Velpalex Tm 300 mg/400 mg/1 g

    Velpalex Tm 300 mg/400 mg/1 g

    S3


    1. What VELPALEX IV is and what it is used for

    VELPALEX IV contains sodium valproate, which belongs to a group of medicines called antiepileptics. These are used to control epileptic seizures. VELPALEX IV solution for injection is used to treat various types of epileptic seizures (fits) when it is not possible to take sodium valproate tablets. VELPALEX IV is also used in mania: where you may feel excited, elated, agitated, enthusiastic or hyperactive. Mania occurs in an illness called ‘bipolar disorder’.

    2. What you need to know before you are given VELPALEX IV

    VELPALEX IV should not be administered to you:

    • if you are hypersensitive (allergic) to sodium valproate or any of the ingredients of VELPALEX IV (listed in Section 6)
    • if you have liver problems, or have a family history of liver problems
    • if you suffer from porphyria (a rare condition that affects the breakdown of components of red blood cells)
    • if you have a genetic problem causing a mitochondrial disorder (e.g. Alpers-Huttenlocher syndrome)
    • if you suffer from urea cycle disorder (a certain metabolic disorder)
    • if you are pregnant or breastfeeding your baby. See “Warnings and precautions” and “Pregnancy, breastfeeding and fertility”.

    Warnings and precautions

    Talk to your doctor or healthcare provider before you are given VELPALEX IV, if you:

    • have diabetes. VELPALEX IV may affect the results of urine tests
    • have a carnitine palmitoyltransferase type II deficiency, which prevents the body from using certain fats for energy, as you may be more prone to serious side effects
    • have kidney problems. Your doctor may give you a lower dose
    • have a brain disease or a metabolic condition affecting your brain
    • have a ‘urea cycle disorder’ where too much ammonia builds up in the body
    • have an illness called ‘systemic lupus erythematosus (SLE)’ – a disease of the immune system which affects skin, bones, joints and internal organs
    • know that there is a genetic problem caused by a mitochondrial disorder in your family. If you are not sure if any of the above apply to you, talk to your doctor or pharmacist before taking VELPALEX IV
    • are having surgery, including dental surgery, tell the doctor or dentist that you are receiving VELPALEX IV. You will need to take extra care in cleaning your teeth to prevent infection, as side effects of VELPALEX IV include bleeding and swelling of the gums (see section 4).

    3. How VELPALEX IV will be administered

    You will not be expected to give yourself VELPALEX IV. It will be given to you by a person who is qualified to do so. VELPALEX IV treatment must be started and supervised by a doctor specialised in the treatment of epilepsy.

    Dosage

    Your doctor will decide on the amount of VELPALEX IV you will be given. This will depend on your age and weight and will be adjusted to achieve adequate control of your seizures. If you have been taking sodium valproate by mouth, the dose given to you will be the same by injection. Your doctor will tell you when you are ready to switch over to an oral dosage form of valproate. If you have been receiving other medicines for epilepsy the dose of VELPALEX IV will be increased gradually over about 2 weeks. The total daily dose will normally be given by three or four slow injections, lasting 3-5 minutes, into your veins during the day, or by a continuous infusion (drip).

    Patients with kidney problems

    Your doctor may decide to adjust your or your child’s dose.

    Patients taking other medicines for fits (epilepsy)

    You or your child may be taking other medicines for epilepsy at the same time as VELPALEX IV. If so, your doctor should gradually initiate treatment depending on your or your child’s condition. If you have any concerns tell your doctor or nurse. It is important for you to keep having your VELPALEX IV treatment until your doctor decides to stop. If you stop, your seizures may return.

    Tests

    Make sure you or your child keep your regular appointments for a check-up. They are very important as your or your child’s dose may need to be changed. VELPALEX IV can change the levels of liver enzymes shown up in blood tests. This can mean that your or your child’s liver is not working properly.

    If you receive more VELPALEX IV than you should

    Since a healthcare provider will administer VELPALEX IV, he/she will control the dosage. However, in the event of overdosage your doctor will manage the overdosage.

    If you miss a dose of VELPALEX IV

    Since a healthcare provider will administer VELPALEX IV, it is unlikely that the dose will be missed.

    4. Possible side effects

    VELPALEX IV can have side effects. Not all side effects reported for VELPALEX IV are included in this leaflet. Should your general health worsen or if you experience any untoward effects while using VELPALEX IV, please consult your doctor healthcare provider for advice.

    If any of the following happens, tell your doctor immediately:

    • You have an allergic reaction. The signs include: a rash, joint pain, fever (systemic lupus erythematosus), swallowing or breathing problems, swelling of your lips, face, throat or tongue. Hands, feet or genitals may also be affected. More severe allergic reactions can lead to lymph node enlargement and possible impairment of other organs (also known as DRESS syndrome).
    • Liver problems and problems of the pancreas: A sudden illness which may happen in the first six months of treatment. It includes feeling and being sick many times; being very tired, sleepy and weak; stomach pain including very bad upper stomach pain; jaundice (yellowing of the skin or whites of the eyes); loss of appetite; swelling (especially of the legs and feet but may include other parts of the body); worsening of your fits or a general feeling of being unwell. It may sometimes even lead to death.

    These are all very serious side effects. If you have them, you may have had a serious reaction to VELPALEX IV. You may need urgent medical attention or further hospitalisation.

    Tell your doctor immediately if you notice any of the following:

    • You have a skin rash or skin lesions with a pink/red ring and a pale centre which may be itchy, scaly or filled with fluid. The rash may appear especially on the palms or soles of your feet. These could be signs of a serious allergy to the medicine called ‘erythema multiforme’.
    • Blistering or bleeding of the skin around the lips, eyes, mouth, nose and genitals. Also, flu-like symptoms and fever. This may be something called ‘Stevens-Johnson syndrome’.
    • Severe blistering rash where layers of the skin may peel off to leave large areas of raw exposed skin over the body. Also, a feeling of being generally unwell, fever, chills, and aching muscles. This may be something called ‘Toxic epidermal necrolysis’.
    • Bruising more easily and getting more infections than usual. This could be a blood problem called ‘thrombocytopenia’. It can also be due to a fall in the number of white blood cells, bone marrow depression or another condition that affects red blood cells, white blood cells and platelets (pancytopenia) or how the blood clots.
    • Blood clotting problems (bleeding for longer than normal), bruising or bleeding for no reason.
    • Changes in mood, loss of memory, lack of concentration and deep loss of consciousness (coma).
    • Underactive thyroid gland, which may cause tiredness or weight gain (hypothyroidism).
    • Breathing difficulty and pain due to inflammation of the lungs (pleural effusion).
    • Changes in behaviour including being very alert, and sometimes also aggressive, hyperactive and unusual or inappropriate behaviour. This is more likely if other medicines to treat fits, such as phenobarbital and topiramate, are taken at the same time or if the starting dose of VELPALEX IV is high or has been suddenly increased.
    • An increase in the number and severity of convulsions.
    • Changes in the amount of ammonia in the blood. Symptoms of this condition are being sick, problems with balance and coordination, feeling lethargic or less alert.
    • Feeling shaky (tremor), sleepy or unsteady when walking or jerky muscle movements.
    • Feeling tired or confused with loss of consciousness sometimes accompanied by hallucinations or fits.

    These are all serious side effects. You may need urgent medical attention.

    Tell your doctor if you notice any of the following:

    • Frequent side effects:
      • Anaemia (the number of red blood cells in your body is too low), causing weakness, fatigue, pale skin)
      • Too low blood sodium concentration (signs may be mental changes, headache, nausea, vomiting, tiredness, muscle spasms)
      • Weight gain (see “Warnings and precautions”)
      • State of confusion, hallucinations (seeing and hearing things that do not exist)
      • Aggression, agitation
      • Attention disturbances
      • Sleepiness
      • Convulsions
      • Trembling of hands and arms, clumsiness or unsteadiness
      • Headache
      • Involuntary eye movements (nystagmus)
      • Dizziness
      • Hearing loss (which may be irreversible)
      • Diarrhoea
      • Nausea, vomiting
      • Indigestion
      • Gum disease (swollen gums)
      • Stomach or abdominal pain.
      • Sore mouth
      • Hair loss or thinning of hair
      • Nail and nail bed disorders
      • Losing bladder control (incontinence)
      • Painful menstrual periods.
    • Less frequent side effects:
      • Hyperandrogenism (excessive presence of male hormones in females including symptoms like excessive hair growth, acne, male pattern hair loss)
      • Double vision (diplopia)

    Frequency unknown:

    • Malformation of the foetus and developmental disorders (see “Pregnancy, breastfeeding and fertility” and “Warnings and precautions”).

    If you notice any side effects not mentioned in this leaflet, please inform your doctor or pharmacist.

    Reporting of side effects

    If you get side effects, talk to your doctor, pharmacist or nurse. You can also report side effects to SAHPRA via the “Adverse drug reaction and quality problem reporting form”, found online under SAHPRA’s publications: https://www.sahpra.org.za/Publications/Index/8. By reporting side effects, you can help provide more information on the safety of VELPALEX IV can help provide more information on the safety of this medicine.

    5. How VELPALEX IV will be stored

    Store all medicines out of reach of children. Store at or below 25 °C. Keep ampoules in their original package until required for use. The contents of the ampoule are for single use only. Do not use VELPALEX IV after the expiry date printed on the label, container or blister. Return any expired or unused medicine to your pharmacist for safe disposal. Do not dispose of unused medicine in drains or sewerage systems (e.g. toilets).

    Important Disclaimer

    The Velpalex Tm 300 mg/400 mg/1 g professional information leaflet below is the property of Abex Pharmaceutica and is provided on Somayeza exactly as issued, with no.. alterations or editorial changes. We make every effort to keep content current by updating documents as soon as new versions become available. Somayeza serves as a trusted access point for healthcare professionals, but does not replace official sources or clinical judgement. For more details, please read our full disclaimer. read more>>

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