n
(pharmacology) A particular antiviral compound.
n
(pharmacology) A drug used especially as the hydrochloride C₁₀H₁₇N·HCl to prevent infection (as by an influenzavirus) by interfering with virus penetration into host cells.
n
A particular oral antiseptic.
n
An antiseptic used to treat minor infections of the mouth and throat.
n
(pharmacology) An antiviral drug.
n
(pharmacology) Abbreviation of atazanavir. [(pharmacology) An antiretroviral drug of the protease inhibitor class that is administered orally in the form of its sulfate C₃₈H₅₂N₆O₇·H₂SO₄ in conjunction with other antiretroviral agents to treat HIV infected patients.]
n
The antiviral drug 4-amino-1-[(2R,3S,4R,5R)-5-azido-3-fluoro-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]pyrimidin-2-one.
n
(pharmacology) A particular antiviral medication used to treat influenza.
n
(neologism) An antiviral drug that is taken orally in the treatment of influenza A and B and there are common side effects.
n
An experimental drug with anticancer and antiviral properties.
n
(pharmacology) A particular antiviral drug.
n
(pharmacology) A nonnucleoside reverse transcriptase inhibitor [5-(3,5-dichlorophenyl)sulfanyl-4-propan-2-yl-1-(pyridin-4-ylmethyl)imidazol-2-yl]methyl carbamate.
n
An antiviral drug and glucosidase inhibitor.
n
(pharmacology) An antiamebic and antidiarrheal drug.
n
A scabicidal and antipruritic drug.
n
A drug used in bile therapy.
n
A DNA derivative used as an anticoagulant.
n
(pharmacology) A particular antiviral drug.
n
A sulfonamide and a carbonic anhydrase inhibitor.
adj
Applied to a diester pivoxil prodrug of adefovir.
n
An antiviral drug effective against herpes simplex.
n
(pharmacology) An antiviral drug.
n
A compound with immunoregulating activity.
n
(pharmacology) An antiviral drug that is nucleoside analog.
n
(pharmacology) An antiviral medication C₉H₁₃N₅O₄ related to acyclovir and used especially to treat or prevent cytomegalovirus retinitis in immunocompromised individuals.
n
(pharmacology) A particular antiviral drug.
n
A particular antiviral drug used to combat herpesvirus.
n
(pharmacology) An antiviral drug against HIV.
n
An antiviral drug that works by inhibiting mRNA and protein synthesis, especially in poxviruses.
n
A phosphodiesterase inhibitor with antitumor activity, derived from dipyridamole.
n
(pharmacology) A particular kind of anti-infection agent.
n
(pharmacology) A drug that acts as a selective inhibitor of the enzyme catechol O-methyl transferase.
n
(pharmacology) An antiviral drug that is taken orally in the form of its phosphate C₁₆H₂₈N₂O₄·H₃PO₄ and is a neuraminidase inhibitor used in the treatment and prevention of influenza. It is a derivative of shikimic acid, and is marketed as Tamiflu.
n
A particular kind of cough suppressant.
n
(pharmacology) A thiazide diuretic.
n
A DNA topoisomerase inhibitor.
n
(pharmacology) A guanine analogue antiviral drug C₁₀H₁₅N₅O₃ that is used mostly topically for the treatment of recurrent herpes labialis.
n
An oral medication for the treatment of interstitial cystitis.
n
(trademark) Alternative form of Pepto-Bismol [(trademark) A brand of medicine used to treat nausea, heartburn, indigestion, upset stomach and diarrhea, and having a bright pink color.]
n
A particular drug used in the treatment of blood disorders.
n
The antiviral drug N-[2-[(2S)-2-[5-[(3S)-3-aminopyrrolidin-1-yl]-6-methylpyrazolo[1,5-a]pyrimidin-2-yl]piperidine-1-carbonyl]-4-chlorophenyl]methanesulfonamide
n
(pharmacology) A particular antiherpetic drug.
n
A drug used in the treatment of tuberculosis.
n
Alternative form of rimantadine [(pharmacology) A synthetic antiviral drug that is chemically related to amantadine and is administered orally in the form of its hydrochloride C₁₂H₂₁N·HCl in the prevention and treatment of influenza A; 1-(1-adamantyl)ethanamine.]
n
A particular antiviral and antimalarial drug.
n
(pharmacology) A drug used in the treatment of gastric and duodenal ulcers. It is a complex of aluminium hydroxide and a sulfate derivative of sucrose, C₁₂HₘAl₁₆OₙS₈ where m and n are approximately 54 and 75.
n
A uricosuric medication used to treat gout.
n
(pharmacology) An investigational drug for the treatment of acne, psoriasis and other keratinization disorders.
n
A medication for the treatment of plaque psoriasis.
n
(pharmacology) A particular antiretroviral drug.
n
A particular antineoplastic drug.
n
A particular drug with neuroprotective and anticonvulsant effects.
n
A particular gastric acid synthesis inhibitor.
n
A medication for the treatment of actinic keratosis on the face or scalp.
n
A toxin-binding polymer that was investigated for the treatment of diarrhoea associated with CDAD.
n
A particular antineoplastic dinitrobenzamide prodrug.
n
(pharmacology) A cell-permeable tricyclic nucleoside used to treat cancer.
n
(pharmacology) An antiviral drug derived from adamantane and used to treat herpes simplex.
n
Alternative spelling of valaciclovir [(pharmacology) An antiviral prodrug used in the management of herpes simplex and herpes zoster.]
n
(pharmacology) An antiviral medication used to treat cytomegalovirus infections, converted to ganciclovir inside the body by intestinal and hepatic esterases.
n
The antiviral drug 4-amino-2-butoxy-8-{[3-(pyrrolidin-1-ylmethyl)phenyl]methyl}-5,7-dihydropteridin-6-one
n
(pharmacology) An anticonvulsant drug C₆H₁₁NO₂ that inhibits enzymatic degradation of gamma-aminobutyric acid.
n
(pharmacology) An antiviral drug C₁₂H₂₀N₄O₇ that is a neuraminidase inhibitor taken by oral inhalation in the treatment and prophylaxis of Influenzavirus.
n
(pharmacology) A nucleoside analog reverse-transcriptase inhibitor C₁₀H₁₃N₅O₄, a type of antiretroviral drug that inhibits replication of some retroviruses (such as HIV) and was first approved for the treatment of AIDS.
n
The antiviral drug N-[(3-aminooxetan-3-yl)methyl]-2-(1,1-dioxo-3,5-dihydro-2H-1λ6,4-benzothiazepin-4-yl)-6-methylquinazolin-4-amine
n
A chimeric toxin that has been engineered by the addition of zymogens
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