Patient Leaflet Updated 23-Apr-2024 | ADVANZ Pharma
Venaxx XL 75 mg and 150 mg
Venaxx XL® 75 mg prolonged-release capsules, hard
Venaxx XL® 150 mg prolonged-release capsules, hard
Venlafaxine
1 What Venaxx XL is and what it is used for
2 What you need to know before you take Venaxx XL
3 How to take Venaxx XL
4 Possible side effects
5 How to store Venaxx XL
6 Contents of the pack and other information
Venaxx XL is an antidepressant that belongs to a group of medicines called serotonin and norepinephrine reuptake inhibitors (SNRIs). This group of medicines is used to treat depression and other conditions such as anxiety disorders. It is thought that people who are depressed and/or anxious have lower levels of serotonin and noradrenaline in the brain. It is not fully understood how antidepressants work, but they may help by increasing the levels of serotonin and noradrenaline in the brain.
Venaxx XL is a treatment for adults with depression. It is also a treatment for adults with the following anxiety disorders: generalized anxiety disorder, social anxiety disorder (fear or avoidance of social situations) and panic disorder (panic attacks).
Treating depression or anxiety disorders properly is important to help you get better. If it is not treated, your condition may not go away and may become more serious and more difficult to treat.
Talk to your doctor or pharmacist before taking Venaxx XL
If you use other medicines (e.g. buprenorphine-containing medicinal products) that taken together with this medicine could increase the risk of developing serotonin syndrome, a potentially life-threatening condition (see section “Other medicines and Venaxx XL”).
Medicines like Venlafaxine (so called SSRIs/SNRIs) may cause symptoms of sexual dysfunction (see section 4). In some cases, these symptoms have continued after stopping treatment
Venlafaxine may cause a sensation of restlessness or an inability to sit or stand still during the first few weeks of treatment. You should tell your doctor if this happens to you.
If any of these conditions apply to you, please talk with your doctor before taking Venlafaxine.
Do not drink alcohol while being treated with Venaxx XL as it can lead to extreme tiredness and unconsciousness. Concomitant use with alcohol and/or certain medicines can make your symptoms of depression and other conditions, such as anxiety disorders worse.
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. These thoughts may also occur when your dose is decreased or during discontinuation of treatment with Venaxx XL.
You may be more likely to think like this:
If you have thoughts about harming or killing yourself at any time, contact your doctor or go to 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.
Dry mouth
Dry mouth is reported in 10% of patients treated with Venaxx XL. This may increase the risk of caries. Therefore, you should take special care in your dental hygiene.
Diabetes
Your blood glucose levels may be altered due to Venaxx XL. Therefore, the dosage of your diabetes medicines may need to be adjusted.
Venaxx XL should normally not be used for children and adolescents under 18 years. Also, you should know that patients under 18 years of age 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. Despite this, your doctor may prescribe Venaxx XL for patients under 18 because he/she decides that this is in their best interests. If your doctor has prescribed this medicine 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 Venaxx XL. Also, the long- term safety effects concerning growth, maturation and cognitive and behavioural development of Venaxx XL in this age group has not yet been demonstrated.
Tell your doctor or pharmacist if you are taking, have recently taken or might take any other medicines.
Your doctor should decide whether you can take this medicine with other medicines.
Do not start or stop taking any medicines, including those bought without a prescription, natural and herbal remedies, before checking with your doctor or pharmacist.
Examples of these medicines include:
Signs and symptoms of serotonin syndrome may include a combination of the following: restlessness, hallucinations, loss of coordination, fast heartbeat, increased body temperature, fast changes in blood pressure, overactive reflexes, diarrhoea, coma, nausea, vomiting.
In its most severe form, serotonin syndrome can resemble Neuroleptic Malignant Syndrome (NMS). Signs and symptoms of NMS may include a combination of fever, fast heartbeat, sweating, severe muscle stiffness, confusion, increased muscle enzymes (determined by a blood test).
Tell your doctor immediately, or go to the casualty department at your nearest hospital if you think serotonin syndrome is happening to you.
You must tell your doctor if you are taking medicines that can affect your heart rhythm.
Examples of these medicines include:
The following medicines may also interact with Venlafaxine and should be used with caution. It is especially important to mention to your doctor or pharmacist if you are taking medicines containing:
Venaxx XL should be taken with food (see section 3 “How to take Venaxx XL”). Do not drink alcohol while being treated with Venaxx XL. Concomitant use with alcohol can lead to extreme tiredness and unconsciousness and can make your symptoms of depression and other conditions, such as anxiety disorders worse.
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.
You should use Venlafaxine only after discussing the potential benefits and the risks to your unborn child with your doctor.
Make sure your midwife and/or doctor know you are on Venlafaxine. When taken during pregnancy, similar drugs (SSRIs) 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.
If you are taking Venaxx XL during pregnancy, in addition to having trouble breathing, another symptom your baby might have when it is born is not feeling properly. If your baby has these symptoms when it is born and you are concerned, contact your doctor and/or midwife who will be able to advise you.
If you take Venaxx XL 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 Venaxx XL so they can advise you.
Venlafaxine passes into breast milk. There is a risk of an effect on the baby. Therefore, you should discuss the matter with your doctor, and he/she will decide whether you should stop breast feeding or stop the therapy with this medicine.
Do not drive or use any tools or machines until you know how Venlafaxine affects you.
This medicinal product contains less than 1 mmol sodium (23 mg) per capsule i.e. essentially 'sodium free'.
Always take this medicine exactly as your doctor or pharmacist has told you. Check with your doctor or pharmacist if you are not sure.
The recommended dose is
The usual recommended starting dose for treatment of depression and social anxiety disorder is 75 mg per day. The dose can be raised by your doctor gradually, and if needed, even up to a maximum dose of 375 mg daily for depression. If you are being treated for panic disorder, your doctor will start with a lower dose (37.5 mg) and then increase the dose gradually. The maximum dose for generalised anxiety disorder, social anxiety disorder and panic disorder is 225 mg/day.
Take Venlafaxine at approximately the same time each day, either in the morning or in the evening. Capsules must be swallowed whole with fluid and not opened, crushed, chewed or dissolved.
Venlafaxine should be taken with food.
If you have liver or kidney problems, talk to your doctor, since your dose of Venaxx XL may need to be different.
Do not stop taking this medicine without talking to your doctor (see the section “If you stop taking Venaxx XL”).
Call your doctor or pharmacist immediately if you take more than the amount of Venlafaxine prescribed by your doctor.
Overdose can be life-threatening, especially with concomitant use of alcohol and/or certain medicines (see “Other medicines and Venaxx XL”).
The symptoms of a possible overdose may include a rapid heartbeat, changes in level of alertness (ranging from sleepiness to coma), blurred vision, seizures or fits, and vomiting.
If you miss a dose, take it as soon as you remember.
However, if it is time for your next dose, skip the missed dose and take only a single dose as usual. Do not take a double dose to make up for a forgotten dose.
Do not take more than the daily amount of Venlafaxine that has been prescribed for you in one day.
Do not stop taking your treatment or reduce the dose without the advice of your doctor even if you feel better. If your doctor thinks that you no longer need Venaxx XL, he/she may ask you to reduce your dose slowly before stopping treatment altogether. Side effects are known to occur when people stop using this medicine, especially when this medicine is stopped suddenly or the dose is reduced too quickly. Some patients may experience symptoms such as suicidal thoughts, aggressiveness, tiredness, dizziness, light-headedness, headache, sleeplessness, nightmares, dry mouth, loss of appetite, nausea, diarrhoea, nervousness, agitation, confusion, ringing in the ears, tingling or rarely electric shock sensation, weakness, sweating, seizures, or flu-like symptoms, problems with eyesight and increase in blood pressure (which can cause headache, dizziness, ringing in the ears, sweating, etc.).
Your doctor will advise you on how you should gradually discontinue this medicine treatment. This can take a period of several weeks or months. In some patients, discontinuation may need to occur very gradually over periods of months or longer. If you experience any of these or other symptoms that are troublesome, ask your doctor for further advice.
If you have any further questions on the use of this medicine, ask your doctor or pharmacist.
Like all medicines, this medicine can cause side effects, although not everybody gets them.
If any of the following happen, do not take more Venlafaxine. Tell your doctor immediately, or go to the casualty department at your nearest hospital:
Uncommon: may affect up to 1 in 100 people
Rare: may affect up to 1 in 1,000 people
Not known: frequency cannot be estimated from the available data
Other side effects that you should tell your doctor about include (The frequency of these side effects are included in the list “Other side effects that may occur” below):
Do not be concerned if you see small white balls or granules in your stools after taking this medicine. Inside Venlafaxine capsules are spheroids (small white balls) that contain the active ingredient (venlafaxine). These spheroids are released from the capsule into your stomach. As they travel through your stomach and intestines, venlafaxine is slowly released. The spheroid “shell” does not dissolve and is passed out in your stools. So, even though you may see spheroids in your stools, your dose of medicine has been absorbed.
Very common: may affect more than 1 in 10 people
Common: may affect up to 1 in 10 people
Uncommon: may affect up to 1 in 100 people
Rare: may affect up to 1 in 1000 people
Very rare: may affect up to 1 in 10,000 people
Not known: frequency cannot be estimated from the available data
Venlafaxine sometimes causes unwanted effects that you may not be aware of, such as increases in blood pressure or abnormal heart beat; slight changes in blood levels or liver enzymes, sodium or cholesterol. More rarely, Venlafaxine may reduce the function of platelets in your blood, leading to an increased risk of bruising or bleeding. Therefore, your doctor may wish to do blood tests occasionally, particularly if you have been taking Venlafaxine for a long time.
If you get any side effects, talk to your doctor, pharmacist. 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.
Keep this medicine out of sight and reach of children.
Do not use this medicine after the expiry date, which is stated on the carton after (EXP).
The expiry date refers to the last day of that month.
Store below 30°C.
Do not throw away any medicines via wastewater or household waste. Ask your pharmacist how to throw away medicines you no longer use. These measures will help protect the environment.
The active substance is Venlafaxine.
Each prolonged-release capsule, hard contains 75 mg or 150 mg of Venlafaxine as venlafaxine hydrochloride.
The other ingredients are:
75 mg prolonged-release capsules, hard:
Capsule content: Hypromellose, ammonio methacrylate copolymer (type B), sodium laurilsulfate, magnesium stearate
Coating: Basic butylated methacrylate copolymer 12.5%
Capsule shell: Gelatin, titanium dioxide (E 171), red iron oxide (E172)
Printing ink: Shellac, black iron oxide (E172), propylene glycol (E1520)
150 mg prolonged-release capsules, hard:
Capsule content: Hypromellose, ammonio methacrylate copolymer (type B), sodium laurilsulfate, magnesium stearate
Coating: Basic butylated methacrylate copolymer 12.5%
Capsule shell: Gelatin, titanium dioxide (E 171), erythrosine (E127), indigotin I (E 132)
Printing ink: Shellac, black iron oxide (E172), propylene glycol (E1520)
75 mg prolonged-release capsules, hard: flesh opaque – flesh opaque size 0 hard gelatin capsules containing two round, biconvex film-coated tablets, with imprint VEN on cap and 75 on body
150 mg prolonged-release capsules, hard: scarlet opaque – scarlet opaque size 00 hard gelatin capsules containing three round, biconvex film-coated tablets, with imprint VEN on cap and 150 on body.
75 mg: 14, 28, 30, 56, 98 and 100 prolonged-release capsules, hard
150 mg: 10, 28, 30, 56, 98 and 100 prolonged-release capsules, hard
Marketing Authorisation Holder:
Manufacturer:
This leaflet was last revised in March 2024
There are a number of organisations that provide help, information and advice for people with depression and their families or carers. You may wish to contact:
For any information about this medicinal product, please contact
Mercury Pharma Group Ltd., medicinal Information by phone at +44 (0) 208 588 9131 or by email to [email protected].
Venaxx is the registered trademark of Mercury Pharma Group Ltd.
Dashwood House, 69 Old Broad Street, London, EC2M 1QS, UK
+44 (0)208 588 9131
www.advanzpharma.com
+44 (0)208 588 9131
+44 (0)208 588 9273