adverse drug reactions Flashcards
What ADR does one worry about in a patient with a newly started statin?
Rhabdomyolysis
What factors an increase the liklihood of a rhabdomyolysis when starting a statin?
- genetic predisposition
- female sex
- acute or chronic kidney injury
- concurrent use of a CCB
How does one treat rhabdomyolysis?
- stop the causative drug
- give IV fluids to reduce risk of kidney injury
- consider sodium bicarbonate to alkanilize the urine
- monitor potassium and correct when necessary
What is the definition pf an adverse drug reaction?
- harmful or unpleasant response/relation to a drug
- predicts if happening again if the drug is still used
- that warrants change in dose or withdrawal of treatment
- can be related to overdose, misuse or administration error
Adverse drug event vs reaction. What’s the dif?
- event is something negative that happens to the patient when they are using the drug
- reaction is something negative that happens to the patient and it’s suspected that the drug in question caused it.
what is a Type A ADR?
-A for augmented reaction
-dose related
-predictable & common
-relating the the pharmacology of the drug
-unlikely to be fatal
(constipation with opiods, brusing with warfarin)
What is a Type B ADR?
-B for bizzare reaction
-no dose related
-unpredictable and uncommon
-not related to pharmacology
-often fatal
(hypersensitivity, hepatitis, angioedema)
What are Type C, D, E and F ADR?
C - Chronic - cumulative dose effect - HPA suppression in long term steroid use
D - Delayed - carcinogenesis later down the line
E - End of Treatment - withdrawal Sx on cessation of opioid Tx
F - Failure - no therapeutic action - OCP failure in presence of an enzyme inducer
What’s the DoTS model of ADRs?
- Dose
- Timing
- Susceptibility
What’s the dose breakdown of the DoTS model?
ADR can occur at three levels of dose
- Hypersensitivity reactions - occuring at subtherapeutic levels of dosing
- Collateral reactions - happens when the dose is in therapeutic range
- Toxicity reactions - happens when there is too much circulating drug in the system
What is the Timing breakdown in the DoTS model?
Can be time dependent or independent
Time dependent
-rapid - ‘red man syndrome’ giving Vanc too fast
-early - nitrate induced headache
-first dose - hypotension in ACEi dose
-intermediate - slightly delayed allergic reaction
-late - withdrawal from long term steroids
-delayed - tetragenicity
What needs to be taken into account for ADR susceptibilities?
- Age
- Sex
- ethnicity
- Genetics - specifically increase risk of ADR haemolytic anaemia in G6P deficiency