Ribavirin Teva
ribavirin
ribavirin
Keep this leaflet. You may need to read it again.
If you have any further questions, ask your doctor, pharmacist or nurse.
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, pharmacist or nurse. This includes any possible side effects not listed in this leaflet. See section 4.
What Ribavirin Teva is and what it is used for
What you need to know before you use Ribavirin Teva
How to use Ribavirin Teva
Possible side effects
How to store Ribavirin Teva
Contents of the pack and other information
Medicinal product no longer authorised
Ribavirin Teva contains the active substance ribavirin. This medicine stops the multiplication of hepatitis C virus. Ribavirin Teva must not be used alone.
Depending on the genotype of the hepatitis C virus that you have, your doctor may choose to treat you with a combination of this medicine with other medicines. There may be some further treatment limitations if you have or have not been previously treated for chronic hepatitis C infection. Your doctor will recommend the best course of therapy.
The combination of Ribavirin Teva and other medicines is used to treat patients who have chronic hepatitis C (HCV).
Ribavirin Teva may be used in paediatric patients (children 3 years of age and older and adolescents) who are not previously treated and without severe liver disease.
For paediatric patients (children and adolescents) weighing less than 47 kg a solution formulation is available.
If you have any further questions on the use of this medicine, ask your doctor or pharmacist.
Do not take Ribavirin Teva if any of the following apply to you or the child you are caring for.
are allergic to ribavirin or any of the other ingredients of this medicine (listed in section 6).
are pregnant or planning to become pregnant. (see section “Pregnancy and breast-feeding”)
are breast-feeding
had a serious heart problem during the past 6 months
have any blood disorders, such as anaemia (low blood count), thalassemia or sickle-cell anaemia.
Reminder: Please read the “Do not take” section of the Package leaflet for the other medicines used in combination with this medicine.
There are several serious adverse reactions associated with the combination therapy of ribavirin with (peg)interferon alfa. These include:
Psychiatric and central nervous system effects (such as depression, suicidal thoughts, attempted
suicide and aggressive behaviour, etc.). 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
Severe eye disorders
Dental and periodontal disorders: Dental and gum disorders have been reported in patients receiving ribavirin in combination with (peg)interferon alfa-2b. 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
Inability to achieve full adult height may occur in some children and adolescents
Increased hormone related to your thyroid (TSH) in children and adolescents
Paediatric population
Medicinal product no longer authorised
If you are caring for a child and your doctor decides not to defer combination treatment with peginterferon alfa-2b or interferon alfa-2b until adulthood, it is important to understand that this combination therapy induces a growth inhibition that may be irreversible in some patients.
In addition these events have occurred in patients taking Ribavirin Teva:
Haemolysis: Ribavirin Teva can cause a break down in red blood cells causing anaemia which may impair your heart function or worsen symptoms of heart disease.
Pancytopenia: Ribavirin Teva can cause a decrease in your platelet and red and white blood cell count
when used in combination with peginterferon.
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 capsules you or the child you are caring for take, prescribe a different pack size of this medicine, 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.
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.
Talk to your doctor if you or the child you are caring for
are a woman of childbearing age (see section “Pregnancy and breast-feeding”).
are a male and your female partner is of childbearing age (see section “Pregnancy and breast- feeding”).
had a previous heart condition or have heart disease.
have another liver problem in addition to hepatitis C infection.
have problems with your kidneys.
have HIV (human immunodeficiency virus) or have ever had any other problems with your immune system.
Please refer to the Package Leaflet of (peg)interferon alfa for more detailed information on these safety issues.
Reminder: Please read the “Warnings and precautions” section of the Package leaflet for the other medicines used in combination with Ribavirin Teva before you begin combination treatment.
If the child is weighing less than 47 kg or unable to swallow capsules an oral solution of ribavirin is available.
Tell your doctor or pharmacist if you or the child you are caring for, are taking, have recently taken or might take:
azathioprine is a medicine that suppresses your immune system, using this medicine in combination with ribavirin may increase your risk of developing severe blood disorders.
anti-Human Immunodeficiency Virus (HIV) medicines – [nucleoside reverse transcriptase inhibitor (NRTI), and/or combined anti-retroviral therapy (cART)]:
Taking this medicine in combination with an alpha interferon and an anti-HIV medicine 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).
With zidovudine or stavudine, it is not certain if this medicine will change the 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 Teva 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.
Medicinal product no longer authorised
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 cART 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 “Other medicines” section of the Package Leaflet for the other medicines used in combination with Ribavirin Teva before you begin combination treatment with this medicine.
If you are pregnant you must not take this medicine. This medicine 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:
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.
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 or your female partner must use an effective contraceptive during the time you are taking this medicine and for 7 months after stopping treatment. This should be discussed with your doctor (see section “Do not take Ribavirin Teva”).
If you are a woman who is breast-feeding, you must not take this medicine. Discontinue breast- feeding before starting to take this medicine.
This medicine does not affect your ability to drive or use machines; however, other medicines used in combination with Ribavirin Teva 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.
This medicine contains less than 1 mmol sodium (23 mg) per hard capsule, that is to say essentially ‘sodium-free’.
General information about taking this medicine:
Always take this medicine exactly as your doctor has told you. 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 this medicine based on how much you or the child you are caring for weighs.
The recommended dose and duration of Ribavirin Teva depends on how much the patient weighs and the medicines that are used in combination.
Medicinal product no longer authorised
Dosing for children above 3 years of age and adolescents depends on how much the person weighs and the medicines that are used in combination. The recommended dose of Ribavirin Teva combined with interferon alfa-2b or peginterferon alfa-2b, is shown in the below table.
Ribavirin Teva dose based on body weight when used in combination with interferon alfa-2b or peginterferon alfa-2b in children above 3 years of age and adolescents | |||
If the child/adolescent weighs (kg) | Usual daily Ribavirin Teva dose | Number of 200 mg capsules | |
47 - 49 | 600 mg | 1 capsule in the morning and 2 capsules in the evening | |
50 - 65 | 800 mg | 2 capsules in the morning and 2 capsules in the evening | |
> 65 | See adult dose | ||
Take your prescribed dose by mouth with water and during your meal. Do not chew the hard capsules. For children or adolescents who cannot swallow a hard capsule, an oral solution of ribavirin is available.
Reminder: This medicine is only to be used in combination with other medicines for hepatitis C virus infection. For complete information be sure to read the “How to use” section of the Package Leaflet for the other medicines used in combination with Ribavirin Teva .
Tell your doctor or pharmacist as soon as possible.
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.
Please read the “Possible side effects” section of the Package Leaflet for the other medicines used in combination with Ribavirin Teva.
Like all medicines, this medicine used in combination with other medicines 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.
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.
Medicinal product no longer authorised
The following side effects have been reported with the combination of this medicine and an alpha interferon product in adults:
Very commonly reported side effects (may affect more than 1 in 10 people):
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, dizziness, fever, flu-like symptoms, headache, nausea, shaking chills, virus infection, vomiting, weakness,
loss of appetite, loss of weight, stomach pain,
dry skin, irritation, hair loss, itching, muscle pain, muscle aches, pain in joints and muscles, rash.
Commonly reported side effects (may affect up to 1 in 10 people):
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 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 (may affect up to 1 in 100 people):
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 (may affect up to 1 in 1,000 people):
seizure (convulsions)
pneumonia,
Medicinal product no longer authorised
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 (may affect up to 1 in 10,000 people):
suicide,
stroke (cerebrovascular events).
Not known side effects (frequency cannot be estimated from the available data):
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,
change in colour of the tongue.
The following side effects have been reported with the combination of this medicine and an interferon alpha-2b product in children and adolescents:
Very commonly reported side effects (may affect more than 1 in 10 people):
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, dizziness, fever, flu-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, itching, muscle pain, muscle aches, pain in joints and muscles, rash.
Commonly reported side effects (may affect up to 1 in 10 people):
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, gastroesophageal or rectal disorder, incontinence, increased appetite, inflammation of the membrane of the stomach and intestine, stomach upset, loose stools,
Medicinal product no longer authorised
urination disorders, urinary tract infection,
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), increased or decreased sensitivity to touch, increased sweating, increase in muscle movement, tense muscle, 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 (may affect up to 1 in 100 people):
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 self-harm has also been reported in adults, children, and adolescents. This medicine in combination with an alpha interferon product may also cause:
aplastic anaemia, pure red cell aplasia (a condition where the body stopped or reduced the
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 this medicine 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),
Vogt-Koyanagi-Harada syndrome (an autoimmune inflammatory disorder affecting 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).
This medicine 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,
Medicinal product no longer authorised
loss of use, drooping or loss of power of facial muscles, loss of feeling sensation,
loss of vision.
If you are a HCV/HIV co-infected adult patient receiving anti-HIV treatment, the addition of this medicine and peginterferon alfa may increase your risk of worsening liver function combined anti- retroviral therapy (cART) 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 cART, 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 you get any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet. You can also report side effects directly via the national reporting system
listed in Appendix V. By reporting side effects you can help provide more information on the safety of this medicine.
Keep this medicine out of the sight and reach of children.
Do not use this medicine after the expiry date which is stated on the carton and blister after EXP. The expiry date refers to the last day of that month.
Do not store above 30oC
Do not use this medicine if you notice any change in the appearance of the capsules.
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 Ribavirin 200 mg
The other ingredients are calcium hydrogen phosphate, croscarmellose sodium, povidone, magnesium stearate. The capsule shell contains titanium dioxide (E171) and gelatin. The capsule shell imprint contains shellac, titanium dioxide (E171) and indigo carmine
Ribavirin Teva is a white, opaque, hard capsule imprinted with blue ink.
Medicinal product no longer authorised
Ribavirin Teva is available in different pack sizes containing 84, 112, 140 or 168 capsules to be swallowed.
Not all pack sizes may be marketed.
Your physician will prescribe the pack size which is best for you.
Teva B.V. Swensweg 5 2031GA Haarlem The Netherlands
Teva Pharmaceutical Works Private Limited Company Pallagi út 13
Debrecen H-4042
Hungary
Pharmachemie B.V. Swensweg 5
2031 GA Haarlem The Netherlands
Teva Pharma SLU C/C, no 4
Poligono Industrial Malpica 50016 Zaragoza
Spain
For any information about this medicinal product, please contact the local representative of the Marketing Authorisation Holder:
Teva Pharma Belgium N.V./S.A./AG Tél/Tel: +32 38207373
UAB Teva Baltics Tel: +370 52660203
Тева Фарма ЕАД Teл: +359 24899585
Teva Pharma Belgium N.V./S.A./AG Belgique/Belgien
Tél/Tel: +32 38207373
Teva Pharmaceuticals CR, s.r.o. Tel: +420 251007111
Teva Gyógyszergyár Zrt.
Tel: +36 12886400
Teva Denmark A/S. Tlf: +45 44985511
Teva Pharmaceuticals Ireland L-Irlanda
Tel: +353 19127700
TEVA GmbH
Tel: +49 73140208
Teva Nederland B.V. Tel: +31 8000228400
Medicinal product no longer authorised
UAB Teva Baltics Eesti filiaal Tel: +372 6610801
Teva Norway AS Tlf: +47 66775590
Specifar A.B.E.E.
Τηλ: +30 2118805000
ratiopharm Arzneimittel Vertriebs-GmbH Tel: +43 1970070
Teva Pharma, S.L.U. Tel: +34 913873280
Teva Pharmaceuticals Polska Sp. z o.o. Tel: +48 223459300
Teva Santé
Tél: +33 155917800
Teva Pharma - Produtos Farmacêuticos, Lda.
Tel: +351 214767550
Pliva Hrvatska d.o.o. Tel: +385 13720000
Teva Pharmaceuticals S.R.L. Tel: +40 212306524
Teva Pharmaceuticals Ireland Tel: +353 19127700
Pliva Ljubljana d.o.o. Tel: +386 15890390
Teva Finland Oy Finnland
Sími: +358 201805900
TEVA Pharmaceuticals Slovakia s.r.o. Tel: +421 257267911
Teva Italia S.r.l. Tel: +39 028917981
Teva Finland Oy
Puh/Tel: +358 201805900
Specifar A.B.E.E.
Ελλάδα
Τηλ: +30 2118805000
Teva Sweden AB Tel: +46 42121100
UAB Teva Baltics filiāle Latvijā
Tel: +371 67323666
Medicinal product no longer authorised
This leaflet is available in all EU/EEA languages on the European Medicines Agency website.