IC16 PK of female endocrine drugs Flashcards
ethinyl estradiol: drug type
synthetic oestrogen
ethinyl estradiol: MOA
- Oestrogen receptor agonist
- Blocks FSH release from pituitary → suppresses development of ovarian follicle
Endometrium unstable for implantation of ovum
ethinyl estradiol: indications
Menopausal symptoms
Gynaecological disorders
(some) Hormone-sensitive cancers
Birth control pill; oral contraceptive
ethinyl estradiol: PK
absorption
route of administration, onset, F
Well absorbed orally; taken OD
Onset: 30-60 mins
F ~0.45
Other Administration methods: parenteral, transdermal, topical
ethinyl estradiol: PK
distribution
protein bidning & Vd
Very highly plasma protein bound (~98% by albumin) ⇒ small Vd
ethinyl estradiol: PK
metabolism
location & phases, t1/2
By liver
Phase I: EE undergoes hydroxylation by CYP3A4
Phase II: conjugation with glucuronide & sulfation into hormonally inert ethinylestradiol glucuronide & ethinylestradiol sulphate
* Formation of EE sulphate → enterohepatic recirculation involved
t1/2 ~13-27 hours
ethinyl estradiol: excretion
Metabolites excreted in faeces & urine
ethinyl estradiol: Adverse effects
Breast tenderness, headache, nausea, fluid retention, dizziness, weight gain
Serious: venous thromboembolism (VTE), MI/ stroke, liver damage
ethinyl estradiol: c/i
- Patients with known hx/ susceptibility to arterial/ venous thrombosis
- Advanced diabetes with vascular disease
- Hypertension >160/100 mmHg
- Avoid in breastfeeding (<21 days postpartum) & breast cancer women
Norethindrone: drug type
synthetic progesterone
Norethindrone: MOA
- Progesterone receptor agonist
- Blocks release of LH → prevents ovulation
Endometrium unstable for implantation of ovum
Norethindrone: Indication
Endometriosis
Abnormal periods/ bleeding → bring on normal menstrual cycle
Birth control pill; oral contraceptive
Norethindrone: PK
absorption
route of administration, F
Well absorbed orally; taken OD
F ~0.64
Norethindrone: PK
distribution
plasma protein binding, Vd
Highly plasma protein bound (ie albumin) ⇒ small Vd
Norethindrone: PK
metabolism
phases, t1/2, EE
- By liver: phase I (reduction) & phase II (glucuronidation & sulfation)
- t1/2 ~8 hours
- Some % may be metabolised in liver to EE
Take note of potential CVS complications (ie VTE) → may have similar SE