Prozep 20mg/5ml Oral Solution

Prozep treats depression and anxiety disorders. Like all medicines it can have unwanted effects. It is therefore important that you and your doctor weigh up the benefits of treatment against the possible unwanted effects, before starting treatment.

Prozep is not for use in children and adolescents under 18. See section 2, Children and adolescents aged 8 to 18 years.

Prozep won’t work straight away. Some people taking antidepressants feel worse before feeling better. Your doctor should ask to see you again a couple of weeks after you first start treatment. Tell your doctor if you haven’t started feeling better. See section 3, How to take Prozep.

Some people who are depressed or anxious think of harming or killing themselves. If you start to feel worse, or think of harming or killing yourself, see your doctor or go to a hospital straight away. See section 2.

Don’t stop taking Prozep without talking to your doctor. If you stop taking Prozep suddenly or miss a dose, you may get withdrawal effects. See section 3 for further information.

If you feel restless and feel like you can’t sit or stand still, tell your doctor. Increasing the dose of Prozep may make these feelings worse. See section 4, Possible side-effects.

Taking some other medicines with Prozep can cause problems. You may need to talk to your doctor. See section 2, Taking other medicines.

If you are pregnant or planning to get pregnant, talk to your doctor. See section 2, Pregnancy, breast-feeding and fertility.

• Keep this leaflet. You may need to read it again.
• If you have any further questions, ask your doctor or pharmacist.
• This medicine has been prescribed for you only. Do not pass it on to others. It may harm them, even if their signs of illness are the same as yours.
• If you get any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet. See section 4.

1. What Prozep is and what it is used for
2. What you need to know before you take Prozep
3. How to take Prozep
4. Possible side effects
5. How to store Prozep
6. Contents of the pack and other information

• if you are allergic to fluoxetine or any of the other ingredients of this medicine (listed in section 6). If you develop a rash or other allergic reactions (like itching, swollen lips or face or shortness of breath), stop taking the oral solution straight away and contact your doctor immediately.
• if you are taking other medicines known as irreversible non-selective monoamine oxidase inhibitors (MAOIs) since serious or even fatal reactions can occur (e.g. iproniazid used to treat depression). Treatment with Prozep should only be started at least 2 weeks after discontinuation of an irreversible, non-selective MAOI.
  Do not take any irreversible, non-selective MAOIs for at least 5 weeks after you stop taking Prozep. If Prozep has been prescribed for a long period and/or at a high dose, a longer interval needs to be considered by your doctor.
• if you are taking metoprolol (to treat heart failure) because there is an increased risk of your heart beat becoming too slow.

Talk to your doctor or pharmacist before taking Prozep if any of the following applies to you:

• heart problems;
• appearance of fever, muscle stiffness or tremor, changes in your mental state like confusion, irritability and extreme agitation; you may suffer from the so-called ‘serotonin syndrome’ or ‘neuroleptic malignant syndrome’. Although this syndrome occurs rarely it may result in potentially life-threatening conditions; contact your doctor immediately, since Prozep might need to be discontinued;
• mania now or in the past; if you have a manic episode, contact your doctor immediately because Prozep might need to be discontinued;
• history of bleeding disorders, appearance of bruises or unusual bleeding, or if you are pregnant (see ‘Pregnancy’);
• ongoing treatment with medicines that thin the blood (see ‘Other medicines and Prozep’);
• epilepsy or fits. If you have a fit (seizures) or experience an increase in seizure frequency, contact your doctor immediately; Prozep might need to be discontinued;
• ongoing ECT (electro-convulsive therapy);
• ongoing treatment with tamoxifen (used to treat breast cancer) (see ‘Other medicines and Prozep’);
• starting to feel restless and cannot sit or stand still (akathisia). Increasing your dose of Prozep may make this worse;
• diabetes (your doctor may need to adjust your dose of insulin or other antidiabetic treatment);
• liver problems (your doctor may need to adjust your dosage);
• low resting heart rate and/or if you know that you may have salt depletion as a result of prolonged severe diarrhoea and vomiting (being sick) or usage of diuretics (water tablets);
• ongoing treatment with diuretics (water tablets), especially if you are elderly;
• glaucoma (increased pressure in the eye).

Medicines like Prozep 20 mg/5 ml Oral Solution (so called SSRIs/SNRIs) may cause symptoms of sexual dysfunction (see section 4). In some cases, these symptoms have continued after stopping treatment.

If you are depressed and/or have anxiety disorders, you can sometimes have thoughts of harming or killing yourself. These may be increased when first starting antidepressants, since these medicines all take time to work, usually about two weeks but sometimes longer.

You may be more likely to think like this:

• if you have previously had thoughts about killing or harming yourself
• if you are a young adult. Information from clinical trials has shown an increased risk of suicidal behaviour in adults aged less than 25 years with psychiatric conditions who were treated with an antidepressant.

If you have thoughts of harming or killing yourself at any time, contact your doctor or go to a hospital straight away.

You may find it helpful to tell a close friend or relative that you are depressed or have an anxiety disorder, and ask them to read this leaflet. You might ask them to tell you if they think your depression or anxiety is getting worse, or if they are worried about changes in your behaviour.

Patients under 18 have an increased risk of side effects such as suicide attempt, suicidal thoughts and hostility (predominantly aggression, oppositional behaviour and anger), when they take this class of medicines.

Prozep should only be used in children and adolescents aged 8 to 18 years for the treatment of moderate to severe major depressive episodes (in combination with psychological therapy) and it should not be used to treat other conditions.

Additionally, only limited information concerning the long-term safety of Prozep on growth, puberty, mental, emotional and behavioural development in this age group is available. Despite this, and if you are a patient under 18, your doctor may prescribe Prozep for moderate to severe major depressive episodes, in combination with psychological therapy, because he/she decides that this is in your best interests.

If your doctor has prescribed Prozep for a patient under 18 and you want to discuss this, please go back to your doctor. You should inform your doctor if any of the symptoms listed above develop or worsen when patients under 18 are taking Prozep.

Prozep should not be used in the treatment of children under the age of 8 years.

Tell your doctor or pharmacist if you are taking, have recently taken or might take any other medicines.

Some medicines may be affected by Prozep or they may affect how well Prozep will work.

Do not take Prozep with:

• Certain irreversible, non-selective monoamine oxidase inhibitors (MAOIs), some used to treat depression. Irreversible, non-selective MAOIs must not be used with Prozep as serious or even fatal reactions (serotonin syndrome) can occur (see section ‘Do not take Prozep’). Treatment with Prozep should only be started at least 2 weeks after discontinuation of an irreversible, non-selective MAOI (for instance tranylcypromine). Do not take any irreversible, non-selective MAOIs for at least 5 weeks after you stop taking Prozep. If Prozep has been prescribed for a long period and/or at a high dose, a longer interval than 5 weeks may need to be considered by your doctor.
• metoprolol when used for heart failure; there is an increased risk of your heart beat becoming too slow.
• pethidine (a painkiller) because it increases the risk of serotonin syndrome when taken with Prozep

Prozep may affect the way the following medicines work (interaction):

• tamoxifen (used to treat breast cancer); because Prozep may change the blood levels of this drug, resulting in the possibility of a reduction in the effect of tamoxifen, your doctor may need to consider prescribing a different antidepressant treatment.
• monoamine oxidase inhibitors A (MAOI-A) including moclobemide, linezolid (an antibiotic) and methylthioninium chloride (also called methylene blue, used for the treatment of medicinal or chemical product induced methaemogobinaemia) due to the risk of serious or even fatal reactions (called serotonin syndrome). Treatment with fluoxetine can be started the day after stopping treatment with reversible MAOIs but the doctor may wish to monitor you carefully and use a lower dose of the MAOI-A drug.
• mequitazine (for allergies); because taking this drug with Prozep may increase the risk of changes in the electrical activity of the heart.
• phenytoin (for epilepsy); because Prozep may influence the blood levels of this drug, your doctor may need to introduce phenytoin more carefully and carry out check-ups when given with Prozep.
• lithium, selegiline, St. John’s Wort, tramadol (a painkiller), triptans (for migraine) and tryptophan there is an increased risk of mild serotonin syndrome when these drugs are taken with Prozep. Your doctor will carry out more frequent check-ups.
• medicines that may affect the heart’s rhythm, e.g. Class IA and III antiarrhythmics, anti-psychotics (e.g. phenothiazine derivatives, pimozide, haloperidol), tricyclic antidepressants, certain antimicrobial agents (e.g. sparfloxacin, moxifloxacin, erythromycin IV, pentamidine), anti-malaria treatment particularly halofantrine, or certain antihistamines (astemizole, mizolastine), because taking one or more of these drugs with Prozep may increase the risk of changes in the electrical activity of the heart.
• Anti-coagulants (such as warfarin), NSAID (such as ibuprofen, diclofenac), aspirin and other medicines which can thin the blood (including clozapine, used to treat certain mental disorders). Prozep may alter the effect of these medicines on the blood. If Prozep treatment is started or stopped when you are taking warfarin, your doctor will need to perform certain tests, adjust your dose and check on you more frequently.
• cyproheptadine (for allergies); because it may reduce the effect of Prozep.
• drugs that lower sodium levels in the blood (including, drug that causes increase in urination, desmopressin, carbamazepine and oxcarbazepine); because these drugs may increase the risk of sodium levels in the blood becoming too low when taken with Prozep.
• antidepressants such as tricyclic antidepressants, other selective serotonin reuptake inhibitors (SSRIs) or bupropion, mefloquine or chloroquine (used to treat malaria), tramadol (used to treat severe pain) or anti-psychotics such as phenothiazines or butyrophenones; because Prozep may increase the risk of seizures when taken with these medicines.
• flecainide, propafenone, nebivolol or encainide (for heart problems), carbamazepine (for epilepsy), atomoxetine or tricyclic antidepressants (for example imipramine, desipramine and amitriptyline) or risperidone (for schizophrenia); because Prozep may possibly change the blood levels of these medicines, your doctor may need to lower their dose when administered with Prozep.

You can take Prozep with or without food, whatever you prefer.

You should avoid alcohol while you are taking this medicine.

If you are pregnant or breast-feeding, think you may be pregnant or are planning to have a baby, ask your doctor or pharmacist for advice before taking this medicine.

Pregnancy

Talk to your doctor as soon as possible if you are pregnant, if you might be pregnant, or if you are planning to become pregnant.

In babies whose mothers took fluoxetine during the first few months of pregnancy, there have been some reports suggesting an increased risk of birth defects affecting the heart. In the general population, about 1 in 100 babies are born with a heart defect. This increased to about 2 in 100 babies in mothers who took fluoxetine. It is preferable not to use this treatment during pregnancy unless the potential benefit outweighs the potential risk. You and your doctor may decide that it is better for you to gradually stop taking Prozep while you are pregnant. However, depending on your circumstances, your doctor may suggest that it is better for you to keep taking Prozep.

When taken during pregnancy, particularly in the last 3 months of pregnancy, medicines like fluoxetine may increase the risk of a serious condition in babies, called persistent pulmonary hypertension of the new born (PPHN), making the baby breathe faster and appear bluish. These symptoms usually begin during the first 24 hours after the baby is born. If this happens to your baby, you should contact your midwife and/or doctor immediately.

Caution should be exercised when used during pregnancy, especially during late pregnancy or just before giving birth since the following effects have been reported in new born children: irritability, tremor, muscle weakness, persistent crying, and difficulty in sucking or in sleeping.

If you take Prozep near the end of your pregnancy there may be an increased risk of heavy vaginal bleeding shortly after birth, especially if you have a history of bleeding disorders. Your doctor or midwife should be aware that you are taking Prozep so they can advise you.

Breast-feeding

Fluoxetine is excreted in breast milk and can cause side effects in babies. You should only breast-feed if it is clearly necessary. If breast-feeding is continued, your doctor may prescribe a lower dose of fluoxetine.

Fertility

Fluoxetine has been shown to reduce the quality of sperm in animal studies. Theoretically, this could affect fertility, but impact on human fertility has not been observed as yet.

Psychotropic drugs such as Prozep may affect your judgment or co-ordination. Do not drive or use machinery until you know how Prozep affects you.

• Prozep contains 2.2 g sorbitol in each 5 ml spoonful of fluoxetine oral solution, which is equivalent to 0.44 g/ml. Sorbitol is a source of fructose. If your doctor has told you that you (or your child) have an intolerance to some sugars or if you have been diagnosed with hereditary fructose intolerance (HFI), a rare genetic disorder in which a person cannot break down fructose, talk to your doctor before you (or your child) take or receive this medicine. Sorbitol may cause gastrointestinal discomfort and mild laxative effect.
• Prozep contains 2.5 mg benzoic acid in each 5ml spoonful of fluoxetine oral solution which is equivalent to 0.5 mg/ml.
• Prozep contains 50 mg polyoxyl 40 hydrogenated castor oil in each 5 ml spoonful of fluoxetine oral solution which is equivalent to 10 mg/ml. Castor oil may cause stomach upset and diarrhoea.

The recommended dose is:

• Depression: The recommended dose is 5 ml oral solution (20 mg) daily. Your doctor will review and adjust your dosage if necessary within 3 to 4 weeks of the start of treatment. If required, the dosage can be gradually increased up to a maximum of 15 ml oral solution (60 mg) daily. The dose should be increased carefully to ensure that you receive the lowest effective dose. You may not feel better immediately when you first start taking your medicine for depression. This is usual because an improvement in depressive symptoms may not occur until after the first few weeks. Patients with depression should be treated for at least 6 months.
• Bulimia: The recommended dose is 15 ml oral solution (60 mg) daily.
• Obsessive-compulsive disorder: The recommended dose is 5 ml oral solution (20 mg) daily. Your doctor will review and adjust your dosage if necessary after 2 weeks of treatment. If required, the dosage can be gradually increased up to a maximum of 15 ml oral solution (60 mg) daily. If no improvement is noted within 10 weeks, your doctor will reconsider your treatment.

Treatment should be started and be supervised by a specialist. The starting dose is 10 mg/day (given as 2.5 ml Prozep). After 1 to 2 weeks, your doctor may increase the dose to 20 mg/day (5 ml).

The dose should be increased carefully to ensure that you receive the lowest effective dose. Lower weight children may need lower doses. If there is a satisfactory response to treatment, your doctor will review the need for continuing treatment beyond 6 months. If you have not improved within 9 weeks, your doctor will reassess your treatment.

Your doctor will increase the dose with more caution and the daily dose should generally not exceed 10 ml oral solution (40 mg). The maximum dose is 15 ml oral solution (60 mg) daily.

If you have a liver problem or are using other medication that might affect Prozep, your doctor may decide to prescribe a lower dose or tell you to use Prozep every other day.

• If you take too much, go to your nearest hospital emergency department (or casualty) or tell your doctor straight away.
• Take the bottle of Prozep with you if you can.

Symptoms of overdose include: nausea, vomiting, seizures, heart problems (like irregular heart beat and cardiac arrest), lung problems and change in mental condition ranging from agitation to coma.

If you miss a dose, do not worry. Take your next dose the next day at the usual time. Do not take a double dose to make up for a forgotten dose.

• Taking your medicine at the same time each day may help you to remember to take it regularly.

• Do not stop taking Prozep without asking your doctor first, even when you start to feel better. It is important that you keep taking your medicine.
• Make sure you do not run out of medicine.

You may notice the following effects (withdrawal effects) when you stop taking Prozep: dizziness; tingling feelings like pins and needles; sleep disturbances (vivid dreams, nightmares, inability to sleep); feeling restless or agitated; unusual tiredness or weakness; feeling anxious; nausea/vomiting (feeling sick or being sick); tremor (shakiness); headaches.

Most people find that any symptoms on stopping Prozep are mild and disappear within a few weeks. If you experience symptoms when you stop treatment, contact your doctor.

When stopping Prozep, your doctor will help you to reduce your dose slowly over one or two weeks – this should help reduce the chance of withdrawal effects.

If you get any side effects, talk to your doctor, pharmacist or nurse. This includes any possible side effects not listed in this leaflet. You can also report side effects directly via the Yellow Card Scheme at: www.mhra.gov.uk/yellowcard or search for MHRA Yellow Card in the Google Play or Apple App Store.

By reporting side effects you can help provide more information on the safety of this medicine.

• The active substance is fluoxetine hydrochloride. Each 5 ml of liquid contains 20 mg fluoxetine (as hydrochloride).
• Other ingredients are: glycerol (E 422), sorbitol (E 420), hydrogenated polyoxyl castor oil, benzoic acid (E 210), peppermint flavour and purified water. (See end of Section 2 for further information on sorbitol, benzoic acid and castor oil).

Prozep is a clear, colourless liquid with the odour of peppermint.

It is available in amber glass bottles of 70 ml with a tamper evident child resistant closure.