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Influenza Type A
Type of Influenza s known to cause pandemics
1. Hemagglutinin
2. Neuraminidase
Influenza Type A is characterized by:
Influenza Type B
generally change more slowly in terms of their genetic and antigenic properties than influenza A viruses
1. Victoria
2. Yamagata
Influenza Type B is characterized by:
Influenza Type C
generally cause mild illness and are not thought to cause human flu epidemics
Influenza Type D
primarily affect cattle and are not known to infect or cause illness in people
Neuraminidase
Responsible for cutting off newly form viral particle
Hemagglutinin
Spike protein that attaches to the cell for entrance
Antigenic Drift
point mutations in certain error-prone regions in the genes. These mutations are ongoing and are responsible for the ability of the virus to evade annually acquired immunity in humans
Antigenic Shift
This happens when two kinds of influenza virus infect the same cell and share their genes to make a new version of influenza
Pneumonia
One of the most serious complications of Influenza, and can be deadly
1918 HIN1 influenza pandemic
Spanish Flu
1957 H2N2 influenza pandemic
Asian Flu
1968 H3N2 influenza pandemic
Hong Kong Flu
2009 H1N1 influenza pandemic
Swine Flu
2014 H5N1 influenza pandemic
Bird flu
1. RT-PCR
2. Rapid Test
3. Non-specific Laboratory Tests (CBC, X-ray)
Laboratory tests for Flu:
1. Oseltamivir
2. Zanamavir
Analogs of sialic acid, interfere with release of progeny influenza A and B virus from infected host cells, thus halting the spread of infection within the respiratory tract.
Neuraminidase inhibitors
Oseltamivir, Zanamivir, & Peramivir Pharmacological class
Oseltamivir carboxylate
Oseltamivir active metabolite
Zanamivir
Neuraminidase inhibitor drug that is administered directly to the respiratory tract via inhalation
Peramivir
cyclopentane analog, active against both influenza A and B viruses. Approved for the treatment of acute uncomplicated influenza in adults
Single 600 mg IV
Approved dose of Peramivir
1. Increased risk of hallucinations
2. Delirium
3. Abnormal Behavior
Peramivir ADRs:
1. Laninamivir octanoate
2. IV formulation of zanamivir
3. DAS181
Investigational Drugs for flu:
Laninamivir octanoate
long-acting neuraminidase inhibitor
IV formulation of zanamivir
This is being evaluated in clinical trials and is available for compassionate use from the manufacturer
DAS181
host-directed antiviral agent with activity against influenza and parainfluenza that acts by removing the virus receptor, sialic acid, from adjacent glycan structures.
Quadrivalent vaccine
Vaccine that protects people from two types of A influenza and two types of type B influenza.
Fluarix Tetra (GSK plc / GlaxoSmithKline plc)
Quadrivalent vaccine Brand name and Manufacturer
Jet Injector
Vaccine given to people ages 18 to 64.
Afluria (Pharmajet)
Jet Injector Brand name and Manufacturer
High-dose vaccine
This type of flu vaccine available in the Philippines is given to people over 65 years old, and its dose is four times more potent than the regular vaccine.
Fluzone high-dose quadrivalent (Sanofi)
High-dose vaccine Brand name and Manufacturer
Adjuvanted vaccine
This provides great protection from the flu for people 65 years old and up
Fluad (Novartis)
Adjuvanted vaccine Brand name and Manufacturer
Cell-based vaccine
This vaccine is made using dead viruses grown in the cells of mammals
Flucelvax (Sequris)
Cell-based vaccine Brand name and Manufacturer
Recombinant vaccine
This virus needed for the vaccine is 'grown' through a technical process, and not in eggs.
Flublok Quadrivalent (Protein Science)
Recombinant vaccine Brand name and Manufacturer
Intranasal Vaccine
Live, attenuated, Administered intranasally, indicated for active immunization to prevent influenza A and B
FluMiist (Medimmune)
Intranasal vaccine brand name & manufacturer
Uricosuric Agent
Agents that inhibit the tubular secretion of the active metabolite of oseltamivir may be used as adjunctive therapy with this antiviral drug.
Probenecid
Inhibits tubular secretion of the active metabolite of oseltamivir, reducing its clearance by approximately 50% and approximately doubling systemic exposure to oseltamivir.