Ribavirin was first made in 1972 under the national cancer institute's Virus-Cancer program. This was done by researchers from International Chemical and Nuclear Corporation including Roberts A. Smith, Joseph T. Witkovski and Roland K. Robins. It was reported that ribavirin was active against a variety of RNA and DNA viruses in culture and in animals, without undue toxicity in the context of cancer chemotherapies. By the late 1970s, the Virus-Cancer program was widely cons… Webb5 juli 2024 · Generic name: ribavirin (oral) [ RYE-ba-VYE-rin ] Brand names: Copegus, Moderiba, Rebetol, RibaPak, Ribasphere, RibaTab Dosage forms: oral capsule (200 mg), …
ClinicoEconomics and Outcomes Research Volume 7 - Dove Press
WebbRibavirin Used for. Ribavirin is used for the treatment of chronic hepatitis C (CHC) virus infection in combination with other antiviral drugs in patients with compensated liver disease not previously treated with interferon alpha and in adult CHC patients coinfected with HIV. Ribavirin should not be used alone. Webb640 rader · Brand Names. Ibavyr, Rebetol, Virazole. Generic Name Ribavirin DrugBank … hanis and stevenson ortho katy
NDC 65862-207-68 Ribavirin Tablet, Film Coated Oral
WebbIt is based on cephapirin sodium and penicillin v potassium (the active ingredients of Cephapirin sodium and Pen-vee k, respectively), and Cephapirin sodium and Pen-vee k (the brand names). Other drugs that have the same active ingredients (e.g. generic drugs) are not considered. Webb5 apr. 2024 · Generic Name: ribavirin Brand Name: Virazole Drug Class: Hepatitis B Hepatitis C Agents, RSV Agents Last updated on RxList: 4/5/2024 home drugs a-z list Virazole (Ribavirin) side effects drug center FDA Monograph Related Drugs Overview Consumer Information Professional Information Virazole Side Effects Center Find … WebbKeywords: Nucleoside, Triazole, Catalysis, Antiviral, Ribavirin, Acyclovir Abstract: Two new regioisomers acyclonucleosides bearing 1,2,4-triazole rings as the base moiety were synthesised with aliphatic side chain [(2-acetoxyethoxy)methyl]-bromide under solid-liquid phase transfer catalysis (S.L.P.T.C.) and under silylation method. hanis acts