Pharmacology Flashcards
How do the following antibiotics work:
Macrolides
Penicillin
Metronidazole
Cephalosporins
Quinolones
Tetracyclines
Nitrofurantoin
Trimethoprim
Macrolides - peptidyltransferase inhibitor, to dow ith protein synthesis
Penicillin - betalactamase inhibitor which disrupts cell wall
Metronidazole - inhibits nucleic acid synthesis by generating radicals
Cephalosporins - betalactamase inhibitor which disrupts cell wall
Quinolones - DNA gyrase inhibitor
Tetracyclines - binds to the 30S subunit of ribosomes which prevents stuff attaching
Nitrofurantoin - damages DNA by generating reactive intermediaries
Trimethoprim - dihydrofolate reductase inhibitor
What type of antibiotic is erythromycin
Macrolide
What type of drug is ciprofloxacin
Quinolone
What type of drug is doxycycline
tetracycline
What are the features of fetal warfarin syndrome?
What are people treated with during pregnancy?
V-PLANTS
Ventriculomegaly
Pectus carinatum
Laryngomalacia
Agenesis of corpus callosum
Nasal bridge hypoplasia
Telybrachydactyly
Short stature
Causess FWS in 5% of fetuses exposed during week 6-12 pregnancy.
Converted to LMWH during pregnancy - an exception can be mechanical heart valve
What is the teratogenic effect of metronidazole
lactose intolerance
What is the teratogenic effect of ACE-i/ARBs
KIDNEY STUFF (and lung)
Renal dysgenesis
Oligohydramnios (not producing any wee)
Renal failure
IUGR
Pulmonary atresia
What is the teratogenic effect of tetracyclines
MOUTH
Yellow teeth
Cleft palate
What is the teratogenic effect of Carbimazole
GUT AND SKIN
Omphalocele
Choanal altresia
Aplasia cutis - no skin
What is the teratogenic effect of sodium valproate AND lithium
cardiac effects
What is the teratogenic effect of gentamicin
ototoxicity
What are the doses for prophylactic for LMWH: enoxaparin, dalteparin
Enoxaparin
50-90 40mg
90-130 mg 60mg
130-170mg 80mg
170mg 0.6mg/kg
Dalteparin
50-90 5000IU
90-130 mg 7500IU
130-170mg 10,000IU
170mg 75 u/kg
Which morphine receptors do the following act on:
Strong opioids
Co-codamol
THEY ARE AGONISTS
Strong ones: morphine/fentanyl/methadone: MU receptors
Mu but also kappa and delta
LIDOCAINE
How does it work?
What is the half life?
What is the maximum dose with and without adrenaline?
It blocks fast voltage gated sodium channels
Half life is 2 hours, metabolised by the liver
Maximum dose without adrenaline is 3mg/kg
Maximum dose with adrenaline is 7mg/kg
How do all the antiemetics work?
They INHIBIT STUFF
REMEMBER H1 and D2
Promethazine and cyclizine - Histamine H1 antagonist
Ondansetron - serotonin antagonist
Prochlorperazine and metoclopramide - Dopamine D2 antagonist