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48 Cards in this Set

  • Front
  • Back
Phenytoin
- For.. and not for?
- MoA
- Side Effects
- Disadv
MoA: Na ch blocker

Good for most seizure except absence seizure

Side Effects
Him RIcbG
-Hirsutism
-impaired muscle co-ord
-Rash
-Impaired cognition & behavior
-Gum Hypertrophy

Disadv:
- non-linear saturation kinetic
- narrow therapeutic range
- difficult to titrate
Carbamazepine
- MoA
- Good for...
- Side Effects
- Disadv
MoA: Na ch blocker

Good for: esp. good for complex partial seizure

Side Effects:
DR NHD
- dizziness
- rash
- nausea
- headache
- double vision

Disadv:
- potent enz inducer
- difficult to titrate
- interact with other common drugs
Drug for rescue tx for hypothyroid coma?
liothyronine (sodium salt of T3)
- acts more quickly than thyroxine
Medication for hyperthyroidism?
Carbimazole (antithyroid)
Main advantage of condom?
the only proven protection against STI
Disadvantage of condom?
• Condoms with spermicide do not protect as effectively against HIV transmission
• Reduces glans sensation
• Occasional leaks/breaks may occur
• Latex allergy (non-latex condoms are available)
How does COC work?
- suppress ovulation
- thickens cervical mucus
- thins endometrium
What is the benefit of COC?
Reduced incidence of:
- menstrual cycle disorder
- endometrial & ovarian cancer
- endometriosis & ovarian cyst
What are the major risk of COC?
- venous thrombosis (PE, DVT)
- thrombotic stroke (CVA)
- MI
- hypertension
- breast, cervical & liver cancer
Low dose Progestogen only pill (POP)
i) give an example
ii) MoA
iii) Risk
iv) Side Effects
i) Noriday

ii)
- thickens cervical mucus
- thins endometrium
- inhibit tubal mobility
- VARIABLE effect on ovulation

iii) ovarian cyst, ?ectopic pregnancy

iv)
Menstrual irregularities
Progestagenic effect
- Amenorrhea (HIGH DOSE)
- Headache
- low Libido
- Acne
- low Mood
- Breast tenderness
High dose POP
i) give an example
ii) MoA
i) cerazette

ii)
- suppress ovulation
- thickens cervical mucus
- thins endometrium
- and inhibit tubal mobility
Depo Provera
i) what is it?
ii) route of admin, duration of efficacy
iii) Safety
iv) Side effects
i) high dose progestogen only contraceptive

ii) IM, 90d intervals

iii)
- long term use: bone density concern
- breast cancer

iv)
progestagenic side-effects
- irreg PV bleeding
HLAMB
- headache
- acne
- low mood
- breast tenderness
Jadelle
i) what is it?
ii) route of admin, duration of efficacy
iii) Risks
iv) Side effects
i) high dose progestogen implant
ii) subdermal 2 rods, effective for 5yrs
iii) insertion risk, ovarian cyst
iv)
irreg PV bleed
amenorrhea
Common progestagenci effects HLAMB:
- headache
- low libido
- acne
- low mood
- breast tenderness
Mirena
i) what is it?
ii) duration of efficacy
iii) Benefits
iv) Risk
v) Side effects
i) IUD with low dose progestogen
*currently unavailable in NZ (2011)
ii) 5yrs
iii) reduce heaviness of menstrual cycle
iv) VIP P
- Vasovagal rxn with insertion
- Infertility
- Perforation uterus
- PID

v)
- irreg spotting initially
- amenorrhea
- progestogenic side effects HLAMB:
headache, low libido, acne, low mood, breast tenderness
Diaphragm
i) Recommended to use in conjunction with?
ii) Contraindication
i) spermicide
ii) vaginal abnormalities, recurrent UTI
IUD Multiload Cu375
i) MoA
ii) Contraindications
iii) Side effect
Available in NZ
i) Cu with foreign body rxn inhibits sperm progression & implantation
ii) MAP UP:
- genital Malignancy
- Active gonorrhea/chlamydia
- PID
- Undiagnosed vaginal bleeding
- Pregnancy

iii) Heavier menstrual period
Characteristics of Patients With Ischemic Stroke Who Could Be Treated With rtPA are:
- Diagnosis of ischemic stroke causing measurable neurological deficit
- The neurological signs should not be clearing spontaneously
- The neurological signs should not be minor and isolated
- Caution should be exercised in treating a patient with major deficits
- The symptoms of stroke should not be suggestive of subarachnoid hemorrhage
- Onset of symptoms 3 hours before beginning treatment
- No head trauma or prior stroke in previous 3 months
- No myocardial infarction in the previous 3 months
- No gastrointestinal or urinary tract hemorrhage in previous 21 days
- No major surgery in the previous 14 days
- No arterial puncture at a noncompressible site in the previous 7 days
- No history of previous intracranial hemorrhage
- Blood pressure not elevated (systolic 185 mm Hg and diastolic 110 mm Hg)
- No evidence of active bleeding or acute trauma (fracture) on examination
- Not taking an oral anticoagulant or if anticoagulant being taken, INR 1.7
- If receiving heparin in previous 48 hours, aPTT must be in normal range
- Platelet count 100 000 mm3
- Blood glucose concentration 50 mg/dL (2.7 mmol/L)
- No seizure with postictal residual neurological impairments
- CT does not show a multilobar infarction (hypodensity 1⁄3 cerebral hemisphere)
- The patient or family understand the potential risks and benefits from treatment
1st line tx for obese T2DM patients
metformin, acarbose or TZD
-latter 2 for metformin-intolerant patients
1st line tx for non-obese T2DM patients
metformin or sulfonylureas
1st line tx: if monotx fails...
metformin, acarbose & TZD recommended
-if target still not achieved, insulin secretagogue may be added
Sulphonylureas (SU)
-e.g.
-MoA
e.g. Gliclazide (2nd gen)
-insulin secretagogue [require pancreatic function]
--inhibits ATP-sensitive K ch on Beta-cell; depol, insulin vesicle release

-ineffective in insulin resistance
-may be ineffective in obesity
Sulphonylureas:
-ADR
-drug-drug interactions
ADR:
-hypoglycemia: esp in elderly
-use other class/adj dose
-use short acting SU
-GI disturbances

Interactions:
-altered metabolism: alcohol, MAOI
-highly prot-bound: altered plasma protein binding -> augment SU's hypoglycemic effect:
-antibacterial (sulfonamide, chloramphenicol)
-NSAIDs
Biguanide
-e.g.
-MoA
e.g. Metformin
-decr hepatic glucose synth, incr insulin-med peripheral glucose uptake (GLUT4)
-MoA unclear

-1st line drug in most cases
-most effective in overwt, obese
-must be taken with food

Benefits:
-doesn't cause hypoglycemia (cf. SU)
-small decr in LDL, cholesterol & TG
-decr macrovasc events (MI)
Metformin ADRs
-GI: diarrhea & abd discomfort
-lactic acidosis:
-contraindicated: impaired renal function, hepatic failure, cardiac failure
alpha-glucosidase inhibitors
-e.g.
-MoA
-ADR
e.g. acarbose
-reduce glucose level by reducing CHO (starch) digestion in SI & reduce CHO absorption

-used to control post-prandial glucose levels not adequately controlled by diet & SU

ADR:
-GI upset & flatulence
Thiazolidinediones
-incr muscle sensitivity to insulin & reduce hepatic glucose synth
Short acting insulin analogues
-e.g.
-features
e.g. Insulin aspart & insulin lispro
Compared to standard insulin:
-less tendency to aggregate
-faster onset & offset of action

-onset ~15min, clearance in 2-5hrs
Describe Insulin aspart
-a.a. substitution (proline to asp) creates charge repulsion & steric hindrance
Long acting insulin analogues
-e.g.
e.g. insulin glargine
-contains 2 extra arginine at end of B-chain
-this alters isoelectric pt, reducing solubility, reducing clearance

Suitable for Once-daily admin:
-insulin lvl rises slowly to a plateau in 6-8hrs and remain unchanged for 24hrs
Describe an Insulin regimen
-basal bolus of glargine (long-acting) in evening

with

-multiple regular doses of aspart (short-acting) before meal times
Insulin injections
-sites of admin
subcut admin: "a tua"
-arms
-thigh
-upper buttocks
-abdomen
NB:
-ROTATE SITE
-absorption rate may be diff
e.g. arm & abdomen faster than thigh & buttock
-SC admin bypasses effect on hepatic metabolic process
-doesn't mimic rapid rise & fall with endogen insulin response to glucose
Insulin ADRs
ADRs mainly related to hypoglycemia due
-insulin OD
-missed meal
-other drug combo affecting caloric intake

Others:
-weight gain
-lipo-atrophy/hypertrophy
-insulin edema (Na retention)
-transient deterioration in retinopathy (VEGF permissive)
-local cutaneous allergy
-IgG-med insulin resistance
Symptoms of hypoglycemia
SHHHITT WAVE

Sweating
Headache
Hunger
HR inc'rd
Irritability
Tiredness
Trembling

Weakness
Anxiety
blurred Vision
ringing in Ears
Frusemide PK
PO: max effect 1-2h, duration 4-6h
-extensively protein bound
*=warfarin, propranolol, nephrotic
-reach glomerular filtrate via organic acid transporter
*=cephalosporins

-high Na load presented to DT also incr loss of H+ & K+
Tx use of Loop diuretics
-Hypertension - in impaired renal function
-Renal failure - acute/chronic
-Nephrotic syndrome - frusemide generally used
-Congestive HF (mod-severe)
-Acute Pulm Edema
-Hyperkalemia
-Hypercalcemia
-Drug OD = incr urine flow
ADR of Loop diuretics
Incr'd Na to DT:
-Metabolic alkalosis (incr'd H+ loss)
-Hypokalemia (incr'd K+ loss)
=>arrythmia & digoxin toxicity

Li retention & toxicity due Na loss

Mg & Ca loss

Prolonged use:
-ototoxicity: loss of endolymph electrolyte = hearing loss
-renal toxicity - cephalosporin antibiotics
-displace plasma prot binding = warfarin, heparin
ADR: mechanism of Ca & Mg loss by Loop diuretic
Normally, apical ROMK and basolat CLC-K2
->lumen-positive transepith potential difference
->drives paraC reabs of cations Ca&Mg

Loop diuretics disrupts this +ve transepith potential
-> Ca&Mg loss
Thiazide
e.g.
-ineffective when...
-2ndary effect...
e.g. bendrofluazide, chlorothiazide
-ineffective when GFR<30-40mL/min
-2ndary effect on PT due inhibiting carbonic anhydrase:
-inhibit NaHCO3 reabs & incr delivery of Na to MD
Thiazide effect on GFR
Thiazide inhibits NaHOC3 reabs at PT, incr Na delivery to MD
->thus acute thiazide tx reduces GFR
= this transient effect can be blocked with ACEI

Chronic use:
-extraC vol decr ->incr Na&water reabs
->decr Na delivery to MD
Resutl: return GFR to baseline
Thiazide PK
-excreted in PT via organic acid transporter = probenicid
-diuresis in 1hr
Tx use of Thiazide
Frontline tx for hypertension along with:
-ACEI & CCB

Acute pulm hypertension

Nephrogenic DI with high urine output:
-low dose thiazide: decr intravasc vol -> decr GFR & conseq modest decr in urine flow & vol

Hypercalciuria = calculus
-promote DT Ca reabs via incr apical Ca ch
Thiazide ADR
Generally due high doses

K loss: digoxin toxicity
H loss: metabolic alkalosis
Na loss: Li toxicity
Hypercalcemia
Uric a retention -> gout

Impaired glucose tolerance:
-exacerbate diabetes via impairing insulin secr or periph insulin sensitivity

QT prolonged - torsade de pointes
Dehydration & postural hypotension
Hyponatremia
Spironolactone ADR
-Hyperkalemia - avoid excessive K+ supplemenation when on this drug
-Androgen-like effects due steroid structure
-gynecomastia
-GI disturbances
Tx use of Spironolocatone
Liver failure
Heart failure
Hyperaldosteronism
Resistant hypertension
Proteinuria
Amiloride
-inhibit eNaC channels under aldosterone influence in CD/late DT
-action complementary with thiazide; augments Na+ loss but limits K+ loss
ACEI ADR
FHK CARD

initial hypotension
hyperKalemia
Fetal anomalies

Cough
Angioedema
Rash
Dysgeusia
ACEI - cautions
Renal impairm: Decr ACEI dose
-enalapril metabolites excreted in urine

Bilat Renal artery stenosis:
-AngII is vital for constr of efferent arteriole to maintain GFR
-inhibiting this can lead to acute renal failure if uncorrected
-in setting of acute renal artery stenosis, there's acute drop in GFR
cf. smaller change in hypertensive setting
ARB ADR
initial hypotension
impaired renal function
fetal morbidity/mortality

low risk of angioedema