Anthropometric Measurements as Predictors of Low Birth Weight Among Tanzanian Neonates: A Hospital-Based Study
November 7, 2025
Brand Name :
Rebetol, RibaTab, Ribasphere, RibaPak
Synonyms :
ribavirin
Class :
Hepatitis B/Hepatitis C Agents, Purine nucleosides
Dosage Forms & Strengths Â
Tablet Â
200mg Â
400mg Â
600mg Â
Inhalation solution Â
6g/vial Â
Oral solution Â
40mg/mL Â
 Â
CAPSULES, ORAL SOLUTION:
In combination with peginterferon alfa-2b:
weight < 66 kg: 400 mg orally two times a day
weight 66-80 kg: 400 mg PO (morning) and 600 mg (evening)
weight 81-105 kg: 600 mg orally two times a day
weight > 105 kg: 600 mg PO (morning) and 800 mg (evening)
In combination with interferon alfa-2b:
weight < 75 kg: 400 mg PO (morning) and 600 mg (evening)
weight >75 kg: 600 mg orally two times a day
Respiratory Syncytial Virus (RSV)Â
(Not approved by FDA) :
6 g/day dissolved and delivered through a Small Particle Aerosol Generator 22-hour period for 5 days
Off-label:
15 - 20
mg/kg
Orally 
divided 3 times a day
3 - 7
days
Note:
ribavirin should only be used under the supervision of a healthcare provider, as it can have potential side effects and may interact with other medications
Dosage Forms & Strengths Â
Tablet Â
200mg Â
400mg Â
600mg Â
Inhalation solution Â
6g/vial Â
Oral solution Â
40mg/mL Â
Respiratory Syncytial Virus (RSV)Â
20
mg/ml
with continuous aerosol administration for 12-18 hours per day for 3-7 days
Age: > 3 years
In combination with peginterferon alfa-2b or interferon alfa-2b: 15 mg/kg orally per day in 2 divided doses
Ribavirin dosages according to weight:
<47 kg: 15 mg/kg orally per day in 2 divided doses
47 -59 kg: 400 mg orally twice a day
60-73 kg: 400 mg orally in the morning and 600 mg in the evening
>73 kg: 600 mg orally twice a day
Off-label
For infants and young children:
6
mg/kg
every 12 hrs
3 - 7
days
refer adult dosing
may enhance the concentration of serum in valsartan
may diminish the concentration of serum when combined with antihepaciviral products
may diminish the concentration of serum when combined with antihepaciviral products
may diminish the concentration of serum when combined with antihepaciviral products
may diminish the concentration of serum when combined with antihepaciviral products
may diminish the concentration of serum when combined with antihepaciviral products
may enhance the serum concentration
may diminish the serum concentration of CYP3A4 Inducers
drospirenone/ethinyl estradiol/levomefolateÂ
may increase the hepatotoxic effect of Ethinyl Estradiol-Containing Products
etonogestrel/ethinyl estradiolÂ
may increase the hepatotoxic effect of each other when combined
may diminish the concentration of serum when combined with antihepaciviral products
may diminish the concentration of serum when combined with antihepaciviral products
may diminish the concentration of serum when combined with antihepaciviral products
may diminish the concentration of serum when combined with antihepaciviral products
may diminish the concentration of serum when combined with antihepaciviral products
it may diminish the excretion rate when combined with gadofosveset, resulting in an enhanced serum level
antiherpetic antivirals decrease the efficacy of talimogene laherparepvec
empagliflozin and linagliptinÂ
may enhance the serum concentration
Actions and Spectrum:
ribavirin is an antiviral medication that exhibits a broad-spectrum activity against a variety of RNA and DNA viruses, including respiratory syncytial virus (RSV), hepatitis C virus (HCV), Lassa fever virus, and some influenza viruses.
The mechanism of action of ribavirin is not entirely understood, but it is thought to interfere with viral replication by inhibiting the synthesis of viral nucleic acids, among other mechanisms. Ribavirin has also been shown to modulate the host immune response, which may contribute to its antiviral effects.
ribavirin is available in various formulations, including oral capsules, oral solution, and inhalation solution. Its clinical use varies depending on the viral infection being treated and the patient population, and it is often used in combination with other antiviral drugs.
Adverse drug reactions:  Â
Frequency Defined Â
>10% Â
Cough Â
1-10% Â
Nausea Â
Vomiting Â
Angina pectoris Â
Dizziness  Â
Diarrhea  Â
Syncope Â
Headache Â
Vertigo Â
<1% Â
Angioedema  Â
 Â
Black Box Warning:
The black box warning for ribavirin states that the drug can cause serious, even fatal, side effects.
Contraindication / Caution:
Contraindications:
Precautions/cautions:
Pregnancy warnings:    Â
AU TGA pregnancy category: N/AÂ
US FDA pregnancy category: N/AÂ
Lactation:Â
Excreted into human milk is unknownÂ
Pregnancy Categories:      Â
Category A: Satisfactory and well-controlled studies show no risk to the fetus in the first or later trimester.      Â
Category B: No evidence shown of risk to the fetus found in animal reproduction studies, and there are not enough studies on pregnant women      Â
Category C: Adverse effects on the fetus found with evidence in animal reproduction studies and no adequate evidence for a result in humans must take care of potential risks in pregnant women      Â
Category D: adequate data available with sufficient evidence of human fetal risk from various platforms, but despite the potential risk, and used only in emergency cases for potential benefits.      Â
Category X: Drugs listed in this category outweigh the risks over benefits. Hence these categories of drugs need to be avoided by pregnant women.      Â
Category N: There is no data available for the drug under this categoryÂ
Pharmacology:
ribavirin is a synthetic nucleoside analogue that resembles the purine nucleotides. It has a broad-spectrum activity against DNA and RNA viruses. Ribavirin inhibits the replication of viruses by disrupting the synthesis of viral RNA and DNA. It also has an immunomodulatory effect, which helps to enhance the antiviral activity of the drug.
Pharmacodynamics:
ribavirin’s precise mechanism of action is not fully understood. However, it is believed to work by inhibiting the synthesis of viral nucleic acids, disrupting viral replication, and inhibiting viral protein synthesis. Ribavirin may also enhance the host’s immune response to the virus, contributing to its antiviral activity.
Pharmacokinetics:
Absorption
ribavirin is rapidly absorbed following oral administration, with peak plasma concentrations occurring within 1-2 hours. Food may delay its absorption but does not significantly affect its overall bioavailability.
Distribution
ribavirin is distributed widely throughout the body, with a volume of distribution of approximately 1.2 L/kg. It crosses the placenta and is distributed into breast milk. It also penetrates into the cerebrospinal fluid, where its concentration is approximately 20% of that in plasma.
Metabolism
ribavirin is metabolized in the liver to several metabolites, including ribavirin mono-, di-, and triphosphate.
Administration:
ribavirin is available in several different formulations, including oral capsules, oral solution, and inhalation solution. The specific administration method and dosing regimen for ribavirin will depend on the condition being treated and the patient population.
For example, in the treatment of hepatitis C virus (HCV), ribavirin is typically administered orally, usually in combination with other antiviral drugs. The recommended dose and duration of treatment will depend on various factors, such as the genotype of the virus, the patient’s medical history, and the severity of liver disease.
In the treatment of respiratory syncytial virus (RSV), ribavirin may be administered via inhalation, usually using a nebulizer. This method of administration allows the drug to be delivered directly to the respiratory tract, where the virus is causing the infection. The recommended dose and duration of treatment will depend on various factors, such as the age of the patient, the severity of illness, and the presence of underlying medical conditions.
Patient Information Leaflet   Â
Generic Name: ribavirinÂ
Why do we use ribavirin?Â
The use of ribavirin for the treatment of Human Metapneumovirus (HMPV) is controversial, and its efficacy in treating HMPV infection has not been clearly established.
However, ribavirin is sometimes used for the treatment of severe or complicated HMPV infections, particularly in immunocompromised patients or those with underlying respiratory conditions. This is because ribavirin has broad-spectrum antiviral activity, and some studies have suggested that it may have in vitro activity against HMPV.
In addition to its antiviral properties, ribavirin has also been shown to have immunomodulatory effects, which may be beneficial in the treatment of certain viral infections. For example, ribavirin has been shown to increase the production of interferon, which is a key component of the host immune response to viral infection.