Consumer medicine information

Duloxetine Sandoz

Duloxetine

BRAND INFORMATION

Brand name

Duloxetine Sandoz (New Formulation)

Active ingredient

Duloxetine

Schedule

S4

 

Consumer medicine information (CMI) leaflet

Please read this leaflet carefully before you start using Duloxetine Sandoz.

SUMMARY CMI

DULOXETINE SANDOZ®

Consumer Medicine Information (CMI) summary

The full CMI on the next page has more details. If you are worried about using this medicine, speak to your doctor or pharmacist.

1. Why am I using DULOXETINE SANDOZ?

DULOXETINE SANDOZ contains the active ingredient duloxetine hydrochloride. DULOXETINE SANDOZ is used to treat major depressive disorder (depression) and Generalized Anxiety Disorder (excessive worry).

For more information, see Section 1. Why am I using DULOXETINE SANDOZ? in the full CMI.

2. What should I know before I use DULOXETINE SANDOZ?

Do not use if you have ever had an allergic reaction to DULOXETINE SANDOZ or any of the ingredients listed at the end of the CMI. Talk to your doctor if you have any other medical conditions, take any other medicines, or are pregnant or plan to become pregnant or are breastfeeding.

For more information, see Section 2. What should I know before I use DULOXETINE SANDOZ? in the full CMI.

3. What if I am taking other medicines?

Some medicines may interfere with DULOXETINE SANDOZ and affect how it works.

A list of these medicines is in Section 3. What if I am taking other medicines? in the full CMI.

4. How do I use DULOXETINE SANDOZ?

  • Your doctor will tell you how much DULOXETINE SANDOZ you need to take each day.
  • Swallow the capsule whole with a full glass of water. It may be taken with or without meals.

More instructions can be found in Section 4. How do I use DULOXETINE SANDOZ? in the full CMI.

5. What should I know while using DULOXETINE SANDOZ?

Things you should do
  • Remind any doctor, dentist or pharmacist you visit that you are using DULOXETINE SANDOZ.
  • If you are going to have surgery, tell the surgeon or anaesthetist that you are taking DULOXETINE SANDOZ.
  • If you become pregnant while taking DULOXETINE SANDOZ, tell your doctor immediately.
  • Tell your doctor immediately if you have any suicidal thoughts or other mental/ mood changes.
Things you should not do
  • Do not stop taking this medicine or lower the dosage without checking with your doctor.
  • Do not take DULOXETINE SANDOZ to treat any other complaints unless your doctor tells you to.
  • Do not give your medicine to anyone else, even if they have the same condition as you.
  • Do not 'binge drink' or drink alcohol excessively during treatment with DULOXETINE SANDOZ.
Driving or using machines
  • Do not drive or operate any machinery until you know how DULOXETINE SANDOZ affects you.
  • DULOXETINE SANDOZ may impair your judgement, affect your thinking or motor skills.
Drinking alcohol
  • Tell your doctor if you drink alcohol. Large amounts during treatment can cause severe liver injury.
  • Drinking alcohol with this medicine may also cause dizziness or drowsiness in some people.
Looking after your medicine
  • Keep your capsules in the pack until it is time to take them.
  • Keep your capsules in a cool dry place where the temperature stays below 25°C.

For more information, see Section 5. What should I know while using DULOXETINE SANDOZ? in the full CMI.

6. Are there any side effects?

Less serious side effects include fatigue, weakness, diarrhoea, chills, headache, nausea, vomiting, weight loss, dry mouth, trouble sleeping, anxiety, abnormal thoughts/dreams, drowsiness, dizziness, sweating, twitches, rash, itch, sexual disturbances, frequent urination, changes in taste and changes in vision. Serious side effects may include: serious allergic reactions, muscle spasms, tremors, seizures, fast, irregular heartbeat, abnormal bleeding, sudden mood swings, confusion, liver problems, loss of coordination, serotonin syndrome and stress cardiomyopathy.

For more information, including what to do if you have any side effects, see Section 6. Are there any side effects? in the full CMI.



FULL CMI

DULOXETINE SANDOZ®

Active ingredient(s): Duloxetine hydrochloride

Consumer Medicine Information (CMI)

This leaflet provides important information about using DULOXETINE SANDOZ. You should also speak to your doctor or pharmacist if you would like further information or if you have any concerns or questions about using DULOXETINE SANDOZ.

Where to find information in this leaflet:

1. Why am I using DULOXETINE SANDOZ?
2. What should I know before I use DULOXETINE SANDOZ?
3. What if I am taking other medicines?
4. How do I use DULOXETINE SANDOZ?
5. What should I know while using DULOXETINE SANDOZ?
6. Are there any side effects?
7. Product details

1. Why am I using DULOXETINE SANDOZ?

DULOXETINE SANDOZ contains the active ingredient duloxetine hydrochloride. DULOXETINE SANDOZ belongs to a group of medicines called Serotonin and Noradrenaline Reuptake Inhibitors (SNRIs).

SNRIs are believed to work by their action on serotonin and noradrenaline in the brain. Serotonin and noradrenaline are the chemical messengers responsible for controlling the psychological and painful physical symptoms of depression.

DULOXETINE SANDOZ is used to treat major depressive disorder (depression) and Generalized Anxiety Disorder (excessive worry).

2. What should I know before I use DULOXETINE SANDOZ?

Warnings

Do not use DULOXETINE SANDOZ if:

  • you are allergic to duloxetine hydrochloride, or any of the ingredients listed at the end of this leaflet. Always check the ingredients to make sure you can use this medicine.
  • you have liver disease. This could increase the chance of you having liver problems during treatment with DULOXETINE SANDOZ.
  • you are taking another medicine for depression called a monoamine oxidase inhibitor (MAOI) or have been taking a MAOI within the last 14 days. Check with your doctor or pharmacist if you are unsure as to whether or not you are taking a MAOI.

Check with your doctor if you:

  • have or have had any other medical conditions, such as:
    - high pressure in the eye (glaucoma)
    - high blood pressure as your doctor may monitor your blood pressure
    - heart conditions
    - kidney problems as you may need to take a lower dose of DULOXETINE SANDOZ
    - fits (seizures)
    - mania
    - bipolar disorder
    - bleeding or clotting disorders
    - diabetes
  • have allergies to any other medicines, foods, preservatives or dyes.
  • take any medicines for any other condition
  • drink alcohol. Talk to your doctor about how much alcohol you drink.

Drug dependence

  • It is not known whether duloxetine causes drug-seeking behaviour in patients.
  • Patients with history of drug abuse should be carefully evaluated by physicians.
  • Also, physicians should follow such patients closely and observe them for signs of misuse or abuse of duloxetine such as development of tolerance, incrementation of dose and drug-seeking behaviour.

During treatment, you may be at risk of developing certain side effects. It is important you understand these risks and how to monitor for them. See additional information under Section 6. Are there any side effects?

Pregnancy and breastfeeding

Check with your doctor if you are pregnant or intend to become pregnant.

Talk to your doctor if you are breastfeeding or intend to breastfeed.

  • Your doctor will discuss the risks and benefits of taking DULOXETINE SANDOZ during pregnancy.
  • When taken during pregnancy, particularly in the last 3 months of pregnancy, medicines like DULOXETINE SANDOZ may affect your newborn baby.
  • Your new born baby may experience irritability, constant crying, feeding difficulties, vomiting, fluctuating temperature, seizures or fits, tremors, jitteriness, bluish appearance (cyanosis), breathing interruptions, wheezing or shallow breathing, low blood sugar, muscle stiffness, muscle weakness, or overresponsive reflexes.
  • These symptoms are uncommon and may be due to the effect of DULOXETINE SANDOZ or the discontinuation of DULOXETINE SANDOZ.
  • These symptoms usually begin immediately after the baby is born, or within a few days of birth, and should only last for a short time.
  • If this happens to your baby, you should contact your doctor and/or midwife immediately.

Taking DULOXETINE SANDOZ during pregnancy may increase the risk of pre-term birth.

If you take DULOXETINE SANDOZ near the end of your pregnancy, there may be an increased risk of heavy vaginal bleeding shortly after birth. Tell your doctor or midwife if you are taking DULOXETINE SANDOZ so that they can advise you.

Talk to your doctor if you are breastfeeding or intend to breastfeed. Breastfeeding while on DULOXETINE SANDOZ is not recommended.

Use in children

  • DULOXETINE SANDOZ is not recommended for use in children and adolescents under the age of 18 years.

3. What if I am taking other medicines?

Tell your doctor or pharmacist if you are taking any other medicines, including any medicines, vitamins or supplements that you buy without a prescription from your pharmacy, supermarket or health food shop.

Some medicines may interfere with DULOXETINE SANDOZ and affect how it works. These include:

  • monoamine oxidase inhibitors (MAOIs), medicines used to treat some types of depression.
  • You should stop taking MAOIs at least two weeks before starting DULOXETINE SANDOZ. If you do take DULOXETINE SANDOZ while you are taking a MAOI, you may experience shaking (tremor), shivering, muscle stiffness, fever, rapid pulse, rapid breathing and mental state from extreme agitation progressing to confusion and coma (a condition called serotonin syndrome). You must stop taking DULOXETINE SANDOZ at least 5 days before you start taking a MAOI.
  • other medicines that strongly interfere with how the liver works (potent CYP1A2 inhibitor), such as another medicine for depression called fluvoxamine.
  • other medicines used to treat depression, panic disorder, anxiety, or obsessive illnesses, including tryptophan
  • strong painkillers such as tramadol, pethidine
  • a type of migraine treatment called 'triptans', such as sumatriptan or zolmitriptan
  • medicines used to treat stress urinary incontinence such as tolteridone
  • tricyclic antidepressants such as nortriptyline, imipramine, and desipramine
  • medicines used to treat heart problems such as flecainide or propafenone
  • phenothiazines such as chlorpromazine and prochlorperazine, used to treat schizophrenia/mood disorders and nausea
  • thioridazine, a medicine used to treat schizophrenia
  • SSRIs used to treat depression (e.g., paroxetine, escitalopram, sertraline)
  • other SNRIs used to treat depression (e.g., venlafaxine, desvenlafaxine)
  • medicines used to treat blood pressure
  • medications to pass urine (diuretics)
  • herbal medicines such as St John's Wort (Hypericum perforatum)
  • warfarin, a medicine used to thin the blood (anticoagulant) or other medicines known to affect blood clotting (NSAIDs, aspirin)
  • antacids or medicines for indigestion

Do not start to take any other medicine unless prescribed or approved by your doctor. You may need different amounts of your medicines, or you may need to take different medicines.

Check with your doctor or pharmacist if you are not sure about what medicines, vitamins or supplements you are taking and if these affect DULOXETINE SANDOZ.

4. How do I use DULOXETINE SANDOZ?

How much to take

  • The usual recommended dose of DULOXETINE SANDOZ in Major Depressive Disorder is one 60 mg capsule taken once daily.
  • The recommended dose of DULOXETINE SANDOZ in Generalised Anxiety Disorder is between 30 mg and 120 mg, taken once daily.
  • Your doctor may start you on a lower dose to help reduce side effects.
  • If you have severe kidney disease, the recommended starting dose of DULOXETINE SANDOZ is one 30 mg capsule taken once daily.
  • Follow the instructions provided and use DULOXETINE SANDOZ until your doctor tells you to stop.

When to take DULOXETINE SANDOZ

  • DULOXETINE SANDOZ should be taken at about the same time each day. Taking it at the same time each day will have the best effect. It will also help you remember when to take it.

How to take DULOXETINE SANDOZ

  • Swallow the capsule whole with a full glass of water.
  • Do not open the capsules and crush the pellets inside because the medicine may not work as well.
  • DULOXETINE SANDOZ may be taken with or without meals.

How long to take DULOXETINE SANDOZ

  • Continue to take DULOXETINE SANDOZ for as long as your doctor recommends, even if you may notice an improvement.
  • The length of treatment with DULOXETINE SANDOZ will depend on how quickly your symptoms improve.
  • Most medicines of this type take time to work so don't be discouraged if you do not feel better right away.

If you forget to use DULOXETINE SANDOZ

If it is almost time for your next dose, skip the dose you missed and take your next dose when you are meant to.

Otherwise, take it as soon as you remember, and then go back to taking your medicine as you would normally.

Do not take a double dose to make up for the dose you missed.

If you are not sure what to do, ask your doctor or pharmacist.

If you take too much DULOXETINE SANDOZ

If you think that you have taken too much DULOXETINE SANDOZ, you may need urgent medical attention. Symptoms of an overdose may include drowsiness, convulsions, and vomiting.

Symptoms may also include some or all of the following: feeling confused, feeling restless, sweating, shaking, shivering, hallucinations, muscle jerks, fast heartbeat.

You should immediately:

  • phone the Poisons Information Centre
    (by calling 13 11 26), or
  • contact your doctor, or
  • go to the Emergency Department at your nearest hospital.

You should do this even if there are no signs of discomfort or poisoning.

5. What should I know while using DULOXETINE SANDOZ?

Things you should do

Tell your doctor if you become pregnant or start breastfeeding while taking DULOXETINE SANDOZ. Your doctor will discuss the risks and benefits of taking DULOXETINE SANDOZ during pregnancy or breastfeeding.

Keep all of your doctor's appointments so that your progress can be checked.

Call your doctor straight away if you:

  • have any suicidal thoughts or other mental/ mood changes.
    - The symptoms of depression or other psychiatric conditions may include thoughts of harming yourself or thoughts of suicide.
    - These symptoms may continue or get worse during the first one or two months of treatment until the full antidepressant effect of DULOXETINE SANDOZ becomes apparent. This is more likely to occur in young adults under 25 years of age.
    - Suicidal thoughts or other mental/mood changes may also worsen when the dose of DULOXETINE SANDOZ is increased or decreased.

If you or someone you know is demonstrating any of the following warning signs, call your doctor straight away or got to the Emergency Department at your nearest hospital:

  • worsening of your depression
  • thoughts or talk of death or suicide or other mental/mood changes
  • thoughts or talk of self-harm or harm to others
  • any recent attempts of self-harm
  • increase in aggressive behaviour, irritability or any other unusual changes in behaviour or mood

All mentions of suicide or violence must be taken seriously.

If you notice any of the following, contact your doctor right away.

  • itchy skin
  • dark urine
  • yellowing of the skin or eyes
  • tenderness over the liver
  • symptoms of the 'flu'

Your doctor may do some blood tests to check your liver or tell you to stop taking your medicine, as these may be signs of serious liver damage.

  • Remind any doctor, dentist or pharmacist you visit or if you are about to start a new medicine that you are taking DULOXETINE SANDOZ.
  • Remind the surgeon/anaesthetist that you are on DULOXETINE SANDOZ if you are having a surgery.

Things you should not do

Do not stop taking DULOXETINE SANDOZ or lower the dosage without checking with your doctor. If you stop taking it suddenly, your condition may worsen or you may have unwanted side effects like dizziness, nausea, headache, tingling or numbness, fatigue, vomiting, irritability, nightmares, difficulty sleeping, diarrhoea, anxiety, excessive sweating, drowsiness, imbalance, and muscle pain. If possible, your doctor will gradually reduce the amount you take each day before stopping the medicine completely.

  • Do not take DULOXETINE SANDOZ to treat any other complaints unless your doctor tells you to.
  • Do not give your medicine to anyone else, even if they have the same condition as you.
  • Do not let yourself run out of DULOXETINE SANDOZ over the weekend or on holidays.
  • Do not take DULOXETINE SANDOZ after the expiry date printed on the pack or if the packaging is torn or shows signs of tampering.

Driving or using machines

Do not drive or use any machines or tools until you know how DULOXETINE SANDOZ affects you.

DULOXETINE SANDOZ may cause dizziness or drowsiness in some people. It may also impair your judgement, affect your thinking or motor skills.

Drinking alcohol

Tell your doctor if you drink alcohol.

You should avoid "binge drinking" or drinking excessively during treatment with DULOXETINE SANDOZ. Excessive drinking while being on DULOXETINE SANDOZ can cause severe liver injury. It may also cause dizziness or drowsiness in some people.

Looking after your medicine

  • Keep your capsules in the pack until it is time to take them. If you take the capsules out of the pack, they may not keep as well.
  • Keep your capsules in a cool dry place where the temperature stays below 25°C.

Follow the instructions in the carton on how to take care of your medicine properly.

Store it in a cool dry place away from moisture, heat or sunlight; for example, do not store it:

  • in the bathroom or near a sink, or
  • in the car or on window sills.

Keep it where young children cannot reach it.

A locked cupboard at least one-and-a-half metres above the ground is a good place to store medicines.

Getting rid of any unwanted medicine

If you no longer need to use this medicine or it is out of date, take it to any pharmacy for safe disposal.

Do not use this medicine after the expiry date.

6. Are there any side effects?

All medicines can have side effects. If you do experience any side effects, most of them are minor and temporary. However, some side effects may need medical attention.

See the information below and, if you need to, ask your doctor or pharmacist if you have any further questions about side effects.

Less serious side effects

Less serious side effectsWhat to do
Gastrointestinal:
  • nausea, vomiting
  • burping or belching, indigestion, stomach pain
  • constipation, diarrhoea, wind (flatulence), loose stools
  • loss of appetite, weight loss
  • throat tightness, difficulty swallowing
  • dry mouth, sore mouth, thirst, changes to taste
  • sore throat, cough
  • bad breath
Nervous system:
  • drowsiness
  • dizziness
  • headache
  • flushing
  • tingling and numbness of hands, arms, face, mouth, legs, and feet
  • feeling anxious, agitated, or restless
Heart related:
  • fast, irregular heart beat (palpitations)
Sleep related:
  • trouble sleeping
  • abnormal dreams (including nightmares)
Skin related:
  • skin rash
Eye related:
  • blurred vision, dry eye, dilated pupils
Muscle related:
  • tremor
  • muscle pain, cramps, stiffness, or twitching
  • changes to the way you walk
  • restless legs
General symptoms:
  • feeling tired, having no energy, or weakness
  • yawning
  • sexual disturbances (decreased sexual drive, problems with orgasm, ejaculation or erection). In some cases, these symptoms have continued after stopping treatment
  • excessive sweating
  • difficulty starting to urinate (urinary hesitation), incomplete emptying of the bladder (urinary retention), urinating more frequently, pain when urinating, or needing to urinate at night
  • hot and cold sweats, fever, chills
  • ringing in ears, ear pain
Speak to your doctor if you have any of these less serious side effects and they worry you.

Serious side effects

Serious side effectsWhat to do
Serious allergic reaction:
  • symptoms of an allergic reaction may include shortness of breath, wheezing or difficulty breathing, swelling of the face, lips, tongue or other parts of the body, or rash, itching or hives on the skin.
Gastrointestinal:
  • abdominal pain, traces of blood in your stools, or dark stools. This may be because you have increased bleeding, possibly in the gastric tract. You may also feel weakness, dizziness and experience nausea and/or vomiting
Liver related:
  • signs of a possible serious liver problem such as nausea, vomiting, loss of appetite, feeling generally unwell, fever, itching, yellowing of the skin and/or eyes, dark urine
General symptoms:
  • abnormal bleeding
Muscle related:
  • stiff neck
Nervous system:
  • fits or seizures
  • feeling tired, dizziness, nausea, vomiting, sleepy, weak or confused and having achy, stiff or uncoordinated muscles, fainting, falls and seizures. This may be because you have low sodium levels in the blood. Elderly and dehydrated patients are at increased risk.
  • feeling confused, feeling restless, agitation, mood swings, sweating, shaking, diarrhoea, shivering, tremor, loss of coordination, overactive reflexes, hallucinations, sudden jerks in your muscles or a fast heart beat (these may be symptoms of a rare condition called serotonin syndrome)
  • Seeing or hearing things (hallucinations)
  • Dizziness or fainting when you stand up, especially from a lying or sitting position
  • Uncontrollable movements
  • Clenching or grinding teeth
  • Mood of excitement, over-activity, and uninhibited behaviour
  • Confusion and attention problems
  • Aggression or anger especially after starting or stopping taking this medicine
Heart-related:
  • Heart rhythm change (arrythmia)
  • Stress cardiomyopathy, signs and symptoms of this condition may include:
    - Chest pain
    - shortness of breath
    - dizziness
    - fainting
    - irregular heartbeat
Call your doctor straight away, or go straight to the Emergency Department at your nearest hospital if you notice any of these serious side effects.

Tell your doctor or pharmacist if you notice anything else that may be making you feel unwell.

Other changes you may not be aware of:

  • increased blood pressure
  • heart rhythm changes
  • underactive thyroid gland
  • liver function changes
  • high pressure in the eye (glaucoma)

This is not a complete list of all possible side effects. Other side effects not listed here may occur in some people.

Reporting side effects

After you have received medical advice for any side effects you experience, you can report side effects to the Therapeutic Goods Administration online at www.tga.gov.au/reporting-problems. By reporting side effects, you can help provide more information on the safety of this medicine.

Always make sure you speak to your doctor or pharmacist before you decide to stop taking any of your medicines.

7. Product details

This medicine is only available with a doctor's prescription.

What DULOXETINE SANDOZ contains

Active ingredient
(main ingredient)		Duloxetine (as hydrochloride)
  • each DULOXETINE SANDOZ 30 mg contains 30 mg of duloxetine
  • each DULOXETINE SANDOZ 60 mg contains 60 mg of duloxetine
Other ingredients
(inactive ingredients)
  • Sugar Spheres
  • ascorbic acid
  • hypromellose
  • purified talc
  • sucrose
  • hypromellose phthalate
  • triethyl citrate
  • gelatin
  • titanium dioxide
  • indigo carmine
  • iron oxide yellow (60 mg only)
  • Tekprint SB-4020 Green Ink (30 mg only)
  • Tekprint SW-0012 White Ink (60 mg only)
Potential allergensDULOXETINE SANDOZ contains sugars as sucrose, phenylalanine and sulfites.

The capsules do not contain gluten and lactose.

Do not take this medicine if you are allergic to any of these ingredients.

What DULOXETINE SANDOZ looks like

DULOXETINE SANDOZ comes in 2 strengths of enteric capsule:

  • DULOXETINE SANDOZ 30 mg – Blue/white, opaque capsules, printed with ‘157’ and ‘A’ in green ink (AUST R 421536)
  • DULOXETINE SANDOZ 60 mg – Blue/green, opaque capsules, printed with ‘157’ and ‘A’ in white ink. (AUST R 421530)

Each blister pack contains 28 enteric capsules.

Who distributes DULOXETINE SANDOZ

Sponsor

Sandoz Pty Ltd
100 Pacific Highway
North Sydney, NSW 2060
Australia
Tel 1800 726 369

This leaflet was prepared in November 2024.

® Registered Trade Mark. The trade marks mentioned in this material are the property of their respective owners.

Published by MIMS January 2025

BRAND INFORMATION

Brand name

Duloxetine Sandoz (New Formulation)

Active ingredient

Duloxetine

Schedule

S4

 

1 Name of Medicine

Duloxetine (present as the hydrochloride).

2 Qualitative and Quantitative Composition

Duloxetine Sandoz enteric capsules come in two strengths and contain enteric-coated pellets of duloxetine hydrochloride equivalent to 30 mg or 60 mg of duloxetine.

Excipient with known effect.

Sucrose.
For the full list of excipients, see Section 6.1 List of Excipients.

3 Pharmaceutical Form

Duloxetine Sandoz 30 mg enteric capsule.

Opaque blue/white hard gelatin capsule '157' on body and 'A' on cap with green ink.

Duloxetine Sandoz 60 mg enteric capsule.

Opaque blue/opaque green hard gelatin capsule '158' on body and 'A' on cap with white ink.

4 Clinical Particulars

4.1 Therapeutic Indications

Duloxetine Sandoz is indicated for the treatment of: major depressive disorder (MDD); generalised anxiety disorder (GAD).

4.2 Dose and Method of Administration

Major depressive disorder.

Duloxetine Sandoz should be administered for the treatment of major depressive disorder at a dose of 60 mg once daily, with or without food. There is no adequate evidence suggesting that patients not responding to 60 mg once daily will benefit from having their dose increased.

Generalised anxiety disorder.

The recommended starting dose of duloxetine in patients with generalized anxiety disorder is 30 mg once daily with or without food. The daily dose should be increased in 30 mg increments until the minimum effective dose is achieved. The maximum dose is 120 mg per day, given as 120 mg once daily. Doses above 120 mg have not been systematically evaluated.

Initial tolerability.

For patients in whom initial tolerability may be a concern, such as treatment-naïve patients or those with a history of adverse events with other medications, use of a lower starting dose such as 30 mg once daily for one week before increasing the dose to 60 mg once daily should be considered. A dose of 30 mg once daily should be used in patients with end stage renal disease (see below). In addition, clinical studies have shown that taking duloxetine with food may improve initial tolerability.

Discontinuation of treatment.

When discontinuing duloxetine after more than one week of therapy it is generally recommended that the dose be tapered to minimise the risk of discontinuation symptoms. As a general recommendation, the dose of duloxetine should be reduced by half or administered on alternate days during a period of not less than two weeks. The precise regimen followed should take into account the individual circumstances of the patient, such as duration of treatment, dose at discontinuation, etc.

Renal impairment.

A lower dose of 30 mg once daily should be used in patients with end stage renal disease (creatinine clearance < 30 mL/min) (see Section 5.2 Pharmacokinetic Properties).

Hepatic impairment.

Duloxetine is contraindicated in patients with liver disease resulting in hepatic impairment (see Section 5.2 Pharmacokinetic Properties).

Patients aged ≥ 65 years.

No dosage adjustment is recommended for elderly patients on the basis of age (see Section 5.2 Pharmacokinetic Properties).

Children and adolescents aged < 18 years.

Duloxetine has not been studied in patients under 18 years of age (see Section 4.4 Special Warnings and Precautions for Use).

4.3 Contraindications

Duloxetine is contraindicated in patients with known hypersensitivity to duloxetine or to any of the excipients in the formulation.

Monoamine oxidase inhibitors (MAOI).

Duloxetine should not be used in combination with monoamine oxidase inhibitors (MAOI) or the reversible MAOI (RIMA), moclobemide, or within 14 days of discontinuing treatment with a MAOI. Similarly, at least 5 days should be allowed after stopping Duloxetine before starting a MAOI. Cases of serious reactions, such as potentially life threatening serotonin syndrome (characterized by neuromuscular excitation, altered mental status and autonomic dysfunction) have been reported in patients receiving an SNRI in combination with MAOIs and RIMA, and in patients who have recently discontinued an SNRI and have been started on a MAOI (see Section 4.4 Special Warnings and Precautions for Use).
Duloxetine is contraindicated in patients with liver disease resulting in hepatic impairment (see Section 5.2 Pharmacokinetic Properties).
Duloxetine should not be used in combination with potent CYP1A2 inhibitors (see Section 4.5 Interactions with Other Medicines and Other Forms of Interactions).

4.4 Special Warnings and Precautions for Use

Clinical worsening and suicide risk.

The risk of suicide attempt is inherent in depression and may persist until significant remission occurs. This risk must be considered in all depressed patients.
Patients with depression may experience worsening of their depressive symptoms and/or the emergence of suicidal ideation and behaviours (suicidality) whether or not they are taking antidepressant medications, and this risk may persist until significant remission occurs. As improvement may not occur during the first few weeks or more of treatment, patients should be closely monitored for clinical worsening and suicidality, especially at the beginning of a course of treatment, or at the time of dose changes, either increases or decreases. Consideration should be given to changing the therapeutic regimen, including possibly discontinuing the medication, in patients whose depression is persistently worse or whose emergent suicidality is severe, abrupt in onset, or was not part of the patient's presenting symptoms. Patients (and caregivers of patients) should be alerted about the need to monitor for any worsening of their condition and/or the emergence of suicidal ideation/behaviour or thoughts of harming themselves and to seek medical advice immediately if these symptoms present. Patients with co-morbid depression associated with other psychiatric disorders being treated with antidepressants should be similarly observed for clinical worsening and suicidality.
Pooled analyses of 24 short-term (4 to 16 weeks), placebo controlled trials of nine antidepressant medicines (SSRIs and others) in 4400 children and adolescents with major depressive disorder (16 trials), obsessive compulsive disorder (4 trials) or other psychiatric disorders (4 trials) have revealed a greater risk of adverse events representing suicidal behaviour or thinking (suicidality) during the first few months of treatment in those receiving antidepressants. The average risk of such events in patients treated with an antidepressant was 4% compared with 2% of patients given placebo. There was considerable variation in risk among the antidepressants, but there was a tendency towards and increase for almost all antidepressants studied. The risk of suicidality was most consistently observed in the major depressive disorder trials, but there were signals of risk arising from trials in other psychiatric indications (obsessive-compulsive disorder and social anxiety disorder) as well. No suicides occurred in these trials. It is unknown whether the suicidality risk in children and adolescent patients extends to use beyond several months. The nine antidepressant medications in the pooled analyses included five SSRIs (citalopram, fluoxetine, fluvoxamine, paroxetine, sertraline) and four non-SSRIs (bupropion, mirtazapine, nefazodone, venlafaxine).
Symptoms of anxiety, agitation, panic attacks, insomnia, irritability, hostility (aggressiveness), impulsivity, akathisia (psychomotor restlessness), hypomania and mania have been reported in adults, adolescents and children being treated with antidepressants for major depressive disorder as well as for other indications, both psychiatric and nonpsychiatric. Although a causal link between the emergence of such symptoms and either worsening of depression and/or emergence of suicidal impulses has not been established, there is concern that such symptoms may be precursors of emerging suicidality.
Families and caregivers of children and adolescents being treated with antidepressants for major depressive disorder or for any other condition (psychiatric or nonpsychiatric) should be informed about the need to monitor these patients for the emergence of agitation, irritability, unusual changes in behaviour and other symptoms described above, as well as the emergence of suicidality, and to report such symptoms immediately to healthcare providers. It is particularly important that monitoring be undertaken during the initial few months of antidepressant treatment or at times of dose increase or decrease.
Duloxetine hydrochloride is not indicated for use in patients under the age of 18. Although a causal role for duloxetine in inducing such events has not been established, some analyses from pooled studies of antidepressants in psychiatric disorders found an increased risk for suicidal ideation and/or suicidal behaviours in paediatric and young adult (< 25 years of age) patients compared to placebo (see Section 4.4 Special Warnings and Precautions for Use).
Physicians should encourage patients to report any distressing thoughts or feelings at any time.
Prescriptions for duloxetine should be written for the smallest quantity of tablets consistent with good patient management, in order to reduce the risk of overdose.

Use in hepatic impairment.

Duloxetine should ordinarily not be prescribed to patients with evidence of acute or chronic liver disease as it is possible that duloxetine may aggravate pre-existing liver disease (see Section 4.3 Contraindications).

Hepatotoxicity.

Duloxetine increases the risk of elevation of serum transaminase levels. Liver transaminase elevations resulted in the discontinuation of 0.3% (82/27,229) of duloxetine-treated patients. In these patients, the median time to detection of the transaminase elevation was about two months. In placebo controlled trials in any indication, elevations of alanine transaminase (ALT) to > 3 times the upper limit of normal occurred in 1.1% (85/7632) of duloxetine-treated patients and in 0.2% (13/5578) of placebo treated patients. In placebo controlled studies using a fixed dose design, there was evidence of a dose-response relationship for ALT and AST elevation of > 3 times the upper limit of normal and > 5 times the upper limit of normal, respectively.
Postmarketing reports have described cases of hepatitis with abdominal pain, hepatomegaly and elevation of transaminase levels to more than twenty times the upper limit of normal with or without jaundice, reflecting a mixed or hepatocellular pattern of liver injury. Cases of cholestatic jaundice with minimal elevation of transaminase levels have also been reported. Isolated cases of liver failure, including fatal cases, have been reported. A majority of these cases have been reported in patients with past or current risk factors for liver injury, including alcohol abuse, hepatitis or exposure to drugs with known adverse effects on the liver.
The combination of transaminase elevations and elevated bilirubin, without evidence of obstruction, is generally recognised as an important predictor of severe liver injury. In clinical trials, 7 duloxetine patients had elevations of transaminases and bilirubin, but 5 of 7 also had elevation of alkaline phosphatase, suggesting an obstructive process; in these patients, in 3 of these 7 patients there was evidence of heavy alcohol use and this may have contributed to the abnormalities seen.
Postmarketing reports indicate that elevated transaminases, bilirubin and alkaline phosphatase have occurred in patients with chronic liver disease or cirrhosis.

Alcohol.

Because it is possible that duloxetine and alcohol may interact to cause liver injury or that duloxetine may aggravate pre-existing liver disease, duloxetine should ordinarily not be prescribed to patients with substantial alcohol use or evidence of chronic liver disease (see Section 4.4 Special Warnings and Precautions for Use, Use in hepatic impairment).

Bipolar disorder.

A major depressive episode may be the initial presentation of bipolar disorder. It is generally believed that treating such an episode with an antidepressant alone can increase the likelihood of precipitation of a mixed/manic episode in patients at risk of bipolar disorder. Prior to initiating treatment with an antidepressant, patients should be adequately screened to determine if they are at risk for bipolar disorder; such screening should include a detailed psychiatric history, including a family history of suicide, bipolar disorder, and depression.

Activation of mania.

In placebo controlled trials in patients with major depressive disorder, activation of hypomania or mania occurred in 0.1% of duloxetine treated patients and 0.1% of placebo treated patients. No activation of mania or hypomania was reported in GAD placebo controlled trials. Activation of mania/hypomania has been reported in a small proportion of patients with mood disorders who were treated with other marketed drugs effective in the treatment of major depressive disorder. As with these other drugs, duloxetine should be used cautiously in patients with a history of mania.

Seizures.

Duloxetine has not been systematically evaluated in patients with a seizure disorder. In placebo controlled clinical trials, seizures/convulsions occurred in 0.03% (3/9445) of patients treated with duloxetine and 0.01% (1/6770) of patients with placebo. As with similar CNS active drugs, duloxetine should be used cautiously in patients with a history of seizure disorder.

Mydriasis.

Mydriasis has been reported in association with duloxetine. Caution should be exercised in patients with raised intraocular pressure or those at risk of acute narrow-angle glaucoma.

Hyponatraemia.

Cases of hyponatraemia (some with serum sodium lower than 110 mmol/Liter) have been reported very rarely when administering duloxetine. The majority of these cases occurred in elderly patients, especially when coupled with a recent history of altered fluid balance or conditions pre-disposing to altered fluid balance. Hyponatremia may present with nonspecific signs and symptoms (such as dizziness, weakness, nausea, vomiting, confusion, somnolence, and lethargy). Signs and symptoms associated with more severe cases have included syncopal episodes, falls, and seizure. Caution is required in patients at increased risk for hyponatraemia; such as elderly, cirrhotic, or dehydrated patients or patients treated with diuretics. Hyponatraemia may be due to a syndrome of inappropriate antidiuretic hormone secretion (SIADH).

Abnormal bleeding.

SSRIs and SNRIs, including duloxetine, may increase the risk of bleeding events, including gastrointestinal bleeding (see Section 4.8 Adverse Effects (Undesirable Effects)). Therefore, caution is advised in patients taking duloxetine concomitantly with anticoagulants and/or medicinal products known to affect platelet function (e.g. NSAIDs, aspirin) and in patients with known bleeding tendencies.

Postpartum haemorrhage.

SSRIs and SNRIs may increase the risk of postpartum haemorrhage (see Section 4.6 Fertility, Pregnancy and Lactation; Section 4.8 Adverse Effects (Undesirable Effects)).

Use in patients with concomitant illness.

Clinical experience with duloxetine in patients with concomitant systemic illnesses is limited. Caution is advisable in using duloxetine in patients with diseases or conditions that produce altered metabolism or haemodynamic responses.
Duloxetine has not been systematically evaluated in patients with a recent history of myocardial infarction or unstable heart disease. Patients with these diagnoses were generally excluded from clinical studies during the product's premarketing testing. However, evaluation of electrocardiograms (ECGs) of 321 patients who received duloxetine in placebo-controlled clinical trials indicated that duloxetine is not associated with the development of clinically significant ECG abnormalities (see Section 4.4 Special Warnings and Precautions for Use, Electrocardiogram changes).
Increased plasma concentrations of duloxetine occur in patients with end stage renal disease (ESRD) and in patients with moderate hepatic impairment (see Section 5.2 Pharmacokinetic Properties).

Drug dependence.

While duloxetine has not been systematically studied in humans for its potential for abuse, there was no indication of drug-seeking behaviour in the clinical trials. However, it is not possible to predict on the basis of premarketing experience the extent to which a CNS active drug will be misused, diverted, and/or abused once marketed. Consequently, physicians should carefully evaluate patients for a history of drug abuse and follow such patients closely, observing them for signs of misuse or abuse of duloxetine (e.g. development of tolerance, incrementation of dose, drug seeking behaviour).

Weight changes.

Weight changes do not appear to be clinically significant outcomes of treatment with duloxetine. In placebo controlled clinical trials, patients treated with duloxetine for up to 9-weeks experienced a mean weight loss of approximately 0.5 kg, compared with a mean weight gain of approximately 0.2 kg in placebo treated patients.

Blood pressure.

Duloxetine is associated with an increase in blood pressure in some patients. In placebo-controlled clinical trials duloxetine treatment was associated with small increases in systolic blood pressure averaging 2 mmHg and small increases in diastolic blood pressure averaging 0.5 mmHg compared to placebo. Large, potentially clinically significant, elevations in blood pressure do not appear to be more common with duloxetine than with placebo. In patients with known hypertension and/or other cardiac disease, blood pressure monitoring is recommended as appropriate. Duloxetine should be used with caution in patients whose conditions could be compromised by an increased heart rate or by an increase in blood pressure.

Orthostatic hypotension and syncope.

Orthostatic hypotension and syncope have been reported with therapeutic doses of duloxetine. Syncope and hypotension tend to occur within the first week of therapy but can occur at any time during duloxetine treatment, particularly after dose increases. The risk of blood pressure decreases may be greater in patients taking concomitant medications that induce orthostatic hypotension (such as antihypertensives) or are potent CYP1A2 inhibitors and in patients taking doses above 60 mg daily. Consideration should be given to discontinuing duloxetine in patients who experience symptomatic orthostatic hypotension and/or syncope during therapy.

Electrocardiogram changes.

ECGs were obtained from 321 duloxetine treated patients with MDD and 169 placebo treated patients in 8 week clinical trials. The rate corrected QT interval in duloxetine treated patients in an 8 week study did not differ from that seen in placebo treated patients. In summary, the data suggest no arrhythmogenic potential with duloxetine. No clinically significant differences were observed for QT, PR and QRS intervals between duloxetine treated and placebo treated patients.

Discontinuing treatment.

As with other drugs effective in the treatment of major depressive disorder, when discontinuing duloxetine after more than 1 week of therapy, it is generally recommended that the dose be tapered to minimise the risk of discontinuation symptoms (see Section 4.2 Dose and Method of Administration). Withdrawal symptoms when treatment is discontinued are common, particularly if discontinuation is abrupt. In clinical trials, adverse events seen on abrupt treatment discontinuation occurred in approximately 45% of patients treated with duloxetine and 23% of patients taking placebo. The most commonly reported symptoms following abrupt discontinuation of duloxetine in clinical trials have included dizziness, nausea, headache, paraesthesia, fatigue, vomiting, irritability, nightmares, insomnia, diarrhoea, anxiety, hyperhidrosis, vertigo, somnolence and myalgia.
The risk of withdrawal symptoms seen with SSRIs and SNRIs may be dependent on several factors, including the duration and dose of therapy and the rate of dose reduction. Generally, these symptoms are mild to moderate; however, in some patients they may be severe in intensity. They usually occur within the first few days of discontinuing treatment, but there have been very rare reports of such symptoms in patients who have inadvertently missed a dose. Generally, these symptoms are self-limiting and usually resolve within 2 weeks, though in some individuals they may be prolonged (2-3 months or more).

Serotonin syndrome.

Development of serotonin syndrome may occur in association with treatment with SSRls and SNRls, particularly when given in combination with MAOls or other serotonergic agents. Symptoms and signs of serotonin syndrome include rapid onset of neuromuscular excitation (hyperreflexia, incoordination, myoclonus, tremor), altered mental status (confusion, agitation, hypomania) and autonomic dysfunction (diaphoresis, diarrhoea, fever, shivering and rapidly fluctuating vital signs). Treatment with duloxetine should be discontinued if such events occur and supportive symptomatic treatment initiated.
Caution is advisable if duloxetine is used concomitantly with serotonergic antidepressants like SSRIs, SNRIs, tricyclic antidepressants like clomipramine or amitriptyline, St. John's wort (Hypericum perforatum), or triptans, tramadol, pethidine and tryptophan.

Sexual dysfunction.

Selective serotonin reuptake inhibitors (SSRIs)/ serotonin norepinephrine reuptake inhibitors (SNRIs) may cause symptoms of sexual dysfunction (see Section 4.8 Adverse Effects (Undesirable Effects)). There have been reports of long-lasting sexual dysfunction where the symptoms have continued despite discontinuation of SSRIs/SNRI.

Use in renal impairment.

Duloxetine Cmax and AUC values were approximately 2-fold higher in patients with ESRD receiving chronic intermittent dialysis, compared with subjects with normal renal function. In contrast, the elimination half-life was similar in both groups. A lower dose should be used for patients with ESRD (see Section 4.2 Dose and Method of Administration). Population pharmacokinetic analyses suggest that mild renal dysfunction has no significant effect on apparent plasma clearance of duloxetine.

Use in the elderly.

Evaluation of patients over the age of 65 who received duloxetine in clinical trials revealed no unusual pattern of adverse events relative to the clinical experience in younger patients, but greater sensitivity of some older individuals cannot be ruled out. SSRIs and SNRIs, including duloxetine, have been associated with cases of clinically significant hyponatraemia in elderly patients, who may be at greater risk for this adverse reaction.

Paediatric use.

Safety and effectiveness in children have not been established. Duloxetine is not indicated for use in patients under the age of 18 and should not be used in children and adolescents aged < 18 years.

Effects on laboratory tests.

There are no data available that shows that duloxetine has an effect on laboratory tests.

4.5 Interactions with Other Medicines and Other Forms of Interactions

Duloxetine is a SNRI with its primary effect on the CNS. Caution should be used when it is administered in combination with other centrally acting drugs and substances, especially those with a similar mechanism of action, including alcohol. Concurrent use with other drugs with serotonergic activity (e.g. SNRIs, SSRIs, triptans or tramadol) may result in serotonin syndrome (see Section 4.4 Special Warnings and Precautions for Use).
Although duloxetine does not increase the impairment of mental and motor skills caused by alcohol, use of duloxetine with substantial alcohol consumption may be associated with severe liver injury. Isolated cases of liver failure, including fatal cases, have been reported (see Section 4.4 Special Warnings and Precautions for Use, Use in hepatic impairment). Duloxetine should only be used in exceptional circumstances with extreme caution in patients who consume substantial amounts of alcohol.

Drugs metabolised by CYP1A2.

Although CYP1A2 is weakly inhibited by duloxetine in vitro, results of a clinical study show that the pharmacokinetics of a CYP1A2 substrate (theophylline) were not significantly affected by coadministration with duloxetine (60 mg twice daily). In vitro studies with human hepatocytes demonstrated that duloxetine does not induce CYP1A2 activity. These studies suggest that duloxetine is unlikely to have a clinically significant effect on the metabolism of CYP1A2 substrates.

Inhibitors of CYP1A2.

As CYP1A2 is involved in duloxetine metabolism, concomitant use of duloxetine with potent inhibitors of CYP1A2 will likely result in higher concentrations of duloxetine. Fluvoxamine (100 mg once daily), a potent inhibitor of CYP1A2, decreased the apparent plasma clearance of duloxetine by about 77%. Duloxetine should not be used in combination with potent inhibitors of CYP1A2 (e.g. fluvoxamine) (see Section 4.3 Contraindications).

Drugs metabolised by CYP2D6.

CYP2D6 is moderately inhibited by duloxetine (in common with tricyclic antidepressants and SSRIs). Duloxetine administered at 60 mg twice daily caused a single 50 mg dose of desipramine (also metabolised through CYP2D6) to have a 3-fold increase in the AUC. Duloxetine administered at 40 mg twice daily increased steady-state AUC of tolterodine (2 mg twice daily) by 71% but did not affect the pharmacokinetics of the 5-hydroxyl metabolite. Therefore, caution should be used if duloxetine is coadministered with medications that are predominantly metabolised by the CYP2D6 system and which have a narrow therapeutic index (e.g. tricyclic antidepressants such as nortriptyline and imipramine, phenothiazines, flecainide, propafenone). Because of the risk of serious ventricular arrhythmias and sudden death potentially associated with elevated plasma concentrations of thioridazine, duloxetine and thioridazine should not be coadministered.

Inhibitors of CYP2D6.

An inhibitor of CYP2D6, paroxetine (20 mg once daily) decreased the oral clearance of duloxetine (40 mg once daily) by about 37%. Because CYP2D6 is involved in duloxetine metabolism, caution is advised if administering duloxetine with inhibitors of CYP2D6 (e.g. SSRIs).

Drugs metabolised by CYP2C9.

Although clinical studies have not been performed, results of in vitro studies demonstrate that duloxetine does not inhibit the enzyme activity of CYP2C9.

Drugs metabolised by CYP3A.

Although clinical studies have not been performed, results of in vitro studies demonstrate that duloxetine does not inhibit or induce the catalytic activity of CYP3A.

Antacids and H2 antagonists.

Coadministration of duloxetine with aluminium- and magnesium-containing antacids or co-administration of duloxetine with famotidine had no significant effect on the rate or extent of duloxetine absorption after administration of a 40 mg oral dose.

Drugs highly bound to plasma protein.

Duloxetine is highly bound to plasma protein (> 90%). Administration of duloxetine with another highly protein bound drug may cause increased free concentrations of either duloxetine or the other drug.

Monoamine oxidase inhibitors (MAOI).

Because duloxetine is an inhibitor of both serotonin and noradrenaline reuptake, it is recommended that duloxetine not be used in combination with an MAOI (see Section 4.3 Contraindications).

St John's wort.

In common with other antidepressants, concomitant administration of duloxetine and the herbal remedy St John's wort (Hypericum perforatum) is not recommended.

Warfarin and INR.

Increases in INR have been reported when duloxetine was coadministered with warfarin.

Drugs that affect gastric acidity.

Duloxetine has an enteric coating that resists dissolution until reaching a segment of the gastrointestinal tract where the pH exceeds 5.5. In extremely acidic conditions, duloxetine, unprotected by the enteric coating, may undergo hydrolysis to form naphthol. Caution is advised in using duloxetine in patients with conditions that may slow gastric emptying (e.g. some diabetics). Drugs that raise the gastrointestinal pH may lead to an earlier release of duloxetine. It is unknown whether the concomitant administration of proton pump inhibitors affects duloxetine absorption.

4.6 Fertility, Pregnancy and Lactation

Effects on fertility.

Duloxetine administered orally to male rats prior to and throughout mating, or to female rats prior to and throughout mating, gestation and lactation, at doses up to 45 mg/kg (3 times the MRHD on a mg/m2 basis) did not alter mating or fertility. In females, this dose was associated with oestrus cycle disruption and signs of maternotoxicity and embryofoetal toxicity.
(Category B3)
Duloxetine and/or its metabolites cross the placenta in rats. There was no evidence of teratogenicity in rats or rabbits following oral administration of duloxetine during the period of organogenesis at doses up to 45 mg/kg/day. In rats, this dose was 3 times the maximum recommended human dose on a mg/m2 basis. In rabbits, the estimated systemic exposure (plasma AUC) at this dose was less than clinical exposure at the maximum recommended dose. In rats receiving the maternotoxic dose of 45 mg/kg/day during organogenesis, there was increased preimplantation loss and resorptions, and reduced foetal weight.
Oral administration of duloxetine to female rats prior to and throughout mating, gestation and lactation at doses of 30-45 mg/kg/day (2-3 times the maximum recommended human dose on a mg/m2 basis) elicited maternal toxicity and reduced live birth indices, birth weight, and postnatal survival and growth of offspring, and altered some indices of offspring behaviour.
Neonates exposed to serotonergic agents late in the third trimester have been uncommonly reported to have clinical findings of respiratory distress, cyanosis, apnoea, seizures, temperature instability, feeding difficulty, vomiting, hypoglycaemia, hypotonia, hypertonia, hyperreflexia, tremor, jitteriness, irritability and constant crying. Such events can arise immediately upon delivery and are usually transient. The majority of cases have occurred either at birth or within a few days of birth. These features could be consistent with either a direct effect of SSRIs and SNRIs or, possibly, a drug discontinuation syndrome. When treating a pregnant woman with duloxetine during the third trimester, the physician should carefully consider the potential risks and benefits of treatment.
The safety of duloxetine in human pregnancy has not been established. This drug should be used during pregnancy only if the potential benefit justifies the potential risk.
Using observational data, there is evidence of an increased risk (less than 2-fold) for postpartum haemorrhage following duloxetine exposure close to delivery.
In an observational study, maternal exposure to duloxetine during pregnancy was associated with an increased risk of pre-term birth (less than 2-fold, corresponding to approximately 6 additional premature births per 100 women treated with duloxetine late in pregnancy). The majority of the premature births occurred between 35 and 36 weeks of gestation.

Labour and delivery.

The effect of duloxetine on labour in humans is unknown.
Observational data indicate an increased risk (less than 2-fold) of postpartum haemorrhage following SSRI/SNRI exposure within the month prior to birth (see Section 4.4 Special Warnings and Precautions for Use; Section 4.8 Adverse Effects (Undesirable Effects)).
 Duloxetine is excreted into the milk of lactating women. The estimated infant dose ranges from approximately 0.1% to 0.3% of the maternal dose, normalised by body weight. Oral administration of duloxetine to female rats prior to and throughout mating, gestation and lactation was associated with maternal toxicity and adverse effects (see Section 4.6 Fertility, Pregnancy and Lactation, Use in pregnancy). Administration of duloxetine to nursing mothers is not recommended.

4.7 Effects on Ability to Drive and Use Machines

In controlled studies, duloxetine has not been shown to impair psychomotor performance, cognitive function or memory. However, as any psychoactive drug may impair judgement, thinking or motor skills, and duloxetine may be associated with undesirable effects such as sedation and dizziness, patients should be cautioned about their ability to perform potentially hazardous tasks until they are reasonably certain that duloxetine therapy does not affect their ability to engage in such activities.

4.8 Adverse Effects (Undesirable Effects)

Clinical trial data.

The data described below reflect exposure to duloxetine in placebo controlled trials for MDD (N = 2327), GAD (N = 668) and DPNP (N = 568). The population studied was 17 to 89 years of age; 64.8%, 64.7% and 38.7%, female; and 85.5%, 77.6%, and 84.6% Caucasian for MDD, GAD and DPNP, respectively. Most patients received doses of a total of 60 to 120 mg per day.
Adverse reactions reported as reasons for discontinuation of treatment in placebo controlled trials.

Major depressive disorder.

Approximately 9% (209/2327) of the patients who received duloxetine in placebo controlled trials for MDD discontinued treatment due to an adverse reaction, compared with 4.7% (68/1460) of the patients receiving placebo. Nausea (duloxetine 1.3%, placebo 0.5%) was the only common adverse reaction reported as a reason for discontinuation and considered to be drug-related (i.e. discontinuation occurring in at least 1% of the duloxetine treated patients and at a rate of at least twice that of placebo).

Generalised anxiety disorder.

Approximately 15.3% (102/668) of the patients who received duloxetine in placebo controlled trials for GAD discontinued treatment due to an adverse reaction, compared with 4.0% (20/495) for placebo. Common adverse reactions reported as a reason for discontinuation and considered to be drug related (as defined above) included nausea (duloxetine 3.7%, placebo 0.2%), vomiting (duloxetine 1.3%, placebo 0.0%), and dizziness (duloxetine 1.0%, placebo 0.2%).

Diabetic peripheral neuropathic pain.

Approximately 14.3% (81/568) of the patients who received duloxetine in placebo controlled trials for DPNP discontinued treatment due to an adverse reaction, compared with 7.2% (16/223) for placebo. Common adverse reactions reported as a reason for discontinuation and considered to be drug-related (as defined above) were nausea (duloxetine 3.5%, placebo 0.4%), dizziness (duloxetine 1.6%, placebo 0.4%), somnolence (duloxetine 1.6%, placebo 0.0%), and fatigue (duloxetine 1.1%, placebo 0.0%).
Adverse reactions occurring at an incidence of 2% or more among duloxetine treated patients in placebo controlled trials.

Pooled MDD and GAD trials.

Table 1 gives the incidence of treatment emergent adverse reactions in MDD and GAD placebo controlled trials that occurred in 2% or more of patients treated with duloxetine and with an incidence greater than placebo.

Diabetic peripheral neuropathic pain.

Table 2 gives the incidence of treatment emergent adverse events that occurred in 2% or more of patients treated with duloxetine in the premarketing acute phase of DPNP placebo-controlled trials (doses of 20 to 120 mg/day) and with an incidence greater than placebo.
The following additional adverse events were reported during placebo-controlled clinical trials of duloxetine for MDD or other indications in 8504 patients. Very common events are defined as those occurring in ≥ 10% of patients, common events are defined as those occurring in ≥ 1% and < 10% of patients, uncommon events are defined as those occurring in ≥ 0.1% and < 1% of patients, and rare events are defined as those occurring in < 0.1% of patients.

Cardiac disorders.

Common: palpitations. Uncommon: tachycardia.

Ear and labyrinth disorders.

Uncommon: vertigo, ear pain, tinnitus.

Endocrine disorders.

Rare: hypothyroidism.

Eye disorders.

Uncommon: mydriasis, visual impairment, dry eye.

Gastrointestinal disorders.

Common: dyspepsia (including stomach discomfort), abdominal pain. Uncommon: eructation, gastroenteritis, stomatitis, halitosis, gastritis, flatulence, gastrointestinal haemorrhage, dysphagia.

General disorders and administration site conditions.

Common: chills (including rigors). Uncommon: feeling abnormal, feeling hot and/or cold, malaise, thirst, falls (more common in the elderly (≥ 65 years old)). Rare: gait disturbance.

Infections and infestations.

Uncommon: laryngitis.

Investigations.

Uncommon: blood pressure increased (including blood pressure systolic increased, blood pressure diastolic increased), hepatic lab related findings (including alanine aminotransferase increased, hepatic enzyme increased, aspartate aminotransferase increased, liver function test abnormal, gamma-glutamyltransferase increased, blood alkaline phosphatase increased, blood bilirubin increased), weight increased, blood cholesterol increased.
Duloxetine treatment in placebo controlled clinical trials was associated with small mean increases from baseline to endpoint in ALT, AST, CPK, and potassium; infrequent, transient, abnormal values were observed for these analytes in duloxetine-treated patients, compared with placebo-treated patients (see Section 4.4 Special Warnings and Precautions for Use).

Metabolism and nutrition disorders.

Uncommon: dehydration.

Musculoskeletal and connective tissue disorders.

Common: musculoskeletal pain (including myalgia, neck pain), muscle spasm. Uncommon: muscle tightness (including musculoskeletal stiffness), muscle twitching.

Nervous system disorders.

Very common: headache (placebo rate was more than duloxetine rate in MDD trials). Common: lethargy, paraesthesia (including hypoaesthesia, hypoaesthesia facia and paraesthesia oral). Uncommon: dysgeusia, disturbance in attention, dyskinesia, poor quality sleep. Rare: myoclonus.

Psychiatric disorders.

Common: anxiety, sleep disorder, agitation (including feeling jittery, nervousness, restlessness, tension, psychomotor agitation). Uncommon: bruxism, disorientation (including confusional state), apathy, abnormal dreams (including nightmares).

Renal and urinary disorders.

Common: urinary frequency. Uncommon: nocturia, urinary hesitation, urinary retention, dysuria, polyuria. Rare: urine odour abnormal, urine flow decreased.

Reproductive system and breast disorders.

Uncommon: ejaculation disorder (includes ejaculation dysfunction, ejaculation failure), sexual dysfunction, menopausal symptoms, testicular pain. Rare: menstrual disorder.

Respiratory, thoracic and mediastinal disorders.

Common: yawning, oropharyngeal pain. Uncommon: throat tightness.

Skin and subcutaneous tissue disorders.

Common: pruritus. Uncommon: night sweats, photosensitivity reaction, cold sweats, dermatitis contact, increased tendency to bruise.

Vascular disorders.

Uncommon: flushing, peripheral coldness, orthostatic hypotension.

Glucose regulation.

In three clinical trials of duloxetine for the treatment of diabetic neuropathic pain, the mean duration of diabetes was approximately 12 years, the mean baseline fasting blood glucose was 176 mg/dL (9.78 mmol/L), and the mean baseline haemoglobin A1c (HbA1c) was 7.81%. In the 12 week acute treatment phase of these studies, small increases in fasting blood glucose were observed in duloxetine-treated patients. HbA1c was stable in both duloxetine treated and placebo treated patients. In the extension phase of these studies, which lasted up to 52 weeks, there was an increase in HbA1c in both the duloxetine and routine care groups, but the mean increase was 0.3% greater in the duloxetine-treated group. There was also a small increase in fasting blood glucose and in total cholesterol in duloxetine treated patients while those laboratory tests showed a slight decrease in the routine care group.

Spontaneous data.

The following list of adverse drug reactions is based on post-marketing spontaneous reports involving use of duloxetine for any indication, and corresponding reporting rates have been provided. Rare events are defined as those occurring in less than 1/1000 patients; very rare events are those occurring in less than 1/10,000 patients.

Endocrine disorders.

Very rare: Syndrome of inappropriate antidiuretic hormone (SIADH).

Cardiac disorders.

Very rare: Supraventricular arrhythmia.
Frequency not known: Stress cardiomyopathy (Takotsubo cardiomyopathy).

Eye disorders.

Very rare: Glaucoma.

Gastrointestinal disorders.

Very rare: Microscopic colitis.

Hepatobiliary disorders.

Very rare: Alanine aminotransferase (ALT) increased, alkaline phosphatase increased, aspartate aminotransferase (AST) increased, bilirubin increased. Very rare: Hepatitis, jaundice.
Isolated cases of liver failure, including fatal cases, have been reported. A majority of these cases have been reported in patients with past or current risk factors for liver injury, including alcohol abuse, hepatitis or exposure to drugs with known adverse effects on the liver (see Section 4.4 Special Warnings and Precautions for Use).

Immune system disorders.

Very rare: Anaphylactic reaction, hypersensitivity.

Metabolism and nutrition disorders.

Very rare: Hyponatraemia. Hyperglycaemia (reported especially in diabetic patients).

Musculoskeletal and connective tissue disorders.

Very rare: Trismus.

Nervous system disorders.

Very rare: Extrapyramidal disorder, paraesthesia (including electric shock-like sensation) upon treatment discontinuation, serotonin syndrome, seizures, restless legs syndrome, seizures upon discontinuation.

Psychiatric disorders.

Rare: Hallucinations. Very rare: Mania, aggression and anger (particularly early in treatment or after treatment discontinuations).

Renal and urinary disorders.

Rare: Urinary retention.

Reproductive system and breast disorders.

Very rare: Gynaecological bleeding, galactorrhoea, hyperprolactinaemia.
Frequency not known: Postpartum haemorrhage*.
*This event has been reported for the therapeutic class of SSRIs and SNRIs (see Section 4.4 Special Warnings and Precautions for Use; Section 4.6 Fertility, Pregnancy and Lactation).

Skin and subcutaneous tissue disorders.

Rare: Rash. Very rare: Angioneurotic oedema, contusion, cutaneous vasculitis (sometimes associated with systemic involvement), Stevens-Johnson syndrome, urticaria.

Vascular disorders.

Very rare: Orthostatic hypotension (especially at the initiation of treatment), syncope (especially at initiation of treatment), hypertensive crisis.

Adverse events - causality not established.

Very rare cases of the following adverse events have been reported in post-marketing experience, but no causal link between these events and duloxetine has been established.
Abnormal bleeding events e.g. intracerebral, gastrointestinal; blood dyscrasias; cardiac events e.g. myocardial infarction and ventricular arrhythmias; pancreatitis; renal impairment; rhabdomyolysis; skin reactions especially in regards to subcutaneous tissue disorder.

Discontinuation symptoms.

The most commonly reported symptoms following abrupt or tapered discontinuation of duloxetine in clinical trials have included dizziness, nausea, headache, paraesthesia, fatigue vomiting, irritability, nightmares, insomnia, diarrhoea, anxiety, hyperhidrosis, vertigo, somnolence and myalgia (see Section 4.4 Special Warnings and Precautions for Use).

Reporting suspected adverse effects.

Reporting suspected adverse reactions after registration of the medicinal product is important. It allows continued monitoring of the benefit-risk balance of the medicinal product. Healthcare professionals are asked to report any suspected adverse reactions at http://www.tga.gov.au/reporting-problems.

4.9 Overdose

On the available evidence, there is a wide margin of safety in overdose. In premarketing clinical trials, cases of acute ingestions up to 1400 mg, alone or in combination with other drugs, have been reported and have not been fatal. However, in postmarketing experience, fatal outcomes have been reported for acute overdoses, primarily with mixed overdoses, but also with duloxetine only, at doses as low as approximately 1000 mg.
Signs and symptoms of overdose (most with mixed drugs) included serotonin syndrome, somnolence, vomiting and seizures. In animal studies, the major signs of overdose toxicity are related to the CNS and gastrointestinal systems. Signs of toxicity include CNS effects such as tremors, clonic convulsions, ataxia, emesis, and decreased appetite.

Management of overdose.

No specific antidote is known, but if serotonin syndrome ensues, specific treatment (such as with cyproheptadine and/or temperature control) may be considered. An airway should be established. Monitoring of cardiac and vital signs is recommended, along with appropriate symptomatic and supportive measures. Activated charcoal may be useful in limiting absorption. Duloxetine has a large volume of distribution and forced diuresis, haemoperfusion, and exchange perfusion are unlikely to be beneficial.
For information on the management of overdose, contact the Poison Information Centre on 131126 (Australia).

5 Pharmacological Properties

5.1 Pharmacodynamic Properties

Duloxetine is a selective serotonin and noradrenaline reuptake inhibitor (SNRI) for oral administration. It is chemically unrelated to tricyclics, alpha-adrenergic receptor agonists or antimuscarinics.

Mechanism of action.

Duloxetine is a selective serotonin and noradrenaline reuptake inhibitor, and weakly inhibits dopamine uptake with no significant affinity for histaminergic, dopaminergic, cholinergic and adrenergic receptors.
Although the mechanism of the antidepressant action of duloxetine in humans is unknown, it is believed to be related to its potentiation of serotonergic and noradrenergic activity in the CNS. Duloxetine dose-dependently increased extracellular levels of serotonin and noradrenaline in selected brain areas of animals, and neurochemical and behavioural studies in animals indicate an enhancement of central serotonin and noradrenaline neurotransmission. Duloxetine undergoes extensive metabolism, but the major circulating metabolites have not been shown to contribute significantly to the pharmacologic activity of duloxetine. Duloxetine displayed analgesic activity in rodent models of persistent, inflammatory or neuropathic pain, but not acute or arthritic pain.

Clinical trials.

Acute treatment of depression.

The efficacy of duloxetine has been evaluated in six double blind, placebo controlled acute Phase 3 studies of 8-9 weeks duration in 1978 adult outpatients (18 to 83 years) meeting the DSM-IV criteria for major depression at doses of 40 mg to 120 mg daily. In four of these studies, duloxetine was significantly superior to placebo as measured by the mean change in the 17 item Hamilton Depression Rating Scale (HAMD17) total score from baseline to endpoint. Duloxetine doses in these four studies were:
60 mg once daily (two studies);
20 mg twice daily and 40 mg twice daily (one study);
40 mg twice daily and 60 mg twice daily (one study).
In the remaining two studies, duloxetine showed numerically superior mean change compared with placebo. The duloxetine doses in these two studies were:
20 mg twice daily and 40 mg twice daily;
40 mg twice daily and 60 mg twice daily.
In both of these latter studies, the active comparator paroxetine also did not separate significantly from placebo on the primary outcome measure. Response (≥ 50% reduction in HAMD17 total score) and remission (HAMD17 total score ≤ 7) were also significantly higher with duloxetine compared with placebo in five out of six and three out of six acute studies, respectively.
While results were positive for improvement in the HAMD17 at a dose of 20 mg twice daily in one of two studies, this dose did not demonstrate statistical superiority on any other measure including response or remission (see Table 3).
In addition to the HAMD17 total score, several other measures were included in the evaluation of efficacy of duloxetine. HAMD17 Depressed Mood Item (Item 1), the Anxiety Subfactor of the HAMD17, the Patient Global Impressions (PGI) Improvement Score, bodily pain as measured by Visual Analog Scale (VAS), and the Quality of Life in Depression rating scales were also examined. In the four studies where duloxetine demonstrated statistical superiority over placebo as measured by improvement in the HAMD17 total score, results were also positive for the additional measures at doses of 60 mg to 120 mg per day.
In each study and in pooled data, the effectiveness of duloxetine was similar regardless of age, gender or racial origin.

Prevention of depressive relapse.

Patients responding to 12 weeks of acute treatment with open-label duloxetine at a dose of 60 mg once daily were randomly assigned to either duloxetine 60 mg once daily or placebo for a further 6 months (continuation phase) and time to relapse in each group was compared. Of 533 subjects who enrolled in the study, 278 responded and were randomised to duloxetine 60 mg once daily (n = 136) or placebo (n = 142). The estimated probability of depressive relapse at 6 months for placebo was 38.3% and for duloxetine 60 mg once daily was 19.7% (p = 0.004). During the 6-month continuation therapy phase of this study, 17.4% of duloxetine-treated patients met the a priori-defined criteria for relapse compared with 28.5% on placebo (p = 0.042).
Of 88 patients who relapsed during the continuation phase, 87 received double-blind rescue therapy. The patients who relapsed on placebo (n = 58) were treated with duloxetine at a dose of 60 mg once daily, and those relapsing on duloxetine 60 mg once daily (n = 29) were treated with duloxetine 60 mg twice daily. Of those patients relapsing on placebo and treated with duloxetine 60 mg once daily, response (50% reduction in HAMD17 total score) occurred in 77% and remission (HAMD17 total score ≤ 7) occurred in 57% at the end of 12 further weeks of treatment. Of those patients who relapsed on duloxetine 60 mg once daily and who were treated with an increased dose of 60 mg twice daily, 62% met response criteria and 38% met remission criteria.

Use in elderly patients with depression.

The efficacy and safety of duloxetine 60 mg once daily (n = 207) and placebo (n = 104) have been compared in the acute treatment (study duration 8 weeks) of elderly patients with MDD (> 65 years of age, mean age 72.9 years). Duloxetine treated patients experienced improvement in depressive symptoms, as assessed by the Geriatric Depression Scale, from week 1, with least-squares mean changes from baseline to endpoint of -1.34 for placebo-treated patients and -4.07 for duloxetine-treated patients (p < 0.001). On the Hamilton Depression Rating Scale, least squares mean changes from baseline to endpoint for total HAMD score were -3.72 for placebo-treated patients and -6.49 for duloxetine-treated patients (p < 0.001). Duloxetine treated patients also experienced a greater improvement in composite cognitive score than the placebo-treated patients. The least-squares mean change from baseline to endpoint for the composite cognitive score was 0.76 in placebo-treated patients and 1.95 for duloxetine-treated patients (p = 0.013).

General anxiety disorder.

The efficacy of duloxetine has been established in 5 Phase 3 clinical trials. Four of the studies were acute placebo-controlled studies and the fifth was a relapse prevention study. Of the four placebo controlled studies one was a fixed dose study while the other three were flexible dose studies.
Study HMBR (fixed dose) was a randomised double blind trial designed to assess whether duloxetine 120 mg once daily (QD) was superior to placebo in the treatment of GAD as measured by the mean change in Hamilton Anxiety Depression Rating Scale (HAMA) during the 9-week, double-blind, acute therapy phase. A key secondary objective was to assess whether duloxetine 60 mg QD was superior to placebo in the treatment of GAD during the 9-week, double blind acute therapy phase.
Studies HMDT, HMDU and HMDW, respectively, were Phase 3 (flexible dose) randomised double-blind placebo-controlled studies that used the same primary objective: to assess whether duloxetine flexibly dosed from 60 mg to 120 mg QD was superior to placebo in the treatment of GAD as measured by mean change in HAMA total score over 10 weeks. Venlafaxine 75 mg to 225 mg QD was used as an active comparator in studies HMDU and HMDW and data from these trials was combined (designed a priori) to have sufficient power for non-inferiority comparison of duloxetine with venlafaxine. For all 3 studies doses were increased at specified visits if the CGI Improvement score remained at 3 or below or minimally improved.
In all 4 acute placebo controlled studies the mean decrease in HAMA total score was significantly greater for duloxetine-treated patients compared with placebo treated patients as shown in Table 4.
Duloxetine at the recommended dose of 60 mg to 120 mg once daily demonstrated statistically significant superiority over placebo as measured by improvement in the Hamilton Anxiety Scale (HAM-A) total score and by the Sheehan Disability Scale (SDS) global functional impairment score.
Response and remission rates were also higher with duloxetine compared to placebo. Duloxetine showed comparable efficacy results to venlafaxine in terms of improvements on the HAM-A total score.
In study HMDV, a relapse prevention study, patients responding to 6 months of acute treatment with open-label duloxetine were randomised to either duloxetine or placebo for a further 6-months. Duloxetine 60 mg to 120 mg once daily demonstrated statistically significant superiority compared to placebo (p < 0.001) on the prevention of relapse, as measured by time to relapse. The incidence of relapse during the 6-months double-blind follow-up period was 14% for duloxetine and 42% for placebo.

5.2 Pharmacokinetic Properties

Absorption.

In humans, orally administered duloxetine hydrochloride is well absorbed with maximal plasma concentrations (Cmax) of duloxetine occurring 6 hours postdose. Food does not affect the Cmax of duloxetine, however food can delay the time to reach peak concentration from 6 to 10 hours and it marginally decreases the extent of absorption (AUC) by about 11%.
Duloxetine plasma exposure increases in proportion to dose for doses up to 60 mg twice a day. Steady-state plasma concentrations are typically achieved after 3 days of dosing. Based upon AUC, multiple once daily doses of 60 mg produce steady-state concentrations that are approximately 1.5 times higher than that predicted from a 60 mg single dose. Average minimum and maximum steady-state concentrations for the 60 mg once daily dose are 27.0 and 89.5 nanogram/mL, respectively. There is no clinically important difference in the pharmacokinetic parameters of morning and evening doses.

Distribution.

Following oral administration, the apparent volume of distribution of duloxetine averages 1640 L. Duloxetine is highly protein bound (> 90%) to plasma proteins but protein binding is not affected by renal or hepatic impairment. Duloxetine binds to both albumin and α1-acid glycoprotein.

Metabolism.

Duloxetine undergoes extensive metabolism. The 2 major metabolites found in plasma and urine are the glucuronide conjugate of 4-hydroxy duloxetine, and the sulfate conjugate of 5-hydroxy, 6-methoxy duloxetine. Both CYP2D6 and CYP1A2 catalyse the formation of the initial oxidation steps to form 4-, 5-, and 6-hydroxy duloxetine. The metabolites circulating in plasma are in the conjugated form and are not pharmacologically active.

Excretion.

The half-life of duloxetine (unchanged drug) is 12.1 hours. Apparent plasma clearance of duloxetine after an oral dose is 101 L/hr. The majority (70%) of the duloxetine dose is recovered in the urine as conjugated metabolites of oxidative metabolites of duloxetine.
Approximately 20% of the dose is recovered in the faeces as unchanged drug, unconjugated metabolites, or unidentified compounds. Only trace (< 1% of the dose) amounts of unchanged duloxetine are present in the urine.

Special populations.

Gender.

Apparent plasma clearance was lower in females; however, this difference in clearance values does not appear to be clinically significant. The mean half-life of duloxetine was similar between males and females. Dosage adjustment based on gender is not necessary.

Elderly.

Population pharmacokinetic analyses suggest no significant effect of age on the pharmacokinetics of duloxetine in adult male and female patients with major depressive disorder. Dosage adjustment based on age is not necessary for elderly patients.

Children and adolescents < 18 years old.

Duloxetine is not indicated for use in patients under 18 years of age.

Race.

No specific pharmacokinetic study was conducted to investigate the effects of race. Due to large interpatient variability, clinically significant differences in drug level exposure among ethnic groups are not likely.

Smoking status.

Duloxetine bioavailability (AUC) appears to be reduced by about one-third in smokers. Dosage modifications are not recommended for smokers.

Renal impairment.

Duloxetine Cmax and AUC values were approximately 2-fold higher in patients with end stage renal disease (ESRD) receiving chronic intermittent dialysis, compared with subjects with normal renal function. In contrast, the elimination half-life was similar in both groups. A lower dose should be used for patients with ESRD (see Section 4.2 Dose and Method of Administration). Population pharmacokinetic analyses suggest that mild renal dysfunction has no significant effect on apparent plasma clearance of duloxetine.

Hepatic impairment.

Mean duloxetine apparent plasma clearance of patients with moderate cirrhosis of the liver was approximately 15% of that of healthy subjects. The Cmax was similar but the half-life was 34 hours longer. Duloxetine is contraindicated in patients with hepatic impairment (see Section 4.3 Contraindications).

5.3 Preclinical Safety Data

Genotoxicity.

Duloxetine demonstrated no genotoxic potential in a battery of in vitro and in vivo tests, including assays for gene mutation, chromosomal effects, unscheduled DNA synthesis, and sister chromatid exchange.

Carcinogenicity.

Duloxetine was administered in the diet to rats and mice for two years. In rats and male mice there was no increase in the incidence of tumours. In female mice, there was an increased incidence of hepatocellular adenomas and carcinomas at the high dose only (144 mg/kg/day which is 5 times the maximum recommended human dose [MRHD] on a mg/m2 basis). These findings were considered to be secondary to hepatic enzyme induction with associated centrilobular hypertrophy and vacuolation and their relevance to humans is unknown.

6 Pharmaceutical Particulars

6.1 List of Excipients

The enteric capsules also contain Sugar Spheres (ARTG 2535), ascorbic acid, hypromellose, purified talc, sucrose, hypromellose phthalate, triethyl citrate, gelatin, titanium dioxide, indigo carmine, iron oxide yellow (60 mg enteric capsule only), Tekprint SB-4020 Green Ink (ARTG 2652, 30 mg enteric capsule only) and TekPrint SW-0012 White Ink (ARTG 13175, 60 mg enteric capsule only). The enteric capsules are gluten free.

6.2 Incompatibilities

Incompatibilities were either not assessed or not identified as part of the registration of this medicine.
For information on interactions with other medicines and other forms of interactions, see Section 4.5.

6.3 Shelf Life

In Australia, information on the shelf life can be found on the public summary of the Australian Register of Therapeutic Goods (ARTG). The expiry date can be found on the packaging.

6.4 Special Precautions for Storage

Store below 25°C.

6.5 Nature and Contents of Container

Duloxetine Sandoz 30 mg and 60 mg enteric capsule.

PVC-Aclar/Alu or Alu/Alu foil blister packs of 28 enteric capsules.
Not all presentations may be marketed in Australia.

6.6 Special Precautions for Disposal

In Australia, any unused medicine or waste material should be disposed of in accordance with local requirements.

6.7 Physicochemical Properties

Duloxetine hydrochloride is a white to slightly brownish white solid, which is slightly soluble in water.

Chemical structure.

The chemical designation of duloxetine hydrochloride is (+)-(S)-N-methyl-γ-(1- naphthalenyloxy)-2-thiophenepropanamine hydrochloride. Its structural formula is C18H19NOS.HCl (Molecular weight: 333.88) and its chemical structure is:

CAS number.

136434-34-9.

7 Medicine Schedule (Poisons Standard)

S4 - Prescription Only Medicine.

Summary Table of Changes