Gyógyszerek Flashcards
2nd generation Fluoroquinolones
Ciprofloxacin Enoxacin Lomefloxacin Nadifloxacin Norfloxacin Ofloxacin Pefloxacin Rufloxacin
1st generation Fluoroquinolones
Flumequine Nalidixic acid Oxolinic acid Piromidic acid Pipemidic acid Rosoxacin
3rd generation Fluoroquinolones
Balofloxacin Gatifloxacin Grepafloxacin Levofloxacin Moxifloxacin Pazufloxacin Sparfloxacin Temafloxacin Tosufloxacin
4th generation fluoroquinolones
Besifloxacin Clinafloxacin Gemifloxacin Sitafloxacin Trovafloxacin Prulifloxacin
Atovaquon/Proguanil (Malarone) hat nur Wechselwirkungen mit…
…antiretroviralen Mittel (?)
Avelox hatóanyag?
Moxifloxacin
Adexor hatóanyag?
Trimetazidine
Xeter hatóanyag?
Rosuvastatin
Vidotin hatóanyag?
Perindopril
Macrolidok
Azithromycin Erythromycin Clarithromycin Dirithromycin Roxithromycin Ketolides: Telithromycin
Aminoglycosidok
Amikacin Gentamicin Kanamycin Neomycin Netilmicin Paromomycin Streptomycin Tobramycin
Invanz hatóanyag
Ertapenem
Brinaldix hatóanyag
Clopamide
Chinotal hatóanyag
Pentoxyphillin
Vessel hatóanyag
Sulodexide
D-penicillamine, used to treat rheumatoid arthritis and Wilson disease, induces production of antibodies to …. This results in a syndrome clinically similar to ….
….acetylcholine receptor….myasthenia gravis
Targocid hatóanyag
Teicoplanin
Glicopeptidek
Vancomycin, Teicoplanin
Bactrim hatóanyag
Trimethoprim-Sulfamethoxazole
Zyvox hatóanyag
Linezolid
Cotrim hatóanyag
Trimethoprim-Sulfamethoxazole
Tarivid hatóanyag
Ofloxacin
Fortum hatóanyag
Ceftazidime
Suprax hatóanyag
Cefixime
Sumetrolim hatóanyag
Trimethoprim-Sulfamethoxazole
Ha túl gyorsan adjuk a protamint…
Hypotonia, keringésleállás lehet.
LT felsz? Pulm. vasoconstr? miatt
Silymarin hatóanyag
Máriatövis kivonat
Drugs that may cause reduced transmission at the neuromuscular junction in cases of overdose, or when used in patients who have underlying disease of the neuromuscular junction…
- D-penicillamine
- Aminoglycoside antibiotics (inhibit both pre- and postsynaptic transmission)
- Fluoroquinolone antibiotics
- Phenytoin (both pre- and postsynaptic effects and prevents the depolarization required for neurotransmission) and other anticonvulsants
- Lithium (with chronic use, it may compete with calcium in the presynaptic region and reduce the release of acetylcholine (ACh) from nerve terminals)
- Beta blockers
- Glucocorticoids
- Magnesium sulfate
Bactroban hatóanyag
Mupirocin
Foster hatóanyag
Formoterol + beclomethasone
Rytmonorm hatóanyag
Propafenone
Lisopress hatóanyag
Lisinopril
DTG
Dolutegravir
EFV
Efavirenz
RAL
Raltegravir
EVG
Elvitegravir
Integrase inhibitors
Dolutegravir, raltegravir, elvitegravir
TDF
Tenofovir
FTC
Emtricitabine
RPV
Rilpivirine
ABC
Abacavir
3TC
Lamivudine
COBI
Cobicistat
DRV/r
Ritonavir-boosted darunavir
TDF/FTC/EVG/COBI how many pills
1
Efient hatóanyag
Prasugrel
Lercaton hatóanyag
Lercanidipine
Mycamine hatóanyag
Mycafungin
Prograf hatóanyag
Tacrolimus
Dexdor hatóanyag
Dexmetotimidin
Cymevene hatóanyag
Ganciclovir
Salbutamol side effects
The most common side effects are fine tremor, anxiety, headache, muscle cramps, dry mouth, and palpitation.
- Other symptoms may include tachycardia, arrhythmia, flushing, myocardial ischemia (rare), and disturbances of sleep and behaviour.
- Rarely occurring, but of importance, are allergic reactions of paradoxical bronchospasm, urticaria, angioedema, hypotension, and collapse.
- hypertension, increased QTc
- metab. acidosis (laktát?)
- hyperglycaemia
- High doses may cause hypokalaemia, which is of concern in patients with renal failure and those on certain diuretics and xanthine derivatives.
Salbutamol cautions
CV disease, glaucoma, hypokalemia, hyperthyreoidism, seizures, diabetes?
Salbutamol duration of action
After inhalation, salbutamol reaches the lungs directly and acts within 3-5 minutes with a peak at 15-20 minutes. Overall duration of action of salbutamol is 4-6 hours
Salbutamol metabolism
Hydrolyzed by esterases in tissue and blood to the active compound colterol. The drug is also conjugatively metabolized to salbutamol 4’-O-sulfate (intestinal tract and in the liver?)
Salbutamol excretion
primarily excreted via the urine. Approximately 50% is excreted as metabolites via the urine and about 30% is excreted as unchanged salbutamol. A small fraction is excreted through the faces.
Approximately 72% of the inhaled dose is excreted in the urine within 24 hours, 28% as unchanged drug and 44% as metabolite?
Gordius hatóanyag
Gabapentin
Salbutamol isomers + their effects
The R-isomer, levalbuterol, is responsible for bronchodilation while the S-isomer increases bronchial reactivity. The R-enantiomer is sold in its pure form as Levalbuterol.
Salbutamol mechanism of action
- beta(2)-adrenergic agonist ->relaxation of bronchial smooth muscles.
- It is believed that salbutamol increases cAMP production by activating adenylate cyclase, and the actions of salbutamol are mediated by cAMP. Increased intracellular cyclic AMP increases the activity of cAMP-dependent protein kinase A, which inhibits the phosphorylation of myosin and lowers intracellular calcium concentrations. A lowered intracellular calcium concentration leads to a smooth muscle relaxation and bronchodilation.
- inhibits the release of bronchoconstricting agents from mast cells
- inhibits microvascular leakage
- enhances mucociliary clearance.
Salbutamol contraindication and warnings
CONTRAINDICATIONS
Tachycardia secondary to heart condition
CAUTIONS
Some inhalers use hydrofluoroalkane (HFA) as propellant instead of chlorofluorocarbons (CFCs); otherwise, devices are equivalent
Risk of hypokalemia (usually transient)
Paradoxical bronchospasm may occur
Use with caution in patients with cardiovascular disease, asthma, glaucoma, diabetes, hypokalemia, hyperthyroidism, or seizures
Use face mask in children <4 years
Serious adverse effects occur when administered dose exceeds recommended dose
Ednyt hatóanyag
Enalapril
Mono mack depot hatóanyag
Izoszorbid-5-nitrát
Epivir hatóanyag
Lamivudine
Norvir hatóanyag
Ritonavir
RTV
Ritonavir
Viread hatóanyag
Tenofovir
Isentress hatóanyag
Raltegravir
CBV
Combivir: zidovudine+lamivudine
LPV/r
Lopinavir + Ritonavir
Kaletra hatóanyag
Lopinavir + Ritonavir
Lipanor hatóanyag
Ciprofibrate
Viramune hatóanyag
Nevirapine
NVP
Nevirapine
Kivexa hatóanyag
Abacavir, lamivudine
Theophylline has significant drug interactions with
ciprofloxacin, digoxin, and warfarin (Coumadin). These interactions may decrease the rate of theophylline clearance by interfering with P-450 site metabolism. On the other hand, phenytoin (Dilantin) and cigarette smoking can increase the rate of metabolism of theophylline and, therefore, can decrease the therapeutic level of the drug.
Prezista hatóanyag
Darunavir
Edurant hatóanyag
Rilpivirine
ATV
Atazanavir
Crixivan hatóanyag
Indinavir
To convert a theophylline dose to aminophylline…
the theophylline dose needs to be divided by 0.80.
Atrovent hatóanyag
Ipratropium bromid
Sultanol hatóanyag
Salbutamol
Berodual hatóanyag
Fenoterol + ipratropium bromid
Pulmicort hatóanyag
Budenoside
Euphylong hatóanyag
Theophyllin
Dormicum hatóanyag
Midazolam
Fortecortin hatóanyag
Dexamethason
anti-leukotrien hatású vegyületek
vagy a cysteinyl-leukotrien 1 (CysLT1) receptor antagonistái (montelukast, pranlukast és zafirlukast) vagy az 5-lipoxygenase (5-LO) enzim inhibitorai (zileuton)
Hosszú-hatású inhalált β2-agonisták (LABA-k)
Formoterol, salmeterol
Symbicort hatóanyag
Formoterol + budesonide
LABA-k hatásideje
salmeterol és a formoterol hörgőtágító hatásának időtartama hasonló, legalább 12 óra, de a formoterol hatása a SABA-khoz hasonlóan gyorsan kialakul, ami miatt alkalmas a rohamoldásra és a tünetek prevenciójára is. - de csak akkor, ha a beteg alapól kap fenntartó ICS-t is (The combination ICS/formoterol inhaler may be taken up to a maximum total formoterol dose of 72 mcg in a day (Evidence A).)
Teofillin mellékhatások
A teofillin hatásszélessége, azaz a legkisebb hatékony dózis és a legnagyobb még tűrt adag közötti különbség kicsi, emiatt a teofillin mellékhatások gyakoriak, bizonyos szérumszint (20 mg/L) felett súlyosak.
A teofillin nagy adagjai (10mg/kg/nap vagy ennél nagyobb adagok) mellékhatásokat okozhatnak, amelyek korlátozzák használatát, ezért fenntartó kezeléshez a dózis gondos beállítása szükséges.
A gyulladáscsökkentő hatás <10 mg/L értékeknél már kialakul, ezért kis napi adagú („gyulladáscsökkentő adagú) terápia esetén szérum szint monitorozás nem szükséges, kivéve panasz esetén.
A mellékhatások súlyossága a teofillin vérszint függvényei. 20mg/L plazmakoncentráció felett fejfájás, hányinger, a diuresis fokozódása, nyugtalanság, álmatlanság, tachycardia, súlyosabb esetben arrythmia, hypotonia, generalizált görcsök jelentkeznek.
A gyógyszer metabolizmusát számos körülmény befolyásolja:
Csökken a teofillin clearance májbetegségekben, jobbszívfél elégtelenségben, lázas állapotok kapcsán, enziminhibitor gyógyszerek (cimetidin, erythromycin, ciprofloxacin, ofloxacin, zileuton) hatására, idős korban, nagy szénhidrát tartalmú diéták esetében. Nő a clearance enziminduktorok (rifampicin, fenobarbital) hatására, dohányosokban, gyermekekben, magas fehérje, kis széhidrát tartalmú diéta mellett.
SABA-k
Salbutamol, terbutalin, fenoterol
Ramace hatóanyag
Ramipril
Rawel hatóanyag
Indapamide
Indapamid CI
?(wiki)
- known hypersensitivity to sulfonamides - severe renal failure
- hepatic encephalopathy or severe hepatic failure
- hypokalemia
Xalacom csepp hatóanyag
Latanoprost+timolol
Xalatan csepp hatoanyag
Latanoprost
Lipidil hatóanyag
Fenofibrate
Delipid hatóanyag
Rosuvastatin
Panangin hatóanyag
Mg aspartate/k aspartate
Oftaquix csepp hatóanyag
Levofloxacin
Combigan csepp hatóanyag
Brimonidine, timolol
Lumigan csepp hatóanyag
Bimatoprost
Yellox csepp hatóanyag
Bromfenac
Vigamox csepp hatóanyag
Moxifloxacin
Efflumidex csepp hatóanyag
Fluorometholone
Fotil csepp hatóanyag
Timolol, pilocarpine
Mydrum csepp hatóanyag
Tropicamide
Sandimmun
Ciclosporin
Corinfar
Nifedipin
Kventiax
Quentiapinr
Kerberan hatóanyag
Clopidogrel
Adimet hatoanyag
Metformin
Scippa hatóanyag
Escitalopram
Asentra hatoanyag
Sertralin
Humapent csepp hatóanyag
Cyclopentolate
Imuran hatóanyag
Azathioprine
Asactal
Acetilszalicilsav
Atrombin
Clopidogrel
Tarka
Verapamil, trandolapril
NSAID side effects
- gastric ulceration
- gastrointestinal (GI) bleeding
- hypertension
- nephrotoxicity
- stroke
- myocardial infarction
- hepatoxicity
- The GI side effects may be reduced when selective cyclooxygenase-2 inhibitors are used
Methotrexate hogyan hat
inhibition of folic acid synthesis and blocks a methylation step necessary for the formation of nucleotide bases used in DNA synthesis.
Methotrexate severe side effects + diet
bone marrow suppression, infection, hepatotoxicity, pulmonary fibrosis, and phototoxicity.
To prevent hepatotoxicity during the course of therapy, considerable dietary and lifestyle modifications are recommended, including limiting acetaminophen use, alcohol use, and the consumption of grapefruit due to its inhibition of cytochrome CYP3A liver enzymes.
Limited sun exposure is also recommended to prevent severe dermatologic reactions.
Azathioprine and MMFhogyan hat
purine synthesis inhibitors
Azathioprine and MMF severe side effects
may cause bone marrow suppression and infection; azathioprine may also cause pancreatitis
Delagil hatóanyag
Chloroquine
Kerberan hatóanyag
Clopidogrel