adverse Reaction Reporting (https://www.canada.ca/en/healthcanada/services/drugs-health-products/medeffectcanada/adverse-reaction-reporting.html) for information on how to report online, by mail or by fax; or
- Calling toll-free at 1-866-234-2345.
NOTE: Contact your health professional if you need information about how to manage your side effects. The Canada Vigilance Program does not provide medical advice.
More information
This document plus the full product monograph, prepared for health
professionals can be found at: http://www.sunovion.ca or by
contacting the sponsor, Sunovion Pharmaceuticals Canada Inc. at:
1-866-260-6291.
This leaflet was prepared by Sunovion Pharmaceuticals Canada Inc.
Last revised: March 18, 2020