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Rebetol Safety Reports
Total Rebetol reports: 65.Rebetol FDA safety alerts: No.
Reported deaths: 7 Reported hospitalizations: 24.
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Reported Rebetol Side Effects: fatigue, depression, haemoglobin decreased, weight decreased, platelet count decreased, pregnancy of partner, vomiting, dehydration, white blood cell count decreased, influenza like illness, alopecia.
Rebetol Usage.
Showing 1-50 of 65 Next >
Rebetol Side Effects Report #5197810-2Physician from FRANCE reported REBETOL problem on Sept 25, 2006. Female patient, 60 years of age, weighting 220.5 lb, was diagnosed with hepatitis c and was treated with REBETOL. After drug was administered, patient experienced the following problems/side effects: eczema, fatigue, insomnia, pain, weight decreased. REBETOL dosage: 12000 MG, QD; PO. During the same period patient was treated with PEGASYS. Patient recovered.
Rebetol Side Effects Report #5198097-7
REBETOL problem was reported by a Physician from UNITED STATES on Dec 18, 2006. Male patient, 21 years of age, weighting 127.9 lb, was diagnosed with hepatitis c, thrombocytopenia and was treated with REBETOL. After drug was administered, patient experienced the following problems/side effects: abnormal behaviour, anaemia, cardiac failure, cardiomyopathy, encephalopathy, infection, multi-organ failure, neutropenia. REBETOL dosage: 1000 MG; QD; PO. During the same period patient was treated with PEGASYS, NEUMEGA, ALDACTONE, RIFAXIMIN, EPOGEN. Patient died on 11/22/2004.
Rebetol Side Effects Report #5199800-2
Physician from SWITZERLAND reported REBETOL problem on Dec 13, 2006. Male patient, 65 years of age, was diagnosed with hepatitis c and was treated with REBETOL. After drug was administered, patient experienced the following problems/side effects: intervertebral disc protrusion, mononeuritis, muscle atrophy. REBETOL dosage: unknown. Patient was hospitalized. Patient recovered.
Rebetol Side Effects Report #5390815-8
REBETOL problem was reported by a Physician from JAPAN on July 05, 2007. Female patient, 42 years of age, weighting 112.4 lb, was diagnosed with hepatitis c and was treated with REBETOL. After drug was administered, patient experienced the following problems/side effects: viith nerve paralysis. REBETOL dosage: 600 MG;PO. During the same period patient was treated with INTRON A, INTRON A. Patient recovered.
Rebetol Side Effects Report #5390997-8
Health Professional from UNITED STATES reported REBETOL problem on July 09, 2007. Male patient, 52 years of age, weighting 224.0 lb, was diagnosed with hepatitis c and was treated with REBETOL. After drug was administered, patient experienced the following problems/side effects: abdominal pain, aspartate aminotransferase increased, diarrhoea, haematocrit decreased, haemoglobin decreased, haemorrhage, influenza like illness, nausea, platelet count decreased. REBETOL dosage: 1200 MG;QD;PO. During the same period patient was treated with INFERGEN. Patient was hospitalized. Patient died on 06/07/2007.
Rebetol Side Effects Report #5397748-1
REBETOL problem was reported by a Physician from JAPAN on July 18, 2007. Female patient, 42 years of age, weighting 112.4 lb, was diagnosed with hepatitis c and was treated with REBETOL. After drug was administered, patient experienced the following problems/side effects: facial palsy. REBETOL dosage: 600 MG;PO. During the same period patient was treated with INTRON A, INTRON A. Patient was hospitalized. Patient recovered.
Rebetol Side Effects Report #5401222-3
Consumer or non-health professional from UNITED STATES reported REBETOL problem on July 18, 2007. Female patient, 46 years of age, was diagnosed with hepatitis and was treated with REBETOL. After drug was administered, patient experienced the following problems/side effects: alopecia, amnesia, gout, immune system disorder. REBETOL dosage: unknown. During the same period patient was treated with INFERGEN. Patient recovered.
Rebetol Side Effects Report #5401834-7
REBETOL problem was reported by a Physician from NETHERLANDS on July 17, 2007. Female patient, 52 years of age, weighting 156.5 lb, was diagnosed with hepatitis c and was treated with REBETOL. After drug was administered, patient experienced the following problems/side effects: malignant melanoma. REBETOL dosage: 1000 MG;. During the same period patient was treated with PEGASYS. Patient recovered.
Rebetol Side Effects Report #5421898-4
Physician from UNITED STATES reported REBETOL problem on Mar 08, 2007. Male patient, 17 years of age, weighting 164.0 lb, was diagnosed with hepatitis c and was treated with REBETOL. After drug was administered, patient experienced the following problems/side effects: suicide attempt. REBETOL dosage: 1200 MG;QD;PO. During the same period patient was treated with INTRON A, CELEXA. Patient recovered.
Rebetol Side Effects Report #5412221-X
REBETOL problem was reported by a Consumer or non-health professional from UNITED STATES on July 31, 2007. Female patient, 33 years of age, was diagnosed with hepatitis c and was treated with REBETOL. After drug was administered, patient experienced the following problems/side effects: blood thyroid stimulating hormone decreased, hyperthyroidism, nausea, palpitations, pancreatitis, red blood cell count decreased, vomiting, white blood cell count decreased. REBETOL dosage: unknown. During the same period patient was treated with PEGASYS, PHENERGAN. Patient was hospitalized. Patient recovered.
Rebetol Side Effects Report #5442601-8
Consumer or non-health professional from UNITED STATES reported REBETOL problem on Aug 21, 2007. Female patient was diagnosed with hepatitis c and was treated with REBETOL. After drug was administered, patient experienced the following problems/side effects: alopecia, asthenia, malaise, pneumonia, pulmonary sarcoidosis, weight decreased. REBETOL dosage: unknown. During the same period patient was treated with INTRON A. Patient recovered.
Rebetol Side Effects Report #5449694-2
REBETOL problem was reported by a Physician from FRANCE on Aug 29, 2007. Male patient, 59 years of age, was diagnosed with hepatitis c and was treated with REBETOL. After drug was administered, patient experienced the following problems/side effects: clonus, confusional state, coordination abnormal, depressed level of consciousness, electroencephalogram abnormal, encephalitis, epilepsy, lumbar puncture abnormal, myoclonus. REBETOL dosage: 800 MG;QD;PO. During the same period patient was treated with ROFERON. Patient was hospitalized. Patient recovered.
Rebetol Side Effects Report #5450680-7
Consumer or non-health professional from UNITED STATES reported REBETOL problem on Sept 04, 2007. Female patient, 47 years of age, was diagnosed with hepatitis c and was treated with REBETOL. After drug was administered, patient experienced the following problems/side effects: alopecia, asthenia, dehydration, headache, malaise, oral intake reduced, pulmonary sarcoidosis, vomiting, weight decreased. REBETOL dosage: unknown. During the same period patient was treated with INTRON A. Patient recovered.
Rebetol Side Effects Report #5466735-7
REBETOL problem was reported by a Physician from FRANCE on Sept 12, 2007. Female patient, 31 years of age, was diagnosed with hepatitis c and was treated with REBETOL. After drug was administered, patient experienced the following problems/side effects: diabetic ketoacidosis, mania, mental disorder. REBETOL dosage: 800 MG;QD;PO. During the same period patient was treated with VIRAFERONPEG, ZOLOFT. Patient was hospitalized. Patient recovered.
Rebetol Side Effects Report #5470307-8
Consumer or non-health professional from UNITED STATES reported REBETOL problem on Sept 17, 2007. Male patient was diagnosed with hepatitis c and was treated with REBETOL. After drug was administered, patient experienced the following problems/side effects: convulsion. REBETOL dosage: unknown. During the same period patient was treated with INTRON A. Patient recovered.
Showing 1-50 of 65 Next >
Drug Information: Ribavirin
URL of this page: http://www.nlm.nih.gov/medlineplus/druginfo/medmaster/a605018.html
(rye ba vye' rin)IMPORTANT WARNING:
| Ribavirin will not treat hepatitis C (a virus that infects the liver and may cause severe liver damage or liver cancer) unless it is taken with another medication. If you have hepatitis C, your doctor will prescribe another medication to take with ribavirin. Take both medications exactly as directed. Ribavirin may cause anemia (condition in which there is a decrease in the number of red blood cells). Tell your doctor if you have ever had a heart attack and if you have or have ever had high blood pressure, breathing problems, any condition that affects your blood such as sickle cell anemia (inherited condition in which the red blood cells are abnormally shaped and cannot bring oxygen to all parts of the body) or thalassemia (Mediterranean anemia; a condition in which the red blood cells do not contain enough of the substance needed to carry oxygen), or heart disease. If you experience any of the following symptoms, call your doctor immediately: excessive tiredness, pale skin, headache, dizziness, confusion, fast heartbeat, weakness, shortness of breath, or chest pain. Keep all appointments with your doctor and the laboratory. Your doctor will order blood tests before you start taking ribavirin and often during the first 4 weeks of your treatment.Your doctor or pharmacist will give you the manufacturer's patient information sheet (Medication Guide) when you begin treatment with ribavirin and each time you refill your prescription. Read the information carefully and ask your doctor or pharmacist if you have any questions. You also can obtain the Medication Guide from the FDA website: http://www.fda.gov/cder/foi/label/2002/21511_Copegus_lbl.pdf.Talk to your doctor about the risks of taking ribavirin.For female patients:Do not take ribavirin if you are pregnant or plan to become pregnant. You should not start taking ribavirin until a pregnancy test has shown that you are not pregnant. You must use two forms of birth control and be tested for pregnancy every month during your treatment and for 6 months afterward. Call your doctor immediately if you become pregnant during this time. Ribavirin may cause harm or death to the fetus.For male patients:Do not take ribavirin if your partner is pregnant or plans to become pregnant. If you have a partner who can become pregnant, you should not start taking ribavirin until a pregnancy test shows that she is not pregnant. You must use two forms of birth control, including a condom with spermicide during your treatment and for 6 months afterward. Your partner must be tested for pregnancy every month during this time. Call your doctor immediately if your partner becomes pregnant. Ribavirin may cause harm or death to the fetus. |
Why is this medication prescribed?
Ribavirin is used with another medication called an interferon to treat hepatitis C. Ribavirin is in a class of antiviral medications called nucleoside analogues. It works by stopping the virus that causes hepatitis C from spreading inside the body. It is not known if treatment that includes ribavirin and another medication cures hepatitis C infection, prevents liver damage that may be caused by hepatitis C, or prevents the spread of hepatitis C to other people.
How should this medicine be used?
Ribavirin comes as a tablet, a capsule and an oral solution (liquid) to take by mouth. It is usually taken twice a day, in the morning and the evening, for 24-48 weeks or longer. Take ribavirin tablets with food. Take ribavirin capsules and oral solution with food, unless your doctor tells you that you may take ribavirin with or without food. In that case, be sure to take the medication the same way every day. It is best to take ribavirin at around the same times every day. Follow the directions on your prescription label carefully, and ask your doctor or pharmacist to explain any part you do not understand. Take ribavirin exactly as directed. Do not take more or less of it or take it more often than prescribed by your doctor.
Shake the liquid well before each use to mix the medication evenly. Be sure to wash the measuring spoon or cup after use each time you measure the liquid.
Your doctor may decrease your dose or tell you to stop taking ribavirin for a short time if you develop side effects of the medication. Call your doctor if you are bothered by side effects of ribavirin. Do not decrease your dose or stop taking ribavirin unless your doctor tells you that you should.
Other uses for this medicine
Ribavirin is also sometimes used to treat viral hemorrhagic fevers (viruses that can cause bleeding inside and outside of the body, problems with many organs, and death). In the event of biological warfare, ribavirin may be used to treat viral hemorrhagic fever that has been spread deliberately. Ribavirin is also sometimes used to treat severe acute respiratory syndrome (SARS; a virus that may cause breathing problems, pneumonia, and death). Talk to your doctor about the possible risks of using this drug for your condition.
This medication may be prescribed for other uses; ask your doctor or pharmacist for more information.
What special precautions should I follow?
Before taking ribavirin,
- tell your doctor and pharmacist if you are allergic to ribavirin or any other medications. If you are taking ribavirin tablets, tell your doctor if you are allergic to corn.
- tell your doctor and pharmacist what other prescription and nonprescription medications, vitamins, nutritional supplements, and herbal products you are taking. Be sure to mention the medications listed in the IMPORTANT WARNING section and any of the following: medications for anxiety, depression,or any other mental illness; medications for human immunodeficiency virus (HIV) or acquired immunodeficiency syndrome (AIDS) such as didanosine (Videx), stavudine (Zerit), and zidovudine (Retrovir); and medications that supress the immune system such as cancer chemotherapy, cyclosporine (Neoral, Sandimmune), sirolimus (Rapamune), and tacrolimus (Prograf). If you are taking ribavirin capsules, tell your doctor if you are taking antacids. Your doctor may need to change the doses of your medications or monitor you carefully for side effects.
- tell your doctor if you drink or have ever drunk large amounts of alcohol, if you use or have ever used street drugs, if you have ever thought about killing yourself or planned or tried to do so, and if you have ever had an organ transplant. Also tell your doctor if you have or have ever had a mental illness such as depression, anxiety, or psychosis (loss of contact with reality); cancer; psoriasis (an inherited skin condition); HIV or AIDS; diabetes; sarcoidosis (a condition in which abnormal tissue grows in parts of the body such as the lungs); Gilbert's syndrome (a mild liver condition that may cause yellowing of the skin or eyes); gout (a type of arthritis caused by crystals deposited in the joints); any type of liver disease other than hepatitis C;or thyroid, kidney, pancreas,eye, or lung disease.
- tell your doctor if you have ever taken any medication to treat hepatitis C. Be sure that your doctor has your complete medical records and knows how well you responded to other treatments for hepatitis C.
- tell your doctor if you are breast-feeding. You should not breastfeed while you are taking ribavirin.
- you should know that ribavirin may make you drowsy, dizzy, or confused. Do not drive a car or operate machinery until you know how this medication affects you.
- do not drink alcoholic beverages while you are taking ribavirin. Alcohol can make your liver disease worse.
What special dietary instructions should I follow?
Be sure to drink plenty of fluids while you are taking ribavirin.
What should I do if I forget a dose?
If you remember the missed dose that same day, take the medication right away. However, if you do not remember the missed dose until the next day, call your doctor to find out what to do. Do not take a double dose to make up for a missed one.
What side effects can this medication cause?
Ribavirin may cause side effects. Tell your doctor if any of these symptoms are severe or do not go away:
- cough
- upset stomach
- vomiting
- diarrhea
- constipation
- heartburn
- loss of appetite
- weight loss
- changes in ability to taste food
- dry mouth
- difficulty concentrating
- difficulty falling asleep or staying asleep
- memory loss
- rash
- dry, irritated, or itchy skin
- sweating
- painful or irregular menstruation (period)
- muscle or bone pain
- hair loss
Some side effects can be serious. The following symptoms are uncommon, but if you experience any of them, or those listed in the IMPORTANT WARNING section, call your doctor immediately:
- hives
- swelling of the face, throat, tongue, lips, eyes, hands, feet, ankles, or lower legs
- hoarseness
- difficulty swallowing or breathing
- pain in the stomach or lower back
- bloody diarrhea
- bright red blood in stools
- black, tarry stools
- unusual bleeding or bruising
- vision changes
- fever, chills, and other signs of infection
- depression
- thinking about hurting or killing yourself
- mood changes
- excessive worry
- irritability
- starting to use street drugs or alcohol again if you used these substances in the past
- worsening of psoriasis that you had before you started to take ribavirin
- intolerance to cold
Ribavirin may slow growth and weight gain in children. Talk to your child's doctor about the risks of giving this medication to your child.
Ribavirin may cause other side effects. Call your doctor if you have any unusual problems while taking this medication.
If you experience a serious side effect, you or your doctor may send a report to the Food and Drug Administration's (FDA) MedWatch Adverse Event Reporting program online [at http://www.fda.gov/MedWatch/index.html] or by phone [1-800-332-1088].
What storage conditions are needed for this medicine?
Keep this medication in the container it came in, tightly closed, and out of reach of children. Store ribavirin tablets and capsules at room temperature and away from excess heat and moisture (not in the bathroom). Store ribavirin oral solution in the refrigerator or at room temperature. Throw away any medication that is outdated or no longer needed. Talk to your pharmacist about the proper disposal of your medication.
In case of emergency/overdose
In case of overdose, call your local poison control center at 1-800-222-1222. If the victim has collapsed or is not breathing, call local emergency services at 911.
What other information should I know?
Do not let anyone else take your medication. Ask your pharmacist any questions you have about refilling your prescription.
It is important for you to keep a written list of all of the prescription and nonprescription (over-the-counter) medicines you are taking, as well as any products such as vitamins, minerals, or other dietary supplements. You should bring this list with you each time you visit a doctor or if you are admitted to a hospital. It is also important information to carry with you in case of emergencies.
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