Ribavirine CT 400 mg, filmomhulde tabletten

Illustratie van Ribavirine CT 400 mg, filmomhulde tabletten
Toelating Nederland
Producent Teva
Verdovend Nee
ATC-Code J05AB04
Farmacologische groep Direct werkende antivirale middelen

Vergunninghouder

Teva

Brochure

Waarvoor wordt dit middel gebruikt?

Ribavirin-CT film-coated tablets contain the active ingredient ribavirin. Your medicine stops the multiplication of many types of viruses, including hepatitis C virus. Ribavirin-CT must not be used without peginterferon alfa-2b or interferon alfa-2b, i.e. your medicine must not be used alone.

Previously untreated patients :

The combination of Ribavirin-CT with peginterferon alfa-2b or interferon alfa-2b is used to treat patients 3 years of age and older who have chronic hepatitis C (HCV) infection.

The combination of Ribavirin-CT with peginterferon alfa-2b is also used to treat patients 18 years of age or older who have chronic hepatitis C, including in patients who are co-infected with clinically stable HIV.

Previously treated adult patients :

The combination of Ribavirin-CT with interferon alfa-2b is used to treat adult patients with chronic hepatitis C, who have previously responded to a treatment with an alpha interferon alone, but whose condition has recurred.

The combination therapy of Ribavirin-CT with peginterferon alfa-2b is used to treat adult patients with chronic hepatitis C who have previously responded to treatment with an alpha interferon (pegylated or non-pegylated), alone or in combination therapy with ribavirin, but whose condition has recurred.

The combination therapy of Ribavirin-CT with peginterferon alfa-2b is used to treat adult patients with chronic hepatitis C who have not responded to previous treatment with an alpha interferon (pegylated or non-pegylated), alone or in combination therapy with ribavirin.

There is no safety or efficacy information on the use of Ribavirin-CT with other forms of interferon (i.e., not alfa-2b).

Advertentie

Wanneer mag u dit middel niet gebruiken of moet u er extra voorzichtig mee zijn?

Ribavirin-CT is not recommended for use in patients under the age of 3 years.

Do not take Ribavirin-CT

If any of the following apply to you or the child you are caring for, do not take Ribavirin-CT and tell your doctor if you:

  • allergicare (hypersensitive) to ribavirin or any of the other ingredients of Ribavirin-CT.
  • pregnantare or planning to become pregnant (see section “Pregnancy and breast-

feeding”).

  • breastare-feeding.
  • had a problem with your heart during the past 6 months.
  • have severe medical conditions that leave you very weak.
- havekidney diseasevereand/or are on haemodialysis.
  • have a serious problem with your liver other than chronic hepatitis C.
- haveblood disordersany , such as anaemia (low blood count), thalassemia, sickle-cell
  anaemia.
  • have autoimmune hepatitis or any other problem with your immune system.
  • are taking medicine that suppresses your immune system (that protects you against infection and some diseases).

Children and adolescents must not take combination therapy with this product and alpha interferon when there is existence or history of serious nervous or mental problems, such as severe depression, thoughts of suicide or attempted suicide.

Reminder: Please read the “Do not take ...” section of the Package Leaflet for peginterferon alfa-2b or interferon alfa-2b before you begin combination treatment with Ribavirin-CT.

Take special care with Ribavirin-CT

Seek medical help immediately if you develop symptoms of a severe allergic reaction (such as difficulty in breathing, wheezing or hives) while taking this treatment.

Children and adolescents weighing less than 47 kg:

The use of Ribavirin-CT film-coated tablets is not recommended.

You should tell your doctor if you or the child you are caring for:

  • are an adult who has or had a severe nervous or mental disorder, confusion, unconsciousness, or have had thoughts of suicide or have attempted suicide.
- have depressionever or develophadsymptoms associated with depression (e.g. feeling of
  sadness, dejection, etc.) while on treatment with ribavirin.
  • are a woman of childbearing age (see section “Pregnancy and breast-feeding”).
  • maleareand yourafemale partner is of childbearing age (see section “Pregnancy and breastfeeding”).
  • had a previous serious heart condition or have cardiac disease.
  • are older than 65 years or if you have problems with your kidneys.
  • have or have had any serious illness.
- have thyroid. problems

During treatment with ribavirin in combination therapy with an alpha interferon, dental and gum disorders, which may lead to loss of teeth, have been reported. In addition, dry mouth that could have a damaging effect on teeth and membranes of the mouth has been reported during long-term treatment with ribavirin in combination therapy with an alpha interferon. You should brush your teeth thoroughly twice daily and have regular dental examinations. In addition some patients may experience vomiting. If you have this reaction, be sure to rinse your mouth thoroughly afterwards.

During treatment with ribavirin in combination therapy with an alpha interferon, patients may experience eye problems, or loss of vision in rare instances. If you receive ribavirin in combination with an alpha interferon, you should have a baseline eye examination. Any patient complaining of

decrease or loss of vision must have a prompt and complete eye examination. Patients with pre64 existing eye disorders (e.g., diabetic or hypertensive retinopathy) should receive periodic eye exams during combination therapy with ribavirin and an alpha interferon. Combination therapy with ribavirin and an alpha interferon should be discontinued in patients who develop new or worsening eye disorders.

Reminder: Please read the “Take special care with...” section of the Package Leaflet for peginterferon alfa-2b or interferon alfa-2b before you begin combination treatment.

Taking other medicines

Please tell your doctor or pharmacist if you or the child you are caring for:

  • are taking or have recently taken any other medicines, including medicines obtained without a prescription.
  • are receiving azathioprine in combination with ribavirin and pegylated alpha interferons and, therefore, may be at an increased risk of developing severe blood disorders.
- are infectedHuman Immunodeficiencywith bothVirus (HIV-positive) and Hepatitis C
Virus (HCV) and are being treated with an anti-HIV medicinal product(s) – [nucleoside
reverse transcriptase inhibitor (NRTI), and/or highly active anti-retroviral therapy
(HAART)]:    
- Taking Ribavirin-CT in combination with an alpha interferon and an anti-HIV
  medicinal product(s) may increase the risk of lactic acidosis, liver failure, and
  blood abnormalities development (reduction in number of red blood cells which
  carry oxygen, certain white blood cells that fight infection, and blood clotting cells
  called platelets). or stavudinezidovudine, it is not certain if Ribavirin-CT will change the
-   With
  way these medicines work. Therefore, your blood will be checked regularly to be

sure that the HIV infection is not getting worse. If it gets worse, your doctor will decide whether or not your Ribavirin-CT treatment needs to be changed. Additionally, patients receiving zidovudine with ribavirin in combination with alpha interferons could be at increased risk of developing anaemia (low number of red blood cells). Therefore the use of zidovudine and ribavirin in combination with alpha interferons is not recommended.

  • Due to the risk of lactic acidosis (a build-up of lactic acid in the body) and pancreatitis, the use of ribavirin and didanosine is not recommended and the use of ribavirin and stavudine should be avoided.
  • Co-infected patients with advanced liver disease receiving HAART may be at increased risk of worsening liver function. Adding treatment with an alpha interferon alone or in combination with ribavirin may increase the risk in this patient subset.

Reminder: Please read the “Taking other medicines” section of the Package Leaflet for peginterferon alfa-2b or interferon alfa-2b before you begin combination treatment with Ribavirin-CT.

Taking Ribavirin-CT with food and drink

Ribavirin-CT must be taken with food.

Pregnancy and breast-feeding

If you are pregnant, you must not take this product. Ribavirin can be very damaging to your unborn baby (embryo).

Both female and male patients must take special precautions in their sexual activity if there is any possibility for pregnancy to occur:

  • Girl or woman of childbearing age: You must have a negative pregnancy test before treatment, each month during treatment, and for the 4 months after treatment is stopped. This should be discussed with your doctor.
  • Men: Do not have sex with a pregnant woman unless you use a condom. This will lessen the possibility for ribavirin to be left in the woman’s body. If your female partner is not pregnant now but is of childbearing age, she must be tested for pregnancy each month during treatment and for the 7 months after treatment has stopped. You and your female partner must each use an effective contraceptive during the time you are taking your medicine and for 7 months after stopping treatment. This should be discussed with your doctor (see section “Do not take Ribavirin-CT”).

If you are a woman who is breast-feeding, you must not take this product. Discontinue breast-feeding before starting to take these tablets.

Driving and using machines

Your medicine does not affect your ability to drive or use machines; however, peginterferon alfa-2b or interferon alfa-2b may affect your ability to drive or use machines. Therefore, do not drive or use machines if you become tired, sleepy, or confused from this treatment.

Advertentie

Hoe gebruikt u dit middel?

General information about taking Ribavirin-CT:

If the child you are caring for is under the age of 3 years, do not administer.

Always take these tablets exactly as your doctor has told you. You should check with your doctor or pharmacist if you are not sure.

Do not take more than the recommended dosage and take the medicine for as long as prescribed. Your doctor has determined the correct dose of Ribavirin-CT based on how much you or the child you are caring for weighs.

Standard blood tests will be taken to check your blood, kidney and liver function.

  • Blood tests will be done regularly to help your doctor to know if this treatment is working.
  • Depending upon the results of these tests, your doctor may change/adjust the number of film- coated tablets you or the child you are caring for take, prescribe a different pack size of Ribavirin-CT, and/or change the length of time to take this treatment.
  • If you have or develop severe kidney or liver problems, this treatment will be stopped.

The usual dose, according to how much the patient weighs, is shown in the table below:

1. Look for the line that shows how much the adult or child/adolescent weighs.

Reminder: If the child is under the age of 3 years, do not administer.

2. Read across on the same line to see how many film-coated tablets to take.

Reminder: If your doctor’s instructions are different from the amounts in the below table, follow your doctor’s instructions.

3. If you have any questions about the dose, ask your doctor.

Ribavirin-CT 400 mg film-coated tablets for oral use - dose based on body weight

If the adult weighs (kg) Usual daily ribavirin Number of 400 mg film-
  dose coated tablets
< 65 800 mg 1 film-coated tablet in
    the morning and 1 film-
    coated tablet in the
    evening
65 – 80 1,000 mg
    200 mg film-coated tablets of
    Ribavirin-CT are available for
    persons weighing 65 – 80 kg.
    Please speak to your doctor or
    pharmacist
81 - 105 1,200 mg 1 film-coated tablet in
    the morning and 2 film-
    coated tablets in the
    evening
> 105 1,400 mg
    200 mg film-coated tablets of
    Ribavirin-CT are available for
    persons weighing > 105 kg.
    Please speak to your doctor or
    pharmacist
If the child/adolescent Usual daily ribavirin Number of 400 mg film-
weighs (kg) dose coated tablets
47 – 49 600 mg
    200 mg film-coated tablets of
    Ribavirin-CT are available for
    persons weighing 47 – 49 kg.
    Please speak to your doctor or
    pharmacist
50 – 65 800 mg 1 film-coated tablet in
    the morning and 1 film-
    coated tablet in the
    evening
> 65 see adult dose and corresponding number of film-coated tablets

Take your prescribed dose by mouth with water and during your meal. Do not chew the film-coated tablets.

Reminder: Ribavirin-CT is only to be used in combination with peginterferon alfa-2b or interferon alfa-2b for hepatitis C virus infection. For complete information be sure to read the “How to use ...” section of the Package Leaflet for peginterferon alfa-2b or interferon alfa-2b.

Interferon medicine that is used in combination with ribavirin may cause unusual tiredness; if you are injecting this medicine yourself or giving it to a child, use it at bedtime.

If you take more Ribavirin-CT than you should

Tell your doctor or pharmacist as soon as possible.

If you forget to take Ribavirin-CT

If you are self-administering treatment, or if you are the caregiver of a child taking this product in combination with interferon alfa-2b or peginterferon alfa-2b, take/administer the missed dose as soon as possible during the same day. If an entire day has gone by, check with your doctor. Do not take a double dose to make up for a forgotten dose.

If you have any further questions on the use of this product, ask your doctor or pharmacist.

Advertentie

Mogelijke bijwerkingen?

Please read the “Possible side effects” section of the Package Leaflet for peginterferon alfa-2b or interferon alfa-2b.

Like all medicines, Ribavirin-CT used in combination with an alpha interferon product can cause side effects, although not everybody gets them. Although not all of these unwanted effects may occur, they may need medical attention if they do occur.

Psychiatric and Central Nervous System:

Some people get depressed when taking ribavirin in combination treatment with an interferon, and in some cases people had thoughts about threatening the life of others, suicidal thoughts or aggressive behaviour (sometimes directed against others). Some patients have actually committed suicide. Be sure to seek emergency care if you notice that you are becoming depressed or have suicidal thoughts or change in your behaviour. You may want to consider asking a family member or close friend to help you stay alert to signs of depression or changes in your behaviour.

Children and adolescents are particularly prone to develop depression when being treated with ribavirin and interferon alpha. Immediately contact the doctor or seek emergency treatment if they display any unusual behavioural symptoms, feel depressed, or feel they want to harm themselves or others.

Growth and development (children and adolescents):

During the one year of treatment with ribavirin in combination with either peginterferon alfa-2b or interferon alfa-2b, some children and adolescents did not grow or gain weight as much as expected. Some children did not reach their projected height within 1-5 years after completing treatment.

Contact your doctor immediately if you notice any of the following side effects occuring during combination treatment with an alpha interferon product:

  • chest pain or persistent cough, changes in the way your heart beats, fainting;
  • confusion, feeling depressed, suicidal thoughts or aggressive behaviour, attempt suicide, thoughts about threatening the life of others;
  • feelings of numbness or tingling;
  • trouble sleeping, thinking or concentrating;
  • severe stomach pain, black or tar-like stools, blood in stool or urine, lower back or side pain;
  • painful or difficult urination;
  • severe bleeding from your nose;
  • fever or chills beginning after a few weeks of treatment;
  • problems with your eyesight or hearing;
  • severe skin rash or redness.

Possible side effects listed below are grouped by frequency of occurrence:

Very common (affects more than 1 user in 10)

Common (affects 1 to 10 users in 100)
Uncommon (affects 1 to 10 users in 1,000)
Rare (affects 1 to 10 users in 10,000)
Very rare (affects less than 1 user in 10,000)
Not known (frequency cannot be estimated from the available data)

The following side effects have been reported with the combination of ribavirin and an alpha interferon product in adults:

Very commonly reported side effects:

  • decreases in the number of red blood cells (that may cause fatigue, shortness of breath, dizziness), decrease in neutrophils(that make you more susceptible to different infections);
  • difficulty concentrating, feeling anxious or nervous, mood swings, feeling depressed or irritable, tired feeling, trouble falling asleep or staying asleep;
  • cough, dry mouth, pharyngitis (sore throat);
- diarrhoea, r,dizzinesflu-like symptoms,feveheadache, nausea, shaking chills, virus
  infection, vomiting, weakness;
  • loss of appetite, loss of weight, stomach pain;
  • dry skin, irritation, pain or redness at the site of injection, hair loss, itching, muscle pain, muscle aches, pain in joints and muscles, rash.

Commonly reported side effects:

  • decrease in blood clotting cells called platelets that may result in easy bruising and spontaneous bleeding, decrease in certain white blood cells called lymphocytes that help fight infection, decrease in thyroid gland activity (which may make you feel tired, depressed, increase your sensitivity to cold and other symptoms), excess of sugar or uric acid (as in gout) in the blood, low calcium level in the blood, severe anaemia;
  • fungal or bacterial infections, crying, agitation, amnesia, memory impaired, nervousness, abnormal behaviour, aggressive behaviour, anger, feeling confused, lack of interest, mental disorder, mood changes, unusual dreams, wanting to harm yourself, feeling sleepy, trouble sleeping, lack of interest in sex or inability to perform, vertigo (spinning feeling);
  • blurred or abnormal vision, eye irritation or pain or infection, dry or teary eyes, changes in your hearing or voice, ringing in ears, ear infection, earache, cold sores (herpes simplex), change in taste, taste loss, bleeding gums or sores in mouth, burning sensation on tongue, sore tongue, inflamed gums, tooth problem, migraine, respiratory infections, sinusitis, nose bleed, nonproductive cough, rapid or difficult breathing, stuffy or runny nose, thirst, tooth disorder;
  • cardiac murmur (abnormal heart beat sounds), chest pain or discomfort, feeling faint, feeling unwell, flushing, increased sweating, heat intolerance and excessive sweating, low or high blood pressure, palpitations (pounding heart beat), rapid heart rate;
  • bloating, constipation, indigestion, intestinal gas (flatus), increased appetite, irritated colon, irritation of prostate gland, jaundice (yellow skin), loose stools, pain on the right side around your ribs, enlarged liver, stomach upset, frequent need to urinate, passing more urine than usual, urinary tract infection, abnormal urine;
  • difficult, irregular, or no menstrual period, abnormally heavy and prolonged menstrual periods, painful menstruation, disorder of ovary or vagina, breast pain, erectile problem;
  • abnormal hair texture, acne, arthritis, bruising, eczema (inflamed, red, itchy and dryness of the skin with possible oozing lesions), hives, increased or decreased sensitivity to touch, nail disorder, muscle spasms, numbness or tingling feeling, limb pain, pain at the site of injection, pain in joints, shaky hands, psoriasis, puffy or swollen hands and ankles, sensitivity to sunlight, rash with raised spotted lesions, redness of skin or skin disorder, swollen face, swollen glands (swollen lymph nodes), tense muscles, tumour (unspecified), unsteady when walking, water impairment.

Uncommonly reported side effects:

  • hearing or seeing images that are not present;
  • heart attack, panic attack;
  • hypersensitivity reaction to the medication;
  • inflammation of pancreas, pain in bone, diabetes mellitus;
- muscle weakness.
Rarely reported side effects:  
- seizure (convulsions);
- pneumonia;
  • rheumatoid arthritis, kidney problems;
  • dark or bloody stools, intense abdominal pain;
  • sarcoidosis (a disease characterised by persistent fever, weight loss, joint pain and swelling, skin lesions and swollen glands);
- vasculitis.

Very rarely reported side effects:

  • suicide.

Not known side effects:

  • thoughts about threatening the life of others;
  • mania (excessive or unreasonable enthusiasm);
  • pericarditis (inflammation of the lining of the heart), pericardial effusion [a fluid collection that develops between the pericardium (the lining of the heart) and the heart itself.

The following side effects have been reported with the combination of ribavirin and an interferon alfa- 2b product in children and adolescents:

Very commonly reported side effects:

  • decreases in the number of red blood cells (that may cause fatigue, shortness of breath, dizziness), decrease in neutrophils (that make you more susceptible to different infections);
  • decrease in thyroid gland activity (which may make you feel tired, depressed, increase your sensitivity to cold and other symptoms);
  • feeling depressed or irritable, feeling sick to stomach, feeling unwell, mood swings, tired feeling, trouble falling asleep or staying asleep, virus infection, weakness;
- diarrhoea, fever,dizzinesflu-like symptoms, headache, loss of or increase in appetite, loss
  of weight, decrease in the rate of growth (height and weight), pain on right side of ribs,
  pharyngitis (sore throat), shaking chills, stomach pain, vomiting;
  • dry skin, hair loss, irritation, pain or redness at the site of injection, itching, muscle pain, muscle aches, pain in joints and muscles, rash.

Commonly reported side effects:

  • decrease in blood clotting cells called platelets (that may result in easy bruising and spontaneous bleeding);
  • excess of triglycerides in the blood, excess of uric acid (as in gout) in the blood, increase in thyroid gland activity (which may cause nervousness, heat intolerance and excessive sweating, weight loss, palpitation, tremors);
  • agitation, anger, aggressive behaviour, behaviour disorder, difficulty concentrating, emotional instability, fainting, feeling anxious or nervous, feeling cold, feeling confused, feeling of restlessness, feeling sleepy, lack of interest or attention, mood changes, pain, poor quality sleep, sleepwalking, suicide attempt, trouble sleeping, unusual dreams, wanting to harm yourself;
  • bacterial infections, common cold, fungal infections, abnormal vision, dry or teary eyes, ear infection, eye irritation or pain or infection, change in taste, changes in your voice, cold sores, coughing, inflamed gums, nose bleed, nose irritation, oral pain, pharyngitis (sore throat), rapid breathing, respiratory infections, scaling lips and clefts in the corners of the mouth, shortness of breath, sinusitis, sneezing, sores in mouth, sore tongue, stuffy or runny nose, throat pain, toothache, tooth abscess, tooth disorder, vertigo (spinning feeling), weakness;
  • chest pain, flushing, palpitations (pounding heart beat), rapid heart rate;
- abnormal liver function;
  • acid reflux, back pain, bedwetting, constipation, gastro-oesophageal or rectal disorder, incontinence, increased appetite, inflammation of the membrane of the stomach and
  intestine, stomach upset, loose stools;
- urination inarydisorders,tract infection; ur
  • difficult, irregular, or no menstrual period, abnormally heavy and prolonged menstrual periods, disorder of vagina, inflammation of the vagina, testis pain, development of male body traits;
  • acne, bruising, eczema (inflamed, red, itchy and dryness of the skin with possible oozing lesions), fingers and toes very sensitive to cold, increased or decreased sensitivity to touch, increased sweating, increase in muscle movement, tense muscle, irritation or itching at the site of injection, limb pain, nail disorder, numbness or tingling feeling, pale skin, rash with raised spotted lesions, shaky hands, redness of skin or skin disorder, skin discolouration, skin sensitive to sunlight, skin wound, swelling due to a build-up of excess water, swollen glands (swollen lymph nodes), tremor, tumour (unspecified).

Uncommonly reported side effects

  • abnormal behaviour, emotional disorder, fear, nightmare;
  • bleeding of the mucous membrane that lines the inner surface of the eyelids, blurred vision, drowsiness, intolerance to light, itchy eyes, facial pain, inflamed gums;
  • chest discomfort, difficult breathing, lung infection, nasal discomfort, pneumonia, wheezing;
- low blood pressure;
- enlarged liver;  
- painful menstruation;
  • itchy anal area (pinworms or ascarids), blistering rash (shingles), decreased sensitivity to touch, muscle twitching, pain in skin, paleness, peeling of skin, redness, swelling.

The attempt to harm yourself has also been reported in adults, children, and adolescents. Ribavirin in combination with an alpha interferon product may also cause:

  • aplastic anaemia, pure red cell aplasia (a condition where the body stopped or reduced them
  production of red blood cells); this causes severe anaemia, symptoms of which would
  include unusual tiredness and a lack of energy;
- delusions;
  • upper and lower respiratory tract infection;
- inflammation of the pancreas;
  • severe rashes which may be associated with blisters in the mouth, nose, eyes and other mucosal membranes (erythema multiforme, Stevens Johnson syndrome), toxic epidermal necrolysis (blistering and peeling of the top layer of skin).

The following other side effects have also been reported with the combination of ribavirin and an alpha interferon product:

  • abnormal thoughts, hearing or seeing images that are not present, altered mental status, disorientation;
  • angioedema (swelling of the hands, feet, ankles, face, lips, mouth, or throat which may cause difficulty in swallowing or breathing), stroke (cerebrovascular events);
- Vogt-Koyanagi-Harada syndrome inflamm(atoryn disorderautoimmuneaffecting the eyes,
  skin and the membranes of the ears, brain and spinal cord);
  • bronchoconstriction and anaphylaxis (a severe, whole-body allergic reaction), constant cough,
  • eye problems including damage to the retina, obstruction of the retinal artery, inflammation of the optic nerve, swelling of the eye and cotton wool spots (white deposits on the retina);
  • enlarged abdominal area, heartburn, trouble having bowel movement or painful bowel movement;
  • acute hypersensitivity reactions including urticaria (hives), bruises, intense pain in a limb, leg or thigh pain, loss of range of motion, stiffness, sarcoidosis (a disease characterised by persistent fever, weight loss, joint pain and swelling, skin lesions and swollen glands).

Ribavirin in combination with peginterferon alfa-2b or interferon alfa-2b may also cause:

  • dark, cloudy or abnormally coloured urine;
  • difficulty breathing, changes in the way your heart beats, chest pain, pain down left arm, jaw pain;
- loss of consciousness;
  • loss of use, drooping or loss of power of facial muscles, loss of feeling sensation;

- loss of vision.

You or your caregiver should call your doctor immediately if you have any of these symptoms.

If you are an HCV/HIV co-infected adult patient receiving anti-HIV treatment, the addition of ribavirin and peginterferon alfa-2b may increase your risk of worsening liver function highly active anti-retroviral therapy (HAART) and increase your risk of lactic acidosis, liver failure, and blood abnormalities development (reduction in number of red blood cells which carry oxygen, certain white blood cells that fight infection, and blood clotting cells called platelets) (NRTI).

In HCV/HIV co-infected patients receiving HAART, the following other side effects have occurred with the combination of ribavirin and peginterferon alfa-2b (not listed above in adults side effects):

- appetite decreased;  
- back pain;  
- CD4 lymphocytes decreased;
  • defective metabolism of fat;
- hepatitis;  
- limb pain;
  • oral candidiasis (oral thrush);
  • various laboratory blood values abnormalities.

If any of the side effects gets serious, or if you notice any side effects not listed in this leaflet, please tell your doctor or pharmacist.

Advertentie

Hoe bewaart u dit middel?

This medicinal product does not require any special storage conditions.

Keep out of the reach and sight of children.

Do not use Ribavirin-CT after the expiry date which is stated on the blister or label and outer carton after EXP. The expiry date refers to the last day of the month.

Tablet container

The shelf life of the tablets after first opening is 8 weeks.

Medicines should not be disposed of via wastewater or household waste. Ask your pharmacist how to dispose of medicines no longer required. These measures will help to protect the environment.

Advertentie

Anvullende Informatie

What Ribavirin-CT contains

  • The active substance is ribavirin. Each film-coated tablet contains 400 mg ribavirin.
  • The other ingredients are: Microcrystalline cellulose, croscarmellose sodium, pregelatinised maize starch, colloidal anhydrous silicia, talc, magnesium stearate, hypromellose, macrogol 6000, titanium dioxide, iron oxide yellow.

What Ribavirin-CT looks like and contents of the pack

Ribavirin-CT are oval, biconvex, yellow film-coated tablets.

Ribavirin-CT is available in different pack sizes containing 14, 20, 28, 42, 56, 60, 84, 112, 140 and 168 film-coated tablets in blister or 14 and 56 film-coated tablets in tablet container.

Not all pack sizes may be marketed.

Ribavirin-CT 400 mg Filmtabletten Ribavirine400 mg,CTfilmomhulde tabletten

Marketing Authorisation Holder

Teva Pharma B.V. Computerweg 10 3542 DR Utrecht Nederland

Manufacturer

Merckle GmbH

Ludwig-Merckle Strasse 3

89143 Blaubeuren-Weiler

Duitsland

HBM Pharma s.r.o. Sklabinská 30 03680 Martin Slowakije

<[To be completed nationally]>

Dit geneesmiddel is geregistreerd onder

Ribavirine CT 400 mg, filmomhulde tabletten RVG 108109

This medicinal product is authorised in the Member States of the EEA under the following names:

Germany:

Netherlands:

This leaflet was last approved in oktober 2013.

Advertentie

Toelating Nederland
Producent Teva
Verdovend Nee
ATC-Code J05AB04
Farmacologische groep Direct werkende antivirale middelen

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