Anthropometric Measurements as Predictors of Low Birth Weight Among Tanzanian Neonates: A Hospital-Based Study
November 7, 2025
Brand Name :
Imunovir
Synonyms :
inosine pranobex
Class :
Antiviral Agent
Dosage Forms & StrengthsÂ
TabletÂ
500 mgÂ
Take daily dose of 50 mg/kg orally in 3 to 4 equally divided doses
Maximum daily dose not more than 3 g
Dosage Forms & StrengthsÂ
TabletÂ
500 mgÂ
Take daily dose of 50 mg/kg orally in 3 to 4 equally divided doses
Maximum daily dose not more than 3 g
Refer to adult dosingÂ
acemetacin may reduce the excretion rate of inosine pranobex, potentially causing a higher serum level
acetaminophen may lower the excretion rate of inosine pranobex, potentially resulting in a higher serum level
Actions and SpectrumÂ
inosine pranobex has antiviral properties and it is effective against different types of viruses, including RNA and DNA viruses.Â
Frequency not defined Â
NervousnessÂ
PruritusÂ
Skin rashÂ
HyperuricemiaÂ
Headache Â
Insomnia Â
DizzinessÂ
ArthralgiaÂ
DiarrheaÂ
Gastric distressÂ
FatigueÂ
Increased urine outputÂ
Black Box WarningÂ
None
Contraindication/Caution:Â
Contraindication:Â
None Â
Caution:Â
Pregnancy consideration:Â
Pregnancy category: N/AÂ
Lactation: Excretion into human milk is unknown Â
Pregnancy Categories:        Â
Category A: well-controlled and Satisfactory studies show no risk to the fetus in the first or later trimester.Â
Category B: there was no evidence of risk to the fetus in animal studies, and there were not enough studies on pregnant women. Â
Category C: there was evidence of risk of adverse effects in animal reproduction studies, and no adequate evidence in human studies must take care of potential risks in pregnant women.Â
Category D: adequate data 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 category.Â
Pharmacology Â
inosine pranobex increases the host’s natural antiviral defense mechanisms, primarily by stimulating the production of interferons including interferon-alpha and interferon-gamma.Â
PharmacodynamicsÂ
inosine pranobex promotes the activation and proliferation of various immune cells, such as T lymphocytes and natural killer (NK) cells. These cells are involved in recognizing and eliminating infected cells.Â
PharmacokineticsÂ
Absorption  Â
inosine pranobex is absorbed from the gastrointestinal tract into the bloodstream. Â
DistributionÂ
inosine pranobex is distributed throughout the body, including different tissues and organs.Â
MetabolismÂ
inosine pranobex undergoes minimal metabolism in the liver. Â
Elimination and excretionÂ
The elimination of inosine pranobex occurs primarily occurs through renal excretion.
AdministrationÂ
inosine pranobex is typically administered orally, and it is available in tables form.
Patient information leafletÂ
Generic Name: inosine pranobexÂ
Why do we use inosine pranobex?Â
inosine pranobex is used to treat certain viral infections, including influenza, Herpes Simplex Virus (HSV), Human Papillomavirus (HPV). inosine pranobex is used in the treatment of slowly progressive subacute sclerosing panencephalitis (PSSP) and due to this delay in neurologic deterioration and prolong life expectancy.Â